PMID-sentid Pub_year Sent_text compound_name comp_offset prot_official_name organism prot_offset 3856016-0 1985 Pin-retained reinforced zinc oxide-eugenol temporary restorations. Zinc Oxide 24-34 dynein light chain LC8-type 1 Homo sapiens 0-3 2656788-2 1989 Adding more zinc-oxide reagent and other anti-bacterial materials to the original Walkhoff"s paste (Kri 1), for pulp canal medication and final filling, seems to improve the pharmacological effect of the paste by reducing the resorption rate. Zinc Oxide 12-22 KRI1 homolog Homo sapiens 100-105 6600397-6 1983 Topical zinc oxide was highly effective in preventing induction of ODC by UV-A irradiation at doses up to 40 J/cm2, and was significantly more effective than either PreSun or Uval. Zinc Oxide 8-18 ornithine decarboxylase, structural 1 Mus musculus 67-70 34039969-0 2021 Interplay of spin-orbit coupling and Coulomb interaction in ZnO-based electron system. Zinc Oxide 60-63 spindlin 1 Homo sapiens 13-17 5248192-0 1968 [Zinc-oxide-eugenol paste as an aid in jaw registration]. Zinc Oxide 1-11 activation induced cytidine deaminase Homo sapiens 32-35 33730632-6 2021 In addition, we found that ZnO NPs exposure caused endoplasmic reticulum stress-mediated apoptosis driven mainly by an increase in intracellular calcium (Ca2+) concentrations, rather than by the activation of three membrane protein receptors (ATF6, IRE-1 and PERK). Zinc Oxide 27-30 endoplasmic reticulum to nucleus signaling 1 Homo sapiens 249-254 33730632-6 2021 In addition, we found that ZnO NPs exposure caused endoplasmic reticulum stress-mediated apoptosis driven mainly by an increase in intracellular calcium (Ca2+) concentrations, rather than by the activation of three membrane protein receptors (ATF6, IRE-1 and PERK). Zinc Oxide 27-30 eukaryotic translation initiation factor 2 alpha kinase 3 Homo sapiens 259-263 34058181-5 2021 The fabricated gas sensor based on CdO-ZnO nanorices exhibited a high response (34.5) towards 300 ppm formaldehyde gas at 350 C compared to ZnO nanoflowers (14.5) under the same experimental conditions. Zinc Oxide 39-42 cell adhesion associated, oncogene regulated Homo sapiens 35-38 34047899-5 2021 By heating the ZnCd-LDH material, some demixtion to ZnO and CdO phases occurred, corresponding to a band gap energy value of 2.93 eV for the formed zinc oxide nanoparticles. Zinc Oxide 148-158 cell adhesion associated, oncogene regulated Homo sapiens 60-63 33894970-5 2021 N2 adsorption/desorption measurements and BET analysis were used to revealed the specific surface area and pore size of Tb2O3-modified ZnO. Zinc Oxide 135-138 delta/notch like EGF repeat containing Homo sapiens 42-45 34014644-0 2021 Functionalization of Zinc Oxide Nanoflowers with Palladium Nanoparticles via Microwave Absorption for Room Temperature-Operating Hydrogen Gas Sensors in the ppb Level. Zinc Oxide 21-31 gastrin Homo sapiens 138-141 33999053-3 2021 The oxidation peak currents of 1-NAP and 2-NAP on a ZnO/ZnCo2O4 modified carbon paste electrode (ZnO/ZnCo2O4/CPE) depended linearly on their concentrations in the range of 0.4-50 muM and 0.06-40 muM with detection limits of 0.13 and 0.02 muM, respectively. Zinc Oxide 52-55 carboxypeptidase E Homo sapiens 109-112 33999053-3 2021 The oxidation peak currents of 1-NAP and 2-NAP on a ZnO/ZnCo2O4 modified carbon paste electrode (ZnO/ZnCo2O4/CPE) depended linearly on their concentrations in the range of 0.4-50 muM and 0.06-40 muM with detection limits of 0.13 and 0.02 muM, respectively. Zinc Oxide 97-100 carboxypeptidase E Homo sapiens 109-112 33999053-4 2021 Their electrooxidation at the ZnO/ZnCo2O4/CPE was a one-electron and one-proton process. Zinc Oxide 30-33 carboxypeptidase E Homo sapiens 42-45 34018472-2 2021 ZnO NPs were remedied with polyethyleneimine (PEI) and modified with bovine serum albumin (BSA). Zinc Oxide 0-3 albumin Homo sapiens 76-89 34014644-1 2021 Microwave-assisted functionalization of zinc oxide nanoflowers (ZnO NFs) with palladium nanoparticles (Pd NPs) is demonstrated to realize high-performance chemiresistive-type hydrogen (H2) gas sensors operating at room temperature (RT). Zinc Oxide 40-50 gastrin Homo sapiens 189-192 34052536-5 2021 Then, the hybrid networks were treated by pyrolysis-oxidation-phosphidation and ZnO-removal processes, leading to the hierarchically porous CoP/NCNs. Zinc Oxide 80-83 caspase recruitment domain family member 16 Homo sapiens 140-143 33545705-1 2021 Zinc oxide (ZnO) nanorod thin films were prepared by CBD onto glass and FTO/glass substrates. Zinc Oxide 0-10 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 72-75 33323305-7 2021 JSH-23 and NAC (a precursor of cysteine) inhibited ZnO NP-induced nuclear translocation of p-NFkappaB p65, cysteine deficiency and apoptosis. Zinc Oxide 51-54 synuclein alpha Homo sapiens 11-14 33323305-8 2021 Additionally, ZnO NPs decreased CD98 level in main pathway and failed to activate transsulfuration pathway in cysteine biosynthesis. Zinc Oxide 14-17 solute carrier family 3 member 2 Homo sapiens 32-36 33545705-1 2021 Zinc oxide (ZnO) nanorod thin films were prepared by CBD onto glass and FTO/glass substrates. Zinc Oxide 12-15 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 72-75 33871882-8 2021 Also nano-ZnO group recorded higher expression levels of genes encoding for metallothionein I and metallothionein II, interleukin-2 and interferon-gamma in the liver of rabbits. Zinc Oxide 10-13 interleukin-2 Oryctolagus cuniculus 118-131 33229261-3 2021 Our results from energy-dispersive spectroscopy, X-ray diffraction and density functional theoretical simulations show that a small amount of ZnO enter C3S and C2S by replacing Ca ions while most incorporate into C4AF by substituting Fe atoms, resulting in a decrease of C3A in OPC as dosage increases. Zinc Oxide 142-145 complement C3 Homo sapiens 271-274 33576698-7 2021 ZnO NPs delivered at 1.0 microg/cm2 in the NACIVT system, mimicking occupational exposure, induced significant increases in metabolic activity and release of the cytokines IL-8 and MCP-1, but no differences were observed using traditional exposures. Zinc Oxide 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 33576698-7 2021 ZnO NPs delivered at 1.0 microg/cm2 in the NACIVT system, mimicking occupational exposure, induced significant increases in metabolic activity and release of the cytokines IL-8 and MCP-1, but no differences were observed using traditional exposures. Zinc Oxide 0-3 C-C motif chemokine ligand 2 Homo sapiens 181-186 33931824-8 2022 The results indicated that inclusion of Nano-ZnO at 60 mg kg-1 was the recommended source to enhance growth, feed utilization, amylase and lipase enzymes activity, intestinal morphology, hemato-biochemical, and oxidative response biomarkers of Nile tilapia compared with Bulk-ZnO in commercial tilapia feeds. Zinc Oxide 45-48 pancreatic alpha-amylase Oreochromis niloticus 127-134 33433689-8 2021 Co-administration of ZnO NPs to CP-treated rats restored the suppressive effects of CP on activities of antioxidant enzymes (SOD, GPX, CAT) and the transcription of the STAR gene. Zinc Oxide 21-24 catalase Rattus norvegicus 135-138 33433689-8 2021 Co-administration of ZnO NPs to CP-treated rats restored the suppressive effects of CP on activities of antioxidant enzymes (SOD, GPX, CAT) and the transcription of the STAR gene. Zinc Oxide 21-24 steroidogenic acute regulatory protein Rattus norvegicus 169-173 33314238-7 2021 Not surprisingly, only ZnO NPs significantly induced the expression of caspase 3. Zinc Oxide 23-26 caspase 3 Homo sapiens 71-80 33934207-12 2021 In silico molecular docking studies of Mg-doped ZnO NRs against DHFR (binding score: - 7.518 kcal/mol), DHPS (binding score: - 6.973 kcal/mol) and FabH (- 6.548 kcal/mol) of E. coli predicted inhibition of given enzymes as possible mechanism behind their bactericidal activity. Zinc Oxide 48-51 dihydrofolate reductase Escherichia coli 64-68 33934207-12 2021 In silico molecular docking studies of Mg-doped ZnO NRs against DHFR (binding score: - 7.518 kcal/mol), DHPS (binding score: - 6.973 kcal/mol) and FabH (- 6.548 kcal/mol) of E. coli predicted inhibition of given enzymes as possible mechanism behind their bactericidal activity. Zinc Oxide 48-51 dihydropteroate synthetase Escherichia coli 104-108 33975099-4 2021 High-dose of ZnO or ZIF-8 NPs co-exposure with Cd2+ would reduce the cell viability while low-dose of ZnO or ZIF-8 NPs co-exposure with Cd2+showed antagonism and the particle size has no remarkable effect on the combined toxicity. Zinc Oxide 13-16 CD2 molecule Homo sapiens 47-50 33975099-4 2021 High-dose of ZnO or ZIF-8 NPs co-exposure with Cd2+ would reduce the cell viability while low-dose of ZnO or ZIF-8 NPs co-exposure with Cd2+showed antagonism and the particle size has no remarkable effect on the combined toxicity. Zinc Oxide 13-16 CD2 molecule Homo sapiens 136-139 33975099-4 2021 High-dose of ZnO or ZIF-8 NPs co-exposure with Cd2+ would reduce the cell viability while low-dose of ZnO or ZIF-8 NPs co-exposure with Cd2+showed antagonism and the particle size has no remarkable effect on the combined toxicity. Zinc Oxide 102-105 CD2 molecule Homo sapiens 136-139 33871882-8 2021 Also nano-ZnO group recorded higher expression levels of genes encoding for metallothionein I and metallothionein II, interleukin-2 and interferon-gamma in the liver of rabbits. Zinc Oxide 10-13 interferon gamma Oryctolagus cuniculus 136-152 33412350-4 2021 Through CdS and CdSe co-sensitization, a layer of CdS/CdSe nanofilm is conformally deposited on ZnO nanorod arrays (NRAs) observed by transmission electron microscopy (TEM). Zinc Oxide 96-99 CDP-diacylglycerol synthase 1 Homo sapiens 8-11 33412350-4 2021 Through CdS and CdSe co-sensitization, a layer of CdS/CdSe nanofilm is conformally deposited on ZnO nanorod arrays (NRAs) observed by transmission electron microscopy (TEM). Zinc Oxide 96-99 CDP-diacylglycerol synthase 1 Homo sapiens 16-19 33412350-0 2021 Fabrication, characterization and photoelectrochemical properties of CdS/CdSe nanofilm co-sensitized ZnO nanorod arrays on Zn foil substrate. Zinc Oxide 101-104 CDP-diacylglycerol synthase 1 Homo sapiens 69-72 33359837-2 2021 Herein, the catalyst dosage was decreased, and the results showed that a dosage of 0.5 g L-1 Ag/ZnO and 4 mM PMS almost completely degraded 30 mg L-1 p-NP after 90 min of irradiation. Zinc Oxide 96-99 S100 calcium binding protein A8 Homo sapiens 89-95 33920931-0 2021 ALD Deposited ZnO:Al Films on Mica for Flexible PDLC Devices. Zinc Oxide 14-17 MHC class I polypeptide-related sequence A Homo sapiens 30-34 33920931-1 2021 In this work, highly conductive Al-doped ZnO (AZO) films are deposited on transparent and flexible muscovite mica substrates by using the atomic layer deposition (ALD) technique. Zinc Oxide 41-44 MHC class I polypeptide-related sequence A Homo sapiens 109-113 33710867-1 2021 Defect influences on the photoactivity of ZnO nanoparticles prepared by a powdered coconut water (ACP) assisted synthesis have been studied. Zinc Oxide 42-45 CPAT1 Homo sapiens 98-101 33291085-1 2021 In this paper, two novel nanostructures with ZnO nanowire and nanosheet arrays vertically growing on the FTO and Al foil has been synthesized by hydrothermal method, which exhibits both the piezoelectric and photocatalytic properties. Zinc Oxide 45-48 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 105-108 33247493-0 2021 Biofabricated zinc oxide nanoparticles impair cognitive function via modulating oxidative stress and acetylcholinesterase level in mice. Zinc Oxide 14-24 acetylcholinesterase Mus musculus 101-121 33500067-0 2021 Using Palladium Nanocubes on ZnO Nanostructures in Hydrogen Gas Sensor for Fast Response and Recovery Time. Zinc Oxide 29-32 Fas activated serine/threonine kinase Homo sapiens 75-79 33624651-0 2021 The suppression of spin-orbit coupling effect by the ZnO layer of La0.7Sr0.3MnO3/ZnO heterostructures grown on (001) oriented Si restores the negative magnetoresistance. Zinc Oxide 53-56 spindlin 1 Homo sapiens 19-23 33683276-0 2021 VPS34 regulates dynamin to determine the endocytosis of mitochondria-targeted zinc oxide nanoparticles in human osteosarcoma cells. Zinc Oxide 78-88 phosphatidylinositol 3-kinase catalytic subunit type 3 Homo sapiens 0-5 33683276-6 2021 Third, we confirmed the key role of dynamin 2 in ZnO NP endocytosis and subsequent autophagic cell death in vitro and in vivo. Zinc Oxide 49-52 dynamin 2 Homo sapiens 36-45 33624651-0 2021 The suppression of spin-orbit coupling effect by the ZnO layer of La0.7Sr0.3MnO3/ZnO heterostructures grown on (001) oriented Si restores the negative magnetoresistance. Zinc Oxide 81-84 spindlin 1 Homo sapiens 19-23 33404429-7 2021 The addition of scavengers to the US/ZnO/peroxodisulfate system through the NF and OTC results in the largest effect of holes. Zinc Oxide 37-40 neurofascin Homo sapiens 76-78 33083954-12 2021 With ZnO NPs (80 mug/mL), with the annexin V/propidium iodide (PI) assay, few apoptotic cells (annexin V+/PI- cells) were detected whereas (annexin V+/PI+ cells) evocating necrotic cells were mainly identified. Zinc Oxide 5-8 annexin A5 Mus musculus 35-44 33404429-0 2021 Aqueous Oxytetracycline and Norfloxacin Sonocatalytic Degradation in the Presence of Peroxydisulfate with Multilayer Sheet-Like Zinc Oxide. Zinc Oxide 128-138 neurofascin Homo sapiens 28-39 33404429-9 2021 In this system, the Na2S2O8 can have two roles to increase the rate of degradation: (1) The SO4- formed by Na2S2O8 under ultrasonic irradiation directly degraded to norfloxacin on ZnO surface; and (2) S2O82- behaved as an electron acceptor, inhibiting recombination of electron hole pairs, enabling the development of more OH. Zinc Oxide 180-183 neurofascin Homo sapiens 165-176 33404429-11 2021 Aqueous norfloxacin sonocatalytic degradation with multilayer flower-like ZnO in the presence of peroxydisulfate. Zinc Oxide 74-77 neurofascin Homo sapiens 8-19 33321673-9 2021 ZnO particles activated ATM, ATR, Chk1, Chk2, gamma-H2AX, ERK and p38 phosphorylation as detected by immunofluorescent staining and western blotting. Zinc Oxide 0-3 ATM serine/threonine kinase Homo sapiens 24-27 33418041-0 2021 Distinguishing normal and aggregated alpha-synuclein interaction on gold nanorod incorporated zinc oxide nanocomposite by electrochemical technique. Zinc Oxide 94-104 synuclein alpha Homo sapiens 37-52 33295340-0 2021 Photoelectrochemical thrombin biosensor based on perylene-3,4,9,10-tetracarboxylic acid and Au co-functionalized ZnO nanorods with signal-off quenching effect of Ag@Ag2S. Zinc Oxide 113-116 coagulation factor II, thrombin Homo sapiens 21-29 33295340-0 2021 Photoelectrochemical thrombin biosensor based on perylene-3,4,9,10-tetracarboxylic acid and Au co-functionalized ZnO nanorods with signal-off quenching effect of Ag@Ag2S. Zinc Oxide 113-116 angiotensin II receptor type 1 Homo sapiens 165-169 33295340-1 2021 In this work, a thrombin photoelectrochemical aptasensor was reported based on a photoanode of perylene-3,4,9,10-tetracarboxylic acid (PTCA), Au nanoparticle co-functionalized ZnO nanorods (ZnO NRs) and the "signal-off" amplification effect of Ag@Ag2S. Zinc Oxide 176-179 coagulation factor II, thrombin Homo sapiens 16-24 33295340-1 2021 In this work, a thrombin photoelectrochemical aptasensor was reported based on a photoanode of perylene-3,4,9,10-tetracarboxylic acid (PTCA), Au nanoparticle co-functionalized ZnO nanorods (ZnO NRs) and the "signal-off" amplification effect of Ag@Ag2S. Zinc Oxide 176-179 angiotensin II receptor type 1 Homo sapiens 247-251 33295340-1 2021 In this work, a thrombin photoelectrochemical aptasensor was reported based on a photoanode of perylene-3,4,9,10-tetracarboxylic acid (PTCA), Au nanoparticle co-functionalized ZnO nanorods (ZnO NRs) and the "signal-off" amplification effect of Ag@Ag2S. Zinc Oxide 190-193 coagulation factor II, thrombin Homo sapiens 16-24 33629325-0 2021 Zinc oxide nanoparticles promotes liver cancer cell apoptosis through inducing autophagy and promoting p53. Zinc Oxide 0-10 tumor protein p53 Homo sapiens 103-106 33533767-0 2021 An enzyme-free electrochemiluminescence insulin probe based on the regular attachment of ZnO nanoparticles on a 3-D nickel foam and H2O2 as an efficient co-reactant. Zinc Oxide 89-92 insulin Homo sapiens 40-47 33533767-1 2021 In this study, a highly sensitive, fast, and enzyme-free electrochemiluminescence (ECL) probe based on the decoration of zinc oxide nanoparticles on nickel foam is proposed for insulin determination. Zinc Oxide 121-131 insulin Homo sapiens 177-184 33718734-4 2021 The photocatalytic performance of the 0.6% PtO-ZnO nanocomposite is 20 and 10 times higher than that of pristine ZnO and commercial P-25, respectively. Zinc Oxide 47-50 tubulin polymerization promoting protein Homo sapiens 132-136 33718734-5 2021 The photodegradation rate of TC over the 0.6% PtO-ZnO nanocomposite is 34 and 12.5 times greater than that of pristine ZnO and commercial P-25, respectively. Zinc Oxide 50-53 tubulin polymerization promoting protein Homo sapiens 138-142 33580353-4 2022 The results revealed that supplementation of nano ZnO at 2.5 ppm recorded significantly (P < 0.05) higher body weight gain, feed intake, and better feed conversion ratio (FCR) compared to control and other treatment groups at 42 days of age. Zinc Oxide 50-53 FCR Gallus gallus 171-174 33670212-0 2021 Enhanced UV Photoresponsivity of ZnO Nanorods Decorated with Ag2S/ZnS Nanoparticles by Successive Ionic Layer Adsorption and Reaction Method. Zinc Oxide 33-36 angiotensin II receptor type 1 Homo sapiens 61-65 33670212-2 2021 In this work, ZnO nanorods were prepared by the hydrothermal method and then decorated with silver sulfide (Ag2S)/zinc sulfide (ZnS) via two-step successive ionic layer adsorption and reaction method. Zinc Oxide 14-17 angiotensin II receptor type 1 Homo sapiens 108-112 33321673-9 2021 ZnO particles activated ATM, ATR, Chk1, Chk2, gamma-H2AX, ERK and p38 phosphorylation as detected by immunofluorescent staining and western blotting. Zinc Oxide 0-3 ATR serine/threonine kinase Homo sapiens 29-32 33321673-9 2021 ZnO particles activated ATM, ATR, Chk1, Chk2, gamma-H2AX, ERK and p38 phosphorylation as detected by immunofluorescent staining and western blotting. Zinc Oxide 0-3 checkpoint kinase 1 Homo sapiens 34-38 33321673-9 2021 ZnO particles activated ATM, ATR, Chk1, Chk2, gamma-H2AX, ERK and p38 phosphorylation as detected by immunofluorescent staining and western blotting. Zinc Oxide 0-3 checkpoint kinase 2 Homo sapiens 40-44 33321673-9 2021 ZnO particles activated ATM, ATR, Chk1, Chk2, gamma-H2AX, ERK and p38 phosphorylation as detected by immunofluorescent staining and western blotting. Zinc Oxide 0-3 mitogen-activated protein kinase 1 Homo sapiens 58-61 33321673-9 2021 ZnO particles activated ATM, ATR, Chk1, Chk2, gamma-H2AX, ERK and p38 phosphorylation as detected by immunofluorescent staining and western blotting. Zinc Oxide 0-3 mitogen-activated protein kinase 14 Homo sapiens 66-69 33321673-14 2021 ZnO particles" toxicity were related to ROS, and DNA damage responses, checkpoint kinases, cell cycle arrest, ERK and p38 signaling, but not IL-8 and ICAM-1. Zinc Oxide 0-3 mitogen-activated protein kinase 1 Homo sapiens 110-113 33321673-14 2021 ZnO particles" toxicity were related to ROS, and DNA damage responses, checkpoint kinases, cell cycle arrest, ERK and p38 signaling, but not IL-8 and ICAM-1. Zinc Oxide 0-3 mitogen-activated protein kinase 14 Homo sapiens 118-121 33502585-1 2021 A sensitive and rapid colorimetric biosensor has been developed for determination of amyloid-beta peptide (Abeta) and study of amyloidogenesis based on the high peroxidase-like activity of porous bimetallic ZnO-Co3O4 nanocages (NCs). Zinc Oxide 207-210 amyloid beta precursor protein Rattus norvegicus 107-112 33502585-2 2021 Due to the high binding ability of Abeta monomer to ZnO-Co3O4 NCs, the catalytic activity of ZnO-Co3O4 NCs can be significantly suppressed by Abeta monomer. Zinc Oxide 52-55 amyloid beta precursor protein Rattus norvegicus 35-40 33502585-2 2021 Due to the high binding ability of Abeta monomer to ZnO-Co3O4 NCs, the catalytic activity of ZnO-Co3O4 NCs can be significantly suppressed by Abeta monomer. Zinc Oxide 52-55 amyloid beta precursor protein Rattus norvegicus 142-147 33502585-2 2021 Due to the high binding ability of Abeta monomer to ZnO-Co3O4 NCs, the catalytic activity of ZnO-Co3O4 NCs can be significantly suppressed by Abeta monomer. Zinc Oxide 93-96 amyloid beta precursor protein Rattus norvegicus 35-40 33502585-2 2021 Due to the high binding ability of Abeta monomer to ZnO-Co3O4 NCs, the catalytic activity of ZnO-Co3O4 NCs can be significantly suppressed by Abeta monomer. Zinc Oxide 93-96 amyloid beta precursor protein Rattus norvegicus 142-147 33502585-6 2021 Critically, the different inhibition effects of monomeric and aggregated Abeta species on the catalytic activity of ZnO-Co3O4 NCs enabled the sensor to be used for tracking the dynamic progress of Abeta aggregation and screening Abeta inhibitors. Zinc Oxide 116-119 amyloid beta precursor protein Rattus norvegicus 73-78 33502585-6 2021 Critically, the different inhibition effects of monomeric and aggregated Abeta species on the catalytic activity of ZnO-Co3O4 NCs enabled the sensor to be used for tracking the dynamic progress of Abeta aggregation and screening Abeta inhibitors. Zinc Oxide 116-119 amyloid beta precursor protein Rattus norvegicus 197-202 33403289-4 2020 Mesoporous 1.5% Ag2O-ZnO nanocomposites indicated the highest degradation efficiency of 100% of TC during 120 min of the visible light exposure compared with 5% and 10% for pristine ZnO NPs and commercial P-25, respectively. Zinc Oxide 21-24 tubulin polymerization promoting protein Homo sapiens 205-209 33403575-6 2021 ZnO-, CuO-, and ZnO+CuO-NPs especially higher doses (5 and 25 mg/kg/day) decreased all serum metabolite (except blood urea nitrogen), ions, and ALP while these nanoparticles increased ALT, AST, LDH, and blood urea nitrogen. Zinc Oxide 0-3 alopecia, recessive Mus musculus 144-147 33403575-6 2021 ZnO-, CuO-, and ZnO+CuO-NPs especially higher doses (5 and 25 mg/kg/day) decreased all serum metabolite (except blood urea nitrogen), ions, and ALP while these nanoparticles increased ALT, AST, LDH, and blood urea nitrogen. Zinc Oxide 0-3 glutamic pyruvic transaminase, soluble Mus musculus 184-187 33403575-6 2021 ZnO-, CuO-, and ZnO+CuO-NPs especially higher doses (5 and 25 mg/kg/day) decreased all serum metabolite (except blood urea nitrogen), ions, and ALP while these nanoparticles increased ALT, AST, LDH, and blood urea nitrogen. Zinc Oxide 0-3 solute carrier family 17 (anion/sugar transporter), member 5 Mus musculus 189-192 33403575-6 2021 ZnO-, CuO-, and ZnO+CuO-NPs especially higher doses (5 and 25 mg/kg/day) decreased all serum metabolite (except blood urea nitrogen), ions, and ALP while these nanoparticles increased ALT, AST, LDH, and blood urea nitrogen. Zinc Oxide 16-19 alopecia, recessive Mus musculus 144-147 33403575-6 2021 ZnO-, CuO-, and ZnO+CuO-NPs especially higher doses (5 and 25 mg/kg/day) decreased all serum metabolite (except blood urea nitrogen), ions, and ALP while these nanoparticles increased ALT, AST, LDH, and blood urea nitrogen. Zinc Oxide 16-19 glutamic pyruvic transaminase, soluble Mus musculus 184-187 33403575-6 2021 ZnO-, CuO-, and ZnO+CuO-NPs especially higher doses (5 and 25 mg/kg/day) decreased all serum metabolite (except blood urea nitrogen), ions, and ALP while these nanoparticles increased ALT, AST, LDH, and blood urea nitrogen. Zinc Oxide 16-19 solute carrier family 17 (anion/sugar transporter), member 5 Mus musculus 189-192 33374659-3 2020 In this work, zinc oxide and carbon co-modified LiFePO4 nanomaterials (LFP/C-ZnO) were prepared by an inorganic-based hydrothermal route, which vastly boosts its performance. Zinc Oxide 14-24 lamin A/C Homo sapiens 71-74 33241835-2 2020 Here, we describe the establishment of a biodegradable ZnO nanoparticle (NP)-assisted asymmetric amplification approach for the simultaneous imaging of microRNA-21 (miRNA-21) and programmed cell death 4 (PDCD4) mRNA at distinct expression levels in live cells. Zinc Oxide 55-58 microRNA 21 Homo sapiens 152-163 33241835-2 2020 Here, we describe the establishment of a biodegradable ZnO nanoparticle (NP)-assisted asymmetric amplification approach for the simultaneous imaging of microRNA-21 (miRNA-21) and programmed cell death 4 (PDCD4) mRNA at distinct expression levels in live cells. Zinc Oxide 55-58 microRNA 21 Homo sapiens 165-173 33241835-2 2020 Here, we describe the establishment of a biodegradable ZnO nanoparticle (NP)-assisted asymmetric amplification approach for the simultaneous imaging of microRNA-21 (miRNA-21) and programmed cell death 4 (PDCD4) mRNA at distinct expression levels in live cells. Zinc Oxide 55-58 programmed cell death 4 Homo sapiens 179-202 33241835-2 2020 Here, we describe the establishment of a biodegradable ZnO nanoparticle (NP)-assisted asymmetric amplification approach for the simultaneous imaging of microRNA-21 (miRNA-21) and programmed cell death 4 (PDCD4) mRNA at distinct expression levels in live cells. Zinc Oxide 55-58 programmed cell death 4 Homo sapiens 204-209 33167227-2 2021 Concretely, CdSe quantum dots (QDs) decorated ZnO networks assembled sensing surface provided outstanding photoelectric properties, on which glucose oxidase (GOx) labeled aptamer was subsequently immobilized via the hybridization chain reaction. Zinc Oxide 46-49 hydroxyacid oxidase 1 Homo sapiens 141-156 33167227-2 2021 Concretely, CdSe quantum dots (QDs) decorated ZnO networks assembled sensing surface provided outstanding photoelectric properties, on which glucose oxidase (GOx) labeled aptamer was subsequently immobilized via the hybridization chain reaction. Zinc Oxide 46-49 hydroxyacid oxidase 1 Homo sapiens 158-161 31994452-3 2021 Therefore, this work was done to evaluate toxicity of Zinc oxide nanoparticles (ZnO NPs) on the structure of human serum albumin (HSA) through in vitro and in silico studies. Zinc Oxide 54-64 albumin Homo sapiens 115-128 32406561-3 2021 A total (100%) RhB removal and COD abatement rates were reached in optimal conditions of treatment time, ZnO dose, and Stirring speed at different concentration of dye. Zinc Oxide 105-108 small nuclear ribonucleoprotein polypeptides B and B1 Homo sapiens 31-34 33403289-6 2020 The mesoporous 1.5% Ag2O-ZnO nanocomposite revealed the highest degradation rate among all synthesized samples, and it was 23 and 8 orders of magnitudes greater than those of pristine ZnO NPs and P-25, respectively. Zinc Oxide 25-28 tubulin polymerization promoting protein Homo sapiens 196-200 32949962-2 2020 Thus, the current study has been designed to analyze the effect of ZnO NPs on the hepatic histopathological and immunohistochemical changes, along with the modulation of the oxidative-stress induced JNK/p38MAPK and the STAT-3 signalling. Zinc Oxide 67-70 signal transducer and activator of transcription 3 Rattus norvegicus 219-225 33299310-0 2020 Oral Exposure to ZnO Nanoparticles Disrupt the Structure of Bone in Young Rats via the OPG/RANK/RANKL/IGF-1 Pathway. Zinc Oxide 17-20 TNF receptor superfamily member 11B Rattus norvegicus 87-90 33299310-0 2020 Oral Exposure to ZnO Nanoparticles Disrupt the Structure of Bone in Young Rats via the OPG/RANK/RANKL/IGF-1 Pathway. Zinc Oxide 17-20 TNF superfamily member 11 Rattus norvegicus 96-101 33299310-0 2020 Oral Exposure to ZnO Nanoparticles Disrupt the Structure of Bone in Young Rats via the OPG/RANK/RANKL/IGF-1 Pathway. Zinc Oxide 17-20 insulin-like growth factor 1 Rattus norvegicus 102-107 33299310-12 2020 Conclusion: We infer that ZnO NPs affect bone growth in young rats directly or indirectly by altering IGF-1 levels. Zinc Oxide 26-29 insulin-like growth factor 1 Rattus norvegicus 102-107 32272856-5 2020 Our results outlined that ZnO/CNT@Fe3O4 decreased the proliferative capacity of K562 cells through induction of G1 arrest and induced apoptosis probably via ROS-dependent upregulation of FOXO3a and SIRT1. Zinc Oxide 26-29 forkhead box O3 Homo sapiens 187-193 32272856-5 2020 Our results outlined that ZnO/CNT@Fe3O4 decreased the proliferative capacity of K562 cells through induction of G1 arrest and induced apoptosis probably via ROS-dependent upregulation of FOXO3a and SIRT1. Zinc Oxide 26-29 sirtuin 1 Homo sapiens 198-203 32272856-6 2020 The results of qRT-PCR analysis also demonstrated that while ZnO/CNT@Fe3O4 significantly increased the expression of pro-apoptotic genes in K562 cells, it had no significant inhibitory effect on the expression levels of anti-apoptotic target genes of NF-kappaB; proposing an attenuating role of NF-kappaB signalling pathway in K562 cell response to ZnO/CNT@Fe3O4. Zinc Oxide 61-64 nuclear factor kappa B subunit 1 Homo sapiens 251-260 32272856-6 2020 The results of qRT-PCR analysis also demonstrated that while ZnO/CNT@Fe3O4 significantly increased the expression of pro-apoptotic genes in K562 cells, it had no significant inhibitory effect on the expression levels of anti-apoptotic target genes of NF-kappaB; proposing an attenuating role of NF-kappaB signalling pathway in K562 cell response to ZnO/CNT@Fe3O4. Zinc Oxide 61-64 nuclear factor kappa B subunit 1 Homo sapiens 295-304 32950875-1 2020 This article aims to explore interaction of nanoparticles ZnO, TiO2 and CeO2 with bovine serum albumin (BSA). Zinc Oxide 58-61 albumin Homo sapiens 89-102 32734545-3 2020 The BET surface area of CeVO4/ZnO is 10.50 m2/g. Zinc Oxide 30-33 delta/notch like EGF repeat containing Homo sapiens 4-7 32842903-5 2020 By virtue of ZnO, the composite scaffolds showed a strong anti-inflammatory response in A549 cells, as demonstrated by a significant decrease of interleukin (IL) IL-1alpha, IL-6 and IL-8 expression in 6 h. In all the scaffold types, but remarkedly in the aligned composite ones, transforming growth factor beta (TGF-beta) and the antimicrobial peptide human beta defensin 2 (HBD-2) were significantly increased. Zinc Oxide 13-16 tumor necrosis factor Homo sapiens 279-310 32842903-5 2020 By virtue of ZnO, the composite scaffolds showed a strong anti-inflammatory response in A549 cells, as demonstrated by a significant decrease of interleukin (IL) IL-1alpha, IL-6 and IL-8 expression in 6 h. In all the scaffold types, but remarkedly in the aligned composite ones, transforming growth factor beta (TGF-beta) and the antimicrobial peptide human beta defensin 2 (HBD-2) were significantly increased. Zinc Oxide 13-16 transforming growth factor alpha Homo sapiens 312-320 32842903-5 2020 By virtue of ZnO, the composite scaffolds showed a strong anti-inflammatory response in A549 cells, as demonstrated by a significant decrease of interleukin (IL) IL-1alpha, IL-6 and IL-8 expression in 6 h. In all the scaffold types, but remarkedly in the aligned composite ones, transforming growth factor beta (TGF-beta) and the antimicrobial peptide human beta defensin 2 (HBD-2) were significantly increased. Zinc Oxide 13-16 defensin beta 4A Homo sapiens 358-373 32842903-5 2020 By virtue of ZnO, the composite scaffolds showed a strong anti-inflammatory response in A549 cells, as demonstrated by a significant decrease of interleukin (IL) IL-1alpha, IL-6 and IL-8 expression in 6 h. In all the scaffold types, but remarkedly in the aligned composite ones, transforming growth factor beta (TGF-beta) and the antimicrobial peptide human beta defensin 2 (HBD-2) were significantly increased. Zinc Oxide 13-16 defensin beta 4A Homo sapiens 375-380 32949962-4 2020 ZnO NPs disrupted the hepatic architecture, elevated the serum liver enzyme alanine transaminase (ALT), aspartate transaminase (AST) and alkaline phosphatase (ALP) levels and caused dose-dependent decrease in the activity of the antioxidant enzymes glutathione-peroxidase, superoxide dismutase and catalase along with an increase in the lipid peroxidation product malondialdehyde. Zinc Oxide 0-3 catalase Rattus norvegicus 298-306 33222098-9 2022 After this examination, it can be concluded that edaravone caused cytoprotective impacts in an HO-1-dependent manner in SH-SY5Y cells against ZnO NPs-induced toxicity. Zinc Oxide 142-145 heme oxygenase 1 Homo sapiens 95-99 33544508-0 2020 Comparison of the effects of zinc oxide and zinc oxide nanoparticles on the expression of hepcidin gene in rat liver. Zinc Oxide 29-39 hepcidin antimicrobial peptide Rattus norvegicus 90-98 33197900-5 2021 Investigating the molecular mechanisms involved in the growth-suppressive effect of ZnO/CNT@Fe3O4-plus-Imatinib clarified that the up-regulation of SIRT1 ceased the progression of the cell cycle, foremost by increasing the expression of p21 and p27 cyclin-dependent kinase inhibitors. Zinc Oxide 84-87 sirtuin 1 Homo sapiens 148-153 33197900-6 2021 Notably, we reported for the first time that either direct or indirect suppression of c-Myc resulted in an enhanced anti-leukemic effect; suggesting that the overexpression of c-Myc could play a contributory role in attenuating the efficacy of ZnO/CNT@Fe3O4-plus-Imatinib in K562. Zinc Oxide 244-247 MYC proto-oncogene, bHLH transcription factor Homo sapiens 86-91 33197900-6 2021 Notably, we reported for the first time that either direct or indirect suppression of c-Myc resulted in an enhanced anti-leukemic effect; suggesting that the overexpression of c-Myc could play a contributory role in attenuating the efficacy of ZnO/CNT@Fe3O4-plus-Imatinib in K562. Zinc Oxide 244-247 MYC proto-oncogene, bHLH transcription factor Homo sapiens 176-181 32540704-1 2020 A ZnO/PEG (polyethylene glycol) -Co(II)-PbO2 nanocomposite electrode was constructed by using the anodic electrodeposition method and used for the electrocatalytic degradation phenol. Zinc Oxide 2-5 mitochondrially encoded cytochrome c oxidase II Homo sapiens 33-39 33273900-2 2020 In this study, the expression of miR-155-5p, miR-203a-3p, and miR-223-3p in the MCF7 cancer cell line was studied when exposed to ZnO nanoparticles synthesized through a green route. Zinc Oxide 130-133 microRNA 155 Homo sapiens 33-40 32866723-1 2020 In this work, a signal amplification competitive-type photoelectrochemical system comprised of bismuth sulfide/bismuth oxyiodide/zinc oxide (Bi2S3/BiOI/ZnO) nano-array as platform and Ag2S-modified aptamers probe DNA (p DNA@Ag2S) as competition content for rapid and sensitive detection of OTA in microfluidic devices. Zinc Oxide 129-139 angiotensin II receptor type 1 Homo sapiens 184-188 32866723-5 2020 After immobilizing with the capture DNA (c DNA) and the sequential hybridization of p DNA@Ag2S, the photocurrent intensity reduced obviously because part photo-generated electron transformed to Ag2S rather than Bi2S3/BiOI/ZnO electrode. Zinc Oxide 222-225 angiotensin II receptor type 1 Homo sapiens 90-94 32937690-0 2020 Dual effects of JNK activation in blood-milk barrier damage induced by zinc oxide nanoparticles. Zinc Oxide 71-81 mitogen-activated protein kinase 8 Homo sapiens 16-19 33544508-0 2020 Comparison of the effects of zinc oxide and zinc oxide nanoparticles on the expression of hepcidin gene in rat liver. Zinc Oxide 44-54 hepcidin antimicrobial peptide Rattus norvegicus 90-98 33544508-4 2020 Given the important role of hepcidin in the development of anemia and iron overload diseases, this study investigated the effect of ZnO nanoparticles on the hepatic expression of the hepcidin gene to help find a way to treat these diseases. Zinc Oxide 132-135 hepcidin antimicrobial peptide Rattus norvegicus 183-191 33544508-9 2020 RESULTS: ZnO and the ZnO nanoparticle significantly increased the expression of the hepcidin gene relative to the control group. Zinc Oxide 9-12 hepcidin antimicrobial peptide Rattus norvegicus 84-92 33544508-9 2020 RESULTS: ZnO and the ZnO nanoparticle significantly increased the expression of the hepcidin gene relative to the control group. Zinc Oxide 21-24 hepcidin antimicrobial peptide Rattus norvegicus 84-92 33544508-10 2020 The increase in expression of the hepcidin gene in ZnO nanoparticles was more significant than in the ZnO. Zinc Oxide 51-54 hepcidin antimicrobial peptide Rattus norvegicus 34-42 33544508-10 2020 The increase in expression of the hepcidin gene in ZnO nanoparticles was more significant than in the ZnO. Zinc Oxide 102-105 hepcidin antimicrobial peptide Rattus norvegicus 34-42 33544508-11 2020 CONCLUSION: ZnO nanoparticles led to significant increase in expression of the hepcidin gene. Zinc Oxide 12-15 hepcidin antimicrobial peptide Rattus norvegicus 79-87 32768851-2 2020 Thus, AgInS2 quantum dots (AIS QDs, 4.0 +- 1.6 nm), have been successfully prepared and loaded onto ZnO nanopyramids (ZnO NPy). Zinc Oxide 100-103 neuropeptide Y Homo sapiens 122-125 33251414-3 2020 Ag nanoparticles play an important role in PAA/ZnO/Ag composite microspheres, conferring new SERS properties and functions to PAA/ZnO/Ag. Zinc Oxide 47-50 seryl-tRNA synthetase 2, mitochondrial Homo sapiens 93-97 33251414-5 2020 The SERS detection limit of R6G obtained was reduced to 1 x 10-6 M. The PAA/ZnO/Ag composite particles show a very good degradation effect on R6G under UV light irradiation. Zinc Oxide 76-79 seryl-tRNA synthetase 2, mitochondrial Homo sapiens 4-8 32650163-5 2020 The results of catalytic activity studies confirmed that the antioxidant enzymes (SOD, CAT, GSH-PX) in midgut cells were expressed in response to ZnO NPs. Zinc Oxide 146-149 superoxide dismutase [Cu-Zn] Bombyx mori 82-85 32671885-5 2020 TiO2 NPs and ZnO NPs individually induced a significant (p < .01) reduction in SOD and CAT activities, while the mixture significantly (p < .001) decreased CAT activity and increased SOD activity. Zinc Oxide 13-16 catalase Mus musculus 87-90 32671885-5 2020 TiO2 NPs and ZnO NPs individually induced a significant (p < .01) reduction in SOD and CAT activities, while the mixture significantly (p < .001) decreased CAT activity and increased SOD activity. Zinc Oxide 13-16 catalase Mus musculus 156-159 32650163-5 2020 The results of catalytic activity studies confirmed that the antioxidant enzymes (SOD, CAT, GSH-PX) in midgut cells were expressed in response to ZnO NPs. Zinc Oxide 146-149 catalase Bombyx mori 87-90 32570030-3 2020 The improved functions of HGnFs over the ZnO@ZnS nanorod-array were attributed to the material"s optimized zinc release, which was decreased from an order of 3.5 mg L-1 to about 0.3 mg L-1 (within the first week). Zinc Oxide 41-44 L1 cell adhesion molecule Mus musculus 165-168 32562731-2 2020 The structural properties were analyzed using FTIR, XRD, SEM, TEM, TGA, and DMA The swelling analysis revealed that SA-poly(AA)/ZnO HNC exhibited high water uptake capacity. Zinc Oxide 128-131 T-box transcription factor 1 Homo sapiens 67-70 32570030-3 2020 The improved functions of HGnFs over the ZnO@ZnS nanorod-array were attributed to the material"s optimized zinc release, which was decreased from an order of 3.5 mg L-1 to about 0.3 mg L-1 (within the first week). Zinc Oxide 41-44 L1 cell adhesion molecule Mus musculus 185-188 33054172-0 2020 HIF-1alpha-Mediated Mitophagy Determines ZnO Nanoparticle-Induced Human Osteosarcoma Cell Death both In Vitro and In Vivo. Zinc Oxide 41-44 hypoxia inducible factor 1 subunit alpha Homo sapiens 0-10 33054172-3 2020 We found that ZnO NPs upregulated HIF-1alpha protein levels when they killed four common human osteosarcoma cell lines. Zinc Oxide 14-17 hypoxia inducible factor 1 subunit alpha Homo sapiens 34-44 33096666-1 2020 This article describes an optical method based on the association of surface plasmon resonance (SPR) with chitosan (CS) film and its nanocomposites, including zinc oxide (ZnO) or graphene oxide (GO) for glyphosate detection. Zinc Oxide 159-169 citrate synthase Homo sapiens 116-118 33149573-10 2020 The conclusions of the present study put forward an evident confirmation of the protective and beneficial effects of zincoxide-loaded syringic acid against the BAP-induced lung cancer model. Zinc Oxide 117-126 prohibitin 2 Mus musculus 160-163 33110140-5 2020 In addition, the electrochemical sensing of the immobilised T1R2-Reb-A complex with zinc oxide nanoparticles (ZnONPs) and graphene oxide (GO) were assessed by testing the performance of multiwalled carbon nanotube (MWCNT) as an adsorbent experimentally. Zinc Oxide 84-94 taste 1 receptor member 2 Homo sapiens 60-64 33096666-1 2020 This article describes an optical method based on the association of surface plasmon resonance (SPR) with chitosan (CS) film and its nanocomposites, including zinc oxide (ZnO) or graphene oxide (GO) for glyphosate detection. Zinc Oxide 171-174 citrate synthase Homo sapiens 116-118 32554261-1 2020 The ZnO + Bi2O3 + BaF2 + B2O3 + TeO2 (ZnBiBaBFTe) host glass was prepared by melt quenching technique with the aim of achieving white light emission from Dy3+ ions. Zinc Oxide 4-7 BANF family member 2 Homo sapiens 18-22 32729488-1 2020 We present a tyrosinase-conjugated zinc oxide-reduced graphene oxide (Tyr/ZnO-rGO) nanocomposite system as a biosensing test-bed for rapid and sensitive detection of dopamine (DA). Zinc Oxide 35-45 tyrosinase Homo sapiens 13-23 32521445-3 2020 As modified by Ag nanoparticles (AgNPs) and ZnO nanoparticles (ZnONPs), the hydrophilic channel exhibited high recyclable SERS detection activity and stability. Zinc Oxide 44-47 seryl-tRNA synthetase 2, mitochondrial Homo sapiens 122-126 33116508-9 2020 Lowering the FC to >=1.5 with p<=0.05 and corrected p<=0.1 showed that ZnO NPs over-expressed the anti-oxidant defense system, drove K562 cells to undergo mitochondrial-dependent apoptosis, and targeted NF-kappaB pathway. Zinc Oxide 71-74 nuclear factor kappa B subunit 1 Homo sapiens 203-212 33115130-4 2020 The presence of the MoOx layer between n-type ZnO and p-type GaN leads to the confinement of electrons and an increase in the electron charge density at n-type ZnO. Zinc Oxide 160-163 gigaxonin Homo sapiens 61-64 32729488-2 2020 The bioelectrodes (Tyr/ZnO-rGO/ITO) were designed by covalently immobilizing tyrosinase enzyme on spin-coated films of ZnO-rGO nanocomposite prepared via self-assembly approach. Zinc Oxide 23-26 tyrosinase Homo sapiens 77-87 32729488-2 2020 The bioelectrodes (Tyr/ZnO-rGO/ITO) were designed by covalently immobilizing tyrosinase enzyme on spin-coated films of ZnO-rGO nanocomposite prepared via self-assembly approach. Zinc Oxide 23-26 spindlin 1 Homo sapiens 98-102 32967362-9 2020 Further, under more acidic conditions (pH 4), the maximum sorption capacities using GO/ZnO as adsorbent were 19.9 mg/g and 33.5 mg/g for Al and Cu, respectively. Zinc Oxide 87-90 prolyl 4-hydroxylase, transmembrane Homo sapiens 39-43 32621200-0 2020 Zinc oxide nanoparticles enhance expression of maspin in human breast cancer cells. Zinc Oxide 0-10 serpin family B member 5 Homo sapiens 47-53 33108324-0 2020 Zinc oxide nanoparticles augment CD4, CD8, and GLUT-4 expression and restrict inflammation response in streptozotocin-induced diabetic rats. Zinc Oxide 0-10 Cd4 molecule Rattus norvegicus 33-36 33108324-0 2020 Zinc oxide nanoparticles augment CD4, CD8, and GLUT-4 expression and restrict inflammation response in streptozotocin-induced diabetic rats. Zinc Oxide 0-10 solute carrier family 2 member 4 Rattus norvegicus 47-53 33281360-3 2020 This study aimed to determine the effect of a wound dressing consisting of zinc oxide and turmeric extract on wound reepithelialization by assessing the expression of cytokeratin 14 (CK14), epidermal growth factor receptor (EGFR), and epithelial cadherin (E-cadherin). Zinc Oxide 75-85 cadherin 1 Rattus norvegicus 256-266 32771442-9 2020 Moreover, we have shown that short time (one day) exposure of SSCs to a low concentration of ZnO NPs (10 microg/ml) promoted expressions of specific genes (Plzf, Gfr alpha1 and Bcl6b) for SSC self-renewal and differentiation genes (Vasa, Dazl, C-kit and Sycp3) expressed by spermatogonia during spermatogenesis. Zinc Oxide 93-96 zinc finger and BTB domain containing 16 Homo sapiens 156-160 32771442-9 2020 Moreover, we have shown that short time (one day) exposure of SSCs to a low concentration of ZnO NPs (10 microg/ml) promoted expressions of specific genes (Plzf, Gfr alpha1 and Bcl6b) for SSC self-renewal and differentiation genes (Vasa, Dazl, C-kit and Sycp3) expressed by spermatogonia during spermatogenesis. Zinc Oxide 93-96 GDNF family receptor alpha 1 Homo sapiens 162-172 32771442-9 2020 Moreover, we have shown that short time (one day) exposure of SSCs to a low concentration of ZnO NPs (10 microg/ml) promoted expressions of specific genes (Plzf, Gfr alpha1 and Bcl6b) for SSC self-renewal and differentiation genes (Vasa, Dazl, C-kit and Sycp3) expressed by spermatogonia during spermatogenesis. Zinc Oxide 93-96 BCL6B transcription repressor Homo sapiens 177-182 32771442-9 2020 Moreover, we have shown that short time (one day) exposure of SSCs to a low concentration of ZnO NPs (10 microg/ml) promoted expressions of specific genes (Plzf, Gfr alpha1 and Bcl6b) for SSC self-renewal and differentiation genes (Vasa, Dazl, C-kit and Sycp3) expressed by spermatogonia during spermatogenesis. Zinc Oxide 93-96 deleted in azoospermia like Homo sapiens 238-242 32771442-9 2020 Moreover, we have shown that short time (one day) exposure of SSCs to a low concentration of ZnO NPs (10 microg/ml) promoted expressions of specific genes (Plzf, Gfr alpha1 and Bcl6b) for SSC self-renewal and differentiation genes (Vasa, Dazl, C-kit and Sycp3) expressed by spermatogonia during spermatogenesis. Zinc Oxide 93-96 KIT proto-oncogene, receptor tyrosine kinase Homo sapiens 244-249 32771442-9 2020 Moreover, we have shown that short time (one day) exposure of SSCs to a low concentration of ZnO NPs (10 microg/ml) promoted expressions of specific genes (Plzf, Gfr alpha1 and Bcl6b) for SSC self-renewal and differentiation genes (Vasa, Dazl, C-kit and Sycp3) expressed by spermatogonia during spermatogenesis. Zinc Oxide 93-96 synaptonemal complex protein 3 Homo sapiens 254-259 32959825-3 2020 This PIERS substrate is composed of a photo-irradiated thin ZnO film on which gold nanoparticles are deposited and allows large photo-induced SERS enhancement to be obtained for the chemical detection of small molecules compared to normal SERS signals. Zinc Oxide 60-63 seryl-tRNA synthetase 2, mitochondrial Homo sapiens 142-146 32959825-3 2020 This PIERS substrate is composed of a photo-irradiated thin ZnO film on which gold nanoparticles are deposited and allows large photo-induced SERS enhancement to be obtained for the chemical detection of small molecules compared to normal SERS signals. Zinc Oxide 60-63 seryl-tRNA synthetase 2, mitochondrial Homo sapiens 239-243 32974847-0 2021 Correction to: Eco-Friendly Mycogenic Synthesis of ZnO and CuO Nanoparticles for In Vitro Antibacterial, Antibiofilm and Antifungal Applications. Zinc Oxide 51-54 ciliogenesis associated kinase 1 Homo sapiens 15-18 32967666-10 2020 In a dose-dependent manner, ZnO-NPs upregulated the mRNA levels of antioxidant enzymes (superoxide dismutase: SOD1; catalase: CAT; glutathione peroxidase-1: GPX 1) and pro-inflammatory cytokines (interferon alpha: IFN-alpha; interleukin 6: IL-6) in liver and brain tissues. Zinc Oxide 28-31 superoxide dismutase [Cu-Zn] Coturnix japonica 110-114 32967666-10 2020 In a dose-dependent manner, ZnO-NPs upregulated the mRNA levels of antioxidant enzymes (superoxide dismutase: SOD1; catalase: CAT; glutathione peroxidase-1: GPX 1) and pro-inflammatory cytokines (interferon alpha: IFN-alpha; interleukin 6: IL-6) in liver and brain tissues. Zinc Oxide 28-31 catalase Coturnix japonica 126-129 32967666-10 2020 In a dose-dependent manner, ZnO-NPs upregulated the mRNA levels of antioxidant enzymes (superoxide dismutase: SOD1; catalase: CAT; glutathione peroxidase-1: GPX 1) and pro-inflammatory cytokines (interferon alpha: IFN-alpha; interleukin 6: IL-6) in liver and brain tissues. Zinc Oxide 28-31 glutathione peroxidase 1 Coturnix japonica 131-155 32967666-10 2020 In a dose-dependent manner, ZnO-NPs upregulated the mRNA levels of antioxidant enzymes (superoxide dismutase: SOD1; catalase: CAT; glutathione peroxidase-1: GPX 1) and pro-inflammatory cytokines (interferon alpha: IFN-alpha; interleukin 6: IL-6) in liver and brain tissues. Zinc Oxide 28-31 glutathione peroxidase 1 Coturnix japonica 157-162 32967666-10 2020 In a dose-dependent manner, ZnO-NPs upregulated the mRNA levels of antioxidant enzymes (superoxide dismutase: SOD1; catalase: CAT; glutathione peroxidase-1: GPX 1) and pro-inflammatory cytokines (interferon alpha: IFN-alpha; interleukin 6: IL-6) in liver and brain tissues. Zinc Oxide 28-31 interleukin-6 Coturnix japonica 225-238 32967666-10 2020 In a dose-dependent manner, ZnO-NPs upregulated the mRNA levels of antioxidant enzymes (superoxide dismutase: SOD1; catalase: CAT; glutathione peroxidase-1: GPX 1) and pro-inflammatory cytokines (interferon alpha: IFN-alpha; interleukin 6: IL-6) in liver and brain tissues. Zinc Oxide 28-31 interleukin-6 Coturnix japonica 240-244 32929172-5 2020 The resulting crystalline and well-aligned ZnO nanorods (NRs) proved their efficiency in immobilizing monoclonal anti-human NKp30 antibodies (mAb), obviating the need for additional procedures for mAb immobilization. Zinc Oxide 43-46 natural cytotoxicity triggering receptor 3 Homo sapiens 124-129 32948194-5 2020 We concluded that autophagic cell death, resulting from zinc ions-ROS-c-Jun N-terminal kinase (JNK)-autophagy positive feedback loop and blockade of autophagosomal-lysosomal fusion, played a major role in the neurotoxicity of ZnO NPs. Zinc Oxide 226-229 mitogen-activated protein kinase 8 Rattus norvegicus 95-98 32387613-2 2020 Herein, chitosan supported zirconium(Zr)/zinc oxide (ZnO)) in the preparation of photo catalyst (Zr-ZnO@CS) for photocatalytic reduction of hexavalent chromium(Cr6+). Zinc Oxide 41-51 teratocarcinoma-derived growth factor 1 pseudogene 6 Homo sapiens 160-163 32387613-2 2020 Herein, chitosan supported zirconium(Zr)/zinc oxide (ZnO)) in the preparation of photo catalyst (Zr-ZnO@CS) for photocatalytic reduction of hexavalent chromium(Cr6+). Zinc Oxide 53-56 teratocarcinoma-derived growth factor 1 pseudogene 6 Homo sapiens 160-163 32957589-5 2020 The PLM test results showed that the micro- and nano-ZnO particles adding decreased the crystal size. Zinc Oxide 53-56 FXYD domain containing ion transport regulator 1 Homo sapiens 4-7 32988057-1 2020 We demonstrate an improvement in the photoresponse characteristics of ultraviolet (UV) photodetectors (PDs) using the N2O plasma-treated ZnO nanorod (NR) gated AlGaN/GaN high electron mobility transistor (HEMT) structure. Zinc Oxide 137-140 gigaxonin Homo sapiens 162-165 32901051-6 2020 Cs1-xFAxPbBr3 QD-LED device structure was optimized by using PVK as a HTL and ZnO modified with b-PEI as an ETL. Zinc Oxide 78-81 chorionic somatomammotropin hormone 1 Homo sapiens 0-3 32915786-0 2020 Zinc oxide nanoparticles modulate the gene expression of ZnT1 and ZIP8 to manipulate zinc homeostasis and stress-induced cytotoxicity in human neuroblastoma SH-SY5Y cells. Zinc Oxide 0-10 solute carrier family 30 member 1 Homo sapiens 57-61 32915786-0 2020 Zinc oxide nanoparticles modulate the gene expression of ZnT1 and ZIP8 to manipulate zinc homeostasis and stress-induced cytotoxicity in human neuroblastoma SH-SY5Y cells. Zinc Oxide 0-10 solute carrier family 39 member 8 Homo sapiens 66-70 32300871-9 2020 The larval and pupal development was delayed at 25 microg mL-1 of Ws-ZnO NPs. Zinc Oxide 69-72 L1 cell adhesion molecule Mus musculus 58-62 32825778-3 2020 Here, we report a hybrid ZnO nanoparticle/graphene phototransistor that exhibits a responsivity up to 4 x 104 AW-1 and gain of up to 1.3 x 105 with high UV wavelength selectivity. Zinc Oxide 25-28 zinc finger protein 174 Homo sapiens 110-114 32640348-5 2020 Sal decreased the expression of ATF4, JNK and Caspase-12, and increased the expression of eNOS and IGF-1caused by the oral ingestion of ZnO NPs. Zinc Oxide 136-139 nitric oxide synthase 3, endothelial cell Mus musculus 90-94 32640348-5 2020 Sal decreased the expression of ATF4, JNK and Caspase-12, and increased the expression of eNOS and IGF-1caused by the oral ingestion of ZnO NPs. Zinc Oxide 136-139 insulin-like growth factor 1 Mus musculus 99-104 32540482-2 2020 This study aims to determine if the use of zinc oxide selects for Extended Spectrum beta-Lactamase (ESBL)-producing E. coli and affects the expression of blaCTX-M-1 in E. coli. Zinc Oxide 43-53 EsbL Escherichia coli 66-98 32882974-1 2020 The aim of this work is to structurally characterize chitosan-zinc oxide nanoparticles (CS-ZnO NPs) films in a wide range of NPs concentration (0-20 wt.%). Zinc Oxide 62-72 citrate synthase Homo sapiens 88-90 32882974-7 2020 The understanding of nanoscale properties of CS-ZnO nanocomposites is important in the development of biocompatible sensors, actuators, nanogenerators for flexible electronics and biomedical applications. Zinc Oxide 48-51 citrate synthase Homo sapiens 45-47 32875247-2 2020 The identification of the reaction scheme governing the gas sensing response is crucial for further development; however, the mechanism of ethanol (EtOH) gas sensing by ZnO is still controversial despite being one of the most intensively studied target gas and sensing material combinations. Zinc Oxide 169-172 gastrin Homo sapiens 154-157 32662629-4 2020 After investigating several C-M-S structures, the SERS blocking mechanism is validated that thick shells (Au, Ag, ZnO and MnO2) can cause significant reduction for the internal SERS signal by obstructing the penetration of the laser or signal. Zinc Oxide 114-117 seryl-tRNA synthetase 2, mitochondrial Homo sapiens 50-54 32662629-4 2020 After investigating several C-M-S structures, the SERS blocking mechanism is validated that thick shells (Au, Ag, ZnO and MnO2) can cause significant reduction for the internal SERS signal by obstructing the penetration of the laser or signal. Zinc Oxide 114-117 seryl-tRNA synthetase 2, mitochondrial Homo sapiens 177-181 32875247-2 2020 The identification of the reaction scheme governing the gas sensing response is crucial for further development; however, the mechanism of ethanol (EtOH) gas sensing by ZnO is still controversial despite being one of the most intensively studied target gas and sensing material combinations. Zinc Oxide 169-172 gastrin Homo sapiens 154-157 32126724-4 2020 The ZnO@CuS core-shell nanocomposites were characterized using different techniques such as XRD, FE-SEM, TEM, FT-IR, UV-Vis, DRS and XPS. Zinc Oxide 4-7 sushi repeat containing protein X-linked Homo sapiens 125-128 32304862-2 2020 In this work, CIP was photocatalytically degraded using a porous ZnO/SnS2 photocatalyst prepared via microwaves. Zinc Oxide 65-68 sodium voltage-gated channel alpha subunit 11 Homo sapiens 69-73 32304862-4 2020 From the study, it was found that visible-light induced degradation of CIP on ZnO/SnS2 is a surface-mediated process and the reaction kinetics followed the Langmuir-Hinshelwood first-order kinetics. Zinc Oxide 78-81 sodium voltage-gated channel alpha subunit 11 Homo sapiens 82-86 32325249-0 2020 Exposure to low dose ZnO nanoparticles induces hyperproliferation and malignant transformation through activating the CXCR2/NF-kappaB/STAT3/ERK and AKT pathways in colonic mucosal cells. Zinc Oxide 21-24 C-X-C motif chemokine receptor 2 Homo sapiens 118-123 32325249-0 2020 Exposure to low dose ZnO nanoparticles induces hyperproliferation and malignant transformation through activating the CXCR2/NF-kappaB/STAT3/ERK and AKT pathways in colonic mucosal cells. Zinc Oxide 21-24 nuclear factor kappa B subunit 1 Homo sapiens 124-133 32325249-0 2020 Exposure to low dose ZnO nanoparticles induces hyperproliferation and malignant transformation through activating the CXCR2/NF-kappaB/STAT3/ERK and AKT pathways in colonic mucosal cells. Zinc Oxide 21-24 signal transducer and activator of transcription 3 Homo sapiens 134-139 32325249-0 2020 Exposure to low dose ZnO nanoparticles induces hyperproliferation and malignant transformation through activating the CXCR2/NF-kappaB/STAT3/ERK and AKT pathways in colonic mucosal cells. Zinc Oxide 21-24 mitogen-activated protein kinase 1 Homo sapiens 140-143 32325249-0 2020 Exposure to low dose ZnO nanoparticles induces hyperproliferation and malignant transformation through activating the CXCR2/NF-kappaB/STAT3/ERK and AKT pathways in colonic mucosal cells. Zinc Oxide 21-24 AKT serine/threonine kinase 1 Homo sapiens 148-151 32325249-6 2020 In conclusion, exposure of ZnO NPs could induce malignant transformation of colonic mucosal cells through the CXCR2/NF-kappaB/STAT3/ERK and AKT pathways. Zinc Oxide 27-30 C-X-C motif chemokine receptor 2 Homo sapiens 110-115 32325249-6 2020 In conclusion, exposure of ZnO NPs could induce malignant transformation of colonic mucosal cells through the CXCR2/NF-kappaB/STAT3/ERK and AKT pathways. Zinc Oxide 27-30 nuclear factor kappa B subunit 1 Homo sapiens 116-125 32325249-6 2020 In conclusion, exposure of ZnO NPs could induce malignant transformation of colonic mucosal cells through the CXCR2/NF-kappaB/STAT3/ERK and AKT pathways. Zinc Oxide 27-30 signal transducer and activator of transcription 3 Homo sapiens 126-131 32325249-6 2020 In conclusion, exposure of ZnO NPs could induce malignant transformation of colonic mucosal cells through the CXCR2/NF-kappaB/STAT3/ERK and AKT pathways. Zinc Oxide 27-30 mitogen-activated protein kinase 1 Homo sapiens 132-135 32325249-6 2020 In conclusion, exposure of ZnO NPs could induce malignant transformation of colonic mucosal cells through the CXCR2/NF-kappaB/STAT3/ERK and AKT pathways. Zinc Oxide 27-30 AKT serine/threonine kinase 1 Homo sapiens 140-143 32199201-3 2020 The beta-cyclodextrin (beta-CD) capped ZnO quantum dots (QDs) were decorated with the vitamin B6 cofactors like pyridoxal 5"-phosphate (PLP) and pyridoxal (Py) by forming host-guest inclusion complexation between the capped beta-CD and PLP/Py. Zinc Oxide 39-42 ACD shelterin complex subunit and telomerase recruitment factor Homo sapiens 23-30 32199201-3 2020 The beta-cyclodextrin (beta-CD) capped ZnO quantum dots (QDs) were decorated with the vitamin B6 cofactors like pyridoxal 5"-phosphate (PLP) and pyridoxal (Py) by forming host-guest inclusion complexation between the capped beta-CD and PLP/Py. Zinc Oxide 39-42 ACD shelterin complex subunit and telomerase recruitment factor Homo sapiens 224-231 32639143-4 2020 A possible growth mechanism of the p-SnO/n-ZnO biaxial nanowires was discussed based on the subsequent growth process: the VLS catalyticgrowth of the ZnO nanowire and subsequent epitaxial SnO growth on the sidewall of the pre-grown ZnO nanowire. Zinc Oxide 43-46 strawberry notch homolog 1 Homo sapiens 188-191 32639143-4 2020 A possible growth mechanism of the p-SnO/n-ZnO biaxial nanowires was discussed based on the subsequent growth process: the VLS catalyticgrowth of the ZnO nanowire and subsequent epitaxial SnO growth on the sidewall of the pre-grown ZnO nanowire. Zinc Oxide 150-153 strawberry notch homolog 1 Homo sapiens 37-40 32639143-5 2020 An epitaxial relationship, (001)SnO//(110)ZnO and [110]SnO//[002]ZnO, was observed in the biaxial p-SnO/n-ZnOheterostructured nanowires. Zinc Oxide 42-45 strawberry notch homolog 1 Homo sapiens 32-35 32639143-5 2020 An epitaxial relationship, (001)SnO//(110)ZnO and [110]SnO//[002]ZnO, was observed in the biaxial p-SnO/n-ZnOheterostructured nanowires. Zinc Oxide 42-45 strawberry notch homolog 1 Homo sapiens 55-58 32639143-5 2020 An epitaxial relationship, (001)SnO//(110)ZnO and [110]SnO//[002]ZnO, was observed in the biaxial p-SnO/n-ZnOheterostructured nanowires. Zinc Oxide 42-45 strawberry notch homolog 1 Homo sapiens 55-58 32639143-5 2020 An epitaxial relationship, (001)SnO//(110)ZnO and [110]SnO//[002]ZnO, was observed in the biaxial p-SnO/n-ZnOheterostructured nanowires. Zinc Oxide 65-68 strawberry notch homolog 1 Homo sapiens 32-35 32639143-5 2020 An epitaxial relationship, (001)SnO//(110)ZnO and [110]SnO//[002]ZnO, was observed in the biaxial p-SnO/n-ZnOheterostructured nanowires. Zinc Oxide 65-68 strawberry notch homolog 1 Homo sapiens 55-58 32639143-5 2020 An epitaxial relationship, (001)SnO//(110)ZnO and [110]SnO//[002]ZnO, was observed in the biaxial p-SnO/n-ZnOheterostructured nanowires. Zinc Oxide 65-68 strawberry notch homolog 1 Homo sapiens 55-58 32353603-8 2020 According to the ATR-FTIR results, Cr(III) ions reacted with hydroxyl groups on nano-ZnO to form ZnO-O bonds, which induced chains of nano-ZnO and Cr(III) complexes, and hence the increased of nano-ZnO aggregates. Zinc Oxide 85-88 ATR serine/threonine kinase Homo sapiens 17-20 32728964-3 2020 Post-deposition thermal annealing is conducted at 300 C in the ambience of oxygen (O2) for 1 h. With strong oxidizing agent O3 and post-deposition TA in growing ZnO, intrinsic strain and stress are reduced to 0.49% and 2.22 GPa, respectively, with extremely low background electron concentration (9.4 x 1015 cm-3). Zinc Oxide 162-165 glycophorin A (MNS blood group) Homo sapiens 225-228 32727153-0 2020 Photocatalytic and Electrocatalytic Properties of NGr-ZnO Hybrid Materials. Zinc Oxide 54-57 reticulon 4 receptor Homo sapiens 50-53 32727153-4 2020 In the case of all NGr-ZnO hybrid materials, the flakes appear heavily decorated with ZnO nanoparticles, having a cauliflower-like morphology. Zinc Oxide 23-26 reticulon 4 receptor Homo sapiens 19-22 32727153-4 2020 In the case of all NGr-ZnO hybrid materials, the flakes appear heavily decorated with ZnO nanoparticles, having a cauliflower-like morphology. Zinc Oxide 86-89 reticulon 4 receptor Homo sapiens 19-22 32727153-10 2020 A high photocatalytic activity of NGr-ZnO samples against rhodamine B solution was observed. Zinc Oxide 38-41 reticulon 4 receptor Homo sapiens 34-37 32353603-9 2020 ATR-FTIR shows merely electrostatic adsorption effects between nano-ZnO and Cu(II) or Cr(VI) ions. Zinc Oxide 68-71 ATR serine/threonine kinase Homo sapiens 0-3 32336537-3 2020 The sensing experimental data indicate that the highest response of the ZnO/CdO/rGO (1.0 wt%) composite to ppm-level NO2 is 8 times and 2 times higher than pure ZnO and ZnO/CdO junction, respectively. Zinc Oxide 72-75 cell adhesion associated, oncogene regulated Homo sapiens 76-79 32336537-3 2020 The sensing experimental data indicate that the highest response of the ZnO/CdO/rGO (1.0 wt%) composite to ppm-level NO2 is 8 times and 2 times higher than pure ZnO and ZnO/CdO junction, respectively. Zinc Oxide 72-75 cell adhesion associated, oncogene regulated Homo sapiens 173-176 32336537-3 2020 The sensing experimental data indicate that the highest response of the ZnO/CdO/rGO (1.0 wt%) composite to ppm-level NO2 is 8 times and 2 times higher than pure ZnO and ZnO/CdO junction, respectively. Zinc Oxide 161-164 cell adhesion associated, oncogene regulated Homo sapiens 76-79 32336537-3 2020 The sensing experimental data indicate that the highest response of the ZnO/CdO/rGO (1.0 wt%) composite to ppm-level NO2 is 8 times and 2 times higher than pure ZnO and ZnO/CdO junction, respectively. Zinc Oxide 161-164 cell adhesion associated, oncogene regulated Homo sapiens 76-79 32336537-5 2020 The enhancement in gas sensing properties is credited to the development of ZnO/CdO heterojunction and the decoration of rGO with high conductivity. Zinc Oxide 76-79 cell adhesion associated, oncogene regulated Homo sapiens 80-83 32339863-2 2020 A microcosm experiment was conducted to explore the chronic effects of ZnO nanoparticle at environmental concentrations (30, 300, 3000 ng L-1) on aquatic fungi associated with the decomposing process of poplar leaf litter (45 days). Zinc Oxide 71-74 L1 cell adhesion molecule Homo sapiens 138-141 32664437-4 2020 Monoclonal antibodies (MABs) anti-CD5 against a cluster of differentiation (CD) proteins on the pathologic cell surface have been used as a bioselective layer on the ZnO surface. Zinc Oxide 166-169 CD5 molecule Homo sapiens 34-37 32664437-9 2020 The increase in the ZnO NRs photoluminescence intensity correlated with the number of CD5-positive MOLT-4 cells in the investigated population (controlled by using flow cytometry). Zinc Oxide 20-23 CD5 molecule Homo sapiens 86-89 32274628-0 2020 TRPC6-Mediated Ca2+ Entry Essential for the Regulation of Nano-ZnO Induced Autophagy in SH-SY5Y Cells. Zinc Oxide 63-66 transient receptor potential cation channel subfamily C member 6 Homo sapiens 0-5 32274628-6 2020 Nano-ZnO increased Ca2+ entry and the expression of TRPC6.The results suggested that nano-ZnO increased [Ca2+] through the TRPC-dependent Ca2+ influx, since Ca2+ influx can be prevented by the TRPC inhibitor. Zinc Oxide 5-8 transient receptor potential cation channel subfamily C member 6 Homo sapiens 52-57 32274628-8 2020 Herein, we demonstrated that the nano-ZnO activated TRPC6 channel, thereby increasing the Ca2+ flux and resulting in increased autophagy. Zinc Oxide 38-41 transient receptor potential cation channel subfamily C member 6 Homo sapiens 52-57 32339863-5 2020 After chronic exposure, the fungal community structure was significantly impacted by ZnO nanoparticles at 300 ng L-1 due to the reduced proportion of Anguillospora, which eventually caused a significant decrease in litter decomposition rate. Zinc Oxide 85-88 L1 cell adhesion molecule Homo sapiens 113-116 32346997-0 2020 From Precursor Chemistry to Gas Sensors: Plasma-Enhanced Atomic Layer Deposition Process Engineering for Zinc Oxide Layers from a Nonpyrophoric Zinc Precursor for Gas Barrier and Sensor Applications. Zinc Oxide 105-115 gastrin Homo sapiens 28-31 32503144-4 2020 The ULBP2 antibody was immobilized onto the screen-printed carbon electrode (SPCE) surfaces of three different sensors: a simple SPCE (ULBP2-SPCE); an SPCE array, which is a series of identical SPCE connected to each other at different arrangements of rows and columns (ULBP2-SPCE-1x2 and ULBP2-SPCE-1x3); and an SPCE combined with ZnO nanoparticles (ULBP2-ZnO/SPCE). Zinc Oxide 332-335 UL16 binding protein 2 Homo sapiens 4-9 32199367-12 2020 Nano and bulk-ZnO also significantly reduced grain Fe, with O-F amendment under drought. Zinc Oxide 14-17 Spi-1 proto-oncogene Homo sapiens 60-63 32570911-6 2020 RESULTS: Our data showed that ZnO was able to reduce the inflammatory response of DECs, in terms of vascular cell adhesion molecule-1 (VCAM-1), interleukin (IL)-8, IL-6, tumor necrosis factor-alpha (TNF-alpha) and monocyte chemoattractant protein-1 (MCP-1) expression induced by TNF-alpha stimulation. Zinc Oxide 30-33 vascular cell adhesion molecule 1 Homo sapiens 100-133 32570911-6 2020 RESULTS: Our data showed that ZnO was able to reduce the inflammatory response of DECs, in terms of vascular cell adhesion molecule-1 (VCAM-1), interleukin (IL)-8, IL-6, tumor necrosis factor-alpha (TNF-alpha) and monocyte chemoattractant protein-1 (MCP-1) expression induced by TNF-alpha stimulation. Zinc Oxide 30-33 vascular cell adhesion molecule 1 Homo sapiens 135-141 32570911-6 2020 RESULTS: Our data showed that ZnO was able to reduce the inflammatory response of DECs, in terms of vascular cell adhesion molecule-1 (VCAM-1), interleukin (IL)-8, IL-6, tumor necrosis factor-alpha (TNF-alpha) and monocyte chemoattractant protein-1 (MCP-1) expression induced by TNF-alpha stimulation. Zinc Oxide 30-33 C-X-C motif chemokine ligand 8 Homo sapiens 144-162 32570911-6 2020 RESULTS: Our data showed that ZnO was able to reduce the inflammatory response of DECs, in terms of vascular cell adhesion molecule-1 (VCAM-1), interleukin (IL)-8, IL-6, tumor necrosis factor-alpha (TNF-alpha) and monocyte chemoattractant protein-1 (MCP-1) expression induced by TNF-alpha stimulation. Zinc Oxide 30-33 interleukin 6 Homo sapiens 164-168 32570911-6 2020 RESULTS: Our data showed that ZnO was able to reduce the inflammatory response of DECs, in terms of vascular cell adhesion molecule-1 (VCAM-1), interleukin (IL)-8, IL-6, tumor necrosis factor-alpha (TNF-alpha) and monocyte chemoattractant protein-1 (MCP-1) expression induced by TNF-alpha stimulation. Zinc Oxide 30-33 tumor necrosis factor Homo sapiens 170-197 32570911-6 2020 RESULTS: Our data showed that ZnO was able to reduce the inflammatory response of DECs, in terms of vascular cell adhesion molecule-1 (VCAM-1), interleukin (IL)-8, IL-6, tumor necrosis factor-alpha (TNF-alpha) and monocyte chemoattractant protein-1 (MCP-1) expression induced by TNF-alpha stimulation. Zinc Oxide 30-33 tumor necrosis factor Homo sapiens 199-208 32570911-6 2020 RESULTS: Our data showed that ZnO was able to reduce the inflammatory response of DECs, in terms of vascular cell adhesion molecule-1 (VCAM-1), interleukin (IL)-8, IL-6, tumor necrosis factor-alpha (TNF-alpha) and monocyte chemoattractant protein-1 (MCP-1) expression induced by TNF-alpha stimulation. Zinc Oxide 30-33 C-C motif chemokine ligand 2 Homo sapiens 214-248 32570911-6 2020 RESULTS: Our data showed that ZnO was able to reduce the inflammatory response of DECs, in terms of vascular cell adhesion molecule-1 (VCAM-1), interleukin (IL)-8, IL-6, tumor necrosis factor-alpha (TNF-alpha) and monocyte chemoattractant protein-1 (MCP-1) expression induced by TNF-alpha stimulation. Zinc Oxide 30-33 C-C motif chemokine ligand 2 Homo sapiens 250-255 32570911-6 2020 RESULTS: Our data showed that ZnO was able to reduce the inflammatory response of DECs, in terms of vascular cell adhesion molecule-1 (VCAM-1), interleukin (IL)-8, IL-6, tumor necrosis factor-alpha (TNF-alpha) and monocyte chemoattractant protein-1 (MCP-1) expression induced by TNF-alpha stimulation. Zinc Oxide 30-33 tumor necrosis factor Homo sapiens 279-288 32169638-5 2020 Binary mixtures of ZnO NPs-HAs (ZnO NPs-HALP or ZnO NPs-LHA) showed negligible alterations of micronuclei (MN) formation in challenged cells, with cytotoxic effects revealed only in case of cells treated with ZnO NPs-LHA at the concentration 5-20 mug mL-1. Zinc Oxide 19-22 L1 cell adhesion molecule Mus musculus 251-255 32512766-1 2020 Zinc oxide nanoparticles were prepared from Zn5(CO3)2(OH)6 precursor, capped with poly(vinylpyrrolidone) (PVP), and annealed at 600 C. The obtained powders were characterized by a powder X-ray diffraction (PXD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), UV-visible spectroscopy (UV-vis), Raman spectroscopy, infrared spectroscopy (IR), thermal analysis (TGA/DTA), and third-order nonlinear (NL) optical measurement. Zinc Oxide 0-10 T-box transcription factor 1 Homo sapiens 389-392 32377776-0 2020 MTH1 is involved in the toxic and carcinogenic long-term effects induced by zinc oxide and cobalt nanoparticles. Zinc Oxide 76-86 nudix hydrolase 1 Homo sapiens 0-4 32377776-5 2020 In the present work, a significantly marked overexpression was found when MTH1 levels were monitored in long-term ZnO and Co NP-exposed cells, a fact that correlates with acquired 2.5-fold and 3.75-fold resistance to the ZnO and Co NPs treatment, respectively. Zinc Oxide 114-117 nudix hydrolase 1 Homo sapiens 74-78 32377776-5 2020 In the present work, a significantly marked overexpression was found when MTH1 levels were monitored in long-term ZnO and Co NP-exposed cells, a fact that correlates with acquired 2.5-fold and 3.75-fold resistance to the ZnO and Co NPs treatment, respectively. Zinc Oxide 221-224 nudix hydrolase 1 Homo sapiens 74-78 32346997-0 2020 From Precursor Chemistry to Gas Sensors: Plasma-Enhanced Atomic Layer Deposition Process Engineering for Zinc Oxide Layers from a Nonpyrophoric Zinc Precursor for Gas Barrier and Sensor Applications. Zinc Oxide 105-115 gastrin Homo sapiens 163-166 32346997-6 2020 As a representative application of the ZnO layers, the gas sensing properties are investigated. Zinc Oxide 39-42 gastrin Homo sapiens 55-58 32126253-5 2020 We next addressed lysosomal function impairment and changes in LC3-II and p62 levels following exposure to TiO2, ZnO, and ZnSO4. Zinc Oxide 113-116 nucleoporin 62 Mus musculus 74-77 32068061-3 2020 CS coated-ZnO nanoparticles were synthesized by a co-precipitation method in the presence of CS. Zinc Oxide 10-13 citrate synthase Homo sapiens 0-2 32319286-2 2020 The present study was designed to determine the effects of silica dioxide (SiO2), titanium dioxide (TiO2), and zinc oxide (ZnO) NPs on cultured THP-1 monocyte-derived macrophages and human epithelial colorectal adenocarcinoma (Caco-2) cells. Zinc Oxide 111-121 GLI family zinc finger 2 Homo sapiens 144-149 32319286-2 2020 The present study was designed to determine the effects of silica dioxide (SiO2), titanium dioxide (TiO2), and zinc oxide (ZnO) NPs on cultured THP-1 monocyte-derived macrophages and human epithelial colorectal adenocarcinoma (Caco-2) cells. Zinc Oxide 123-126 GLI family zinc finger 2 Homo sapiens 144-149 32319286-3 2020 Exposure to ZnO NPs for 24 hours increased the production of redox response species (ROS) and reduced cell viability in a dose-dependent manner in THP-1 macrophages and Caco-2 cells. Zinc Oxide 12-15 GLI family zinc finger 2 Homo sapiens 147-152 32068061-3 2020 CS coated-ZnO nanoparticles were synthesized by a co-precipitation method in the presence of CS. Zinc Oxide 10-13 citrate synthase Homo sapiens 93-95 32252911-0 2020 A sandwich-type ECL immunosensor based on signal amplification using a ZnO nanorods-L-cysteine-luminol nanocomposite for ultrasensitive detection of prostate specific antigen. Zinc Oxide 71-74 kallikrein related peptidase 3 Homo sapiens 149-174 32297504-4 2020 To overcome these issues and enhance the functionalities, we envision the substantial piezopotential in a zinc oxide (ZnO)/muscovite (mica) heteroepitaxy system based on theoretical consideration and realize it in practice. Zinc Oxide 106-116 MHC class I polypeptide-related sequence A Homo sapiens 134-138 32297504-4 2020 To overcome these issues and enhance the functionalities, we envision the substantial piezopotential in a zinc oxide (ZnO)/muscovite (mica) heteroepitaxy system based on theoretical consideration and realize it in practice. Zinc Oxide 118-121 MHC class I polypeptide-related sequence A Homo sapiens 134-138 32252911-1 2020 An ultrasensitive sandwich-type electrochemiluminescence (ECL) immunosensor was developed for detection of prostate specific antigen (PSA) using an amplification strategy based on ZnO nanorods-l-cysteine-luminol nanocomposites and the biotin-streptavidin system. Zinc Oxide 180-183 kallikrein related peptidase 3 Homo sapiens 107-132 32252911-1 2020 An ultrasensitive sandwich-type electrochemiluminescence (ECL) immunosensor was developed for detection of prostate specific antigen (PSA) using an amplification strategy based on ZnO nanorods-l-cysteine-luminol nanocomposites and the biotin-streptavidin system. Zinc Oxide 180-183 kallikrein related peptidase 3 Homo sapiens 134-137 32368048-14 2020 Conclusion: Our findings unveiled the potential harmful effects of ZnO NPs to human cardiomyocytes that involve mitochondrial biogenesis and the PGC-1alpha pathway that could affect cardiac electrophysiological function. Zinc Oxide 67-70 PPARG coactivator 1 alpha Homo sapiens 145-155 32337854-5 2020 Ag, CuO, and ZnO induced caspase 3 generated apoptosis in both cell types is accompanied by ion shedding and generation of mitochondrial reactive oxygen species (ROS) in both cell types. Zinc Oxide 13-16 caspase 3 Mus musculus 25-34 32391486-4 2020 The ZnO nanorods of the gas-sensing material were directly grown on 2 inch AlGaN-based LEDs containing thousands of independent light-emitting chips, leading to photosensitive materials with uniform and controllable, as well as a sensor with low power consumption and mass manufacture with low cost. Zinc Oxide 4-7 gastrin Homo sapiens 24-27 32004598-0 2020 Interaction with zinc oxide nanoparticle kinetically traps alpha-synuclein fibrillation into off-pathway non-toxic intermediates. Zinc Oxide 17-27 synuclein alpha Homo sapiens 59-74 32004598-6 2020 In this context, our study explores the zinc oxide nanoparticle (ZnONP) with negative surface potential interface interaction with alpha-synuclein, and subsequent impact of the interaction on the protein fibrillation and the fibril-mediated cytotoxicity. Zinc Oxide 40-50 synuclein alpha Homo sapiens 131-146 32032711-0 2020 Chitosan and chitosan-zinc oxide nanocomposite inhibit expression of LasI and RhlI genes and quorum sensing dependent virulence factors of Pseudomonas aeruginosa. Zinc Oxide 22-32 acyl-homoserine-lactone synthase Pseudomonas aeruginosa PAO1 78-82 32326005-0 2020 Nanostructured ZnO/Ag Film Prepared by Magnetron Sputtering Method for Fast Response of Ammonia Gas Detection. Zinc Oxide 15-18 gastrin Homo sapiens 96-99 32326005-2 2020 Here, we propose a fast-response ammonia gas sensor based on porous nanostructured zinc oxide (ZnO) film, which is fabricated through physical vapor deposition and subsequent thermal annealing. Zinc Oxide 83-93 gastrin Homo sapiens 41-44 32326005-2 2020 Here, we propose a fast-response ammonia gas sensor based on porous nanostructured zinc oxide (ZnO) film, which is fabricated through physical vapor deposition and subsequent thermal annealing. Zinc Oxide 95-98 gastrin Homo sapiens 41-44 32326005-5 2020 Different thicknesses of the Ag layer help the formation of different sizes and quantities of hollows uniformly distributed in the ZnO film, which is demonstrated to hold superior gas sensing abilities than the compact ZnO film. Zinc Oxide 131-134 gastrin Homo sapiens 180-183 32326005-7 2020 Experimental results demonstrate that the ZnO/Ag(3 nm) sensor possesses a good electrical resistance variation of 85.74% after exposing the sample to 300 ppm ammonia gas for 310 s. Interestingly, a fast response of 61.18% in 60 s for 300 ppm ammonia gas has been achieved from the ZnO/Ag(5 nm) sensor, which costs only 6 s for the response increase to 10%. Zinc Oxide 42-45 gastrin Homo sapiens 166-169 32326005-7 2020 Experimental results demonstrate that the ZnO/Ag(3 nm) sensor possesses a good electrical resistance variation of 85.74% after exposing the sample to 300 ppm ammonia gas for 310 s. Interestingly, a fast response of 61.18% in 60 s for 300 ppm ammonia gas has been achieved from the ZnO/Ag(5 nm) sensor, which costs only 6 s for the response increase to 10%. Zinc Oxide 42-45 gastrin Homo sapiens 250-253 32326005-8 2020 Therefore, this controllable, porous, nanostructured ZnO film maintaining a sensitive gas response, fabricated by the physical deposition approach, will be of great interest to the gas-sensing community. Zinc Oxide 53-56 gastrin Homo sapiens 86-89 32326005-8 2020 Therefore, this controllable, porous, nanostructured ZnO film maintaining a sensitive gas response, fabricated by the physical deposition approach, will be of great interest to the gas-sensing community. Zinc Oxide 53-56 gastrin Homo sapiens 181-184 32112740-8 2020 Exposure of HTFs to ZnO nanoparticles could also induce the elevated Caspase-3, Caspase-9, and Apaf-1 expression, decrease the levels of FSP-1, collagen III, and E-cadherin expression, leading to HTFs apoptosis. Zinc Oxide 20-23 caspase 3 Homo sapiens 69-78 32112740-8 2020 Exposure of HTFs to ZnO nanoparticles could also induce the elevated Caspase-3, Caspase-9, and Apaf-1 expression, decrease the levels of FSP-1, collagen III, and E-cadherin expression, leading to HTFs apoptosis. Zinc Oxide 20-23 caspase 9 Homo sapiens 80-89 32112740-8 2020 Exposure of HTFs to ZnO nanoparticles could also induce the elevated Caspase-3, Caspase-9, and Apaf-1 expression, decrease the levels of FSP-1, collagen III, and E-cadherin expression, leading to HTFs apoptosis. Zinc Oxide 20-23 apoptotic peptidase activating factor 1 Homo sapiens 95-101 32112740-8 2020 Exposure of HTFs to ZnO nanoparticles could also induce the elevated Caspase-3, Caspase-9, and Apaf-1 expression, decrease the levels of FSP-1, collagen III, and E-cadherin expression, leading to HTFs apoptosis. Zinc Oxide 20-23 S100 calcium binding protein A4 Homo sapiens 137-142 32112740-8 2020 Exposure of HTFs to ZnO nanoparticles could also induce the elevated Caspase-3, Caspase-9, and Apaf-1 expression, decrease the levels of FSP-1, collagen III, and E-cadherin expression, leading to HTFs apoptosis. Zinc Oxide 20-23 cadherin 1 Homo sapiens 162-172 32112740-9 2020 Our results suggested that elevated ROS and activated Caspase signaling play a fundamental role in ZnO nanoparticle-induced HTFs apoptosis. Zinc Oxide 99-102 caspase 9 Homo sapiens 54-61 32308073-4 2021 The level of TGF (transforming growth factor)-beta1 cytokine was also elevated significantly in the burn tissue treated with ROCEN almost the same as zinc oxide cream. Zinc Oxide 150-160 transforming growth factor, beta 1 Rattus norvegicus 18-51 32112740-0 2020 Zinc oxide nanoparticles induce human tenon fibroblast apoptosis through reactive oxygen species and caspase signaling pathway. Zinc Oxide 0-10 caspase 9 Homo sapiens 101-108 32112740-3 2020 Our previous study has revealed that zinc oxide (ZnO) nanoparticles could efficiently decrease the expressions of TGF-beta1 and inhibit fibroblast-mediated collagen lattice contraction. Zinc Oxide 37-47 transforming growth factor beta 1 Homo sapiens 114-123 32112740-3 2020 Our previous study has revealed that zinc oxide (ZnO) nanoparticles could efficiently decrease the expressions of TGF-beta1 and inhibit fibroblast-mediated collagen lattice contraction. Zinc Oxide 49-52 transforming growth factor beta 1 Homo sapiens 114-123 32112740-6 2020 Moreover, we also explored the influence of ZnO nanoparticles on the expression of Caspase-3, Caspase-9, apoptotic protease-activating factor-1 (Apaf-1), fibroblast-specific protein-1 (FSP-1), collagen III, and E-cadherin. Zinc Oxide 44-47 caspase 3 Homo sapiens 83-92 32337421-1 2020 A robust synthesis approach to develop CuO/ZnO nanocomposites using microwave-epoxide-assisted hydrothermal synthesis and their proficiency toward H2S gas-sensing application are reported. Zinc Oxide 43-46 gastrin Homo sapiens 151-154 32294608-12 2020 At the lower ZnO nanoparticle concentration, only Slc30a7 mRNA levels in the lungs were up (1.74 fold). Zinc Oxide 13-16 solute carrier family 30 (zinc transporter), member 7 Mus musculus 50-57 32433029-0 2020 High-performance immunosensor for urine albumin using hybrid architectures of ZnO nanowire/carbon nanotube. Zinc Oxide 78-81 albumin Homo sapiens 40-47 32433029-1 2020 In this work, the authors reported the hybrid architecture of carbon nanotube (CNT)-zinc oxide (ZnO) nanowire as a multi-functional probe in amperometric immunosensor for the detection of urine albumin. Zinc Oxide 84-94 albumin Homo sapiens 194-201 32433029-1 2020 In this work, the authors reported the hybrid architecture of carbon nanotube (CNT)-zinc oxide (ZnO) nanowire as a multi-functional probe in amperometric immunosensor for the detection of urine albumin. Zinc Oxide 96-99 albumin Homo sapiens 194-201 32230816-7 2020 At the studied concentrations (40 mg L-1, 80 mg L-1, 120 mg L-1), ZnO NPs had obvious impacts on the activity of Proteobacteria. Zinc Oxide 66-69 L1 cell adhesion molecule Homo sapiens 37-40 32230816-7 2020 At the studied concentrations (40 mg L-1, 80 mg L-1, 120 mg L-1), ZnO NPs had obvious impacts on the activity of Proteobacteria. Zinc Oxide 66-69 L1 cell adhesion molecule Homo sapiens 48-51 32230816-7 2020 At the studied concentrations (40 mg L-1, 80 mg L-1, 120 mg L-1), ZnO NPs had obvious impacts on the activity of Proteobacteria. Zinc Oxide 66-69 L1 cell adhesion molecule Homo sapiens 48-51 32193477-4 2020 Herein, we account for a novel electrocatalyst as electrode material that comprised ZnO nanoparticles decorated on the surface of polyindole (PIn)-multi-walled carbon nanotube (MWCNT), for the immobilization of glucose oxidase (GOx) enzyme and mediator (Ferritin). Zinc Oxide 84-87 hydroxyacid oxidase 1 Homo sapiens 211-226 32193477-4 2020 Herein, we account for a novel electrocatalyst as electrode material that comprised ZnO nanoparticles decorated on the surface of polyindole (PIn)-multi-walled carbon nanotube (MWCNT), for the immobilization of glucose oxidase (GOx) enzyme and mediator (Ferritin). Zinc Oxide 84-87 hydroxyacid oxidase 1 Homo sapiens 228-231 32124101-7 2020 Quantitative real-time PCR data showed that the mRNA levels of apoptotic marker genes such as p53, bax, and caspase-3 were upregulated, whereas bcl-2, an anti-apoptotic gene, was downregulated; therefore, apoptosis was mediated through the p53, bax, caspase-3, and bcl-2 pathways, suggesting a possible mechanism by which QDs and NPs of ZnO mediate their toxicity.Graphic abstract. Zinc Oxide 337-340 tumor protein p53 Homo sapiens 94-97 32050064-3 2020 Herein, for the first time we report that pro-angiogenic nanomaterials, zinc oxide nanoflowers (ZONF), exhibit neuritogenic activity by elevating mRNA expression of different neurotrophins, following PI3K/Akt-MAPK/ERK signaling pathways. Zinc Oxide 72-82 AKT serine/threonine kinase 1 Rattus norvegicus 205-208 32050064-3 2020 Herein, for the first time we report that pro-angiogenic nanomaterials, zinc oxide nanoflowers (ZONF), exhibit neuritogenic activity by elevating mRNA expression of different neurotrophins, following PI3K/Akt-MAPK/ERK signaling pathways. Zinc Oxide 72-82 Eph receptor B1 Rattus norvegicus 214-217 32168923-0 2020 Highly Rectifying Heterojunctions Formed by Annealed ZnO Nanorods on GaN Substrates. Zinc Oxide 53-56 gigaxonin Homo sapiens 69-72 32168923-2 2020 The ZnO nanorods are prepared by chemical bath deposition on both plain GaN substrates and on the substrates locally patterned by focused ion beam lithography. Zinc Oxide 4-7 gigaxonin Homo sapiens 72-75 32168923-5 2020 The specific configuration of the interface between the ZnO nanorods and GaN substrate created by the focused ion beam suppresses the surface leakage current and improves the current-voltage characteristics. Zinc Oxide 56-59 gigaxonin Homo sapiens 73-76 31727532-5 2020 Combined with DRS, PL and BET, the influence of calcination temperature on photocatalytic activities of as-synthesized zinc oxide were discussed as compared with commercial zinc oxide. Zinc Oxide 119-129 sushi repeat containing protein X-linked Homo sapiens 14-17 31727532-5 2020 Combined with DRS, PL and BET, the influence of calcination temperature on photocatalytic activities of as-synthesized zinc oxide were discussed as compared with commercial zinc oxide. Zinc Oxide 119-129 delta/notch like EGF repeat containing Homo sapiens 26-29 31732340-5 2020 Upon incorporating with ZnO NPs, the electrosorption efficiency was enhanced from 17% to 33% for Pb2+, from 21% to 29% for Cd2+ and from 21% to 35% for mixed Pb2+ and Cd2+ ions. Zinc Oxide 24-27 CD2 molecule Homo sapiens 123-126 31732340-5 2020 Upon incorporating with ZnO NPs, the electrosorption efficiency was enhanced from 17% to 33% for Pb2+, from 21% to 29% for Cd2+ and from 21% to 35% for mixed Pb2+ and Cd2+ ions. Zinc Oxide 24-27 CD2 molecule Homo sapiens 167-170 30938584-0 2020 Effects of nanoparticle size on the interaction between zinc oxide nanoparticles and bovine serum albumin. Zinc Oxide 56-66 albumin Homo sapiens 92-105 32124101-7 2020 Quantitative real-time PCR data showed that the mRNA levels of apoptotic marker genes such as p53, bax, and caspase-3 were upregulated, whereas bcl-2, an anti-apoptotic gene, was downregulated; therefore, apoptosis was mediated through the p53, bax, caspase-3, and bcl-2 pathways, suggesting a possible mechanism by which QDs and NPs of ZnO mediate their toxicity.Graphic abstract. Zinc Oxide 337-340 BCL2 apoptosis regulator Homo sapiens 144-149 31922397-3 2020 Gas-sensitive zinc oxide (ZnO) nanowires were directly synthesized on top of the muLED through a hydrothermal reaction. Zinc Oxide 14-24 gastrin Homo sapiens 0-3 32129155-0 2020 Samarium enriches antitumor activity of ZnO nanoparticles via downregulation of CXCR4 receptor and cytochrome P450. Zinc Oxide 40-43 C-X-C motif chemokine receptor 4 Homo sapiens 80-85 32129155-0 2020 Samarium enriches antitumor activity of ZnO nanoparticles via downregulation of CXCR4 receptor and cytochrome P450. Zinc Oxide 40-43 cytochrome P450 family 4 subfamily F member 3 Homo sapiens 99-114 32129155-2 2020 Zinc oxide nanoparticles play an effective role in tumor treatment but with some cautions, such as overexpression of cytochrome P450, hepatic overload, and the mammalian target of rapamycin pathway resistance. Zinc Oxide 0-10 cytochrome P450 family 4 subfamily F member 3 Homo sapiens 117-132 32129155-2 2020 Zinc oxide nanoparticles play an effective role in tumor treatment but with some cautions, such as overexpression of cytochrome P450, hepatic overload, and the mammalian target of rapamycin pathway resistance. Zinc Oxide 0-10 mechanistic target of rapamycin kinase Homo sapiens 160-189 32129155-6 2020 The in vivo experiment on mice bearing Ehrlich solid tumor revealed that intramuscular injection of samarium/zinc oxide downregulates the expressions of CXCR4 and PI3K/Akt/mammalian target of rapamycin pathway in respect to Ehrlich solid tumor group. Zinc Oxide 109-119 chemokine (C-X-C motif) receptor 4 Mus musculus 153-158 32129155-6 2020 The in vivo experiment on mice bearing Ehrlich solid tumor revealed that intramuscular injection of samarium/zinc oxide downregulates the expressions of CXCR4 and PI3K/Akt/mammalian target of rapamycin pathway in respect to Ehrlich solid tumor group. Zinc Oxide 109-119 thymoma viral proto-oncogene 1 Mus musculus 168-171 32129155-6 2020 The in vivo experiment on mice bearing Ehrlich solid tumor revealed that intramuscular injection of samarium/zinc oxide downregulates the expressions of CXCR4 and PI3K/Akt/mammalian target of rapamycin pathway in respect to Ehrlich solid tumor group. Zinc Oxide 109-119 mechanistic target of rapamycin kinase Homo sapiens 172-201 32129155-7 2020 Regarding the apoptotic biomarkers, samarium/zinc oxide upregulates the apoptotic biomarker; Bax accompanied with the mitotic catastrophe which was indicated by cell cycle arrest in G2 phase. Zinc Oxide 45-55 BCL2 associated X, apoptosis regulator Homo sapiens 93-96 32129155-8 2020 Moreover, samarium:zinc oxide nanoparticles exhibited minimum toxicity which was indicated by suppressed activities of cytochrome P450 and hepatic enzymes, including alanine transaminase and aspartate transaminase. Zinc Oxide 19-29 cytochrome P450 family 4 subfamily F member 3 Homo sapiens 119-134 32597415-8 2020 The Ag (0.02%)-Ni doped ZnO NPs exhibits highest photocatalytic activity of 77% under pH 4. Zinc Oxide 24-27 prolyl 4-hydroxylase, transmembrane Homo sapiens 86-90 31922397-3 2020 Gas-sensitive zinc oxide (ZnO) nanowires were directly synthesized on top of the muLED through a hydrothermal reaction. Zinc Oxide 26-29 gastrin Homo sapiens 0-3 32180717-5 2020 Several gene expression involved in apoptosis was regulated by ZnO QDs, including bcl-2 gene and caspase. Zinc Oxide 63-66 BCL2 apoptosis regulator Homo sapiens 82-87 32033506-5 2020 Our results show that non-functionalized spherical zinc oxide nanoparticles with surface density N = 5.89 x 10-6 mol/m2, protonation and deprotonation rates pKa = 10.9 and pKb = -5.5, and NP size in the range of 20-50 nm are the most effective, smart anti-cancer agents for biomedical treatments. Zinc Oxide 51-61 AKT serine/threonine kinase 1 Homo sapiens 172-175 32399224-8 2020 Results: The results indicated that the penicillin G removal efficiency of photocatalytic process [UV/ZnO] using ZnO was 74.65% at the concentration of 10 mgL-1, the pH value of 5, the ZnO NP dosage of 0.1 gL-1 and the contact time of 180 min, as well as the kinetics of degradation followed the pseudo-first-order kinetic model. Zinc Oxide 102-105 LLGL scribble cell polarity complex component 1 Homo sapiens 155-160 32399224-8 2020 Results: The results indicated that the penicillin G removal efficiency of photocatalytic process [UV/ZnO] using ZnO was 74.65% at the concentration of 10 mgL-1, the pH value of 5, the ZnO NP dosage of 0.1 gL-1 and the contact time of 180 min, as well as the kinetics of degradation followed the pseudo-first-order kinetic model. Zinc Oxide 113-116 LLGL scribble cell polarity complex component 1 Homo sapiens 155-160 31748192-0 2020 Resonance Raman scattering-infrared absorption dual-mode immunosensing for carcinoembryonic antigen based on ZnO@SiO2 nanocomposites. Zinc Oxide 109-112 CEA cell adhesion molecule 3 Homo sapiens 75-99 31748192-3 2020 In this work, a reliable and sensitive dual-mode immunosensing method is described for carcinoembryonic antigen (CEA) detection using a biofunctional ZnO@SiO2 nanocomposite as a resonance Raman scattering (RRS)-infrared (IR) absorption nanoprobe. Zinc Oxide 150-153 CEA cell adhesion molecule 3 Homo sapiens 87-111 31748192-3 2020 In this work, a reliable and sensitive dual-mode immunosensing method is described for carcinoembryonic antigen (CEA) detection using a biofunctional ZnO@SiO2 nanocomposite as a resonance Raman scattering (RRS)-infrared (IR) absorption nanoprobe. Zinc Oxide 150-153 CEA cell adhesion molecule 3 Homo sapiens 113-116 32111101-0 2020 ZnO Nanoparticles Induced Caspase-Dependent Apoptosis in Gingival Squamous Cell Carcinoma through Mitochondrial Dysfunction and p70S6K Signaling Pathway. Zinc Oxide 0-3 ribosomal protein S6 kinase B1 Homo sapiens 128-134 32111101-12 2020 Collectively, these results suggest that ZnO-NPs induce apoptosis through the mitochondrial oxidative damage and p70S6K signaling pathway in human GSCC. Zinc Oxide 41-44 ribosomal protein S6 kinase B1 Homo sapiens 113-119 31385191-8 2020 In addition, the levels of serum IL-1beta and LPS-binding protein were also decreased by ZnO treatment. Zinc Oxide 89-92 interleukin 1 beta Mus musculus 33-41 31918281-0 2020 Zinc oxide nanoparticles induce human multiple myeloma cell death via reactive oxygen species and Cyt-C/Apaf-1/Caspase-9/Caspase-3 signaling pathway in vitro. Zinc Oxide 0-10 cytochrome c, somatic Homo sapiens 98-103 31918281-0 2020 Zinc oxide nanoparticles induce human multiple myeloma cell death via reactive oxygen species and Cyt-C/Apaf-1/Caspase-9/Caspase-3 signaling pathway in vitro. Zinc Oxide 0-10 apoptotic peptidase activating factor 1 Homo sapiens 104-110 31918281-0 2020 Zinc oxide nanoparticles induce human multiple myeloma cell death via reactive oxygen species and Cyt-C/Apaf-1/Caspase-9/Caspase-3 signaling pathway in vitro. Zinc Oxide 0-10 caspase 9 Homo sapiens 111-120 31918281-0 2020 Zinc oxide nanoparticles induce human multiple myeloma cell death via reactive oxygen species and Cyt-C/Apaf-1/Caspase-9/Caspase-3 signaling pathway in vitro. Zinc Oxide 0-10 caspase 3 Homo sapiens 121-130 31383118-1 2020 ZnO nanorods were grown on silicon (Si) substrates by two techniques: (i) Chemical Bath Deposition (CBD) and (ii) a CBD seed layer combined with Carbothermal Reduction Vapor Phase Transport (CTR-VPT). Zinc Oxide 0-3 calcitonin receptor Homo sapiens 191-194 31383118-6 2020 The presence of ZnO was further confirmed by XPS and contact angle measurements showed that ZnO grown by CBD (ZnO/CBD) had a slightly hydrophobic behavior while ZnO grown by CTR-VPT (ZnO/CTR-VPT) is hydrophilic. Zinc Oxide 16-19 calcitonin receptor Homo sapiens 174-177 31383118-6 2020 The presence of ZnO was further confirmed by XPS and contact angle measurements showed that ZnO grown by CBD (ZnO/CBD) had a slightly hydrophobic behavior while ZnO grown by CTR-VPT (ZnO/CTR-VPT) is hydrophilic. Zinc Oxide 16-19 calcitonin receptor Homo sapiens 187-190 31762255-1 2020 This work reports a ZIF-8 (ZIF: Zeolitic Imidazolate Framework)-assisted NaYF4:Yb,Tm@ZnO upconverter for the photoelectrochemical (PEC) biosensing of carcinoembryonic antigen (CEA) under near-infrared (NIR) irradiation on a homemade 3D-printed device with DNA walker-based amplification strategy. Zinc Oxide 85-88 CEA cell adhesion molecule 3 Homo sapiens 150-174 31676262-9 2020 MgO and ZnO NPs in the presence of stress increased the glutamate level and ZnO NPs increased the zinc and the NR2A expression. Zinc Oxide 8-11 glutamate ionotropic receptor NMDA type subunit 2A Rattus norvegicus 111-115 31676262-9 2020 MgO and ZnO NPs in the presence of stress increased the glutamate level and ZnO NPs increased the zinc and the NR2A expression. Zinc Oxide 76-79 glutamate ionotropic receptor NMDA type subunit 2A Rattus norvegicus 111-115 31940100-0 2020 New Immunosensing-Fluorescence Detection of Tumor Marker Cytokeratin-19 Fragment (CYFRA 21-1) Via Carbon Quantum Dots/Zinc Oxide Nanocomposite. Zinc Oxide 118-128 keratin 19 Homo sapiens 57-71 31762255-1 2020 This work reports a ZIF-8 (ZIF: Zeolitic Imidazolate Framework)-assisted NaYF4:Yb,Tm@ZnO upconverter for the photoelectrochemical (PEC) biosensing of carcinoembryonic antigen (CEA) under near-infrared (NIR) irradiation on a homemade 3D-printed device with DNA walker-based amplification strategy. Zinc Oxide 85-88 CEA cell adhesion molecule 3 Homo sapiens 176-179 31762255-7 2020 Under optimal conditions, NaYF4:Yb,Tm@ZnO-based NIR light-driven PEC biosensor presented high sensitivity and selectivity for CEA sensing with a detection limit of 0.032 ng mL-1. Zinc Oxide 38-41 CEA cell adhesion molecule 3 Homo sapiens 126-129 31412311-0 2020 Preparation of the plasmonic Ag/AgBr/ZnO film substrate for reusable SERS detection: Implication to the Z-scheme photocatalytic mechanism. Zinc Oxide 37-40 seryl-tRNA synthetase 1 Homo sapiens 69-73 31412311-2 2020 The SERS performances of Ag/AgBr/ZnO substrates were evaluated using aqueous crystal violet (CV) and Rhodamine 6G (R6G) as target analytes. Zinc Oxide 33-36 seryl-tRNA synthetase 1 Homo sapiens 4-8 31412311-10 2020 This study reveals that the Ag/AgBr/ZnO film on glass is practically applicable as an ultra-highly sensitive SERS substrate that can be readily regenerated. Zinc Oxide 36-39 seryl-tRNA synthetase 1 Homo sapiens 109-113 31746300-0 2020 Sm doped ZnO nanowires@PAN nanofibrous membranes for photo-catalytic degradation of dye. Zinc Oxide 9-12 adenosine deaminase 2 Homo sapiens 23-26 31383170-2 2020 Moreover, ZnO nanorods (NR1) obtained on the seed layer prepared by oxidation of Zn films exhibited the faster growth rate than those (NR2) synthesized on the seed layer prepared by spin-coating method due to having access to a sufficient amount of Zn2+ ions. Zinc Oxide 10-13 glutamate ionotropic receptor NMDA type subunit 1 Homo sapiens 24-27 31383170-3 2020 The ZnO nanorods obtained at a precursor concentration of 0.025 M exhibited the highest photocurrent, dark current, and photoresponsivity, with the photoresponsivity and photosensitivity of ZnO NR1 exceeding those of ZnO NR2, owing to the larger surface area. Zinc Oxide 4-7 glutamate ionotropic receptor NMDA type subunit 1 Homo sapiens 194-197 31746300-7 2020 ZnO nanowires showed the optimum morphologies when the ratio of PAN/Zn (Ac)2 was 10:1.5, the decomposition temperature was 150 oC, NH4OH was added in the hydrothermal reaction, respectively. Zinc Oxide 0-3 adenosine deaminase 2 Homo sapiens 64-76 31746300-9 2020 The photodegradation ability of the ZnO @PAN membrane doped with cerium (Sm) was also investigated. Zinc Oxide 36-39 adenosine deaminase 2 Homo sapiens 41-44 31662252-0 2020 Early-life long-term exposure to ZnO nanoparticles suppresses innate immunity regulated by SKN-1/Nrf and the p38 MAPK signaling pathway in Caenorhabditis elegans. Zinc Oxide 33-36 BZIP domain-containing protein;Protein skinhead-1 Caenorhabditis elegans 91-96 32863303-4 2020 Compared with the NC group, porous ZnO at both doses (750 or 1,500 mg/kg) increased serum alkaline phosphatase (ALP), immunoglobulin G (IgG) and insulin-like growth factor 1 (IGF-1) concentrations, but decreased serum glucose (GLU). Zinc Oxide 35-38 alkaline phosphatase, placental Homo sapiens 90-110 32863303-4 2020 Compared with the NC group, porous ZnO at both doses (750 or 1,500 mg/kg) increased serum alkaline phosphatase (ALP), immunoglobulin G (IgG) and insulin-like growth factor 1 (IGF-1) concentrations, but decreased serum glucose (GLU). Zinc Oxide 35-38 alkaline phosphatase, placental Homo sapiens 112-115 32863303-4 2020 Compared with the NC group, porous ZnO at both doses (750 or 1,500 mg/kg) increased serum alkaline phosphatase (ALP), immunoglobulin G (IgG) and insulin-like growth factor 1 (IGF-1) concentrations, but decreased serum glucose (GLU). Zinc Oxide 35-38 insulin like growth factor 1 Homo sapiens 145-173 32863303-4 2020 Compared with the NC group, porous ZnO at both doses (750 or 1,500 mg/kg) increased serum alkaline phosphatase (ALP), immunoglobulin G (IgG) and insulin-like growth factor 1 (IGF-1) concentrations, but decreased serum glucose (GLU). Zinc Oxide 35-38 insulin like growth factor 1 Homo sapiens 175-180 32863303-5 2020 Moreover, the mRNA expression of anti-inflammation cytokine (TGF-beta), tight junction (Occludin, ZO-1) in the jejunum by different ZnO administration were significantly increased compared with the NC group, while mRNA expression of pro-inflammatory (IL-8), membrane channels that transport water (AQP3) and miR-122a were significantly decreased. Zinc Oxide 132-135 transforming growth factor alpha Homo sapiens 61-69 32863303-5 2020 Moreover, the mRNA expression of anti-inflammation cytokine (TGF-beta), tight junction (Occludin, ZO-1) in the jejunum by different ZnO administration were significantly increased compared with the NC group, while mRNA expression of pro-inflammatory (IL-8), membrane channels that transport water (AQP3) and miR-122a were significantly decreased. Zinc Oxide 132-135 occludin Homo sapiens 88-96 32863303-5 2020 Moreover, the mRNA expression of anti-inflammation cytokine (TGF-beta), tight junction (Occludin, ZO-1) in the jejunum by different ZnO administration were significantly increased compared with the NC group, while mRNA expression of pro-inflammatory (IL-8), membrane channels that transport water (AQP3) and miR-122a were significantly decreased. Zinc Oxide 132-135 tight junction protein 1 Homo sapiens 98-102 32863303-5 2020 Moreover, the mRNA expression of anti-inflammation cytokine (TGF-beta), tight junction (Occludin, ZO-1) in the jejunum by different ZnO administration were significantly increased compared with the NC group, while mRNA expression of pro-inflammatory (IL-8), membrane channels that transport water (AQP3) and miR-122a were significantly decreased. Zinc Oxide 132-135 C-X-C motif chemokine ligand 8 Homo sapiens 251-255 32863303-5 2020 Moreover, the mRNA expression of anti-inflammation cytokine (TGF-beta), tight junction (Occludin, ZO-1) in the jejunum by different ZnO administration were significantly increased compared with the NC group, while mRNA expression of pro-inflammatory (IL-8), membrane channels that transport water (AQP3) and miR-122a were significantly decreased. Zinc Oxide 132-135 aquaporin 3 (Gill blood group) Homo sapiens 298-302 32863303-5 2020 Moreover, the mRNA expression of anti-inflammation cytokine (TGF-beta), tight junction (Occludin, ZO-1) in the jejunum by different ZnO administration were significantly increased compared with the NC group, while mRNA expression of pro-inflammatory (IL-8), membrane channels that transport water (AQP3) and miR-122a were significantly decreased. Zinc Oxide 132-135 microRNA 122 Homo sapiens 308-316 31746300-12 2020 CONCLUSION: Sm doped ZnO nanowires @PAN nanofibrous membranes were easily produced and could provide a novel process for degradation on dye decontamination. Zinc Oxide 21-24 adenosine deaminase 2 Homo sapiens 36-39 31746300-3 2020 OBJECTIVE: Polyacrylonitrile (PAN) nanofibrous membranes loaded with zinc oxide (ZnO) nanowires were fabricated and evaluated for photocatalytic degradation. Zinc Oxide 69-79 adenosine deaminase 2 Homo sapiens 30-33 31746300-3 2020 OBJECTIVE: Polyacrylonitrile (PAN) nanofibrous membranes loaded with zinc oxide (ZnO) nanowires were fabricated and evaluated for photocatalytic degradation. Zinc Oxide 81-84 adenosine deaminase 2 Homo sapiens 30-33 31746300-4 2020 METHOD: In this work, polyacrylonitrile (PAN) nanofibrous membranes loaded with ZnO seeds were prepared by electrospinning PAN/Zn (Ac)2 solution followed by a thermal decomposition process. Zinc Oxide 80-83 adenosine deaminase 2 Homo sapiens 41-44 31746300-4 2020 METHOD: In this work, polyacrylonitrile (PAN) nanofibrous membranes loaded with ZnO seeds were prepared by electrospinning PAN/Zn (Ac)2 solution followed by a thermal decomposition process. Zinc Oxide 80-83 adenosine deaminase 2 Homo sapiens 123-135 31746300-5 2020 ZnO nanowires were hydrothermally grown on the surface of PAN nanofibers. Zinc Oxide 0-3 adenosine deaminase 2 Homo sapiens 58-61 31746300-6 2020 The effects of the ratio of PAN and zinc acetate in solution, decomposition temperature and ammonia (NH4OH) on the morphologies of ZnO nanowires were observed. Zinc Oxide 131-134 adenosine deaminase 2 Homo sapiens 28-31 31766842-9 2019 The composite of longer ZnO NRs and CNF showed 2.8 x 103 times higher photocurrent and responsivity performance. Zinc Oxide 24-27 NPHS1 adhesion molecule, nephrin Homo sapiens 36-39 31888596-7 2019 The group comparison between filtered air and ZnO exposures showed statistically significant increases of neutrophils and interleukin-8 (IL-8), interleukin-6 (IL-6), matrix metalloproteinase (MMP-9) and tissue inhibitors of metalloproteinases (TIMP-1) in sputum starting at the lowest ZnO concentration of 0.5 mg/m3. Zinc Oxide 46-49 C-X-C motif chemokine ligand 8 Homo sapiens 122-135 31888596-7 2019 The group comparison between filtered air and ZnO exposures showed statistically significant increases of neutrophils and interleukin-8 (IL-8), interleukin-6 (IL-6), matrix metalloproteinase (MMP-9) and tissue inhibitors of metalloproteinases (TIMP-1) in sputum starting at the lowest ZnO concentration of 0.5 mg/m3. Zinc Oxide 46-49 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 31888596-7 2019 The group comparison between filtered air and ZnO exposures showed statistically significant increases of neutrophils and interleukin-8 (IL-8), interleukin-6 (IL-6), matrix metalloproteinase (MMP-9) and tissue inhibitors of metalloproteinases (TIMP-1) in sputum starting at the lowest ZnO concentration of 0.5 mg/m3. Zinc Oxide 46-49 interleukin 6 Homo sapiens 144-157 31888596-7 2019 The group comparison between filtered air and ZnO exposures showed statistically significant increases of neutrophils and interleukin-8 (IL-8), interleukin-6 (IL-6), matrix metalloproteinase (MMP-9) and tissue inhibitors of metalloproteinases (TIMP-1) in sputum starting at the lowest ZnO concentration of 0.5 mg/m3. Zinc Oxide 46-49 interleukin 6 Homo sapiens 159-163 31888596-7 2019 The group comparison between filtered air and ZnO exposures showed statistically significant increases of neutrophils and interleukin-8 (IL-8), interleukin-6 (IL-6), matrix metalloproteinase (MMP-9) and tissue inhibitors of metalloproteinases (TIMP-1) in sputum starting at the lowest ZnO concentration of 0.5 mg/m3. Zinc Oxide 46-49 matrix metallopeptidase 9 Homo sapiens 192-197 31888596-7 2019 The group comparison between filtered air and ZnO exposures showed statistically significant increases of neutrophils and interleukin-8 (IL-8), interleukin-6 (IL-6), matrix metalloproteinase (MMP-9) and tissue inhibitors of metalloproteinases (TIMP-1) in sputum starting at the lowest ZnO concentration of 0.5 mg/m3. Zinc Oxide 46-49 TIMP metallopeptidase inhibitor 1 Homo sapiens 244-250 31849474-0 2019 Heterozygous Disruption of Beclin 1 Alleviates Zinc Oxide Nanoparticles-Induced Disturbance of Cholesterol Biosynthesis in Mouse Liver. Zinc Oxide 47-57 beclin 1, autophagy related Mus musculus 27-35 31842927-0 2019 Role of Nrf2 in inflammatory response in lung of mice exposed to zinc oxide nanoparticles. Zinc Oxide 65-75 nuclear factor, erythroid derived 2, like 2 Mus musculus 8-12 31539365-0 2019 Sputtering control of Ag2O decoration configurations on ZnO nanorods and their surface arrangement effects on photodegradation ability toward methyl orange. Zinc Oxide 56-59 anterior gradient 2, protein disulphide isomerase family member Homo sapiens 22-25 31307228-6 2019 The annealed micro/nanostructured TiO2/ZnO coating exhibited higher hydrophilicity and fibronectin adsorption ability compared to the micro-arc oxidation modified TiO2 coating. Zinc Oxide 39-42 fibronectin 1 Homo sapiens 87-98 31824151-5 2019 The results showed that increased dosage of ZnO NPs correspondingly up-regulated the IRE1alpha, XBP1s, BIP, and CHOP (P<0.05) which are genes related to ER stress. Zinc Oxide 44-47 endoplasmic reticulum (ER) to nucleus signalling 1 Mus musculus 85-94 31824151-5 2019 The results showed that increased dosage of ZnO NPs correspondingly up-regulated the IRE1alpha, XBP1s, BIP, and CHOP (P<0.05) which are genes related to ER stress. Zinc Oxide 44-47 heat shock protein 5 Mus musculus 103-106 31824151-5 2019 The results showed that increased dosage of ZnO NPs correspondingly up-regulated the IRE1alpha, XBP1s, BIP, and CHOP (P<0.05) which are genes related to ER stress. Zinc Oxide 44-47 DNA-damage inducible transcript 3 Mus musculus 112-116 31307228-7 2019 SaOS-2 cells grown on the annealed micro/nanostructured TiO2/ZnO coating showed increased alkaline phosphatase activity and collagen secretion, and immunofluorescence labeling revealed an upregulation of osteopontin, collagen type iota and osteocalcin. Zinc Oxide 61-64 secreted phosphoprotein 1 Homo sapiens 204-215 31529764-3 2019 Herein, a 3D conductive carbon nanofiber framework with gradient-distributed ZnO particles as nucleation seeds (G-CNF) to regulate lithium deposition is proposed. Zinc Oxide 77-80 NPHS1 adhesion molecule, nephrin Homo sapiens 114-117 30997657-3 2019 Two cements have long been used in endodontics-IRM, which is a reinforced zinc oxide cement and Cavit G, a calcium sulphate based cement. Zinc Oxide 74-84 maternally expressed 8, small nucleolar RNA host gene Homo sapiens 47-50 31771091-12 2019 Molecular dynamic simulations revealed association of LL37 onto ZnO NP confirmed by gel shift assay. Zinc Oxide 64-67 cathelicidin antimicrobial peptide Homo sapiens 54-58 31437644-6 2019 The photodegradation followed the first-order kinetics with degradation rate constants (k) ranging between 1.19 x 10-1 and 2.52 x 10-1 min-1 at 20-80 mg L-1 ZnO nanowires. Zinc Oxide 157-160 CD59 molecule (CD59 blood group) Homo sapiens 135-140 31520953-6 2019 Toxic effects of ZnO NPs were observed by a dose-dependent reduction of bacterial growth at >=1 mug ml-1, by teratogenicity and genotoxicity in zebrafish embryos (from 3 to 90 mug ml-1) and by a significant nanoparticle uptake (0.5 ng mul-1) by a fish serum. Zinc Oxide 17-20 mitochondrial E3 ubiquitin protein ligase 1a Danio rerio 237-242 31787980-0 2019 Zinc Oxide Nanowires Exposure Induces a Distinct Inflammatory Response via CCL11-Mediated Eosinophil Recruitment. Zinc Oxide 0-10 chemokine (C-C motif) ligand 11 Mus musculus 75-80 31411486-2 2019 The Zn+-O- surface electronic states of semiconductor oxides were formed on the ZnO surface by Zn 4s and O 2p orbital coupling with the diboron compound"s B 2p orbitals. Zinc Oxide 4-9 immunoglobulin kappa variable 5-2 Homo sapiens 155-159 31411486-2 2019 The Zn+-O- surface electronic states of semiconductor oxides were formed on the ZnO surface by Zn 4s and O 2p orbital coupling with the diboron compound"s B 2p orbitals. Zinc Oxide 80-83 immunoglobulin kappa variable 5-2 Homo sapiens 155-159 31394149-0 2019 Highly selective inhibition of alpha-glucosidase by green synthesised ZnO nanoparticles - In-vitro screening and in-silico docking studies. Zinc Oxide 70-73 sucrase-isomaltase Homo sapiens 31-48 31401269-0 2019 Fabrication of chitosan-based MCS/ZnO@Alg gel microspheres for efficient adsorption of As(V). Zinc Oxide 34-37 SRC proto-oncogene, non-receptor tyrosine kinase Homo sapiens 87-92 31394149-3 2019 Present study investigates the in-vitro antidiabetic activity of ZnO nanoparticles assessing their inhibition efficiency on alpha-glucosidase and alpha-amylase. Zinc Oxide 65-68 sucrase-isomaltase Homo sapiens 124-141 31401269-4 2019 Then, MCS/ZnO@Alg gel beads were fabricated by combining MCS with ZnO and Alg, and crosslinking the composite material in the presence of Ca2+ ions. Zinc Oxide 10-13 Miles-Carpenter X-linked mental retardation syndrome Homo sapiens 57-60 31401269-4 2019 Then, MCS/ZnO@Alg gel beads were fabricated by combining MCS with ZnO and Alg, and crosslinking the composite material in the presence of Ca2+ ions. Zinc Oxide 66-69 Miles-Carpenter X-linked mental retardation syndrome Homo sapiens 6-9 31401269-6 2019 The adsorption experiments revealed that the MCS/ZnO@Alg magnetic gel beads have high stability and As(V) adsorption capability, and adsorbed As(V) through chemical adsorption. Zinc Oxide 49-52 Miles-Carpenter X-linked mental retardation syndrome Homo sapiens 45-48 31401269-6 2019 The adsorption experiments revealed that the MCS/ZnO@Alg magnetic gel beads have high stability and As(V) adsorption capability, and adsorbed As(V) through chemical adsorption. Zinc Oxide 49-52 SRC proto-oncogene, non-receptor tyrosine kinase Homo sapiens 100-105 31401269-6 2019 The adsorption experiments revealed that the MCS/ZnO@Alg magnetic gel beads have high stability and As(V) adsorption capability, and adsorbed As(V) through chemical adsorption. Zinc Oxide 49-52 SRC proto-oncogene, non-receptor tyrosine kinase Homo sapiens 142-147 31401269-8 2019 In addition, MCS/ZnO@Alg exhibited good recyclability and high sustainability. Zinc Oxide 17-20 Miles-Carpenter X-linked mental retardation syndrome Homo sapiens 13-16 31401269-9 2019 This work proves that the MCS/ZnO@Alg gel beads are an ideal candidate for addressing the grievous environmental threats caused by water pollution. Zinc Oxide 30-33 Miles-Carpenter X-linked mental retardation syndrome Homo sapiens 26-29 31394149-9 2019 Molecular docking models were generated for ZnO association with alpha-glucosidase and possible binding sites were recognized. Zinc Oxide 44-47 sucrase-isomaltase Homo sapiens 65-82 31202320-1 2019 In this work, we report a develop of electrochemical immunosensor based on ZnO nanostructures immobilized with ZIKV-NS1 antibody on Printed Circuit Board (PCB). Zinc Oxide 75-78 influenza virus NS1A binding protein Homo sapiens 116-119 31096129-0 2019 UCH-L1 mitigates neurotoxicity induced by ZnO particles via stabilizing the inhibitor of NF-kappa B signaling, IkappaB-alpha. Zinc Oxide 42-45 nuclear factor kappa B subunit 1 Homo sapiens 89-99 31096129-0 2019 UCH-L1 mitigates neurotoxicity induced by ZnO particles via stabilizing the inhibitor of NF-kappa B signaling, IkappaB-alpha. Zinc Oxide 42-45 NFKB inhibitor alpha Homo sapiens 111-124 31096129-1 2019 Our study determined the toxic effects of zinc oxide (ZnO) particles with different diameters on dopaminergic (DA) neurons, the role of ubiquitin C-terminal hydrolase L1 (UCH-L1) for ZnO particles-induced neurotoxicity, and corresponding molecular mechanisms. Zinc Oxide 183-186 ubiquitin C-terminal hydrolase L1 Homo sapiens 136-169 31096129-1 2019 Our study determined the toxic effects of zinc oxide (ZnO) particles with different diameters on dopaminergic (DA) neurons, the role of ubiquitin C-terminal hydrolase L1 (UCH-L1) for ZnO particles-induced neurotoxicity, and corresponding molecular mechanisms. Zinc Oxide 183-186 ubiquitin C-terminal hydrolase L1 Homo sapiens 171-177 31096129-5 2019 Furthermore, ZnO particles exposure resulted in a significant decrease in UCH-L1 expression in SH-SY5Y; whereas UCH-L1 overexpression led to a significant increase in cell viability and a sharp decrease in ROS level. Zinc Oxide 13-16 ubiquitin C-terminal hydrolase L1 Homo sapiens 74-80 31096129-6 2019 Western blotting and adenovirus transfection found that exposure to ZnO particles with different diameters all activate the NF-kappaB signaling in SH-SY5Y cells; whereas UCH-L1 over-expression resulted in increased levels of IkappaBalpha, an endogenous inhibitor of NF-kappaB signaling pathway. Zinc Oxide 68-71 NFKB inhibitor alpha Homo sapiens 225-237 31096129-8 2019 Regarding the neurotoxic effect of ZnO particles, UCH-L1 protects against and/or alleviates neuronal damage, possibly by deubiquitination of the endogenous inhibitor, IkappaBalpha, which leads to activation of NF-kappaB signaling. Zinc Oxide 35-38 ubiquitin C-terminal hydrolase L1 Homo sapiens 50-56 31096129-9 2019 Therefore, one possible mechanism for ZnO particle-induced neurotoxicity may be mediated via the down-regulation of UCH-L1 expression in DA cells. Zinc Oxide 38-41 ubiquitin C-terminal hydrolase L1 Homo sapiens 116-122 31202320-3 2019 ZIKV-NS1 antibody was immobilized on the ZnO nanostructures surface via cystamine and glutaraldehyde. Zinc Oxide 41-44 influenza virus NS1A binding protein Homo sapiens 5-8 31500273-5 2019 Besides, the ZnO HS2 sensor showed a shorter response time (14 s) compared with the ZnO NFs (25 s) and ZnO HS1 (19 s) gas sensors. Zinc Oxide 13-16 spectrin beta, erythrocytic Homo sapiens 17-20 31271644-2 2019 This study has been attempted to elucidate the DNA damage response mechanism in a dermal model exposed to ZnO NPs through Ataxia Telangiectasia Mutated (ATM)-mediated ChK1-dependent G2/M arrest. Zinc Oxide 106-109 ATM serine/threonine kinase Homo sapiens 122-151 31271644-2 2019 This study has been attempted to elucidate the DNA damage response mechanism in a dermal model exposed to ZnO NPs through Ataxia Telangiectasia Mutated (ATM)-mediated ChK1-dependent G2/M arrest. Zinc Oxide 106-109 ATM serine/threonine kinase Homo sapiens 153-156 31271644-2 2019 This study has been attempted to elucidate the DNA damage response mechanism in a dermal model exposed to ZnO NPs through Ataxia Telangiectasia Mutated (ATM)-mediated ChK1-dependent G2/M arrest. Zinc Oxide 106-109 checkpoint kinase 1 Homo sapiens 167-171 31500273-1 2019 Firecracker-like ZnO hierarchical structures (ZnO HS1) were synthesized by combining electrospinning with hydrothermal methods. Zinc Oxide 17-20 eukaryotic translation elongation factor 1 alpha 2 Homo sapiens 50-53 31500273-2 2019 Flower-like ZnO hierarchical structures (ZnO HS2) were prepared by a hydrothermal method using ultrasound-treated ZnO nanofibers (ZnO NFs) as raw material which has rarely been reported in previous papers. Zinc Oxide 12-15 spectrin beta, erythrocytic Homo sapiens 45-48 31271644-6 2019 Subsequently, ZnO NPs treatment created DNA damage as confirmed via Comet assay (increase in olive tail moment), micronucleus assay (increase in micronucleus formation), double-strand breaks (increase in ATM and Ataxia Telangiectasia and Rad3 related (ATR) expression), DNA fragmentation and cell cycle (G2/M arrest) studies. Zinc Oxide 14-17 ATM serine/threonine kinase Homo sapiens 204-207 31271644-6 2019 Subsequently, ZnO NPs treatment created DNA damage as confirmed via Comet assay (increase in olive tail moment), micronucleus assay (increase in micronucleus formation), double-strand breaks (increase in ATM and Ataxia Telangiectasia and Rad3 related (ATR) expression), DNA fragmentation and cell cycle (G2/M arrest) studies. Zinc Oxide 14-17 ATR serine/threonine kinase Homo sapiens 252-255 31500273-7 2019 Apart from the synergistic effect of nanoparticles and nanoflowers, more point-point contacts between flower-like ZnO nanorods were advantageous for the excellent H2S sensing properties of ZnO HS2 material. Zinc Oxide 114-117 spectrin beta, erythrocytic Homo sapiens 193-196 31500273-2 2019 Flower-like ZnO hierarchical structures (ZnO HS2) were prepared by a hydrothermal method using ultrasound-treated ZnO nanofibers (ZnO NFs) as raw material which has rarely been reported in previous papers. Zinc Oxide 41-44 spectrin beta, erythrocytic Homo sapiens 45-48 31500273-3 2019 Scanning electron microscope (SEM) and transmission electron microscope"s (TEM) images clearly indicated the existence of nanoparticles on the ZnO HS2 material. Zinc Oxide 143-146 spectrin beta, erythrocytic Homo sapiens 147-150 31500273-4 2019 Both gas sensors exhibited high selectivity toward H2S gas over various other gases at 180 C. The ZnO HS2 gas sensor exhibited higher H2S sensitivity response (50 ppm H2S, 42.298) at 180 C than ZnO NFs (50 ppm H2S, 9.223) and ZnO HS1 (50 ppm H2S, 17.506) gas sensors. Zinc Oxide 99-102 spectrin beta, erythrocytic Homo sapiens 103-106 31500273-4 2019 Both gas sensors exhibited high selectivity toward H2S gas over various other gases at 180 C. The ZnO HS2 gas sensor exhibited higher H2S sensitivity response (50 ppm H2S, 42.298) at 180 C than ZnO NFs (50 ppm H2S, 9.223) and ZnO HS1 (50 ppm H2S, 17.506) gas sensors. Zinc Oxide 99-102 eukaryotic translation elongation factor 1 alpha 2 Homo sapiens 232-235 31212046-0 2019 Chitosan capped ZnO nanoparticles with cell specific apoptosis induction through P53 activation and G2/M arrest in breast cancer cells - In vitro approaches. Zinc Oxide 16-19 tumor protein p53 Homo sapiens 81-84 32042215-0 2019 Zinc Oxide nanoparticles induce oxidative and proteotoxic stress in ovarian cancer cells and trigger apoptosis Independent of p53-mutation status. Zinc Oxide 0-10 tumor protein p53 Homo sapiens 126-129 31173826-6 2019 Hence a novel, cost-effective and eco-friendly ZnO incorporated into aminated chitosan Schiff"s base (ACSSB@ZnO) has been synthesized, characterized (BET, XRD, FTIR, SEM, TEM and 1H NMR), and utilized as an adsorbent for the removal of Pb(II) ions from the aqueous environment. Zinc Oxide 47-50 submaxillary gland androgen regulated protein 3B Homo sapiens 236-242 31173826-6 2019 Hence a novel, cost-effective and eco-friendly ZnO incorporated into aminated chitosan Schiff"s base (ACSSB@ZnO) has been synthesized, characterized (BET, XRD, FTIR, SEM, TEM and 1H NMR), and utilized as an adsorbent for the removal of Pb(II) ions from the aqueous environment. Zinc Oxide 108-111 submaxillary gland androgen regulated protein 3B Homo sapiens 236-242 31173826-8 2019 The maximum sorption capacity of Pb(II) onto ACSSB@ZnO was found to be 55.55 mg/g. Zinc Oxide 51-54 submaxillary gland androgen regulated protein 3B Homo sapiens 33-39 31420568-0 2019 Reaction Route Selection for Cellulose Hydrogenolysis into C2/C3 Glycols by ZnO-Modified Ni-W/beta-zeolite Catalysts. Zinc Oxide 76-79 complement C2 Homo sapiens 59-72 31040175-6 2019 Indeed, direct intratumoral injection of ZnO NPs or a complex of ZnO with RNA significantly suppresses ERK and AKT phosphorylation. Zinc Oxide 41-44 mitogen-activated protein kinase 1 Homo sapiens 103-106 31040175-6 2019 Indeed, direct intratumoral injection of ZnO NPs or a complex of ZnO with RNA significantly suppresses ERK and AKT phosphorylation. Zinc Oxide 41-44 AKT serine/threonine kinase 1 Homo sapiens 111-114 31040175-6 2019 Indeed, direct intratumoral injection of ZnO NPs or a complex of ZnO with RNA significantly suppresses ERK and AKT phosphorylation. Zinc Oxide 65-68 mitogen-activated protein kinase 1 Homo sapiens 103-106 31040175-6 2019 Indeed, direct intratumoral injection of ZnO NPs or a complex of ZnO with RNA significantly suppresses ERK and AKT phosphorylation. Zinc Oxide 65-68 AKT serine/threonine kinase 1 Homo sapiens 111-114 31067518-2 2019 Aero-GaN is made up of randomly arranged hollow GaN microtetrapods, which are obtained by direct growth using hydride vapor phase epitaxy of GaN on the sacrificial network of ZnO microtetrapods. Zinc Oxide 175-178 gigaxonin Homo sapiens 5-8 31147016-5 2019 When the concentration of BQ-788/EA@ZnO was 12.5 mug/mL, the inhibition rate on tyrosinase activity and melanin deposition were up to 44.23 +- 4.97% and 37.50 +- 5.23%, respectively. Zinc Oxide 36-39 tyrosinase Homo sapiens 80-90 31379173-10 2019 While adding Triton X-100 still induced leakage of the encapsulated liposomes, the shell protected the liposomes from leakage induced by ZnO NPs, suggesting a porous structure of the Gd3+/AMP shell which allowed penetration of Triton X-100 but not the larger ZnO NPs. Zinc Oxide 137-140 GRDX Homo sapiens 183-186 31379173-10 2019 While adding Triton X-100 still induced leakage of the encapsulated liposomes, the shell protected the liposomes from leakage induced by ZnO NPs, suggesting a porous structure of the Gd3+/AMP shell which allowed penetration of Triton X-100 but not the larger ZnO NPs. Zinc Oxide 259-262 GRDX Homo sapiens 183-186 31276364-7 2019 As expected, the SASP/ZnO NPs enhanced ROS production because of ZnO and impaired GSH synthesis because of SASP-induced inhibition of xCT (SLC7A11) transport function. Zinc Oxide 22-25 solute carrier family 7 (cationic amino acid transporter, y+ system), member 11 Mus musculus 134-137 31078877-4 2019 The nano-ZnO inhibited the expression of the cyclins (Cycs), cyclin-dependent kinases (CDK) and the minichromosome maintenance (MCM), making the activation of Cyc/CDK complexs (CycD/CDK4, 6; CycE/CDK2; CycA/CDK2) and MCM fail and resulting in DNA replication disorder in different periods (G1, M and G2 phase). Zinc Oxide 9-12 nodal-related 2 Danio rerio 54-57 31078877-4 2019 The nano-ZnO inhibited the expression of the cyclins (Cycs), cyclin-dependent kinases (CDK) and the minichromosome maintenance (MCM), making the activation of Cyc/CDK complexs (CycD/CDK4, 6; CycE/CDK2; CycA/CDK2) and MCM fail and resulting in DNA replication disorder in different periods (G1, M and G2 phase). Zinc Oxide 9-12 cyclin-dependent kinase 4 Danio rerio 182-189 31078877-4 2019 The nano-ZnO inhibited the expression of the cyclins (Cycs), cyclin-dependent kinases (CDK) and the minichromosome maintenance (MCM), making the activation of Cyc/CDK complexs (CycD/CDK4, 6; CycE/CDK2; CycA/CDK2) and MCM fail and resulting in DNA replication disorder in different periods (G1, M and G2 phase). Zinc Oxide 9-12 cyclin E1 Danio rerio 191-195 31026756-4 2019 Moreover, the incorporation of CIN or ZnO NPs to SPI matrix affected differently color parameters, oxygen permeability and storage modulus of the resulting composite films. Zinc Oxide 38-41 chromogranin A Homo sapiens 49-52 31026756-5 2019 Among regular SPI film and composite film with one added ingredient, SPI-based bionanocomposite film containing CIN and ZnO NPs displayed the best barrier capacities, mechanical properties and antifungal activities. Zinc Oxide 120-123 chromogranin A Homo sapiens 69-72 31026756-7 2019 Meanwhile, the oxygen permeability and water permeability for SPI + CIN + ZnO film are 66.1% and 54.8% of that in regular SPI film, respectively. Zinc Oxide 74-77 chromogranin A Homo sapiens 62-65 31026756-7 2019 Meanwhile, the oxygen permeability and water permeability for SPI + CIN + ZnO film are 66.1% and 54.8% of that in regular SPI film, respectively. Zinc Oxide 74-77 chromogranin A Homo sapiens 122-125 31220582-0 2019 The role of ATF3 in ZnO nanoparticle-induced genotoxicity and cytotoxicity in bronchial epithelial cells. Zinc Oxide 20-23 activating transcription factor 3 Homo sapiens 12-16 31220582-6 2019 Moreover, ATF3 also contributed to ZnO NP-induced cell apoptosis. Zinc Oxide 35-38 activating transcription factor 3 Homo sapiens 10-14 31078877-4 2019 The nano-ZnO inhibited the expression of the cyclins (Cycs), cyclin-dependent kinases (CDK) and the minichromosome maintenance (MCM), making the activation of Cyc/CDK complexs (CycD/CDK4, 6; CycE/CDK2; CycA/CDK2) and MCM fail and resulting in DNA replication disorder in different periods (G1, M and G2 phase). Zinc Oxide 9-12 cyclin-dependent kinase 2 Danio rerio 196-200 31078877-4 2019 The nano-ZnO inhibited the expression of the cyclins (Cycs), cyclin-dependent kinases (CDK) and the minichromosome maintenance (MCM), making the activation of Cyc/CDK complexs (CycD/CDK4, 6; CycE/CDK2; CycA/CDK2) and MCM fail and resulting in DNA replication disorder in different periods (G1, M and G2 phase). Zinc Oxide 9-12 cyclin-dependent kinase 2 Danio rerio 207-211 31432799-3 2019 The haemolysis and bovine serum albumin adsorption assays showed that the modification of ZnO QDs on the mesoporous silica nanoparticles modified by mercapto groups (CMS-SH)(ZnO@CMS) had better biocompatibility compared to CMS-SH. Zinc Oxide 90-93 albumin Homo sapiens 26-39 31017309-6 2019 Ap and Bl exposure to 100 mug/mL sono ZnO NPs and Ap exposure to 50 mug/mL commercial ZnO NPs induced a significant (P < 0.05) release of interleukin-6. Zinc Oxide 86-89 interleukin 6 Homo sapiens 141-154 31017309-7 2019 A significant (P < 0.05) release of interleukin-8 was observed after Ap exposure to ZnO NPs at 100 mug/mL and after Bl exposure to sono ZnO NPs at 100 mug/mL. Zinc Oxide 87-90 C-X-C motif chemokine ligand 8 Homo sapiens 39-52 31372825-0 2019 ZnO nanoparticles on MoS2 microflowers for ultrasensitive SERS detection of bisphenol A. Zinc Oxide 0-3 seryl-tRNA synthetase 2, mitochondrial Homo sapiens 58-62 31372825-7 2019 Graphical abstract MoS2/ZnO MCs SERS substrate broke through the application barrier of semiconductor composite materials in SERS substrates. Zinc Oxide 24-27 seryl-tRNA synthetase 2, mitochondrial Homo sapiens 32-36 31372825-7 2019 Graphical abstract MoS2/ZnO MCs SERS substrate broke through the application barrier of semiconductor composite materials in SERS substrates. Zinc Oxide 24-27 seryl-tRNA synthetase 2, mitochondrial Homo sapiens 125-129 31036196-2 2019 In this work, we report a method for the separation and size characterization of ZnO-NPs by asymmetrical flow field-flow fractionation (AF4) coupled to UV-vis detector. Zinc Oxide 81-84 AF4/FMR2 family member 1 Homo sapiens 136-139 31036199-9 2019 This study illustrate that ZnO-NRs exhibit a photoluminescence signal suitable for the determination of anti-CD19-FITC* labeled IM9 cell line at concentrations - from 10 till 500 cells adsorbed per 1 mm2 of ZnO-NRs platform. Zinc Oxide 27-30 CD19 molecule Homo sapiens 109-113 31036199-9 2019 This study illustrate that ZnO-NRs exhibit a photoluminescence signal suitable for the determination of anti-CD19-FITC* labeled IM9 cell line at concentrations - from 10 till 500 cells adsorbed per 1 mm2 of ZnO-NRs platform. Zinc Oxide 207-210 CD19 molecule Homo sapiens 109-113 31460417-4 2019 Ternary Ag2S/NiO-ZnO nanocomposites showed excellent visible light photocatalytic property which increases further with the concentration of Ag2S. Zinc Oxide 17-20 angiotensin II receptor type 1 Homo sapiens 8-12 31460417-4 2019 Ternary Ag2S/NiO-ZnO nanocomposites showed excellent visible light photocatalytic property which increases further with the concentration of Ag2S. Zinc Oxide 17-20 angiotensin II receptor type 1 Homo sapiens 141-145 31276364-7 2019 As expected, the SASP/ZnO NPs enhanced ROS production because of ZnO and impaired GSH synthesis because of SASP-induced inhibition of xCT (SLC7A11) transport function. Zinc Oxide 22-25 solute carrier family 7 (cationic amino acid transporter, y+ system), member 11 Mus musculus 139-146 31330912-3 2019 At 24 h after exposure to the ZnO NPs, transmission electron microscopy revealed swelling of the endoplasmic reticulum (ER) and increased numbers of autophagolysosomes in the cultured astrocytes, and increased levels of LC3 (microtubule-associated protein 1 light chain 3)-mediated autophagy were identified by flow cytometry. Zinc Oxide 30-33 microtubule associated protein 1 light chain 3 alpha Homo sapiens 220-223 31330912-6 2019 Phosphatidylinositol 3-kinase (PI3K)/mitogen-activated protein kinase (MAPK) dual activation was induced by ZnO NPs in a dose-dependent manner. Zinc Oxide 108-111 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha Homo sapiens 0-29 31259510-2 2019 First, ZnO was modified by doping of tetraalkylammonium salts (TRAX) into polyethylenimine ethoxylated (PEIE) for the WF control. Zinc Oxide 7-10 translin associated factor X Homo sapiens 63-67 31259510-9 2019 Finally, the ZnO/PEIE:TRAX bilayers were applied as electron injection layers in poly[2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylenevinylene] emissive-layer-based OLEDs with an inverted structure. Zinc Oxide 13-16 translin associated factor X Homo sapiens 22-26 30951608-11 2019 CONCLUSION: In general, in the current study, the antitumor effects of ZnO-NPs were confirmed by the enhancement of P53 and Bax genes expression profile, which are indicated the apoptotic induction in HUH7 cell line. Zinc Oxide 71-74 tumor protein p53 Homo sapiens 116-119 31112708-8 2019 ZnO nanoparticles can also decrease the expressions of TGF-beta1, ED-A, and PICP at mRNA and protein levels; significantly prevent fibroblast-mediated collagen lattice contraction. Zinc Oxide 0-3 transforming growth factor beta 1 Homo sapiens 55-64 31112708-8 2019 ZnO nanoparticles can also decrease the expressions of TGF-beta1, ED-A, and PICP at mRNA and protein levels; significantly prevent fibroblast-mediated collagen lattice contraction. Zinc Oxide 0-3 ectodysplasin A Homo sapiens 66-70 31346463-10 2019 Furthermore, pigs fed ZnO had less ETEC-F4 diarrhoea (P = 0.009) than pigs fed other diets, however faecal shedding of ETEC was similar (P > 0.05) between diets. Zinc Oxide 22-25 ETEC Sus scrofa 35-39 31157349-0 2019 Frizzled-7-targeted delivery of zinc oxide nanoparticles to drug-resistant breast cancer cells. Zinc Oxide 32-42 frizzled class receptor 7 Homo sapiens 0-10 31157349-11 2019 This study shows that ZnO-MSs are promising tools to treat triple-negative and drug-resistant breast cancers and highlights the potential clinical utility of FZD-7 for delivery of nanomedicines and imaging probes specifically to these cancer types. Zinc Oxide 22-25 frizzled class receptor 7 Homo sapiens 158-163 30951608-11 2019 CONCLUSION: In general, in the current study, the antitumor effects of ZnO-NPs were confirmed by the enhancement of P53 and Bax genes expression profile, which are indicated the apoptotic induction in HUH7 cell line. Zinc Oxide 71-74 BCL2 associated X, apoptosis regulator Homo sapiens 124-127 30951608-11 2019 CONCLUSION: In general, in the current study, the antitumor effects of ZnO-NPs were confirmed by the enhancement of P53 and Bax genes expression profile, which are indicated the apoptotic induction in HUH7 cell line. Zinc Oxide 71-74 MIR7-3 host gene Homo sapiens 201-205 30778562-6 2019 Compared with the CTC group, COS/ZnO/PAL enhanced serum catalase (CAT) activity at 21 d (P < 0.05), and decreased serum malondialdehyde (MDA) content at 42 d (P < 0.05). Zinc Oxide 33-36 catalase Gallus gallus 56-64 30778562-6 2019 Compared with the CTC group, COS/ZnO/PAL enhanced serum catalase (CAT) activity at 21 d (P < 0.05), and decreased serum malondialdehyde (MDA) content at 42 d (P < 0.05). Zinc Oxide 33-36 catalase Gallus gallus 66-69 31341558-5 2019 Generation of reactive oxygen species was observed, and expression of apoptosis related biomarkers including Bax and Bcl-2 were changed after treatment of zinc oxide nanoparticles, while no other significant toxicity- related changes were observed in cornea cells treated with Ag, CeO2, SiO2 and TiO2 nanoparticles. Zinc Oxide 155-165 apoptosis regulator BAX Oryctolagus cuniculus 109-112 31341558-5 2019 Generation of reactive oxygen species was observed, and expression of apoptosis related biomarkers including Bax and Bcl-2 were changed after treatment of zinc oxide nanoparticles, while no other significant toxicity- related changes were observed in cornea cells treated with Ag, CeO2, SiO2 and TiO2 nanoparticles. Zinc Oxide 155-165 BCL-2 Oryctolagus cuniculus 117-122 31195378-0 2019 Fluorescent ZnO quantum dots synthesized with urea for the selective detection of Cr6+ ion in water with a wide range of concentrations. Zinc Oxide 12-15 teratocarcinoma-derived growth factor 1 pseudogene 6 Homo sapiens 82-85 31195378-2 2019 In this paper, urea-ZnO QDs were used as fluorescent probe to detect Cr6+ in solution. Zinc Oxide 20-23 teratocarcinoma-derived growth factor 1 pseudogene 6 Homo sapiens 69-72 31195378-3 2019 The emission from the as-synthesized urea-ZnO QDs is selectively quenched when Cr6+ ions were added. Zinc Oxide 42-45 teratocarcinoma-derived growth factor 1 pseudogene 6 Homo sapiens 79-82 30423365-0 2019 Cytotoxicity and global transcriptional responses induced by zinc oxide nanoparticles NM 110 in PMA-differentiated THP-1 cells. Zinc Oxide 61-71 GLI family zinc finger 2 Homo sapiens 115-120 30981028-1 2019 In this work, the ZnO nanostars with excellent catalytic performance were firstly used as the coreaction accelerator of luminol-O2 system to construct a biosensor for ultrasensitively detecting microRNA-21 (miRNA-21) in cancer cells. Zinc Oxide 18-21 microRNA 21 Homo sapiens 194-205 30981028-1 2019 In this work, the ZnO nanostars with excellent catalytic performance were firstly used as the coreaction accelerator of luminol-O2 system to construct a biosensor for ultrasensitively detecting microRNA-21 (miRNA-21) in cancer cells. Zinc Oxide 18-21 microRNA 21 Homo sapiens 207-215 30423365-2 2019 Thus, we have used, as a model, zinc oxide nanoparticle NM110 (ZnO110NP) exposure to PMA-differentiated THP-1 macrophages. Zinc Oxide 32-42 GLI family zinc finger 2 Homo sapiens 104-109 31173148-5 2019 In contrast, aged ZnO NPs induced more reactive oxygen species (ROS) production and endoplasmic reticulum (ER) stress marker protein (BIP/GRP78) expression and their genotoxicity could be dramatically suppressed by either ROS scavengers (DMSO, CAT and NaN3) or ER stress inhibitor (4-PBA). Zinc Oxide 18-21 heat shock protein family A (Hsp70) member 5 Homo sapiens 134-137 30972400-12 2019 The observed apparent rate constant for the photocatalytic MB degradation using 10 mol% Ag-ZnO (Kapp = 6.01 x 10-2 min-1) was six times that of pure ZnO (Kapp = 1.09 x 10-2 min-1). Zinc Oxide 91-94 CD59 molecule (CD59 blood group) Homo sapiens 115-120 30972400-12 2019 The observed apparent rate constant for the photocatalytic MB degradation using 10 mol% Ag-ZnO (Kapp = 6.01 x 10-2 min-1) was six times that of pure ZnO (Kapp = 1.09 x 10-2 min-1). Zinc Oxide 91-94 CD59 molecule (CD59 blood group) Homo sapiens 173-178 31173148-5 2019 In contrast, aged ZnO NPs induced more reactive oxygen species (ROS) production and endoplasmic reticulum (ER) stress marker protein (BIP/GRP78) expression and their genotoxicity could be dramatically suppressed by either ROS scavengers (DMSO, CAT and NaN3) or ER stress inhibitor (4-PBA). Zinc Oxide 18-21 heat shock protein family A (Hsp70) member 5 Homo sapiens 138-143 30959244-0 2019 Potential use of ZnO@activated carbon nanocomposites for the adsorptive removal of Cd2+ ions in aqueous solutions. Zinc Oxide 17-20 CD2 molecule Homo sapiens 83-86 31159486-4 2019 The p-type ZnO nanowire film has a well-preferred orientation along the (100) direction and a wurtzite structure, thereby displaying an effective photocatalytic capability for carcinogenic Cr6+ ions and CO2 greenhouse gas reduction under visible light irradiation. Zinc Oxide 11-14 teratocarcinoma-derived growth factor 1 pseudogene 6 Homo sapiens 189-192 30959244-6 2019 The ratio of ZnO nanoparticles and activated carbon was optimized to achieve enhanced electrostatic interactions for the effective adsorption of cadmium ions (Cd2+). Zinc Oxide 13-16 CD2 molecule Homo sapiens 159-162 30959244-9 2019 The favourable adsorption capacity of the synthesized ZnO/activated carbon (9:1) nanocomposites supported their use as an efficient sorbent material in practical performance metrics (e.g., partition coefficient of 0.54 mg g-1muM-1) for the adsorption of Cd2+ ions. Zinc Oxide 54-57 PWWP domain containing 3A, DNA repair factor Homo sapiens 225-230 30959244-9 2019 The favourable adsorption capacity of the synthesized ZnO/activated carbon (9:1) nanocomposites supported their use as an efficient sorbent material in practical performance metrics (e.g., partition coefficient of 0.54 mg g-1muM-1) for the adsorption of Cd2+ ions. Zinc Oxide 54-57 CD2 molecule Homo sapiens 254-257 31086927-0 2019 Ferroelectric field manipulated nonvolatile resistance switching in Al:ZnO/Pb(Mg1/3Nb2/3)0.7Ti0.3O3 heterostructures at room temperature. Zinc Oxide 71-74 mucin 5B, oligomeric mucus/gel-forming Homo sapiens 78-81 30901700-0 2019 Novel rare earth (RE-La, Er, Sm) metal doped ZnO photocatalysts for degradation of Congo-Red dye: Synthesis, characterization and kinetic studies. Zinc Oxide 45-48 RELA proto-oncogene, NF-kB subunit Homo sapiens 18-23 30901700-3 2019 TEM results showed the formation of a unidimensional structure (ZnO) with an average fiber diameter of 600 nm and a morphology consisting of interconnected nanoparticles having dimensions in the range 25-134 nm (ZnO doped with RE). Zinc Oxide 64-67 MFT2 Homo sapiens 0-3 30901700-3 2019 TEM results showed the formation of a unidimensional structure (ZnO) with an average fiber diameter of 600 nm and a morphology consisting of interconnected nanoparticles having dimensions in the range 25-134 nm (ZnO doped with RE). Zinc Oxide 212-215 MFT2 Homo sapiens 0-3 31086927-4 2019 The results indicate that the carrier density in the Al:ZnO films is modulated under external electric fields, due to the accumulation and depletion of charge at the interface between Al:ZnO and Pb(Mg1/3Nb2/3)0.7Ti0.3O3. Zinc Oxide 56-59 mucin 5B, oligomeric mucus/gel-forming Homo sapiens 198-201 31002239-7 2019 Similar enhancement on gas-sensing performance is also observed for the ZnO-nanosheet-based monolayer sensors prepared by the same self-assembly method. Zinc Oxide 72-75 galactosamine (N-acetyl)-6-sulfatase Homo sapiens 23-26 31213808-6 2019 Results: Data revealed a significant reduction in tumor size with a significant increase in p53 and Bax and decrease in Bcl2 expression levels in the tissues of ZnO-NPs treated ESC bearing mice. Zinc Oxide 161-164 B cell leukemia/lymphoma 2 Mus musculus 120-124 30461332-0 2019 Toxicity of ZnO nanoparticles (NPs) to THP-1 macrophages: interactions with saturated or unsaturated free fatty acids. Zinc Oxide 12-15 GLI family zinc finger 2 Homo sapiens 39-44 30618096-0 2019 Zinc oxide nanoparticles induced gene mutation at the HGPRT locus and cell cycle arrest associated with apoptosis in V-79 cells. Zinc Oxide 0-10 hypoxanthine-guanine phosphoribosyltransferase Cricetulus griseus 54-59 30620997-3 2019 In this study, we investigated the combined toxicity of ZnO NRs/Mini-NRs and palmitate (PA) to THP-1 macrophages. Zinc Oxide 56-59 GLI family zinc finger 2 Homo sapiens 95-100 30620997-7 2019 ZnO NRs and ZnO Mini-NRs significantly promoted the expression of ER stress genes HSPA5, DDIT3, XBP-1s and apoptotic gene CASP3, whereas PA also modestly promoted the expression of HSPA5, DDIT3 and CASP3. Zinc Oxide 0-3 heat shock protein family A (Hsp70) member 5 Homo sapiens 82-87 30620997-7 2019 ZnO NRs and ZnO Mini-NRs significantly promoted the expression of ER stress genes HSPA5, DDIT3, XBP-1s and apoptotic gene CASP3, whereas PA also modestly promoted the expression of HSPA5, DDIT3 and CASP3. Zinc Oxide 0-3 DNA damage inducible transcript 3 Homo sapiens 89-94 30620997-7 2019 ZnO NRs and ZnO Mini-NRs significantly promoted the expression of ER stress genes HSPA5, DDIT3, XBP-1s and apoptotic gene CASP3, whereas PA also modestly promoted the expression of HSPA5, DDIT3 and CASP3. Zinc Oxide 0-3 X-box binding protein 1 Homo sapiens 96-101 30620997-7 2019 ZnO NRs and ZnO Mini-NRs significantly promoted the expression of ER stress genes HSPA5, DDIT3, XBP-1s and apoptotic gene CASP3, whereas PA also modestly promoted the expression of HSPA5, DDIT3 and CASP3. Zinc Oxide 0-3 caspase 3 Homo sapiens 122-127 30620997-7 2019 ZnO NRs and ZnO Mini-NRs significantly promoted the expression of ER stress genes HSPA5, DDIT3, XBP-1s and apoptotic gene CASP3, whereas PA also modestly promoted the expression of HSPA5, DDIT3 and CASP3. Zinc Oxide 0-3 heat shock protein family A (Hsp70) member 5 Homo sapiens 181-186 30620997-7 2019 ZnO NRs and ZnO Mini-NRs significantly promoted the expression of ER stress genes HSPA5, DDIT3, XBP-1s and apoptotic gene CASP3, whereas PA also modestly promoted the expression of HSPA5, DDIT3 and CASP3. Zinc Oxide 0-3 DNA damage inducible transcript 3 Homo sapiens 188-193 30620997-7 2019 ZnO NRs and ZnO Mini-NRs significantly promoted the expression of ER stress genes HSPA5, DDIT3, XBP-1s and apoptotic gene CASP3, whereas PA also modestly promoted the expression of HSPA5, DDIT3 and CASP3. Zinc Oxide 0-3 caspase 3 Homo sapiens 198-203 30620997-7 2019 ZnO NRs and ZnO Mini-NRs significantly promoted the expression of ER stress genes HSPA5, DDIT3, XBP-1s and apoptotic gene CASP3, whereas PA also modestly promoted the expression of HSPA5, DDIT3 and CASP3. Zinc Oxide 12-15 heat shock protein family A (Hsp70) member 5 Homo sapiens 82-87 30620997-7 2019 ZnO NRs and ZnO Mini-NRs significantly promoted the expression of ER stress genes HSPA5, DDIT3, XBP-1s and apoptotic gene CASP3, whereas PA also modestly promoted the expression of HSPA5, DDIT3 and CASP3. Zinc Oxide 12-15 DNA damage inducible transcript 3 Homo sapiens 89-94 30620997-7 2019 ZnO NRs and ZnO Mini-NRs significantly promoted the expression of ER stress genes HSPA5, DDIT3, XBP-1s and apoptotic gene CASP3, whereas PA also modestly promoted the expression of HSPA5, DDIT3 and CASP3. Zinc Oxide 12-15 X-box binding protein 1 Homo sapiens 96-101 30620997-7 2019 ZnO NRs and ZnO Mini-NRs significantly promoted the expression of ER stress genes HSPA5, DDIT3, XBP-1s and apoptotic gene CASP3, whereas PA also modestly promoted the expression of HSPA5, DDIT3 and CASP3. Zinc Oxide 12-15 caspase 3 Homo sapiens 122-127 30620997-7 2019 ZnO NRs and ZnO Mini-NRs significantly promoted the expression of ER stress genes HSPA5, DDIT3, XBP-1s and apoptotic gene CASP3, whereas PA also modestly promoted the expression of HSPA5, DDIT3 and CASP3. Zinc Oxide 12-15 heat shock protein family A (Hsp70) member 5 Homo sapiens 181-186 30620997-7 2019 ZnO NRs and ZnO Mini-NRs significantly promoted the expression of ER stress genes HSPA5, DDIT3, XBP-1s and apoptotic gene CASP3, whereas PA also modestly promoted the expression of HSPA5, DDIT3 and CASP3. Zinc Oxide 12-15 DNA damage inducible transcript 3 Homo sapiens 188-193 30620997-7 2019 ZnO NRs and ZnO Mini-NRs significantly promoted the expression of ER stress genes HSPA5, DDIT3, XBP-1s and apoptotic gene CASP3, whereas PA also modestly promoted the expression of HSPA5, DDIT3 and CASP3. Zinc Oxide 12-15 caspase 3 Homo sapiens 198-203 30461332-6 2019 Moreover, only co-exposure to ZnO NPs and SA significantly promoted the release of interleukin-8. Zinc Oxide 30-33 C-X-C motif chemokine ligand 8 Homo sapiens 83-96 31096382-0 2019 Promoting charge separation of biochar-based Zn-TiO2/pBC in the presence of ZnO for efficient sulfamethoxazole photodegradation under visible light irradiation. Zinc Oxide 76-79 dihydrolipoamide S-acetyltransferase Homo sapiens 53-56 31011810-7 2019 The results of cell viability were supported by ALP activity and mineralization assay, wherein, PCL/nHA/ZnO scaffolds showed higher ALP activity and better mineralization capacity as compared to pristine PCL. Zinc Oxide 104-107 PHD finger protein 1 Homo sapiens 96-99 31011810-7 2019 The results of cell viability were supported by ALP activity and mineralization assay, wherein, PCL/nHA/ZnO scaffolds showed higher ALP activity and better mineralization capacity as compared to pristine PCL. Zinc Oxide 104-107 alkaline phosphatase, placental Homo sapiens 132-135 31011810-8 2019 Although, the PCL/nHA/ZnO scaffolds with 10, 15 and 30wt% of ZnO particles exhibited superior antimicrobial efficacy against both gram-negative (E. coli) and gram-positive (S. aureus) bacteria, a significant decrease in the cell viability and mechanical properties was observed at higher concentrations of ZnO namely 15 and 30%. Zinc Oxide 61-64 PHD finger protein 1 Homo sapiens 14-17 31011810-8 2019 Although, the PCL/nHA/ZnO scaffolds with 10, 15 and 30wt% of ZnO particles exhibited superior antimicrobial efficacy against both gram-negative (E. coli) and gram-positive (S. aureus) bacteria, a significant decrease in the cell viability and mechanical properties was observed at higher concentrations of ZnO namely 15 and 30%. Zinc Oxide 61-64 PHD finger protein 1 Homo sapiens 14-17 31011810-10 2019 Thus, the present study revealed that the biomimetic tri-component PCL/nHA/ZnO scaffolds with ZnO concentration range of <= 10% could be ideal for achieving optimal biocompatibility (cell proliferation, biomineralization, and antimicrobial capacity) and mechanical stability thus making it a promising biomaterial substrate for bone tissue regeneration. Zinc Oxide 75-78 PHD finger protein 1 Homo sapiens 67-70 31011810-10 2019 Thus, the present study revealed that the biomimetic tri-component PCL/nHA/ZnO scaffolds with ZnO concentration range of <= 10% could be ideal for achieving optimal biocompatibility (cell proliferation, biomineralization, and antimicrobial capacity) and mechanical stability thus making it a promising biomaterial substrate for bone tissue regeneration. Zinc Oxide 94-97 PHD finger protein 1 Homo sapiens 67-70 30826647-1 2019 This article is clearly presenting the development of a biosensor for human factor IX (FIX) to diagnose the blood clotting deficiency, a so-called "Royal disease" using an interdigitated electrode (IDE) with the zinc oxide surface modification. Zinc Oxide 212-222 coagulation factor IX Homo sapiens 76-85 30669078-11 2019 Superoxide dismutase (SOD) and catalase (CAT) activities of wheat seedling roots decreased at 1000 mg L-1 ZnO (NPs and bulk), especially in the co-exposure treatments. Zinc Oxide 106-109 SOD Triticum aestivum 0-20 30669078-11 2019 Superoxide dismutase (SOD) and catalase (CAT) activities of wheat seedling roots decreased at 1000 mg L-1 ZnO (NPs and bulk), especially in the co-exposure treatments. Zinc Oxide 106-109 SOD Triticum aestivum 22-25 30669078-11 2019 Superoxide dismutase (SOD) and catalase (CAT) activities of wheat seedling roots decreased at 1000 mg L-1 ZnO (NPs and bulk), especially in the co-exposure treatments. Zinc Oxide 106-109 catalase-1 Triticum aestivum 31-39 30669078-11 2019 Superoxide dismutase (SOD) and catalase (CAT) activities of wheat seedling roots decreased at 1000 mg L-1 ZnO (NPs and bulk), especially in the co-exposure treatments. Zinc Oxide 106-109 catalase-1 Triticum aestivum 41-44 30708053-6 2019 This protective mechanism of ZnO NPs was signaled through hepatic SIRT1-LKB1-AMPK which restricted SREBP-1c within the cytosol limiting its transcriptional ability and thereby ameliorating HFD mediated DNL. Zinc Oxide 29-32 sirtuin 1 Mus musculus 66-71 30708053-6 2019 This protective mechanism of ZnO NPs was signaled through hepatic SIRT1-LKB1-AMPK which restricted SREBP-1c within the cytosol limiting its transcriptional ability and thereby ameliorating HFD mediated DNL. Zinc Oxide 29-32 serine/threonine kinase 11 Mus musculus 72-76 30708053-6 2019 This protective mechanism of ZnO NPs was signaled through hepatic SIRT1-LKB1-AMPK which restricted SREBP-1c within the cytosol limiting its transcriptional ability and thereby ameliorating HFD mediated DNL. Zinc Oxide 29-32 sterol regulatory element binding transcription factor 1 Mus musculus 99-107 31016942-0 2019 [Synthesis of transdermal aloesin loaded zinc oxide nanoparticles and its inhibitory effect on the activity of tyrosinase]. Zinc Oxide 41-51 tyrosinase Homo sapiens 111-121 31011810-6 2019 The PCL/nHA scaffolds exhibited a 1.2-fold increase in cell viability and proliferation, while incorporation of ZnO nanoparticles to PCL/nHA imparted antimicrobial activity to the scaffolds with a progressive increase in the antimicrobial efficacy with increasing ZnO concentration. Zinc Oxide 112-115 PHD finger protein 1 Homo sapiens 133-136 32172745-4 2019 Results showed that nano-ZnO at most of the levels and 1microM bulk-ZnO positively affected growth (root and shoot length/dry weight), leaf surface area and its metabolites (auxin, phenolic compounds, flavonoids), leaf enzymatic activities (CAT, APX, SOD, POX, GPX, PPO and PAL) and anatomical properties (root, stem, cortex and central cylinder diameters), while bulk-ZnO caused decreases at other levels. Zinc Oxide 25-28 L-ascorbate peroxidase 2, cytosolic Nicotiana tabacum 246-249 30650222-0 2019 Visualizing Formation of Intermetallic PdZn in a Palladium/Zinc Oxide Catalyst: Interfacial Fertilization by PdHx. Zinc Oxide 59-69 pyruvate dehydrogenase complex component X Homo sapiens 109-113 30650222-6 2019 The evolution of PdHx in the PdZn catalyst initializes at the PdHx /ZnO interfaces, and proceeds along the PdHx (111) direction. Zinc Oxide 68-71 pyruvate dehydrogenase complex component X Homo sapiens 17-21 30543963-0 2019 A synergistic heterostructured ZnO/BaTiO3 loaded carbon photoanode in photocatalytic fuel cell for degradation of Reactive Red 120 and electricity generation. Zinc Oxide 31-34 RNA binding motif protein 25 Homo sapiens 123-130 32172745-4 2019 Results showed that nano-ZnO at most of the levels and 1microM bulk-ZnO positively affected growth (root and shoot length/dry weight), leaf surface area and its metabolites (auxin, phenolic compounds, flavonoids), leaf enzymatic activities (CAT, APX, SOD, POX, GPX, PPO and PAL) and anatomical properties (root, stem, cortex and central cylinder diameters), while bulk-ZnO caused decreases at other levels. Zinc Oxide 25-28 protoporphyrinogen oxidase, chloroplastic Nicotiana tabacum 266-269 32172745-4 2019 Results showed that nano-ZnO at most of the levels and 1microM bulk-ZnO positively affected growth (root and shoot length/dry weight), leaf surface area and its metabolites (auxin, phenolic compounds, flavonoids), leaf enzymatic activities (CAT, APX, SOD, POX, GPX, PPO and PAL) and anatomical properties (root, stem, cortex and central cylinder diameters), while bulk-ZnO caused decreases at other levels. Zinc Oxide 25-28 phenylalanine ammonia-lyase Nicotiana tabacum 274-277 32172745-4 2019 Results showed that nano-ZnO at most of the levels and 1microM bulk-ZnO positively affected growth (root and shoot length/dry weight), leaf surface area and its metabolites (auxin, phenolic compounds, flavonoids), leaf enzymatic activities (CAT, APX, SOD, POX, GPX, PPO and PAL) and anatomical properties (root, stem, cortex and central cylinder diameters), while bulk-ZnO caused decreases at other levels. Zinc Oxide 68-71 L-ascorbate peroxidase 2, cytosolic Nicotiana tabacum 246-249 32172745-4 2019 Results showed that nano-ZnO at most of the levels and 1microM bulk-ZnO positively affected growth (root and shoot length/dry weight), leaf surface area and its metabolites (auxin, phenolic compounds, flavonoids), leaf enzymatic activities (CAT, APX, SOD, POX, GPX, PPO and PAL) and anatomical properties (root, stem, cortex and central cylinder diameters), while bulk-ZnO caused decreases at other levels. Zinc Oxide 68-71 protoporphyrinogen oxidase, chloroplastic Nicotiana tabacum 266-269 32172745-4 2019 Results showed that nano-ZnO at most of the levels and 1microM bulk-ZnO positively affected growth (root and shoot length/dry weight), leaf surface area and its metabolites (auxin, phenolic compounds, flavonoids), leaf enzymatic activities (CAT, APX, SOD, POX, GPX, PPO and PAL) and anatomical properties (root, stem, cortex and central cylinder diameters), while bulk-ZnO caused decreases at other levels. Zinc Oxide 68-71 phenylalanine ammonia-lyase Nicotiana tabacum 274-277 32172745-4 2019 Results showed that nano-ZnO at most of the levels and 1microM bulk-ZnO positively affected growth (root and shoot length/dry weight), leaf surface area and its metabolites (auxin, phenolic compounds, flavonoids), leaf enzymatic activities (CAT, APX, SOD, POX, GPX, PPO and PAL) and anatomical properties (root, stem, cortex and central cylinder diameters), while bulk-ZnO caused decreases at other levels. Zinc Oxide 68-71 L-ascorbate peroxidase 2, cytosolic Nicotiana tabacum 246-249 32172745-4 2019 Results showed that nano-ZnO at most of the levels and 1microM bulk-ZnO positively affected growth (root and shoot length/dry weight), leaf surface area and its metabolites (auxin, phenolic compounds, flavonoids), leaf enzymatic activities (CAT, APX, SOD, POX, GPX, PPO and PAL) and anatomical properties (root, stem, cortex and central cylinder diameters), while bulk-ZnO caused decreases at other levels. Zinc Oxide 68-71 protoporphyrinogen oxidase, chloroplastic Nicotiana tabacum 266-269 32172745-4 2019 Results showed that nano-ZnO at most of the levels and 1microM bulk-ZnO positively affected growth (root and shoot length/dry weight), leaf surface area and its metabolites (auxin, phenolic compounds, flavonoids), leaf enzymatic activities (CAT, APX, SOD, POX, GPX, PPO and PAL) and anatomical properties (root, stem, cortex and central cylinder diameters), while bulk-ZnO caused decreases at other levels. Zinc Oxide 68-71 phenylalanine ammonia-lyase Nicotiana tabacum 274-277 30611108-2 2019 Firstly, Ag and N co-doped zinc oxide (Ag-N@ZnO) was produced by sol-gel method, and then Ag-N@ZnO was ultrasonically supported on activated carbon prepared from coconut husk (Ag-N@ZnO/CHAC). Zinc Oxide 27-37 vacuolar protein sorting 13 homolog A Homo sapiens 185-189 30248023-0 2019 MgCl2 passivated ZnO electron transporting layer to improve PbS quantum dot solar cells. Zinc Oxide 17-20 cholinergic receptor muscarinic 3 Homo sapiens 60-63 30248023-5 2019 The MgCl2 treated ZnO electron transporting layers boost the PbS colloidal quantum dot cell efficiency from 6.3% to 8.2%. Zinc Oxide 18-21 cholinergic receptor muscarinic 3 Homo sapiens 61-64 30611108-9 2019 The DMMIP-Ag-N@ZnO/CHAC electrochemical sensor proposed in this paper has great potential in food safety, drug residue determination and environmental monitoring. Zinc Oxide 15-18 vacuolar protein sorting 13 homolog A Homo sapiens 19-23 30628002-4 2019 It has proven that ZnO photocatalyst degraded the three contaminants very efficiently under almost all the studied experimental conditions, with efficiency rates of 92.3, 94.5, and 98.7 % for PSG, IBU, and NAP, respectively. Zinc Oxide 19-22 pregnancy specific beta-1-glycoprotein 5 Homo sapiens 192-195 30699223-0 2019 A sensitive photoelectrochemical assay of miRNA-155 based on a CdSe QDs//NPC-ZnO polyhedra photocurrent-direction switching system and target-triggered strand displacement amplification strategy. Zinc Oxide 77-80 microRNA 155 Homo sapiens 42-51 30497009-2 2019 The aim of this study was to develop and assess a simple procedure for surface functionalization of ZnO NPs by N-acetyl-l-cysteine (NAC) for anticancer camptothecin (CPT) delivery. Zinc Oxide 100-103 X-linked Kx blood group Homo sapiens 132-135 30497009-3 2019 NAC capped ZnO NPs were successfully made using ZnCl2 and NaOH in the presence of NAC. Zinc Oxide 11-14 X-linked Kx blood group Homo sapiens 0-3 30497009-3 2019 NAC capped ZnO NPs were successfully made using ZnCl2 and NaOH in the presence of NAC. Zinc Oxide 11-14 X-linked Kx blood group Homo sapiens 82-85 30497009-5 2019 To characterize the synthesized conjugate product (ZnO-NAC-CPT NPs), X-ray diffraction, Fourier Transform Infrared spectroscopy, transmission electron microscopy, scanning electron microscopy, and dynamic light scattering method were used. Zinc Oxide 51-54 X-linked Kx blood group Homo sapiens 55-58 30497009-6 2019 Our results indicated that the ZnO-NAC-CPT NPs exhibit near-spherical morphology and uniform dispersion with an average diameter of ~70 nm. Zinc Oxide 31-34 X-linked Kx blood group Homo sapiens 35-38 30159912-5 2019 The expression of endoplasmic reticulum stress marker DDIT3 was induced following an order of ZnO NRs > a-ZnO MS > c-ZnO MS > ZnO Mini-NRs, and the apoptosis gene CASP12 was induced following an order of a-ZnO MS > ZnO NRs > c-ZnO MS > ZnO Mini-NRs. Zinc Oxide 94-97 DNA damage inducible transcript 3 Homo sapiens 54-59 30503572-6 2019 The findings show that a physiologically relevant dose of ZnO NP can cause a significant decrease in glucose transport, which is consistent with gene expression changes for the basolateral glucose transporter GLUT2. Zinc Oxide 58-61 solute carrier family 2 member 2 Homo sapiens 209-214 30159912-5 2019 The expression of endoplasmic reticulum stress marker DDIT3 was induced following an order of ZnO NRs > a-ZnO MS > c-ZnO MS > ZnO Mini-NRs, and the apoptosis gene CASP12 was induced following an order of a-ZnO MS > ZnO NRs > c-ZnO MS > ZnO Mini-NRs. Zinc Oxide 109-112 DNA damage inducible transcript 3 Homo sapiens 54-59 30159912-5 2019 The expression of endoplasmic reticulum stress marker DDIT3 was induced following an order of ZnO NRs > a-ZnO MS > c-ZnO MS > ZnO Mini-NRs, and the apoptosis gene CASP12 was induced following an order of a-ZnO MS > ZnO NRs > c-ZnO MS > ZnO Mini-NRs. Zinc Oxide 109-112 DNA damage inducible transcript 3 Homo sapiens 54-59 30159912-5 2019 The expression of endoplasmic reticulum stress marker DDIT3 was induced following an order of ZnO NRs > a-ZnO MS > c-ZnO MS > ZnO Mini-NRs, and the apoptosis gene CASP12 was induced following an order of a-ZnO MS > ZnO NRs > c-ZnO MS > ZnO Mini-NRs. Zinc Oxide 109-112 DNA damage inducible transcript 3 Homo sapiens 54-59 30573230-9 2019 The properties of ZnO nanoparticles and its derivatives were detected by power XRD, TEM, EDS, FTIR, TGA, DLS, Zeta potential and UV. Zinc Oxide 18-21 T-box transcription factor 1 Homo sapiens 100-103 30679528-7 2019 With A549 cells, we have demonstrated that epithelial to mesenchymal transition and an increased duration of phosphorylation of eIF2alpha are crucial mechanisms routing better tolerance to TiO2 NP treatment over exposure to ZnO. Zinc Oxide 224-227 eukaryotic translation initiation factor 2A Homo sapiens 128-137 30620176-7 2019 Such a bioinspired ZnO nanocone-decorated 3D fiber network (i.e., N3D) has potential application to harvest fog water for production or living, for example, water recondensation in cooling water towers and in agricultural irrigation systems, even in water-deficient countries. Zinc Oxide 19-22 zinc finger protein, FOG family member 1 Homo sapiens 108-111 30342768-0 2019 Retraction notice to "Facile, Eco-friendly and template free phytosynthesis of Cauliflower like ZnO nanoparticles using leaf extract of Tamarindus indica (L.) and its biological evolution of antibacterial and antifungal activities" [Spectrochim. Zinc Oxide 96-99 ciliogenesis associated kinase 1 Homo sapiens 30-33 30576595-4 2019 We report herein the development of a mass tag covalently bonded with glutamate or N-methyl-d-aspartate that functions as both an electron acceptor to generate mass spectrometric signals on irradiated (Bi2O3)0.07(CoO)0.03(ZnO)0.9 nanoparticles with the third harmonic (355 nm) of Nd3+:YAG laser and as the core component to target bilobed clamshell-like structures of GluRs. Zinc Oxide 222-225 glutamyl-tRNA synthetase 2, mitochondrial Mus musculus 368-373 30340083-5 2019 Exposure to pristine ZnO NPs significantly promoted the expression of ER stress-apoptosis genes, namely DDIT3, XBP-1s, CASP9, CASP12 and BAX (p < 0.05), but hydrophobic ZnO NPs only significantly promoted the expression of BAX (p < 0.05). Zinc Oxide 21-24 DNA damage inducible transcript 3 Homo sapiens 104-109 30340083-5 2019 Exposure to pristine ZnO NPs significantly promoted the expression of ER stress-apoptosis genes, namely DDIT3, XBP-1s, CASP9, CASP12 and BAX (p < 0.05), but hydrophobic ZnO NPs only significantly promoted the expression of BAX (p < 0.05). Zinc Oxide 21-24 caspase 9 Homo sapiens 119-124 30340083-5 2019 Exposure to pristine ZnO NPs significantly promoted the expression of ER stress-apoptosis genes, namely DDIT3, XBP-1s, CASP9, CASP12 and BAX (p < 0.05), but hydrophobic ZnO NPs only significantly promoted the expression of BAX (p < 0.05). Zinc Oxide 21-24 caspase 12 (gene/pseudogene) Homo sapiens 126-132 30340083-5 2019 Exposure to pristine ZnO NPs significantly promoted the expression of ER stress-apoptosis genes, namely DDIT3, XBP-1s, CASP9, CASP12 and BAX (p < 0.05), but hydrophobic ZnO NPs only significantly promoted the expression of BAX (p < 0.05). Zinc Oxide 21-24 BCL2 associated X, apoptosis regulator Homo sapiens 137-140 30340083-5 2019 Exposure to pristine ZnO NPs significantly promoted the expression of ER stress-apoptosis genes, namely DDIT3, XBP-1s, CASP9, CASP12 and BAX (p < 0.05), but hydrophobic ZnO NPs only significantly promoted the expression of BAX (p < 0.05). Zinc Oxide 21-24 BCL2 associated X, apoptosis regulator Homo sapiens 226-229 30340083-6 2019 Exposure to pristine ZnO NPs also significantly reduced the expression of autophagic gene BECN1 (p < 0.05) but not ATG7 (p > 0.05), whereas hydrophobic ZnO NPs significantly reduced the expression of ATG7 and BECN1 (p < 0.01). Zinc Oxide 21-24 beclin 1 Homo sapiens 90-95 30340083-6 2019 Exposure to pristine ZnO NPs also significantly reduced the expression of autophagic gene BECN1 (p < 0.05) but not ATG7 (p > 0.05), whereas hydrophobic ZnO NPs significantly reduced the expression of ATG7 and BECN1 (p < 0.01). Zinc Oxide 21-24 autophagy related 7 Homo sapiens 118-122 30340083-6 2019 Exposure to pristine ZnO NPs also significantly reduced the expression of autophagic gene BECN1 (p < 0.05) but not ATG7 (p > 0.05), whereas hydrophobic ZnO NPs significantly reduced the expression of ATG7 and BECN1 (p < 0.01). Zinc Oxide 21-24 autophagy related 7 Homo sapiens 206-210 30340083-6 2019 Exposure to pristine ZnO NPs also significantly reduced the expression of autophagic gene BECN1 (p < 0.05) but not ATG7 (p > 0.05), whereas hydrophobic ZnO NPs significantly reduced the expression of ATG7 and BECN1 (p < 0.01). Zinc Oxide 21-24 beclin 1 Homo sapiens 215-220 30288931-4 2019 The ion- and electron-conductive Li2 O-Zn middle layer can be ingeniously introduced by means of the poor reversed conversion reaction between ZnO and Li+ ions after the first cycle. Zinc Oxide 143-146 ATP binding cassette subfamily A member 12 Homo sapiens 33-36 31458461-4 2018 By the characterization of BET, XRD, TPR, FTIR, and in situ XAFS, the optimal calcination temperature leads to the small crystallite of NiO and ZnO species. Zinc Oxide 144-147 delta/notch like EGF repeat containing Homo sapiens 27-30 30766660-2 2019 Previously, we found that zinc oxide (ZnO) NPs that are neurotoxic to human dopaminergic neuroblastoma SH-SY5Y cells are mediated by lipoxygenase (LOX), not cyclooxygenase-2 (COX-2). Zinc Oxide 26-36 prostaglandin-endoperoxide synthase 2 Homo sapiens 175-180 30766660-2 2019 Previously, we found that zinc oxide (ZnO) NPs that are neurotoxic to human dopaminergic neuroblastoma SH-SY5Y cells are mediated by lipoxygenase (LOX), not cyclooxygenase-2 (COX-2). Zinc Oxide 38-41 prostaglandin-endoperoxide synthase 2 Homo sapiens 175-180 30766660-7 2019 ZnO NPs and ZnO showed similar dose-dependent and significant cytotoxic effects at concentrations >= 15 mug/mL, in accordance with annexin V expression, caspase-3/7 activity, and MMP results. Zinc Oxide 0-3 annexin A5 Homo sapiens 134-143 30766660-7 2019 ZnO NPs and ZnO showed similar dose-dependent and significant cytotoxic effects at concentrations >= 15 mug/mL, in accordance with annexin V expression, caspase-3/7 activity, and MMP results. Zinc Oxide 0-3 caspase 3 Homo sapiens 156-165 30766660-7 2019 ZnO NPs and ZnO showed similar dose-dependent and significant cytotoxic effects at concentrations >= 15 mug/mL, in accordance with annexin V expression, caspase-3/7 activity, and MMP results. Zinc Oxide 12-15 annexin A5 Homo sapiens 134-143 30766660-7 2019 ZnO NPs and ZnO showed similar dose-dependent and significant cytotoxic effects at concentrations >= 15 mug/mL, in accordance with annexin V expression, caspase-3/7 activity, and MMP results. Zinc Oxide 12-15 caspase 3 Homo sapiens 156-165 30766660-8 2019 Human MSCs exhibited both COX-2 and LOX-mediated cytotoxicity after exposure to ZnO NPs, which was different from human neuroblastoma cells. Zinc Oxide 80-83 prostaglandin-endoperoxide synthase 2 Homo sapiens 26-31 30766660-10 2019 Conclusively, these results suggest that ZnO NPs exhibit both COX-2- and LOX-mediated apoptosis by the participation of mitochondrial dysfunction in human MSC cultures. Zinc Oxide 41-44 prostaglandin-endoperoxide synthase 2 Homo sapiens 62-67 30315849-0 2019 Insulin adsorption onto zinc oxide nanoparticle mediates conformational rearrangement into amyloid-prone structure with enhanced cytotoxic propensity. Zinc Oxide 24-34 insulin Homo sapiens 0-7 30315849-3 2019 Hence, the present study deals with the effect of zinc oxide nanoparticles (ZnONP) on the amyloidogenicity and cytotoxicity of insulin. Zinc Oxide 50-60 insulin Homo sapiens 127-134 30298533-6 2019 Transepithelial electrical resistance of distal small intestinal mucosa was higher for pigs fed the alternative ZnO source as compared with groups fed 110 mg/kg Zn of conventional ZnO, in line with a trend for higher gene expression of claudin-1 and zona occludens-1. Zinc Oxide 112-115 claudin 1 Sus scrofa 236-266 31217912-6 2019 Odontogenic potential of ZnO and ZrO2 particles in combination with WPC was investigated by alkaline phosphatase (ALP) activity and ionized calcium level of supernatant culture media at different time intervals. Zinc Oxide 25-28 alkaline phosphatase, placental Homo sapiens 92-112 31217912-6 2019 Odontogenic potential of ZnO and ZrO2 particles in combination with WPC was investigated by alkaline phosphatase (ALP) activity and ionized calcium level of supernatant culture media at different time intervals. Zinc Oxide 25-28 alkaline phosphatase, placental Homo sapiens 114-117 31217912-14 2019 WPC enriched with ZnO and ZrO2 increased ALP activity and calcium ion release of human dental pulp stem cells over a period of 21 days in vitro. Zinc Oxide 18-21 alkaline phosphatase, placental Homo sapiens 41-44 30207239-0 2019 ZnO Nanoparticles Catalyst in the Synthesis of Bioactive Fused Pyrimidines as Anti-breast Cancer Agents Targeting VEGFR-2. Zinc Oxide 0-3 kinase insert domain receptor Homo sapiens 114-121 30207239-11 2019 CONCLUSION: We succeeded in this context to synthesize new fused pyrimidines using ZnO(NPs) as anti-breast cancer agents targeting VEGFR-2. Zinc Oxide 83-86 kinase insert domain receptor Homo sapiens 131-138 31089315-7 2019 The coadministration of ZnO NPs ameliorated most of the undesirable effects of CPF, through elevation of macrophage and serum lysozyme activities, increased the levels of IL-2 and IL-6, corrected the oxidative stress markers, and alleviated most of the adverse effect exerted by CPF in liver and spleen tissues. Zinc Oxide 24-27 interleukin 2 Rattus norvegicus 171-175 31089315-7 2019 The coadministration of ZnO NPs ameliorated most of the undesirable effects of CPF, through elevation of macrophage and serum lysozyme activities, increased the levels of IL-2 and IL-6, corrected the oxidative stress markers, and alleviated most of the adverse effect exerted by CPF in liver and spleen tissues. Zinc Oxide 24-27 interleukin 6 Rattus norvegicus 180-184 30419705-0 2018 [The role of heme oxygenase-1 on oxidative stress injury induced by zinc oxide nanoparticles in human umbilical vein endothelial cells line EA.hy926 cells]. Zinc Oxide 68-78 heme oxygenase 1 Homo sapiens 13-29 30568444-3 2018 Results: Only ZnO NPs significantly induced cytotoxicity, accompanied by increased intracellular reactive oxygen species, Zn ions, and endoplasmic reticulum stress biomarkers (DDIT3 expression and p-Chop proteins). Zinc Oxide 14-17 DNA damage inducible transcript 3 Homo sapiens 176-181 30568444-5 2018 Furthermore, KLF4 expression (a transcription factor for SMC-phenotype switch) was significantly induced by TiO2 NPs and modestly by ZnO NPs, but the expression of CD68 remained unaltered. Zinc Oxide 133-136 Kruppel like factor 4 Homo sapiens 13-17 30423876-7 2018 Hybrid composites of SAN/PANI/FLG coatings have demonstrated better performances compared to ZnO/GO in the corrosive environments under investigation. Zinc Oxide 93-96 filaggrin Homo sapiens 30-33 30419705-8 2018 In all groups ROS levels were detected after exposed to ZnO-NPs for 4 hours, the protein expression of HO-1 was detected after exposed to ZnO-NPs for 24 hours. Zinc Oxide 138-141 heme oxygenase 1 Homo sapiens 103-107 30419705-10 2018 HO-1 expression in ZnPPIx pretreatment group decreased compared with ZnO-NPs group (1.05+-0.05 vs. 1.12+-0.01, P<0.05), meanwhile ROS level enhanced (62 683.95+-2 589.59 vs. 53 654.53+-2 229.01, P<0.05). Zinc Oxide 69-72 heme oxygenase 1 Homo sapiens 0-4 30419705-13 2018 HO-1 regulated ZnO-NPs-induced oxidative stress. Zinc Oxide 15-18 heme oxygenase 1 Homo sapiens 0-4 30226471-2 2018 Here, we report the fabrication of ZnO/CdS self-biased heterojunction photodetectors on soft lithographically patterned PEDOT:PSS layers with grating geometry. Zinc Oxide 35-38 CDP-diacylglycerol synthase 1 Homo sapiens 39-42 30419522-5 2018 UV-DRS spectrum of nano-ZnO particles showed below at wave length 400 nm. Zinc Oxide 24-27 sushi repeat containing protein X-linked Homo sapiens 3-6 30428752-0 2018 Human keratinocytes adapt to ZnO nanoparticles induced toxicity via complex paracrine crosstalk and Nrf2-proteasomal signal transduction. Zinc Oxide 29-32 NFE2 like bZIP transcription factor 2 Homo sapiens 100-104 30207296-4 2018 More than 60% of electrons are effectively blocked by the ZnO interface barrier compared with the standard device, resulting in increasing the maximum luminance of the device from 25 390 to 48 220 cd m-2 and the current efficiency from 1.5 to 3.2 cd A-1. Zinc Oxide 58-61 BCL2 related protein A1 Homo sapiens 250-253 30419705-1 2018 Objective: To explore the effect of heme oxygenase-1 (HO-1) on level of reactive oxygen species (ROS) induced by zinc oxide nanoparticles (ZnO-NPs) in Human umbilical vein endothelial cells line EA.hy926. Zinc Oxide 113-123 heme oxygenase 1 Homo sapiens 36-52 30419705-1 2018 Objective: To explore the effect of heme oxygenase-1 (HO-1) on level of reactive oxygen species (ROS) induced by zinc oxide nanoparticles (ZnO-NPs) in Human umbilical vein endothelial cells line EA.hy926. Zinc Oxide 113-123 heme oxygenase 1 Homo sapiens 54-58 30419705-3 2018 The ROS level, reflected by mean fluorescence intensity (MFI), was examined by flow cytometer after 4 hours exposure, the protein expression of HO-1 which was determined by Western Blot after exposed to ZnO-NPs for 24 hours. Zinc Oxide 203-206 heme oxygenase 1 Homo sapiens 144-148 30419705-6 2018 15 mg/L ZnO-NPs was chosen to conduct the experiment of HO-1 activation and inhibition. Zinc Oxide 8-11 heme oxygenase 1 Homo sapiens 56-60 30419705-8 2018 In all groups ROS levels were detected after exposed to ZnO-NPs for 4 hours, the protein expression of HO-1 was detected after exposed to ZnO-NPs for 24 hours. Zinc Oxide 56-59 heme oxygenase 1 Homo sapiens 103-107 30500804-0 2018 Photocatalytic performance of Ag2S/ZnO/ZnS nanocomposites with high visible light response prepared via microwave-assisted hydrothermal two-step method. Zinc Oxide 35-38 angiotensin II receptor type 1 Homo sapiens 30-34 29064322-0 2018 Interaction mechanism of insulin with ZnO nanoparticles by replica exchange molecular dynamics simulation. Zinc Oxide 38-41 insulin Homo sapiens 25-32 29064322-3 2018 In the present work, the interaction mechanism of insulin with ZnO nanoparticles was studied. Zinc Oxide 63-66 insulin Homo sapiens 50-57 29064322-5 2018 According to the results obtained by REMD simulation, it was found that insulin interacts with ZnO nanoparticle surface via its polar and charged amino acids. Zinc Oxide 95-98 insulin Homo sapiens 72-79 29064322-6 2018 Unfolding insulin at ZnO nanoparticle surface, the terminal parts of its chains play the main role. Zinc Oxide 21-24 insulin Homo sapiens 10-17 30500804-6 2018 Meanwhile, 1% Ag2S/ZnO/ZnS also showed a good degradation effect on other dyes with different structures, and its degradation efficiency did not change significantly after three cycles, showing certain stability. Zinc Oxide 19-22 angiotensin II receptor type 1 Homo sapiens 14-18 30500804-3 2018 At the same time, due to the introduction of narrow band gap Ag2S, the synthesized composite can effectively increase the visible optical absorption of ZnO/ZnS composites. Zinc Oxide 152-155 angiotensin II receptor type 1 Homo sapiens 61-65 30500804-4 2018 Among them, 1% Ag2S/ZnO/ZnS showed a mixed structure of nano-line and nano-particle, of which BET value increased significantly, and the morphology was more excellent. Zinc Oxide 20-23 angiotensin II receptor type 1 Homo sapiens 15-19 30352603-6 2018 By contrast, intratracheal instillation of low toxicity TiO2 (P90), TiO2 (Rutile), ZnO, and toner increased the concentration of MPO in BALF only transiently, and inhalation of TiO2 (Rutile) and ZnO induced almost no increase of the MPO. Zinc Oxide 83-86 myeloperoxidase Rattus norvegicus 129-132 30417860-6 2018 To obtain the requisite Zn-polarity, careful surface treatment of GaN templates and control over the VI/II ratio during the growth of low temperature ZnO nucleation layer are utilized. Zinc Oxide 150-153 cytochrome c oxidase subunit 8A Homo sapiens 101-106 30352603-6 2018 By contrast, intratracheal instillation of low toxicity TiO2 (P90), TiO2 (Rutile), ZnO, and toner increased the concentration of MPO in BALF only transiently, and inhalation of TiO2 (Rutile) and ZnO induced almost no increase of the MPO. Zinc Oxide 195-198 myeloperoxidase Rattus norvegicus 129-132 29691881-4 2018 Surprisingly, H3 markedly decreased the initial concentration of ZnO NPs required to induce cytotoxicity to Caco-2, HepG2, THP-1 and human umbilical vein endothelial cells, which suggested that H3 could promote the toxicity of ZnO NPs to both cancerous and normal cells. Zinc Oxide 65-68 GLI family zinc finger 2 Homo sapiens 123-128 29783874-0 2018 Influence of bovine serum albumin pre-incubation on toxicity and ER stress-apoptosis gene expression in THP-1 macrophages exposed to ZnO nanoparticles. Zinc Oxide 133-136 GLI family zinc finger 2 Homo sapiens 104-109 29783874-7 2018 However, ZnO NPs with or without pre-incubation of BSA resulted in comparable intracellular Zn ions, glutathione and reactive oxygen species in THP-1 macrophages. Zinc Oxide 9-12 GLI family zinc finger 2 Homo sapiens 144-149 29783874-8 2018 Exposure to ZnO NPs promoted the expression of endoplasmic reticulum (ER) stress markers (DDIT3 and XBP-1s) and apoptosis genes (CASP9 and CASP12). Zinc Oxide 12-15 DNA damage inducible transcript 3 Homo sapiens 90-95 29783874-8 2018 Exposure to ZnO NPs promoted the expression of endoplasmic reticulum (ER) stress markers (DDIT3 and XBP-1s) and apoptosis genes (CASP9 and CASP12). Zinc Oxide 12-15 caspase 9 Homo sapiens 129-134 29783874-8 2018 Exposure to ZnO NPs promoted the expression of endoplasmic reticulum (ER) stress markers (DDIT3 and XBP-1s) and apoptosis genes (CASP9 and CASP12). Zinc Oxide 12-15 caspase 12 (gene/pseudogene) Homo sapiens 139-145 30206611-7 2018 In the detection of carcinoembryonic antigen, the limit of detection reached 100 fg mL-1, which indicated that the ZnO@PAA nanorod array-based microfluidic device exhibits remarkable fluorescence detection performance towards protein markers and possesses potential to be applied to point-of-care diagnostics and high throughput cancer biomarker detection. Zinc Oxide 115-118 L1 cell adhesion molecule Mus musculus 84-88 30141818-5 2018 Furthermore, the photocatalytic H2 evolution activities of ZnO and C3N4 can also be improved by introducing SnO via simple mechanical mixing. Zinc Oxide 59-62 strawberry notch homolog 2 Homo sapiens 108-111 30213055-10 2018 Synthesized ZnO exhibited BET surface area of 9.2629 m2/g and showed absorption of light in the UV region. Zinc Oxide 12-15 delta/notch like EGF repeat containing Homo sapiens 26-29 30340606-8 2018 The mechanism underlying how ZnO NPs induce neuroinflammation via the Ca2+-dependent NF-kappaB, ERK and p38 activation pathways was verified at the cytological level. Zinc Oxide 29-32 mitogen activated protein kinase 14 Rattus norvegicus 104-107 30209460-1 2018 By adjusting the content of ZnF2-SrF2/ZnO-SrO, a series of SiO2-Al2O3-B2O3-Na2O-ZnO/ZnF2-SrO/SrF2-Ag multiphase glasses was designed and prepared via a melt-quenching method. Zinc Oxide 80-83 zinc finger protein 2 Homo sapiens 28-32 30209460-5 2018 The ZnO-Al2O3-rich or ZnO-SiO2-rich (i.e. SiO2-rich in GZnOSrO) phase has a relatively high solubility for [Ag2]2+ pairs. Zinc Oxide 4-7 anterior gradient 2, protein disulphide isomerase family member Homo sapiens 108-111 30209460-5 2018 The ZnO-Al2O3-rich or ZnO-SiO2-rich (i.e. SiO2-rich in GZnOSrO) phase has a relatively high solubility for [Ag2]2+ pairs. Zinc Oxide 22-25 anterior gradient 2, protein disulphide isomerase family member Homo sapiens 108-111 29870809-2 2018 In order to determine possible protein target, interaction of ZnO QDs was studied with CRP (Cyclic AMP Receptor Protein), a global transcription regulator protein. Zinc Oxide 62-65 catabolite gene activator protein Escherichia coli 87-90 29870809-2 2018 In order to determine possible protein target, interaction of ZnO QDs was studied with CRP (Cyclic AMP Receptor Protein), a global transcription regulator protein. Zinc Oxide 62-65 catabolite gene activator protein Escherichia coli 92-119 29870809-3 2018 Binding between ZnO QDs and E. coli CRP was mainly studied by isothermal titration calorimetry (ITC), structural changes of protein were monitored by fluorescence and circular dichroism spectroscopy, and in-vitro transcription assay was used to asses CRP activity. Zinc Oxide 16-19 catabolite gene activator protein Escherichia coli 36-39 29870809-3 2018 Binding between ZnO QDs and E. coli CRP was mainly studied by isothermal titration calorimetry (ITC), structural changes of protein were monitored by fluorescence and circular dichroism spectroscopy, and in-vitro transcription assay was used to asses CRP activity. Zinc Oxide 16-19 catabolite gene activator protein Escherichia coli 251-254 29870809-4 2018 Result shows that both electrostatic and hydrophobic interactions are involved in CRP-ZnO binding. Zinc Oxide 86-89 catabolite gene activator protein Escherichia coli 82-85 29870809-5 2018 Different spectroscopic investigation revealed that ZnO binding to CRP leads to extensive unfolding and destabilization, which ultimately leads to protein aggregation. Zinc Oxide 52-55 catabolite gene activator protein Escherichia coli 67-70 29870809-6 2018 It was also observed that in presence of ZnO dimerization ability of CRP was sharply reduced. Zinc Oxide 41-44 catabolite gene activator protein Escherichia coli 69-72 29870809-7 2018 In-vitro transcription assay also shows that CRP activity gets severely compromised on ZnO binding. Zinc Oxide 87-90 catabolite gene activator protein Escherichia coli 45-48 29870809-8 2018 All our data suggests that ZnO QD binding to CRP and consequent structural and functional changes most probably plays a crucial role in ZnO QD induced antimicrobial action. Zinc Oxide 27-30 catabolite gene activator protein Escherichia coli 45-48 29870809-8 2018 All our data suggests that ZnO QD binding to CRP and consequent structural and functional changes most probably plays a crucial role in ZnO QD induced antimicrobial action. Zinc Oxide 136-139 catabolite gene activator protein Escherichia coli 45-48 29894783-1 2018 Phospholipase D (PLD) was effectively immobilized on a ZnO nanowires/macroporous SiO2 composite support through an in-situ cross-linking method. Zinc Oxide 55-58 glycosylphosphatidylinositol specific phospholipase D1 Homo sapiens 0-15 29894783-1 2018 Phospholipase D (PLD) was effectively immobilized on a ZnO nanowires/macroporous SiO2 composite support through an in-situ cross-linking method. Zinc Oxide 55-58 glycosylphosphatidylinositol specific phospholipase D1 Homo sapiens 17-20 29882686-10 2018 ZnO and CuO nanoparticles displayed severe cytotoxicity and enhanced gene expression of heme oxygenase-1 (HO-1) and interleukin-8 (IL-8). Zinc Oxide 0-3 heme oxygenase 1 Homo sapiens 88-104 29882686-10 2018 ZnO and CuO nanoparticles displayed severe cytotoxicity and enhanced gene expression of heme oxygenase-1 (HO-1) and interleukin-8 (IL-8). Zinc Oxide 0-3 heme oxygenase 1 Homo sapiens 106-110 29882686-10 2018 ZnO and CuO nanoparticles displayed severe cytotoxicity and enhanced gene expression of heme oxygenase-1 (HO-1) and interleukin-8 (IL-8). Zinc Oxide 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 116-129 29882686-10 2018 ZnO and CuO nanoparticles displayed severe cytotoxicity and enhanced gene expression of heme oxygenase-1 (HO-1) and interleukin-8 (IL-8). Zinc Oxide 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 29882686-12 2018 Additionally, the gene expression of metallothionein 2A (MT2A) was enhanced in the ZnO, CuO, and Bi2O3 exposed cells. Zinc Oxide 83-86 metallothionein 2A Homo sapiens 37-55 29882686-12 2018 Additionally, the gene expression of metallothionein 2A (MT2A) was enhanced in the ZnO, CuO, and Bi2O3 exposed cells. Zinc Oxide 83-86 metallothionein 2A Homo sapiens 57-61 30462061-3 2018 Results show that the sensor with ZnO nanoflowers exhibits a high sensitivity of 5.75 pm/(mug L-1) for ammonia concentration ranging from 0 to 5460 mug L-1, which is more than 2.6 times higher than that of the sensor with a coating of ZnO microspheres [2.2 pm/(mug L-1)]. Zinc Oxide 34-37 immunoglobulin kappa variable 1-16 Homo sapiens 95-98 30462061-3 2018 Results show that the sensor with ZnO nanoflowers exhibits a high sensitivity of 5.75 pm/(mug L-1) for ammonia concentration ranging from 0 to 5460 mug L-1, which is more than 2.6 times higher than that of the sensor with a coating of ZnO microspheres [2.2 pm/(mug L-1)]. Zinc Oxide 34-37 immunoglobulin kappa variable 1-16 Homo sapiens 154-157 30462061-3 2018 Results show that the sensor with ZnO nanoflowers exhibits a high sensitivity of 5.75 pm/(mug L-1) for ammonia concentration ranging from 0 to 5460 mug L-1, which is more than 2.6 times higher than that of the sensor with a coating of ZnO microspheres [2.2 pm/(mug L-1)]. Zinc Oxide 34-37 immunoglobulin kappa variable 1-16 Homo sapiens 154-157 30462061-3 2018 Results show that the sensor with ZnO nanoflowers exhibits a high sensitivity of 5.75 pm/(mug L-1) for ammonia concentration ranging from 0 to 5460 mug L-1, which is more than 2.6 times higher than that of the sensor with a coating of ZnO microspheres [2.2 pm/(mug L-1)]. Zinc Oxide 237-240 immunoglobulin kappa variable 1-16 Homo sapiens 95-98 30124901-0 2018 Zinc oxide nanoparticles affect the expression of p53, Ras p21 and JNKs: an ex vivo/in vitro exposure study in respiratory disease patients. Zinc Oxide 0-10 tumor protein p53 Homo sapiens 50-53 30124901-0 2018 Zinc oxide nanoparticles affect the expression of p53, Ras p21 and JNKs: an ex vivo/in vitro exposure study in respiratory disease patients. Zinc Oxide 0-10 H3 histone pseudogene 16 Homo sapiens 59-62 30213995-2 2018 The prepared ZnO nanorods were used as an amperometric enzyme electrode, in which glucose oxidase (GOx) was immobilised through physical adsorption. Zinc Oxide 13-16 hydroxyacid oxidase 1 Homo sapiens 82-97 30213995-2 2018 The prepared ZnO nanorods were used as an amperometric enzyme electrode, in which glucose oxidase (GOx) was immobilised through physical adsorption. Zinc Oxide 13-16 hydroxyacid oxidase 1 Homo sapiens 99-102 30213995-9 2018 The Nafion/GOx/ZnO NRs/ITO electrode also displayed a linear response to glucose ranging from 0.05 mM to 1 mM, with a sensitivity of 48.75 microA/mM and a low Michaelis-Menten constant of 0.34 mM. Zinc Oxide 15-18 hydroxyacid oxidase 1 Homo sapiens 11-14 29691881-7 2018 Exposure to ZnO NPs at 3 hours induced the expression of endoplasmic reticulum stress markers DDIT3 and XBP-1 s, which was suppressed by H3. Zinc Oxide 12-15 DNA damage inducible transcript 3 Homo sapiens 94-99 29691881-7 2018 Exposure to ZnO NPs at 3 hours induced the expression of endoplasmic reticulum stress markers DDIT3 and XBP-1 s, which was suppressed by H3. Zinc Oxide 12-15 X-box binding protein 1 Homo sapiens 104-109 30140055-0 2018 Facile and inexpensive fabrication of zinc oxide based bio-surfaces for C-reactive protein detection. Zinc Oxide 38-48 C-reactive protein Homo sapiens 72-90 29677731-4 2018 While physisorbed water or oxygen-related ions can detach from the ZnO surface during evacuation, exposure to high energy in the electron beam is believed to detach the chemisorbed anions of O- and O-2 from the surface of ZnO nanorods, which releases more electrons into the channel. Zinc Oxide 222-225 immunoglobulin kappa variable 1D-39 Homo sapiens 191-201 29677828-0 2018 Influence of Post-Heat Treatment of ZnO:Al Transparent Electrode for Copper Indium Gallium Selenide Thin Film Solar Cell. Zinc Oxide 36-39 solute carrier family 35 member G1 Homo sapiens 13-17 29677828-3 2018 In this study, ZnO:Al films were deposited on glass under various post-heat temperature using RF sputtering to observe the characteristics of ZnO:Al films such as Hall mobility, carrier concentration, and resistivity; subsequently, the ZnO:Al films were applied to a CIGS solar cell as a window. Zinc Oxide 15-18 solute carrier family 35 member G1 Homo sapiens 66-70 29697006-0 2018 Toxicity of ZnO nanoparticles (NPs) with or without hydrophobic surface coating to THP-1 macrophages: interactions with BSA or oleate-BSA. Zinc Oxide 12-15 GLI family zinc finger 2 Homo sapiens 83-88 29697006-6 2018 Exposure to both types of ZnO NPs was associated with cytotoxicity to THP-1 macrophages, which was equally mitigated by BSA or OA-BSA associated with decreased cellular Zn elements. Zinc Oxide 26-29 GLI family zinc finger 2 Homo sapiens 70-75 29985599-4 2018 The detailed mechanism was investigated, showing that ascorbic acid can not only act as the electron donor to capture the holes in CdS/ZnO-HNRs, leading to the increase photocurrent, but also as the reductant to form silver shells on Au nanobipyramids, generating multiply vivid color variations and blue shifts. Zinc Oxide 135-138 CDP-diacylglycerol synthase 1 Homo sapiens 131-134 29458646-7 2018 The electronegativity differences between the metal and oxygen was ZnO (1.79) > CdO (1.75) > CuO (1.54) > AgO (1.51). Zinc Oxide 67-70 cell adhesion associated, oncogene regulated Homo sapiens 83-86 29863331-0 2018 Suppressed Interfacial Charge Recombination of PbS Quantum Dot Photovoltaics by Graphene Incorporated into ZnO Nanoparticles. Zinc Oxide 107-110 cholinergic receptor muscarinic 3 Homo sapiens 47-50 33435116-8 2018 MeHA/ELP hydrogels were then rendered antimicrobial through the incorporation of zinc oxide (ZnO) nanoparticles, and were shown to significantly inhibit the growth of methicillin-resistant Staphylococcus aureus (MRSA), as compared to controls. Zinc Oxide 81-91 nuclear receptor subfamily 5 group A member 1 Homo sapiens 5-8 31458911-3 2018 High-resolution transmission electron microscopy images show the close contacts between SnO2-ZnO QDs with the g-C3N4 in the ternary SnO2-ZnO QDs/g-C3N4 hybrid. Zinc Oxide 93-96 strawberry notch homolog 1 Homo sapiens 88-91 31458911-5 2018 The enriched charge-carrier separation and transportation in the SnO2-ZnO QDs/g-C3N4 hybrid was determined based on electrochemical impedance and photocurrent analyses. Zinc Oxide 70-73 strawberry notch homolog 1 Homo sapiens 65-68 31458911-6 2018 This remarkable photoactivity is ascribed to the "smart" heterostructure, which yields numerous benefits, such as visible-light-driven fast electron and hole transfer, due to the strong interaction between the SnO2-ZnO QDs with the g-C3N4 matrix. Zinc Oxide 215-218 strawberry notch homolog 1 Homo sapiens 210-213 33435111-0 2018 Microneedles Integrated with ZnO Quantum-Dot-Capped Mesoporous Bioactive Glasses for Glucose-Mediated Insulin Delivery. Zinc Oxide 29-32 insulin Homo sapiens 102-109 29768979-6 2018 In utero exposure of ZnO NPs increased the relative expression of StAR in 100 mg/kg body weight (BW) ZnO NP-treated and bulk ZnO-treated groups and P450 side-chain cleavage enzyme (P450scc) in 50 mg/kg BW ZnO NP-treated and 100 mg/kg of bulk ZnO-treated male offspring. Zinc Oxide 21-24 steroidogenic acute regulatory protein Mus musculus 66-70 29768979-6 2018 In utero exposure of ZnO NPs increased the relative expression of StAR in 100 mg/kg body weight (BW) ZnO NP-treated and bulk ZnO-treated groups and P450 side-chain cleavage enzyme (P450scc) in 50 mg/kg BW ZnO NP-treated and 100 mg/kg of bulk ZnO-treated male offspring. Zinc Oxide 21-24 cytochrome P450, family 11, subfamily a, polypeptide 1 Mus musculus 148-179 29768979-6 2018 In utero exposure of ZnO NPs increased the relative expression of StAR in 100 mg/kg body weight (BW) ZnO NP-treated and bulk ZnO-treated groups and P450 side-chain cleavage enzyme (P450scc) in 50 mg/kg BW ZnO NP-treated and 100 mg/kg of bulk ZnO-treated male offspring. Zinc Oxide 21-24 cytochrome P450, family 11, subfamily a, polypeptide 1 Mus musculus 181-188 29768979-6 2018 In utero exposure of ZnO NPs increased the relative expression of StAR in 100 mg/kg body weight (BW) ZnO NP-treated and bulk ZnO-treated groups and P450 side-chain cleavage enzyme (P450scc) in 50 mg/kg BW ZnO NP-treated and 100 mg/kg of bulk ZnO-treated male offspring. Zinc Oxide 101-104 steroidogenic acute regulatory protein Mus musculus 66-70 29768979-6 2018 In utero exposure of ZnO NPs increased the relative expression of StAR in 100 mg/kg body weight (BW) ZnO NP-treated and bulk ZnO-treated groups and P450 side-chain cleavage enzyme (P450scc) in 50 mg/kg BW ZnO NP-treated and 100 mg/kg of bulk ZnO-treated male offspring. Zinc Oxide 101-104 steroidogenic acute regulatory protein Mus musculus 66-70 29768979-6 2018 In utero exposure of ZnO NPs increased the relative expression of StAR in 100 mg/kg body weight (BW) ZnO NP-treated and bulk ZnO-treated groups and P450 side-chain cleavage enzyme (P450scc) in 50 mg/kg BW ZnO NP-treated and 100 mg/kg of bulk ZnO-treated male offspring. Zinc Oxide 101-104 steroidogenic acute regulatory protein Mus musculus 66-70 29768979-6 2018 In utero exposure of ZnO NPs increased the relative expression of StAR in 100 mg/kg body weight (BW) ZnO NP-treated and bulk ZnO-treated groups and P450 side-chain cleavage enzyme (P450scc) in 50 mg/kg BW ZnO NP-treated and 100 mg/kg of bulk ZnO-treated male offspring. Zinc Oxide 101-104 steroidogenic acute regulatory protein Mus musculus 66-70 33435116-8 2018 MeHA/ELP hydrogels were then rendered antimicrobial through the incorporation of zinc oxide (ZnO) nanoparticles, and were shown to significantly inhibit the growth of methicillin-resistant Staphylococcus aureus (MRSA), as compared to controls. Zinc Oxide 93-96 nuclear receptor subfamily 5 group A member 1 Homo sapiens 5-8 29904768-4 2018 The highly stable and reusable sample CIS/ZO-2 possesses the highest photocatalytic activity (94.04%), and its rate constant (k = 0.06357 min-1) is about 4.96 and 22.31 times as high as those of pure CdIn2S4 and ZnO. Zinc Oxide 212-215 tight junction protein 2 Homo sapiens 42-46 29365097-2 2018 4F2, a camelid VHH antibody, recognizes ZnO surface and has been applied for sensor applications. Zinc Oxide 40-43 solute carrier family 3 member 2 Homo sapiens 0-3 30127816-8 2018 In contrast, lymphocytes treated with different concentrations of ZnO NPs showed a significant decrease in the percent of mortality as well as the levels of TNF-alpha, as compared with CP-treated lymphocytes. Zinc Oxide 66-69 tumor necrosis factor Homo sapiens 157-166 30127816-9 2018 Besides, ZnO NPs increased the levels of AChE and TAP at 1 microg/mL. Zinc Oxide 9-12 acetylcholinesterase (Cartwright blood group) Homo sapiens 41-45 29622477-0 2018 Zinc oxide nanoparticles induce HIF-1alpha protein stabilization through increased reactive oxygen species generation from electron transfer chain complex III of mitochondria. Zinc Oxide 0-10 hypoxia inducible factor 1 subunit alpha Homo sapiens 32-42 29914155-0 2018 Hazy Al2O3-FTO Nanocomposites: A Comparative Study with FTO-Based Nanocomposites Integrating ZnO and S:TiO2 Nanostructures. Zinc Oxide 93-96 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 56-59 29950828-0 2018 Zinc oxide nanoparticles induce toxicity in CAL 27 oral cancer cell lines by activating PINK1/Parkin-mediated mitophagy. Zinc Oxide 0-10 PTEN induced kinase 1 Homo sapiens 88-93 29950828-9 2018 The ZnO NPs increased the intracellular reactive oxygen species levels and decreased the mitochondrial membrane potential in a time-dependent manner as well as activated the PINK1/Parkin-mediated mitophagy process in CAL 27 cells. Zinc Oxide 4-7 PTEN induced kinase 1 Homo sapiens 174-179 29845983-3 2018 Here, ZnO nanoparticles were used as the electron-transporting material (ETM) and methylammonium lead iodide (MAPbI3) perovskite was used as the light-absorbing material to form an FTO/ZnO/MAPbI3/copolymer/Ag device, of which the power conversion efficiency (PCE) was found to be dependent on the copolymer composition and reached a maximum (~10%) at a P3TAA content of 43 mol% in the copolymer (P3). Zinc Oxide 185-188 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 181-184 29442795-7 2018 The energy levels caused by the surface defects of ZnO NPs by Ni doping have influence on the charge-transfer process and have benefit for the SERS performance. Zinc Oxide 51-54 seryl-tRNA synthetase 1 Homo sapiens 143-147 32254340-6 2018 An in ovo xenograft assay revealed that the MoS2-ZnO nanocomposite retards tumor growth by specifically activating caspase-3 and thereby inducing cellular apoptosis. Zinc Oxide 49-52 caspase 3 Homo sapiens 115-124 29875670-3 2018 Main focus of this study was to evaluate acute exposure of n-butanol fraction of Prosopis cineraria (L.) Druce hydroethanolic extract (BuPC) and green synthesized zinc oxide nanoparticles of BuPC (ZnOPC) on spatial cognition behavior, and to assess underlying mechanism by estimation of enzymatic antioxidative status along with acetylcholinesterase (AChE) activity in mice brain. Zinc Oxide 163-173 acetylcholinesterase Mus musculus 329-349 29875670-3 2018 Main focus of this study was to evaluate acute exposure of n-butanol fraction of Prosopis cineraria (L.) Druce hydroethanolic extract (BuPC) and green synthesized zinc oxide nanoparticles of BuPC (ZnOPC) on spatial cognition behavior, and to assess underlying mechanism by estimation of enzymatic antioxidative status along with acetylcholinesterase (AChE) activity in mice brain. Zinc Oxide 163-173 acetylcholinesterase Mus musculus 351-355 30310656-0 2018 Effect of the calcination process on CdO-ZnO nanocomposites by a honey-assisted combustion method for antimicrobial performance. Zinc Oxide 41-44 cell adhesion associated, oncogene regulated Homo sapiens 37-40 29475166-1 2018 A novel hybrid layered material-Schiff Base-Zinc Complexes intercalated ZnCr-LDHs-supported ZnO-was synthesized by one-step coprecipitation method and characterized by XRD, UV-vis DRS, SEM, TEM, BET, ICP-AES and XPS analysis. Zinc Oxide 92-95 MFT2 Homo sapiens 190-193 29475166-1 2018 A novel hybrid layered material-Schiff Base-Zinc Complexes intercalated ZnCr-LDHs-supported ZnO-was synthesized by one-step coprecipitation method and characterized by XRD, UV-vis DRS, SEM, TEM, BET, ICP-AES and XPS analysis. Zinc Oxide 92-95 delta/notch like EGF repeat containing Homo sapiens 195-198 29641897-0 2018 Design, Synthesis, and Enzymatic Evaluation of Novel ZnO Quantum Dot-Based Assay for Detection of Proteinase 3 Activity. Zinc Oxide 53-56 proteinase 3 Homo sapiens 98-110 30310656-4 2018 The electrical conductivity of the CdO : ZnO nanoparticles was investigated. Zinc Oxide 41-44 cell adhesion associated, oncogene regulated Homo sapiens 35-38 30310656-5 2018 The antimicrobial activity of CdO : ZnO nanocomposites was tested for various bacterial and fungal organisms using a zone inhibition method. Zinc Oxide 36-39 cell adhesion associated, oncogene regulated Homo sapiens 30-33 29634249-3 2018 In this work, we take advantage of energy band engineering to synthesize (GaN)1- x(ZnO) x solid solution nanowires with ZnO contents ranging from 10.3% to 47.6% and corresponding band gap tailoring from 3.08 to 2.77 eV on the basis of the Au-assisted VLS mechanism. Zinc Oxide 83-86 gigaxonin Homo sapiens 74-79 29747457-3 2018 Then, Zn-Sal-MCM-3 and Zn-Sal-MCM-9 were calcined to obtain nano-zinc oxide loaded on mesoporous silica (ZnO-MCM-3 and ZnO-MCM-9). Zinc Oxide 65-75 minichromosome maintenance complex component 3 Homo sapiens 13-18 29747457-3 2018 Then, Zn-Sal-MCM-3 and Zn-Sal-MCM-9 were calcined to obtain nano-zinc oxide loaded on mesoporous silica (ZnO-MCM-3 and ZnO-MCM-9). Zinc Oxide 65-75 minichromosome maintenance 9 homologous recombination repair factor Homo sapiens 30-35 29747457-5 2018 Methyl orange (MO) was used to investigate the photocatalysis behavior of ZnO-MCM-3 and ZnO-MCM-9. Zinc Oxide 74-77 minichromosome maintenance complex component 3 Homo sapiens 78-83 29747457-5 2018 Methyl orange (MO) was used to investigate the photocatalysis behavior of ZnO-MCM-3 and ZnO-MCM-9. Zinc Oxide 88-91 minichromosome maintenance 9 homologous recombination repair factor Homo sapiens 92-97 29747457-8 2018 When the modification amount of salicylaldimine was one-ninth and one-third of the mass of the silicon source, respectively, the load of nano ZnO on ZnO-MCM-9 and ZnO-MCM-3 had atomic concentrations of 1.27 and 2.03, respectively. Zinc Oxide 142-145 minichromosome maintenance 9 homologous recombination repair factor Homo sapiens 153-158 29747457-8 2018 When the modification amount of salicylaldimine was one-ninth and one-third of the mass of the silicon source, respectively, the load of nano ZnO on ZnO-MCM-9 and ZnO-MCM-3 had atomic concentrations of 1.27 and 2.03, respectively. Zinc Oxide 142-145 minichromosome maintenance complex component 3 Homo sapiens 167-172 29747457-9 2018 ZnO loaded on ZnO-MCM-9 had a wurtzite structure, while ZnO loaded on ZnO-MCM-3 was not in the same crystalline group. Zinc Oxide 0-3 minichromosome maintenance 9 homologous recombination repair factor Homo sapiens 18-23 29747457-9 2018 ZnO loaded on ZnO-MCM-9 had a wurtzite structure, while ZnO loaded on ZnO-MCM-3 was not in the same crystalline group. Zinc Oxide 14-17 minichromosome maintenance 9 homologous recombination repair factor Homo sapiens 18-23 29543406-0 2018 Organic-Free, ZnO-Assisted Synthesis of Zeolite FAU with Tunable SiO2 /Al2 O3 Molar Ratio. Zinc Oxide 14-17 FAU ubiquitin like and ribosomal protein S30 fusion Homo sapiens 48-51 29479853-3 2018 10 microg mL-1 ZnO uniquely increases the amplitude of the steady-state current, decreases the rate of hERG current inactivation during steady-state depolarization, accelerates channel deactivation during resurgent tail currents, and shows no significant alteration of current activation rate or voltage dependence. Zinc Oxide 15-18 L1 cell adhesion molecule Mus musculus 10-14 31458706-1 2018 This work uniquely reports the synthesis of Zn x Mg1-x O nanowires and submicron columns by utilizing a traditional carbothermal reduction process toward forming ZnO nanowire ultraviolet detectors, while simultaneously utilizing Mg3N2 as the source of Mg. Zinc Oxide 162-165 mucin 5B, oligomeric mucus/gel-forming Homo sapiens 49-52 31458706-3 2018 Postanneal scanning electron micrographs revealed a reduction of the average ensemble nanowire dimensions, which was correlated to the modification of ZnO lattice parameters stemming from Zn2+ dissociation and Mg2+ substitution (confirmed via Raman spectroscopy). Zinc Oxide 151-154 mucin 7, secreted Homo sapiens 210-213 29498203-4 2018 Uniquely revealed for a high-performance model PSC are the often overlooked porosity distributions of the ZnO-based CBL and the differential diffusions of the polymer PTB7-Th and fullerene derivative PC71 BM of the active layer into the CBL. Zinc Oxide 106-109 Cbl proto-oncogene Homo sapiens 116-119 28759296-6 2018 The increase of inflammatory markers, tumor necrosis factor-alpha (TNF-alpha) and interleukin-6 (IL-6) by ZnO-NPs suggests that deleterious effects of ZnO-NPs on bone turnover were, in part, due to inflammation. Zinc Oxide 106-109 tumor necrosis factor Rattus norvegicus 38-65 28759296-6 2018 The increase of inflammatory markers, tumor necrosis factor-alpha (TNF-alpha) and interleukin-6 (IL-6) by ZnO-NPs suggests that deleterious effects of ZnO-NPs on bone turnover were, in part, due to inflammation. Zinc Oxide 106-109 tumor necrosis factor Rattus norvegicus 67-76 28759296-6 2018 The increase of inflammatory markers, tumor necrosis factor-alpha (TNF-alpha) and interleukin-6 (IL-6) by ZnO-NPs suggests that deleterious effects of ZnO-NPs on bone turnover were, in part, due to inflammation. Zinc Oxide 106-109 interleukin 6 Rattus norvegicus 82-95 28759296-6 2018 The increase of inflammatory markers, tumor necrosis factor-alpha (TNF-alpha) and interleukin-6 (IL-6) by ZnO-NPs suggests that deleterious effects of ZnO-NPs on bone turnover were, in part, due to inflammation. Zinc Oxide 106-109 interleukin 6 Rattus norvegicus 97-101 28759296-6 2018 The increase of inflammatory markers, tumor necrosis factor-alpha (TNF-alpha) and interleukin-6 (IL-6) by ZnO-NPs suggests that deleterious effects of ZnO-NPs on bone turnover were, in part, due to inflammation. Zinc Oxide 151-154 interleukin 6 Rattus norvegicus 82-95 28759296-6 2018 The increase of inflammatory markers, tumor necrosis factor-alpha (TNF-alpha) and interleukin-6 (IL-6) by ZnO-NPs suggests that deleterious effects of ZnO-NPs on bone turnover were, in part, due to inflammation. Zinc Oxide 151-154 interleukin 6 Rattus norvegicus 97-101 29658693-1 2018 In this work, we adopted polyacrylamide gel-contained zinc finger peptide (PZF) as a "lock" of Raman signal and zinc ions (Zn2+) as a sensitive "key", which was converted from target-captured ZnO NPs, to achieve the measurement of prostate-specific antigen (PSA). Zinc Oxide 192-195 ZFP91 zinc finger protein, atypical E3 ubiquitin ligase Homo sapiens 75-78 29658693-1 2018 In this work, we adopted polyacrylamide gel-contained zinc finger peptide (PZF) as a "lock" of Raman signal and zinc ions (Zn2+) as a sensitive "key", which was converted from target-captured ZnO NPs, to achieve the measurement of prostate-specific antigen (PSA). Zinc Oxide 192-195 kallikrein related peptidase 3 Homo sapiens 231-262 29658693-3 2018 Meanwhile, target PSA can specifically connect with antibody 2-coupled ZnO nanocomplexes (ZnO@Au@Ab2) and antibody 1-coupled magnetic (CoFe2O4@Au@Ab1) nanocomposite through sandwich immunoassay. Zinc Oxide 71-74 kallikrein related peptidase 3 Homo sapiens 18-21 29658693-3 2018 Meanwhile, target PSA can specifically connect with antibody 2-coupled ZnO nanocomplexes (ZnO@Au@Ab2) and antibody 1-coupled magnetic (CoFe2O4@Au@Ab1) nanocomposite through sandwich immunoassay. Zinc Oxide 90-93 kallikrein related peptidase 3 Homo sapiens 18-21 29658693-4 2018 In the presence of HCl, the ZnO NPs would convert into Zn2+ to open the PZF because Zn2+ can specifically react with zinc finger peptide to destroy the PZF structure forming abundant pores. Zinc Oxide 28-31 ZFP91 zinc finger protein, atypical E3 ubiquitin ligase Homo sapiens 72-75 29658693-4 2018 In the presence of HCl, the ZnO NPs would convert into Zn2+ to open the PZF because Zn2+ can specifically react with zinc finger peptide to destroy the PZF structure forming abundant pores. Zinc Oxide 28-31 ZFP91 zinc finger protein, atypical E3 ubiquitin ligase Homo sapiens 152-155 29548697-7 2018 A mixture of silver and zinc oxide nanoparticles showed synergy against resistant Pseudomonas spp. Zinc Oxide 24-34 histocompatibility minor 13 Homo sapiens 94-97 29565440-2 2018 C dots are incorporated into an annealing-free ZnO layer to innovatively construct a local built-in electric field (Ebi) using the difference in the work functions; this simultaneously overcomes the drawbacks of the pristine ZnO photosensitive layer. Zinc Oxide 47-50 transducin beta like 1 X-linked Homo sapiens 116-119 29565440-2 2018 C dots are incorporated into an annealing-free ZnO layer to innovatively construct a local built-in electric field (Ebi) using the difference in the work functions; this simultaneously overcomes the drawbacks of the pristine ZnO photosensitive layer. Zinc Oxide 225-228 transducin beta like 1 X-linked Homo sapiens 116-119 28813612-4 2018 ZnO-NPs relieved the decrease of hepatic or renal reduced glutathione (GSH), catalase (CAT), and superoxide dismutase (SOD) induced by TAA. Zinc Oxide 0-3 catalase Rattus norvegicus 77-85 28813612-4 2018 ZnO-NPs relieved the decrease of hepatic or renal reduced glutathione (GSH), catalase (CAT), and superoxide dismutase (SOD) induced by TAA. Zinc Oxide 0-3 catalase Rattus norvegicus 87-90 29498203-5 2018 Interface modification of the ZnO-based CBL with fullerene derivative PCBE OH for size-selective nanochannels can selectively improve the diffusion of PC71 BM more than that of the polymer. Zinc Oxide 30-33 Cbl proto-oncogene Homo sapiens 40-43 29498203-6 2018 The deeper penetration of PC71 BM establishes a gradient distribution of fullerene derivatives over the ZnO/PCBE-OH CBL, resulting in markedly improved electron mobility and device efficiency of the inverted PSC. Zinc Oxide 104-107 Cbl proto-oncogene Homo sapiens 116-119 29479853-3 2018 10 microg mL-1 ZnO uniquely increases the amplitude of the steady-state current, decreases the rate of hERG current inactivation during steady-state depolarization, accelerates channel deactivation during resurgent tail currents, and shows no significant alteration of current activation rate or voltage dependence. Zinc Oxide 15-18 ETS transcription factor ERG Homo sapiens 103-107 29327688-0 2018 Empirical optimization of DFT + U and HSE for the band structure of ZnO. Zinc Oxide 70-73 hydroxysteroid 17-beta dehydrogenase 6 Homo sapiens 40-43 29353012-6 2018 Fabricated drug delivery system (F-P-M-ZnO@Fe2O3) was characterized by FT-IR, TGA, zeta potential, and UV-Visible spectroscopy. Zinc Oxide 39-42 T-box transcription factor 1 Homo sapiens 78-81 29593572-5 2018 ZnO-NPs induced significant increases in the serum levels of interleukin 8 (IL-8), interleukin-1 beta (IL-1beta), and tumor necrosis factor alpha (TNF-alpha), and elevated the number of cells and the percentage of neutrophils in the blood. Zinc Oxide 0-3 interleukin 1 beta Rattus norvegicus 83-101 29593572-5 2018 ZnO-NPs induced significant increases in the serum levels of interleukin 8 (IL-8), interleukin-1 beta (IL-1beta), and tumor necrosis factor alpha (TNF-alpha), and elevated the number of cells and the percentage of neutrophils in the blood. Zinc Oxide 0-3 interleukin 1 beta Rattus norvegicus 103-111 29593572-5 2018 ZnO-NPs induced significant increases in the serum levels of interleukin 8 (IL-8), interleukin-1 beta (IL-1beta), and tumor necrosis factor alpha (TNF-alpha), and elevated the number of cells and the percentage of neutrophils in the blood. Zinc Oxide 0-3 tumor necrosis factor Rattus norvegicus 118-145 29593572-5 2018 ZnO-NPs induced significant increases in the serum levels of interleukin 8 (IL-8), interleukin-1 beta (IL-1beta), and tumor necrosis factor alpha (TNF-alpha), and elevated the number of cells and the percentage of neutrophils in the blood. Zinc Oxide 0-3 tumor necrosis factor Rattus norvegicus 147-156 29268571-8 2018 CONCLUSION: The present results are interpreted to suggest that dietary ZnO provided by SZ may play a role in intestinal mucosal growth and immune function by modulating the expression of IGF-I, IL-6, and IL-10 genes. Zinc Oxide 72-75 insulin like growth factor 1 Sus scrofa 188-193 29268571-8 2018 CONCLUSION: The present results are interpreted to suggest that dietary ZnO provided by SZ may play a role in intestinal mucosal growth and immune function by modulating the expression of IGF-I, IL-6, and IL-10 genes. Zinc Oxide 72-75 interleukin 6 Sus scrofa 195-199 29268571-8 2018 CONCLUSION: The present results are interpreted to suggest that dietary ZnO provided by SZ may play a role in intestinal mucosal growth and immune function by modulating the expression of IGF-I, IL-6, and IL-10 genes. Zinc Oxide 72-75 IL10 Sus scrofa 205-210 29310213-0 2018 Electrogenerated chemiluminescence of ZnO nanorods and its sensitive detection of cytochrome C. Zinc Oxide 38-41 cytochrome c, somatic Homo sapiens 82-94 32704689-14 2018 Feeding ZnO increased (P < 0.05) ADG, ADFI, and BW during the treatment period and increased (P < 0.05) ADG and ADFI overall (d 5 to 47). Zinc Oxide 8-11 ADG Sus scrofa 33-36 32704689-14 2018 Feeding ZnO increased (P < 0.05) ADG, ADFI, and BW during the treatment period and increased (P < 0.05) ADG and ADFI overall (d 5 to 47). Zinc Oxide 8-11 ADG Sus scrofa 104-107 29137802-0 2018 Nanocomposite materials based on poly(vinyl chloride) and bovine serum albumin modified ZnO through ultrasonic irradiation as a green technique: Optical, thermal, mechanical and morphological properties. Zinc Oxide 88-91 albumin Homo sapiens 65-78 29137802-2 2018 Firstly, ZnO NPs were modified with bovine serum albumin (BSA) as an organo-modifier and biocompatible substance through ultrasound irradiation as environmental friendly, low cost and rapid means. Zinc Oxide 9-12 albumin Homo sapiens 43-56 29327688-7 2018 In this work, both DFT + U and HSE methods were parametrized to fit almost exactly the binding energies of electrons in ZnO obtained by XPS. Zinc Oxide 122-125 hydroxysteroid 17-beta dehydrogenase 6 Homo sapiens 33-36 29399718-5 2018 In another observation, the high sensitivity of the HCN molecule for the Fe-incorporated ZnO nanotube suggests it as a potential gas sensor. Zinc Oxide 89-92 metastasis associated lung adenocarcinoma transcript 1 Homo sapiens 52-55 29277990-1 2018 We report the effect of Y2O3 passivation by atomic layer deposition (ALD) using various oxidants, such as H2O, O2 plasma, and O3, on In-Ga-Zn-O thin-film transistors (IGZO TFTs). Zinc Oxide 139-143 immunoglobulin kappa variable 2D-38 (pseudogene) Homo sapiens 106-128 29166623-0 2018 Anticancer potential of ZnO nanoparticle-ferulic acid conjugate on Huh-7 and HepG2 cells and diethyl nitrosamine induced hepatocellular cancer on Wistar albino rat. Zinc Oxide 24-27 MIR7-3 host gene Homo sapiens 67-72 29448596-7 2018 The power factor increased significantly from 2.58 x 10-5 W/mK2 in un-doped ZnO film to 2.63 x 10-4 W/mK2 in 2% Al doped ZnO film. Zinc Oxide 76-79 paired related homeobox 1 Mus musculus 60-63 30416185-0 2018 Amperometric Glucose Biosensor Utilizing Zinc Oxide-chitosan-glucose Oxidase Hybrid Composite Films on Electrodeposited Pt-Fe(III). Zinc Oxide 41-51 hydroxyacid oxidase 1 Homo sapiens 61-76 28802749-7 2018 We further used the optimized ZnO nanowires to demonstrate multiple detection of cancer biomarkers, achieving a superior limit of detection (LOD) as low as 1pg/mL in human alpha-fetoprotein (AFP) assay and 100 fg/mL in carcinoembryonic antigen (CEA) assay with large dynamic range of 6-7 orders, which suggests that ZnO nanowire integrated microfluidic chips are promising for high-throughput fluorescence-based diagnostic assays. Zinc Oxide 30-33 alpha fetoprotein Homo sapiens 172-189 28802749-7 2018 We further used the optimized ZnO nanowires to demonstrate multiple detection of cancer biomarkers, achieving a superior limit of detection (LOD) as low as 1pg/mL in human alpha-fetoprotein (AFP) assay and 100 fg/mL in carcinoembryonic antigen (CEA) assay with large dynamic range of 6-7 orders, which suggests that ZnO nanowire integrated microfluidic chips are promising for high-throughput fluorescence-based diagnostic assays. Zinc Oxide 30-33 alpha fetoprotein Homo sapiens 191-194 28802749-7 2018 We further used the optimized ZnO nanowires to demonstrate multiple detection of cancer biomarkers, achieving a superior limit of detection (LOD) as low as 1pg/mL in human alpha-fetoprotein (AFP) assay and 100 fg/mL in carcinoembryonic antigen (CEA) assay with large dynamic range of 6-7 orders, which suggests that ZnO nanowire integrated microfluidic chips are promising for high-throughput fluorescence-based diagnostic assays. Zinc Oxide 30-33 CEA cell adhesion molecule 3 Homo sapiens 219-243 28802749-7 2018 We further used the optimized ZnO nanowires to demonstrate multiple detection of cancer biomarkers, achieving a superior limit of detection (LOD) as low as 1pg/mL in human alpha-fetoprotein (AFP) assay and 100 fg/mL in carcinoembryonic antigen (CEA) assay with large dynamic range of 6-7 orders, which suggests that ZnO nanowire integrated microfluidic chips are promising for high-throughput fluorescence-based diagnostic assays. Zinc Oxide 30-33 CEA cell adhesion molecule 3 Homo sapiens 245-248 29235608-5 2018 This research not only further confirms the SPR-assisted electron transfer process but also offers an approach to improve the intrinsic UV emission even for heavily-defected ZnO through visible light excitation via a nonlinear process. Zinc Oxide 174-177 sepiapterin reductase Homo sapiens 44-47 29243754-8 2018 Our simplified kinetic model on the HCl + ZnO system concurs very well with experimentally reported TGA weight loss profiles on two grounds: accumulation of oxyhalides until ~700 K and desorption of ZnCl2 at higher temperatures. Zinc Oxide 42-45 T-box transcription factor 1 Homo sapiens 100-103 28873527-2 2018 In the present study, polyamine oxidase specific for spermine and spermidine and diamine oxidase specific for putrescine, were co-immobilized onto a novel chitosan/coconut fibre/zinc oxide nanoparticles (CS/CF/nZnO) hybrid support to yield a polyamine sensing strip. Zinc Oxide 178-188 polyamine oxidase Homo sapiens 22-39 30416185-1 2018 We developed an amperometric glucose biosensor based on glucose oxidase (GOx) embedded in zinc oxide (ZnO)-chitosan (CS) hybrid composite films on electrodeposited Pt-Fe(III). Zinc Oxide 90-100 hydroxyacid oxidase 1 Homo sapiens 73-76 29488395-5 2018 Our results show that ZnO nanoparticles induce the release of cytochorme c, decrease the intracellular ATP level, collapse the mitochondrial membrane potential, elevate the ROS level, inhibit total antioxidant enzyme activities and increase the Bax and Caspase 3 levels whereas it decrease the Bcl-2 expression, leading to cell death. Zinc Oxide 22-25 BCL2-associated X protein Mus musculus 245-248 29488395-5 2018 Our results show that ZnO nanoparticles induce the release of cytochorme c, decrease the intracellular ATP level, collapse the mitochondrial membrane potential, elevate the ROS level, inhibit total antioxidant enzyme activities and increase the Bax and Caspase 3 levels whereas it decrease the Bcl-2 expression, leading to cell death. Zinc Oxide 22-25 caspase 3 Mus musculus 253-262 29488395-5 2018 Our results show that ZnO nanoparticles induce the release of cytochorme c, decrease the intracellular ATP level, collapse the mitochondrial membrane potential, elevate the ROS level, inhibit total antioxidant enzyme activities and increase the Bax and Caspase 3 levels whereas it decrease the Bcl-2 expression, leading to cell death. Zinc Oxide 22-25 B cell leukemia/lymphoma 2 Mus musculus 294-299 28946431-3 2018 Successful synthesis of CdO-ZnO photocatalyst in crystalline form was confirmed by XRD analysis resulting lower crystallite sizes for ZnO compared to CdO in the composites. Zinc Oxide 28-31 cell adhesion associated, oncogene regulated Homo sapiens 24-27 28946431-3 2018 Successful synthesis of CdO-ZnO photocatalyst in crystalline form was confirmed by XRD analysis resulting lower crystallite sizes for ZnO compared to CdO in the composites. Zinc Oxide 28-31 cell adhesion associated, oncogene regulated Homo sapiens 150-153 28946431-4 2018 The FESEM analysis demonstrated a nanostructured catalyst with a distinct decrease in particle size by addition of CdO to ZnO photocatalyst. Zinc Oxide 122-125 cell adhesion associated, oncogene regulated Homo sapiens 115-118 29164854-5 2017 Taking alkaline phosphatase (ALP) as a model, a NPC-ZnO nanopolyhedra-based PEC sensor was developed and showed good performance for ALP assay with a wide linear response range from 2 to 1500 U L-1 and a low detection limit of 1.7 U L-1. Zinc Oxide 52-55 alkaline phosphatase, placental Homo sapiens 7-27 29164854-5 2017 Taking alkaline phosphatase (ALP) as a model, a NPC-ZnO nanopolyhedra-based PEC sensor was developed and showed good performance for ALP assay with a wide linear response range from 2 to 1500 U L-1 and a low detection limit of 1.7 U L-1. Zinc Oxide 52-55 alkaline phosphatase, placental Homo sapiens 29-32 28888009-11 2017 Furthermore, our data suggested that ZnO QDs regulated apoptosis via Bax and Bcl-2 proteins as validated by immunofluorescence and western blot. Zinc Oxide 37-40 BCL2 associated X, apoptosis regulator Homo sapiens 69-72 29164854-5 2017 Taking alkaline phosphatase (ALP) as a model, a NPC-ZnO nanopolyhedra-based PEC sensor was developed and showed good performance for ALP assay with a wide linear response range from 2 to 1500 U L-1 and a low detection limit of 1.7 U L-1. Zinc Oxide 52-55 alkaline phosphatase, placental Homo sapiens 133-136 29028602-5 2017 In A549 epithelium model, exposure to ZnO NPs induced cytotoxicity and decreased the release of interleukin 6 (IL-6) without a significant effect on epithelial permeability rate. Zinc Oxide 38-41 interleukin 6 Homo sapiens 96-109 29028602-5 2017 In A549 epithelium model, exposure to ZnO NPs induced cytotoxicity and decreased the release of interleukin 6 (IL-6) without a significant effect on epithelial permeability rate. Zinc Oxide 38-41 interleukin 6 Homo sapiens 111-115 29028602-6 2017 Co-exposure of A549 cells or A549 epithelium model to DPPC and ZnO NPs induced a higher release of lactate dehydrogenase (LDH) and interleukin-6 (IL-6) compared with the exposure of ZnO NPs alone. Zinc Oxide 63-66 interleukin 6 Homo sapiens 131-144 29028602-6 2017 Co-exposure of A549 cells or A549 epithelium model to DPPC and ZnO NPs induced a higher release of lactate dehydrogenase (LDH) and interleukin-6 (IL-6) compared with the exposure of ZnO NPs alone. Zinc Oxide 63-66 interleukin 6 Homo sapiens 146-150 30263719-2 2018 Hence, in this work, glyoxalase 1(GLO 1) based, zinc oxide (ZnO) flakes interfaced mediator free electrochemical biosensor was developed to detect MG in grilled chicken. Zinc Oxide 48-58 glyoxalase I Gallus gallus 34-39 28888009-11 2017 Furthermore, our data suggested that ZnO QDs regulated apoptosis via Bax and Bcl-2 proteins as validated by immunofluorescence and western blot. Zinc Oxide 37-40 BCL2 apoptosis regulator Homo sapiens 77-82 28235370-0 2017 Low-Temperature PLD-Growth of Ultrathin ZnO Nanowires by Using Zn x Al1-x O and Zn x Ga1-x O Seed Layers. Zinc Oxide 40-43 ephrin A5 Homo sapiens 68-71 29052675-2 2017 Herein we demonstrate the preparation of novel and high-quality ZnO inverse opal photonic crystals (IOPCs)/Ag/NaYF4:Yb,Tm hybrid films by different advanced film techniques, including colloidal self-assembling, vapor phase deposition and pulsed laser deposition and its application to sensitive detection of alpha-fetoprotein (AFP). Zinc Oxide 64-67 alpha fetoprotein Homo sapiens 308-325 28974419-6 2017 Significantly higher levels of MT1 were observed in the duodenums of bulk ZnO and ZnO NPs groups than those of the control (9.8 and 5660.11 fold increases, respectively). Zinc Oxide 74-77 metallothionein 1 Mus musculus 31-34 28974419-6 2017 Significantly higher levels of MT1 were observed in the duodenums of bulk ZnO and ZnO NPs groups than those of the control (9.8 and 5660.11 fold increases, respectively). Zinc Oxide 82-85 metallothionein 1 Mus musculus 31-34 28974419-7 2017 The MT4 levels in the bulk ZnO and ZnO NPs groups also showed 4.07 and 43.21fold increases, respectively. Zinc Oxide 27-30 metallothionein 4 Mus musculus 4-7 28974419-7 2017 The MT4 levels in the bulk ZnO and ZnO NPs groups also showed 4.07 and 43.21fold increases, respectively. Zinc Oxide 35-38 metallothionein 4 Mus musculus 4-7 29076344-7 2017 More importantly, we demonstrated that ZnO NPs could effectively downregulate CD44, a key CSC surface marker, and decrease the stemness of CSCs, leading to the sensitization of the Dox treatment, inhibition of the cancer cell adhesion and migration, and prevention of the tumor (3D cancer cell spheroid) formation. Zinc Oxide 39-42 CD44 molecule (Indian blood group) Homo sapiens 78-82 28920580-0 2017 Sandwiched ZnO@Au@CdS nanorod arrays with enhanced visible-light-driven photocatalytical performance. Zinc Oxide 11-14 CDP-diacylglycerol synthase 1 Homo sapiens 18-21 28920580-3 2017 Here, sandwiched ZnO@Au@CdS nanorod films were synthesized via successive ZnO nanorod electrodeposition, Au sputtering and CdS electrodeposition. Zinc Oxide 17-20 CDP-diacylglycerol synthase 1 Homo sapiens 24-27 28920580-3 2017 Here, sandwiched ZnO@Au@CdS nanorod films were synthesized via successive ZnO nanorod electrodeposition, Au sputtering and CdS electrodeposition. Zinc Oxide 17-20 CDP-diacylglycerol synthase 1 Homo sapiens 123-126 28920580-3 2017 Here, sandwiched ZnO@Au@CdS nanorod films were synthesized via successive ZnO nanorod electrodeposition, Au sputtering and CdS electrodeposition. Zinc Oxide 74-77 CDP-diacylglycerol synthase 1 Homo sapiens 24-27 28920580-6 2017 ZnO@Au@CdS exhibited better photocatalytic performance than ZnO@CdS throughout the visible light region, and the corresponding enhancement factor of Au nanoparticles was measured as a function of CdS loading amount, and it could reach 190% with CdS deposition for 1 min. Zinc Oxide 0-3 CDP-diacylglycerol synthase 1 Homo sapiens 7-10 28920580-7 2017 The normalized rate constant could reach 0.387 h-1 for ZnO@Au@CdS-1min, which was equivalent to or better than results in reference photocatalysts. Zinc Oxide 55-58 CDP-diacylglycerol synthase 1 Homo sapiens 62-67 28920580-8 2017 The enhancement mechanism of Au nanoparticles was estimated by comparing the monochromatic photocatalytic action spectra with the absorption spectrum of ZnO@Au@CdS, and it was mainly determined by incident photon energy. Zinc Oxide 153-156 CDP-diacylglycerol synthase 1 Homo sapiens 160-163 28735192-5 2017 Utilization of nozzle-jet printing methods resulted in highly reproducible electrodes with well-defined vertical grown ZnO NRs for high GOx loading and enhanced glucose sensing performance in a wide glucose detection range. Zinc Oxide 119-122 hydroxyacid oxidase 1 Homo sapiens 136-139 28795445-3 2017 Adsorption experiments at pH 6.8 with 2 mg ZnO@MC as adsorbent illustrated an adsorption efficiency of 92.3 % in 5 mL hemoglobin (Hb) solution with a concentration of 100 mg L-1 . Zinc Oxide 43-46 immunoglobulin kappa variable 1-16 Homo sapiens 174-177 29052675-2 2017 Herein we demonstrate the preparation of novel and high-quality ZnO inverse opal photonic crystals (IOPCs)/Ag/NaYF4:Yb,Tm hybrid films by different advanced film techniques, including colloidal self-assembling, vapor phase deposition and pulsed laser deposition and its application to sensitive detection of alpha-fetoprotein (AFP). Zinc Oxide 64-67 alpha fetoprotein Homo sapiens 327-330 29052675-5 2017 Furthermore, because of the high specific surface area of ZnO IOPCs and the conductivity of Ag films, ZnO IOPCs/Ag/NaYF4:Yb,Tm hybrid films based near-infrared light-triggered PEC sensors showed ultrasensitive detection of AFP with a linear range from 0.05 ng mL-1 to 100 ng mL-1 and a low detection limit of ~0.04 ng mL-1 (40 pg mL-1). Zinc Oxide 102-105 alpha fetoprotein Homo sapiens 223-226 29022694-5 2017 The small weight ratio of Ag2S QDs to ZnO@C at 1:180 shows the best performance in lithium storage. Zinc Oxide 38-41 angiotensin II receptor type 1 Homo sapiens 26-30 28990751-0 2017 MOF-Derived ZnO Nanoparticles Covered by N-Doped Carbon Layers and Hybridized on Carbon Nanotubes for Lithium-Ion Battery Anodes. Zinc Oxide 12-15 lysine acetyltransferase 8 Homo sapiens 0-3 29022694-7 2017 At low current densities (200 mA g-1), treatment of ZnO@C with Ag2S QDs results in a 38% increase in the specific capacity. Zinc Oxide 52-55 angiotensin II receptor type 1 Homo sapiens 63-67 29022694-0 2017 Enhancing Distorted Metal-Organic Framework-Derived ZnO as Anode Material for Lithium Storage by the Addition of Ag2S Quantum Dots. Zinc Oxide 52-55 angiotensin II receptor type 1 Homo sapiens 113-117 28668561-5 2017 Results showed that the ZnO NPs with low concentration (<=5mgL-1) was profitable for nitrogen removal while the high concentration performed inhibition, and it lowered the abundance of both AOB and NOB while enhanced that of AAOB. Zinc Oxide 24-27 LLGL scribble cell polarity complex component 1 Homo sapiens 62-67 29022694-1 2017 The lithium storage properties of the distorted metal-organic framework-derived nanosized ZnO@C are significantly improved by the introduction of Ag2S quantum dots (QDs) during the processing of the material. Zinc Oxide 90-93 angiotensin II receptor type 1 Homo sapiens 146-150 28668561-7 2017 The inhibition threshold of ZnO NPs on CANON process was 10mgL-1, and the profitable concentration was 1mgL-1. Zinc Oxide 28-31 LLGL scribble cell polarity complex component 1 Homo sapiens 59-64 28668561-7 2017 The inhibition threshold of ZnO NPs on CANON process was 10mgL-1, and the profitable concentration was 1mgL-1. Zinc Oxide 28-31 LLGL scribble cell polarity complex component 1 Homo sapiens 104-109 28957153-8 2017 The PL spectrum of ZnS:Mn/ZnO/GaN covers the visible region from the blue light to the red light (400-700 nm), and its color coordinate and color temperature are (0.3103,0.3063) and 6869 K, respectively, presenting strong white light emission. Zinc Oxide 26-29 gigaxonin Homo sapiens 30-33 28582753-4 2017 In this work, we will shed light on this observation using small angle X-ray and neutron scattering (SAXS, SANS) by demonstrating that after the first washing cycle the content of acetate in the ligand shell around the ZnO NPs increases. Zinc Oxide 219-222 USH1 protein network component sans Homo sapiens 107-111 28834273-0 2017 Hollow ZnO Nanospheres Enhance Anticancer Immunity by Promoting CD4+ and CD8+ T Cell Populations In Vivo. Zinc Oxide 7-10 CD4 antigen Mus musculus 64-67 28870124-0 2017 Reactive oxygen species trigger NF-kappaB-mediated NLRP3 inflammasome activation induced by zinc oxide nanoparticles in A549 cells. Zinc Oxide 92-102 nuclear factor kappa B subunit 1 Homo sapiens 32-41 28651203-5 2017 Lithium-ion battery devices based on the carbon-coated ZnO mat passivation by atomic layer deposited HfO2 exhibit an excellent initial discharge and charge capacities of 2684.01 and 963.21mAhg-1, respectively, at a current density of 100mAg-1 in the voltage range of 0.01-3V. Zinc Oxide 55-58 dentin matrix protein 1 Mus musculus 237-242 28697814-4 2017 Silver and zinc oxide nanoparticles at concentration of 10 and 5 ng mL-1 killed 100 and 97% of theronts, respectively and inhibited reproduction of tomonts after 2 h exposure. Zinc Oxide 11-21 L1 cell adhesion molecule Mus musculus 68-72 29084556-8 2017 The amounts of albumin, transferrin and alpha-1 antitrypsin were greater in the coronas of BaSO4 and ZnO than that of the two CeO2 NPs. Zinc Oxide 101-104 transferrin Rattus norvegicus 24-35 29053567-10 2017 Annexin V/propidium iodide (PI) flow cytometry analysis confirmed that ZnO NPs induce apoptosis in MCF-7 cells. Zinc Oxide 71-74 annexin A5 Homo sapiens 0-9 28993638-2 2017 It was found that the critical thickness of the m-plane GaN films grown on ZnO lies between 25 and 62 nm, whereas 180-nm-thick m-plane In0.12Ga0.88N can be coherently grown on ZnO substrates, which is explained well by theoretical calculations based on an energy-balance model. Zinc Oxide 75-78 gigaxonin Homo sapiens 56-59 28993638-3 2017 The coherently grown m-plane InGaN on ZnO exhibited narrow X-ray rocking curves compared with the m-plane GaN grown on ZnO. Zinc Oxide 38-41 gigaxonin Homo sapiens 31-34 28771048-10 2017 In conclusion, dietary supplementation of nanoZnO and gamma-PGA-nanoZnO increased Zn content in eggshells, serum Zn concentration, ghrelin and IgG levels of aged layers when compared to regular ZnO. Zinc Oxide 46-49 ghrelin/obestatin prepropeptide Gallus gallus 131-138 28957153-0 2017 Effects of the ZnO layer on the structure and white light emission properties of a ZnS:Mn/GaN nanocomposite system. Zinc Oxide 15-18 gigaxonin Homo sapiens 90-93 28957153-1 2017 ZnO films were inserted between the ZnS:Mn films and GaN substrates by pulsed laser deposition (PLD). Zinc Oxide 0-3 gigaxonin Homo sapiens 53-56 28957153-4 2017 Due to the insertion of ZnO films, the diffraction peak intensity of ZnS:Mn in ZnS:Mn/ZnO/GaN is stronger than that of ZnS:Mn in ZnS:Mn/GaN, and the full width at half-maximum is smaller. Zinc Oxide 24-27 gigaxonin Homo sapiens 90-93 28957153-4 2017 Due to the insertion of ZnO films, the diffraction peak intensity of ZnS:Mn in ZnS:Mn/ZnO/GaN is stronger than that of ZnS:Mn in ZnS:Mn/GaN, and the full width at half-maximum is smaller. Zinc Oxide 24-27 gigaxonin Homo sapiens 136-139 28957153-4 2017 Due to the insertion of ZnO films, the diffraction peak intensity of ZnS:Mn in ZnS:Mn/ZnO/GaN is stronger than that of ZnS:Mn in ZnS:Mn/GaN, and the full width at half-maximum is smaller. Zinc Oxide 86-89 gigaxonin Homo sapiens 90-93 28870124-6 2017 ZnO-NPs stimulation induced ROS generation and NF-kappaB p65 phosphorylation. Zinc Oxide 0-3 nuclear factor kappa B subunit 1 Homo sapiens 47-56 28870124-7 2017 Similarly, the expression of NLRP3 and caspase-1 p10 and the release of IL-1beta and IL-18 were significantly increased after ZnO-NPs treatment, which indicated that the NLRP3 inflammasome was activated by ZnO-NPs. Zinc Oxide 126-129 NLR family pyrin domain containing 3 Homo sapiens 29-34 28870124-7 2017 Similarly, the expression of NLRP3 and caspase-1 p10 and the release of IL-1beta and IL-18 were significantly increased after ZnO-NPs treatment, which indicated that the NLRP3 inflammasome was activated by ZnO-NPs. Zinc Oxide 126-129 caspase 1 Homo sapiens 39-48 28870124-7 2017 Similarly, the expression of NLRP3 and caspase-1 p10 and the release of IL-1beta and IL-18 were significantly increased after ZnO-NPs treatment, which indicated that the NLRP3 inflammasome was activated by ZnO-NPs. Zinc Oxide 126-129 S100 calcium binding protein A10 Homo sapiens 49-52 28870124-0 2017 Reactive oxygen species trigger NF-kappaB-mediated NLRP3 inflammasome activation induced by zinc oxide nanoparticles in A549 cells. Zinc Oxide 92-102 NLR family pyrin domain containing 3 Homo sapiens 51-56 28919752-6 2017 Furthermore, the cells treated with ZnO NPs showed significant double-strand DNA breaks, which are gained evidences from significant number of gamma-H2AX and Rad51 expressed cells. Zinc Oxide 36-39 RAD51 recombinase Homo sapiens 158-163 28870124-7 2017 Similarly, the expression of NLRP3 and caspase-1 p10 and the release of IL-1beta and IL-18 were significantly increased after ZnO-NPs treatment, which indicated that the NLRP3 inflammasome was activated by ZnO-NPs. Zinc Oxide 126-129 interleukin 1 beta Homo sapiens 72-80 28870124-7 2017 Similarly, the expression of NLRP3 and caspase-1 p10 and the release of IL-1beta and IL-18 were significantly increased after ZnO-NPs treatment, which indicated that the NLRP3 inflammasome was activated by ZnO-NPs. Zinc Oxide 126-129 interleukin 18 Homo sapiens 85-90 28870124-7 2017 Similarly, the expression of NLRP3 and caspase-1 p10 and the release of IL-1beta and IL-18 were significantly increased after ZnO-NPs treatment, which indicated that the NLRP3 inflammasome was activated by ZnO-NPs. Zinc Oxide 126-129 NLR family pyrin domain containing 3 Homo sapiens 170-175 28870124-7 2017 Similarly, the expression of NLRP3 and caspase-1 p10 and the release of IL-1beta and IL-18 were significantly increased after ZnO-NPs treatment, which indicated that the NLRP3 inflammasome was activated by ZnO-NPs. Zinc Oxide 206-209 NLR family pyrin domain containing 3 Homo sapiens 29-34 28870124-7 2017 Similarly, the expression of NLRP3 and caspase-1 p10 and the release of IL-1beta and IL-18 were significantly increased after ZnO-NPs treatment, which indicated that the NLRP3 inflammasome was activated by ZnO-NPs. Zinc Oxide 206-209 caspase 1 Homo sapiens 39-48 28870124-7 2017 Similarly, the expression of NLRP3 and caspase-1 p10 and the release of IL-1beta and IL-18 were significantly increased after ZnO-NPs treatment, which indicated that the NLRP3 inflammasome was activated by ZnO-NPs. Zinc Oxide 206-209 S100 calcium binding protein A10 Homo sapiens 49-52 28870124-7 2017 Similarly, the expression of NLRP3 and caspase-1 p10 and the release of IL-1beta and IL-18 were significantly increased after ZnO-NPs treatment, which indicated that the NLRP3 inflammasome was activated by ZnO-NPs. Zinc Oxide 206-209 NLR family pyrin domain containing 3 Homo sapiens 170-175 28870124-8 2017 Meanwhile, NAC pretreatment inhibited ZnO-NPs-induced activation of NF-kappaB and NLRP3 inflammasome. Zinc Oxide 38-41 X-linked Kx blood group Homo sapiens 11-14 28870124-8 2017 Meanwhile, NAC pretreatment inhibited ZnO-NPs-induced activation of NF-kappaB and NLRP3 inflammasome. Zinc Oxide 38-41 nuclear factor kappa B subunit 1 Homo sapiens 68-77 28870124-8 2017 Meanwhile, NAC pretreatment inhibited ZnO-NPs-induced activation of NF-kappaB and NLRP3 inflammasome. Zinc Oxide 38-41 NLR family pyrin domain containing 3 Homo sapiens 82-87 28870124-10 2017 Furthermore, the ability of ZnO-NPs to increase the production of IL-1beta and IL-18 was significantly inhibited by GEL. Zinc Oxide 28-31 interleukin 1 beta Homo sapiens 66-74 28870124-10 2017 Furthermore, the ability of ZnO-NPs to increase the production of IL-1beta and IL-18 was significantly inhibited by GEL. Zinc Oxide 28-31 interleukin 18 Homo sapiens 79-84 28870124-11 2017 The ZnO-NPs induced the activation of the NLRP3 inflammasome in A549 cells, which might be via a ROS-NF-kappaB-NLRP3 signaling pathway. Zinc Oxide 4-7 NLR family pyrin domain containing 3 Homo sapiens 42-47 28870124-11 2017 The ZnO-NPs induced the activation of the NLRP3 inflammasome in A549 cells, which might be via a ROS-NF-kappaB-NLRP3 signaling pathway. Zinc Oxide 4-7 nuclear factor kappa B subunit 1 Homo sapiens 101-110 28870124-11 2017 The ZnO-NPs induced the activation of the NLRP3 inflammasome in A549 cells, which might be via a ROS-NF-kappaB-NLRP3 signaling pathway. Zinc Oxide 4-7 NLR family pyrin domain containing 3 Homo sapiens 111-116 28919752-7 2017 ZnO NP-treated cells showed upregulation of p53 and LC3, indicating that ZnO NPs are able to upregulate apoptosis and autophagy. Zinc Oxide 0-3 tumor protein p53 Homo sapiens 44-47 28919752-7 2017 ZnO NP-treated cells showed upregulation of p53 and LC3, indicating that ZnO NPs are able to upregulate apoptosis and autophagy. Zinc Oxide 0-3 microtubule associated protein 1 light chain 3 alpha Homo sapiens 52-55 28710015-10 2017 Based on previous research, ZnO NPs had strong anti-tubercular impact against H37RvMTB to in-vitro condition, but it was toxic in concentration of ~ 0.468 ppm to both of THP-1 and normal lung (MRC-5) cell lines. Zinc Oxide 28-31 GLI family zinc finger 2 Homo sapiens 170-175 28500885-4 2017 The presence of ZnO NPs caused significant inhibition of gene expressions and catalytic activities of nitrate reductase and nitrite reductase, which finally led to delayed nitrate reduction and high nitrite accumulation. Zinc Oxide 16-19 periplasmic nitrate reductase, NapE protein Pseudomonas stutzeri 102-119 28500885-4 2017 The presence of ZnO NPs caused significant inhibition of gene expressions and catalytic activities of nitrate reductase and nitrite reductase, which finally led to delayed nitrate reduction and high nitrite accumulation. Zinc Oxide 16-19 nitrite reductase small subunit NirD Pseudomonas stutzeri 124-141 28570896-1 2017 A mechano-/photo- bi-catalyst of piezoelectric-ZnO@photoelectric-TiO2 core-shell nanofibers was hydrothermally synthesized for Methyl Orange (10 mg L-1) decomposition. Zinc Oxide 47-50 L1 cell adhesion molecule Homo sapiens 148-151 28768420-5 2017 GOx showed a higher immobilization on ZnO/PC with an activity of 9.2 +- 1.7 mU cm-2 compared to Chl.Ox. Zinc Oxide 38-41 hydroxyacid oxidase 1 Homo sapiens 0-3 28805859-3 2017 In a typical procedure, the Ag nanoparticles (NPs) were reduced on the surface of ZnO nanorods (NRs), and the ZnO/Ag heterostructures were used as the SERS substrates. Zinc Oxide 110-113 seryl-tRNA synthetase 1 Homo sapiens 151-155 30090548-5 2017 IC50 values for undoped and 1 wt% Fe-doped ZnO NPs were found to be 400 and 600 mug mL-1, respectively. Zinc Oxide 43-46 L1 cell adhesion molecule Mus musculus 84-88 28792520-9 2017 Compared with nano ZnO, porous ZnO had better performance on reducing diarrhea but less effect on up-regulation of intestinal TFF3 and Nrf2. Zinc Oxide 31-34 trefoil factor 3 Homo sapiens 126-130 28792520-9 2017 Compared with nano ZnO, porous ZnO had better performance on reducing diarrhea but less effect on up-regulation of intestinal TFF3 and Nrf2. Zinc Oxide 31-34 NFE2 like bZIP transcription factor 2 Homo sapiens 135-139 28768420-7 2017 This is attributed to the larger crystallite size and higher Zn per unit area on PC as compared to glass which enabled a higher activity of GOx on ZnO/PC compared to ZnO/glass. Zinc Oxide 147-150 hydroxyacid oxidase 1 Homo sapiens 140-143 28768420-15 2017 But under stirring condition, the diffusion limitation was overcome, and the sensitivity for Chl.Ox./ZnO was 11.2 muA cm-2 mM-1 as compared to GOx/ZnO/PC with 3.5 muA cm-2 mM-1. Zinc Oxide 101-104 hydroxyacid oxidase 1 Homo sapiens 143-146 28768420-15 2017 But under stirring condition, the diffusion limitation was overcome, and the sensitivity for Chl.Ox./ZnO was 11.2 muA cm-2 mM-1 as compared to GOx/ZnO/PC with 3.5 muA cm-2 mM-1. Zinc Oxide 147-150 hydroxyacid oxidase 1 Homo sapiens 143-146 28723962-0 2017 Surface functionalization-specific binding of coagulation factors by zinc oxide nanoparticles delays coagulation time and reduces thrombin generation potential in vitro. Zinc Oxide 69-79 coagulation factor II Rattus norvegicus 130-138 28646756-1 2017 Zinc oxide nanostructure (ZnONS) was chemically synthesized and functionalized (FZnONSBLA) with a small protein bovine alpha-lactalbumin (BLA) by chemical cross-linking methods. Zinc Oxide 0-10 lactalbumin alpha Bos taurus 119-136 28773209-12 2017 On the other hand, the magnetoelastic measurements show a small linear mass increase versus the H2O2 concentration with a slope of 152 ng/muM, which is probably due to H2O2 adsorption in ZnO during the electrochemical reaction. Zinc Oxide 187-190 latexin Homo sapiens 138-141 28576013-6 2017 The expression of Runx-2 was significantly up regulated (P<0.05) in the case of cells seeded on monetite prepared with beta-TCP doped with 0.03 moles of ZnO. Zinc Oxide 156-159 RUNX family transcription factor 2 Homo sapiens 18-24 28723962-6 2017 The kinetics data of thrombin generation showed that ZnO NPs reduced the thrombin generation potential with functionalization-specificity in the order of pristine > citrate > L-serine but there was no size-specificity. Zinc Oxide 53-56 coagulation factor II Rattus norvegicus 21-29 28723962-6 2017 The kinetics data of thrombin generation showed that ZnO NPs reduced the thrombin generation potential with functionalization-specificity in the order of pristine > citrate > L-serine but there was no size-specificity. Zinc Oxide 53-56 coagulation factor II Rattus norvegicus 73-81 28589695-8 2017 While the immunohistochemical analysis of the ZnO NPs treated group revealed a decrease in the number of cells expressed positive reactions of anti-PCNA and an increase in the number of cells expressed positive reaction of anti-p53 in the thymus and spleen. Zinc Oxide 46-49 proliferating cell nuclear antigen Rattus norvegicus 148-152 28589695-8 2017 While the immunohistochemical analysis of the ZnO NPs treated group revealed a decrease in the number of cells expressed positive reactions of anti-PCNA and an increase in the number of cells expressed positive reaction of anti-p53 in the thymus and spleen. Zinc Oxide 46-49 Wistar clone pR53P1 p53 pseudogene Rattus norvegicus 228-231 28421223-6 2017 The UV-vis absorption diagrams and the Ct/C0 curves reveal that 8PbS/ZnO NTs have the highest catalytic activity, which can degrade MO (20 mg L-1) into a colorless solution within 30 min. Zinc Oxide 69-72 immunoglobulin kappa variable 1-16 Homo sapiens 142-145 28502431-2 2017 Herein, we present a simple photoelectrochemical immunosensor based on ZnO nanorod arrays for the sensitive detection of NDPK-A. Zinc Oxide 71-74 NME/NM23 nucleoside diphosphate kinase 1 Homo sapiens 121-127 28273533-5 2017 In addition, P1, P2, and P3 promoted the transformation of ZnO NPs into zinc phosphate (Zn-P) precipitates via interactions with dissolved Zn2+. Zinc Oxide 59-62 crystallin gamma F, pseudogene Homo sapiens 13-27 28039809-0 2017 Selective staining of CdS on ZnO biolabel for ultrasensitive sandwich-type amperometric immunoassay of human heart-type fatty-acid-binding protein and immunoglobulin G. We report on an ultrasensitive metal-labeled amperometric immunoassay of proteins, which is based on the selective staining of nanocrystalline cadmium sulfide (CdS) on ZnO nanocrystals and in-situ microliter-droplet anodic stripping voltammetry (ASV) detection on the immunoelectrode. Zinc Oxide 29-32 fatty acid binding protein 3 Homo sapiens 109-146 27927285-11 2017 Here, the acrylic resin, zinc oxide (eugenol), and zinc phosphate cements significantly reduced cellular viability after exposure with respect to HGF cells only. Zinc Oxide 25-35 hepatocyte growth factor Mus musculus 146-149 28482492-0 2017 Electrochemical immunosensor based on ZnO nanorods-Au nanoparticles nanohybrids for ovarian cancer antigen CA-125 detection. Zinc Oxide 38-41 mucin 16, cell surface associated Homo sapiens 107-113 28482492-1 2017 In this research, ZnO nanorods - Au nanoparticles nanohybrids have been fabricated and employed to sensitive electrochemical strategy for the specific detection of the ovarian cancer antigen CA-125/MUC126. Zinc Oxide 18-21 mucin 16, cell surface associated Homo sapiens 191-197 28482492-4 2017 The Au NPs onto ZnO nanorods surface provides a favorable platform for efficient loading of anti-CA-125 antibody via binding with cystamine and glutaraldehyde. Zinc Oxide 16-19 mucin 16, cell surface associated Homo sapiens 97-103 29267767-1 2017 OBJECTIVES: To evaluate the effect of ZnO, TiO2 and SiO2 nanoparticles on cell viability and expression of the interleukin 7, interleukin 3, and granulocyte-macrophage colony stimulating factor (GM-CSF) genes in Mus musculus. Zinc Oxide 38-41 interleukin 7 Mus musculus 111-124 29267767-7 2017 ZnO nanoparticles reduced the expression of GM-CSF starting at doses of 20 mg/kg and 25 mg/kg. Zinc Oxide 0-3 colony stimulating factor 2 (granulocyte-macrophage) Mus musculus 44-50 28516178-1 2017 We report the fabrication of a flexible, lightweight and disposable multi walled carbon nanotube (MWCNT)-zinc oxide (ZnO) nanofiber based chemiresistive biosensor for label free detection of the malaria biomarker, histidine rich protein II (HRP2). Zinc Oxide 105-115 HDGF like 2 Homo sapiens 241-245 28516178-1 2017 We report the fabrication of a flexible, lightweight and disposable multi walled carbon nanotube (MWCNT)-zinc oxide (ZnO) nanofiber based chemiresistive biosensor for label free detection of the malaria biomarker, histidine rich protein II (HRP2). Zinc Oxide 117-120 HDGF like 2 Homo sapiens 241-245 28540719-0 2017 One Step Toward a New Generation of C-MOS Compatible Oxide P-N Junctions: Structure of the LSMO/ZnO Interface Elucidated by an Experimental and Theoretical Synergic Work. Zinc Oxide 96-99 MOS proto-oncogene, serine/threonine kinase Homo sapiens 36-41 27652582-6 2017 The addition of 1.4 wt% Ag2O on ZnO followed by calcination at 500 C resulted in an increase of 11% in the value of the reaction rate constant (kap) for COD reduction under UV radiation. Zinc Oxide 32-35 cyclin dependent kinase inhibitor 3 Homo sapiens 145-148 28652743-6 2017 Pretreatment of A549 cells on the apical side of the coculture system with the phagocytosis inhibitor cytochalasin B (CB) blocked ZnO-NP-induced HO-1 and PECAM-1 expression in HCAEC, indicating that endocytosis of ZnO-NPs by alveolar epithelial cells was involved in ZnO-NP-induced HO-1 or PECAM-1 expression in endothelial cells. Zinc Oxide 130-133 heme oxygenase 1 Homo sapiens 145-149 28652743-6 2017 Pretreatment of A549 cells on the apical side of the coculture system with the phagocytosis inhibitor cytochalasin B (CB) blocked ZnO-NP-induced HO-1 and PECAM-1 expression in HCAEC, indicating that endocytosis of ZnO-NPs by alveolar epithelial cells was involved in ZnO-NP-induced HO-1 or PECAM-1 expression in endothelial cells. Zinc Oxide 130-133 platelet and endothelial cell adhesion molecule 1 Homo sapiens 154-161 28652743-6 2017 Pretreatment of A549 cells on the apical side of the coculture system with the phagocytosis inhibitor cytochalasin B (CB) blocked ZnO-NP-induced HO-1 and PECAM-1 expression in HCAEC, indicating that endocytosis of ZnO-NPs by alveolar epithelial cells was involved in ZnO-NP-induced HO-1 or PECAM-1 expression in endothelial cells. Zinc Oxide 130-133 heme oxygenase 1 Homo sapiens 282-286 28652743-6 2017 Pretreatment of A549 cells on the apical side of the coculture system with the phagocytosis inhibitor cytochalasin B (CB) blocked ZnO-NP-induced HO-1 and PECAM-1 expression in HCAEC, indicating that endocytosis of ZnO-NPs by alveolar epithelial cells was involved in ZnO-NP-induced HO-1 or PECAM-1 expression in endothelial cells. Zinc Oxide 130-133 platelet and endothelial cell adhesion molecule 1 Homo sapiens 290-297 28594362-1 2017 In the present study, ZnO nanoparticles (NPs) were synthesized in zerumbone solution by a green approach and appraised for their ability to absorb Pb(II) ions from aqueous solution. Zinc Oxide 22-25 submaxillary gland androgen regulated protein 3B Homo sapiens 147-153 28459695-1 2017 This paper reports a novel electrochemical method for detection of Glutathione (GSH) using Glutathione-S-Transferase (GST) - ZnO composite nanoparticles to investigate the prospects of the method for detection of cancer at an early stage. Zinc Oxide 125-128 glutathione S-transferase kappa 1 Homo sapiens 91-116 28459695-1 2017 This paper reports a novel electrochemical method for detection of Glutathione (GSH) using Glutathione-S-Transferase (GST) - ZnO composite nanoparticles to investigate the prospects of the method for detection of cancer at an early stage. Zinc Oxide 125-128 glutathione S-transferase kappa 1 Homo sapiens 118-121 28459695-2 2017 The purified GST enzyme was bound with ZnO nanoparticles by electrostatic interactions and the nanocomposite was dropcast on a silicon dioxide wafer. Zinc Oxide 39-42 glutathione S-transferase kappa 1 Homo sapiens 13-16 28459695-9 2017 The kinetic parameters of both GST and nanoconjugate of ZnO nanoparticles andGSTwere determinedwith respect to its substrates, GSH and CDNB, using Michaelis-Mentenmodel. Zinc Oxide 56-59 glutathione S-transferase kappa 1 Homo sapiens 31-34 28322516-2 2017 Herein, ZnO nanoparticles encapsulated into N-doped porous carbon has been rationally prepared by the pyrolysis of a metal-organic framework (MOF) followed by a moderate oxidation treatment. Zinc Oxide 8-11 lysine acetyltransferase 8 Homo sapiens 117-146 27441385-0 2017 Synergistic toxicity of zno nanoparticles and dimethoate in mice: Enhancing their biodistribution by synergistic binding of serum albumin and dimethoate to zno nanoparticles. Zinc Oxide 24-27 albumin Mus musculus 130-137 28441756-6 2017 Paradoxically, the release of inflammatory cytokine interleukin-6 (IL-6) was decreased, which indicated the anti-inflammatory effects of ZnO NPs when BSA was present. Zinc Oxide 137-140 interleukin 6 Homo sapiens 52-65 28441756-6 2017 Paradoxically, the release of inflammatory cytokine interleukin-6 (IL-6) was decreased, which indicated the anti-inflammatory effects of ZnO NPs when BSA was present. Zinc Oxide 137-140 interleukin 6 Homo sapiens 67-71 27441385-0 2017 Synergistic toxicity of zno nanoparticles and dimethoate in mice: Enhancing their biodistribution by synergistic binding of serum albumin and dimethoate to zno nanoparticles. Zinc Oxide 156-159 albumin Mus musculus 130-137 27441385-8 2017 Nano ZnO had 3-fold or 2.4-fold higher binding capability for serum albumin or DM, respectively, than bulk ZnO. Zinc Oxide 5-8 albumin Mus musculus 68-75 27441385-9 2017 In addition, serum albumin significantly increased the binding capability of nano ZnO for DM by approximately four times via the interaction of serum albumin and DM. Zinc Oxide 82-85 albumin Mus musculus 19-26 27441385-9 2017 In addition, serum albumin significantly increased the binding capability of nano ZnO for DM by approximately four times via the interaction of serum albumin and DM. Zinc Oxide 82-85 albumin Mus musculus 150-157 27441385-10 2017 The uptake of serum albumin- and DM-bound nano ZnO by the macrophages significantly increased DM accumulation in mice. Zinc Oxide 47-50 albumin Mus musculus 20-27 28911670-3 2017 By combining the benefits of Pp-ABSA, ZnO NPs, and CPE, the resulted modified electrode exhibited outstanding electrocatalytic activity in terms of tartrazine oxidation by giving much higher peak currents than those obtained for the unmodified CPE and also other constructed electrodes. Zinc Oxide 38-41 carboxypeptidase E Homo sapiens 244-247 28476991-5 2017 The inhibitory action of thioglycerol capped ZnO nanoparticles (SP1) and acarbose drug (used for diabetes type II) capped ZnO (SP2) for HSA was observed to 61 and72%, respectively. Zinc Oxide 122-125 Sp2 transcription factor Homo sapiens 127-130 28476991-5 2017 The inhibitory action of thioglycerol capped ZnO nanoparticles (SP1) and acarbose drug (used for diabetes type II) capped ZnO (SP2) for HSA was observed to 61 and72%, respectively. Zinc Oxide 122-125 albumin Homo sapiens 136-139 28285566-0 2017 Involvement of the cytokine-IDO1-AhR loop in zinc oxide nanoparticle-induced acute pulmonary inflammation. Zinc Oxide 45-55 indoleamine 2,3-dioxygenase 1 Mus musculus 28-32 28911670-2 2017 A fast and easy method for the fabrication of poly p-ABSA (Pp-ABSA)/ZnO NPs-carbon paste electrode (Pp-ABSA/ZnO NPs-CPE) by cyclic voltammetry was used. Zinc Oxide 68-71 carboxypeptidase E Homo sapiens 116-119 28911670-2 2017 A fast and easy method for the fabrication of poly p-ABSA (Pp-ABSA)/ZnO NPs-carbon paste electrode (Pp-ABSA/ZnO NPs-CPE) by cyclic voltammetry was used. Zinc Oxide 108-111 carboxypeptidase E Homo sapiens 116-119 28285566-0 2017 Involvement of the cytokine-IDO1-AhR loop in zinc oxide nanoparticle-induced acute pulmonary inflammation. Zinc Oxide 45-55 aryl-hydrocarbon receptor Mus musculus 33-36 28366952-6 2017 Furthermore, several apoptosis pathway related genes such as Bax, p53, caspase-3 and caspase-9 were significantly up-regulated in the PFOS plus ZnO-NPs exposure groups, while anti-apoptotic gene Bcl-2 was significantly down-regulated in the PFOS plus ZnO-NPs exposure groups. Zinc Oxide 144-147 BCL2 associated X, apoptosis regulator a Danio rerio 61-64 28003440-9 2017 Therefore, the increased apoptosis resulting from ZnO NPs exposure is likely cep-1/p53 dependent. Zinc Oxide 50-53 Transcription factor cep-1 Caenorhabditis elegans 77-82 28126643-6 2017 The results showed that all the tested zinc compounds induced similar concentration-dependent cytotoxicity, but only ZnO NPs significantly elevated DNA and chromosomal damage, which was accompanied by a reduction of GST and CAT activity. Zinc Oxide 117-120 catalase Canis lupus familiaris 224-227 28366952-6 2017 Furthermore, several apoptosis pathway related genes such as Bax, p53, caspase-3 and caspase-9 were significantly up-regulated in the PFOS plus ZnO-NPs exposure groups, while anti-apoptotic gene Bcl-2 was significantly down-regulated in the PFOS plus ZnO-NPs exposure groups. Zinc Oxide 144-147 tumor protein p53 Danio rerio 66-69 28366952-6 2017 Furthermore, several apoptosis pathway related genes such as Bax, p53, caspase-3 and caspase-9 were significantly up-regulated in the PFOS plus ZnO-NPs exposure groups, while anti-apoptotic gene Bcl-2 was significantly down-regulated in the PFOS plus ZnO-NPs exposure groups. Zinc Oxide 144-147 caspase 3, apoptosis-related cysteine peptidase a Danio rerio 71-80 28366952-6 2017 Furthermore, several apoptosis pathway related genes such as Bax, p53, caspase-3 and caspase-9 were significantly up-regulated in the PFOS plus ZnO-NPs exposure groups, while anti-apoptotic gene Bcl-2 was significantly down-regulated in the PFOS plus ZnO-NPs exposure groups. Zinc Oxide 144-147 caspase 9, apoptosis-related cysteine peptidase Danio rerio 85-94 28366952-6 2017 Furthermore, several apoptosis pathway related genes such as Bax, p53, caspase-3 and caspase-9 were significantly up-regulated in the PFOS plus ZnO-NPs exposure groups, while anti-apoptotic gene Bcl-2 was significantly down-regulated in the PFOS plus ZnO-NPs exposure groups. Zinc Oxide 144-147 BCL2 apoptosis regulator a Danio rerio 195-200 28366952-7 2017 In addition, some oxidative stress-related genes such as Cat, GSH peroxidase 1 (Gpx1a) and superoxide dismutase 1 (Sod1) were also significantly down-regulated after the PFOS plus ZnO-NPs co-treatments. Zinc Oxide 180-183 catalase Danio rerio 57-60 28366952-7 2017 In addition, some oxidative stress-related genes such as Cat, GSH peroxidase 1 (Gpx1a) and superoxide dismutase 1 (Sod1) were also significantly down-regulated after the PFOS plus ZnO-NPs co-treatments. Zinc Oxide 180-183 glutathione peroxidase 1a Danio rerio 80-85 28366952-7 2017 In addition, some oxidative stress-related genes such as Cat, GSH peroxidase 1 (Gpx1a) and superoxide dismutase 1 (Sod1) were also significantly down-regulated after the PFOS plus ZnO-NPs co-treatments. Zinc Oxide 180-183 superoxide dismutase 1, soluble Danio rerio 91-113 28366952-7 2017 In addition, some oxidative stress-related genes such as Cat, GSH peroxidase 1 (Gpx1a) and superoxide dismutase 1 (Sod1) were also significantly down-regulated after the PFOS plus ZnO-NPs co-treatments. Zinc Oxide 180-183 superoxide dismutase 1, soluble Danio rerio 115-119 28772691-6 2017 We prove that LiF-doped ZnO is the only codoped system that exhibits a p-type character in the presence of Zn vacancies. Zinc Oxide 24-27 LIF interleukin 6 family cytokine Homo sapiens 14-17 27914333-6 2017 The step wise modification in the synthesis ZnO-GO/NC was characterized using FT-IR, XRD, SEM, EDS, AFM, DRS-UV and BET N2 adsorption isotherm techniques. Zinc Oxide 44-47 sushi repeat containing protein X-linked Homo sapiens 105-108 27818043-4 2017 A flexible disposable electrochemical biosensor device comprising of vertically oriented zinc oxide (ZnO) nanostructures was developed for rapid and simultaneous screening of cardiac Troponin-I (cTnI) and cardiac-Troponin-T (cTnT) in a point-of-care sensor format. Zinc Oxide 89-99 troponin I3, cardiac type Homo sapiens 175-193 27818043-4 2017 A flexible disposable electrochemical biosensor device comprising of vertically oriented zinc oxide (ZnO) nanostructures was developed for rapid and simultaneous screening of cardiac Troponin-I (cTnI) and cardiac-Troponin-T (cTnT) in a point-of-care sensor format. Zinc Oxide 101-104 troponin I3, cardiac type Homo sapiens 175-193 27818043-4 2017 A flexible disposable electrochemical biosensor device comprising of vertically oriented zinc oxide (ZnO) nanostructures was developed for rapid and simultaneous screening of cardiac Troponin-I (cTnI) and cardiac-Troponin-T (cTnT) in a point-of-care sensor format. Zinc Oxide 101-104 troponin I3, cardiac type Homo sapiens 195-199 27818043-4 2017 A flexible disposable electrochemical biosensor device comprising of vertically oriented zinc oxide (ZnO) nanostructures was developed for rapid and simultaneous screening of cardiac Troponin-I (cTnI) and cardiac-Troponin-T (cTnT) in a point-of-care sensor format. Zinc Oxide 101-104 troponin T2, cardiac type Homo sapiens 205-223 27818043-4 2017 A flexible disposable electrochemical biosensor device comprising of vertically oriented zinc oxide (ZnO) nanostructures was developed for rapid and simultaneous screening of cardiac Troponin-I (cTnI) and cardiac-Troponin-T (cTnT) in a point-of-care sensor format. Zinc Oxide 101-104 troponin T2, cardiac type Homo sapiens 225-229 28287492-2 2017 Through modulating the operating temperature and the processing response signal with a pattern recognition algorithm, a gas sensor consisting of a single sensing electrode, i.e., ZnO/In2O3 composite, is designed to differentiate NO2, NH3, C3H6, CO within the level of 50-400 ppm. Zinc Oxide 179-182 galactosamine (N-acetyl)-6-sulfatase Homo sapiens 120-123 28331313-0 2017 Involvement of PINK1/parkin-mediated mitophagy in ZnO nanoparticle-induced toxicity in BV-2 cells. Zinc Oxide 50-53 PTEN induced putative kinase 1 Mus musculus 15-20 28331313-9 2017 The present study demonstrated that apart from autophagy, PINK1/parkin-mediated mitophagy plays a protective role in ZnO NP-induced cytotoxicity. Zinc Oxide 117-120 PTEN induced putative kinase 1 Mus musculus 58-63 28280330-11 2017 Removal of one copy of the D. melanogaster Nrf2 alleles further decreased the ZnO NPs-induced lethality due to increased production of ROS, indicating that nuclear factor E2-related factor 2 (Nrf2) plays important role in ZnO NPs-mediated ROS production. Zinc Oxide 78-81 cap-n-collar Drosophila melanogaster 43-47 28252113-3 2017 In the present study, we report a novel Zinc oxide nanorods functionalized paper platform for the preconcentration of Myoglobin, a cardiac biomarker. Zinc Oxide 40-50 myoglobin Homo sapiens 118-127 28252113-8 2017 Paper-based ELISA was performed for determination of pre-concentration of cardiac marker protein Myoglobin using the new ZnO-NRs/WFP platform. Zinc Oxide 121-124 myoglobin Homo sapiens 97-106 28171821-3 2017 In this study, the effects of ER stress inducer thapsigargin (TG) on the toxicity of ZnO NPs to THP-1 macrophages were investigated. Zinc Oxide 85-88 GLI family zinc finger 2 Homo sapiens 96-101 28171821-6 2017 In the co-culture, exposure of THP-1 macrophages in the upper chamber to ZnO NPs and TG significantly reduced the viability of human umbilical vein endothelial cells (HUVECs) in the lower chamber, but the release of tumor necrosis factor alpha (TNFalpha) was not induced. Zinc Oxide 73-76 GLI family zinc finger 2 Homo sapiens 31-36 28171821-6 2017 In the co-culture, exposure of THP-1 macrophages in the upper chamber to ZnO NPs and TG significantly reduced the viability of human umbilical vein endothelial cells (HUVECs) in the lower chamber, but the release of tumor necrosis factor alpha (TNFalpha) was not induced. Zinc Oxide 73-76 tumor necrosis factor Homo sapiens 216-243 28171821-6 2017 In the co-culture, exposure of THP-1 macrophages in the upper chamber to ZnO NPs and TG significantly reduced the viability of human umbilical vein endothelial cells (HUVECs) in the lower chamber, but the release of tumor necrosis factor alpha (TNFalpha) was not induced. Zinc Oxide 73-76 tumor necrosis factor Homo sapiens 245-253 28171821-7 2017 In summary, our data showed that stressing THP-1 macrophages with TG enhanced the cytotoxicity of ZnO NPs to macrophages and macrophage-endothelial co-cultures. Zinc Oxide 98-101 GLI family zinc finger 2 Homo sapiens 43-48 28280330-11 2017 Removal of one copy of the D. melanogaster Nrf2 alleles further decreased the ZnO NPs-induced lethality due to increased production of ROS, indicating that nuclear factor E2-related factor 2 (Nrf2) plays important role in ZnO NPs-mediated ROS production. Zinc Oxide 78-81 cap-n-collar Drosophila melanogaster 156-190 28280330-11 2017 Removal of one copy of the D. melanogaster Nrf2 alleles further decreased the ZnO NPs-induced lethality due to increased production of ROS, indicating that nuclear factor E2-related factor 2 (Nrf2) plays important role in ZnO NPs-mediated ROS production. Zinc Oxide 78-81 cap-n-collar Drosophila melanogaster 192-196 28280330-11 2017 Removal of one copy of the D. melanogaster Nrf2 alleles further decreased the ZnO NPs-induced lethality due to increased production of ROS, indicating that nuclear factor E2-related factor 2 (Nrf2) plays important role in ZnO NPs-mediated ROS production. Zinc Oxide 222-225 cap-n-collar Drosophila melanogaster 43-47 28280330-11 2017 Removal of one copy of the D. melanogaster Nrf2 alleles further decreased the ZnO NPs-induced lethality due to increased production of ROS, indicating that nuclear factor E2-related factor 2 (Nrf2) plays important role in ZnO NPs-mediated ROS production. Zinc Oxide 222-225 cap-n-collar Drosophila melanogaster 156-190 28280330-11 2017 Removal of one copy of the D. melanogaster Nrf2 alleles further decreased the ZnO NPs-induced lethality due to increased production of ROS, indicating that nuclear factor E2-related factor 2 (Nrf2) plays important role in ZnO NPs-mediated ROS production. Zinc Oxide 222-225 cap-n-collar Drosophila melanogaster 192-196 28233796-0 2017 ZnO nanoparticles act as supportive therapy in DSS-induced ulcerative colitis in mice by maintaining gut homeostasis and activating Nrf2 signaling. Zinc Oxide 0-3 nuclear factor, erythroid derived 2, like 2 Mus musculus 132-136 27339255-12 2017 The pro-inflammatory cytokine interleukin-lbeta (IL-1beta) mRNA expression in the jejunum mucosa was downregulated in the ZnO-supplemented group, compared with the control (P < 0.05). Zinc Oxide 122-125 interleukin 1 beta Homo sapiens 49-57 28029108-3 2017 In the current study, we report on a combination of zinc oxide (ZnO) nanowires with monolayers of photosynthetic reaction centers which are self-assembled, via a cytochrome c linker, as photoactive electrode. Zinc Oxide 52-62 cytochrome c, somatic Homo sapiens 162-174 28029108-3 2017 In the current study, we report on a combination of zinc oxide (ZnO) nanowires with monolayers of photosynthetic reaction centers which are self-assembled, via a cytochrome c linker, as photoactive electrode. Zinc Oxide 64-67 cytochrome c, somatic Homo sapiens 162-174 27339255-13 2017 Both in-feed antibiotics and ZnO supplementation decreased the mRNA expression of interferon-gamma (IFN-gamma), but increased the mRNA expression of transforming growth factor-beta (TGF-beta), in the jejunum mucosa of piglets, when compared to those in the control (P < 0.05). Zinc Oxide 29-32 interferon gamma Homo sapiens 82-98 27339255-13 2017 Both in-feed antibiotics and ZnO supplementation decreased the mRNA expression of interferon-gamma (IFN-gamma), but increased the mRNA expression of transforming growth factor-beta (TGF-beta), in the jejunum mucosa of piglets, when compared to those in the control (P < 0.05). Zinc Oxide 29-32 interferon gamma Homo sapiens 100-109 28094367-7 2017 The number of spins calculated per one CNP (NSOP) was found to depend on carbon content in ZnO + xC samples. Zinc Oxide 91-94 2',3'-cyclic nucleotide 3' phosphodiesterase Homo sapiens 39-42 27984146-0 2017 Deciphering the interaction of bovine heart cystatin with ZnO nanoparticles: Spectroscopic and thermodynamic approach. Zinc Oxide 58-61 probable cystatin-15 Bos taurus 44-52 27984146-4 2017 In the present study zinc oxide nanoparticles (ZnO-NPs) were synthesized and subjected to interact with buffalo heart cystatin (BHC), purified from buffalo heart, to assess the effect(s) of ZnO-NPs on the structure and function of BHC. Zinc Oxide 21-31 probable cystatin-15 Bos taurus 118-126 26717901-6 2017 Both LA and ZnO treatments enhanced intestinal homeostatic and architecture, significantly decreased urinary lactulose to mannitol ratios (p < 0.05) and increased the expression of the intestinal mucosal tight junction proteins occludin (OCLN) and zonula occludens protein-1 (ZO-1) (p < 0.05). Zinc Oxide 12-15 occludin Rattus norvegicus 231-239 26717901-6 2017 Both LA and ZnO treatments enhanced intestinal homeostatic and architecture, significantly decreased urinary lactulose to mannitol ratios (p < 0.05) and increased the expression of the intestinal mucosal tight junction proteins occludin (OCLN) and zonula occludens protein-1 (ZO-1) (p < 0.05). Zinc Oxide 12-15 occludin Rattus norvegicus 241-245 26717901-6 2017 Both LA and ZnO treatments enhanced intestinal homeostatic and architecture, significantly decreased urinary lactulose to mannitol ratios (p < 0.05) and increased the expression of the intestinal mucosal tight junction proteins occludin (OCLN) and zonula occludens protein-1 (ZO-1) (p < 0.05). Zinc Oxide 12-15 tight junction protein 1 Rattus norvegicus 251-277 26717901-6 2017 Both LA and ZnO treatments enhanced intestinal homeostatic and architecture, significantly decreased urinary lactulose to mannitol ratios (p < 0.05) and increased the expression of the intestinal mucosal tight junction proteins occludin (OCLN) and zonula occludens protein-1 (ZO-1) (p < 0.05). Zinc Oxide 12-15 tight junction protein 1 Rattus norvegicus 279-283 27933497-8 2017 Furthermore, the highest phenolic compound"s removal rate was 99% at the optimal condition (pH 5, ZnO dosage of 0.1 g L-1 at the 30 min with UV-C illumination of 125 W). Zinc Oxide 98-101 immunoglobulin kappa variable 1-16 Homo sapiens 118-121 27940348-0 2017 PEG-functionalized zinc oxide nanoparticles induce apoptosis in breast cancer cells through reactive oxygen species-dependent impairment of DNA damage repair enzyme NEIL2. Zinc Oxide 19-29 nei like DNA glycosylase 2 Homo sapiens 165-170 27810506-9 2017 The light emission properties of the ZnO:CdO thin films were studied by photoluminescence spectra recorded at room temperature. Zinc Oxide 37-40 cell adhesion associated, oncogene regulated Homo sapiens 41-44 28331785-2 2017 Herein, UV-vis-NIR sensitive ZnO photodetectors consisting of ZnO nanowires (NW) array/PbS quantum dots (QDs) heterostructures are fabricated through modified electrospining method and an exchanging process. Zinc Oxide 29-32 cholinergic receptor muscarinic 3 Homo sapiens 87-90 28115650-0 2017 Ion-shedding zinc oxide nanoparticles induce microglial BV2 cell proliferation via the ERK and Akt signaling pathways. Zinc Oxide 13-23 mitogen-activated protein kinase 1 Mus musculus 87-90 28115650-0 2017 Ion-shedding zinc oxide nanoparticles induce microglial BV2 cell proliferation via the ERK and Akt signaling pathways. Zinc Oxide 13-23 thymoma viral proto-oncogene 1 Mus musculus 95-98 28115650-8 2017 ZnO NPs significantly induced the phosphorylation of ERK and Akt, which might be involved in promoting cell proliferation. Zinc Oxide 0-3 mitogen-activated protein kinase 1 Mus musculus 53-56 28115650-8 2017 ZnO NPs significantly induced the phosphorylation of ERK and Akt, which might be involved in promoting cell proliferation. Zinc Oxide 0-3 thymoma viral proto-oncogene 1 Mus musculus 61-64 28115650-9 2017 In conclusion, our results demonstrated that ZnO NPs induced BV2 microglial cell proliferation probably via the release of zinc ions from ZnO, which could then activate the ERK and Akt signaling pathways. Zinc Oxide 45-48 mitogen-activated protein kinase 1 Mus musculus 173-176 28115650-9 2017 In conclusion, our results demonstrated that ZnO NPs induced BV2 microglial cell proliferation probably via the release of zinc ions from ZnO, which could then activate the ERK and Akt signaling pathways. Zinc Oxide 45-48 thymoma viral proto-oncogene 1 Mus musculus 181-184 28115650-9 2017 In conclusion, our results demonstrated that ZnO NPs induced BV2 microglial cell proliferation probably via the release of zinc ions from ZnO, which could then activate the ERK and Akt signaling pathways. Zinc Oxide 138-141 mitogen-activated protein kinase 1 Mus musculus 173-176 28115650-9 2017 In conclusion, our results demonstrated that ZnO NPs induced BV2 microglial cell proliferation probably via the release of zinc ions from ZnO, which could then activate the ERK and Akt signaling pathways. Zinc Oxide 138-141 thymoma viral proto-oncogene 1 Mus musculus 181-184 27871387-0 2017 Mediator-free interaction of glucose oxidase, as model enzyme for immobilization, with Al-doped and undoped ZnO thin films laser-deposited on polycarbonate supports. Zinc Oxide 108-111 hydroxyacid oxidase 1 Homo sapiens 29-44 27871387-9 2017 The limit of detection (LoD) was 167muM of glucose for GOx/AZO, as compared to 360muM for GOx/ZnO. Zinc Oxide 94-97 hydroxyacid oxidase 1 Homo sapiens 90-93 27871387-10 2017 The linearity was 0.28-28mM for GOx/AZO whereas it was 0.6-28mM for GOx/ZnO with a response time of 10s. Zinc Oxide 72-75 hydroxyacid oxidase 1 Homo sapiens 68-71 27871387-11 2017 Possibly due to higher enzyme loading, the decrease of impedance in presence of glucose was larger for GOx/ZnO as compared to GOx/AZO in electrochemical impedance spectroscopy (EIS). Zinc Oxide 107-110 hydroxyacid oxidase 1 Homo sapiens 103-106 27871387-13 2017 The characteristics of novel ZnO and AZO thin films with GOx as a model enzyme, should prove useful for the future fabrication of inexpensive, highly sensitive, disposable electrochemical biosensors for high throughput diagnostics. Zinc Oxide 29-32 hydroxyacid oxidase 1 Homo sapiens 57-60 29630810-6 2017 This results show that the MEH-PPV/ZnO thin films gives good performance and is relevant for applications in optoelectronic devices such as a negative differential resistance. Zinc Oxide 35-38 epoxide hydrolase 1 Homo sapiens 27-30 28573081-7 2017 Moreover, pulmonary surfactant-associated protein D and gelsolin, biomarkers of idiopathic pulmonary fibrosis, were significantly up-regulated in rat BALF after ZnO NPs exposure (2.42- and 2.84-fold, respectively). Zinc Oxide 161-164 surfactant protein D Rattus norvegicus 10-51 28573081-7 2017 Moreover, pulmonary surfactant-associated protein D and gelsolin, biomarkers of idiopathic pulmonary fibrosis, were significantly up-regulated in rat BALF after ZnO NPs exposure (2.42- and 2.84-fold, respectively). Zinc Oxide 161-164 gelsolin Rattus norvegicus 56-64 27783247-5 2017 The optimal operating conditions for the degradation of 0.12 mM (74 mg L-1) dye concentration and mineralization of its aqueous solution were determined as GrF-ZnO-TiO2 thin film anode, 100 mA current intensity, and 0.1 mM Fe2+ (catalyst) concentration. Zinc Oxide 160-163 L1 cell adhesion molecule Homo sapiens 71-74 28717102-0 2017 Human lung adenocarcinoma cells with an EGFR mutation are sensitive to non-autophagic cell death induced by zinc oxide and aluminium-doped zinc oxide nanoparticles. Zinc Oxide 108-118 epidermal growth factor receptor Homo sapiens 40-44 28717102-0 2017 Human lung adenocarcinoma cells with an EGFR mutation are sensitive to non-autophagic cell death induced by zinc oxide and aluminium-doped zinc oxide nanoparticles. Zinc Oxide 139-149 epidermal growth factor receptor Homo sapiens 40-44 28717102-2 2017 The objective of this study was to investigate the effects of an epidermal growth factor receptor (EGFR) mutation on autophagic cell death in human lung adenocarcinoma cells by 20-nm zinc oxide nanoparticles (ZnONP20) and aluminum-doped ZnONPs (Al-ZnONP20). Zinc Oxide 183-193 epidermal growth factor receptor Homo sapiens 65-97 28717102-2 2017 The objective of this study was to investigate the effects of an epidermal growth factor receptor (EGFR) mutation on autophagic cell death in human lung adenocarcinoma cells by 20-nm zinc oxide nanoparticles (ZnONP20) and aluminum-doped ZnONPs (Al-ZnONP20). Zinc Oxide 183-193 epidermal growth factor receptor Homo sapiens 99-103 27922086-0 2016 Photoelectrochemical detection of alpha-fetoprotein based on ZnO inverse opals structure electrodes modified by Ag2S nanoparticles. Zinc Oxide 61-64 alpha fetoprotein Homo sapiens 34-51 28024321-3 2016 Here, we report the investigation of strain-gradient induced symmetry-breaking effect on excitonic states in pure bending ZnO microwires by high spatial-resolved cathodoluminescence at low temperature of 80 K. In addition to the local-strain induced light emission peak shift, the bound exciton emission photon energy shows an extraordinary jump of ~16.6 meV at a high strain-gradient of 1.22% mum-1, which is ascribed to the strain gradient induced symmetry-breaking. Zinc Oxide 122-125 PWWP domain containing 3A, DNA repair factor Homo sapiens 394-399 28144552-6 2016 Improved sensing performance was achieved for the ZnO (98 wt %)-SnO2 (2 wt %) composite as compared to the sensors containing only the pristine oxides. Zinc Oxide 50-53 strawberry notch homolog 2 Homo sapiens 64-67 28144552-8 2016 The high sensitivity (RS = 1.21) to low amounts of CO (5 ppm) was reported for the sensor containing a composite sensitive film with ZnO (98 wt %)-SnO2 (2 wt %). Zinc Oxide 133-136 strawberry notch homolog 2 Homo sapiens 147-150 27922086-1 2016 In this work, a new photoelectrochemical biosensor based on Ag2S nanoparticles (NPs) modified macroporous ZnO inverse opals structure (IOs) was developed for sensitive and rapid detection of alpha fetal protein (AFP). Zinc Oxide 106-109 angiotensin II receptor type 1 Homo sapiens 60-64 27922086-1 2016 In this work, a new photoelectrochemical biosensor based on Ag2S nanoparticles (NPs) modified macroporous ZnO inverse opals structure (IOs) was developed for sensitive and rapid detection of alpha fetal protein (AFP). Zinc Oxide 106-109 alpha fetoprotein Homo sapiens 191-210 27922086-1 2016 In this work, a new photoelectrochemical biosensor based on Ag2S nanoparticles (NPs) modified macroporous ZnO inverse opals structure (IOs) was developed for sensitive and rapid detection of alpha fetal protein (AFP). Zinc Oxide 106-109 alpha fetoprotein Homo sapiens 212-215 27922086-2 2016 Small size and uniformly dispersed Ag2S NPs were prepared using the Successive Ionic Layer Adsorption And Reaction (SILAR) method, which were adsorbed on ZnO IOs surface and frame work as matrix for immobilization of AFP. Zinc Oxide 154-157 angiotensin II receptor type 1 Homo sapiens 35-39 27922086-3 2016 The composite structure of ZnO/Ag2S expanded the scope of light absorption to long wavelength, which can make full use of the light energy. Zinc Oxide 27-30 angiotensin II receptor type 1 Homo sapiens 31-35 27922086-5 2016 The biosensors based on FTO (fluorine-doped tinoxide) ZnO/Ag2S electrode showed enough sensitivity and a wide linear range from 0.05 ng/mL to 200 ng/mL with a low detection limit of 8 pg/mL for the detection of AFP. Zinc Oxide 54-57 alpha fetoprotein Homo sapiens 211-214 27922092-2 2016 The as-prepared ZnO micro/nanomaterials are characterized by XRD, SEM, TEM, HRTEM, XPS, BET, and UV-Vis. Zinc Oxide 16-19 delta/notch like EGF repeat containing Homo sapiens 88-91 27770658-7 2016 Taken together, the results of the present study showed a combined toxicity of low levels of PA and ZnO NPs especially to lysosomes in THP-1 macrophages. Zinc Oxide 100-103 GLI family zinc finger 2 Homo sapiens 135-140 27770658-0 2016 Combined effects of low levels of palmitate on toxicity of ZnO nanoparticles to THP-1 macrophages. Zinc Oxide 59-62 GLI family zinc finger 2 Homo sapiens 80-85 30895007-2 2016 This study aimed to investigate the dentin disinfection and cytotoxicity of a novel zinc oxide (ZnO) based medicament, Z-Mix. Zinc Oxide 84-94 Mix paired-like homeobox Homo sapiens 121-124 27770658-6 2016 In addition, ZnO NPs dose-dependently increased intracellular Zn ions in THP-1 macrophages, which was not significantly affected by PA. Zinc Oxide 13-16 GLI family zinc finger 2 Homo sapiens 73-78 30895007-2 2016 This study aimed to investigate the dentin disinfection and cytotoxicity of a novel zinc oxide (ZnO) based medicament, Z-Mix. Zinc Oxide 96-99 Mix paired-like homeobox Homo sapiens 121-124 27726336-5 2016 A simple and cost-effective ASC construction was demonstrated with ZnO@MnO2 NFs as a battery-type cathode material and a commercial-quality activated carbon as a capacitor-type anode material. Zinc Oxide 67-70 PYD and CARD domain containing Homo sapiens 28-31 27896788-0 2016 Facile Synthesis and High Photocatalytic Degradation Performance of ZnO-SnO2 Hollow Spheres. Zinc Oxide 68-71 strawberry notch homolog 2 Homo sapiens 72-75 27801574-0 2016 Nano Zinc Oxide Inhibits Fibrillar Growth and Suppresses Cellular Toxicity of Lysozyme Amyloid. Zinc Oxide 5-15 lysozyme Homo sapiens 78-86 27624339-0 2016 Streptavidin Modified ZnO Film Bulk Acoustic Resonator for Detection of Tumor Marker Mucin 1. Zinc Oxide 22-25 mucin 1, cell surface associated Homo sapiens 85-92 27624339-1 2016 A ZnO-based film bulk acoustic resonator has been fabricated using a magnetron sputtering technology, which was employed as a biosensor for detection of mucin 1. Zinc Oxide 2-5 mucin 1, cell surface associated Homo sapiens 153-160 27162145-0 2016 Ultrasensitive photoelectrochemical aptasensing of miR-155 using efficient and stable CH3NH3PbI3 quantum dots sensitized ZnO nanosheets as light harvester. Zinc Oxide 121-124 microRNA 155 Homo sapiens 51-58 28774047-2 2016 The structure and morphology of ZnO-LDH@C3N4 composite were characterized using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopes/transmission electron microscopes (SEM/TEM), N2 adsorption/desorption, ultraviolet visible diffuse reflectance spectroscopy (UV-Vis-DRS), photoluminescence spectrometer (PL) and electrochemical impedance spectroscopy (EIS). Zinc Oxide 32-35 sushi repeat containing protein X-linked Homo sapiens 316-319 27262279-6 2016 The ER stress marker of PERK, eIF2alpha, ATF4, Chop, JNK, caspase-12, caspase-9, GRP94, and Bax at the mRNA levels were higher expression in 30nm ZnO NP than that in bulk or 90nm ZnO. Zinc Oxide 146-149 eukaryotic translation initiation factor 2 alpha kinase 3 Mus musculus 24-28 27262279-6 2016 The ER stress marker of PERK, eIF2alpha, ATF4, Chop, JNK, caspase-12, caspase-9, GRP94, and Bax at the mRNA levels were higher expression in 30nm ZnO NP than that in bulk or 90nm ZnO. Zinc Oxide 146-149 eukaryotic translation initiation factor 2A Mus musculus 30-39 27262279-6 2016 The ER stress marker of PERK, eIF2alpha, ATF4, Chop, JNK, caspase-12, caspase-9, GRP94, and Bax at the mRNA levels were higher expression in 30nm ZnO NP than that in bulk or 90nm ZnO. Zinc Oxide 146-149 activating transcription factor 4 Mus musculus 41-45 27262279-6 2016 The ER stress marker of PERK, eIF2alpha, ATF4, Chop, JNK, caspase-12, caspase-9, GRP94, and Bax at the mRNA levels were higher expression in 30nm ZnO NP than that in bulk or 90nm ZnO. Zinc Oxide 146-149 mitogen-activated protein kinase 8 Mus musculus 53-56 27262279-6 2016 The ER stress marker of PERK, eIF2alpha, ATF4, Chop, JNK, caspase-12, caspase-9, GRP94, and Bax at the mRNA levels were higher expression in 30nm ZnO NP than that in bulk or 90nm ZnO. Zinc Oxide 146-149 caspase 12 Mus musculus 58-68 27262279-6 2016 The ER stress marker of PERK, eIF2alpha, ATF4, Chop, JNK, caspase-12, caspase-9, GRP94, and Bax at the mRNA levels were higher expression in 30nm ZnO NP than that in bulk or 90nm ZnO. Zinc Oxide 146-149 caspase 9 Mus musculus 70-79 27262279-6 2016 The ER stress marker of PERK, eIF2alpha, ATF4, Chop, JNK, caspase-12, caspase-9, GRP94, and Bax at the mRNA levels were higher expression in 30nm ZnO NP than that in bulk or 90nm ZnO. Zinc Oxide 146-149 heat shock protein 90, beta (Grp94), member 1 Mus musculus 81-86 27404512-6 2016 However, both ZnO and AgNP20 induced cytoskeletal breakdown as evidenced by the cleavage of lamin B1. Zinc Oxide 14-17 lamin B1 Homo sapiens 92-100 26805551-7 2016 In conclusion, nanosize zinc oxide for dietary supplementation can increase zinc digestibility, serum growth hormone levels and carbonic anhydrase activity and enhance the immune response of weanling piglets. Zinc Oxide 24-34 growth hormone Capra hircus 102-116 27658222-12 2016 In this study, exposure of zebrafish embryos to nano-ZnO triggered an excessive production of ROS, which was followed by several phenomena: the up-regulation of p53, a reduction in the bcl-2/bax ratio,a reduction in the mitochondrial membrane potential (psim), the release of cytochrome c into the cytosolic fraction, and the activation of caspases 9 and 3. Zinc Oxide 53-56 tumor protein p53 Danio rerio 161-164 27658222-12 2016 In this study, exposure of zebrafish embryos to nano-ZnO triggered an excessive production of ROS, which was followed by several phenomena: the up-regulation of p53, a reduction in the bcl-2/bax ratio,a reduction in the mitochondrial membrane potential (psim), the release of cytochrome c into the cytosolic fraction, and the activation of caspases 9 and 3. Zinc Oxide 53-56 BCL2 apoptosis regulator a Danio rerio 185-190 27658222-12 2016 In this study, exposure of zebrafish embryos to nano-ZnO triggered an excessive production of ROS, which was followed by several phenomena: the up-regulation of p53, a reduction in the bcl-2/bax ratio,a reduction in the mitochondrial membrane potential (psim), the release of cytochrome c into the cytosolic fraction, and the activation of caspases 9 and 3. Zinc Oxide 53-56 BCL2 associated X, apoptosis regulator a Danio rerio 191-194 27658222-12 2016 In this study, exposure of zebrafish embryos to nano-ZnO triggered an excessive production of ROS, which was followed by several phenomena: the up-regulation of p53, a reduction in the bcl-2/bax ratio,a reduction in the mitochondrial membrane potential (psim), the release of cytochrome c into the cytosolic fraction, and the activation of caspases 9 and 3. Zinc Oxide 53-56 cytochrome c, somatic b Danio rerio 276-288 27658222-12 2016 In this study, exposure of zebrafish embryos to nano-ZnO triggered an excessive production of ROS, which was followed by several phenomena: the up-regulation of p53, a reduction in the bcl-2/bax ratio,a reduction in the mitochondrial membrane potential (psim), the release of cytochrome c into the cytosolic fraction, and the activation of caspases 9 and 3. Zinc Oxide 53-56 caspase 9, apoptosis-related cysteine peptidase Danio rerio 340-356 27658222-13 2016 Collectively, our data imply that nano-ZnO induce an excessive production of ROS which then activate the apoptosis pathway mediated by mitochondria and caspases. Zinc Oxide 39-42 caspase 9, apoptosis-related cysteine peptidase Danio rerio 152-160 27559998-6 2016 Compared with GO-COOH and the control group, ZnO/GO-COOH nanocomposites significantly enhanced ALP activity, osteocalcin production and extracellular matrix mineralization as well as up-regulated osteogenic-related genes (ALP, OCN, and Runx2) in MG63 osteoblast-like cells. Zinc Oxide 45-48 ATHS Homo sapiens 95-98 27559998-6 2016 Compared with GO-COOH and the control group, ZnO/GO-COOH nanocomposites significantly enhanced ALP activity, osteocalcin production and extracellular matrix mineralization as well as up-regulated osteogenic-related genes (ALP, OCN, and Runx2) in MG63 osteoblast-like cells. Zinc Oxide 45-48 bone gamma-carboxyglutamate protein Homo sapiens 109-120 27559998-6 2016 Compared with GO-COOH and the control group, ZnO/GO-COOH nanocomposites significantly enhanced ALP activity, osteocalcin production and extracellular matrix mineralization as well as up-regulated osteogenic-related genes (ALP, OCN, and Runx2) in MG63 osteoblast-like cells. Zinc Oxide 45-48 ATHS Homo sapiens 222-225 27559998-6 2016 Compared with GO-COOH and the control group, ZnO/GO-COOH nanocomposites significantly enhanced ALP activity, osteocalcin production and extracellular matrix mineralization as well as up-regulated osteogenic-related genes (ALP, OCN, and Runx2) in MG63 osteoblast-like cells. Zinc Oxide 45-48 RUNX family transcription factor 2 Homo sapiens 236-241 27404512-7 2016 Using an ELISArray approach for the simultaneous detection of several analytes (cytokines/chemokines), it was found that only ZnO and AgNP20 increased the production of different analytes including the potent pro-inflammatory CXCL8 (IL-8) chemokine. Zinc Oxide 126-129 C-X-C motif chemokine ligand 8 Homo sapiens 226-231 27404512-7 2016 Using an ELISArray approach for the simultaneous detection of several analytes (cytokines/chemokines), it was found that only ZnO and AgNP20 increased the production of different analytes including the potent pro-inflammatory CXCL8 (IL-8) chemokine. Zinc Oxide 126-129 C-X-C motif chemokine ligand 8 Homo sapiens 233-237 27622344-2 2016 The CS/Ag/ZnO nanocomposite exhibited antibacterial activity against Gram positive (B. licheniformis and B. cereus) bacteria at 8 mug mL-1 compared to Gram negative (V. parahaemolyticus. Zinc Oxide 10-13 L1 cell adhesion molecule Mus musculus 134-138 27622344-4 2016 CS/Ag/ZnO nanocomposite effectively inhibited the biofilm growth of Gram positive bacteria compared to Gram negative bacteria at 30 mug mL-1. Zinc Oxide 6-9 L1 cell adhesion molecule Mus musculus 136-140 27622344-5 2016 The hydrophobicity index and EPS (extracellular polysaccharide) production of both Gram positive and Gram negative bacteria was decreased after treatment with 30 mug mL-1 of CS/Ag/ZnO nanocomposite. Zinc Oxide 180-183 L1 cell adhesion molecule Mus musculus 166-170 27622344-6 2016 CS/Ag/ZnO nanocomposite showed effective control of fungal C. albicans biofilm (92%) at 50 mug mL-1. Zinc Oxide 6-9 L1 cell adhesion molecule Mus musculus 95-99 27678081-6 2016 Interestingly, the ROS-induced hypoxia-inducible factor-1alpha (HIF-1alpha) signaling pathway was significantly increased following ZnO NPs exposure. Zinc Oxide 132-135 hypoxia inducible factor 1 subunit alpha Homo sapiens 31-62 27872576-0 2016 The alteration of mRNA expression of SOD and GPX genes, and proteins in tomato (Lycopersicon esculentum Mill) under stress of NaCl and/or ZnO nanoparticles. Zinc Oxide 138-141 iron superoxide dismutase Solanum lycopersicum 37-40 27872576-0 2016 The alteration of mRNA expression of SOD and GPX genes, and proteins in tomato (Lycopersicon esculentum Mill) under stress of NaCl and/or ZnO nanoparticles. Zinc Oxide 138-141 glutathione peroxidase Solanum lycopersicum 45-48 27872576-2 2016 Treatments with NaCl at both 3 and 6 g L-1 suppressed the mRNA levels of superoxide dismutase (SOD) and glutathione peroxidase (GPX) genes in all cultivars while plants treated with ZnO-NPs in the presence of NaCl, showed increments in the mRNA expression levels. Zinc Oxide 182-185 iron superoxide dismutase Solanum lycopersicum 73-93 27872576-2 2016 Treatments with NaCl at both 3 and 6 g L-1 suppressed the mRNA levels of superoxide dismutase (SOD) and glutathione peroxidase (GPX) genes in all cultivars while plants treated with ZnO-NPs in the presence of NaCl, showed increments in the mRNA expression levels. Zinc Oxide 182-185 glutathione peroxidase Solanum lycopersicum 104-126 27872576-2 2016 Treatments with NaCl at both 3 and 6 g L-1 suppressed the mRNA levels of superoxide dismutase (SOD) and glutathione peroxidase (GPX) genes in all cultivars while plants treated with ZnO-NPs in the presence of NaCl, showed increments in the mRNA expression levels. Zinc Oxide 182-185 glutathione peroxidase Solanum lycopersicum 128-131 27678081-0 2016 The role of hypoxia-inducible factor-1alpha in zinc oxide nanoparticle-induced nephrotoxicity in vitro and in vivo. Zinc Oxide 47-57 hypoxia inducible factor 1 subunit alpha Homo sapiens 12-43 27544635-0 2016 Role of Cyt-C/caspases-9,3, Bax/Bcl-2 and the FAS death receptor pathway in apoptosis induced by zinc oxide nanoparticles in human aortic endothelial cells and the protective effect by alpha-lipoic acid. Zinc Oxide 97-107 BCL2 associated X, apoptosis regulator Homo sapiens 28-31 27544635-0 2016 Role of Cyt-C/caspases-9,3, Bax/Bcl-2 and the FAS death receptor pathway in apoptosis induced by zinc oxide nanoparticles in human aortic endothelial cells and the protective effect by alpha-lipoic acid. Zinc Oxide 97-107 BCL2 apoptosis regulator Homo sapiens 32-37 27544635-6 2016 Exposure to ZnO NPs was found to induce apoptosis at 12 h and necrosis after 24 h. Apoptosis was confirmed using reactive oxygen species that triggered a decrease in mitochondria membrane potential, increase in Cyt-C release, activation of caspases 3 and caspases9 and increase in the ratio of Bax/Bcl-2. Zinc Oxide 12-15 BCL2 associated X, apoptosis regulator Homo sapiens 294-297 27544635-6 2016 Exposure to ZnO NPs was found to induce apoptosis at 12 h and necrosis after 24 h. Apoptosis was confirmed using reactive oxygen species that triggered a decrease in mitochondria membrane potential, increase in Cyt-C release, activation of caspases 3 and caspases9 and increase in the ratio of Bax/Bcl-2. Zinc Oxide 12-15 BCL2 apoptosis regulator Homo sapiens 298-303 27452280-0 2016 Human eosinophils are direct targets to nanoparticles: Zinc oxide nanoparticles (ZnO) delay apoptosis and increase the production of the pro-inflammatory cytokines IL-1beta and IL-8. Zinc Oxide 55-65 interleukin 1 beta Homo sapiens 164-172 27452280-0 2016 Human eosinophils are direct targets to nanoparticles: Zinc oxide nanoparticles (ZnO) delay apoptosis and increase the production of the pro-inflammatory cytokines IL-1beta and IL-8. Zinc Oxide 55-65 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 27452280-0 2016 Human eosinophils are direct targets to nanoparticles: Zinc oxide nanoparticles (ZnO) delay apoptosis and increase the production of the pro-inflammatory cytokines IL-1beta and IL-8. Zinc Oxide 81-84 interleukin 1 beta Homo sapiens 164-172 27452280-0 2016 Human eosinophils are direct targets to nanoparticles: Zinc oxide nanoparticles (ZnO) delay apoptosis and increase the production of the pro-inflammatory cytokines IL-1beta and IL-8. Zinc Oxide 81-84 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 27452280-5 2016 We found that ZnO delay human eosinophil apoptosis, partially by inhibiting caspases and by preventing caspase-4 and Bcl-xL degradation. Zinc Oxide 14-17 caspase 1 Homo sapiens 76-84 27452280-5 2016 We found that ZnO delay human eosinophil apoptosis, partially by inhibiting caspases and by preventing caspase-4 and Bcl-xL degradation. Zinc Oxide 14-17 caspase 4 Homo sapiens 103-112 27452280-5 2016 We found that ZnO delay human eosinophil apoptosis, partially by inhibiting caspases and by preventing caspase-4 and Bcl-xL degradation. Zinc Oxide 14-17 BCL2 like 1 Homo sapiens 117-123 27452280-7 2016 In addition, ZnO were found to increase the production of the proinflammatory IL-1beta and IL-8 cytokines. Zinc Oxide 13-16 interleukin 1 beta Homo sapiens 78-86 27452280-7 2016 In addition, ZnO were found to increase the production of the proinflammatory IL-1beta and IL-8 cytokines. Zinc Oxide 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 27452280-8 2016 Using a pharmacological approach, we demonstrated that inhibition of caspase-1 reversed the ability of ZnO to induce IL-1beta and IL-8 production, whereas inhibition of caspase-4 only reversed that of IL-8. Zinc Oxide 103-106 caspase 1 Homo sapiens 69-78 27452280-8 2016 Using a pharmacological approach, we demonstrated that inhibition of caspase-1 reversed the ability of ZnO to induce IL-1beta and IL-8 production, whereas inhibition of caspase-4 only reversed that of IL-8. Zinc Oxide 103-106 interleukin 1 beta Homo sapiens 117-125 27452280-8 2016 Using a pharmacological approach, we demonstrated that inhibition of caspase-1 reversed the ability of ZnO to induce IL-1beta and IL-8 production, whereas inhibition of caspase-4 only reversed that of IL-8. Zinc Oxide 103-106 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 27678081-6 2016 Interestingly, the ROS-induced hypoxia-inducible factor-1alpha (HIF-1alpha) signaling pathway was significantly increased following ZnO NPs exposure. Zinc Oxide 132-135 hypoxia inducible factor 1 subunit alpha Homo sapiens 64-74 27678081-7 2016 Additionally, connective tissue growth factor (CTGF) and plasminogen activator inhibitor-1 (PAI-1), which are directly regulated by HIF-1 and are involved in the pathogenesis of kidney diseases, displayed significantly increased levels following ZnO NPs exposure in HEK-293 cells. Zinc Oxide 246-249 cellular communication network factor 2 Homo sapiens 14-45 27678081-7 2016 Additionally, connective tissue growth factor (CTGF) and plasminogen activator inhibitor-1 (PAI-1), which are directly regulated by HIF-1 and are involved in the pathogenesis of kidney diseases, displayed significantly increased levels following ZnO NPs exposure in HEK-293 cells. Zinc Oxide 246-249 cellular communication network factor 2 Homo sapiens 47-51 27678081-7 2016 Additionally, connective tissue growth factor (CTGF) and plasminogen activator inhibitor-1 (PAI-1), which are directly regulated by HIF-1 and are involved in the pathogenesis of kidney diseases, displayed significantly increased levels following ZnO NPs exposure in HEK-293 cells. Zinc Oxide 246-249 serpin family E member 1 Homo sapiens 57-90 27678081-7 2016 Additionally, connective tissue growth factor (CTGF) and plasminogen activator inhibitor-1 (PAI-1), which are directly regulated by HIF-1 and are involved in the pathogenesis of kidney diseases, displayed significantly increased levels following ZnO NPs exposure in HEK-293 cells. Zinc Oxide 246-249 serpin family E member 1 Homo sapiens 92-97 27678081-7 2016 Additionally, connective tissue growth factor (CTGF) and plasminogen activator inhibitor-1 (PAI-1), which are directly regulated by HIF-1 and are involved in the pathogenesis of kidney diseases, displayed significantly increased levels following ZnO NPs exposure in HEK-293 cells. Zinc Oxide 246-249 hypoxia inducible factor 1 subunit alpha Homo sapiens 132-137 27678081-9 2016 Therefore, our results suggest that HIF-1alpha may have a protective role in adaptation to the toxicity of ZnO NPs in kidney cells. Zinc Oxide 107-110 hypoxia inducible factor 1 subunit alpha Homo sapiens 36-46 27678081-12 2016 Moreover, ZnO NPs enhanced the HIF-1alpha signaling pathway, apoptosis and autophagy in mouse kidney tissues. Zinc Oxide 10-13 hypoxia inducible factor 1, alpha subunit Mus musculus 31-41 27247145-7 2016 In TM4 cells, the expressions of BTB proteins (ZO-1, occludin, claudin-5, and connexin-43) were lower in the ZnO NPs group. Zinc Oxide 109-112 tight junction protein 1 Mus musculus 33-51 27660443-7 2016 The investigation was designed to evaluate global DNA methylation, estimating the corresponding methyltransferase activity and expression of Dnmt gene using lung fibroblast (MRC5) cell line as lungs are the primary route of entry and target of occupational exposure to TiO2 and ZnO NPs. Zinc Oxide 278-281 DNA methyltransferase 1 Homo sapiens 141-145 27672670-8 2016 San Biagio, 2012) [2] "Effect of zinc oxide nanomaterials induced oxidative stress on the p53 pathway" (M.I. Zinc Oxide 33-43 tumor protein p53 Homo sapiens 90-93 27593282-8 2016 Compared with the exposure to PFOS alone, exposure to both PFOS (0.8mg/L) and nano-ZnO (50mg/L) significantly up-regulated the expression of corticotropin-releasing factor, sodium/iodidesymporter, iodothyronine deiodinases and thyroid receptors and significantly down-regulated the expression of thyroid-stimulating hormone, thyroglobulin (TG), transthyretin (TTR) and thyroid receptors. Zinc Oxide 83-86 transthyretin (prealbumin, amyloidosis type I) Danio rerio 345-358 27593282-8 2016 Compared with the exposure to PFOS alone, exposure to both PFOS (0.8mg/L) and nano-ZnO (50mg/L) significantly up-regulated the expression of corticotropin-releasing factor, sodium/iodidesymporter, iodothyronine deiodinases and thyroid receptors and significantly down-regulated the expression of thyroid-stimulating hormone, thyroglobulin (TG), transthyretin (TTR) and thyroid receptors. Zinc Oxide 83-86 transthyretin (prealbumin, amyloidosis type I) Danio rerio 360-363 27464704-3 2016 In the present study, we hypothesized that ZnO nanorods have promising potential for the enhancement of ASC proliferation. Zinc Oxide 43-46 PYD and CARD domain containing Homo sapiens 104-107 27464704-5 2016 The physicochemical properties of the nanorods such as their crystallinity, morphology, size, and solvent compatibility were evaluated, and then, the ability of the synthesized ZnO nanorods to enhance ASC proliferation was investigated. Zinc Oxide 177-180 PYD and CARD domain containing Homo sapiens 201-204 27464704-10 2016 These results collectively suggest that ZnO nanorods have promising potential for use as an agent for the enhancement of ASC proliferation. Zinc Oxide 40-43 PYD and CARD domain containing Homo sapiens 121-124 27463610-4 2016 Moreover, a targeting ligand, hyaluronic acid (HA), was conjugated to ZnO QDs for specifically binding to the overexpressed glycoprotein CD44 by cancer cells. Zinc Oxide 70-73 CD44 molecule (Indian blood group) Homo sapiens 137-141 27621621-7 2016 Although the expression of mRNA for CYP 2C11 and 3A2 enzymes was induced by ZnO nanoparticles, the activities of CYP 2C11 and 3A2 were suppressed. Zinc Oxide 76-79 cytochrome P450, subfamily 2, polypeptide 11 Rattus norvegicus 36-44 27247145-7 2016 In TM4 cells, the expressions of BTB proteins (ZO-1, occludin, claudin-5, and connexin-43) were lower in the ZnO NPs group. Zinc Oxide 109-112 occludin Mus musculus 53-61 27247145-7 2016 In TM4 cells, the expressions of BTB proteins (ZO-1, occludin, claudin-5, and connexin-43) were lower in the ZnO NPs group. Zinc Oxide 109-112 claudin 5 Mus musculus 63-72 27247145-7 2016 In TM4 cells, the expressions of BTB proteins (ZO-1, occludin, claudin-5, and connexin-43) were lower in the ZnO NPs group. Zinc Oxide 109-112 gap junction protein, alpha 1 Mus musculus 78-89 27247145-8 2016 The increased cell permeability and increased TNF-alpha secretion were also observed in ZnO NPs group. Zinc Oxide 88-91 tumor necrosis factor Mus musculus 46-55 27527337-0 2016 ZnO-Au-SnO2 Z-scheme photoanodes for remarkable photoelectrochemical water splitting. Zinc Oxide 0-3 strawberry notch homolog 2 Homo sapiens 7-10 27247145-9 2016 In GC2-spd cells, S phase arrest and DNA damage occurred in ZnO NPs group, which could be partially rescued by NAC. Zinc Oxide 60-63 NLR family, pyrin domain containing 1A Mus musculus 111-114 27363512-5 2016 Soluble NPs (Ag, CdS and ZnO) showed the highest acute and sublethal toxicity, with LC50 values as low as 0.529 mg Ag l(-1) for Ag NPs of 20 nm, and a significant increase in the malformation prevalence in embryos exposed to 0.1 mg Cd l(-1) of CdS NPs of ~4 nm. Zinc Oxide 25-28 extra spindle pole bodies like 1, separase Danio rerio 244-247 27504894-9 2016 Several genes that were differentially regulated following ZnO NP exposure shared similar biological pathways with those observed with ZnSO4 exposure, but six genes (aicda, cyb5d1, edar, intl2, ogfrl2 and tnfsf13b) associated with inflammation and the immune system responded specifically to ZnO NPs (either in the opposite direction or were unchanged in ZnSO4 exposure). Zinc Oxide 59-62 TNF superfamily member 13b Danio rerio 205-213 27570453-4 2016 The mRNA expression of the methyltransferase genes G9a and GLP was also increased upon treatment with ZnO NPs, and the acetyltransferase genes GCN5, P300, and CBP were downregulated. Zinc Oxide 102-105 lysine acetyltransferase 2A Homo sapiens 143-147 27570453-4 2016 The mRNA expression of the methyltransferase genes G9a and GLP was also increased upon treatment with ZnO NPs, and the acetyltransferase genes GCN5, P300, and CBP were downregulated. Zinc Oxide 102-105 E1A binding protein p300 Homo sapiens 149-153 27570453-4 2016 The mRNA expression of the methyltransferase genes G9a and GLP was also increased upon treatment with ZnO NPs, and the acetyltransferase genes GCN5, P300, and CBP were downregulated. Zinc Oxide 102-105 CREB binding protein Homo sapiens 159-162 27570453-8 2016 These findings suggest that the ZnO NPs induced cell cycle arrest at G2/M, which was associated with epigenetic changes and accompanied by p53-Bax mitochondrial pathway-mediated apoptosis. Zinc Oxide 32-35 tumor protein p53 Homo sapiens 139-142 27570453-8 2016 These findings suggest that the ZnO NPs induced cell cycle arrest at G2/M, which was associated with epigenetic changes and accompanied by p53-Bax mitochondrial pathway-mediated apoptosis. Zinc Oxide 32-35 BCL2 associated X, apoptosis regulator Homo sapiens 143-146 27490535-6 2016 In the intratracheal instillation study, both the 0.2 and the 1.0 mg ZnO groups had a transient increase in the total cell and neutrophil count in the BALF and in the expression of cytokine-induced neutrophil chemoattractant (CINC)-1, CINC-2, chemokine for neutrophil, and heme oxygenase-1 (HO-1), an oxidative stress marker, in the BALF. Zinc Oxide 69-72 C-X-C motif chemokine ligand 1 Rattus norvegicus 181-233 27490535-6 2016 In the intratracheal instillation study, both the 0.2 and the 1.0 mg ZnO groups had a transient increase in the total cell and neutrophil count in the BALF and in the expression of cytokine-induced neutrophil chemoattractant (CINC)-1, CINC-2, chemokine for neutrophil, and heme oxygenase-1 (HO-1), an oxidative stress marker, in the BALF. Zinc Oxide 69-72 C-X-C motif chemokine ligand 3 Rattus norvegicus 235-241 27490535-6 2016 In the intratracheal instillation study, both the 0.2 and the 1.0 mg ZnO groups had a transient increase in the total cell and neutrophil count in the BALF and in the expression of cytokine-induced neutrophil chemoattractant (CINC)-1, CINC-2, chemokine for neutrophil, and heme oxygenase-1 (HO-1), an oxidative stress marker, in the BALF. Zinc Oxide 69-72 heme oxygenase 1 Rattus norvegicus 273-289 26581431-9 2016 We also found that the protein corona formed on silica-coated ZnO NPs had higher amounts of plasma proteins, particularly albumin, transferrin, A1 inhibitor 3, alpha-2-hs-glycoprotein, apoprotein E and alpha-1 antitrypsin. Zinc Oxide 62-65 transferrin Rattus norvegicus 131-142 26581431-9 2016 We also found that the protein corona formed on silica-coated ZnO NPs had higher amounts of plasma proteins, particularly albumin, transferrin, A1 inhibitor 3, alpha-2-hs-glycoprotein, apoprotein E and alpha-1 antitrypsin. Zinc Oxide 62-65 alpha-2-HS-glycoprotein Rattus norvegicus 160-183 27443692-6 2016 As a result, the optimal solar-to-hydrogen efficiency of ZnO/Au/Al2O3 with 5 cycles was 6.7 times that of pristine ZnO, ascribed to the synergistic effect of SPR and surface passivation. Zinc Oxide 57-60 sepiapterin reductase Homo sapiens 158-161 27555781-9 2016 Using fluorescent dyes and flow cytometry analysis, HA/ZnO nanocomposite caused G2/M cell cycle arrest and stimulated apoptosis-related increase in caspase-3 and -7 activities of the HL-60 cells. Zinc Oxide 55-58 caspase 3 Homo sapiens 148-164 27443692-6 2016 As a result, the optimal solar-to-hydrogen efficiency of ZnO/Au/Al2O3 with 5 cycles was 6.7 times that of pristine ZnO, ascribed to the synergistic effect of SPR and surface passivation. Zinc Oxide 115-118 sepiapterin reductase Homo sapiens 158-161 27142998-0 2016 Enhanced field emission properties of ZnO-Ag2S core-shell heterojunction nanowires. Zinc Oxide 38-41 angiotensin II receptor type 1 Homo sapiens 42-46 27142998-2 2016 By a simple and facile successive ionic layer adsorption and reaction (SILAR) approach, Ag2S QDs were uniformly and densely packed on ZnO nanowires (NWs) to form ZnO-Ag2S core-shell heterojunction structures. Zinc Oxide 162-165 angiotensin II receptor type 1 Homo sapiens 166-170 27142998-3 2016 The FE properties of ZnO NWAs were effectively tuned by controlling the amount of Ag2S QDs. Zinc Oxide 21-24 angiotensin II receptor type 1 Homo sapiens 82-86 27401693-3 2016 Aqueous experiments (CO2 saturated KCl) using the optimized ZnO-functionalized device exhibited H(+) H2 (FY = 66%) and CO2 CO (FY = 6%). Zinc Oxide 60-63 complement C2 Homo sapiens 21-24 27401693-3 2016 Aqueous experiments (CO2 saturated KCl) using the optimized ZnO-functionalized device exhibited H(+) H2 (FY = 66%) and CO2 CO (FY = 6%). Zinc Oxide 60-63 complement C2 Homo sapiens 121-124 27278808-15 2016 CONCLUSIONS: Pulmonary exposure to ZnO-coated MWCNTs produces a systemic acute phase response that involves the release of Zn(+2), lung epithelial growth arrest, and increased IL-6. Zinc Oxide 35-38 interleukin 6 Homo sapiens 176-180 27142998-1 2016 A simple approach to Ag2S quantum dot (QD) modification was used to tune the field emission (FE) properties of ZnO nanowire arrays (NWAs). Zinc Oxide 111-114 angiotensin II receptor type 1 Homo sapiens 21-25 27142998-2 2016 By a simple and facile successive ionic layer adsorption and reaction (SILAR) approach, Ag2S QDs were uniformly and densely packed on ZnO nanowires (NWs) to form ZnO-Ag2S core-shell heterojunction structures. Zinc Oxide 134-137 angiotensin II receptor type 1 Homo sapiens 88-92 27142998-2 2016 By a simple and facile successive ionic layer adsorption and reaction (SILAR) approach, Ag2S QDs were uniformly and densely packed on ZnO nanowires (NWs) to form ZnO-Ag2S core-shell heterojunction structures. Zinc Oxide 162-165 angiotensin II receptor type 1 Homo sapiens 88-92 26774095-0 2016 Electrochemical sensing of nuclear matrix protein 22 in urine with molecularly imprinted poly(ethylene-co-vinyl alcohol) coated zinc oxide nanorod arrays for clinical studies of bladder cancer diagnosis. Zinc Oxide 128-138 nuclear mitotic apparatus protein 1 Homo sapiens 27-52 27094462-0 2016 Zinc oxide nanoparticles inhibit expression of manganese superoxide dismutase via amplification of oxidative stress, in murine photoreceptor cells. Zinc Oxide 0-10 superoxide dismutase 2, mitochondrial Mus musculus 47-77 27094462-2 2016 In the present study, we aimed to investigate inhibitory effects of zinc oxide (ZnO) nanoparticles on expression of manganese superoxide dismutase (MnSOD) in murine photoreceptor-derived cells. Zinc Oxide 68-78 superoxide dismutase 2, mitochondrial Mus musculus 116-146 27094462-2 2016 In the present study, we aimed to investigate inhibitory effects of zinc oxide (ZnO) nanoparticles on expression of manganese superoxide dismutase (MnSOD) in murine photoreceptor-derived cells. Zinc Oxide 68-78 superoxide dismutase 2, mitochondrial Mus musculus 148-153 27094462-2 2016 In the present study, we aimed to investigate inhibitory effects of zinc oxide (ZnO) nanoparticles on expression of manganese superoxide dismutase (MnSOD) in murine photoreceptor-derived cells. Zinc Oxide 80-83 superoxide dismutase 2, mitochondrial Mus musculus 116-146 27094462-2 2016 In the present study, we aimed to investigate inhibitory effects of zinc oxide (ZnO) nanoparticles on expression of manganese superoxide dismutase (MnSOD) in murine photoreceptor-derived cells. Zinc Oxide 80-83 superoxide dismutase 2, mitochondrial Mus musculus 148-153 27094462-5 2016 Moreover, ZnO nanoparticles also significantly reduced expression of MnSOD at both the mRNA and protein levels, reduced its activity, and further aggravated oxidative stress-mediated cell damage. Zinc Oxide 10-13 superoxide dismutase 2, mitochondrial Mus musculus 69-74 27094462-6 2016 CONCLUSION: Overall, ZnO nanoparticle-induced cytotoxicity was associated with elevated levels of oxidative stress due to overproduction of ROS and reduced expression and activity of MnSOD. Zinc Oxide 21-24 superoxide dismutase 2, mitochondrial Mus musculus 183-188 26100656-15 2016 Zinc oxide cement caused a significant up-regulation in IL-1alpha and TNF-alpha (P < 0.05). Zinc Oxide 0-10 interleukin 1 alpha Homo sapiens 56-65 26100656-15 2016 Zinc oxide cement caused a significant up-regulation in IL-1alpha and TNF-alpha (P < 0.05). Zinc Oxide 0-10 tumor necrosis factor Homo sapiens 70-79 26774095-6 2016 Finally, in phase 0 clinical trials, measurements were made of samples from a few patients with bladder cancer using the NMP22 MIP-coated ZnO nanorods electrodes that were integrated into a portable potentiostat, revealing NMP 22 concentrations in the range 128 +- 19 to 588 +- 53 ng/mL. Zinc Oxide 138-141 nuclear mitotic apparatus protein 1 Homo sapiens 121-126 27483897-0 2016 Effects of Precursor Concentration on Structural and Optical Properties of ZnO Thin Films Grown on Muscovite Mica Substrates by Sol-Gel Spin-Coating. Zinc Oxide 75-78 MHC class I polypeptide-related sequence A Homo sapiens 109-113 26812116-0 2016 Unfolding of insulin at the surface of ZnO quantum dots. Zinc Oxide 39-42 insulin Homo sapiens 13-20 26812116-3 2016 Interaction of ZnO QDs with insulin was investigated by fluorescence quenching, circular dichroism (CD), isothermal titration calorimetry (ITC) and thermal aggregation tests. Zinc Oxide 15-18 insulin Homo sapiens 28-35 26812116-5 2016 CD spectroscopy results also confirmed this unfolding and show a reduction in alpha helices content of insulin in contact with ZnO QDs and their conversion to random coils. Zinc Oxide 127-130 insulin Homo sapiens 103-110 26812116-7 2016 Thermal aggregation test showed fast aggregation of insulin in the presence of ZnO QDs. Zinc Oxide 79-82 insulin Homo sapiens 52-59 26812116-8 2016 Therefore in biological application of ZnO QDs such as bioimaging, presence of such QDs in vicinity of insulin could unfold this protein. Zinc Oxide 39-42 insulin Homo sapiens 103-110 27242821-9 2016 Furthermore, the activities of key antioxidant enzymes such as superoxide dismutase (SOD), catalase, ascorbate peroxidase and glutathione reductase were increased by combined treatment of BR and ZnO NPs compared with ZnO NPs only treatment. Zinc Oxide 195-198 catalase isozyme 1 Solanum lycopersicum 91-99 27242821-9 2016 Furthermore, the activities of key antioxidant enzymes such as superoxide dismutase (SOD), catalase, ascorbate peroxidase and glutathione reductase were increased by combined treatment of BR and ZnO NPs compared with ZnO NPs only treatment. Zinc Oxide 195-198 peroxidase Solanum lycopersicum 111-121 27483877-2 2016 ZnO films between transparent conductive oxide (TCO) and the CdS films can improve the performances of CIGS thin-film solar cells. Zinc Oxide 0-3 CDP-diacylglycerol synthase 1 Homo sapiens 61-64 27483897-1 2016 The structural and optical properties of the ZnO thin films grown on mica substrates for different precursor concentrations were investigated. Zinc Oxide 45-48 MHC class I polypeptide-related sequence A Homo sapiens 69-73 27030646-3 2016 The specific surface area of the resultant ZnO measured by BET was 1.3 m(2) g(-1). Zinc Oxide 43-46 delta/notch like EGF repeat containing Homo sapiens 59-62 26964013-0 2016 Gate-Tunable Spin Exchange Interactions and Inversion of Magnetoresistance in Single Ferromagnetic ZnO Nanowires. Zinc Oxide 99-102 spindlin 1 Homo sapiens 13-17 26985734-6 2016 The mRNA expression of apoptotic gene p53 and caspase 3 was up-regulated following ZnO nanoparticle exposure, which confirms the occurrence of apoptosis at the transcriptional level. Zinc Oxide 83-86 tumor protein p53 Homo sapiens 38-41 26985734-6 2016 The mRNA expression of apoptotic gene p53 and caspase 3 was up-regulated following ZnO nanoparticle exposure, which confirms the occurrence of apoptosis at the transcriptional level. Zinc Oxide 83-86 caspase 3 Homo sapiens 46-55 27451766-1 2016 CdS decorated ZnO nanorods have been grown by a combination of hydrothermal method and successive ion layer absorption and reaction (SILAR) method. Zinc Oxide 14-17 CDP-diacylglycerol synthase 1 Homo sapiens 0-3 26649489-1 2016 In this work, a nanohybrid of platinum nanoparticles-porous ZnO spheres-hemin (Pt-pZnO-hemin) was synthesized for construction of alkaline phosphatase-based immunosensor for detection of influenza. Zinc Oxide 60-63 alkaline phosphatase, placental Homo sapiens 130-150 27003470-3 2016 In this work, we report on a general methodology for improving the selectivity of SMOx nanowires sensors, based on the coverage of ZnO nanowires with a thin ZIF-8 molecular sieve membrane. Zinc Oxide 131-134 spermine oxidase Homo sapiens 82-86 27137000-2 2016 The threshold and driving electric fields of PDLC film doped with 2.44 wt% ZnO NPs were 0.13 and 0.31 V/mum, respectively, with a contrast ratio of 26. Zinc Oxide 75-78 latexin Homo sapiens 104-107 28031965-5 2016 ZnO and Al2O3 Nps activated the NFkappaB pathway and induced the release of inflammatory cytokines. Zinc Oxide 0-3 nuclear factor kappa B subunit 1 Homo sapiens 32-40 33465853-7 2016 In vivo application of ZnO chips to mouse calvarial bone induced bone resorption, presumably due to the activation of osteoclasts by zinc ion-induced TNF-alpha release. Zinc Oxide 23-26 tumor necrosis factor Mus musculus 150-159 26825457-0 2016 Aluminum-doped zinc oxide nanoparticles attenuate the TSLP levels via suppressing caspase-1 in activated mast cells. Zinc Oxide 15-25 thymic stromal lymphopoietin Homo sapiens 54-58 26825457-0 2016 Aluminum-doped zinc oxide nanoparticles attenuate the TSLP levels via suppressing caspase-1 in activated mast cells. Zinc Oxide 15-25 caspase 1 Homo sapiens 82-91 27451766-0 2016 Spectral Dependent Photoelectrochemical Behaviors of CdS Sensitized ZnO Nanorods. Zinc Oxide 68-71 CDP-diacylglycerol synthase 1 Homo sapiens 53-56 27451766-2 2016 Optical absorption and emission properties of ZnO nanorods have been studied after sensitization with CdS nanoparticles. Zinc Oxide 46-49 CDP-diacylglycerol synthase 1 Homo sapiens 102-105 27451766-3 2016 Current-voltage characteristics of ZnO nanorods and CdS sensitized ZnO nanorods have been studied in an electrochemical cell. Zinc Oxide 67-70 CDP-diacylglycerol synthase 1 Homo sapiens 52-55 27451766-4 2016 The spectral dependent photocurrent and photopotential behaviors of ZnO nanorods and CdS sensitized ZnO nanorods have been investigated using monochromatic light of wavelength 300-700 nm. Zinc Oxide 100-103 CDP-diacylglycerol synthase 1 Homo sapiens 85-88 28959565-5 2016 Molecular analysis of cells treated with ZnO chips revealed that zinc ions released from the chips increased cellular levels of reactive oxygen species, including hydrogen peroxide, which led to the down-regulation of anti-apoptotic molecules (such as HIF-1alpha, survivin, cIAP-2, claspin, p-53, and XIAP) and caspase-dependent apoptosis. Zinc Oxide 41-44 baculoviral IAP repeat containing 3 Homo sapiens 274-280 26841231-0 2016 Degradation of refractory pollutants under solar light irradiation by a robust and self-protected ZnO/CdS/TiO2 hybrid photocatalyst. Zinc Oxide 98-101 CDP-diacylglycerol synthase 1 Homo sapiens 102-105 26841231-3 2016 In this work, we developed a synergistic ZnO/CdS/TiO2 hybrid, which could act as a robust and self-protected photocatalyst for water purification without additional sacrificial reagents. Zinc Oxide 41-44 CDP-diacylglycerol synthase 1 Homo sapiens 45-48 26841231-5 2016 Photons were selectively adsorbed by ZnO and CdS, then, the electrons with a low reductive activity in ZnO recombined directly with the holes with a low oxidative activity in CdS, whereas the holes with a high oxidative activity in ZnO and the electrons with a high reductive activity in CdS were captured for catalytic reaction. Zinc Oxide 37-40 CDP-diacylglycerol synthase 1 Homo sapiens 175-178 26841231-5 2016 Photons were selectively adsorbed by ZnO and CdS, then, the electrons with a low reductive activity in ZnO recombined directly with the holes with a low oxidative activity in CdS, whereas the holes with a high oxidative activity in ZnO and the electrons with a high reductive activity in CdS were captured for catalytic reaction. Zinc Oxide 37-40 CDP-diacylglycerol synthase 1 Homo sapiens 175-178 26841231-5 2016 Photons were selectively adsorbed by ZnO and CdS, then, the electrons with a low reductive activity in ZnO recombined directly with the holes with a low oxidative activity in CdS, whereas the holes with a high oxidative activity in ZnO and the electrons with a high reductive activity in CdS were captured for catalytic reaction. Zinc Oxide 103-106 CDP-diacylglycerol synthase 1 Homo sapiens 45-48 26841231-5 2016 Photons were selectively adsorbed by ZnO and CdS, then, the electrons with a low reductive activity in ZnO recombined directly with the holes with a low oxidative activity in CdS, whereas the holes with a high oxidative activity in ZnO and the electrons with a high reductive activity in CdS were captured for catalytic reaction. Zinc Oxide 103-106 CDP-diacylglycerol synthase 1 Homo sapiens 175-178 26841231-5 2016 Photons were selectively adsorbed by ZnO and CdS, then, the electrons with a low reductive activity in ZnO recombined directly with the holes with a low oxidative activity in CdS, whereas the holes with a high oxidative activity in ZnO and the electrons with a high reductive activity in CdS were captured for catalytic reaction. Zinc Oxide 103-106 CDP-diacylglycerol synthase 1 Homo sapiens 175-178 26841231-5 2016 Photons were selectively adsorbed by ZnO and CdS, then, the electrons with a low reductive activity in ZnO recombined directly with the holes with a low oxidative activity in CdS, whereas the holes with a high oxidative activity in ZnO and the electrons with a high reductive activity in CdS were captured for catalytic reaction. Zinc Oxide 103-106 CDP-diacylglycerol synthase 1 Homo sapiens 45-48 26841231-5 2016 Photons were selectively adsorbed by ZnO and CdS, then, the electrons with a low reductive activity in ZnO recombined directly with the holes with a low oxidative activity in CdS, whereas the holes with a high oxidative activity in ZnO and the electrons with a high reductive activity in CdS were captured for catalytic reaction. Zinc Oxide 103-106 CDP-diacylglycerol synthase 1 Homo sapiens 175-178 26841231-5 2016 Photons were selectively adsorbed by ZnO and CdS, then, the electrons with a low reductive activity in ZnO recombined directly with the holes with a low oxidative activity in CdS, whereas the holes with a high oxidative activity in ZnO and the electrons with a high reductive activity in CdS were captured for catalytic reaction. Zinc Oxide 103-106 CDP-diacylglycerol synthase 1 Homo sapiens 175-178 26841231-6 2016 The superiority of the novel ZnO/CdS/TiO2 hybrid over the traditional CdS/TiO2 hybrid in both photocatalytic activity and anti-photocorrosion capacity was demonstrated in the degradation of Atrazine and Rhodamine B, two typical refractory organic pollutants, and the treatment of real textile wastewater under solar light irradiation. Zinc Oxide 29-32 CDP-diacylglycerol synthase 1 Homo sapiens 33-36 26841231-6 2016 The superiority of the novel ZnO/CdS/TiO2 hybrid over the traditional CdS/TiO2 hybrid in both photocatalytic activity and anti-photocorrosion capacity was demonstrated in the degradation of Atrazine and Rhodamine B, two typical refractory organic pollutants, and the treatment of real textile wastewater under solar light irradiation. Zinc Oxide 29-32 CDP-diacylglycerol synthase 1 Homo sapiens 70-73 26841231-7 2016 The developed ZnO/CdS/TiO2 hybrid exhibited an excellent potential for the degradation of refractory pollutants, and provided a new way to advance intrinsically solar-susceptible catalyst for photochemical wastewater treatment. Zinc Oxide 14-17 CDP-diacylglycerol synthase 1 Homo sapiens 18-21 28959565-5 2016 Molecular analysis of cells treated with ZnO chips revealed that zinc ions released from the chips increased cellular levels of reactive oxygen species, including hydrogen peroxide, which led to the down-regulation of anti-apoptotic molecules (such as HIF-1alpha, survivin, cIAP-2, claspin, p-53, and XIAP) and caspase-dependent apoptosis. Zinc Oxide 41-44 claspin Homo sapiens 282-289 28959565-5 2016 Molecular analysis of cells treated with ZnO chips revealed that zinc ions released from the chips increased cellular levels of reactive oxygen species, including hydrogen peroxide, which led to the down-regulation of anti-apoptotic molecules (such as HIF-1alpha, survivin, cIAP-2, claspin, p-53, and XIAP) and caspase-dependent apoptosis. Zinc Oxide 41-44 tumor protein p53 Homo sapiens 291-295 28959565-5 2016 Molecular analysis of cells treated with ZnO chips revealed that zinc ions released from the chips increased cellular levels of reactive oxygen species, including hydrogen peroxide, which led to the down-regulation of anti-apoptotic molecules (such as HIF-1alpha, survivin, cIAP-2, claspin, p-53, and XIAP) and caspase-dependent apoptosis. Zinc Oxide 41-44 X-linked inhibitor of apoptosis Homo sapiens 301-305 26815888-0 2016 Enhanced visible light photocatalytic performance of ZnO nanowires integrated with CdS and Ag2S. Zinc Oxide 53-56 CDP-diacylglycerol synthase 1 Homo sapiens 83-86 26436325-3 2016 Co(2+) doping has a beneficial effect in extending the band width of light absorption of ZnO into the visible region and to promote the separation of the photoinduced carriers due to the sp-d exchange interactions existing between the band electrons and the localized d electrons of Co(2+). Zinc Oxide 89-92 surfactant protein D Homo sapiens 187-191 26763156-6 2016 Furthermore, this sensory array can discriminate ppb-level TNT and ppt-level RDX from structurally similar and high-concentration interfering aromatic gases in less than 12 s. Through comparison with the previously reported chemiresistor or Schottky sensors for explosive detection, the present transition-metal-doping method resulting ZnO sensor stands out and undoubtedly challenges the best. Zinc Oxide 336-339 chromosome 16 open reading frame 82 Homo sapiens 59-62 26763156-6 2016 Furthermore, this sensory array can discriminate ppb-level TNT and ppt-level RDX from structurally similar and high-concentration interfering aromatic gases in less than 12 s. Through comparison with the previously reported chemiresistor or Schottky sensors for explosive detection, the present transition-metal-doping method resulting ZnO sensor stands out and undoubtedly challenges the best. Zinc Oxide 336-339 tachykinin precursor 1 Homo sapiens 67-70 26763156-6 2016 Furthermore, this sensory array can discriminate ppb-level TNT and ppt-level RDX from structurally similar and high-concentration interfering aromatic gases in less than 12 s. Through comparison with the previously reported chemiresistor or Schottky sensors for explosive detection, the present transition-metal-doping method resulting ZnO sensor stands out and undoubtedly challenges the best. Zinc Oxide 336-339 radixin Homo sapiens 77-80 26815888-0 2016 Enhanced visible light photocatalytic performance of ZnO nanowires integrated with CdS and Ag2S. Zinc Oxide 53-56 angiotensin II receptor type 1 Homo sapiens 91-95 26815888-2 2016 The ZnO nanowires, with a diameter of ~ 100 nm and a length of ~ 1 mum, were modified by coating CdS and Ag2S. Zinc Oxide 4-7 CDP-diacylglycerol synthase 1 Homo sapiens 97-100 26815888-2 2016 The ZnO nanowires, with a diameter of ~ 100 nm and a length of ~ 1 mum, were modified by coating CdS and Ag2S. Zinc Oxide 4-7 angiotensin II receptor type 1 Homo sapiens 105-109 26815888-3 2016 CdS has a high absorption coefficient and can efficiently match with the energy levels of ZnO, which can enhance the light absorption ability of the nanostructures. Zinc Oxide 90-93 CDP-diacylglycerol synthase 1 Homo sapiens 0-3 26815888-5 2016 The photocatalytic activity of the ZnO-CdS-Ag2S ternary nanostructures was investigated using the degradation of methyl orange (MO) in an aqueous solution under visible light. Zinc Oxide 35-38 CDP-diacylglycerol synthase 1 Homo sapiens 39-42 26815888-5 2016 The photocatalytic activity of the ZnO-CdS-Ag2S ternary nanostructures was investigated using the degradation of methyl orange (MO) in an aqueous solution under visible light. Zinc Oxide 35-38 angiotensin II receptor type 1 Homo sapiens 43-47 26815888-6 2016 The ZnO-CdS-Ag2S ternary nanostructures were found to be more efficient than ZnO nanowires, ZnO-CdS nanowires, and ZnO-Ag2S nanowires. Zinc Oxide 4-7 CDP-diacylglycerol synthase 1 Homo sapiens 8-11 26815888-6 2016 The ZnO-CdS-Ag2S ternary nanostructures were found to be more efficient than ZnO nanowires, ZnO-CdS nanowires, and ZnO-Ag2S nanowires. Zinc Oxide 4-7 angiotensin II receptor type 1 Homo sapiens 12-16 26815888-6 2016 The ZnO-CdS-Ag2S ternary nanostructures were found to be more efficient than ZnO nanowires, ZnO-CdS nanowires, and ZnO-Ag2S nanowires. Zinc Oxide 4-7 CDP-diacylglycerol synthase 1 Homo sapiens 96-99 26815888-6 2016 The ZnO-CdS-Ag2S ternary nanostructures were found to be more efficient than ZnO nanowires, ZnO-CdS nanowires, and ZnO-Ag2S nanowires. Zinc Oxide 4-7 angiotensin II receptor type 1 Homo sapiens 119-123 26815888-6 2016 The ZnO-CdS-Ag2S ternary nanostructures were found to be more efficient than ZnO nanowires, ZnO-CdS nanowires, and ZnO-Ag2S nanowires. Zinc Oxide 77-80 CDP-diacylglycerol synthase 1 Homo sapiens 8-11 26815888-6 2016 The ZnO-CdS-Ag2S ternary nanostructures were found to be more efficient than ZnO nanowires, ZnO-CdS nanowires, and ZnO-Ag2S nanowires. Zinc Oxide 77-80 angiotensin II receptor type 1 Homo sapiens 12-16 26815888-6 2016 The ZnO-CdS-Ag2S ternary nanostructures were found to be more efficient than ZnO nanowires, ZnO-CdS nanowires, and ZnO-Ag2S nanowires. Zinc Oxide 77-80 CDP-diacylglycerol synthase 1 Homo sapiens 8-11 26815888-6 2016 The ZnO-CdS-Ag2S ternary nanostructures were found to be more efficient than ZnO nanowires, ZnO-CdS nanowires, and ZnO-Ag2S nanowires. Zinc Oxide 77-80 angiotensin II receptor type 1 Homo sapiens 12-16 26815888-6 2016 The ZnO-CdS-Ag2S ternary nanostructures were found to be more efficient than ZnO nanowires, ZnO-CdS nanowires, and ZnO-Ag2S nanowires. Zinc Oxide 77-80 CDP-diacylglycerol synthase 1 Homo sapiens 8-11 26815888-6 2016 The ZnO-CdS-Ag2S ternary nanostructures were found to be more efficient than ZnO nanowires, ZnO-CdS nanowires, and ZnO-Ag2S nanowires. Zinc Oxide 77-80 angiotensin II receptor type 1 Homo sapiens 12-16 26815888-7 2016 There is 7.68 times more photocatalytic activity for MO degradation in terms of the rate constant for ZnO-CdS-Ag2S 15-cycle ternary nanostructure compared to the as-grown ZnO. Zinc Oxide 102-105 CDP-diacylglycerol synthase 1 Homo sapiens 106-109 26815888-7 2016 There is 7.68 times more photocatalytic activity for MO degradation in terms of the rate constant for ZnO-CdS-Ag2S 15-cycle ternary nanostructure compared to the as-grown ZnO. Zinc Oxide 102-105 angiotensin II receptor type 1 Homo sapiens 110-114 26815888-8 2016 Furthermore, the effect of the amount of Ag2S and CdS on the ZnO surface on the photocatalytic activity was analyzed. Zinc Oxide 61-64 angiotensin II receptor type 1 Homo sapiens 41-45 26815888-8 2016 Furthermore, the effect of the amount of Ag2S and CdS on the ZnO surface on the photocatalytic activity was analyzed. Zinc Oxide 61-64 CDP-diacylglycerol synthase 1 Homo sapiens 50-53 26815888-9 2016 The superior photo-absorption properties and photocatalytic performance of the ZnO-CdS-Ag2S ternary nanostructures can be ascribed to the heterostructure, which enhanced the separation of the photo-induced electron-hole pairs. Zinc Oxide 79-82 CDP-diacylglycerol synthase 1 Homo sapiens 83-86 26815888-9 2016 The superior photo-absorption properties and photocatalytic performance of the ZnO-CdS-Ag2S ternary nanostructures can be ascribed to the heterostructure, which enhanced the separation of the photo-induced electron-hole pairs. Zinc Oxide 79-82 angiotensin II receptor type 1 Homo sapiens 87-91 26815888-10 2016 In addition, visible light could be absorbed by ZnO-CdS-Ag2S ternary nanostructures rather than by ZnO. Zinc Oxide 48-51 CDP-diacylglycerol synthase 1 Homo sapiens 52-55 26815888-10 2016 In addition, visible light could be absorbed by ZnO-CdS-Ag2S ternary nanostructures rather than by ZnO. Zinc Oxide 48-51 angiotensin II receptor type 1 Homo sapiens 56-60 27455697-4 2016 X-ray diffraction data, TEM images confirm that the materials synthesized in optimal conditions are ZnO:Co single crystalline solid solution without any impurities related to Co. Zinc Oxide 100-103 MFT2 Homo sapiens 24-27 26271306-5 2016 The quantitative PCR (qPCR) analysis showed that the PPARgamma, FABP4, C/EBPalpha, and SREBP1 messenger RNA (mRNA) expression was significantly increased in the ZnO nanoparticle-treated 3T3-L1 adipocytes. Zinc Oxide 161-164 peroxisome proliferator activated receptor gamma Mus musculus 53-62 26271306-5 2016 The quantitative PCR (qPCR) analysis showed that the PPARgamma, FABP4, C/EBPalpha, and SREBP1 messenger RNA (mRNA) expression was significantly increased in the ZnO nanoparticle-treated 3T3-L1 adipocytes. Zinc Oxide 161-164 fatty acid binding protein 4, adipocyte Mus musculus 64-69 26271306-5 2016 The quantitative PCR (qPCR) analysis showed that the PPARgamma, FABP4, C/EBPalpha, and SREBP1 messenger RNA (mRNA) expression was significantly increased in the ZnO nanoparticle-treated 3T3-L1 adipocytes. Zinc Oxide 161-164 CCAAT/enhancer binding protein (C/EBP), alpha Mus musculus 71-81 26271306-5 2016 The quantitative PCR (qPCR) analysis showed that the PPARgamma, FABP4, C/EBPalpha, and SREBP1 messenger RNA (mRNA) expression was significantly increased in the ZnO nanoparticle-treated 3T3-L1 adipocytes. Zinc Oxide 161-164 sterol regulatory element binding transcription factor 1 Mus musculus 87-93 27455660-0 2016 Zinc Oxide Nanoparticles Demoted MDM2 Expression to Suppress TSLP-Induced Mast Cell Proliferation. Zinc Oxide 0-10 transformed mouse 3T3 cell double minute 2 Mus musculus 33-37 27455660-0 2016 Zinc Oxide Nanoparticles Demoted MDM2 Expression to Suppress TSLP-Induced Mast Cell Proliferation. Zinc Oxide 0-10 thymic stromal lymphopoietin Mus musculus 61-65 26977526-3 2016 This work demonstrates a rational and elegant design of TFT, composed of poly crystalline ZnO:H/ZnO bilayer structure without using other metal elements for doping. Zinc Oxide 90-93 T-box transcription factor T Homo sapiens 56-59 26977526-3 2016 This work demonstrates a rational and elegant design of TFT, composed of poly crystalline ZnO:H/ZnO bilayer structure without using other metal elements for doping. Zinc Oxide 96-99 T-box transcription factor T Homo sapiens 56-59 26846189-2 2016 Here, we successfully demonstrate the novel use of zinc oxide nanorods (ZnO NRs) in the ultrasensitive and quantitative detection of two acute kidney injury (AKI)-related protein biomarkers, tumor necrosis factor (TNF)-alpha and interleukin (IL)-8, directly from patient samples. Zinc Oxide 51-61 tumor necrosis factor Homo sapiens 191-224 26846189-2 2016 Here, we successfully demonstrate the novel use of zinc oxide nanorods (ZnO NRs) in the ultrasensitive and quantitative detection of two acute kidney injury (AKI)-related protein biomarkers, tumor necrosis factor (TNF)-alpha and interleukin (IL)-8, directly from patient samples. Zinc Oxide 51-61 C-X-C motif chemokine ligand 8 Homo sapiens 229-247 26846189-2 2016 Here, we successfully demonstrate the novel use of zinc oxide nanorods (ZnO NRs) in the ultrasensitive and quantitative detection of two acute kidney injury (AKI)-related protein biomarkers, tumor necrosis factor (TNF)-alpha and interleukin (IL)-8, directly from patient samples. Zinc Oxide 72-75 tumor necrosis factor Homo sapiens 191-224 26821250-0 2016 Controllable in situ photo-assisted chemical deposition of CdSe quantum dots on ZnO/CdS nanorod arrays and its photovoltaic application. Zinc Oxide 80-83 CDP-diacylglycerol synthase 1 Homo sapiens 59-62 26846189-2 2016 Here, we successfully demonstrate the novel use of zinc oxide nanorods (ZnO NRs) in the ultrasensitive and quantitative detection of two acute kidney injury (AKI)-related protein biomarkers, tumor necrosis factor (TNF)-alpha and interleukin (IL)-8, directly from patient samples. Zinc Oxide 72-75 C-X-C motif chemokine ligand 8 Homo sapiens 229-247 26821250-3 2016 In this work, we have grown a uniform CdSe layer on ZnO/CdS nanorod arrays by a novel in situ photo-assisted chemical deposition method. Zinc Oxide 52-55 CDP-diacylglycerol synthase 1 Homo sapiens 38-41 26846189-3 2016 We first validate the ZnO NRs-based IL-8 results via comparison with those obtained from using a conventional enzyme-linked immunosorbent method in samples from 38 individuals. Zinc Oxide 22-25 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 26846189-4 2016 We further assess the full detection capability of the ZnO NRs-based technique by quantifying TNF-alpha, whose levels in human urine are often below the detection limits of conventional methods. Zinc Oxide 55-58 tumor necrosis factor Homo sapiens 94-103 26846189-5 2016 Using the ZnO NR platforms, we determine the TNF-alpha concentrations of all 46 patient samples tested, down to the fg per mL level. Zinc Oxide 10-13 tumor necrosis factor Homo sapiens 45-54 26891290-5 2016 The release of the fourth generation cephalosporin Cfp in a biologically active form from the ZnO matrix could help preventing the bacterial adhesion and the subsequent colonization and biofilm development on various surfaces, and thus decreasing the risk of biofilm-related infections. Zinc Oxide 94-97 complement factor properdin Homo sapiens 51-54 26840501-1 2016 The effect of incorporation of rigid zinc oxide (ZnO) nanostructures on carbonization behavior of electrospun special acrylic fiber grade poly(acrylonitrile) (PAN-SAF) nanofibers was investigated. Zinc Oxide 49-52 FAS antisense RNA 1 Homo sapiens 163-166 26611369-1 2016 A novel bio-analytical method has been devised based on the change in catalytic activity of acetylcholinesterase (AChE) enzyme induced by captan, carbosulfan, 2,3,7,8-tetrachlorodibenzodioxin (TCDD) and pentachlorophenol (PCP) for the investigation of inhibition efficiency and sensitivity using Pt/ZnO/AChE/Chitosan bioelectrode. Zinc Oxide 299-302 acetylcholinesterase (Cartwright blood group) Homo sapiens 92-112 26815407-2 2016 In this work, we report the preparation of (GaN)1-x(ZnO)x solid-solution nanorods with a high ZnO solubility up to 95% via a two-step synthetic route, which starts from a sol-gel reaction and follows with a nitridation process. Zinc Oxide 52-55 gigaxonin Homo sapiens 44-47 26815407-4 2016 Correspondingly, the ZnO content in the GaN lattice can be achieved in the range of ~25%-95%. Zinc Oxide 21-24 gigaxonin Homo sapiens 40-43 26815407-5 2016 Room-temperature cathodoluminescence (CL) measurements on the three types of (GaN)1-x(ZnO)x solid-solution nanorods indicate that the minimum band-gap of 2.46 eV of the solid-solution nanorods is achieved under a ZnO solubility of 25%. Zinc Oxide 86-89 gigaxonin Homo sapiens 78-81 26796532-0 2016 Enhancement of Trap-Assisted Green Electroluminescence Efficiency in ZnO/SiO2/Si Nanowire Light-Emitting Diodes on Bendable Substrates by Piezophototronic Effect. Zinc Oxide 69-72 TRAP Homo sapiens 15-19 26796532-1 2016 The trap-assisted green electroluminescence (EL) efficiency of a light-emitting diode (LED) consisting of a ZnO nanowire (NW), a SiO2 layer, and a Si NW on a bendable substrate is enhanced by piezophototronic effect. Zinc Oxide 108-111 TRAP Homo sapiens 4-8 26523294-2 2016 Initially, the transferrin receptor antibody (TfR Ab) functionalized Fe3O4@ZnO nanocomposites, followed by loading with doxorubicin (Dox) and denoted as Fe3O4@ZnO/Dox/TfR Ab, were prepared as an all-in-one system allowing for a targeted drug delivery with simultaneous concurrent chemoradiotherapy and magnetic resonance imaging (MRI) monitoring. Zinc Oxide 75-78 transferrin receptor Homo sapiens 15-35 26523294-2 2016 Initially, the transferrin receptor antibody (TfR Ab) functionalized Fe3O4@ZnO nanocomposites, followed by loading with doxorubicin (Dox) and denoted as Fe3O4@ZnO/Dox/TfR Ab, were prepared as an all-in-one system allowing for a targeted drug delivery with simultaneous concurrent chemoradiotherapy and magnetic resonance imaging (MRI) monitoring. Zinc Oxide 159-162 transferrin receptor Homo sapiens 15-35 26611369-1 2016 A novel bio-analytical method has been devised based on the change in catalytic activity of acetylcholinesterase (AChE) enzyme induced by captan, carbosulfan, 2,3,7,8-tetrachlorodibenzodioxin (TCDD) and pentachlorophenol (PCP) for the investigation of inhibition efficiency and sensitivity using Pt/ZnO/AChE/Chitosan bioelectrode. Zinc Oxide 299-302 acetylcholinesterase (Cartwright blood group) Homo sapiens 114-118 26618499-1 2016 A CdS/reduced graphene oxide (RGO)/ZnO nanowire array (NWAs) heterostructure is designed, which exhibits enhanced photoelectrochemical (PEC) activity compared to pure ZnO, RGO/ZnO, and CdS/ZnO. Zinc Oxide 167-170 CDP-diacylglycerol synthase 1 Homo sapiens 2-5 26652440-2 2016 The ZnO nanoparticles and multi-walled carbon nanotubes modified CPE (ZnO-MWCNT/CPE) electrode was prepared by incorporation of the ZnO nanoparticles and multi-walled carbon nanotubes (MWCNT) in carbon paste electrode. Zinc Oxide 4-7 carboxypeptidase E Homo sapiens 65-68 26652440-2 2016 The ZnO nanoparticles and multi-walled carbon nanotubes modified CPE (ZnO-MWCNT/CPE) electrode was prepared by incorporation of the ZnO nanoparticles and multi-walled carbon nanotubes (MWCNT) in carbon paste electrode. Zinc Oxide 4-7 carboxypeptidase E Homo sapiens 70-83 26652440-2 2016 The ZnO nanoparticles and multi-walled carbon nanotubes modified CPE (ZnO-MWCNT/CPE) electrode was prepared by incorporation of the ZnO nanoparticles and multi-walled carbon nanotubes (MWCNT) in carbon paste electrode. Zinc Oxide 70-73 carboxypeptidase E Homo sapiens 65-68 26618499-1 2016 A CdS/reduced graphene oxide (RGO)/ZnO nanowire array (NWAs) heterostructure is designed, which exhibits enhanced photoelectrochemical (PEC) activity compared to pure ZnO, RGO/ZnO, and CdS/ZnO. Zinc Oxide 35-38 CDP-diacylglycerol synthase 1 Homo sapiens 185-188 26618499-1 2016 A CdS/reduced graphene oxide (RGO)/ZnO nanowire array (NWAs) heterostructure is designed, which exhibits enhanced photoelectrochemical (PEC) activity compared to pure ZnO, RGO/ZnO, and CdS/ZnO. Zinc Oxide 167-170 CDP-diacylglycerol synthase 1 Homo sapiens 2-5 26322591-7 2016 The surfaces of these ZnO NWs were modified with mouse immunoglobulin G (IgG), infused through the second microfluidic channels with dye-conjugated (Alexa 546) anti-mouse IgG in different concentrations. Zinc Oxide 22-25 immunoglobulin heavy variable V1-62 Mus musculus 55-71 26322591-7 2016 The surfaces of these ZnO NWs were modified with mouse immunoglobulin G (IgG), infused through the second microfluidic channels with dye-conjugated (Alexa 546) anti-mouse IgG in different concentrations. Zinc Oxide 22-25 immunoglobulin heavy variable V1-62 Mus musculus 73-76 26322591-7 2016 The surfaces of these ZnO NWs were modified with mouse immunoglobulin G (IgG), infused through the second microfluidic channels with dye-conjugated (Alexa 546) anti-mouse IgG in different concentrations. Zinc Oxide 22-25 immunoglobulin heavy variable V1-62 Mus musculus 171-174 26322591-10 2016 Fluorescence images present clear multiple detections at the crossover areas when using the sharp ZnO NWs for simultaneous dye-conjugated anti-mouse IgG and dye-conjugated anti-rabbit IgG (Alexa 647) detection. Zinc Oxide 98-101 immunoglobulin heavy variable V1-62 Mus musculus 149-152 26322591-10 2016 Fluorescence images present clear multiple detections at the crossover areas when using the sharp ZnO NWs for simultaneous dye-conjugated anti-mouse IgG and dye-conjugated anti-rabbit IgG (Alexa 647) detection. Zinc Oxide 98-101 immunoglobulin heavy variable V1-62 Mus musculus 184-187 26433085-2 2016 In this paper, two kinds of 3D flower-like ZnO architectures assembled with numerous nanosheets were successfully synthesized by a simple hydrothermal route assisted by sodium dodecyl sulfate (SDS), origining from the different alkali environment created by urea and hexamine (HMT). Zinc Oxide 43-46 histamine N-methyltransferase Homo sapiens 277-280 26618499-4 2016 Subsequently, the CdS/RGO/ZnO heterostructure is successfully utilized for the PEC bioanalysis of glutathione at 0 V (vs Ag/AgCl). Zinc Oxide 26-29 CDP-diacylglycerol synthase 1 Homo sapiens 18-21 26618499-6 2016 Therefore, the CdS/RGO/ZnO heterostructure has opened up a promising channel for the development of PEC biosensors. Zinc Oxide 23-26 CDP-diacylglycerol synthase 1 Homo sapiens 15-18 26618499-1 2016 A CdS/reduced graphene oxide (RGO)/ZnO nanowire array (NWAs) heterostructure is designed, which exhibits enhanced photoelectrochemical (PEC) activity compared to pure ZnO, RGO/ZnO, and CdS/ZnO. Zinc Oxide 167-170 CDP-diacylglycerol synthase 1 Homo sapiens 2-5 27398497-6 2016 ZnO doped with Eu3+ and Dy3+ ions exhibited a strong blue (483 nm) emission from the 4F9/2 --> 6H15/2 transition of Dy3+ ions, a yellowish-green (575 nm) emission from the 4F9/2 --> 6H13/2 transition of Dy3+ ions and a red (612 nm) emission from the 5D0 --> 7F2 transition of Eu3+ ions, without a defect background. Zinc Oxide 0-3 CD82 molecule Homo sapiens 85-90 26738698-4 2016 Transient photocurrent and photovoltage decay measurements (TCD/TVD) were applied to systematically study the charge transport and recombination kinetics in these devices, showing the electron life time (tauR) of B18 dye in ZnO and TiO2 based DSSCs is higher than CPTD-R and BTD-R based DSSCs, which is consistent with the photovoltaic performances. Zinc Oxide 224-227 NADH:ubiquinone oxidoreductase subunit B7 Homo sapiens 213-216 26747815-4 2016 Based on the interface models and GGA-1/2 calculations, we find that the valence band maximum and conduction band minimum of ZnO, respectively, lie 0.64 eV and 0.57 eV above those of anatase TiO2, while lie 0.84 eV and 1.09 eV below those of GaN, which agree well with the experimental data. Zinc Oxide 125-128 golgi associated, gamma adaptin ear containing, ARF binding protein 1 Homo sapiens 34-41 27398497-6 2016 ZnO doped with Eu3+ and Dy3+ ions exhibited a strong blue (483 nm) emission from the 4F9/2 --> 6H15/2 transition of Dy3+ ions, a yellowish-green (575 nm) emission from the 4F9/2 --> 6H13/2 transition of Dy3+ ions and a red (612 nm) emission from the 5D0 --> 7F2 transition of Eu3+ ions, without a defect background. Zinc Oxide 0-3 CD82 molecule Homo sapiens 175-180 27112401-5 2016 Lipase, glycerol kinase, and glycerol-3-phosphate oxidase are required for lipid analysis in a cascade reaction, and we describe the co-immobilization of these three enzymes on nanocomposites of zinc oxide nanoparticles (ZnONPs)-chitosan (CHIT) and gold nanoparticles-polypyrrole-polyindole carboxylic acid (AuPPy-Pin5COOH) which are electrodeposited on Pt and Au electrodes, respectively. Zinc Oxide 195-205 glycerol kinase Homo sapiens 8-23 26119758-0 2015 A visible light induced photoelectrochemical aptsensor constructed by aligned ZnO@CdTe core shell nanocable arrays/carboxylated g-C3N4 for the detection of Proprotein convertase subtilisin/kexin type 6 gene. Zinc Oxide 78-81 proprotein convertase subtilisin/kexin type 6 Homo sapiens 156-201 26600002-4 2015 low turn-on field of 2.62 V/mum with high FE current density of 4.57 mA/cm(2) (corresponding to a applied field of 6.43 V/mum) and prominently high lifetime stability lasting for 1092 min revealing their superiority on comparison with the other commonly used field emitters such as carbon nanotubes, graphene, and zinc oxide nanorods. Zinc Oxide 314-324 latexin Homo sapiens 28-31 26548406-1 2015 To remedy the problems caused by the introduction of an additional electron mediator and realize signal amplification, a new strategy has been presented to construct an electrochemical aptasensor for thrombin detection based on the cascade electrocatalysis of alkaline phosphatase (ALP) and Pt nanoparticle (PtNP)-functionalized ZnO nanoflowers. Zinc Oxide 329-332 coagulation factor II, thrombin Homo sapiens 200-208 26548406-1 2015 To remedy the problems caused by the introduction of an additional electron mediator and realize signal amplification, a new strategy has been presented to construct an electrochemical aptasensor for thrombin detection based on the cascade electrocatalysis of alkaline phosphatase (ALP) and Pt nanoparticle (PtNP)-functionalized ZnO nanoflowers. Zinc Oxide 329-332 alkaline phosphatase, placental Homo sapiens 260-280 26548406-1 2015 To remedy the problems caused by the introduction of an additional electron mediator and realize signal amplification, a new strategy has been presented to construct an electrochemical aptasensor for thrombin detection based on the cascade electrocatalysis of alkaline phosphatase (ALP) and Pt nanoparticle (PtNP)-functionalized ZnO nanoflowers. Zinc Oxide 329-332 alkaline phosphatase, placental Homo sapiens 282-285 26162328-2 2015 In this study, new approaches were applied to measure quantitatively the kinetics and affinities of fibrinogen and human serum albumin (HSA) for TiO2, CeO2, Al2O3 and ZnO NPs immobilized on a sensor chip. Zinc Oxide 167-170 fibrinogen beta chain Homo sapiens 100-110 26162328-2 2015 In this study, new approaches were applied to measure quantitatively the kinetics and affinities of fibrinogen and human serum albumin (HSA) for TiO2, CeO2, Al2O3 and ZnO NPs immobilized on a sensor chip. Zinc Oxide 167-170 albumin Homo sapiens 121-134 26588414-0 2015 Spin-Selective Electron Quantum Transport in Nonmagnetic MgZnO/ZnO Heterostructures. Zinc Oxide 59-62 spindlin 1 Homo sapiens 0-4 26164013-0 2015 A sensitive photoelectrochemical biosensor for AFP detection based on ZnO inverse opal electrodes with signal amplification of CdS-QDs. Zinc Oxide 70-73 alpha fetoprotein Homo sapiens 47-50 26164013-1 2015 In this work, ZnO inverse opals structure (IOs) based photoelectrochemical (PEC) electrode was fabricated for alpha-fetoprotein (AFP) detection. Zinc Oxide 14-17 alpha fetoprotein Homo sapiens 110-127 26164013-1 2015 In this work, ZnO inverse opals structure (IOs) based photoelectrochemical (PEC) electrode was fabricated for alpha-fetoprotein (AFP) detection. Zinc Oxide 14-17 alpha fetoprotein Homo sapiens 129-132 26439450-4 2015 Reactions of Cu(NO3 )2 2.5 H2 O, CuO, and ZnO with the neat 2:1 1-mim/4,5-DCNIm melt resulted in the isolation of entirely N-donor ligated complexes of the formula M(4,5-DCNIm)2 (1-mim)4 (M=Cu, Zn). Zinc Oxide 43-46 NBL1, DAN family BMP antagonist Homo sapiens 13-19 26744884-5 2015 The mRNA transcript levels of inflammatory-related genes (TNF-alpha and IL1-beta) were elevated in the spleen cells of mice treated with ZnO NPs at 12h. Zinc Oxide 137-140 tumor necrosis factor Mus musculus 58-67 26744884-5 2015 The mRNA transcript levels of inflammatory-related genes (TNF-alpha and IL1-beta) were elevated in the spleen cells of mice treated with ZnO NPs at 12h. Zinc Oxide 137-140 interleukin 1 beta Mus musculus 72-80 26744884-6 2015 RESULTS: The elevated levels of TNF-alpha and IL1-beta in supernatants of spleen cell cultures of mice treated with ZnO NPs were also observed at 24h. Zinc Oxide 116-119 tumor necrosis factor Mus musculus 32-41 26744884-6 2015 RESULTS: The elevated levels of TNF-alpha and IL1-beta in supernatants of spleen cell cultures of mice treated with ZnO NPs were also observed at 24h. Zinc Oxide 116-119 interleukin 1 beta Mus musculus 46-54 26527454-4 2015 A synergistic reaction between aging and ZnO NP exposure occurred regarding serum interleukin 1 (IL-1) and interleukin 6 (IL-6). Zinc Oxide 41-44 interleukin 1 complex Mus musculus 82-102 26527454-4 2015 A synergistic reaction between aging and ZnO NP exposure occurred regarding serum interleukin 1 (IL-1) and interleukin 6 (IL-6). Zinc Oxide 41-44 interleukin 6 Mus musculus 107-120 26527454-4 2015 A synergistic reaction between aging and ZnO NP exposure occurred regarding serum interleukin 1 (IL-1) and interleukin 6 (IL-6). Zinc Oxide 41-44 interleukin 6 Mus musculus 122-126 26527454-7 2015 The contents of hippocampal cAMP response element binding protein (CREB), phosphorylated CREB, synapsin I, and cAMP were decreased in an age-dependent manner, and the most substantial decrease occurred in old mice treated with ZnO NPs. Zinc Oxide 227-230 cAMP responsive element binding protein 1 Mus musculus 28-65 26527454-7 2015 The contents of hippocampal cAMP response element binding protein (CREB), phosphorylated CREB, synapsin I, and cAMP were decreased in an age-dependent manner, and the most substantial decrease occurred in old mice treated with ZnO NPs. Zinc Oxide 227-230 synapsin I Mus musculus 95-105 26726535-0 2015 Effect of Oxidation Temperature on Characteristics of Thermally Oxidized ZnO Thin Films on Mica Substrates. Zinc Oxide 73-76 MHC class I polypeptide-related sequence A Homo sapiens 91-95 26189883-8 2015 In mZnO-800 group, interferon-gamma mRNA was the lowest (P=0.02), and both pharmacological ZnO and mZnO reduced tumor necrosis factor-alpha protein level (P<0.0001). Zinc Oxide 4-7 interferon gamma Sus scrofa 19-35 26189883-10 2015 At day 42, both groups receiving microencapsulated ZnO had 1.7 kg greater BW than control and did not differ from pZnO group (P=0.01); ileum villi height and V:C ratio were the greatest for pZnO compared with the other groups, whereas PCNA-positive cells were the most numerous in mZnO-800 group (P<0.001). Zinc Oxide 51-54 proliferating cell nuclear antigen Sus scrofa 235-239 26997697-0 2015 Comparison of Calcium Phosphate and Zinc Oxide Nanoparticles as Dermal Penetration Enhancers for Albumin. Zinc Oxide 36-46 albumin Mus musculus 97-104 26997697-3 2015 Since dermal delivery of proteins encounter problems, in this investigation, zinc oxide nanoparticles and calcium phosphate nanoparticles were compared as enhancers for dermal permeation of albumin. Zinc Oxide 77-87 albumin Mus musculus 190-197 26997697-7 2015 Zinc oxide nanoparticles and calcium phosphate nanoparticles acted as enhancers for skin permeation of albumin. Zinc Oxide 0-10 albumin Mus musculus 103-110 26997697-10 2015 After 0.5 or 1 h, the permeated albumin in presence of calcium phosphate nanoparticles was more than that in presence of zinc oxide nanoparticles and after 1.5 h the permeated albumin in presence of zinc oxide nanoparticles was more than that in presence of calcium phosphate nanoparticles. Zinc Oxide 121-131 albumin Mus musculus 176-183 26997697-10 2015 After 0.5 or 1 h, the permeated albumin in presence of calcium phosphate nanoparticles was more than that in presence of zinc oxide nanoparticles and after 1.5 h the permeated albumin in presence of zinc oxide nanoparticles was more than that in presence of calcium phosphate nanoparticles. Zinc Oxide 199-209 albumin Mus musculus 32-39 26997697-10 2015 After 0.5 or 1 h, the permeated albumin in presence of calcium phosphate nanoparticles was more than that in presence of zinc oxide nanoparticles and after 1.5 h the permeated albumin in presence of zinc oxide nanoparticles was more than that in presence of calcium phosphate nanoparticles. Zinc Oxide 199-209 albumin Mus musculus 176-183 26997697-12 2015 The profiles of albumin permeation (in presence of each of the nanoparticles) versus time was delayed and linear for both nanoparticles while the slope for calcium phosphate nanoparticles was higher than zinc oxide nanoparticles. Zinc Oxide 204-214 albumin Mus musculus 16-23 26997697-14 2015 Maximum cumulative (total) permeated albumin in presence of zinc oxide nanoparticles was obtained at time of 1.5 h, which was 40.2+-3.6 mg, while in presence of calcium phosphate nanoparticles, it was obtained at 1 h, which was 33.8+-5.5 mg. Zinc Oxide 60-70 albumin Mus musculus 37-44 33210899-0 2015 Comparison of Calcium Phosphate and Zinc Oxide Nanoparticles as Dermal Penetration Enhancers for Albumin. Zinc Oxide 36-46 albumin Homo sapiens 97-104 26364578-13 2015 These results suggest that ZnO NPs induce apoptosis via the PI3K/Akt/caspase-3/7 pathway and necrosis by LOX-mediated ROS production elevation. Zinc Oxide 27-30 AKT serine/threonine kinase 1 Homo sapiens 65-68 26364578-13 2015 These results suggest that ZnO NPs induce apoptosis via the PI3K/Akt/caspase-3/7 pathway and necrosis by LOX-mediated ROS production elevation. Zinc Oxide 27-30 caspase 3 Homo sapiens 69-78 26010476-8 2015 However, the expression levels of the T helper 2 (Th2) cytokines IL-4, IL-5, and IL-13 increased significantly after 24h of exposure to only ZnO NPs and then decreased gradually. Zinc Oxide 141-144 interleukin 4 Mus musculus 65-69 26586993-0 2015 ZnO nanoparticles augment ALT, AST, ALP and LDH expressions in C2C12 cells. Zinc Oxide 0-3 glutamic pyruvic transaminase, soluble Mus musculus 26-29 26586993-0 2015 ZnO nanoparticles augment ALT, AST, ALP and LDH expressions in C2C12 cells. Zinc Oxide 0-3 solute carrier family 17 (anion/sugar transporter), member 5 Mus musculus 31-34 26586993-1 2015 The present study aimed to investigate the effect of ZnO nanoparticles on alanine transaminase (ALT), aspartate transaminase (AST), alkaline phosphatase (ALP) and lactate dehydrogenase (LDH) enzyme expressions in C2C12 cells. Zinc Oxide 53-56 glutamic pyruvic transaminase, soluble Mus musculus 74-94 26586993-5 2015 A cytotoxicity assay was carried out to determine the effect of ZnO nanoparticles (1-5 mg/ml) on C2C12 cell viability at 48 and 72 h. ZnO nanoparticles increased ALT, AST, ALP and LDH enzyme mRNA expression and their activities in C2C12 cells. Zinc Oxide 134-137 glutamic pyruvic transaminase, soluble Mus musculus 162-165 26586993-5 2015 A cytotoxicity assay was carried out to determine the effect of ZnO nanoparticles (1-5 mg/ml) on C2C12 cell viability at 48 and 72 h. ZnO nanoparticles increased ALT, AST, ALP and LDH enzyme mRNA expression and their activities in C2C12 cells. Zinc Oxide 134-137 solute carrier family 17 (anion/sugar transporter), member 5 Mus musculus 167-170 26010476-8 2015 However, the expression levels of the T helper 2 (Th2) cytokines IL-4, IL-5, and IL-13 increased significantly after 24h of exposure to only ZnO NPs and then decreased gradually. Zinc Oxide 141-144 interleukin 5 Mus musculus 71-75 26010476-8 2015 However, the expression levels of the T helper 2 (Th2) cytokines IL-4, IL-5, and IL-13 increased significantly after 24h of exposure to only ZnO NPs and then decreased gradually. Zinc Oxide 141-144 interleukin 13 Mus musculus 81-86 26226935-0 2015 Bovine serum albumin surface imprinted polymer fabricated by surface grafting copolymerization on zinc oxide rods and its application for protein recognition. Zinc Oxide 98-108 albumin Homo sapiens 7-20 26327311-3 2015 The CZTS/CdS/ZnO hetero-NRs have cascade band gaps decreasing from 3.15 to 1.82 eV, which gives them efficient charge transfer and broad photoresponse in the UV to near-IR region, resulting in 47% IPCE in a wide light region from 400 to 500 nm; and the stainless steel mesh serves not only as a conductor for charge transport, but also as a skeleton of the grid structure for absorbing more light. Zinc Oxide 13-16 CDP-diacylglycerol synthase 1 Homo sapiens 9-12 26327311-4 2015 The related mechanism has been investigated, which demonstrates that the two-storey CZTS/CdS/ZnO@steel composite nanostructure would have great potential as a promising photoelectrode with high efficiency and low cost for PEC hydrogen generation. Zinc Oxide 93-96 CDP-diacylglycerol synthase 1 Homo sapiens 89-92 26226935-1 2015 A novel bovine serum albumin (BSA) surface imprinted polymer based on ZnO rods was synthesized by surface grafting copolymerization. Zinc Oxide 70-73 albumin Homo sapiens 15-28 25935283-0 2015 ZnO/Ag/CdO nanocomposite for visible light-induced photocatalytic degradation of industrial textile effluents. Zinc Oxide 0-3 cell adhesion associated, oncogene regulated Homo sapiens 7-10 26716206-0 2015 Zinc Oxide Nanoparticles Suppress LPS-Induced NF-kappaB Activation by Inducing A20, a Negative Regulator of NF-kappaB, in RAW 264.7 Macrophages. Zinc Oxide 0-10 nuclear factor kappa B subunit 1 Homo sapiens 46-55 26716206-0 2015 Zinc Oxide Nanoparticles Suppress LPS-Induced NF-kappaB Activation by Inducing A20, a Negative Regulator of NF-kappaB, in RAW 264.7 Macrophages. Zinc Oxide 0-10 TNF alpha induced protein 3 Homo sapiens 79-82 26716206-0 2015 Zinc Oxide Nanoparticles Suppress LPS-Induced NF-kappaB Activation by Inducing A20, a Negative Regulator of NF-kappaB, in RAW 264.7 Macrophages. Zinc Oxide 0-10 nuclear factor kappa B subunit 1 Homo sapiens 108-117 26196359-1 2015 ZnO/CdS heterostructured nanocomposites were fabricated with enhanced light harvesting capability and photostability using sequential sonochemical and hydrothermal methods from ZnO rods and particles. Zinc Oxide 177-180 CDP-diacylglycerol synthase 1 Homo sapiens 4-7 26196359-2 2015 Interestingly, in the composite made up of CdS sensitized ZnO rods, both ZnO and CdS exist in the hexagonal wurtzite form with different morphologies. Zinc Oxide 58-61 CDP-diacylglycerol synthase 1 Homo sapiens 43-46 26196359-2 2015 Interestingly, in the composite made up of CdS sensitized ZnO rods, both ZnO and CdS exist in the hexagonal wurtzite form with different morphologies. Zinc Oxide 58-61 CDP-diacylglycerol synthase 1 Homo sapiens 81-84 26196359-2 2015 Interestingly, in the composite made up of CdS sensitized ZnO rods, both ZnO and CdS exist in the hexagonal wurtzite form with different morphologies. Zinc Oxide 73-76 CDP-diacylglycerol synthase 1 Homo sapiens 43-46 26196359-3 2015 On the other hand, in the composite made up of CdS sensitized ZnO particles, ZnO exists in the hexagonal wurtzite form, whereas CdS in the cubic form but with a similar morphology. Zinc Oxide 62-65 CDP-diacylglycerol synthase 1 Homo sapiens 47-50 26196359-3 2015 On the other hand, in the composite made up of CdS sensitized ZnO particles, ZnO exists in the hexagonal wurtzite form, whereas CdS in the cubic form but with a similar morphology. Zinc Oxide 62-65 CDP-diacylglycerol synthase 1 Homo sapiens 128-131 26196359-3 2015 On the other hand, in the composite made up of CdS sensitized ZnO particles, ZnO exists in the hexagonal wurtzite form, whereas CdS in the cubic form but with a similar morphology. Zinc Oxide 77-80 CDP-diacylglycerol synthase 1 Homo sapiens 47-50 26196359-4 2015 The synthesized photocatalysts under simulated solar irradiation exhibited hydrogen evolution rates of 870 and 1007 mumol h(-1) g(-1) for the ZnO rod/CdS and ZnO nanoparticle/CdS composites, respectively, compared to the native ZnO (40 mumol h(-1) g(-1) for rods and 154 mumol h(-1) g(-1) for particles) and CdS (208 mumol h(-1) g(-1)) structures. Zinc Oxide 158-161 CDP-diacylglycerol synthase 1 Homo sapiens 175-178 26196359-4 2015 The synthesized photocatalysts under simulated solar irradiation exhibited hydrogen evolution rates of 870 and 1007 mumol h(-1) g(-1) for the ZnO rod/CdS and ZnO nanoparticle/CdS composites, respectively, compared to the native ZnO (40 mumol h(-1) g(-1) for rods and 154 mumol h(-1) g(-1) for particles) and CdS (208 mumol h(-1) g(-1)) structures. Zinc Oxide 158-161 CDP-diacylglycerol synthase 1 Homo sapiens 175-178 26196359-4 2015 The synthesized photocatalysts under simulated solar irradiation exhibited hydrogen evolution rates of 870 and 1007 mumol h(-1) g(-1) for the ZnO rod/CdS and ZnO nanoparticle/CdS composites, respectively, compared to the native ZnO (40 mumol h(-1) g(-1) for rods and 154 mumol h(-1) g(-1) for particles) and CdS (208 mumol h(-1) g(-1)) structures. Zinc Oxide 158-161 CDP-diacylglycerol synthase 1 Homo sapiens 175-178 26196359-4 2015 The synthesized photocatalysts under simulated solar irradiation exhibited hydrogen evolution rates of 870 and 1007 mumol h(-1) g(-1) for the ZnO rod/CdS and ZnO nanoparticle/CdS composites, respectively, compared to the native ZnO (40 mumol h(-1) g(-1) for rods and 154 mumol h(-1) g(-1) for particles) and CdS (208 mumol h(-1) g(-1)) structures. Zinc Oxide 158-161 CDP-diacylglycerol synthase 1 Homo sapiens 175-178 26196359-6 2015 Our results confirmed that the morphology of the host matrix ZnO played a crucial role in forming ZnO/CdS heterostructures with improved interface for the direct Z-scheme mechanism with enhanced hydrogen evolution efficiency. Zinc Oxide 61-64 CDP-diacylglycerol synthase 1 Homo sapiens 102-105 26196359-6 2015 Our results confirmed that the morphology of the host matrix ZnO played a crucial role in forming ZnO/CdS heterostructures with improved interface for the direct Z-scheme mechanism with enhanced hydrogen evolution efficiency. Zinc Oxide 98-101 CDP-diacylglycerol synthase 1 Homo sapiens 102-105 26335275-7 2015 The increased accumulations of dimethoate and Zn in the liver reduced its cholinesterase activity from 5.64 +- 0.45 U/mg protein to 4.67 +- 0.42 U/mg protein or 4.76 +- 0.45 U/mg protein for nano or bulk ZnO, respectively. Zinc Oxide 204-207 butyrylcholinesterase Mus musculus 74-88 26347142-7 2015 Up-regulation of apoptotic genes (e.g. p53, bax/bcl2 ratio, caspase-3 &caspase-9) along with loss of mitochondrial membrane potential suggested that Al-doped ZnO nanoparticles induced apoptosis in MCF-7 cells through mitochondrial pathway. Zinc Oxide 162-165 caspase 3 Homo sapiens 60-69 26347142-7 2015 Up-regulation of apoptotic genes (e.g. p53, bax/bcl2 ratio, caspase-3 &caspase-9) along with loss of mitochondrial membrane potential suggested that Al-doped ZnO nanoparticles induced apoptosis in MCF-7 cells through mitochondrial pathway. Zinc Oxide 162-165 caspase 9 Homo sapiens 75-84 26203893-7 2015 Furthermore, by thermal treatment in air, ZIF-8 nanocrystals can be transformed into ZnO coating on SOS silica microspheres. Zinc Oxide 85-88 xylosyltransferase 2 Homo sapiens 100-103 26203893-8 2015 The SOS@ZnO microspheres show excellent photocatalytic activity, as measured by degradation of methyl orange in water, when compared to ZnO nanoparticles. Zinc Oxide 8-11 xylosyltransferase 2 Homo sapiens 4-7 25935283-3 2015 The ZnO/Ag/CdO nanocomposite exhibited enhanced photocatalytic activity under visible light irradiation for the degradation of methyl orange and methylene blue compared with binary ZnO/Ag and ZnO/CdO nanocomposites. Zinc Oxide 4-7 cell adhesion associated, oncogene regulated Homo sapiens 11-14 25935283-3 2015 The ZnO/Ag/CdO nanocomposite exhibited enhanced photocatalytic activity under visible light irradiation for the degradation of methyl orange and methylene blue compared with binary ZnO/Ag and ZnO/CdO nanocomposites. Zinc Oxide 4-7 cell adhesion associated, oncogene regulated Homo sapiens 196-199 25935283-3 2015 The ZnO/Ag/CdO nanocomposite exhibited enhanced photocatalytic activity under visible light irradiation for the degradation of methyl orange and methylene blue compared with binary ZnO/Ag and ZnO/CdO nanocomposites. Zinc Oxide 181-184 cell adhesion associated, oncogene regulated Homo sapiens 11-14 25935283-3 2015 The ZnO/Ag/CdO nanocomposite exhibited enhanced photocatalytic activity under visible light irradiation for the degradation of methyl orange and methylene blue compared with binary ZnO/Ag and ZnO/CdO nanocomposites. Zinc Oxide 181-184 cell adhesion associated, oncogene regulated Homo sapiens 11-14 25935283-4 2015 The ZnO/Ag/CdO nanocomposite was also used for the degradation of the industrial textile effluent (real sample analysis) and degraded more than 90% in 210 min under visible light irradiation. Zinc Oxide 4-7 cell adhesion associated, oncogene regulated Homo sapiens 11-14 25935283-5 2015 The small size, high surface area and synergistic effect in the ZnO/Ag/CdO nanocomposite is responsible for high photocatalytic activity. Zinc Oxide 64-67 cell adhesion associated, oncogene regulated Homo sapiens 71-74 25935283-6 2015 These results also showed that the Ag nanoparticles induced visible light activity and facilitated efficient charge separation in the ZnO/Ag/CdO nanocomposite, thereby improving the photocatalytic performance. Zinc Oxide 134-137 cell adhesion associated, oncogene regulated Homo sapiens 141-144 26171978-0 2015 Double-Shelled CdS- and CdSe-Cosensitized ZnO Porous Nanotube Arrays for Superior Photoelectrocatalytic Applications. Zinc Oxide 42-45 CDP-diacylglycerol synthase 1 Homo sapiens 15-18 28347066-8 2015 At 100 mg/mL concentration, the synthesized ZnO NPs exhibited significant cytotoxic effects and the apoptotic features were confirmed through caspase-3 activation and DNA fragmentation assays. Zinc Oxide 44-47 caspase 3 Homo sapiens 142-151 26171978-2 2015 Here, a facile and effective two-step strategy is developed to fabricate double-shelled ZnO/CdS/CdSe porous nanotube photoanodes from ZnO nanorod arrays (NRAs). Zinc Oxide 88-91 CDP-diacylglycerol synthase 1 Homo sapiens 92-95 26171978-2 2015 Here, a facile and effective two-step strategy is developed to fabricate double-shelled ZnO/CdS/CdSe porous nanotube photoanodes from ZnO nanorod arrays (NRAs). Zinc Oxide 134-137 CDP-diacylglycerol synthase 1 Homo sapiens 92-95 26171978-3 2015 Surprisingly, after the process of the deposition of CdS and CdSe, the ZnO nanorod arrays are partially dissolved, resulting in the formation of ZnO/CdS/CdSe porous nanotube arrays (NTAs). Zinc Oxide 71-74 CDP-diacylglycerol synthase 1 Homo sapiens 53-56 26171978-3 2015 Surprisingly, after the process of the deposition of CdS and CdSe, the ZnO nanorod arrays are partially dissolved, resulting in the formation of ZnO/CdS/CdSe porous nanotube arrays (NTAs). Zinc Oxide 71-74 CDP-diacylglycerol synthase 1 Homo sapiens 61-64 26171978-3 2015 Surprisingly, after the process of the deposition of CdS and CdSe, the ZnO nanorod arrays are partially dissolved, resulting in the formation of ZnO/CdS/CdSe porous nanotube arrays (NTAs). Zinc Oxide 145-148 CDP-diacylglycerol synthase 1 Homo sapiens 53-56 26171978-3 2015 Surprisingly, after the process of the deposition of CdS and CdSe, the ZnO nanorod arrays are partially dissolved, resulting in the formation of ZnO/CdS/CdSe porous nanotube arrays (NTAs). Zinc Oxide 145-148 CDP-diacylglycerol synthase 1 Homo sapiens 61-64 26171978-4 2015 By virtue of their unique porous nanotube structure and cosensitization effect, the ZnO/CdS/CdSe porous NTAs show superior photoelectrochemical water-splitting performance and organic-pollutant-degradation ability under visible light irradiation, as well as excellent long-term photostability. Zinc Oxide 84-87 CDP-diacylglycerol synthase 1 Homo sapiens 88-91 26369059-1 2015 This paper reported ternary MEH-PPV-CuInS2/ZnO solar cells, which were fabricated with the mixture of poly(2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylene vinylene) (MEH-PPV) and CuInS2 quantum dots (QDs) as photovoltaic layer and ZnO nanorod arrays (ZnO-NAs) as electron acceptor. Zinc Oxide 43-46 epoxide hydrolase 1 Homo sapiens 28-31 26024212-0 2015 Novel ferrocene-anchored ZnO nanoparticle/carbon nanotube assembly for glucose oxidase wiring: application to a glucose/air fuel cell. Zinc Oxide 25-28 hydroxyacid oxidase 1 Homo sapiens 71-86 26024212-1 2015 Glucose oxidase (GOx) is immobilized on ZnO nanoparticle-modified electrodes. Zinc Oxide 40-43 hydroxyacid oxidase 1 Homo sapiens 0-15 26024212-1 2015 Glucose oxidase (GOx) is immobilized on ZnO nanoparticle-modified electrodes. Zinc Oxide 40-43 hydroxyacid oxidase 1 Homo sapiens 17-20 26024212-2 2015 The immobilized glucose oxidase shows efficient mediated electron transfer with ZnO nanoparticles to which the ferrocenyl moiety is pi-stacked into a supramolecular architecture. Zinc Oxide 80-83 hydroxyacid oxidase 1 Homo sapiens 16-31 26042713-9 2015 The proliferation of mesenchymal stem cells (MSCs) and their alkaline phosphatase activity (ALP) on GCs was revealed to be Zn-dose dependent with the highest performance being observed for 4 mol% ZnO. Zinc Oxide 196-199 alkaline phosphatase, placental Homo sapiens 92-95 25771180-10 2015 Exposure of RBL-2H3 and primary mouse BMMC to ZnO NPs markedly inhibited both histamine and beta-hexosaminidase release. Zinc Oxide 46-49 O-GlcNAcase Mus musculus 92-111 25746190-5 2015 Furthermore, the growth of ZnO involved a phase transformation from intermediate compound ZnF(OH) to ZnO. Zinc Oxide 27-30 zinc finger protein 763 Homo sapiens 90-93 32262403-0 2015 Surface defect rich ZnO quantum dots as antioxidants inhibiting alpha-amylase and alpha-glucosidase: a potential anti-diabetic nanomedicine. Zinc Oxide 20-23 sucrase-isomaltase Homo sapiens 82-99 26369059-1 2015 This paper reported ternary MEH-PPV-CuInS2/ZnO solar cells, which were fabricated with the mixture of poly(2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylene vinylene) (MEH-PPV) and CuInS2 quantum dots (QDs) as photovoltaic layer and ZnO nanorod arrays (ZnO-NAs) as electron acceptor. Zinc Oxide 227-230 epoxide hydrolase 1 Homo sapiens 28-31 25902878-1 2015 A novel route called thermal replacement reaction was demonstrated for synthesizing eco-friendly ZnO@gamma-In2Se3 hetero-structural nanowires on FTO glass by replacing the element cadmium with indium for the first time. Zinc Oxide 97-100 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 145-148 25907247-0 2015 ZnO@Ag2S core-shell nanowire arrays for environmentally friendly solid-state quantum dot-sensitized solar cells with panchromatic light capture and enhanced electron collection. Zinc Oxide 0-3 angiotensin II receptor type 1 Homo sapiens 4-8 25907268-5 2015 We implemented gold-nanoparticle-decorated zinc oxide nanoflowers (Au-ZnO) as the matrix for immobilizing ALP and TB aptamer (TBA) and then labeled it with hemin to form hemin/G-quadruplex/ALP/Au-ZnO bioconjugates (TBA II bioconjugates). Zinc Oxide 43-53 alkaline phosphatase, placental Homo sapiens 106-109 25907247-3 2015 Ag2S quantum dots (QDs) were directly grown on the ZnO nanowires by the successive ionic layer adsorption and reaction (SILAR) method to obtain the core-shell nanostructure. Zinc Oxide 51-54 angiotensin II receptor type 1 Homo sapiens 0-4 25907268-5 2015 We implemented gold-nanoparticle-decorated zinc oxide nanoflowers (Au-ZnO) as the matrix for immobilizing ALP and TB aptamer (TBA) and then labeled it with hemin to form hemin/G-quadruplex/ALP/Au-ZnO bioconjugates (TBA II bioconjugates). Zinc Oxide 70-73 alkaline phosphatase, placental Homo sapiens 106-109 25740574-3 2015 A model cell with a FTO/ZnO/CdS photoanode produced by SILAR and FTO/ZnO/CuxS films as counter-electrode showed a light conversion efficiency, eta = 1.73%, which is 25% higher than a similar cell where copper sulfide was deposited onto ZnO in "dark" conditions. Zinc Oxide 69-72 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 20-23 24917655-0 2015 Zinc oxide influences mitogen-activated protein kinase and TGF-beta1 signaling pathways, and enhances intestinal barrier integrity in weaned pigs. Zinc Oxide 0-10 transforming growth factor beta 1 Sus scrofa 59-68 24917655-3 2015 We examined whether ZnO protects the intestinal barrier via mitogen-activated protein kinases and TGF-beta1 signaling pathways. Zinc Oxide 20-23 transforming growth factor beta 1 Sus scrofa 98-107 24917655-7 2015 ZnO decreased the ratios of the phosphorylated to total JNK and p38 (p-JNK/JNK and p-p38/p38), while it increased the ratio of ERK (p-ERK/ERK). Zinc Oxide 0-3 mitogen-activated protein kinase 8 Sus scrofa 56-59 24917655-7 2015 ZnO decreased the ratios of the phosphorylated to total JNK and p38 (p-JNK/JNK and p-p38/p38), while it increased the ratio of ERK (p-ERK/ERK). Zinc Oxide 0-3 mitogen-activated protein kinase 8 Sus scrofa 71-74 24917655-7 2015 ZnO decreased the ratios of the phosphorylated to total JNK and p38 (p-JNK/JNK and p-p38/p38), while it increased the ratio of ERK (p-ERK/ERK). Zinc Oxide 0-3 mitogen-activated protein kinase 8 Sus scrofa 71-74 24917655-8 2015 Supplementation with ZnO increased intestinal TGF-beta1 expression. Zinc Oxide 21-24 transforming growth factor beta 1 Sus scrofa 46-55 24917655-9 2015 The results indicate that supplementation with ZnO activates ERK 1/2, and inhibits JNK and p38 signaling pathways, and increases intestinal TGF-beta1 expression in weaned pigs. Zinc Oxide 47-50 mitogen-activated protein kinase 3 Sus scrofa 61-68 24917655-9 2015 The results indicate that supplementation with ZnO activates ERK 1/2, and inhibits JNK and p38 signaling pathways, and increases intestinal TGF-beta1 expression in weaned pigs. Zinc Oxide 47-50 mitogen-activated protein kinase 8 Sus scrofa 83-86 24917655-9 2015 The results indicate that supplementation with ZnO activates ERK 1/2, and inhibits JNK and p38 signaling pathways, and increases intestinal TGF-beta1 expression in weaned pigs. Zinc Oxide 47-50 transforming growth factor beta 1 Sus scrofa 140-149 25740574-3 2015 A model cell with a FTO/ZnO/CdS photoanode produced by SILAR and FTO/ZnO/CuxS films as counter-electrode showed a light conversion efficiency, eta = 1.73%, which is 25% higher than a similar cell where copper sulfide was deposited onto ZnO in "dark" conditions. Zinc Oxide 24-27 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 65-68 25740574-3 2015 A model cell with a FTO/ZnO/CdS photoanode produced by SILAR and FTO/ZnO/CuxS films as counter-electrode showed a light conversion efficiency, eta = 1.73%, which is 25% higher than a similar cell where copper sulfide was deposited onto ZnO in "dark" conditions. Zinc Oxide 69-72 CDP-diacylglycerol synthase 1 Homo sapiens 28-31 25740574-3 2015 A model cell with a FTO/ZnO/CdS photoanode produced by SILAR and FTO/ZnO/CuxS films as counter-electrode showed a light conversion efficiency, eta = 1.73%, which is 25% higher than a similar cell where copper sulfide was deposited onto ZnO in "dark" conditions. Zinc Oxide 69-72 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 20-23 25740574-3 2015 A model cell with a FTO/ZnO/CdS photoanode produced by SILAR and FTO/ZnO/CuxS films as counter-electrode showed a light conversion efficiency, eta = 1.73%, which is 25% higher than a similar cell where copper sulfide was deposited onto ZnO in "dark" conditions. Zinc Oxide 69-72 CDP-diacylglycerol synthase 1 Homo sapiens 28-31 25740574-4 2015 Varying the conditions of the photocatalytic deposition of the starting copper nanoparticles slightly affects the electrocatalytic properties of the final FTO/ZnO/CuxS heterostructures. Zinc Oxide 159-162 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 155-158 25835084-4 2015 With the protection of polyvinylpyrrolidone (PVP) on the surface, the interior of metal oxide solid colloidal spheres (c-MOs) that possess radially divergent structures could be selectively etched with acid/alkali as an etchant, forming h-MO of Al2O3 and ZnO. Zinc Oxide 255-258 MOS proto-oncogene, serine/threonine kinase Homo sapiens 119-124 25785476-2 2015 Here we introduce plasmonic Ag nanocubes (NCs) to colloidal PbS quantum dot/ZnO nanowire (PbS QD/ZnO NW) bulk-heterojunction solar cells, which are characterized by high photocurrents, for further improvement in the photocurrent and power conversion efficiency (PCE) in the visible and near-infrared regions. Zinc Oxide 76-79 cholinergic receptor muscarinic 3 Homo sapiens 90-93 25680694-8 2015 Our results showed that exposure to Nano-ZnO caused liver injury that was reflected by focal hepatocellular necrosis, congestive dilation of central veins, and significantly increased alanine transaminase (ALT) and aspartate transaminase (AST) levels. Zinc Oxide 41-44 glutamic pyruvic transaminase, soluble Mus musculus 184-204 25977654-0 2015 Facile synthesis of composition-tuned ZnO/Zn x Cd1-x Se nanowires for photovoltaic applications. Zinc Oxide 38-41 CD1c molecule Homo sapiens 47-50 25875377-6 2015 The eta improvement can be attributed primarily to the morphology effect of ZnO nanocones on light-trapping and effectively passivating the interface surface recombination sites of ZnO nanocones by coating with a ZnS shell layer. Zinc Oxide 76-79 endothelin receptor type A Homo sapiens 4-7 25875377-6 2015 The eta improvement can be attributed primarily to the morphology effect of ZnO nanocones on light-trapping and effectively passivating the interface surface recombination sites of ZnO nanocones by coating with a ZnS shell layer. Zinc Oxide 181-184 endothelin receptor type A Homo sapiens 4-7 25530535-0 2015 CuO-induced signal amplification strategy for multiplexed photoelectrochemical immunosensing using CdS sensitized ZnO nanotubes arrays as photoactive material and AuPd alloy nanoparticles as electron sink. Zinc Oxide 114-117 CDP-diacylglycerol synthase 1 Homo sapiens 99-102 25530535-7 2015 The introduction of CuO brings signal amplification because of the conduction band (CB) of both CuO and ZnO are lower than that of CdS, CuO will compete the photo-induced electrons in CB of CdS with ZnO, leading to the decrease of the photocurrent intensity. Zinc Oxide 104-107 CDP-diacylglycerol synthase 1 Homo sapiens 131-134 25530535-7 2015 The introduction of CuO brings signal amplification because of the conduction band (CB) of both CuO and ZnO are lower than that of CdS, CuO will compete the photo-induced electrons in CB of CdS with ZnO, leading to the decrease of the photocurrent intensity. Zinc Oxide 104-107 CDP-diacylglycerol synthase 1 Homo sapiens 190-193 25530535-7 2015 The introduction of CuO brings signal amplification because of the conduction band (CB) of both CuO and ZnO are lower than that of CdS, CuO will compete the photo-induced electrons in CB of CdS with ZnO, leading to the decrease of the photocurrent intensity. Zinc Oxide 199-202 CDP-diacylglycerol synthase 1 Homo sapiens 131-134 25530535-7 2015 The introduction of CuO brings signal amplification because of the conduction band (CB) of both CuO and ZnO are lower than that of CdS, CuO will compete the photo-induced electrons in CB of CdS with ZnO, leading to the decrease of the photocurrent intensity. Zinc Oxide 199-202 CDP-diacylglycerol synthase 1 Homo sapiens 190-193 25680694-8 2015 Our results showed that exposure to Nano-ZnO caused liver injury that was reflected by focal hepatocellular necrosis, congestive dilation of central veins, and significantly increased alanine transaminase (ALT) and aspartate transaminase (AST) levels. Zinc Oxide 41-44 glutamic pyruvic transaminase, soluble Mus musculus 206-209 25680694-8 2015 Our results showed that exposure to Nano-ZnO caused liver injury that was reflected by focal hepatocellular necrosis, congestive dilation of central veins, and significantly increased alanine transaminase (ALT) and aspartate transaminase (AST) levels. Zinc Oxide 41-44 solute carrier family 17 (anion/sugar transporter), member 5 Mus musculus 215-237 25680694-8 2015 Our results showed that exposure to Nano-ZnO caused liver injury that was reflected by focal hepatocellular necrosis, congestive dilation of central veins, and significantly increased alanine transaminase (ALT) and aspartate transaminase (AST) levels. Zinc Oxide 41-44 solute carrier family 17 (anion/sugar transporter), member 5 Mus musculus 239-242 25680694-11 2015 The mRNA expression levels of ER stress-associated genes (grp78, grp94, pdi-3, xbp-1) were also up-regulated in Nano-ZnO-treated mice. Zinc Oxide 117-120 heat shock protein 5 Mus musculus 58-63 25680694-11 2015 The mRNA expression levels of ER stress-associated genes (grp78, grp94, pdi-3, xbp-1) were also up-regulated in Nano-ZnO-treated mice. Zinc Oxide 117-120 heat shock protein 90, beta (Grp94), member 1 Mus musculus 65-70 25680694-11 2015 The mRNA expression levels of ER stress-associated genes (grp78, grp94, pdi-3, xbp-1) were also up-regulated in Nano-ZnO-treated mice. Zinc Oxide 117-120 peptidyl arginine deiminase, type III Mus musculus 72-77 25680694-11 2015 The mRNA expression levels of ER stress-associated genes (grp78, grp94, pdi-3, xbp-1) were also up-regulated in Nano-ZnO-treated mice. Zinc Oxide 117-120 X-box binding protein 1 Mus musculus 79-84 25680694-12 2015 Nano-ZnO caused increased phosphorylation of RNA-dependent protein kinase-like ER kinase (PERK) and eukaryotic initiation factor 2alpha (eIF2alpha). Zinc Oxide 5-8 eukaryotic translation initiation factor 2 alpha kinase 3 Mus musculus 59-88 25680694-12 2015 Nano-ZnO caused increased phosphorylation of RNA-dependent protein kinase-like ER kinase (PERK) and eukaryotic initiation factor 2alpha (eIF2alpha). Zinc Oxide 5-8 eukaryotic translation initiation factor 2 alpha kinase 3 Mus musculus 90-94 25680694-12 2015 Nano-ZnO caused increased phosphorylation of RNA-dependent protein kinase-like ER kinase (PERK) and eukaryotic initiation factor 2alpha (eIF2alpha). Zinc Oxide 5-8 eukaryotic translation initiation factor 2A Mus musculus 137-146 25680694-13 2015 Finally, we found that exposure to Nano-ZnO caused increased ER stress-associated apoptotic protein levels, such as caspase-3, caspase-9, caspase-12, phosphorylation of JNK, and CHOP/GADD153, and up-regulation of pro-apoptotic genes (chop and bax). Zinc Oxide 40-43 caspase 3 Mus musculus 116-125 25680694-13 2015 Finally, we found that exposure to Nano-ZnO caused increased ER stress-associated apoptotic protein levels, such as caspase-3, caspase-9, caspase-12, phosphorylation of JNK, and CHOP/GADD153, and up-regulation of pro-apoptotic genes (chop and bax). Zinc Oxide 40-43 caspase 9 Mus musculus 127-136 25680694-13 2015 Finally, we found that exposure to Nano-ZnO caused increased ER stress-associated apoptotic protein levels, such as caspase-3, caspase-9, caspase-12, phosphorylation of JNK, and CHOP/GADD153, and up-regulation of pro-apoptotic genes (chop and bax). Zinc Oxide 40-43 caspase 12 Mus musculus 138-148 25680694-13 2015 Finally, we found that exposure to Nano-ZnO caused increased ER stress-associated apoptotic protein levels, such as caspase-3, caspase-9, caspase-12, phosphorylation of JNK, and CHOP/GADD153, and up-regulation of pro-apoptotic genes (chop and bax). Zinc Oxide 40-43 DNA-damage inducible transcript 3 Mus musculus 178-182 25680694-13 2015 Finally, we found that exposure to Nano-ZnO caused increased ER stress-associated apoptotic protein levels, such as caspase-3, caspase-9, caspase-12, phosphorylation of JNK, and CHOP/GADD153, and up-regulation of pro-apoptotic genes (chop and bax). Zinc Oxide 40-43 DNA-damage inducible transcript 3 Mus musculus 183-190 25680694-13 2015 Finally, we found that exposure to Nano-ZnO caused increased ER stress-associated apoptotic protein levels, such as caspase-3, caspase-9, caspase-12, phosphorylation of JNK, and CHOP/GADD153, and up-regulation of pro-apoptotic genes (chop and bax). Zinc Oxide 40-43 DNA-damage inducible transcript 3 Mus musculus 234-238 25680694-13 2015 Finally, we found that exposure to Nano-ZnO caused increased ER stress-associated apoptotic protein levels, such as caspase-3, caspase-9, caspase-12, phosphorylation of JNK, and CHOP/GADD153, and up-regulation of pro-apoptotic genes (chop and bax). Zinc Oxide 40-43 BCL2-associated X protein Mus musculus 243-246 25758259-4 2015 Owing to the unique hydrophobic feature of a ZnO NW that provides a desirable "microenvironment" for the immobilization of biomolecules, our device can effectively stimulate the tolbutamide metabolism by decorating a ZnO NW with cytochrome P4502C9/CYPs reductase (CYP2C9/CPR) microsomes. Zinc Oxide 45-48 cytochrome P450 family 2 subfamily C member 9 Homo sapiens 264-270 25615023-0 2015 Zinc oxide nanoparticles inhibit murine photoreceptor-derived cell proliferation and migration via reducing TGF-beta and MMP-9 expression in vitro. Zinc Oxide 0-10 transforming growth factor, beta 1 Mus musculus 108-116 25615023-0 2015 Zinc oxide nanoparticles inhibit murine photoreceptor-derived cell proliferation and migration via reducing TGF-beta and MMP-9 expression in vitro. Zinc Oxide 0-10 matrix metallopeptidase 9 Mus musculus 121-126 25615023-1 2015 OBJECTIVES: To investigate behaviour and expression of transforming growth factor-beta (TGF-beta) and matrix metalloproteinases (MMP-9) in murine photoreceptor-derived cells (661W) after incubation with zinc oxide (ZnO) nanoparticles. Zinc Oxide 203-213 transforming growth factor, beta 1 Mus musculus 88-96 25615023-1 2015 OBJECTIVES: To investigate behaviour and expression of transforming growth factor-beta (TGF-beta) and matrix metalloproteinases (MMP-9) in murine photoreceptor-derived cells (661W) after incubation with zinc oxide (ZnO) nanoparticles. Zinc Oxide 203-213 matrix metallopeptidase 9 Mus musculus 129-134 25615023-3 2015 RESULTS: Our results indicate that ZnO nanoparticles induced overload of calcium and reactive oxygen species within cells, causing formation of apoptotic bodies, disruption of cell cycle distribution, and reduction in expression of TGF-beta and MMP-9, to suppress cell proliferation and migration. Zinc Oxide 35-38 transforming growth factor, beta 1 Mus musculus 232-240 25615023-3 2015 RESULTS: Our results indicate that ZnO nanoparticles induced overload of calcium and reactive oxygen species within cells, causing formation of apoptotic bodies, disruption of cell cycle distribution, and reduction in expression of TGF-beta and MMP-9, to suppress cell proliferation and migration. Zinc Oxide 35-38 matrix metallopeptidase 9 Mus musculus 245-250 25615023-4 2015 Our findings show that disruption of intracellular calcium homoeostasis and overproduction of reactive oxygen species were closely associated with reduction of TGF-beta and MMP-9 in 661W cells under ZnO nanoparticle treatment. Zinc Oxide 199-202 transforming growth factor, beta 1 Mus musculus 160-168 25615023-4 2015 Our findings show that disruption of intracellular calcium homoeostasis and overproduction of reactive oxygen species were closely associated with reduction of TGF-beta and MMP-9 in 661W cells under ZnO nanoparticle treatment. Zinc Oxide 199-202 matrix metallopeptidase 9 Mus musculus 173-178 25615023-5 2015 CONCLUSIONS: Results of our study indicate that ZnO nanoparticles suppressed cell proliferation and migration, and reduced production of TGF-beta and MMP-9 at both gene and protein levels. Zinc Oxide 48-51 transforming growth factor, beta 1 Mus musculus 137-145 25615023-5 2015 CONCLUSIONS: Results of our study indicate that ZnO nanoparticles suppressed cell proliferation and migration, and reduced production of TGF-beta and MMP-9 at both gene and protein levels. Zinc Oxide 48-51 matrix metallopeptidase 9 Mus musculus 150-155 25615023-6 2015 Our findings contribute to the understanding of the molecular mechanisms that reduced TGF-beta and MMP-9 levels inhibit cell proliferation and migration under ZnO nanoparticle influence. Zinc Oxide 159-162 transforming growth factor, beta 1 Mus musculus 86-94 25615023-6 2015 Our findings contribute to the understanding of the molecular mechanisms that reduced TGF-beta and MMP-9 levels inhibit cell proliferation and migration under ZnO nanoparticle influence. Zinc Oxide 159-162 matrix metallopeptidase 9 Mus musculus 99-104 26020182-0 2015 Diosmectite-zinc oxide composite improves intestinal barrier restoration and modulates TGF-beta1, ERK1/2, and Akt in piglets after acetic acid challenge. Zinc Oxide 12-22 transforming growth factor beta 1 Homo sapiens 87-96 26020182-0 2015 Diosmectite-zinc oxide composite improves intestinal barrier restoration and modulates TGF-beta1, ERK1/2, and Akt in piglets after acetic acid challenge. Zinc Oxide 12-22 mitogen-activated protein kinase 3 Homo sapiens 98-104 26020182-0 2015 Diosmectite-zinc oxide composite improves intestinal barrier restoration and modulates TGF-beta1, ERK1/2, and Akt in piglets after acetic acid challenge. Zinc Oxide 12-22 AKT serine/threonine kinase 1 Homo sapiens 110-113 25553547-11 2015 Inflammatory responses were at a low level but macrophage inflammatory protein 2 reached a statistically significant level after exposure of RAW 264.7 macrophages to ZnO containing emission particles. Zinc Oxide 166-169 chemokine (C-X-C motif) ligand 2 Mus musculus 47-80 25555257-10 2015 Our results show the heterogeneous reaction accelerated in the fog and haze episodes indicated by more zinc nitrate or zinc sulfate instead of zinc oxide or carbonate. Zinc Oxide 143-153 zinc finger protein, FOG family member 1 Homo sapiens 63-66 26020182-8 2015 Diosmectite-zinc oxide composite supplementation also increased (P < 0.05) TGF-beta1 expression and ERK1/2 and Akt activation. Zinc Oxide 12-22 transforming growth factor beta 1 Homo sapiens 78-87 26020182-8 2015 Diosmectite-zinc oxide composite supplementation also increased (P < 0.05) TGF-beta1 expression and ERK1/2 and Akt activation. Zinc Oxide 12-22 mitogen-activated protein kinase 3 Homo sapiens 103-109 26020182-8 2015 Diosmectite-zinc oxide composite supplementation also increased (P < 0.05) TGF-beta1 expression and ERK1/2 and Akt activation. Zinc Oxide 12-22 AKT serine/threonine kinase 1 Homo sapiens 114-117 25758259-4 2015 Owing to the unique hydrophobic feature of a ZnO NW that provides a desirable "microenvironment" for the immobilization of biomolecules, our device can effectively stimulate the tolbutamide metabolism by decorating a ZnO NW with cytochrome P4502C9/CYPs reductase (CYP2C9/CPR) microsomes. Zinc Oxide 217-220 cytochrome P450 family 2 subfamily C member 9 Homo sapiens 264-270 25381309-0 2015 Zinc oxide nanoparticles affect the expression of p53, Ras p21 and JNKs: an ex vivo/in vitro exposure study in respiratory disease patients. Zinc Oxide 0-10 tumor protein p53 Homo sapiens 50-53 25381309-0 2015 Zinc oxide nanoparticles affect the expression of p53, Ras p21 and JNKs: an ex vivo/in vitro exposure study in respiratory disease patients. Zinc Oxide 0-10 H3 histone pseudogene 16 Homo sapiens 59-62 25381309-5 2015 Using the differential expression analysis, we observed a significant (P < 0.05) dose-dependent (10, 20 and 40 microg/ml for 6h) increase in the expression of tumour suppressor protein p53 (40, 60 and 110%); Ras p21 (30, 52 and 80%); c-Jun N-terminal kinases; JNKs) (28, 47 and 78%) in lung cancer patient samples treated with ZnO ENPs compared to healthy controls. Zinc Oxide 330-333 tumor protein p53 Homo sapiens 188-191 25051535-0 2015 Sensitive electrochemiluminescence detection for CA15-3 based on immobilizing luminol on dendrimer functionalized ZnO nanorods. Zinc Oxide 114-117 mucin 1, cell surface associated Homo sapiens 49-55 25381309-6 2015 A similar trend was also seen in COPD patient samples where a significant (P < 0.05) dose-dependent increase in the expression of tumour suppressor protein p53 (26, 45 and 84%), Ras p21 (21, 40 and 77%), JNKs (17, 32 and 69%) was observed after 6h of ZnO ENPs treatment at the aforesaid concentrations. Zinc Oxide 254-257 tumor protein p53 Homo sapiens 159-162 25645871-10 2015 This was confirmed by up-regulation of eotaxin mRNA in the lung tissue and release of pro-inflammatory cytokines in the sera of mice exposed to ZnO NPs. Zinc Oxide 144-147 chemokine (C-C motif) ligand 11 Mus musculus 39-46 25864991-8 2015 After inhalation of OVA, the concentrations of total IgE, OVA-specific IgE and OVA-specific IgG1 in serum increased in the mice treated with ZnO. Zinc Oxide 141-144 LOC105243590 Mus musculus 92-96 25546020-1 2015 A ruthenium polypyridyl dye containing a hexasulfanyl-styryl modified bipyridyl group as ancillary ligand, coded TG6, is investigated as a sensitizer for ZnO-based dye-sensitized solar cells (DSSCs). Zinc Oxide 154-157 transglutaminase 6 Homo sapiens 113-116 25546020-3 2015 TG6 has been used to sensitize ZnO nanorod particle layers of high structural quality and ZnO layers made of submicrometer spheres composed of aggregated nanocrystallites and that develop an internal surface area. Zinc Oxide 31-34 transglutaminase 6 Homo sapiens 0-3 25546020-3 2015 TG6 has been used to sensitize ZnO nanorod particle layers of high structural quality and ZnO layers made of submicrometer spheres composed of aggregated nanocrystallites and that develop an internal surface area. Zinc Oxide 90-93 transglutaminase 6 Homo sapiens 0-3 32261984-8 2015 Complete bacterial inactivation was achieved for specific amino- and ionic liquid-modifications at 0.125 g L-1, revealing the synergistic effect of ZnO and its modifications, exhibiting up to 2-fold improvement compared to unmodified ZnO. Zinc Oxide 148-151 L1 cell adhesion molecule Homo sapiens 107-110 25607242-3 2015 Here we developed novel red fluorescent ZnO NPs and described the successful conjugation of 64Cu (t1/2=12.7 h) and TRC105, a chimeric monoclonal antibody against CD105, to these ZnO NPs via well-developed surface engineering procedures. Zinc Oxide 178-181 endoglin Mus musculus 162-167 25078460-1 2015 ZnO nanoparticles were doped with Ce(3+) by sol-gel synthesis and characterized by high-resolution scanning electron microscopy (HR-SEM), powder X-ray diffraction (XRD) and UV-visible diffuse reflectance (DRS) and photoluminescence (PL) spectroscopies. Zinc Oxide 0-3 sushi repeat containing protein X-linked Homo sapiens 205-208 28787941-3 2015 Thus, the photocatalytic degradation of 4-CPA in aqueous medium assisted by ultraviolet-active ZnO photocatalyst was systematically investigated. Zinc Oxide 95-98 carboxypeptidase A1 Homo sapiens 42-45 28787941-5 2015 Based on the results obtained, it was found that a maximum of 91% of 4-CPA was successfully degraded under optimal conditions (0.02 g ZnO dosage, 20.00 mg/L of 4-CPA and pH 7.71). Zinc Oxide 134-137 carboxypeptidase A1 Homo sapiens 71-74 25051535-1 2015 In this study, we constructed a novel electrochemiluminescence (ECL) immunosensor for sensitive and selective detection of carbohydrate antigen 15-3 (CA15-3) by using polyamidoamine (PAMAM)-functionalized ZnO nanorods (ZNs-PAMAM) as carriers. Zinc Oxide 205-208 mucin 1, cell surface associated Homo sapiens 123-156 25304748-1 2015 Investigations were made to evaluate and distinguish the photocatalytic decolorization of Reactive Red 2 (RR) dye using zinc oxide (ZnO) and zinc oxide impregnated chitosan beads (ZCB) under UV and visible light irradiations. Zinc Oxide 120-130 adenosine deaminase RNA specific B2 (inactive) Homo sapiens 99-104 25291796-0 2015 Synthesis of ZnO nanosphere for picomolar level detection of bovine serum albumin. Zinc Oxide 13-16 albumin Homo sapiens 68-81 25291796-1 2015 In this paper, we demonstrate an electrical detection technique based on solution processed zinc oxide nanosphere for ultra-low level detection of bovine serum albumin (BSA). Zinc Oxide 92-102 albumin Homo sapiens 154-167 25304748-1 2015 Investigations were made to evaluate and distinguish the photocatalytic decolorization of Reactive Red 2 (RR) dye using zinc oxide (ZnO) and zinc oxide impregnated chitosan beads (ZCB) under UV and visible light irradiations. Zinc Oxide 132-135 adenosine deaminase RNA specific B2 (inactive) Homo sapiens 99-104 25378273-10 2015 Exposure of immune cells to ZnO NPs resulted in autophagic death and increased levels of LC3A, an essential component of autophagic vacuoles. Zinc Oxide 28-31 microtubule-associated protein 1 light chain 3 alpha Mus musculus 89-93 25589205-0 2015 Anticancer activity of fungal L-asparaginase conjugated with zinc oxide nanoparticles. Zinc Oxide 61-71 asparaginase and isoaspartyl peptidase 1 Homo sapiens 30-44 25589205-3 2015 Nanobiocomposite of zinc oxide nanoparticles conjugated with L-asparaginase was produced by Aspergillus terreus and was confirmed using maximum UV-Vis absorption at 340 nm in the present work. Zinc Oxide 20-30 asparaginase and isoaspartyl peptidase 1 Homo sapiens 61-75 25589205-8 2015 The anti-cancerous nature of the synthesized zinc oxide conjugated L-asparaginase nanobiocomposite on MCF-7 cell line was studied using MTT assay. Zinc Oxide 45-55 asparaginase and isoaspartyl peptidase 1 Homo sapiens 67-81 25589205-9 2015 The viability of the MCF-7 cells was decreased to 35.02 % when it was treated with L-asparaginase conjugated zinc oxide nanobiocomposite. Zinc Oxide 109-119 asparaginase and isoaspartyl peptidase 1 Homo sapiens 83-97 25589205-10 2015 Hence it is proved that the synthesized nanobiocomposites of zinc oxide conjugated L-asparaginase has good anti-cancerous activity. Zinc Oxide 61-71 asparaginase and isoaspartyl peptidase 1 Homo sapiens 83-97 25405261-4 2015 There were major differences between the types of NMs; exposure to ZnO and Ag resulted in cytotoxicity and increased gene expression levels of HMOX1 and IL8. Zinc Oxide 67-70 heme oxygenase 1 Homo sapiens 143-148 25405261-4 2015 There were major differences between the types of NMs; exposure to ZnO and Ag resulted in cytotoxicity and increased gene expression levels of HMOX1 and IL8. Zinc Oxide 67-70 C-X-C motif chemokine ligand 8 Homo sapiens 153-156 25561223-9 2014 At Day 10, the synergistic effect of BLM and ZnO exposure was detected on IL-1beta and monocyte chemotactic protein (MCP)-1 in BALF. Zinc Oxide 45-48 interleukin 1 beta Mus musculus 74-82 25876966-0 2015 [The protein expression of heme oxygenase-1 and platelet endothelial cell adhesion molecules-1 in human coronary artery endothelial cell induced by zinc oxide nanoparticle]. Zinc Oxide 148-158 heme oxygenase 1 Homo sapiens 27-43 25876966-1 2015 OBJECTIVE: To explore the protein expression of heme oxygenase-1 (HO-1) and platelet endothelial cell adhesion molecules-1 (PECAM-1) in human coronary artery endothelial cells induced with Zinc Oxide Nanoparticle (ZnO-NPs). Zinc Oxide 189-199 heme oxygenase 1 Homo sapiens 48-64 25876966-1 2015 OBJECTIVE: To explore the protein expression of heme oxygenase-1 (HO-1) and platelet endothelial cell adhesion molecules-1 (PECAM-1) in human coronary artery endothelial cells induced with Zinc Oxide Nanoparticle (ZnO-NPs). Zinc Oxide 189-199 heme oxygenase 1 Homo sapiens 66-70 25876966-1 2015 OBJECTIVE: To explore the protein expression of heme oxygenase-1 (HO-1) and platelet endothelial cell adhesion molecules-1 (PECAM-1) in human coronary artery endothelial cells induced with Zinc Oxide Nanoparticle (ZnO-NPs). Zinc Oxide 189-199 platelet and endothelial cell adhesion molecule 1 Homo sapiens 124-131 25876966-1 2015 OBJECTIVE: To explore the protein expression of heme oxygenase-1 (HO-1) and platelet endothelial cell adhesion molecules-1 (PECAM-1) in human coronary artery endothelial cells induced with Zinc Oxide Nanoparticle (ZnO-NPs). Zinc Oxide 214-217 heme oxygenase 1 Homo sapiens 48-64 25876966-1 2015 OBJECTIVE: To explore the protein expression of heme oxygenase-1 (HO-1) and platelet endothelial cell adhesion molecules-1 (PECAM-1) in human coronary artery endothelial cells induced with Zinc Oxide Nanoparticle (ZnO-NPs). Zinc Oxide 214-217 platelet and endothelial cell adhesion molecule 1 Homo sapiens 124-131 25876966-4 2015 Protein levels of HO-1 (ng/L) in each group were 0.041+-0.011, 0.512+-0.076, 0.906+-0.059, 1.062+-0.089 respectively after the stimulation of different concentrations of ZnO-NPs (0, 10, 20, 40microg/ml). Zinc Oxide 170-173 heme oxygenase 1 Homo sapiens 18-22 25876966-6 2015 Protein levels of PECAM-1 (microg/L) in each group were 7.966 +- 0.046, 7.993 +- 0.036, 8.629 +- 0.052, 8.811 +- 0.039 respectively after the stimulation of different concentrations of ZnO-NPs (0, 10, 20, 40 microg/ml). Zinc Oxide 185-188 platelet and endothelial cell adhesion molecule 1 Homo sapiens 18-25 25876966-7 2015 Compared with the control group, protein levels of PECAM-1 increased (P < 0.05) when the concentration of ZnO-NPs was 20microg/ml or 40 microg/ml. Zinc Oxide 109-112 platelet and endothelial cell adhesion molecule 1 Homo sapiens 51-58 25561223-9 2014 At Day 10, the synergistic effect of BLM and ZnO exposure was detected on IL-1beta and monocyte chemotactic protein (MCP)-1 in BALF. Zinc Oxide 45-48 chemokine (C-C motif) ligand 2 Mus musculus 87-123 25565829-1 2014 PURPOSE: The study reported here was conducted to determine the systemic oral toxicity and to find the no-observed-adverse-effect level of 20 nm positively charged zinc oxide (ZnO(SM20(+))) nanoparticles in Sprague Dawley rats for 90 days. Zinc Oxide 164-174 egl-9 family hypoxia-inducible factor 3 Rattus norvegicus 180-184 24997365-3 2014 The GOx immobilized on GR-CNT-ZnO composite exhibits well-defined redox peaks with a peak potential separation (DeltaEp) of about 26 mV with enhanced peak currents, indicating a fast electron transfer at the modified electrode surface. Zinc Oxide 30-33 hydroxyacid oxidase 1 Homo sapiens 4-7 25565829-1 2014 PURPOSE: The study reported here was conducted to determine the systemic oral toxicity and to find the no-observed-adverse-effect level of 20 nm positively charged zinc oxide (ZnO(SM20(+))) nanoparticles in Sprague Dawley rats for 90 days. Zinc Oxide 176-179 egl-9 family hypoxia-inducible factor 3 Rattus norvegicus 180-184 25565829-4 2014 A distributional study was also carried out for the systemic distribution of ZnO(SM20(+)) NPs. Zinc Oxide 77-80 egl-9 family hypoxia-inducible factor 3 Rattus norvegicus 81-85 25565837-8 2014 The CD4(+)/CD8(+) ratio, a marker for matured T-cells was slightly reduced, which implies the alteration of immune status induced by ZnO NPs. Zinc Oxide 133-136 CD4 antigen Mus musculus 4-7 25565841-6 2014 Both SiO2 and ZnO nanoparticles activated caspase-3 and induced DNA fragmentation in U373MG cells, suggesting the induction of apoptosis. Zinc Oxide 14-17 caspase 3 Homo sapiens 42-51 25380639-0 2014 Microwave-mediated extracellular synthesis of metallic silver and zinc oxide nanoparticles using macro-algae (Gracilaria edulis) extracts and its anticancer activity against human PC3 cell lines. Zinc Oxide 66-76 chromobox 8 Homo sapiens 180-183 25464507-6 2014 Results of the selectivity study demonstrated that Ag2O3-ZnO NC phase was the most selective towards Co(II) ion. Zinc Oxide 57-60 mitochondrially encoded cytochrome c oxidase II Homo sapiens 101-107 25464507-9 2014 Kinetic study revealed that the adsorption of Co(II) on Ag2O3-ZnO NCs phase followed the pseudo-second-order kinetic model. Zinc Oxide 62-65 mitochondrially encoded cytochrome c oxidase II Homo sapiens 46-52 25464507-10 2014 In addition, thermodynamic results provided that the adsorption mechanism of Co(II) ions on Ag2O3-ZnO NCs was a spontaneous process and thermodynamically favorable. Zinc Oxide 98-101 mitochondrially encoded cytochrome c oxidase II Homo sapiens 77-83 25380639-1 2014 A rapid and novel microwave-mediated protocol was established for extracellular synthesis of metallic silver (Ag) and zinc oxide (ZnO) nanoparticles using the extracts of macro-algae Gracilaria edulis (GE) and also examined its anticancer activity against human prostate cancer cell lines (PC3). Zinc Oxide 130-133 chromobox 8 Homo sapiens 290-293 25324138-0 2014 Formation of a CdO layer on CdS/ZnO nanorod arrays to enhance their photoelectrochemical performance. Zinc Oxide 32-35 cell adhesion associated, oncogene regulated Homo sapiens 15-18 25324138-1 2014 The performance and photocatalytic activity of the well-known CdS/ZnO nanorod array system were improved significantly by the layer-by-layer heterojunction structure fabrication of a transparent conductive oxide (TCO) CdO layer on the CdS/ZnO nanorods. Zinc Oxide 66-69 CDP-diacylglycerol synthase 1 Homo sapiens 62-65 25324138-3 2014 At an external potential of 0.0 V vs. Ag/AgCl, the CdO/CdS/ZnO nanorod array electrodes exhibit an increased incident photon to conversion efficiency, which is significantly higher than that of the CdS/ZnO nanorod array electrodes. Zinc Oxide 59-62 cell adhesion associated, oncogene regulated Homo sapiens 51-54 25324138-1 2014 The performance and photocatalytic activity of the well-known CdS/ZnO nanorod array system were improved significantly by the layer-by-layer heterojunction structure fabrication of a transparent conductive oxide (TCO) CdO layer on the CdS/ZnO nanorods. Zinc Oxide 66-69 cell adhesion associated, oncogene regulated Homo sapiens 218-221 25324138-3 2014 At an external potential of 0.0 V vs. Ag/AgCl, the CdO/CdS/ZnO nanorod array electrodes exhibit an increased incident photon to conversion efficiency, which is significantly higher than that of the CdS/ZnO nanorod array electrodes. Zinc Oxide 59-62 CDP-diacylglycerol synthase 1 Homo sapiens 55-58 25324138-3 2014 At an external potential of 0.0 V vs. Ag/AgCl, the CdO/CdS/ZnO nanorod array electrodes exhibit an increased incident photon to conversion efficiency, which is significantly higher than that of the CdS/ZnO nanorod array electrodes. Zinc Oxide 59-62 CDP-diacylglycerol synthase 1 Homo sapiens 198-201 25324138-3 2014 At an external potential of 0.0 V vs. Ag/AgCl, the CdO/CdS/ZnO nanorod array electrodes exhibit an increased incident photon to conversion efficiency, which is significantly higher than that of the CdS/ZnO nanorod array electrodes. Zinc Oxide 202-205 cell adhesion associated, oncogene regulated Homo sapiens 51-54 25324138-3 2014 At an external potential of 0.0 V vs. Ag/AgCl, the CdO/CdS/ZnO nanorod array electrodes exhibit an increased incident photon to conversion efficiency, which is significantly higher than that of the CdS/ZnO nanorod array electrodes. Zinc Oxide 202-205 CDP-diacylglycerol synthase 1 Homo sapiens 55-58 25324138-1 2014 The performance and photocatalytic activity of the well-known CdS/ZnO nanorod array system were improved significantly by the layer-by-layer heterojunction structure fabrication of a transparent conductive oxide (TCO) CdO layer on the CdS/ZnO nanorods. Zinc Oxide 66-69 CDP-diacylglycerol synthase 1 Homo sapiens 235-238 25324138-1 2014 The performance and photocatalytic activity of the well-known CdS/ZnO nanorod array system were improved significantly by the layer-by-layer heterojunction structure fabrication of a transparent conductive oxide (TCO) CdO layer on the CdS/ZnO nanorods. Zinc Oxide 239-242 CDP-diacylglycerol synthase 1 Homo sapiens 62-65 25324138-1 2014 The performance and photocatalytic activity of the well-known CdS/ZnO nanorod array system were improved significantly by the layer-by-layer heterojunction structure fabrication of a transparent conductive oxide (TCO) CdO layer on the CdS/ZnO nanorods. Zinc Oxide 239-242 cell adhesion associated, oncogene regulated Homo sapiens 218-221 25324138-2 2014 Accordingly, a CdO layer with a thickness of approximately 5-10 nm can be formed that surrounds the CdS/ZnO nanorod arrays after annealing at 500 C under air. Zinc Oxide 104-107 cell adhesion associated, oncogene regulated Homo sapiens 15-18 25127755-0 2014 ZnO nanoparticles induced adjuvant effect via toll-like receptors and Src signaling in Balb/c mice. Zinc Oxide 0-3 Rous sarcoma oncogene Mus musculus 70-73 25324138-4 2014 The high charge separation between the electrons and holes at the interfaces of the heterojunction structure results from the specific band energy structure of the photoanode materials, and the unique high conductivity of the CdO layer is attributed to the suppression of electron-hole recombination; this suppression enhances the photocurrent density of the CdO/CdS/ZnO nanorod arrays. Zinc Oxide 367-370 cell adhesion associated, oncogene regulated Homo sapiens 226-229 25324138-5 2014 The photoresponse of the electrodes in an electrolytic solution without sacrificial agents indicated that the CdO layer also has the ability to suppress the well-known photocorrosive behavior of CdS/ZnO nanorods. Zinc Oxide 199-202 cell adhesion associated, oncogene regulated Homo sapiens 110-113 25394423-6 2014 In contrast, the ZnO NPs seemed to suppress the inflammatory (decreased neutrophils in Bmal1(-/-) mice) and oxidative response (increased total glutathione in Bmal1(-/-) mice), but were also procoagulant with a significant increase of FVIII. Zinc Oxide 17-20 aryl hydrocarbon receptor nuclear translocator-like Mus musculus 87-92 25394423-6 2014 In contrast, the ZnO NPs seemed to suppress the inflammatory (decreased neutrophils in Bmal1(-/-) mice) and oxidative response (increased total glutathione in Bmal1(-/-) mice), but were also procoagulant with a significant increase of FVIII. Zinc Oxide 17-20 aryl hydrocarbon receptor nuclear translocator-like Mus musculus 159-164 25394423-6 2014 In contrast, the ZnO NPs seemed to suppress the inflammatory (decreased neutrophils in Bmal1(-/-) mice) and oxidative response (increased total glutathione in Bmal1(-/-) mice), but were also procoagulant with a significant increase of FVIII. Zinc Oxide 17-20 coagulation factor VIII Mus musculus 235-240 25307611-5 2014 Corresponding ZnO nanocones and nanoplates have been further obtained through the thermal calcination of NO3(-)-intercalating zinc hydroxide nanocones/nanoplates. Zinc Oxide 14-17 NBL1, DAN family BMP antagonist Homo sapiens 105-108 25127755-1 2014 Our previous studies indicated that zinc oxide nanoparticles (ZnO NPs) have adjuvant properties to a known allergen ovalbumin (OVA) in Balb/c mice. Zinc Oxide 36-46 serine (or cysteine) peptidase inhibitor, clade B, member 1, pseudogene Mus musculus 116-125 25127755-1 2014 Our previous studies indicated that zinc oxide nanoparticles (ZnO NPs) have adjuvant properties to a known allergen ovalbumin (OVA) in Balb/c mice. Zinc Oxide 62-65 serine (or cysteine) peptidase inhibitor, clade B, member 1, pseudogene Mus musculus 116-125 25127755-3 2014 The eosinophil counts in the Peyers" patches of intestine and ICAM-1, Cox2 protein expressions were enhanced in the ZnO NPs/OVA group. Zinc Oxide 116-119 intercellular adhesion molecule 1 Mus musculus 62-68 25127755-3 2014 The eosinophil counts in the Peyers" patches of intestine and ICAM-1, Cox2 protein expressions were enhanced in the ZnO NPs/OVA group. Zinc Oxide 116-119 cytochrome c oxidase II, mitochondrial Mus musculus 70-74 25127755-5 2014 Accordingly, we found that downstream proteins of TLRs such as myeloid differentiation primary response protein-88 (MyD88), IL-1 receptor associated kinase 1 (IRAK 1), and TNFR-associated factor 6 (TRAF 6) were also found to be enhanced in the ZnO NPs/OVA-induced group. Zinc Oxide 244-247 myeloid differentiation primary response gene 88 Mus musculus 116-121 25127755-5 2014 Accordingly, we found that downstream proteins of TLRs such as myeloid differentiation primary response protein-88 (MyD88), IL-1 receptor associated kinase 1 (IRAK 1), and TNFR-associated factor 6 (TRAF 6) were also found to be enhanced in the ZnO NPs/OVA-induced group. Zinc Oxide 244-247 interleukin-1 receptor-associated kinase 1 Mus musculus 124-157 25127755-5 2014 Accordingly, we found that downstream proteins of TLRs such as myeloid differentiation primary response protein-88 (MyD88), IL-1 receptor associated kinase 1 (IRAK 1), and TNFR-associated factor 6 (TRAF 6) were also found to be enhanced in the ZnO NPs/OVA-induced group. Zinc Oxide 244-247 interleukin-1 receptor-associated kinase 1 Mus musculus 159-165 25127755-5 2014 Accordingly, we found that downstream proteins of TLRs such as myeloid differentiation primary response protein-88 (MyD88), IL-1 receptor associated kinase 1 (IRAK 1), and TNFR-associated factor 6 (TRAF 6) were also found to be enhanced in the ZnO NPs/OVA-induced group. Zinc Oxide 244-247 TNF receptor-associated factor 6 Mus musculus 172-196 25127755-5 2014 Accordingly, we found that downstream proteins of TLRs such as myeloid differentiation primary response protein-88 (MyD88), IL-1 receptor associated kinase 1 (IRAK 1), and TNFR-associated factor 6 (TRAF 6) were also found to be enhanced in the ZnO NPs/OVA-induced group. Zinc Oxide 244-247 TNF receptor-associated factor 6 Mus musculus 198-204 25127755-7 2014 ZnO NPs increased the mRNA levels of inflammatory cytokine IL-1beta and protein expression of several mediators, including Cox2, PGE2, MMP-9 and finally caspase 1 in macrophages. Zinc Oxide 0-3 interleukin 1 beta Mus musculus 59-67 25127755-7 2014 ZnO NPs increased the mRNA levels of inflammatory cytokine IL-1beta and protein expression of several mediators, including Cox2, PGE2, MMP-9 and finally caspase 1 in macrophages. Zinc Oxide 0-3 cytochrome c oxidase II, mitochondrial Mus musculus 123-127 25127755-7 2014 ZnO NPs increased the mRNA levels of inflammatory cytokine IL-1beta and protein expression of several mediators, including Cox2, PGE2, MMP-9 and finally caspase 1 in macrophages. Zinc Oxide 0-3 matrix metallopeptidase 9 Mus musculus 135-140 25127755-7 2014 ZnO NPs increased the mRNA levels of inflammatory cytokine IL-1beta and protein expression of several mediators, including Cox2, PGE2, MMP-9 and finally caspase 1 in macrophages. Zinc Oxide 0-3 caspase 1 Mus musculus 153-162 25127755-11 2014 We therefore, conclude that ZnO NPs have significant adjuvant effect via following Src kinase and TLRs signaling that ascribed to inflammatory responses due to recruitment and activation of adhesion molecules and inflammatory cells. Zinc Oxide 28-31 Rous sarcoma oncogene Mus musculus 83-86 25253808-11 2014 High dietary Zn treatment led to a reduced abundance of CD8(+) gammadelta T-cells (P < 0.05). Zinc Oxide 13-15 CD8a molecule Homo sapiens 56-59 25253808-15 2014 High Zn intakes resulted in a reduced gene expression of beta-defensin 3 (P < 0.05), but did not affect the expression of TFF3. Zinc Oxide 5-7 defensin beta 103B Homo sapiens 57-72 25082708-8 2014 Uptake of these particles was further strengthened by the ZnO-induced activation of the Src-kinase p-Lyn, phospho-tyrosine kinases Syk (spleen tyrosine kinase), p-PLC-gamma and PI3K (phosphatidylinositol 3-kinase). Zinc Oxide 58-61 spleen associated tyrosine kinase Homo sapiens 131-134 25771730-11 2014 Significant depletion of SOD level, variation in GSH level and release of ROS in cells treated by ZnO NPs were observed, which suggests that cytotoxicity of ZnO NPs in intestine cells might be mediated through cellular oxidative stress. Zinc Oxide 98-101 superoxide dismutase 1 Homo sapiens 25-28 25379929-4 2014 The application to the specific cases of nonpolar (101 0) facets of GaN and ZnO reveals a significant role for the structural motifs at the interface, including the degree of interface water dissociation and the dynamical fluctuations in the interface Zn-O and O-H bond orientations. Zinc Oxide 252-256 gigaxonin Homo sapiens 68-71 25226166-3 2014 Morphology of the sample was studied by scanning electron microscopy and it was observed that ZnO nanoplates were covered with ZnS and Ag2S nanoparticles. Zinc Oxide 94-97 angiotensin II receptor type 1 Homo sapiens 135-139 25082708-8 2014 Uptake of these particles was further strengthened by the ZnO-induced activation of the Src-kinase p-Lyn, phospho-tyrosine kinases Syk (spleen tyrosine kinase), p-PLC-gamma and PI3K (phosphatidylinositol 3-kinase). Zinc Oxide 58-61 spleen associated tyrosine kinase Homo sapiens 136-158 24752145-3 2014 The biosensing properties toward glucose of the Nafion/GOD/ZnO IOPCs modified FTO electrodes were carefully studied and the results indicated that the sensitivity of ZnO IOPCs modified electrode was 18 times than reference electrode due to the large surface area and uniform porous structure of ZnO IOPCs. Zinc Oxide 166-169 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 78-81 24973873-6 2014 Catalase activity in serum samples was significantly higher in the 20- and 60-nano-ZnO groups relative to the control and 100-nano-ZnO birds, but catalase activity in liver tissue was not affected by different nano-ZnO levels. Zinc Oxide 83-86 catalase Homo sapiens 0-8 24727606-3 2014 meningitides onto the nanostructured ZnO (ZNF) matrix surface have been investigated using cyclic voltammetry (CV) and electrochemical impeadance spectroscopy (EIS). Zinc Oxide 51-54 zinc finger protein 763 Homo sapiens 56-59 24752145-3 2014 The biosensing properties toward glucose of the Nafion/GOD/ZnO IOPCs modified FTO electrodes were carefully studied and the results indicated that the sensitivity of ZnO IOPCs modified electrode was 18 times than reference electrode due to the large surface area and uniform porous structure of ZnO IOPCs. Zinc Oxide 59-62 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 78-81 24998074-0 2014 The influence of annealing temperature on the interface and photovoltaic properties of CdS/CdSe quantum dots sensitized ZnO nanorods solar cells. Zinc Oxide 120-123 CDP-diacylglycerol synthase 1 Homo sapiens 87-90 24998074-2 2014 CdS/CdSe quantum dots were synthesized on the surface of ZnO nanorods that serve as the scaffold via a simple ion-exchange approach. Zinc Oxide 57-60 CDP-diacylglycerol synthase 1 Homo sapiens 0-3 25043592-2 2014 The results indicated that ZnO particles dispersed uniformly on the mpg-C3N4 sheet. Zinc Oxide 27-30 N-methylpurine DNA glycosylase Homo sapiens 68-71 25043592-4 2014 The optimal ZnO content for the photocatalytic activity of the ZnO/mpg-C3N4 composites is 24.9%, which is almost 2.3 times as high as that of pure mpg-C3N4 under visible light, and 1.9 times higher than that under simulated solar irradiation. Zinc Oxide 12-15 N-methylpurine DNA glycosylase Homo sapiens 67-70 25043592-4 2014 The optimal ZnO content for the photocatalytic activity of the ZnO/mpg-C3N4 composites is 24.9%, which is almost 2.3 times as high as that of pure mpg-C3N4 under visible light, and 1.9 times higher than that under simulated solar irradiation. Zinc Oxide 12-15 N-methylpurine DNA glycosylase Homo sapiens 147-150 25043592-4 2014 The optimal ZnO content for the photocatalytic activity of the ZnO/mpg-C3N4 composites is 24.9%, which is almost 2.3 times as high as that of pure mpg-C3N4 under visible light, and 1.9 times higher than that under simulated solar irradiation. Zinc Oxide 63-66 N-methylpurine DNA glycosylase Homo sapiens 67-70 25043592-4 2014 The optimal ZnO content for the photocatalytic activity of the ZnO/mpg-C3N4 composites is 24.9%, which is almost 2.3 times as high as that of pure mpg-C3N4 under visible light, and 1.9 times higher than that under simulated solar irradiation. Zinc Oxide 63-66 N-methylpurine DNA glycosylase Homo sapiens 147-150 25043592-5 2014 The enhancement in photocatalytic activity should be assigned to the effective separation and transfer of photogenerated charges coming from the well-matched overlapping band-structure between mpg-C3N4 and ZnO. Zinc Oxide 206-209 N-methylpurine DNA glycosylase Homo sapiens 193-196 25043592-6 2014 Radical trap experiments show that both ZnO/mpg-C3N4 composites and mpg-C3N4 have the same photodegradation mechanism, and the holes are their main oxidative species for MB degradation. Zinc Oxide 40-43 N-methylpurine DNA glycosylase Homo sapiens 44-47 25144692-0 2014 Band gap engineering of ZnO using core/shell morphology with environmentally benign Ag2S sensitizer for efficient light harvesting and enhanced visible-light photocatalysis. Zinc Oxide 24-27 angiotensin II receptor type 1 Homo sapiens 84-88 25144692-3 2014 We engineered the band gap of ZnO nanorods by introducing the core/shell geometry with Ag2S sensitizer as the shell. Zinc Oxide 30-33 angiotensin II receptor type 1 Homo sapiens 87-91 25144692-5 2014 To unveil the superiority of Ag2S as a sensitizer in engineering the band gap of ZnO in comparison to the Cd-based sensitizers, we also designed ZnO/CdS core/shell nanostructures having the same shell thickness. Zinc Oxide 81-84 angiotensin II receptor type 1 Homo sapiens 29-33 25144692-7 2014 The results imply that the ZnO/Ag2S core/shell nanostructures reveal 40- and 2-fold enhancement in degradation constant in comparison to the pure ZnO and ZnO/CdS core/shell nanostructures, respectively. Zinc Oxide 27-30 angiotensin II receptor type 1 Homo sapiens 31-35 25144692-7 2014 The results imply that the ZnO/Ag2S core/shell nanostructures reveal 40- and 2-fold enhancement in degradation constant in comparison to the pure ZnO and ZnO/CdS core/shell nanostructures, respectively. Zinc Oxide 146-149 angiotensin II receptor type 1 Homo sapiens 31-35 25144692-7 2014 The results imply that the ZnO/Ag2S core/shell nanostructures reveal 40- and 2-fold enhancement in degradation constant in comparison to the pure ZnO and ZnO/CdS core/shell nanostructures, respectively. Zinc Oxide 146-149 angiotensin II receptor type 1 Homo sapiens 31-35 25144692-8 2014 This high efficiency is elucidated in terms of (i) efficient light harvesting owing to the incorporation of Ag2S and (ii) smaller conduction band offset between ZnO and Ag2S, promoting more efficient charge separation at the core/shell interface. Zinc Oxide 161-164 angiotensin II receptor type 1 Homo sapiens 108-112 25144692-9 2014 A credible photodegradation mechanism for the MB dye deploying ZnO/Ag2S core/shell nanostructures is proposed from the analysis of involved active species such as hydroxyl radicals (OH( )), electrons (e(-)(CB)), holes (h(+)(VB)), and superoxide radical anions (O2( -)) in the photodegradation process utilizing various active species scavengers and EPR spectroscopy. Zinc Oxide 63-66 angiotensin II receptor type 1 Homo sapiens 67-71 24973873-6 2014 Catalase activity in serum samples was significantly higher in the 20- and 60-nano-ZnO groups relative to the control and 100-nano-ZnO birds, but catalase activity in liver tissue was not affected by different nano-ZnO levels. Zinc Oxide 131-134 catalase Homo sapiens 0-8 24973873-6 2014 Catalase activity in serum samples was significantly higher in the 20- and 60-nano-ZnO groups relative to the control and 100-nano-ZnO birds, but catalase activity in liver tissue was not affected by different nano-ZnO levels. Zinc Oxide 131-134 catalase Homo sapiens 0-8 24878115-6 2014 Cells on ZnO thin films exhibited a 43% and 68% decrease in cell viability using the MTT and 7-AAD/Annexin V flow cytometry assays, respectively, after a 24-h exposure as compared to controls. Zinc Oxide 9-12 annexin A5 Homo sapiens 99-108 25008783-5 2014 Interestingly, the BGE and DE from oxygen vacancies of ZnO in the ZnO/CdS nano-composites are almost entirely quenched, while DE from zinc vacancies changes little. Zinc Oxide 55-58 CDP-diacylglycerol synthase 1 Homo sapiens 70-73 25232299-4 2014 Highly efficient ZnO excitonic recombination at reverse bias is caused by electrons tunneling from deep-level states near the n-ZnO/p-GaN interface to the conduction band in n-ZnO. Zinc Oxide 17-20 gigaxonin Homo sapiens 134-137 25008783-3 2014 The XEOL from ZnO/CdS NW arrays exhibits one weak ultraviolet (UV) emission at 375 nm, one strong green emission at 512 nm, and two broad infrared (IR) emissions at 750 and 900 nm. Zinc Oxide 14-17 CDP-diacylglycerol synthase 1 Homo sapiens 18-21 25008783-5 2014 Interestingly, the BGE and DE from oxygen vacancies of ZnO in the ZnO/CdS nano-composites are almost entirely quenched, while DE from zinc vacancies changes little. Zinc Oxide 66-69 CDP-diacylglycerol synthase 1 Homo sapiens 70-73 24946839-0 2014 Promising ZnO-based DSSC performance using HMP molecular dyes of high extinction coefficients. Zinc Oxide 10-13 inner membrane mitochondrial protein Homo sapiens 43-46 24919039-0 2014 Ag-ZnO nanoreactor grown on FTO substrate exhibiting high heterogeneous photocatalytic efficiency. Zinc Oxide 3-6 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 28-31 24650882-2 2014 Metal oxide NPs (ZnO, CeO2, TiO2 and Al2O3) induced changes in the expression levels of adhesion molecules and the C-X-C chemokine receptor type 4 (CXCR4) in these cells. Zinc Oxide 17-20 C-X-C motif chemokine receptor 4 Homo sapiens 115-146 24650882-2 2014 Metal oxide NPs (ZnO, CeO2, TiO2 and Al2O3) induced changes in the expression levels of adhesion molecules and the C-X-C chemokine receptor type 4 (CXCR4) in these cells. Zinc Oxide 17-20 C-X-C motif chemokine receptor 4 Homo sapiens 148-153 24424259-7 2014 For larval locomotor activity, co-exposure to NAC rescued the behavioral effect caused by ZnO NP, but co-exposure to BSO did not exacerbate the effect. Zinc Oxide 90-93 melanocyte inducing transcription factor a Danio rerio 46-49 25030846-0 2014 CdS sensitized 3D hierarchical TiO2/ZnO heterostructure for efficient solar energy conversion. Zinc Oxide 36-39 CDP-diacylglycerol synthase 1 Homo sapiens 0-3 25030846-3 2014 Here, a three dimensional (3D) hierarchical heterostructure, consisting of CdS sensitized one dimensional (1D) ZnO nanorods deposited on two dimensional (2D) TiO2 (001) nanosheet, is prepared via a solution-process method. Zinc Oxide 111-114 CDP-diacylglycerol synthase 1 Homo sapiens 75-78 25030846-4 2014 Such heterstructure exhibits significantly enhanced photoelectric and photocatalytic H2 evolution performance compared with CdS sensitized 1D ZnO nanorods/1D TiO2 nanorods photoanode, as a result of the more efficient light harvesting over the entire visible light spectrum and the effective electron transport through a highly connected 3D network. Zinc Oxide 142-145 CDP-diacylglycerol synthase 1 Homo sapiens 124-127 25046356-1 2014 Adsorption of H2O and CO2 on zinc oxide surfaces was studied by gas adsorption calorimetry on nanocrystalline samples prepared by laser evaporation in oxygen to minimize surface impurities and degassed at 450 C. Differential enthalpies of H2O and CO2 chemisorption are in the range -150 +-10 kJ/mol and -110 +-10 kJ/mol up to a coverage of 2 molecules per nm(2). Zinc Oxide 29-39 complement C2 Homo sapiens 14-25 24919039-1 2014 This Research Article reports an unusually high efficiency heterogeneous photodegradation of methyl orange (MO) in the presence of Ag nanoparticle-loaded ZnO quasi-nanotube or nanoreactor (A-ZNRs) nanocatalyst grown on FTO substrate. Zinc Oxide 154-157 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 219-222 23946240-0 2014 Effects of SiO2, SrO, MgO, and ZnO dopants in tricalcium phosphates on osteoblastic Runx2 expression. Zinc Oxide 31-34 RUNX family transcription factor 2 Homo sapiens 84-89 24567946-4 2014 The present study was designed to evaluate the intraperitoneal administration of an opioidergic receptor agonist and antagonist of as well as the intra CA1 administration of an opioidergic receptor antagonist on the anxiolytic properties of nano and conventional ZnO in adult male Wistar rats. Zinc Oxide 263-266 carbonic anhydrase 1 Rattus norvegicus 152-155 24593842-0 2014 Toll-like receptor 6 mediated inflammatory and functional responses of zinc oxide nanoparticles primed macrophages. Zinc Oxide 71-81 toll like receptor 6 Homo sapiens 0-20 25045341-0 2014 Efficiency improvement of InGaP/GaAs/Ge solar cells by hydrothermal-deposited ZnO nanotube structure. Zinc Oxide 78-81 regenerating family member 3 alpha Homo sapiens 26-31 24910333-0 2014 Immobilized Candida antarctica lipase B on ZnO nanowires/macroporous silica composites for catalyzing chiral resolution of (R,S)-2-octanol. Zinc Oxide 43-46 PAN0_003d1715 Moesziomyces antarcticus 31-37 23956359-0 2014 Zinc oxide influences intestinal integrity, the expressions of genes associated with inflammation and TLR4-myeloid differentiation factor 88 signaling pathways in weanling pigs. Zinc Oxide 0-10 toll like receptor 4 Sus scrofa 102-106 23956359-3 2014 The results showed that supplemental ZnO improved daily gain and feed intake, decreased post weaning scour scores, increased villus height and villus height:crypt depth ratio at the jejunal mucosa, and decreased diamine oxidase activity and endotoxin concentration in plasma. Zinc Oxide 37-40 amine oxidase copper containing 1 Sus scrofa 212-227 23956359-4 2014 The intestinal mRNA levels of TLR4 and its downstream signals, including MyD88, IL-1 receptor-associated kinase 1 and TNF-alpha receptor-associated factor 6, were decreased, and the expressions of intestinal pro-inflammatory cytokines and chemokines were decreased simultaneously in the ZnO-supplemented piglets. Zinc Oxide 287-290 toll like receptor 4 Sus scrofa 30-34 23956359-7 2014 The results indicated that the protective effects of ZnO on intestinal integrity were closely related to decreasing the expressions of genes associated with inflammation through inhibiting the TLR4-MyD88 signaling pathways. Zinc Oxide 53-56 toll like receptor 4 Sus scrofa 193-197 23956359-7 2014 The results indicated that the protective effects of ZnO on intestinal integrity were closely related to decreasing the expressions of genes associated with inflammation through inhibiting the TLR4-MyD88 signaling pathways. Zinc Oxide 53-56 MYD88 innate immune signal transduction adaptor Sus scrofa 198-203 24801357-5 2014 The results reveal that the exposed (0001) planes of the ZnO nanoplates promote better ethanol adsorption by interacting with the surface oxygen p (O2p) orbitals and stretching the O-H bond to lower the adsorption energy, leading to the sensitivity enhancement of the nanoplates. Zinc Oxide 57-60 immunoglobulin kappa variable 1D-39 Homo sapiens 148-151 24746987-5 2014 The 16-hour exposure to ZnO particles increased the level of monocyte chemotactic protein-1 (MCP-1) and induced the migration of THP-1 monocyte mediated by increased MCP-1. Zinc Oxide 24-27 C-C motif chemokine ligand 2 Homo sapiens 61-91 24746987-5 2014 The 16-hour exposure to ZnO particles increased the level of monocyte chemotactic protein-1 (MCP-1) and induced the migration of THP-1 monocyte mediated by increased MCP-1. Zinc Oxide 24-27 C-C motif chemokine ligand 2 Homo sapiens 93-98 24746987-5 2014 The 16-hour exposure to ZnO particles increased the level of monocyte chemotactic protein-1 (MCP-1) and induced the migration of THP-1 monocyte mediated by increased MCP-1. Zinc Oxide 24-27 GLI family zinc finger 2 Homo sapiens 129-134 24746987-5 2014 The 16-hour exposure to ZnO particles increased the level of monocyte chemotactic protein-1 (MCP-1) and induced the migration of THP-1 monocyte mediated by increased MCP-1. Zinc Oxide 24-27 C-C motif chemokine ligand 2 Homo sapiens 166-171 24746987-6 2014 Exposure to ZnO particles also induced adhesion of THP-1 cells to HUVECs. Zinc Oxide 12-15 GLI family zinc finger 2 Homo sapiens 51-56 24746987-7 2014 Moreover, exposure to ZnO particles, but not TiO2 particles, upregulated the expression of membrane scavenger receptors of modified LDL and increased cholesterol uptake in THP-1 monocytes/macrophages. Zinc Oxide 22-25 GLI family zinc finger 2 Homo sapiens 172-177 24872799-2 2014 ZnO nanostructures were grown in both tree-like and nanorod (NR) arrays on an AZO/FTO film structure by using a hydrothermal method. Zinc Oxide 0-3 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 82-85 24508815-2 2014 In this study, a photoelectrochemical sensor based on flower-like ZnO nanostructures was developed for Pb(2+) detection, using a Pb(2+)-dependent DNAzyme as the recognition unit and a double-strand DNA intercalator, Ru(bpy)2(dppz)(2+) (bpy=2,2"-bipyridine, dppz=dipyrido[3,2-a:2",3"-c] phenazine) as the photoelectrochemical signal reporter. Zinc Oxide 66-69 basic charge Y-linked 2 Homo sapiens 216-224 24362079-3 2014 The obtained results demonstrate that nitrogen doping in ZnO matrix offers a striking electrocatalytic activity to the immobilized uricase towards the oxidation of analyte (uric acid) and promotes the direct transfer of electrons from active sites of enzyme onto the electrode without any mediator. Zinc Oxide 57-60 urate oxidase (pseudogene) Homo sapiens 131-138 24384261-5 2014 In addition, we demonstrated the QD-based immunoassay of carcinoembryonic antigen (CEA) on a ZnO nanowire substrate, showing an excellent immunoassay performance with a very low detection limit (0.001 ng/mL) and a large detection range up to 100 ng/mL. Zinc Oxide 93-96 CEA cell adhesion molecule 3 Homo sapiens 57-81 24384261-5 2014 In addition, we demonstrated the QD-based immunoassay of carcinoembryonic antigen (CEA) on a ZnO nanowire substrate, showing an excellent immunoassay performance with a very low detection limit (0.001 ng/mL) and a large detection range up to 100 ng/mL. Zinc Oxide 93-96 CEA cell adhesion molecule 3 Homo sapiens 83-86 24525258-4 2014 20 wt% ZnO-TiO2 photocatalyst exhibited much higher photocatalytic activity than pure TiO2, ZnO and P-25 in the degradation of 4-chlorophenol under low UV irradiation. Zinc Oxide 7-10 tubulin polymerization promoting protein Homo sapiens 100-104 24766196-3 2014 In this work, an inexpensive ZnO nanomulberry (NMB) decorated glass slide is investigated as a superior substrate to nonenzymatically amplify the signal of protein microarray for sensitive detection, accomplishing a limit of detection (LOD) of 1 pg mL(-1) and a broad dynamic range of 1 pg mL(-1) to 1 mug mL(-1) to detect an important cancer biomarker, carcinoembryonic antigen (CEA) in 10% human serum. Zinc Oxide 29-32 CEA cell adhesion molecule 3 Homo sapiens 354-378 24766196-3 2014 In this work, an inexpensive ZnO nanomulberry (NMB) decorated glass slide is investigated as a superior substrate to nonenzymatically amplify the signal of protein microarray for sensitive detection, accomplishing a limit of detection (LOD) of 1 pg mL(-1) and a broad dynamic range of 1 pg mL(-1) to 1 mug mL(-1) to detect an important cancer biomarker, carcinoembryonic antigen (CEA) in 10% human serum. Zinc Oxide 29-32 CEA cell adhesion molecule 3 Homo sapiens 380-383 24614525-0 2014 Zinc oxide nanoparticles induce apoptosis by enhancement of autophagy via PI3K/Akt/mTOR inhibition. Zinc Oxide 0-10 AKT serine/threonine kinase 1 Homo sapiens 79-82 24614525-0 2014 Zinc oxide nanoparticles induce apoptosis by enhancement of autophagy via PI3K/Akt/mTOR inhibition. Zinc Oxide 0-10 mechanistic target of rapamycin kinase Homo sapiens 83-87 24614525-4 2014 ZnO NPs also activated the cleavage of apoptosis markers like caspases 3, 8 and 9. Zinc Oxide 0-3 caspase 3 Homo sapiens 62-81 24614525-7 2014 Phosphorylated Akt, PI3K and mTOR were significantly decreased on ZnO NPs exposure. Zinc Oxide 66-69 AKT serine/threonine kinase 1 Homo sapiens 15-18 24614525-7 2014 Phosphorylated Akt, PI3K and mTOR were significantly decreased on ZnO NPs exposure. Zinc Oxide 66-69 mechanistic target of rapamycin kinase Homo sapiens 29-33 24718232-1 2014 Heterogenous nanostructures shaped with CdS covered ZnO (ZnO/CdS) core/shell nanorods (NRs) are fabricated on indium-tin-oxide by pulsed laser deposition of CdS on hydrothermally grown ZnO NRs and characterized through morphology examination, structure characterization, photoluminescence and optical absorption measurements. Zinc Oxide 52-55 CDP-diacylglycerol synthase 1 Homo sapiens 40-43 24510408-6 2014 The results also showed that responses of candidate genes to different chemicals were distinct, 18S rRNA was the best for BalphaP and chlorpyrifos, tba-1 was the most stable gene for diazinon and gossypol treatments, while pmp-3 was more stable for zinc oxide exposure. Zinc Oxide 249-259 Tubulin alpha chain Caenorhabditis elegans 148-153 24510408-6 2014 The results also showed that responses of candidate genes to different chemicals were distinct, 18S rRNA was the best for BalphaP and chlorpyrifos, tba-1 was the most stable gene for diazinon and gossypol treatments, while pmp-3 was more stable for zinc oxide exposure. Zinc Oxide 249-259 Peroxisomal Membrane Protein related Caenorhabditis elegans 223-228 24291267-3 2014 The biosensor is functionalized by first applying ZnO nanorods to increase the surface area for attracting electrical charges of EGFR (epidermal growth factor receptor) antibodies. Zinc Oxide 50-53 epidermal growth factor receptor Homo sapiens 129-133 24291267-3 2014 The biosensor is functionalized by first applying ZnO nanorods to increase the surface area for attracting electrical charges of EGFR (epidermal growth factor receptor) antibodies. Zinc Oxide 50-53 epidermal growth factor receptor Homo sapiens 135-167 24632943-1 2014 With the help of density functional calculations using the HSE and PBE functionals, it is shown that incorporation of nitrogen into ZnO nanoparticles is energetically less costly compared to ZnO bulk, due to charge transfer between Zn dangling bonds and the NO impurity. Zinc Oxide 132-135 enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase Homo sapiens 67-70 24718232-1 2014 Heterogenous nanostructures shaped with CdS covered ZnO (ZnO/CdS) core/shell nanorods (NRs) are fabricated on indium-tin-oxide by pulsed laser deposition of CdS on hydrothermally grown ZnO NRs and characterized through morphology examination, structure characterization, photoluminescence and optical absorption measurements. Zinc Oxide 57-60 CDP-diacylglycerol synthase 1 Homo sapiens 40-43 24718232-1 2014 Heterogenous nanostructures shaped with CdS covered ZnO (ZnO/CdS) core/shell nanorods (NRs) are fabricated on indium-tin-oxide by pulsed laser deposition of CdS on hydrothermally grown ZnO NRs and characterized through morphology examination, structure characterization, photoluminescence and optical absorption measurements. Zinc Oxide 57-60 CDP-diacylglycerol synthase 1 Homo sapiens 40-43 24718232-3 2014 Compared with bare ZnO NRs, the fabricated ZnO/CdS core/shell NRs present an extended photo-response and have optical properties corresponding to the two excitonic band-gaps of ZnO and CdS as well as the effective band-gap formed between the conduction band minimum of ZnO and the valence band maximum of CdS. Zinc Oxide 19-22 CDP-diacylglycerol synthase 1 Homo sapiens 47-50 24718232-3 2014 Compared with bare ZnO NRs, the fabricated ZnO/CdS core/shell NRs present an extended photo-response and have optical properties corresponding to the two excitonic band-gaps of ZnO and CdS as well as the effective band-gap formed between the conduction band minimum of ZnO and the valence band maximum of CdS. Zinc Oxide 43-46 CDP-diacylglycerol synthase 1 Homo sapiens 47-50 24718232-3 2014 Compared with bare ZnO NRs, the fabricated ZnO/CdS core/shell NRs present an extended photo-response and have optical properties corresponding to the two excitonic band-gaps of ZnO and CdS as well as the effective band-gap formed between the conduction band minimum of ZnO and the valence band maximum of CdS. Zinc Oxide 43-46 CDP-diacylglycerol synthase 1 Homo sapiens 185-188 24718232-3 2014 Compared with bare ZnO NRs, the fabricated ZnO/CdS core/shell NRs present an extended photo-response and have optical properties corresponding to the two excitonic band-gaps of ZnO and CdS as well as the effective band-gap formed between the conduction band minimum of ZnO and the valence band maximum of CdS. Zinc Oxide 43-46 CDP-diacylglycerol synthase 1 Homo sapiens 185-188 24718232-3 2014 Compared with bare ZnO NRs, the fabricated ZnO/CdS core/shell NRs present an extended photo-response and have optical properties corresponding to the two excitonic band-gaps of ZnO and CdS as well as the effective band-gap formed between the conduction band minimum of ZnO and the valence band maximum of CdS. Zinc Oxide 43-46 CDP-diacylglycerol synthase 1 Homo sapiens 47-50 24718232-3 2014 Compared with bare ZnO NRs, the fabricated ZnO/CdS core/shell NRs present an extended photo-response and have optical properties corresponding to the two excitonic band-gaps of ZnO and CdS as well as the effective band-gap formed between the conduction band minimum of ZnO and the valence band maximum of CdS. Zinc Oxide 43-46 CDP-diacylglycerol synthase 1 Homo sapiens 185-188 24718232-3 2014 Compared with bare ZnO NRs, the fabricated ZnO/CdS core/shell NRs present an extended photo-response and have optical properties corresponding to the two excitonic band-gaps of ZnO and CdS as well as the effective band-gap formed between the conduction band minimum of ZnO and the valence band maximum of CdS. Zinc Oxide 43-46 CDP-diacylglycerol synthase 1 Homo sapiens 185-188 24718232-3 2014 Compared with bare ZnO NRs, the fabricated ZnO/CdS core/shell NRs present an extended photo-response and have optical properties corresponding to the two excitonic band-gaps of ZnO and CdS as well as the effective band-gap formed between the conduction band minimum of ZnO and the valence band maximum of CdS. Zinc Oxide 43-46 CDP-diacylglycerol synthase 1 Homo sapiens 47-50 24718232-3 2014 Compared with bare ZnO NRs, the fabricated ZnO/CdS core/shell NRs present an extended photo-response and have optical properties corresponding to the two excitonic band-gaps of ZnO and CdS as well as the effective band-gap formed between the conduction band minimum of ZnO and the valence band maximum of CdS. Zinc Oxide 43-46 CDP-diacylglycerol synthase 1 Homo sapiens 185-188 24718232-3 2014 Compared with bare ZnO NRs, the fabricated ZnO/CdS core/shell NRs present an extended photo-response and have optical properties corresponding to the two excitonic band-gaps of ZnO and CdS as well as the effective band-gap formed between the conduction band minimum of ZnO and the valence band maximum of CdS. Zinc Oxide 43-46 CDP-diacylglycerol synthase 1 Homo sapiens 185-188 24554449-0 2014 Transcriptional and posttranscriptional regulation and endocytosis were involved in zinc oxide nanoparticle-induced interleukin-8 overexpression in human bronchial epithelial cells. Zinc Oxide 84-94 C-X-C motif chemokine ligand 8 Homo sapiens 116-129 24554449-1 2014 Inhaled zinc oxide nanoparticles (ZnO-NPs) can induce lung inflammation through released inflammatory mediators, such as interleukin 8 (IL-8), from airways. Zinc Oxide 8-18 C-X-C motif chemokine ligand 8 Homo sapiens 121-134 24554449-1 2014 Inhaled zinc oxide nanoparticles (ZnO-NPs) can induce lung inflammation through released inflammatory mediators, such as interleukin 8 (IL-8), from airways. Zinc Oxide 8-18 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 24554449-4 2014 The effect of ZnO-NPs on IL-8 mRNA stability was examined using mRNA decay assay. Zinc Oxide 14-17 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 24554449-7 2014 Exposure to ZnO-NPs significantly increased the expression of IL-8 mRNA and protein in a dose-dependent manner. Zinc Oxide 12-15 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 24554449-12 2014 Exposure to ZnO-NPs induced IL-8 gene expression through transcriptional activation and mRNA stabilization. Zinc Oxide 12-15 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 24734682-9 2014 EXAFS spectra indicate that Co2(BDC)2dabco has the Co--O bond distance of 2.030 A with the coordination number of 4.2 while Zn2(BDC)2dabco has 2.015 angstroms bond distance of Zn--O with the coordination number of 3.4. Zinc Oxide 176-181 complement C2 Homo sapiens 28-37 24490819-5 2014 More importantly, ZnO NPs at noncytotoxic concentration, but not CeO2 NPs, can induce significant cellular ER stress response with higher expression of spliced xbp-1, chop, and caspase-12 at the mRNA level, and associated ER marker proteins including BiP, Chop, GADD34, p-PERK, p-eIF2alpha, and cleaved Caspase-12 at the protein levels. Zinc Oxide 18-21 X-box binding protein 1 Homo sapiens 160-165 24002615-10 2014 Immunofluorescence staining on lung tissue slices from animals exposed to ZnO NPs showed an increase in CD11b reactivity at days 1 and 7, followed by a decrease in CD11b positive cells at 28 days. Zinc Oxide 74-77 integrin subunit alpha M Homo sapiens 104-109 24002615-10 2014 Immunofluorescence staining on lung tissue slices from animals exposed to ZnO NPs showed an increase in CD11b reactivity at days 1 and 7, followed by a decrease in CD11b positive cells at 28 days. Zinc Oxide 74-77 integrin subunit alpha M Homo sapiens 164-169 24684892-10 2014 Sub-acute exposure to ZnO NPs caused an increase of macrophages in BAL fluid and a moderate increase in IL-12(p40) and MIP-1alpha, but no other inflammatory or toxic responses were observed. Zinc Oxide 22-25 interleukin 12b Mus musculus 110-113 24684892-10 2014 Sub-acute exposure to ZnO NPs caused an increase of macrophages in BAL fluid and a moderate increase in IL-12(p40) and MIP-1alpha, but no other inflammatory or toxic responses were observed. Zinc Oxide 22-25 chemokine (C-C motif) ligand 3 Mus musculus 119-129 24490819-5 2014 More importantly, ZnO NPs at noncytotoxic concentration, but not CeO2 NPs, can induce significant cellular ER stress response with higher expression of spliced xbp-1, chop, and caspase-12 at the mRNA level, and associated ER marker proteins including BiP, Chop, GADD34, p-PERK, p-eIF2alpha, and cleaved Caspase-12 at the protein levels. Zinc Oxide 18-21 DNA damage inducible transcript 3 Homo sapiens 167-171 24490819-5 2014 More importantly, ZnO NPs at noncytotoxic concentration, but not CeO2 NPs, can induce significant cellular ER stress response with higher expression of spliced xbp-1, chop, and caspase-12 at the mRNA level, and associated ER marker proteins including BiP, Chop, GADD34, p-PERK, p-eIF2alpha, and cleaved Caspase-12 at the protein levels. Zinc Oxide 18-21 heat shock protein family A (Hsp70) member 5 Homo sapiens 251-254 24490819-5 2014 More importantly, ZnO NPs at noncytotoxic concentration, but not CeO2 NPs, can induce significant cellular ER stress response with higher expression of spliced xbp-1, chop, and caspase-12 at the mRNA level, and associated ER marker proteins including BiP, Chop, GADD34, p-PERK, p-eIF2alpha, and cleaved Caspase-12 at the protein levels. Zinc Oxide 18-21 DNA damage inducible transcript 3 Homo sapiens 256-260 24490819-5 2014 More importantly, ZnO NPs at noncytotoxic concentration, but not CeO2 NPs, can induce significant cellular ER stress response with higher expression of spliced xbp-1, chop, and caspase-12 at the mRNA level, and associated ER marker proteins including BiP, Chop, GADD34, p-PERK, p-eIF2alpha, and cleaved Caspase-12 at the protein levels. Zinc Oxide 18-21 protein phosphatase 1 regulatory subunit 15A Homo sapiens 262-268 24624962-7 2014 In addition, exposure of the cultured cells to ZnO NPs led to phosphorylation of c-Jun N-terminal kinase (JNK), extracellular signal-related kinase (ERK), and p38 mitogen-activated protein kinase (p38 MAPK). Zinc Oxide 47-50 mitogen-activated protein kinase 1 Homo sapiens 112-147 24528697-2 2014 Characterization of functionalized ZnO nanoparticles were carried out by Fourier transform infrared spectra (FT-IR), elemental analysis (CHN), Thermogravimetric analysis (TGA), X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM) and transmission electron microscopy (TEM). Zinc Oxide 35-38 chimerin 1 Homo sapiens 137-140 24528697-3 2014 The amount of MCT-beta-CD bonded to the ZnO surface was determined by CHN and TGA analysis. Zinc Oxide 40-43 chimerin 1 Homo sapiens 70-73 24624962-0 2014 ZnO nanoparticle-induced oxidative stress triggers apoptosis by activating JNK signaling pathway in cultured primary astrocytes. Zinc Oxide 0-3 mitogen-activated protein kinase 8 Homo sapiens 75-78 24624962-7 2014 In addition, exposure of the cultured cells to ZnO NPs led to phosphorylation of c-Jun N-terminal kinase (JNK), extracellular signal-related kinase (ERK), and p38 mitogen-activated protein kinase (p38 MAPK). Zinc Oxide 47-50 mitogen-activated protein kinase 1 Homo sapiens 149-152 24624962-7 2014 In addition, exposure of the cultured cells to ZnO NPs led to phosphorylation of c-Jun N-terminal kinase (JNK), extracellular signal-related kinase (ERK), and p38 mitogen-activated protein kinase (p38 MAPK). Zinc Oxide 47-50 mitogen-activated protein kinase 8 Homo sapiens 81-104 24624962-7 2014 In addition, exposure of the cultured cells to ZnO NPs led to phosphorylation of c-Jun N-terminal kinase (JNK), extracellular signal-related kinase (ERK), and p38 mitogen-activated protein kinase (p38 MAPK). Zinc Oxide 47-50 mitogen-activated protein kinase 14 Homo sapiens 159-195 24624962-7 2014 In addition, exposure of the cultured cells to ZnO NPs led to phosphorylation of c-Jun N-terminal kinase (JNK), extracellular signal-related kinase (ERK), and p38 mitogen-activated protein kinase (p38 MAPK). Zinc Oxide 47-50 mitogen-activated protein kinase 8 Homo sapiens 106-109 24624962-7 2014 In addition, exposure of the cultured cells to ZnO NPs led to phosphorylation of c-Jun N-terminal kinase (JNK), extracellular signal-related kinase (ERK), and p38 mitogen-activated protein kinase (p38 MAPK). Zinc Oxide 47-50 mitogen-activated protein kinase 14 Homo sapiens 197-205 24618047-0 2014 ZnO nanosheet arrays constructed on weaved titanium wire for CdS-sensitized solar cells. Zinc Oxide 0-3 CDP-diacylglycerol synthase 1 Homo sapiens 61-64 24249633-1 2014 Two flame-based synthesis methods are presented for fabricating ZnO-nanostructure-based UV photodetectors: burner flame transport synthesis (B-FTS)and crucible flame transport synthesis (C-FTS). Zinc Oxide 64-67 AKT interacting protein Homo sapiens 143-146 24249633-1 2014 Two flame-based synthesis methods are presented for fabricating ZnO-nanostructure-based UV photodetectors: burner flame transport synthesis (B-FTS)and crucible flame transport synthesis (C-FTS). Zinc Oxide 64-67 AKT interacting protein Homo sapiens 189-192 24249633-2 2014 B-FTS allows rapid growth of ZnO nanotetrapods and in situ bridging of them into electrical contacts. Zinc Oxide 29-32 AKT interacting protein Homo sapiens 2-5 24618047-2 2014 CdS nanoparticles were deposited onto the ZnO nanosheet arrays using the successive ionic layer adsorption and reaction method to make a photoanode. Zinc Oxide 42-45 CDP-diacylglycerol synthase 1 Homo sapiens 0-3 24333255-0 2014 Metalloproteins and phytochelatin synthase may confer protection against zinc oxide nanoparticle induced toxicity in Caenorhabditis elegans. Zinc Oxide 73-83 Glutathione gamma-glutamylcysteinyltransferase Caenorhabditis elegans 20-42 24594662-4 2014 As a result, the sensitivity of the PCB-orientated SPV sensor is much improved by showing amplified variation of the SPV-signals perturbed by PCBs adsorbed on the ZnO-CuPc@porous-ZnO sensitive material. Zinc Oxide 163-166 pyruvate carboxylase Homo sapiens 36-39 24374571-4 2014 ZnO Nps could synergistically potentiate ISO to induce apoptosis through resulting in mitochondrial dysfunction, inhibiting the phosphorylation of Akt and ERK1/2, and enhancing the phosphorylation of JNK and P38. Zinc Oxide 0-3 AKT serine/threonine kinase 1 Homo sapiens 147-150 24374571-4 2014 ZnO Nps could synergistically potentiate ISO to induce apoptosis through resulting in mitochondrial dysfunction, inhibiting the phosphorylation of Akt and ERK1/2, and enhancing the phosphorylation of JNK and P38. Zinc Oxide 0-3 mitogen-activated protein kinase 3 Homo sapiens 155-161 24374571-4 2014 ZnO Nps could synergistically potentiate ISO to induce apoptosis through resulting in mitochondrial dysfunction, inhibiting the phosphorylation of Akt and ERK1/2, and enhancing the phosphorylation of JNK and P38. Zinc Oxide 0-3 mitogen-activated protein kinase 8 Homo sapiens 200-203 24374571-4 2014 ZnO Nps could synergistically potentiate ISO to induce apoptosis through resulting in mitochondrial dysfunction, inhibiting the phosphorylation of Akt and ERK1/2, and enhancing the phosphorylation of JNK and P38. Zinc Oxide 0-3 mitogen-activated protein kinase 1 Homo sapiens 208-211 24555677-7 2014 Exposure of THP-1 cells to both sizes of ZnO stimulated and increased release of proinflammatory cytokines interleukin (IL)-1beta, tumor necrosis factor (TNF)-alpha, and IL-6, as well as chemokine IL-8, and upregulated the expression of monocyte chemoattractant protein-1 and cyclooxygenase-2 genes. Zinc Oxide 41-44 interleukin 1 beta Homo sapiens 107-129 24184009-2 2014 In this paper, we report a simple method for the synthesis of a new (101) high-energy plane bounded ZnO nanocubes photocatalyst directly on the FTO surface, using a seed-mediated ultrasonic assisted hydrolysis process. Zinc Oxide 100-103 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 144-147 24569599-4 2014 Here we show how to probe the charge carrier density of zinc oxide thin films by Scanning Kelvin Probe Microscopy, a technique that allows measuring the contact potential difference between the tip and the sample surface with high spatial resolution. Zinc Oxide 56-66 TOR signaling pathway regulator Homo sapiens 194-197 24572004-0 2014 Deposition of F-doped ZnO transparent thin films using ZnF2-doped ZnO target under different sputtering substrate temperatures. Zinc Oxide 22-25 zinc finger protein 2 Homo sapiens 55-59 24572004-0 2014 Deposition of F-doped ZnO transparent thin films using ZnF2-doped ZnO target under different sputtering substrate temperatures. Zinc Oxide 66-69 zinc finger protein 2 Homo sapiens 55-59 24572004-1 2014 Highly transparent and conducting fluorine-doped ZnO (FZO) thin films were deposited onto glass substrates by radio-frequency (RF) magnetron sputtering, using 1.5 wt% zinc fluoride (ZnF2)-doped ZnO as sputtering target. Zinc Oxide 194-197 zinc finger protein 2 Homo sapiens 182-186 24001511-2 2014 ZnO nanorod matrix was synthesized by low temperature aqueous method and provided a favorable environment for the immobilization of glucose oxidase (GOx). Zinc Oxide 0-3 hydroxyacid oxidase 1 Homo sapiens 132-147 24001511-2 2014 ZnO nanorod matrix was synthesized by low temperature aqueous method and provided a favorable environment for the immobilization of glucose oxidase (GOx). Zinc Oxide 0-3 hydroxyacid oxidase 1 Homo sapiens 149-152 24225181-0 2014 Zinc oxide nanoparticles provide an adjuvant effect to ovalbumin via a Th2 response in Balb/c mice. Zinc Oxide 0-10 serine (or cysteine) peptidase inhibitor, clade B, member 1, pseudogene Mus musculus 55-64 24225181-0 2014 Zinc oxide nanoparticles provide an adjuvant effect to ovalbumin via a Th2 response in Balb/c mice. Zinc Oxide 0-10 heart and neural crest derivatives expressed 2 Mus musculus 71-74 24745255-2 2014 The obtained ZnO nanostructures were characterized by X-ray diffraction (XRD), high resolution scanning electron microscopy (HR-SEM), high resolution transmission electron microscopy (HR-TEM), energy dispersive X-ray analysis (EDX), diffuse reflectance (DRS) and photoluminescence (PL) spectroscopy. Zinc Oxide 13-16 sushi repeat containing protein X-linked Homo sapiens 254-257 24477262-5 2014 Zinc oxide and silver nanoparticles induce a significant reduced blood glucose, higher serum insulin, higher glucokinase activity higher expression level of insulin, insulin receptor, GLUT-2 and glucokinase genes in diabetic rats treated with zinc oxide, silver nanoparticles and insulin. Zinc Oxide 0-10 insulin receptor Rattus norvegicus 166-182 24477262-5 2014 Zinc oxide and silver nanoparticles induce a significant reduced blood glucose, higher serum insulin, higher glucokinase activity higher expression level of insulin, insulin receptor, GLUT-2 and glucokinase genes in diabetic rats treated with zinc oxide, silver nanoparticles and insulin. Zinc Oxide 0-10 solute carrier family 2 member 2 Rattus norvegicus 184-190 24477262-5 2014 Zinc oxide and silver nanoparticles induce a significant reduced blood glucose, higher serum insulin, higher glucokinase activity higher expression level of insulin, insulin receptor, GLUT-2 and glucokinase genes in diabetic rats treated with zinc oxide, silver nanoparticles and insulin. Zinc Oxide 243-253 insulin receptor Rattus norvegicus 166-182 24477262-5 2014 Zinc oxide and silver nanoparticles induce a significant reduced blood glucose, higher serum insulin, higher glucokinase activity higher expression level of insulin, insulin receptor, GLUT-2 and glucokinase genes in diabetic rats treated with zinc oxide, silver nanoparticles and insulin. Zinc Oxide 243-253 solute carrier family 2 member 2 Rattus norvegicus 184-190 24095988-5 2014 For ZnO Nps, a strong interaction was observed, which induced a decrease in the thermal stability of both fibrinogen and albumin at a low temperature, interfering with the clotting activity of fibrinogen. Zinc Oxide 4-7 fibrinogen beta chain Homo sapiens 106-116 24095988-5 2014 For ZnO Nps, a strong interaction was observed, which induced a decrease in the thermal stability of both fibrinogen and albumin at a low temperature, interfering with the clotting activity of fibrinogen. Zinc Oxide 4-7 fibrinogen beta chain Homo sapiens 193-203 24992626-6 2014 Reduced glutathione level was decreased while caspase3 level was elevated in liver tissues of ZnO-NPs treated group compared with intoxicated one. Zinc Oxide 94-97 caspase 3 Rattus norvegicus 46-54 24555677-7 2014 Exposure of THP-1 cells to both sizes of ZnO stimulated and increased release of proinflammatory cytokines interleukin (IL)-1beta, tumor necrosis factor (TNF)-alpha, and IL-6, as well as chemokine IL-8, and upregulated the expression of monocyte chemoattractant protein-1 and cyclooxygenase-2 genes. Zinc Oxide 41-44 tumor necrosis factor Homo sapiens 131-164 24555677-7 2014 Exposure of THP-1 cells to both sizes of ZnO stimulated and increased release of proinflammatory cytokines interleukin (IL)-1beta, tumor necrosis factor (TNF)-alpha, and IL-6, as well as chemokine IL-8, and upregulated the expression of monocyte chemoattractant protein-1 and cyclooxygenase-2 genes. Zinc Oxide 41-44 interleukin 6 Homo sapiens 170-174 24555677-7 2014 Exposure of THP-1 cells to both sizes of ZnO stimulated and increased release of proinflammatory cytokines interleukin (IL)-1beta, tumor necrosis factor (TNF)-alpha, and IL-6, as well as chemokine IL-8, and upregulated the expression of monocyte chemoattractant protein-1 and cyclooxygenase-2 genes. Zinc Oxide 41-44 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 24555677-7 2014 Exposure of THP-1 cells to both sizes of ZnO stimulated and increased release of proinflammatory cytokines interleukin (IL)-1beta, tumor necrosis factor (TNF)-alpha, and IL-6, as well as chemokine IL-8, and upregulated the expression of monocyte chemoattractant protein-1 and cyclooxygenase-2 genes. Zinc Oxide 41-44 C-C motif chemokine ligand 2 Homo sapiens 237-271 24555677-7 2014 Exposure of THP-1 cells to both sizes of ZnO stimulated and increased release of proinflammatory cytokines interleukin (IL)-1beta, tumor necrosis factor (TNF)-alpha, and IL-6, as well as chemokine IL-8, and upregulated the expression of monocyte chemoattractant protein-1 and cyclooxygenase-2 genes. Zinc Oxide 41-44 prostaglandin-endoperoxide synthase 2 Homo sapiens 276-292 24187959-3 2013 In this study, rapid scanning X-ray fluorescence microscopy was used to assay the number ZnO nanoparticles associated with ~1000 individual THP-1 monocyte-derived human macrophages. Zinc Oxide 89-92 GLI family zinc finger 2 Homo sapiens 140-145 23867351-0 2013 rhEPO/EPO discrimination with ultrasensitive electrochemical biosensor based on sandwich-type nano-Au/ZnO sol-gel/nano-Au signal amplification. Zinc Oxide 102-105 erythropoietin Homo sapiens 2-5 24354393-5 2013 The improvement can be ascribed to the deposited Ag2O forming the p-n junction at the interface of ZnO and Ag2O, resulting in the transfer of photocarriers and suppressing the electron-hole recombination rate. Zinc Oxide 99-102 anterior gradient 2, protein disulphide isomerase family member Homo sapiens 49-52 23867351-5 2013 By combining the advantages of both ZnO sol-gel and nano-Au, the amount of erythropoietin receptor (EPOR) increased substantially, and electron transfer of EPOR protein and electrode surface increased accordingly. Zinc Oxide 36-39 erythropoietin receptor Homo sapiens 75-98 23867351-5 2013 By combining the advantages of both ZnO sol-gel and nano-Au, the amount of erythropoietin receptor (EPOR) increased substantially, and electron transfer of EPOR protein and electrode surface increased accordingly. Zinc Oxide 36-39 erythropoietin receptor Homo sapiens 100-104 23867351-5 2013 By combining the advantages of both ZnO sol-gel and nano-Au, the amount of erythropoietin receptor (EPOR) increased substantially, and electron transfer of EPOR protein and electrode surface increased accordingly. Zinc Oxide 36-39 erythropoietin receptor Homo sapiens 156-160 24060544-9 2013 ZnO nanoparticles can increase the intracellular calcium ion level, disrupt the intracellular calcium homeostasis, and decrease the expression level of PMCA1. Zinc Oxide 0-3 ATPase plasma membrane Ca2+ transporting 1 Homo sapiens 152-157 24090840-4 2013 At low level of ZnO NMs induced ROS, p53 triggers expression of antioxidant genes such as SOD2, GPX1, SESN1, SESN2 and ALDH4A1 to restore oxidative homeostasis while at high concentration of ZnO NMs, the elevated level of intracellular ROS activated the apoptotic pathway through p53. Zinc Oxide 16-19 tumor protein p53 Homo sapiens 37-40 24090840-4 2013 At low level of ZnO NMs induced ROS, p53 triggers expression of antioxidant genes such as SOD2, GPX1, SESN1, SESN2 and ALDH4A1 to restore oxidative homeostasis while at high concentration of ZnO NMs, the elevated level of intracellular ROS activated the apoptotic pathway through p53. Zinc Oxide 16-19 superoxide dismutase 2 Homo sapiens 90-94 24090840-4 2013 At low level of ZnO NMs induced ROS, p53 triggers expression of antioxidant genes such as SOD2, GPX1, SESN1, SESN2 and ALDH4A1 to restore oxidative homeostasis while at high concentration of ZnO NMs, the elevated level of intracellular ROS activated the apoptotic pathway through p53. Zinc Oxide 16-19 glutathione peroxidase 1 Homo sapiens 96-100 24090840-4 2013 At low level of ZnO NMs induced ROS, p53 triggers expression of antioxidant genes such as SOD2, GPX1, SESN1, SESN2 and ALDH4A1 to restore oxidative homeostasis while at high concentration of ZnO NMs, the elevated level of intracellular ROS activated the apoptotic pathway through p53. Zinc Oxide 16-19 sestrin 1 Homo sapiens 102-107 24090840-4 2013 At low level of ZnO NMs induced ROS, p53 triggers expression of antioxidant genes such as SOD2, GPX1, SESN1, SESN2 and ALDH4A1 to restore oxidative homeostasis while at high concentration of ZnO NMs, the elevated level of intracellular ROS activated the apoptotic pathway through p53. Zinc Oxide 16-19 sestrin 2 Homo sapiens 109-114 24090840-4 2013 At low level of ZnO NMs induced ROS, p53 triggers expression of antioxidant genes such as SOD2, GPX1, SESN1, SESN2 and ALDH4A1 to restore oxidative homeostasis while at high concentration of ZnO NMs, the elevated level of intracellular ROS activated the apoptotic pathway through p53. Zinc Oxide 16-19 aldehyde dehydrogenase 4 family member A1 Homo sapiens 119-126 24090840-4 2013 At low level of ZnO NMs induced ROS, p53 triggers expression of antioxidant genes such as SOD2, GPX1, SESN1, SESN2 and ALDH4A1 to restore oxidative homeostasis while at high concentration of ZnO NMs, the elevated level of intracellular ROS activated the apoptotic pathway through p53. Zinc Oxide 16-19 tumor protein p53 Homo sapiens 280-283 24090840-4 2013 At low level of ZnO NMs induced ROS, p53 triggers expression of antioxidant genes such as SOD2, GPX1, SESN1, SESN2 and ALDH4A1 to restore oxidative homeostasis while at high concentration of ZnO NMs, the elevated level of intracellular ROS activated the apoptotic pathway through p53. Zinc Oxide 191-194 tumor protein p53 Homo sapiens 37-40 24090840-4 2013 At low level of ZnO NMs induced ROS, p53 triggers expression of antioxidant genes such as SOD2, GPX1, SESN1, SESN2 and ALDH4A1 to restore oxidative homeostasis while at high concentration of ZnO NMs, the elevated level of intracellular ROS activated the apoptotic pathway through p53. Zinc Oxide 191-194 superoxide dismutase 2 Homo sapiens 90-94 24090840-4 2013 At low level of ZnO NMs induced ROS, p53 triggers expression of antioxidant genes such as SOD2, GPX1, SESN1, SESN2 and ALDH4A1 to restore oxidative homeostasis while at high concentration of ZnO NMs, the elevated level of intracellular ROS activated the apoptotic pathway through p53. Zinc Oxide 191-194 glutathione peroxidase 1 Homo sapiens 96-100 24090840-4 2013 At low level of ZnO NMs induced ROS, p53 triggers expression of antioxidant genes such as SOD2, GPX1, SESN1, SESN2 and ALDH4A1 to restore oxidative homeostasis while at high concentration of ZnO NMs, the elevated level of intracellular ROS activated the apoptotic pathway through p53. Zinc Oxide 191-194 sestrin 1 Homo sapiens 102-107 24090840-4 2013 At low level of ZnO NMs induced ROS, p53 triggers expression of antioxidant genes such as SOD2, GPX1, SESN1, SESN2 and ALDH4A1 to restore oxidative homeostasis while at high concentration of ZnO NMs, the elevated level of intracellular ROS activated the apoptotic pathway through p53. Zinc Oxide 191-194 sestrin 2 Homo sapiens 109-114 24090840-4 2013 At low level of ZnO NMs induced ROS, p53 triggers expression of antioxidant genes such as SOD2, GPX1, SESN1, SESN2 and ALDH4A1 to restore oxidative homeostasis while at high concentration of ZnO NMs, the elevated level of intracellular ROS activated the apoptotic pathway through p53. Zinc Oxide 191-194 aldehyde dehydrogenase 4 family member A1 Homo sapiens 119-126 24090840-5 2013 The implication of our finding that p53 can function as an important regulator in determining ZnO induced cytotoxicity is highlighted by the differential action of ZnO on p53 deficient and proficient colorectal cell lines. Zinc Oxide 94-97 tumor protein p53 Homo sapiens 36-39 24090840-5 2013 The implication of our finding that p53 can function as an important regulator in determining ZnO induced cytotoxicity is highlighted by the differential action of ZnO on p53 deficient and proficient colorectal cell lines. Zinc Oxide 164-167 tumor protein p53 Homo sapiens 36-39 24090840-5 2013 The implication of our finding that p53 can function as an important regulator in determining ZnO induced cytotoxicity is highlighted by the differential action of ZnO on p53 deficient and proficient colorectal cell lines. Zinc Oxide 164-167 tumor protein p53 Homo sapiens 171-174 24090840-6 2013 p53 deficient cells cancer cells such as DLD-1 and SW480 are more susceptible to ZnO induced cell death compared to p53 proficient cells such as colon epithelial cells NCM460 and HCT116 cells in a ROS dependent manner. Zinc Oxide 81-84 tumor protein p53 Homo sapiens 0-3 24396300-5 2013 Partial density states calculation further suggests that the appearance of the half-metallic ferromagnetism in ZnO nanorod with V(Zn) originates from the hybridization of the O2p states with Zn 3d states. Zinc Oxide 111-114 immunoglobulin kappa variable 1D-39 Homo sapiens 175-178 24090840-0 2013 Effect of zinc oxide nanomaterials-induced oxidative stress on the p53 pathway. Zinc Oxide 10-20 tumor protein p53 Homo sapiens 67-70 24090840-3 2013 Here, using a BJ fibroblast p53 knockdown system, we showed that p53 may be implicated in playing a dual regulatory role to determine cell survivability in response to oxidative stress induced by ZnO NMs. Zinc Oxide 196-199 tumor protein p53 Homo sapiens 28-31 24090840-3 2013 Here, using a BJ fibroblast p53 knockdown system, we showed that p53 may be implicated in playing a dual regulatory role to determine cell survivability in response to oxidative stress induced by ZnO NMs. Zinc Oxide 196-199 tumor protein p53 Homo sapiens 65-68 24001789-0 2013 ZnO nanoparticles induce TNF-alpha expression via ROS-ERK-Egr-1 pathway in human keratinocytes. Zinc Oxide 0-3 tumor necrosis factor Homo sapiens 25-34 24001789-0 2013 ZnO nanoparticles induce TNF-alpha expression via ROS-ERK-Egr-1 pathway in human keratinocytes. Zinc Oxide 0-3 mitogen-activated protein kinase 1 Homo sapiens 54-57 24001789-0 2013 ZnO nanoparticles induce TNF-alpha expression via ROS-ERK-Egr-1 pathway in human keratinocytes. Zinc Oxide 0-3 early growth response 1 Homo sapiens 58-63 24001789-9 2013 The up-regulation of Egr-1 expression by ZnO-NPs stimulation was found to be inhibited by an ERK inhibitor, but by neither c-Jun-N-terminal kinase (JNK) nor p38 inhibitor. Zinc Oxide 41-44 early growth response 1 Homo sapiens 21-26 24001789-9 2013 The up-regulation of Egr-1 expression by ZnO-NPs stimulation was found to be inhibited by an ERK inhibitor, but by neither c-Jun-N-terminal kinase (JNK) nor p38 inhibitor. Zinc Oxide 41-44 mitogen-activated protein kinase 1 Homo sapiens 93-96 24001789-10 2013 Antioxidative N-acetyl-cysteine (NAC) strongly inhibited the level of Egr-1 and phosphorylated ERK expression in ZnO-NPs treated cells. Zinc Oxide 113-116 early growth response 1 Homo sapiens 70-75 24001789-10 2013 Antioxidative N-acetyl-cysteine (NAC) strongly inhibited the level of Egr-1 and phosphorylated ERK expression in ZnO-NPs treated cells. Zinc Oxide 113-116 mitogen-activated protein kinase 1 Homo sapiens 95-98 24001789-11 2013 ZnO NPs also increased tumor necrosis factor (TNF)-alpha expression and secretion, which were inhibited by the blockade of Egr-1 expression. Zinc Oxide 0-3 tumor necrosis factor Homo sapiens 23-56 24001789-11 2013 ZnO NPs also increased tumor necrosis factor (TNF)-alpha expression and secretion, which were inhibited by the blockade of Egr-1 expression. Zinc Oxide 0-3 early growth response 1 Homo sapiens 123-128 24001789-12 2013 CONCLUSIONS: The present study demonstrated that ZnO-NPs might induce inflammatory response via ROS-ERK-Egr-1 pathway in human keratinocytes. Zinc Oxide 49-52 mitogen-activated protein kinase 1 Homo sapiens 100-103 24001789-12 2013 CONCLUSIONS: The present study demonstrated that ZnO-NPs might induce inflammatory response via ROS-ERK-Egr-1 pathway in human keratinocytes. Zinc Oxide 49-52 early growth response 1 Homo sapiens 104-109 23078188-6 2013 However, only ZnO NPs increased ROS and induced IL-8 release both after 6 and 24 h. Experimental data indicate a main role of chemical composition and solubility in ZnO NPs toxicity. Zinc Oxide 14-17 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 24175740-3 2013 The ZnO nanoparticle-doped active layer (ITO\PEDOT:PSS(DMF) \ZnO:P3HT:PCBM\LiF\Al) exhibited a higher efficiency of 3.39% due to the modulated PEDOT:PSS buffer layer with low resistivity and the hybrid active layer containing ZnO nanoparticles. Zinc Oxide 4-7 LIF interleukin 6 family cytokine Homo sapiens 75-78 24147760-4 2013 The interaction between the cbp ligands on the surface of ZnO and CdS QDs and cyanobiphenyl side-chain mesogens of diblock copolymers promoted the cooperative self-assembly and controllable well-dispersion of QDs in the polymer matrix and, as a consequence, yielded an intimately contacted polymer-QD nanocomposites. Zinc Oxide 58-61 CREB binding protein Homo sapiens 28-31 24175740-3 2013 The ZnO nanoparticle-doped active layer (ITO\PEDOT:PSS(DMF) \ZnO:P3HT:PCBM\LiF\Al) exhibited a higher efficiency of 3.39% due to the modulated PEDOT:PSS buffer layer with low resistivity and the hybrid active layer containing ZnO nanoparticles. Zinc Oxide 61-64 LIF interleukin 6 family cytokine Homo sapiens 75-78 24175740-3 2013 The ZnO nanoparticle-doped active layer (ITO\PEDOT:PSS(DMF) \ZnO:P3HT:PCBM\LiF\Al) exhibited a higher efficiency of 3.39% due to the modulated PEDOT:PSS buffer layer with low resistivity and the hybrid active layer containing ZnO nanoparticles. Zinc Oxide 61-64 LIF interleukin 6 family cytokine Homo sapiens 75-78 24555346-4 2013 And the intensity of near ultraviolet emission from ZnO is stronger than that of the orange-red emission belonging to MEH-PPV. Zinc Oxide 52-55 epoxide hydrolase 1 Homo sapiens 118-121 24096940-1 2013 A novel ZnO/reduced graphene oxide (RGO)/CdS heterostructure was successfully synthesized via a facile three-step solution method. Zinc Oxide 8-11 CDP-diacylglycerol synthase 1 Homo sapiens 41-44 24096940-3 2013 Under UV light irradiation, the photocatalytic activity of the ZnO/RGO/CdS heterostructure is 4.0 times and 1.9 times as high as those of pure ZnO and ZnO/RGO, respectively. Zinc Oxide 63-66 CDP-diacylglycerol synthase 1 Homo sapiens 71-74 24096940-3 2013 Under UV light irradiation, the photocatalytic activity of the ZnO/RGO/CdS heterostructure is 4.0 times and 1.9 times as high as those of pure ZnO and ZnO/RGO, respectively. Zinc Oxide 143-146 CDP-diacylglycerol synthase 1 Homo sapiens 71-74 24096940-3 2013 Under UV light irradiation, the photocatalytic activity of the ZnO/RGO/CdS heterostructure is 4.0 times and 1.9 times as high as those of pure ZnO and ZnO/RGO, respectively. Zinc Oxide 143-146 CDP-diacylglycerol synthase 1 Homo sapiens 71-74 24096940-4 2013 Under visible light irradiation, the ZnO/RGO/CdS heterostructure shows a dramatic visible light photocatalytic activity which is 2.3 times higher than that of the ZnO/CdS photocatalyst. Zinc Oxide 37-40 CDP-diacylglycerol synthase 1 Homo sapiens 45-48 24096940-4 2013 Under visible light irradiation, the ZnO/RGO/CdS heterostructure shows a dramatic visible light photocatalytic activity which is 2.3 times higher than that of the ZnO/CdS photocatalyst. Zinc Oxide 37-40 CDP-diacylglycerol synthase 1 Homo sapiens 167-170 24096940-4 2013 Under visible light irradiation, the ZnO/RGO/CdS heterostructure shows a dramatic visible light photocatalytic activity which is 2.3 times higher than that of the ZnO/CdS photocatalyst. Zinc Oxide 163-166 CDP-diacylglycerol synthase 1 Homo sapiens 45-48 24096940-4 2013 Under visible light irradiation, the ZnO/RGO/CdS heterostructure shows a dramatic visible light photocatalytic activity which is 2.3 times higher than that of the ZnO/CdS photocatalyst. Zinc Oxide 163-166 CDP-diacylglycerol synthase 1 Homo sapiens 167-170 24096940-5 2013 The photocurrent of the ZnO/RGO/CdS heterostructure under UV light irradiation was greatly enhanced and a photocurrent under visible light irradiation was observed. Zinc Oxide 24-27 CDP-diacylglycerol synthase 1 Homo sapiens 32-35 24096940-6 2013 The enhanced photocatalytic activity and the extended light adsorption spectrum originate from the type-II ZnO/CdS band alignment and the introduction of RGO as a charge mediator. Zinc Oxide 107-110 CDP-diacylglycerol synthase 1 Homo sapiens 111-114 24555346-0 2013 [Tunneling electroluminescence of the ZnO nanorods/MEH-PPV heterojunction devices]. Zinc Oxide 38-41 epoxide hydrolase 1 Homo sapiens 51-54 24245326-0 2013 Structural and electrical properties of ZnO films deposited with low-temperature facing targets magnetron sputtering (FTS) system with changes in H2 and O2 flow rate. Zinc Oxide 40-43 relaxin 2 Homo sapiens 146-155 24555346-3 2013 When a reverse bias exceeding 17 volts was applied to the ZnO-NRs/ MEH-PPV heterojunction, both emissions of ZnO and MEH-PPV were detected. Zinc Oxide 58-61 epoxide hydrolase 1 Homo sapiens 67-70 24555346-3 2013 When a reverse bias exceeding 17 volts was applied to the ZnO-NRs/ MEH-PPV heterojunction, both emissions of ZnO and MEH-PPV were detected. Zinc Oxide 58-61 epoxide hydrolase 1 Homo sapiens 117-120 24555346-3 2013 When a reverse bias exceeding 17 volts was applied to the ZnO-NRs/ MEH-PPV heterojunction, both emissions of ZnO and MEH-PPV were detected. Zinc Oxide 109-112 epoxide hydrolase 1 Homo sapiens 67-70 24044753-0 2013 The effect of the binding of ZnO nanoparticle on the structure and stability of alpha-lactalbumin: a comparative study. Zinc Oxide 29-32 lactalbumin alpha Homo sapiens 80-97 24044753-3 2013 We have carried out a detailed study on the interaction of alpha-lactalbumin (a protein which forms the regulatory subunit of lactose synthase) with zinc oxide nanoparticles. Zinc Oxide 149-159 lactalbumin alpha Homo sapiens 59-76 24044753-3 2013 We have carried out a detailed study on the interaction of alpha-lactalbumin (a protein which forms the regulatory subunit of lactose synthase) with zinc oxide nanoparticles. Zinc Oxide 149-159 beta-1,4-galactosyltransferase 1 Homo sapiens 126-142 24044753-9 2013 Finally, a comparison of structure, function, and stability of the alpha-lactalbumin-NP complex has been made by binding ZnO to other model proteins to get a better insight into the process of protein nanoparticle interaction. Zinc Oxide 121-124 lactalbumin alpha Homo sapiens 67-84 24245326-4 2013 To control the electrical conductivity of ZnO, this study was performed using an FTS system with H2 and O2 addition at low processing temperature. Zinc Oxide 42-45 relaxin 2 Homo sapiens 97-106 24245326-5 2013 The structural and electrical properties of ZnO thin films deposited at various H2 and O2 flow rates were investigated using XRD and a sheet resistance meter. Zinc Oxide 44-47 relaxin 2 Homo sapiens 80-89 24245326-6 2013 In response to changes in H2 and O2 flow rates, the crystallization and related grain size of the ZnO films were somewhat changed. Zinc Oxide 98-101 relaxin 2 Homo sapiens 26-35 23628581-2 2013 In this paper we studied the conjugation of horse heart cytochrome c with ZnO nanoparticles modified by mercaptoacetic acid (MAA) which may be a material with great potential in anticancer therapy as a consequence of synergic effect of both components. Zinc Oxide 74-77 cytochrome c, somatic Equus caballus 56-68 23836722-0 2013 Low-cost fully transparent ultraviolet photodetectors based on electrospun ZnO-SnO2 heterojunction nanofibers. Zinc Oxide 75-78 strawberry notch homolog 2 Homo sapiens 79-82 23352990-0 2013 Involvement of MyD88 in zinc oxide nanoparticle-induced lung inflammation. Zinc Oxide 24-34 myeloid differentiation primary response gene 88 Mus musculus 15-20 23563288-3 2013 From the BET and SEM micrographs, the introduction of ZnO nanoparticles into chitosan-polyaniline hybrid could obviously increase the porosity due to good possibility for dye adsorption. Zinc Oxide 54-57 delta/notch like EGF repeat containing Homo sapiens 9-12 23945632-5 2013 Herein we use an all-electrochemical approach to directly deposit ZnO NWs onto FTO followed by electrochemical doping with Ga to produce a heterojunction solar cell. Zinc Oxide 66-69 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 79-82 23882462-2 2013 Zinc oxide (ZnO) nanoparticles were employed as the carriers for immobilizing the capture AFP antibody (Ab1) and CdSe quantum dots (QDs). Zinc Oxide 0-10 alpha fetoprotein Homo sapiens 90-93 23882462-2 2013 Zinc oxide (ZnO) nanoparticles were employed as the carriers for immobilizing the capture AFP antibody (Ab1) and CdSe quantum dots (QDs). Zinc Oxide 12-15 alpha fetoprotein Homo sapiens 90-93 23882462-3 2013 CdSe QDs-functionalized ZnO nanoparticles were used as the tracer to label the signal AFP antibody (Ab2). Zinc Oxide 24-27 alpha fetoprotein Homo sapiens 86-89 23889004-0 2013 Transmission electron microscopy and time resolved optical spectroscopy study of the electronic and structural interactions of ZnO nanorods with bovine serum albumin. Zinc Oxide 127-130 albumin Homo sapiens 152-165 23889004-1 2013 The adsorption behavior and electronic interactions of bovine serum albumin (BSA) with ZnO nanorod surfaces were investigated using high-resolution transmission electron microscopy as well as stationary and time-resolved optical spectroscopy techniques. Zinc Oxide 87-90 albumin Homo sapiens 62-75 23808529-1 2013 Dye sensitization of zinc oxide single crystals by a carbazole thiophene cyanoacrylate (MK-2) sensitizer deposited from THF and mixtures of THF and water was investigated. Zinc Oxide 21-31 MAPK activated protein kinase 2 Homo sapiens 88-92 23773013-3 2013 The TFTs based on the 10 mol % LiF-doped ZnO thin films annealed at 300 C revealed a good device performance with an average electron mobility of 8.9 cm(2) V(-1) s(-1) and a high on/off current ratio of 4 x 10(7), superior to the devices based on the nondoped ZnO TFTs (1.6 cm(2) V(-1) s(-1)). Zinc Oxide 41-44 LIF interleukin 6 family cytokine Homo sapiens 31-34 23773013-3 2013 The TFTs based on the 10 mol % LiF-doped ZnO thin films annealed at 300 C revealed a good device performance with an average electron mobility of 8.9 cm(2) V(-1) s(-1) and a high on/off current ratio of 4 x 10(7), superior to the devices based on the nondoped ZnO TFTs (1.6 cm(2) V(-1) s(-1)). Zinc Oxide 261-264 LIF interleukin 6 family cytokine Homo sapiens 31-34 23773013-0 2013 Solution-processed LiF-doped ZnO films for high performance low temperature field effect transistors and inverted solar cells. Zinc Oxide 29-32 LIF interleukin 6 family cytokine Homo sapiens 19-22 23773013-5 2013 The inverted bulk heterojunction solar cells based on P3HT:PCBM blend system fabricated using 10 mol % LiF doped ZnO as electron selective layer showed higher power conversion efficiency (eta = 3.3%) than that from undoped ZnO thin films (eta = 2.94%) due to enhanced short circuit current (Jsc = 10.55 mA/cm(2)). Zinc Oxide 113-116 LIF interleukin 6 family cytokine Homo sapiens 103-106 23773013-1 2013 This paper reports that high performance metal oxide thin film transistors (TFTs) can be achieved by using LiF-doped ZnO thin films processed from aqueous solution. Zinc Oxide 117-120 LIF interleukin 6 family cytokine Homo sapiens 107-110 23773013-5 2013 The inverted bulk heterojunction solar cells based on P3HT:PCBM blend system fabricated using 10 mol % LiF doped ZnO as electron selective layer showed higher power conversion efficiency (eta = 3.3%) than that from undoped ZnO thin films (eta = 2.94%) due to enhanced short circuit current (Jsc = 10.55 mA/cm(2)). Zinc Oxide 223-226 LIF interleukin 6 family cytokine Homo sapiens 103-106 23643724-9 2013 Moreover, the transcriptional expression of mitochondrial inner membrane genes related to ROS production, such as Bcl-2, in response to oxidative damage, such as Nqo1, and related to antioxidant response element such as Gstp2 were significantly down-regulated in the nano-ZnO treatment groups. Zinc Oxide 272-275 BCL2 apoptosis regulator a Danio rerio 114-119 23726862-3 2013 TiO2, CeO2 and ZnO NPs slightly down-regulated cell surface expression of the granule marker CD35, but increased CD66b and CD63 expression, as assessed by flow cytometry. Zinc Oxide 15-18 complement C3b/C4b receptor 1 (Knops blood group) Homo sapiens 93-97 23726862-3 2013 TiO2, CeO2 and ZnO NPs slightly down-regulated cell surface expression of the granule marker CD35, but increased CD66b and CD63 expression, as assessed by flow cytometry. Zinc Oxide 15-18 CEA cell adhesion molecule 8 Homo sapiens 113-118 23726862-3 2013 TiO2, CeO2 and ZnO NPs slightly down-regulated cell surface expression of the granule marker CD35, but increased CD66b and CD63 expression, as assessed by flow cytometry. Zinc Oxide 15-18 CD63 molecule Homo sapiens 123-127 23643724-9 2013 Moreover, the transcriptional expression of mitochondrial inner membrane genes related to ROS production, such as Bcl-2, in response to oxidative damage, such as Nqo1, and related to antioxidant response element such as Gstp2 were significantly down-regulated in the nano-ZnO treatment groups. Zinc Oxide 272-275 NAD(P)H dehydrogenase, quinone 1 Danio rerio 162-166 23643724-9 2013 Moreover, the transcriptional expression of mitochondrial inner membrane genes related to ROS production, such as Bcl-2, in response to oxidative damage, such as Nqo1, and related to antioxidant response element such as Gstp2 were significantly down-regulated in the nano-ZnO treatment groups. Zinc Oxide 272-275 glutathione S-transferase pi 1.1 Danio rerio 220-225 23643724-10 2013 However, the nano-ZnO up-regulated the transcriptional expression of Ucp2-related to ROS production. Zinc Oxide 18-21 uncoupling protein 2 Danio rerio 69-73 23675744-3 2013 In fact, ETA cells suffer from a very low Voc/Egap ratio, such as in ZnO/CdS/CuSCN cells. Zinc Oxide 69-72 N-alpha-acetyltransferase 35, NatC auxiliary subunit Homo sapiens 46-50 23849302-2 2013 Herein, we have developed heterojunction LEDs based on the well-aligned ZnO nanorods and nanotubes on the p-type GaN with the insertion of the NiO buffer layer that showed enhancement in the light emission. Zinc Oxide 72-75 gigaxonin Homo sapiens 113-116 23849302-4 2013 X-ray diffraction study describes the wurtzite crystal structure array of ZnO nanorods with the involvement of GaN at the (002) peak. Zinc Oxide 74-77 gigaxonin Homo sapiens 111-114 23849302-7 2013 Introducing a sandwich-thin layer of NiO between the n-type ZnO and the p-type GaN will possibly block the injection of electrons from the ZnO to the GaN. Zinc Oxide 60-63 gigaxonin Homo sapiens 150-153 23680782-2 2013 ZnO nanoparticles (NPs), a UV filter, were synthesized and characterized to be the carrier for benzophenone-3 (Bp-3), a UV-absorption medicine, by varying the molar ratio of ZnO NPs to Bp-3 ranging from 300 : 1 to 20 : 1. Zinc Oxide 0-3 BP3 Homo sapiens 95-115 23680782-2 2013 ZnO nanoparticles (NPs), a UV filter, were synthesized and characterized to be the carrier for benzophenone-3 (Bp-3), a UV-absorption medicine, by varying the molar ratio of ZnO NPs to Bp-3 ranging from 300 : 1 to 20 : 1. Zinc Oxide 174-177 BP3 Homo sapiens 95-115 23849302-7 2013 Introducing a sandwich-thin layer of NiO between the n-type ZnO and the p-type GaN will possibly block the injection of electrons from the ZnO to the GaN. Zinc Oxide 139-142 gigaxonin Homo sapiens 79-82 23849302-7 2013 Introducing a sandwich-thin layer of NiO between the n-type ZnO and the p-type GaN will possibly block the injection of electrons from the ZnO to the GaN. Zinc Oxide 139-142 gigaxonin Homo sapiens 150-153 23862406-0 2013 Zinc oxide nanoparticles induce rat retinal ganglion cell damage through bcl-2, caspase-9 and caspase-12 pathways. Zinc Oxide 0-10 BCL2, apoptosis regulator Rattus norvegicus 73-78 23644717-2 2013 An overall light-to-electricity conversion efficiency (eta) of 2.70% was achieved for the DSSC under 100 mW cm(-2) illumination, and this eta was found to be much higher than that of the DSSC with ZnO nanowire (NW) as the photoanode (0.71%). Zinc Oxide 197-200 endothelin receptor type A Homo sapiens 55-58 23755271-0 2013 Zinc oxide nanoparticles induce necrosis and apoptosis in macrophages in a p47phox- and Nrf2-independent manner. Zinc Oxide 0-10 neutrophil cytosolic factor 1 Mus musculus 75-82 23755271-0 2013 Zinc oxide nanoparticles induce necrosis and apoptosis in macrophages in a p47phox- and Nrf2-independent manner. Zinc Oxide 0-10 nuclear factor, erythroid derived 2, like 2 Mus musculus 88-92 23755271-4 2013 The involvement of the essential effector caspase-3 in ZnO-mediated apoptosis could be demonstrated by immunocytochemical detection of activated caspase-3 in RAW 264.7 cells. Zinc Oxide 55-58 caspase 3 Mus musculus 42-51 23755271-4 2013 The involvement of the essential effector caspase-3 in ZnO-mediated apoptosis could be demonstrated by immunocytochemical detection of activated caspase-3 in RAW 264.7 cells. Zinc Oxide 55-58 caspase 3 Mus musculus 145-154 23755271-5 2013 ZnO specifically triggered the intrinsic apoptotic pathway, because Jurkat T lymphocytes deficient in the key mediator caspase-9 were protected against ZnO-mediated toxicity whereas reconstituted cells were not. Zinc Oxide 0-3 caspase 9 Mus musculus 119-128 23755271-5 2013 ZnO specifically triggered the intrinsic apoptotic pathway, because Jurkat T lymphocytes deficient in the key mediator caspase-9 were protected against ZnO-mediated toxicity whereas reconstituted cells were not. Zinc Oxide 152-155 caspase 9 Mus musculus 119-128 23755271-8 2013 Taken together, our data demonstrate that ZnO nanoparticles trigger p47(phox) NADPH oxidase-mediated ROS formation in macrophages, but that this is dispensable for caspase-9/3-mediated apoptosis. Zinc Oxide 42-45 NSFL1 (p97) cofactor (p47) Mus musculus 68-71 23755271-9 2013 Execution of apoptotic cell death by ZnO nanoparticles appears to be NADPH oxidase and Nrf2-independent but rather triggered by alternative routes. Zinc Oxide 37-40 nuclear factor, erythroid derived 2, like 2 Mus musculus 87-91 23862406-0 2013 Zinc oxide nanoparticles induce rat retinal ganglion cell damage through bcl-2, caspase-9 and caspase-12 pathways. Zinc Oxide 0-10 caspase 9 Rattus norvegicus 80-89 23862406-0 2013 Zinc oxide nanoparticles induce rat retinal ganglion cell damage through bcl-2, caspase-9 and caspase-12 pathways. Zinc Oxide 0-10 caspase 12 Rattus norvegicus 94-104 23862406-6 2013 Moreover, our results also demonstrated that the overproduction of reactive oxygen species (ROS) and elevated level of caspase-12 as well as decreased levels of bcl-2 and caspase-9 occurred after treatment with different concentrations of ZnO nanoparticles when compared to those in untreated cells. Zinc Oxide 239-242 caspase 12 Rattus norvegicus 119-129 23862406-6 2013 Moreover, our results also demonstrated that the overproduction of reactive oxygen species (ROS) and elevated level of caspase-12 as well as decreased levels of bcl-2 and caspase-9 occurred after treatment with different concentrations of ZnO nanoparticles when compared to those in untreated cells. Zinc Oxide 239-242 BCL2, apoptosis regulator Rattus norvegicus 161-166 23862406-6 2013 Moreover, our results also demonstrated that the overproduction of reactive oxygen species (ROS) and elevated level of caspase-12 as well as decreased levels of bcl-2 and caspase-9 occurred after treatment with different concentrations of ZnO nanoparticles when compared to those in untreated cells. Zinc Oxide 239-242 caspase 9 Rattus norvegicus 171-180 23862406-7 2013 In summary, our findings suggest that ZnO nanoparticles could lead to the over generations of ROS and caspase-12 as well as decreased levels of bcl-2 and caspase-9. Zinc Oxide 38-41 caspase 12 Rattus norvegicus 102-112 23862406-7 2013 In summary, our findings suggest that ZnO nanoparticles could lead to the over generations of ROS and caspase-12 as well as decreased levels of bcl-2 and caspase-9. Zinc Oxide 38-41 BCL2, apoptosis regulator Rattus norvegicus 144-149 23862406-7 2013 In summary, our findings suggest that ZnO nanoparticles could lead to the over generations of ROS and caspase-12 as well as decreased levels of bcl-2 and caspase-9. Zinc Oxide 38-41 caspase 9 Rattus norvegicus 154-163 23862406-8 2013 These results indicate that bcl-2, caspase-9 and caspase-12 may play significant roles in ZnO nanoparticle-induced RGC-5 cell damage. Zinc Oxide 90-93 B cell leukemia/lymphoma 2 Mus musculus 28-33 23862406-8 2013 These results indicate that bcl-2, caspase-9 and caspase-12 may play significant roles in ZnO nanoparticle-induced RGC-5 cell damage. Zinc Oxide 90-93 caspase 9 Mus musculus 35-44 23862406-8 2013 These results indicate that bcl-2, caspase-9 and caspase-12 may play significant roles in ZnO nanoparticle-induced RGC-5 cell damage. Zinc Oxide 90-93 caspase 12 Mus musculus 49-59 23532625-7 2013 Moreover, either of the 2 used agents successfully alleviated the alteration in nitric oxide (NO) and vascular endothelial growth factor (VEGF) in ZnO-NPs in sera of intoxicated group. Zinc Oxide 147-150 vascular endothelial growth factor A Rattus norvegicus 102-136 23592178-1 2013 The adsorption of O2/H2O molecules on the ZnO nanowire (NW) surface results in the long lifetime of photo-generated carriers and thus benefits ZnO NW-based ultraviolet photodetectors by suppressing the dark current and improving the photocurrent gain, but the slow adsorption process also leads to slow detector response time. Zinc Oxide 42-45 immunoglobulin kappa variable 1D-39 Homo sapiens 18-24 23592178-1 2013 The adsorption of O2/H2O molecules on the ZnO nanowire (NW) surface results in the long lifetime of photo-generated carriers and thus benefits ZnO NW-based ultraviolet photodetectors by suppressing the dark current and improving the photocurrent gain, but the slow adsorption process also leads to slow detector response time. Zinc Oxide 143-146 immunoglobulin kappa variable 1D-39 Homo sapiens 18-24 23321926-0 2013 Serum albumin enhances the membrane activity of ZnO nanoparticles. Zinc Oxide 48-51 albumin Homo sapiens 0-13 23321926-1 2013 We investigate the effect of serum albumin on the interaction of ZnO nanoparticles with DOPC lipid membranes and show that the size-stabilizing effect of the protein corona enhances their interaction with lipid membranes, which manifests, in part, as an increased ordering in the lipid packing. Zinc Oxide 65-68 albumin Homo sapiens 29-42 23501721-0 2013 Synthesis and structural characterization of Co2+ ions doped ZnO nanopowders by solid state reaction through sonication. Zinc Oxide 61-64 complement C2 Homo sapiens 45-48 23532625-7 2013 Moreover, either of the 2 used agents successfully alleviated the alteration in nitric oxide (NO) and vascular endothelial growth factor (VEGF) in ZnO-NPs in sera of intoxicated group. Zinc Oxide 147-150 vascular endothelial growth factor A Rattus norvegicus 138-142 23233308-4 2013 Compared to CdS-ZnO QDSSCs, Ag(2)S-ZnO QDSSCs exhibit a considerably higher short-circuit current density (J(sc)) and a strongly enhanced light-harvesting efficiency, but lower open-circuit voltages (V(oc)), resulting in almost the same power-conversion efficiency of 1.2 %. Zinc Oxide 35-38 angiotensin II receptor type 1 Homo sapiens 28-34 23380398-0 2013 Fibrinogen adsorption on zinc oxide nanoparticles: a Micro-Differential Scanning Calorimetry analysis. Zinc Oxide 25-35 fibrinogen beta chain Homo sapiens 0-10 23380398-2 2013 The aim of this work is the study of the interaction of fibrinogen (Fib) with zinc oxide nanoparticles. Zinc Oxide 78-88 fibrinogen beta chain Homo sapiens 56-66 23380398-2 2013 The aim of this work is the study of the interaction of fibrinogen (Fib) with zinc oxide nanoparticles. Zinc Oxide 78-88 fibrinogen beta chain Homo sapiens 68-71 23380398-9 2013 The discrepancy between the Fib adsorption percentages on homemade and commercially available zinc oxide nanoparticles can be attributed to their different size. Zinc Oxide 94-104 fibrinogen beta chain Homo sapiens 28-31 23318775-3 2013 Ag(2)S-ZnO is found to be more efficient than commercial ZnO, prepared ZnO and TiO(2)-P25 at pH 9 for the mineralization of Acid Black 1. Zinc Oxide 7-10 angiotensin II receptor type 1 Homo sapiens 0-6 23318775-3 2013 Ag(2)S-ZnO is found to be more efficient than commercial ZnO, prepared ZnO and TiO(2)-P25 at pH 9 for the mineralization of Acid Black 1. Zinc Oxide 57-60 angiotensin II receptor type 1 Homo sapiens 0-6 23318775-3 2013 Ag(2)S-ZnO is found to be more efficient than commercial ZnO, prepared ZnO and TiO(2)-P25 at pH 9 for the mineralization of Acid Black 1. Zinc Oxide 57-60 angiotensin II receptor type 1 Homo sapiens 0-6 23318775-5 2013 Mechanism of degradation by Ag(2)S-ZnO is proposed. Zinc Oxide 35-38 angiotensin II receptor type 1 Homo sapiens 28-34 23232460-6 2013 Our studies indicate that ZnO nanoparticles could apparently decrease the mitochondrial membrane potential, increase the production of ROS and lead to the overexpression of caspase-12 in RGC-5 cells, suggesting that ZnO nanoparticle-induced toxicity via ROS overproduction will trigger endoplasmic reticulum stress, lead to the RGC-5 cell damage and finally induce apoptosis/necrosis, the overexpression of caspase-12 may be involved in cell death in RGC-5 cells. Zinc Oxide 26-29 caspase 12 Mus musculus 173-183 23232460-6 2013 Our studies indicate that ZnO nanoparticles could apparently decrease the mitochondrial membrane potential, increase the production of ROS and lead to the overexpression of caspase-12 in RGC-5 cells, suggesting that ZnO nanoparticle-induced toxicity via ROS overproduction will trigger endoplasmic reticulum stress, lead to the RGC-5 cell damage and finally induce apoptosis/necrosis, the overexpression of caspase-12 may be involved in cell death in RGC-5 cells. Zinc Oxide 26-29 caspase 12 Mus musculus 407-417 23232460-6 2013 Our studies indicate that ZnO nanoparticles could apparently decrease the mitochondrial membrane potential, increase the production of ROS and lead to the overexpression of caspase-12 in RGC-5 cells, suggesting that ZnO nanoparticle-induced toxicity via ROS overproduction will trigger endoplasmic reticulum stress, lead to the RGC-5 cell damage and finally induce apoptosis/necrosis, the overexpression of caspase-12 may be involved in cell death in RGC-5 cells. Zinc Oxide 216-219 caspase 12 Mus musculus 173-183 23232460-6 2013 Our studies indicate that ZnO nanoparticles could apparently decrease the mitochondrial membrane potential, increase the production of ROS and lead to the overexpression of caspase-12 in RGC-5 cells, suggesting that ZnO nanoparticle-induced toxicity via ROS overproduction will trigger endoplasmic reticulum stress, lead to the RGC-5 cell damage and finally induce apoptosis/necrosis, the overexpression of caspase-12 may be involved in cell death in RGC-5 cells. Zinc Oxide 216-219 caspase 12 Mus musculus 407-417 23339573-2 2013 However, up to date, the external quantum efficiency of UV LED based on ZnO nanostructures has been limited by a lack of efficient methods to achieve a balance between electron contributed current and hole contributed current that reduces the nonradiative recombination at interface. Zinc Oxide 72-75 small integral membrane protein 10 like 2A Homo sapiens 59-62 23339573-3 2013 Here we demonstrate that the piezo-phototronic effect can largely enhance the efficiency of a hybridized inorganic/organic LED made of a ZnO nanowire/p-polymer structure, by trimming the electron current to match the hole current and increasing the localized hole density near the interface through a carrier channel created by piezoelectric polarization charges on the ZnO side. Zinc Oxide 137-140 small integral membrane protein 10 like 2A Homo sapiens 123-126 23339573-3 2013 Here we demonstrate that the piezo-phototronic effect can largely enhance the efficiency of a hybridized inorganic/organic LED made of a ZnO nanowire/p-polymer structure, by trimming the electron current to match the hole current and increasing the localized hole density near the interface through a carrier channel created by piezoelectric polarization charges on the ZnO side. Zinc Oxide 370-373 small integral membrane protein 10 like 2A Homo sapiens 123-126 23295026-4 2013 In this paper, optimized mats of ZnO nanofibers with an average fiber diameter of 60 nm are shown to be highly effective in the photocatalytic degradation of the PAH dyes--naphthalene and anthracene. Zinc Oxide 33-36 phenylalanine hydroxylase Homo sapiens 162-165 23318775-0 2013 Ag2S-ZnO--an efficient photocatalyst for the mineralization of Acid Black 1 with UV light. Zinc Oxide 5-8 angiotensin II receptor type 1 Homo sapiens 0-4 23318775-1 2013 The Ag(2)S loaded ZnO (Ag(2)S-ZnO) was successfully synthesized by precipitation of zinc oxalate and Ag(2)S and calcination of the mixed precipitate at 400 C for 12 h. The catalyst was characterized by X-ray diffraction (XRD), scanning electron microscope (SEM) images, energy dispersive spectra (EDS), diffuse reflectance spectra (DRS) photoluminescence spectra (PL) and BET surface area measurements. Zinc Oxide 18-21 angiotensin II receptor type 1 Homo sapiens 4-10 23318775-1 2013 The Ag(2)S loaded ZnO (Ag(2)S-ZnO) was successfully synthesized by precipitation of zinc oxalate and Ag(2)S and calcination of the mixed precipitate at 400 C for 12 h. The catalyst was characterized by X-ray diffraction (XRD), scanning electron microscope (SEM) images, energy dispersive spectra (EDS), diffuse reflectance spectra (DRS) photoluminescence spectra (PL) and BET surface area measurements. Zinc Oxide 18-21 angiotensin II receptor type 1 Homo sapiens 23-29 23318775-1 2013 The Ag(2)S loaded ZnO (Ag(2)S-ZnO) was successfully synthesized by precipitation of zinc oxalate and Ag(2)S and calcination of the mixed precipitate at 400 C for 12 h. The catalyst was characterized by X-ray diffraction (XRD), scanning electron microscope (SEM) images, energy dispersive spectra (EDS), diffuse reflectance spectra (DRS) photoluminescence spectra (PL) and BET surface area measurements. Zinc Oxide 18-21 angiotensin II receptor type 1 Homo sapiens 23-29 23318775-1 2013 The Ag(2)S loaded ZnO (Ag(2)S-ZnO) was successfully synthesized by precipitation of zinc oxalate and Ag(2)S and calcination of the mixed precipitate at 400 C for 12 h. The catalyst was characterized by X-ray diffraction (XRD), scanning electron microscope (SEM) images, energy dispersive spectra (EDS), diffuse reflectance spectra (DRS) photoluminescence spectra (PL) and BET surface area measurements. Zinc Oxide 18-21 delta/notch like EGF repeat containing Homo sapiens 373-376 23318775-1 2013 The Ag(2)S loaded ZnO (Ag(2)S-ZnO) was successfully synthesized by precipitation of zinc oxalate and Ag(2)S and calcination of the mixed precipitate at 400 C for 12 h. The catalyst was characterized by X-ray diffraction (XRD), scanning electron microscope (SEM) images, energy dispersive spectra (EDS), diffuse reflectance spectra (DRS) photoluminescence spectra (PL) and BET surface area measurements. Zinc Oxide 30-33 angiotensin II receptor type 1 Homo sapiens 4-10 23318775-1 2013 The Ag(2)S loaded ZnO (Ag(2)S-ZnO) was successfully synthesized by precipitation of zinc oxalate and Ag(2)S and calcination of the mixed precipitate at 400 C for 12 h. The catalyst was characterized by X-ray diffraction (XRD), scanning electron microscope (SEM) images, energy dispersive spectra (EDS), diffuse reflectance spectra (DRS) photoluminescence spectra (PL) and BET surface area measurements. Zinc Oxide 30-33 angiotensin II receptor type 1 Homo sapiens 23-29 23318775-1 2013 The Ag(2)S loaded ZnO (Ag(2)S-ZnO) was successfully synthesized by precipitation of zinc oxalate and Ag(2)S and calcination of the mixed precipitate at 400 C for 12 h. The catalyst was characterized by X-ray diffraction (XRD), scanning electron microscope (SEM) images, energy dispersive spectra (EDS), diffuse reflectance spectra (DRS) photoluminescence spectra (PL) and BET surface area measurements. Zinc Oxide 30-33 angiotensin II receptor type 1 Homo sapiens 23-29 23318775-1 2013 The Ag(2)S loaded ZnO (Ag(2)S-ZnO) was successfully synthesized by precipitation of zinc oxalate and Ag(2)S and calcination of the mixed precipitate at 400 C for 12 h. The catalyst was characterized by X-ray diffraction (XRD), scanning electron microscope (SEM) images, energy dispersive spectra (EDS), diffuse reflectance spectra (DRS) photoluminescence spectra (PL) and BET surface area measurements. Zinc Oxide 30-33 delta/notch like EGF repeat containing Homo sapiens 373-376 23318775-2 2013 The photocatalytic activity of Ag(2)S-ZnO was investigated for the degradation of Acid Black (AB 1) in aqueous solution using UV light. Zinc Oxide 38-41 angiotensin II receptor type 1 Homo sapiens 31-37 23274157-0 2013 Interaction of cytochrome c with zinc oxide nanoparticles. Zinc Oxide 33-43 cytochrome c, somatic Equus caballus 15-27 23654106-5 2013 RESULTS: At 8h exposure to ZnO-NPs, there was no significant difference in the activity of LDH in the cell culture media among the ZnO-NPs-treated and control groups, but the activity of caspase-1 and the levels of IL-1beta in A549 cells were significantly increased in 20 microg/ml ZnO-NPs group compared to that in the control group (P < 0.05). Zinc Oxide 27-30 caspase 1 Homo sapiens 187-196 23654106-5 2013 RESULTS: At 8h exposure to ZnO-NPs, there was no significant difference in the activity of LDH in the cell culture media among the ZnO-NPs-treated and control groups, but the activity of caspase-1 and the levels of IL-1beta in A549 cells were significantly increased in 20 microg/ml ZnO-NPs group compared to that in the control group (P < 0.05). Zinc Oxide 27-30 interleukin 1 beta Homo sapiens 215-223 23654106-6 2013 Levels of IL-1beta and activity of LDH in the groups treated with ZnO-NPs (10 or 20 microg/ml) were significantly higher than that in the control group after 24 h exposure to ZnO-NPs, but there was no significant difference in the activity of caspase-1 among ZnO-NPs and control group. Zinc Oxide 66-69 interleukin 1 beta Homo sapiens 10-18 23654106-6 2013 Levels of IL-1beta and activity of LDH in the groups treated with ZnO-NPs (10 or 20 microg/ml) were significantly higher than that in the control group after 24 h exposure to ZnO-NPs, but there was no significant difference in the activity of caspase-1 among ZnO-NPs and control group. Zinc Oxide 66-69 caspase 1 Homo sapiens 243-252 23654106-6 2013 Levels of IL-1beta and activity of LDH in the groups treated with ZnO-NPs (10 or 20 microg/ml) were significantly higher than that in the control group after 24 h exposure to ZnO-NPs, but there was no significant difference in the activity of caspase-1 among ZnO-NPs and control group. Zinc Oxide 175-178 interleukin 1 beta Homo sapiens 10-18 23654106-6 2013 Levels of IL-1beta and activity of LDH in the groups treated with ZnO-NPs (10 or 20 microg/ml) were significantly higher than that in the control group after 24 h exposure to ZnO-NPs, but there was no significant difference in the activity of caspase-1 among ZnO-NPs and control group. Zinc Oxide 175-178 interleukin 1 beta Homo sapiens 10-18 23288043-4 2013 The CdSe/CdS co-sensitized QDSSCs using these nanosheet branched (NB) ZnO nanorods (NRs) as a photoanode exhibit a highly enhanced solar-energy conversion efficiency of 4.4% under conditions of 1 sun illumination. Zinc Oxide 70-73 CDP-diacylglycerol synthase 1 Homo sapiens 4-7 23233308-0 2013 Environmentally benign and efficient Ag2S-ZnO nanowires as photoanodes for solar cells: comparison with CdS-ZnO nanowires. Zinc Oxide 42-45 angiotensin II receptor type 1 Homo sapiens 37-41 23233308-1 2013 In this work, we develop a low-temperature, facile solution reaction route for the fabrication of quantum-dot-sensitized solar cells (QDSSCs) containing Ag(2)S-ZnO nanowires (NWs), simultaneously ensuring low manufacturing costs and environmental safety. Zinc Oxide 160-163 angiotensin II receptor type 1 Homo sapiens 153-159 23233308-4 2013 Compared to CdS-ZnO QDSSCs, Ag(2)S-ZnO QDSSCs exhibit a considerably higher short-circuit current density (J(sc)) and a strongly enhanced light-harvesting efficiency, but lower open-circuit voltages (V(oc)), resulting in almost the same power-conversion efficiency of 1.2 %. Zinc Oxide 16-19 angiotensin II receptor type 1 Homo sapiens 28-34 23331623-7 2013 Introduction of ZnO nanorod on the SnO(2) nanoparticle layer improved significantly electron transport and lifetime compared to the SnO(2) only film. Zinc Oxide 16-19 strawberry notch homolog 2 Homo sapiens 35-38 23000680-0 2013 Interaction of colloidal zinc oxide nanoparticles with bovine serum albumin and its adsorption isotherms and kinetics. Zinc Oxide 25-35 albumin Homo sapiens 62-75 23331623-7 2013 Introduction of ZnO nanorod on the SnO(2) nanoparticle layer improved significantly electron transport and lifetime compared to the SnO(2) only film. Zinc Oxide 16-19 strawberry notch homolog 2 Homo sapiens 132-135 23000680-3 2013 The aim of this study was to stabilize and biofunctionalize ZnO NPs using bovine serum albumin (BSA). Zinc Oxide 60-63 albumin Homo sapiens 81-94 23646550-1 2013 Fabrication and characterization of a heterojunction structured by CdS quantum dots@ZnO nanowire-array panels were presented. Zinc Oxide 84-87 CDP-diacylglycerol synthase 1 Homo sapiens 67-70 23646550-3 2013 Secondly, CdS quantum dots were deposited onto the surface of the ZnO nanowire-arrays by using successive ion layer absorption and reaction method, and the CdS shell/ZnO core heterojunction were thus obtained. Zinc Oxide 66-69 CDP-diacylglycerol synthase 1 Homo sapiens 10-13 23646550-3 2013 Secondly, CdS quantum dots were deposited onto the surface of the ZnO nanowire-arrays by using successive ion layer absorption and reaction method, and the CdS shell/ZnO core heterojunction were thus obtained. Zinc Oxide 66-69 CDP-diacylglycerol synthase 1 Homo sapiens 156-159 23646550-3 2013 Secondly, CdS quantum dots were deposited onto the surface of the ZnO nanowire-arrays by using successive ion layer absorption and reaction method, and the CdS shell/ZnO core heterojunction were thus obtained. Zinc Oxide 166-169 CDP-diacylglycerol synthase 1 Homo sapiens 10-13 23646550-4 2013 Field emission scanning electron microscopy and transmission electron microscope were employed to characterize the morphological properties of the as-obtained CdS quantum dots@ZnO nanowire-array panels. Zinc Oxide 176-179 CDP-diacylglycerol synthase 1 Homo sapiens 159-162 23646550-5 2013 X-ray diffraction was adopted to characterize the crystalline properties of the as-obtained CdS quantum dots@ZnO nanowire-array panels. Zinc Oxide 109-112 CDP-diacylglycerol synthase 1 Homo sapiens 92-95 23646550-6 2013 Methyl orange was taken as a model compound to confirm the photocatalytic activities of the CdS shell/ZnO core heterojunction. Zinc Oxide 102-105 CDP-diacylglycerol synthase 1 Homo sapiens 92-95 23646580-1 2013 In this work, periodic arrays of various ZnO nanostructures were fabricated on both Si and GaN substrates via a facile hydrothermal process. Zinc Oxide 41-44 gigaxonin Homo sapiens 91-94 23646580-8 2013 It is found that the highly ordered and vertically aligned ZnO nanorods epitaxially grow on the GaN substrate, while the ZnO nanoflowers on Si substrates are random oriented. Zinc Oxide 59-62 gigaxonin Homo sapiens 96-99 23433213-0 2013 [Inductive effect of zinc oxide nanoparticles on interleukin 8 gene expression in human bronchial epithelial cells and its regulatory mechanism]. Zinc Oxide 21-31 C-X-C motif chemokine ligand 8 Homo sapiens 49-62 23433213-1 2013 OBJECTIVE: To clarify the effect of zinc oxide nanoparticles (ZnO-NPs) (30 nm in diameter) on the interleukin 8 (IL-8) gene expression in human bronchial epithelial cells (BEAS-2B) and its regulatory mechanism. Zinc Oxide 36-46 C-X-C motif chemokine ligand 8 Homo sapiens 98-111 23433213-1 2013 OBJECTIVE: To clarify the effect of zinc oxide nanoparticles (ZnO-NPs) (30 nm in diameter) on the interleukin 8 (IL-8) gene expression in human bronchial epithelial cells (BEAS-2B) and its regulatory mechanism. Zinc Oxide 36-46 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 23433213-4 2013 RT-PCR and ELISA were used to measure the mRNA and protein expression levels of IL-8 in the BEAS-2B cells exposed to ZnO-NPs. Zinc Oxide 117-120 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 23433213-5 2013 The IL-8 mRNA decay assay was used to determine the effect of ZnO-NPs on IL-8 mRNA stability. Zinc Oxide 62-65 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 23433213-6 2013 RESULTS: Exposure to ZnO-NPs significantly increased the level of IL-8 mRNA in BEAS-2B cells and the level of IL-8 protein in supernatant medium. Zinc Oxide 21-24 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 23433213-6 2013 RESULTS: Exposure to ZnO-NPs significantly increased the level of IL-8 mRNA in BEAS-2B cells and the level of IL-8 protein in supernatant medium. Zinc Oxide 21-24 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 23433213-7 2013 The transcription inhibitor significantly reduced the mRNA expression of IL-8 induced by ZnO-NPs. Zinc Oxide 89-92 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 23433213-8 2013 ZnO-NPs significantly delayed IL-8 mRNA degradation in the BEAS-2B cells that were pretreated with actinomycin D for terminating IL-8 mRNA synthesis. Zinc Oxide 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 23433213-8 2013 ZnO-NPs significantly delayed IL-8 mRNA degradation in the BEAS-2B cells that were pretreated with actinomycin D for terminating IL-8 mRNA synthesis. Zinc Oxide 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 23234536-1 2013 The different wt % of Zr-codoped Ag-ZnO catalysts were prepared by the simple precipitation-thermal decomposition method and used for degradation of anionic azo dye Reactive Red 120 (RR 120) under natural sunlight. Zinc Oxide 36-39 RNA binding motif protein 25 Homo sapiens 175-182 23259506-1 2013 Remote plasma in situ atomic layer doping technique was applied to prepare an n-type nitrogen-doped ZnO (n-ZnO:N) layer upon p-type magnesium-doped GaN (p-GaN:Mg) to fabricate the n-ZnO:N/p-GaN:Mg heterojuntion light-emitting diodes. Zinc Oxide 100-103 gigaxonin Homo sapiens 153-161 23259506-1 2013 Remote plasma in situ atomic layer doping technique was applied to prepare an n-type nitrogen-doped ZnO (n-ZnO:N) layer upon p-type magnesium-doped GaN (p-GaN:Mg) to fabricate the n-ZnO:N/p-GaN:Mg heterojuntion light-emitting diodes. Zinc Oxide 100-103 gigaxonin Homo sapiens 188-196 23259506-2 2013 The room-temperature electroluminescence exhibits a dominant ultraviolet peak at lambda 370 nm from ZnO band-edge emission and suppressed luminescence from GaN, as a result of the decrease in electron concentration in ZnO and reduced electron injection from n-ZnO:N to p-GaN:Mg because of the nitrogen incorporation. Zinc Oxide 220-223 gigaxonin Homo sapiens 158-161 23259506-2 2013 The room-temperature electroluminescence exhibits a dominant ultraviolet peak at lambda 370 nm from ZnO band-edge emission and suppressed luminescence from GaN, as a result of the decrease in electron concentration in ZnO and reduced electron injection from n-ZnO:N to p-GaN:Mg because of the nitrogen incorporation. Zinc Oxide 220-223 gigaxonin Homo sapiens 271-279 23259506-2 2013 The room-temperature electroluminescence exhibits a dominant ultraviolet peak at lambda 370 nm from ZnO band-edge emission and suppressed luminescence from GaN, as a result of the decrease in electron concentration in ZnO and reduced electron injection from n-ZnO:N to p-GaN:Mg because of the nitrogen incorporation. Zinc Oxide 220-223 gigaxonin Homo sapiens 158-161 23270955-6 2013 Size effects of ZnO nanoparticles on bovine serum albumin and keratinocyte cells are different. Zinc Oxide 16-19 albumin Homo sapiens 44-57 23259506-2 2013 The room-temperature electroluminescence exhibits a dominant ultraviolet peak at lambda 370 nm from ZnO band-edge emission and suppressed luminescence from GaN, as a result of the decrease in electron concentration in ZnO and reduced electron injection from n-ZnO:N to p-GaN:Mg because of the nitrogen incorporation. Zinc Oxide 220-223 gigaxonin Homo sapiens 271-279 22842014-6 2012 Interestingly, ZnO but not TiO(2) nanoparticles induced a down regulation of FcgammaRIII (CD16) expression on NK-cells in the PBMC population, suggesting that subtoxic concentrations of ZnO nanoparticles might have an effect on FcgammaR-mediated immune responses. Zinc Oxide 15-18 Fc gamma receptor IIIa Homo sapiens 77-88 23383938-1 2013 High-spin paramagnetic manganese defects in polar piezoelectric zinc oxide exhibit a simple, almost axial anisotropy and phase coherence times of the order of a millisecond at low temperatures. Zinc Oxide 64-74 spindlin 1 Homo sapiens 5-9 23646734-1 2013 High ordered one-dimensional (1D) Zinc oxide (ZnO) nanowires were grown on FTO substrate by using the hydrothermal method. Zinc Oxide 34-44 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 75-78 23646734-1 2013 High ordered one-dimensional (1D) Zinc oxide (ZnO) nanowires were grown on FTO substrate by using the hydrothermal method. Zinc Oxide 46-49 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 75-78 23646734-3 2013 Solar cell made from ZnO nanowire at 50 nm radius and several tens micron lengths showed high solar conversion efficiency (eta) of 2.1% and incident photon current efficiency (IPCE) 35% using nanowire/N719 dye/I-/I3- electrolyte. Zinc Oxide 21-24 endothelin receptor type A Homo sapiens 123-126 23646734-5 2013 In the case of the N3 dye on ZnO nanowire conversion efficiency (eta) of 1.32% and IPCE 23% were obtained under an illumination of 100 mW/cm2. Zinc Oxide 29-32 endothelin receptor type A Homo sapiens 65-68 23174455-0 2013 Alkaline transition of horse heart cytochrome c in the presence of ZnO nanoparticles. Zinc Oxide 67-70 cytochrome c, somatic Equus caballus 35-47 23174455-1 2013 The effect of zinc oxide nanoparticles (ZnO NPs) on cytochrome c (cyt c) in alkaline pH was studied with absorption spectroscopy and UV circular dichroism (CD). Zinc Oxide 14-24 cytochrome c, somatic Equus caballus 52-64 23174455-1 2013 The effect of zinc oxide nanoparticles (ZnO NPs) on cytochrome c (cyt c) in alkaline pH was studied with absorption spectroscopy and UV circular dichroism (CD). Zinc Oxide 14-24 cytochrome c, somatic Equus caballus 66-71 23174455-1 2013 The effect of zinc oxide nanoparticles (ZnO NPs) on cytochrome c (cyt c) in alkaline pH was studied with absorption spectroscopy and UV circular dichroism (CD). Zinc Oxide 40-43 cytochrome c, somatic Equus caballus 52-64 23174455-1 2013 The effect of zinc oxide nanoparticles (ZnO NPs) on cytochrome c (cyt c) in alkaline pH was studied with absorption spectroscopy and UV circular dichroism (CD). Zinc Oxide 40-43 cytochrome c, somatic Equus caballus 66-71 23174455-3 2013 The stability around the heme crevice of cyt c and therefore the switch of the axial ligand Met80 to Lys which occurs in conditions of higher pH was proven following the interaction of cytochrome c with ZnO nanoparticles. Zinc Oxide 203-206 cytochrome c, somatic Equus caballus 41-46 23174455-3 2013 The stability around the heme crevice of cyt c and therefore the switch of the axial ligand Met80 to Lys which occurs in conditions of higher pH was proven following the interaction of cytochrome c with ZnO nanoparticles. Zinc Oxide 203-206 cytochrome c, somatic Equus caballus 185-197 23627071-5 2013 The aim of the present study was to analyze functional impairment of hMSC by ZnO- and TiO2-NPs. Zinc Oxide 77-80 musculin Homo sapiens 69-73 23142470-1 2013 Zinc oxide (ZnO) particle induced cytotoxicity was dependent on size, charge and solubility, factors which at sublethal concentrations may influence the activation of the human monocytic cell line THP1. Zinc Oxide 0-10 GLI family zinc finger 2 Homo sapiens 197-201 23142470-1 2013 Zinc oxide (ZnO) particle induced cytotoxicity was dependent on size, charge and solubility, factors which at sublethal concentrations may influence the activation of the human monocytic cell line THP1. Zinc Oxide 12-15 GLI family zinc finger 2 Homo sapiens 197-201 23142470-5 2013 This association with protein may influence interaction of the ZnO particles and NP with THP1 cells. Zinc Oxide 63-66 GLI family zinc finger 2 Homo sapiens 89-93 23142470-6 2013 After 24h exposure to the ZnO particles and NP at sublethal concentrations there was little effect on immunological markers of inflammation such as HLA DR and CD14, although they may induce a modest increase in the adhesion molecule CD11b. Zinc Oxide 26-29 integrin subunit alpha M Homo sapiens 233-238 22981930-0 2012 Development of an Au/ZnO thin film surface plasmon resonance-based biosensor immunoassay for the detection of carbohydrate antigen 15-3 in human saliva. Zinc Oxide 21-24 mucin 1, cell surface associated Homo sapiens 110-135 22981930-4 2012 RESULTS: The linear detection range of CA15-3 in human saliva with the SPR system based on thin-film Au/ZnO was 2.5-20 U/mL (the cut-off point in cancer patients is around 4 U/mL). Zinc Oxide 104-107 mucin 1, cell surface associated Homo sapiens 39-45 22981930-6 2012 CONCLUSIONS: These results show that thin-film Au/ZnO-based SPR systems have higher sensitivity and can be used for measuring the levels of CA15-3 in human saliva without concentrating the samples. Zinc Oxide 50-53 mucin 1, cell surface associated Homo sapiens 140-146 23030004-8 2012 Cell membrane damage (significant increase in lactate dehydrogenase release and annexin V staining) was observed in the concentration of ZnO nanoparticles above 30 microg/ml. Zinc Oxide 137-140 annexin A5 Homo sapiens 80-89 22842014-6 2012 Interestingly, ZnO but not TiO(2) nanoparticles induced a down regulation of FcgammaRIII (CD16) expression on NK-cells in the PBMC population, suggesting that subtoxic concentrations of ZnO nanoparticles might have an effect on FcgammaR-mediated immune responses. Zinc Oxide 15-18 Fc gamma receptor IIIa Homo sapiens 90-94 22842014-6 2012 Interestingly, ZnO but not TiO(2) nanoparticles induced a down regulation of FcgammaRIII (CD16) expression on NK-cells in the PBMC population, suggesting that subtoxic concentrations of ZnO nanoparticles might have an effect on FcgammaR-mediated immune responses. Zinc Oxide 186-189 Fc gamma receptor IIIa Homo sapiens 77-88 22842014-6 2012 Interestingly, ZnO but not TiO(2) nanoparticles induced a down regulation of FcgammaRIII (CD16) expression on NK-cells in the PBMC population, suggesting that subtoxic concentrations of ZnO nanoparticles might have an effect on FcgammaR-mediated immune responses. Zinc Oxide 186-189 Fc gamma receptor IIIa Homo sapiens 90-94 22967553-1 2012 A potentiometrically tuned-glucose biosensor was fabricated using core-shell nanocomposite based on zinc oxide encapsulated chitosan-graft-poly(vinyl alcohol) (ZnO/CHIT-g-PVAL). Zinc Oxide 100-110 chitinase 1 Homo sapiens 164-168 22743779-0 2012 Low-temperature synthesis of ZnO/CdS hierarchical nanostructure for photovoltaic application. Zinc Oxide 29-32 CDP-diacylglycerol synthase 1 Homo sapiens 33-36 22743779-2 2012 In the present work, we developed a low-temperature process for facile synthesis of ZnO/CdS hierarchical nanowires, where the primary ZnO nanowires were first prepared via a hydrothermal route and then the secondary single-crystal CdS tips were grown on the ZnO nanowires by electrochemical deposition. Zinc Oxide 84-87 CDP-diacylglycerol synthase 1 Homo sapiens 88-91 22743779-2 2012 In the present work, we developed a low-temperature process for facile synthesis of ZnO/CdS hierarchical nanowires, where the primary ZnO nanowires were first prepared via a hydrothermal route and then the secondary single-crystal CdS tips were grown on the ZnO nanowires by electrochemical deposition. Zinc Oxide 134-137 CDP-diacylglycerol synthase 1 Homo sapiens 88-91 22743779-2 2012 In the present work, we developed a low-temperature process for facile synthesis of ZnO/CdS hierarchical nanowires, where the primary ZnO nanowires were first prepared via a hydrothermal route and then the secondary single-crystal CdS tips were grown on the ZnO nanowires by electrochemical deposition. Zinc Oxide 134-137 CDP-diacylglycerol synthase 1 Homo sapiens 88-91 22743779-3 2012 The as-grown hierarchical ZnO/CdS nanowires are superior in charge separation as well as carrier transport, thus achieving higher open circuit voltage, short circuit current and final conversion efficiency than the common coaxial nanocables with CdS nanocrystal shell on core ZnO nanowires. Zinc Oxide 276-279 CDP-diacylglycerol synthase 1 Homo sapiens 30-33 22331639-2 2012 Due to the polarization of ions in a crystal that has non-central symmetry in materials such as the wurtzite structured ZnO, GaN and InN, a piezoelectric potential (piezopotential) is created in the crystal by applying a stress. Zinc Oxide 120-123 growth hormone releasing hormone Homo sapiens 133-136 25780643-4 2012 The effect of ZnO NP HPPS on NF-kappa B was measured by using a luciferase assay. Zinc Oxide 14-17 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 Mus musculus 29-39 23035478-2 2012 The crystal structure, morphology and chemical compositions of the as-prepared ZnO nanoparticles were examined by X-ray powder diffraction (XRD), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), scanning electron microscopy (SEM), Brunauer-Emmett-Teller specific surface area (BET). Zinc Oxide 79-82 delta/notch like EGF repeat containing Homo sapiens 308-311 25780643-9 2012 However, ZnO NP HPPS, the combined form of ZnO NPs and HPPS, did induce the intracellular ROS production, as well as prominently activating NF-kappa B and it"s dependent genes. Zinc Oxide 9-12 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 Mus musculus 140-150 25780643-9 2012 However, ZnO NP HPPS, the combined form of ZnO NPs and HPPS, did induce the intracellular ROS production, as well as prominently activating NF-kappa B and it"s dependent genes. Zinc Oxide 43-46 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 Mus musculus 140-150 25780643-13 2012 The ZnO NP HPPS, however, significantly activated NF-kappa B and up-regulated its dependent genes such as TNF-alpha, IL-1, and MCP-1. Zinc Oxide 4-7 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 Mus musculus 50-60 25780643-13 2012 The ZnO NP HPPS, however, significantly activated NF-kappa B and up-regulated its dependent genes such as TNF-alpha, IL-1, and MCP-1. Zinc Oxide 4-7 tumor necrosis factor Mus musculus 106-115 25780643-13 2012 The ZnO NP HPPS, however, significantly activated NF-kappa B and up-regulated its dependent genes such as TNF-alpha, IL-1, and MCP-1. Zinc Oxide 4-7 interleukin 1 complex Mus musculus 117-121 25780643-13 2012 The ZnO NP HPPS, however, significantly activated NF-kappa B and up-regulated its dependent genes such as TNF-alpha, IL-1, and MCP-1. Zinc Oxide 4-7 mast cell protease 1 Mus musculus 127-132 22544331-1 2012 Hydrogenated ZnO nanorod arrays (NRAs) grown on F-doped SnO(2) (FTO) glass substrates yield a benchmark specific hydrogen production rate of 122,500 mumol h(-1) g(-1), and exhibit excellent stability and recyclability. Zinc Oxide 13-16 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 64-67 22033421-6 2012 Interestingly, inverse dose-dependent increase was noted in aspartate aminotransferase, alanine aminotransferase serum levels of nano-size zinc oxide groups when compared with their micro-sized zinc oxide. Zinc Oxide 139-149 glutamic-oxaloacetic transaminase 2 Rattus norvegicus 60-86 22901679-6 2012 RESULTS: Off-gases released as by-product of flame ZnO synthesis caused a significant decrease of total reduced GSH and induced further the release of the cytokine TNFalpha, demonstrating the influence of the gas phase on aerosol toxicology. Zinc Oxide 51-54 tumor necrosis factor Homo sapiens 164-172 22901679-9 2012 Other parameters such as LDH and HO-1 were not influenced by gaseous compounds: Following aerosol exposure, LDH levels appeared elevated at both timepoints and the HO-1 transcript correlated positively with deposited ZnO-dose. Zinc Oxide 217-220 heme oxygenase 1 Homo sapiens 164-168 22617216-2 2012 The morphology of the CdZnO films depends on the amount of ZnO and CdO in the films. Zinc Oxide 24-27 cell adhesion associated, oncogene regulated Homo sapiens 67-70 22617216-3 2012 The optical band gap of the CdZnO films depends on the compositions of CdO and ZnO. Zinc Oxide 30-33 cell adhesion associated, oncogene regulated Homo sapiens 71-74 22617216-4 2012 Films having higher amount of CdO shows the presence of grains along with the fiber nature of ZnO, whereas the film with lower percentage of CdO shows fiber nature of the film very similar to pure ZnO film. Zinc Oxide 197-200 cell adhesion associated, oncogene regulated Homo sapiens 141-144 22395444-8 2012 In addition, ZnO nanoparticles activated JNK, p38 and induced p53(Ser15) phosphorylation. Zinc Oxide 13-16 mitogen-activated protein kinase 14 Homo sapiens 46-49 22395444-8 2012 In addition, ZnO nanoparticles activated JNK, p38 and induced p53(Ser15) phosphorylation. Zinc Oxide 13-16 tumor protein p53 Homo sapiens 62-65 22746363-0 2012 Interaction of polyethyleneimine-functionalized ZnO nanoparticles with bovine serum albumin. Zinc Oxide 48-51 albumin Homo sapiens 78-91 22852476-0 2012 Regulation of c-Myc and Bcl-2 induced apoptosis of human bronchial epithelial cells by zinc oxide nanoparticles. Zinc Oxide 87-97 MYC proto-oncogene, bHLH transcription factor Homo sapiens 14-19 22852476-0 2012 Regulation of c-Myc and Bcl-2 induced apoptosis of human bronchial epithelial cells by zinc oxide nanoparticles. Zinc Oxide 87-97 BCL2 apoptosis regulator Homo sapiens 24-29 22852476-5 2012 It demonstrated that following the exposure of 16HBE cells to ZnO NPs, both levels of mRNA and protein expression of c-Myc were significantly up-regulated, whereas the expressions of Bcl-2 mRNA and protein were down-regulated. Zinc Oxide 62-65 MYC proto-oncogene, bHLH transcription factor Homo sapiens 117-122 22852476-5 2012 It demonstrated that following the exposure of 16HBE cells to ZnO NPs, both levels of mRNA and protein expression of c-Myc were significantly up-regulated, whereas the expressions of Bcl-2 mRNA and protein were down-regulated. Zinc Oxide 62-65 BCL2 apoptosis regulator Homo sapiens 183-188 22852476-6 2012 Our results suggested that apoptosis induced by ZnO NPs might primarily involve the regulations of c-Myc and Bcl-2 gene expressions besides decline of MMP in 16HBE cells. Zinc Oxide 48-51 MYC proto-oncogene, bHLH transcription factor Homo sapiens 99-104 22852476-6 2012 Our results suggested that apoptosis induced by ZnO NPs might primarily involve the regulations of c-Myc and Bcl-2 gene expressions besides decline of MMP in 16HBE cells. Zinc Oxide 48-51 BCL2 apoptosis regulator Homo sapiens 109-114 22522300-0 2012 Spectroscopic analyses on sonocatalytic damage to bovine serum albumin (BSA) induced by ZnO/hydroxylapatite (ZnO/HA) composite under ultrasonic irradiation. Zinc Oxide 88-91 albumin Homo sapiens 57-70 22522300-2 2012 The sonocatalytic activities of ZnO/HA composite was carried out through the damage of bovine serum albumin (BSA) in aqueous solution. Zinc Oxide 32-35 albumin Homo sapiens 94-107 22746363-3 2012 We have carried out a detailed investigation on the interaction of bovine serum albumin (BSA) with polyethyleneimine-functionalized ZnO nanoparticles (ZnO-PEI). Zinc Oxide 132-135 albumin Homo sapiens 74-87 22734686-3 2012 According to UV-visible diffuse reflectance spectroscopy, the evident energy band gap value of the SnO(2)-ZnO photocatalyst was estimated to be 3.23 eV to be compared with those of pure SnO(2), that is, 3.7 eV, and ZnO, that is, 3.2 eV, analogues. Zinc Oxide 106-109 strawberry notch homolog 2 Homo sapiens 99-102 22812506-3 2012 RESULTS: We noted a dose dependant decrease in the cellular glutathione content following exposure of the C3A cells to Ag, the ZnO and the MWCNTs. Zinc Oxide 127-130 complement C3 Homo sapiens 106-109 22734686-3 2012 According to UV-visible diffuse reflectance spectroscopy, the evident energy band gap value of the SnO(2)-ZnO photocatalyst was estimated to be 3.23 eV to be compared with those of pure SnO(2), that is, 3.7 eV, and ZnO, that is, 3.2 eV, analogues. Zinc Oxide 106-109 strawberry notch homolog 2 Homo sapiens 186-189 22734686-4 2012 The energy band diagram of the SnO(2)-ZnO heterostructure was directly determined by combining XPS and the energy band gap values. Zinc Oxide 38-41 strawberry notch homolog 2 Homo sapiens 31-34 22734686-6 2012 Moreover, the heterostructure SnO(2)-ZnO photocatalyst showed much higher photocatalytic activities for the degradation of methylene blue than those of individual SnO(2) and ZnO nanomaterials. Zinc Oxide 37-40 strawberry notch homolog 2 Homo sapiens 30-33 22734686-6 2012 Moreover, the heterostructure SnO(2)-ZnO photocatalyst showed much higher photocatalytic activities for the degradation of methylene blue than those of individual SnO(2) and ZnO nanomaterials. Zinc Oxide 37-40 strawberry notch homolog 2 Homo sapiens 163-166 22734686-7 2012 This behavior was rationalized in terms of better charge separation and the suppression of charge recombination in the SnO(2)-ZnO photocatalyst because of the energy difference between the conduction band edges of SnO(2) and ZnO as evidenced by the band alignment determination. Zinc Oxide 126-129 strawberry notch homolog 2 Homo sapiens 119-122 22734686-7 2012 This behavior was rationalized in terms of better charge separation and the suppression of charge recombination in the SnO(2)-ZnO photocatalyst because of the energy difference between the conduction band edges of SnO(2) and ZnO as evidenced by the band alignment determination. Zinc Oxide 126-129 strawberry notch homolog 2 Homo sapiens 214-217 22734686-7 2012 This behavior was rationalized in terms of better charge separation and the suppression of charge recombination in the SnO(2)-ZnO photocatalyst because of the energy difference between the conduction band edges of SnO(2) and ZnO as evidenced by the band alignment determination. Zinc Oxide 225-228 strawberry notch homolog 2 Homo sapiens 119-122 22849192-1 2012 ZnO films co-doped with fluorine and hydrogen were prepared on Corning glass by radio frequency magnetron sputtering of ZnO targets with varying amounts of ZnF2 in H2/Ar gas mixtures of varying H2 content. Zinc Oxide 0-3 zinc finger protein 2 Homo sapiens 156-160 22966712-2 2012 Well-aligned high-quality ZnO nanorods were synthesized on FTO glass by the sonochemical decomposition of zinc acetate dihydrate using a ZnO thin-film as the catalytic layer. Zinc Oxide 26-29 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 59-62 22966712-3 2012 The ZnO thin-films were deposited on the FTO glass by a sputtering method. Zinc Oxide 4-7 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 41-44 22551404-0 2012 Nanointerlayer induced electroluminescence transition from ultraviolet- to red-dominant mode for n-Mn:ZnO/N-GaN heterojunction. Zinc Oxide 102-105 gigaxonin Homo sapiens 108-111 22422051-2 2012 Herein, we report a large-scale synthesis of a SnO(2)/alpha-Fe(2)O(3) composite nanotube array on a stainless steel substrate via a ZnO nanowire array as an in situ sacrificial template without using any strong acid or alkali. Zinc Oxide 132-135 strawberry notch homolog 1 Homo sapiens 47-50 22966608-1 2012 This paper presents the fabrication and characteristics of a new aptamer-based electrochemical immunosensor on the patterned zinc oxide nanorod networks (ZNNs) for detecting thrombin. Zinc Oxide 125-135 coagulation factor II, thrombin Homo sapiens 174-182 22642360-0 2012 Spin-assisted multilayers of poly(methyl methacrylate) and zinc oxide quantum dots for ultraviolet-blocking applications. Zinc Oxide 59-69 spindlin 1 Homo sapiens 0-4 22642360-1 2012 Thin UV-blocking films of poly(methyl methacrylate) (PMMA) and ZnO quantum dots (QDs) were built-up by spin-coating. Zinc Oxide 63-66 spindlin 1 Homo sapiens 103-107 22673046-0 2012 Direct synthesis of vertically aligned ZnO nanowires on FTO substrates using a CVD method and the improvement of photovoltaic performance. Zinc Oxide 39-42 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 56-59 22341990-1 2012 A multifunctional ZnO/Ag nanorod arrays has been prepared to construct SERS-active and photocatalytic substrate by a hydrothermal method. Zinc Oxide 18-21 seryl-tRNA synthetase 2, mitochondrial Homo sapiens 71-75 22341990-4 2012 The mechanism of SERS enhancement was discussed due to the formation of interfacial electric field between ZnO nanorods and Ag. Zinc Oxide 107-110 seryl-tRNA synthetase 2, mitochondrial Homo sapiens 17-21 22607485-5 2012 Optimum power conversion efficiency (eta) of 1.49% was obtained in a DSSC with the ZnO nanowires length of 3 mum. Zinc Oxide 83-86 endothelin receptor type A Homo sapiens 37-40 22551254-7 2012 RESULTS: Nano zinc oxide-induced nephrotoxicity was confirmed by the elevation in serum inflammatory markers including: tumor necrosis factor alpha (TNF-alpha), interleukin-6 (IL-6); and C-reactive protein (CRP). Zinc Oxide 14-24 tumor necrosis factor Rattus norvegicus 120-147 22551254-7 2012 RESULTS: Nano zinc oxide-induced nephrotoxicity was confirmed by the elevation in serum inflammatory markers including: tumor necrosis factor alpha (TNF-alpha), interleukin-6 (IL-6); and C-reactive protein (CRP). Zinc Oxide 14-24 tumor necrosis factor Rattus norvegicus 149-158 22551254-7 2012 RESULTS: Nano zinc oxide-induced nephrotoxicity was confirmed by the elevation in serum inflammatory markers including: tumor necrosis factor alpha (TNF-alpha), interleukin-6 (IL-6); and C-reactive protein (CRP). Zinc Oxide 14-24 interleukin 6 Rattus norvegicus 161-174 22551254-7 2012 RESULTS: Nano zinc oxide-induced nephrotoxicity was confirmed by the elevation in serum inflammatory markers including: tumor necrosis factor alpha (TNF-alpha), interleukin-6 (IL-6); and C-reactive protein (CRP). Zinc Oxide 14-24 interleukin 6 Rattus norvegicus 176-180 22551254-7 2012 RESULTS: Nano zinc oxide-induced nephrotoxicity was confirmed by the elevation in serum inflammatory markers including: tumor necrosis factor alpha (TNF-alpha), interleukin-6 (IL-6); and C-reactive protein (CRP). Zinc Oxide 14-24 C-reactive protein Rattus norvegicus 187-205 22551254-7 2012 RESULTS: Nano zinc oxide-induced nephrotoxicity was confirmed by the elevation in serum inflammatory markers including: tumor necrosis factor alpha (TNF-alpha), interleukin-6 (IL-6); and C-reactive protein (CRP). Zinc Oxide 14-24 C-reactive protein Rattus norvegicus 207-210 22309190-6 2012 Direct electron transfer of GOx is achieved at ZnO/Cu nanocomposite with a high heterogeneous electron transfer rate constant of 0.67 +- 0.06 s(-1). Zinc Oxide 47-50 hydroxyacid oxidase 1 Homo sapiens 28-31 22054034-5 2012 Through targeted analysis during this response period and the use of a novel image analysis approach, we show how the ZnO and CuO nanoparticles trigger the active export of intracellular glutathione via an increase in the activity of the ATP dependent MRP/1 efflux pumps. Zinc Oxide 118-121 ATP binding cassette subfamily C member 1 Homo sapiens 252-257 22755124-1 2012 Herein we describe synthesis of ZnO nanoparticles by using alkaline solution of ZnX2 (X = NO3, Cl) under ultrasound energy of 20 KHz. Zinc Oxide 32-35 NBL1, DAN family BMP antagonist Homo sapiens 90-93 22166487-0 2012 Zinc oxide nanoparticles-induced intercellular adhesion molecule 1 expression requires Rac1/Cdc42, mixed lineage kinase 3, and c-Jun N-terminal kinase activation in endothelial cells. Zinc Oxide 0-10 mitogen-activated protein kinase 8 Homo sapiens 127-150 22166487-3 2012 Within the testing concentrations of 0.1-10 mug/ml, which did not cause a marked drop in cell viability, zinc oxide NPs (ZnO-NPs) induced intercellular adhesion molecule-1 (ICAM-1) messenger RNA, and protein expression in both concentration- and time-dependent manner in treated human umbilical vein endothelial cells (HUVECs). Zinc Oxide 105-115 intercellular adhesion molecule 1 Homo sapiens 138-171 22166487-3 2012 Within the testing concentrations of 0.1-10 mug/ml, which did not cause a marked drop in cell viability, zinc oxide NPs (ZnO-NPs) induced intercellular adhesion molecule-1 (ICAM-1) messenger RNA, and protein expression in both concentration- and time-dependent manner in treated human umbilical vein endothelial cells (HUVECs). Zinc Oxide 105-115 intercellular adhesion molecule 1 Homo sapiens 173-179 22166487-3 2012 Within the testing concentrations of 0.1-10 mug/ml, which did not cause a marked drop in cell viability, zinc oxide NPs (ZnO-NPs) induced intercellular adhesion molecule-1 (ICAM-1) messenger RNA, and protein expression in both concentration- and time-dependent manner in treated human umbilical vein endothelial cells (HUVECs). Zinc Oxide 121-124 intercellular adhesion molecule 1 Homo sapiens 138-171 22166487-3 2012 Within the testing concentrations of 0.1-10 mug/ml, which did not cause a marked drop in cell viability, zinc oxide NPs (ZnO-NPs) induced intercellular adhesion molecule-1 (ICAM-1) messenger RNA, and protein expression in both concentration- and time-dependent manner in treated human umbilical vein endothelial cells (HUVECs). Zinc Oxide 121-124 intercellular adhesion molecule 1 Homo sapiens 173-179 22166487-4 2012 ZnO-NPs treatment cause the activation of Ras-related C3 botulinum toxin substrate 1 (Rac1)/cell division control protein 42 homolog (Cdc42) and protein accumulation of mixed lineage kinase 3 (MLK3), followed by c-Jun N-terminal kinase (JNK) and transcription factor c-Jun activation. Zinc Oxide 0-3 Rac family small GTPase 1 Homo sapiens 42-84 22166487-4 2012 ZnO-NPs treatment cause the activation of Ras-related C3 botulinum toxin substrate 1 (Rac1)/cell division control protein 42 homolog (Cdc42) and protein accumulation of mixed lineage kinase 3 (MLK3), followed by c-Jun N-terminal kinase (JNK) and transcription factor c-Jun activation. Zinc Oxide 0-3 Rac family small GTPase 1 Homo sapiens 86-90 22166487-4 2012 ZnO-NPs treatment cause the activation of Ras-related C3 botulinum toxin substrate 1 (Rac1)/cell division control protein 42 homolog (Cdc42) and protein accumulation of mixed lineage kinase 3 (MLK3), followed by c-Jun N-terminal kinase (JNK) and transcription factor c-Jun activation. Zinc Oxide 0-3 cell division cycle 42 Homo sapiens 134-139 22166487-4 2012 ZnO-NPs treatment cause the activation of Ras-related C3 botulinum toxin substrate 1 (Rac1)/cell division control protein 42 homolog (Cdc42) and protein accumulation of mixed lineage kinase 3 (MLK3), followed by c-Jun N-terminal kinase (JNK) and transcription factor c-Jun activation. Zinc Oxide 0-3 mitogen-activated protein kinase kinase kinase 11 Homo sapiens 169-191 22166487-4 2012 ZnO-NPs treatment cause the activation of Ras-related C3 botulinum toxin substrate 1 (Rac1)/cell division control protein 42 homolog (Cdc42) and protein accumulation of mixed lineage kinase 3 (MLK3), followed by c-Jun N-terminal kinase (JNK) and transcription factor c-Jun activation. Zinc Oxide 0-3 mitogen-activated protein kinase kinase kinase 11 Homo sapiens 193-197 22166487-4 2012 ZnO-NPs treatment cause the activation of Ras-related C3 botulinum toxin substrate 1 (Rac1)/cell division control protein 42 homolog (Cdc42) and protein accumulation of mixed lineage kinase 3 (MLK3), followed by c-Jun N-terminal kinase (JNK) and transcription factor c-Jun activation. Zinc Oxide 0-3 mitogen-activated protein kinase 8 Homo sapiens 212-235 22166487-4 2012 ZnO-NPs treatment cause the activation of Ras-related C3 botulinum toxin substrate 1 (Rac1)/cell division control protein 42 homolog (Cdc42) and protein accumulation of mixed lineage kinase 3 (MLK3), followed by c-Jun N-terminal kinase (JNK) and transcription factor c-Jun activation. Zinc Oxide 0-3 mitogen-activated protein kinase 8 Homo sapiens 237-240 22166487-4 2012 ZnO-NPs treatment cause the activation of Ras-related C3 botulinum toxin substrate 1 (Rac1)/cell division control protein 42 homolog (Cdc42) and protein accumulation of mixed lineage kinase 3 (MLK3), followed by c-Jun N-terminal kinase (JNK) and transcription factor c-Jun activation. Zinc Oxide 0-3 Jun proto-oncogene, AP-1 transcription factor subunit Homo sapiens 212-217 22166487-6 2012 In addition, pretreatment with NSC23766 significantly reduced MLK3 accumulation, suggesting the involvement of Rac1/Cdc42-MLK3-JNK-c-Jun signaling in the regulation of ZnO-NPs-induced ICAM-1 expression, whereas these signaling factors were not activated in zinc oxide microparticles (ZnO-MPs)-treated HUVECs. Zinc Oxide 168-171 mitogen-activated protein kinase kinase kinase 11 Homo sapiens 62-66 22166487-6 2012 In addition, pretreatment with NSC23766 significantly reduced MLK3 accumulation, suggesting the involvement of Rac1/Cdc42-MLK3-JNK-c-Jun signaling in the regulation of ZnO-NPs-induced ICAM-1 expression, whereas these signaling factors were not activated in zinc oxide microparticles (ZnO-MPs)-treated HUVECs. Zinc Oxide 168-171 Rac family small GTPase 1 Homo sapiens 111-115 22166487-6 2012 In addition, pretreatment with NSC23766 significantly reduced MLK3 accumulation, suggesting the involvement of Rac1/Cdc42-MLK3-JNK-c-Jun signaling in the regulation of ZnO-NPs-induced ICAM-1 expression, whereas these signaling factors were not activated in zinc oxide microparticles (ZnO-MPs)-treated HUVECs. Zinc Oxide 168-171 cell division cycle 42 Homo sapiens 116-121 22166487-6 2012 In addition, pretreatment with NSC23766 significantly reduced MLK3 accumulation, suggesting the involvement of Rac1/Cdc42-MLK3-JNK-c-Jun signaling in the regulation of ZnO-NPs-induced ICAM-1 expression, whereas these signaling factors were not activated in zinc oxide microparticles (ZnO-MPs)-treated HUVECs. Zinc Oxide 168-171 mitogen-activated protein kinase kinase kinase 11 Homo sapiens 122-126 22166487-6 2012 In addition, pretreatment with NSC23766 significantly reduced MLK3 accumulation, suggesting the involvement of Rac1/Cdc42-MLK3-JNK-c-Jun signaling in the regulation of ZnO-NPs-induced ICAM-1 expression, whereas these signaling factors were not activated in zinc oxide microparticles (ZnO-MPs)-treated HUVECs. Zinc Oxide 168-171 mitogen-activated protein kinase 8 Homo sapiens 127-130 22166487-6 2012 In addition, pretreatment with NSC23766 significantly reduced MLK3 accumulation, suggesting the involvement of Rac1/Cdc42-MLK3-JNK-c-Jun signaling in the regulation of ZnO-NPs-induced ICAM-1 expression, whereas these signaling factors were not activated in zinc oxide microparticles (ZnO-MPs)-treated HUVECs. Zinc Oxide 168-171 Jun proto-oncogene, AP-1 transcription factor subunit Homo sapiens 131-136 22166487-6 2012 In addition, pretreatment with NSC23766 significantly reduced MLK3 accumulation, suggesting the involvement of Rac1/Cdc42-MLK3-JNK-c-Jun signaling in the regulation of ZnO-NPs-induced ICAM-1 expression, whereas these signaling factors were not activated in zinc oxide microparticles (ZnO-MPs)-treated HUVECs. Zinc Oxide 257-267 Rac family small GTPase 1 Homo sapiens 111-115 22166487-6 2012 In addition, pretreatment with NSC23766 significantly reduced MLK3 accumulation, suggesting the involvement of Rac1/Cdc42-MLK3-JNK-c-Jun signaling in the regulation of ZnO-NPs-induced ICAM-1 expression, whereas these signaling factors were not activated in zinc oxide microparticles (ZnO-MPs)-treated HUVECs. Zinc Oxide 284-287 Rac family small GTPase 1 Homo sapiens 111-115 22166487-7 2012 The increase of ICAM-1 expression on ZnO-NPs-treated HUVECs enables leukocytes to adhere and has been identified as an indicator of vascular inflammation. Zinc Oxide 37-40 intercellular adhesion molecule 1 Homo sapiens 16-22 22238275-3 2012 Our experiment shows that antibodies toward epidermal growth factor receptor (EGFR) can be connected to ZnO nanorods and to EGFR receptors of SCC (squamous cell carcinoma). Zinc Oxide 104-107 epidermal growth factor receptor Homo sapiens 44-76 22238275-3 2012 Our experiment shows that antibodies toward epidermal growth factor receptor (EGFR) can be connected to ZnO nanorods and to EGFR receptors of SCC (squamous cell carcinoma). Zinc Oxide 104-107 epidermal growth factor receptor Homo sapiens 78-82 22238275-6 2012 From the photoluminescent spectra, the peak intensity ratio between the purple light (from ZnO at the wavelength 377 nm) and the green band (from the autofluorescence of cells) is much higher with the presence in SCC, as compared with Hs68. Zinc Oxide 91-94 serpin family B member 3 Homo sapiens 213-216 22629981-4 2012 To demonstrate its usefulness, we used the water-mediated mTP to fabricate low voltage ZnO thin-film transistors. Zinc Oxide 87-90 lysosomal-associated protein transmembrane 4A Mus musculus 58-61 22213372-2 2012 The roles of ZnO nanowalls and GaN intermediate layers in the heteroepitaxial growth of GaN on graphene, revealed by cross-sectional transmission electron microscopy, are also discussed. Zinc Oxide 13-16 gigaxonin Homo sapiens 88-91 22166487-0 2012 Zinc oxide nanoparticles-induced intercellular adhesion molecule 1 expression requires Rac1/Cdc42, mixed lineage kinase 3, and c-Jun N-terminal kinase activation in endothelial cells. Zinc Oxide 0-10 intercellular adhesion molecule 1 Homo sapiens 33-66 22166487-0 2012 Zinc oxide nanoparticles-induced intercellular adhesion molecule 1 expression requires Rac1/Cdc42, mixed lineage kinase 3, and c-Jun N-terminal kinase activation in endothelial cells. Zinc Oxide 0-10 Rac family small GTPase 1 Homo sapiens 87-91 22166487-0 2012 Zinc oxide nanoparticles-induced intercellular adhesion molecule 1 expression requires Rac1/Cdc42, mixed lineage kinase 3, and c-Jun N-terminal kinase activation in endothelial cells. Zinc Oxide 0-10 cell division cycle 42 Homo sapiens 92-97 22166487-0 2012 Zinc oxide nanoparticles-induced intercellular adhesion molecule 1 expression requires Rac1/Cdc42, mixed lineage kinase 3, and c-Jun N-terminal kinase activation in endothelial cells. Zinc Oxide 0-10 mitogen-activated protein kinase kinase kinase 11 Homo sapiens 99-121 22208722-6 2012 The strain-induced piezopotential can thus tune the transport process of the charge carriers inside the InN nanorod over a larger range than in ZnO. Zinc Oxide 144-147 growth hormone releasing hormone Homo sapiens 104-107 22148364-6 2012 For the ZnO/ZnS core/shell nanostructures, the J(SC) and eta can reach a maximum of 8.38 mA/cm(2) and 1.92% after 6 h conversion time, corresponding to 12- and 16-fold increments of as-synthesized ZnO, respectively. Zinc Oxide 8-11 endothelin receptor type A Homo sapiens 57-60 22148364-6 2012 For the ZnO/ZnS core/shell nanostructures, the J(SC) and eta can reach a maximum of 8.38 mA/cm(2) and 1.92% after 6 h conversion time, corresponding to 12- and 16-fold increments of as-synthesized ZnO, respectively. Zinc Oxide 197-200 endothelin receptor type A Homo sapiens 57-60 22393286-8 2012 ZnO NPs were also found to induce activity of caspase-3 enzyme, DNA fragmentation, reactive oxygen species generation, and oxidative stress in HepG2 cells. Zinc Oxide 0-3 caspase 3 Homo sapiens 46-55 21944543-0 2012 Detection of HCG-antigen based on enhanced photoluminescence of hierarchical ZnO arrays. Zinc Oxide 77-80 chorionic gonadotropin subunit beta 5 Homo sapiens 13-16 21944543-1 2012 Specific antibody of Human chorionic gonadotrophin (HCG) was conjugated onto hierarchical ZnO arrays through the carbodiimide technique, and the photoluminescence (PL) intensity of ZnO arrays were enhanced linearly with the linked antibody concentration in the range of 40-160 ng/mL, which resulted from the nano sheet structure and rough surface in hierarchical ZnO columns. Zinc Oxide 90-93 chorionic gonadotropin subunit beta 5 Homo sapiens 21-50 21944543-1 2012 Specific antibody of Human chorionic gonadotrophin (HCG) was conjugated onto hierarchical ZnO arrays through the carbodiimide technique, and the photoluminescence (PL) intensity of ZnO arrays were enhanced linearly with the linked antibody concentration in the range of 40-160 ng/mL, which resulted from the nano sheet structure and rough surface in hierarchical ZnO columns. Zinc Oxide 90-93 chorionic gonadotropin subunit beta 5 Homo sapiens 52-55 21944543-1 2012 Specific antibody of Human chorionic gonadotrophin (HCG) was conjugated onto hierarchical ZnO arrays through the carbodiimide technique, and the photoluminescence (PL) intensity of ZnO arrays were enhanced linearly with the linked antibody concentration in the range of 40-160 ng/mL, which resulted from the nano sheet structure and rough surface in hierarchical ZnO columns. Zinc Oxide 181-184 chorionic gonadotropin subunit beta 5 Homo sapiens 21-50 21944543-1 2012 Specific antibody of Human chorionic gonadotrophin (HCG) was conjugated onto hierarchical ZnO arrays through the carbodiimide technique, and the photoluminescence (PL) intensity of ZnO arrays were enhanced linearly with the linked antibody concentration in the range of 40-160 ng/mL, which resulted from the nano sheet structure and rough surface in hierarchical ZnO columns. Zinc Oxide 181-184 chorionic gonadotropin subunit beta 5 Homo sapiens 52-55 21944543-1 2012 Specific antibody of Human chorionic gonadotrophin (HCG) was conjugated onto hierarchical ZnO arrays through the carbodiimide technique, and the photoluminescence (PL) intensity of ZnO arrays were enhanced linearly with the linked antibody concentration in the range of 40-160 ng/mL, which resulted from the nano sheet structure and rough surface in hierarchical ZnO columns. Zinc Oxide 181-184 chorionic gonadotropin subunit beta 5 Homo sapiens 21-50 21944543-1 2012 Specific antibody of Human chorionic gonadotrophin (HCG) was conjugated onto hierarchical ZnO arrays through the carbodiimide technique, and the photoluminescence (PL) intensity of ZnO arrays were enhanced linearly with the linked antibody concentration in the range of 40-160 ng/mL, which resulted from the nano sheet structure and rough surface in hierarchical ZnO columns. Zinc Oxide 181-184 chorionic gonadotropin subunit beta 5 Homo sapiens 52-55 21944543-2 2012 After the specific combination between antigen and antibody on hierarchical ZnO arrays, the enhanced PL intensity of ZnO arrays was also basically linear with the concentration of HCG antigen. Zinc Oxide 76-79 chorionic gonadotropin subunit beta 5 Homo sapiens 180-183 21944543-2 2012 After the specific combination between antigen and antibody on hierarchical ZnO arrays, the enhanced PL intensity of ZnO arrays was also basically linear with the concentration of HCG antigen. Zinc Oxide 117-120 chorionic gonadotropin subunit beta 5 Homo sapiens 180-183 21944543-3 2012 Thus, detection of HCG antigen in the range of 2-20 ng/mL was achieved based on PL intensity enhancement, suggesting that the prepared ZnO arrays are envisioned to be applied in the detection of early tumor markers in future. Zinc Oxide 135-138 chorionic gonadotropin subunit beta 5 Homo sapiens 19-22 22393286-9 2012 CONCLUSION: Overall, our data demonstrated that ZnO NPs selectively induce apoptosis in cancer cells, which is likely to be mediated by reactive oxygen species via p53 pathway, through which most of the anticancer drugs trigger apoptosis. Zinc Oxide 48-51 tumor protein p53 Homo sapiens 164-167 21656222-7 2011 Exposure of primary dendritic cells to ZnO nanoparticles upregulated expression of CD80 and CD86 (well-known markers of DC activation and maturation) and stimulated release of pro-inflammatory cytokines--IL-6 and TNF-alpha, thus pointing to the potential of ZnO nanoparticles in inducing inflammation. Zinc Oxide 39-42 CD80 molecule Homo sapiens 83-87 22524012-6 2012 A fast current response time is within 9 s. It was also found that the uricase/T-ZnO biosensor presented a high and reproducible sensitivity of 80.0 microA cm(-2) mM(-1) and an experiment limit of detection of 0.8 microM. Zinc Oxide 81-84 urate oxidase (pseudogene) Homo sapiens 71-78 22736977-2 2012 The enzyme uricase was electrostatically immobilized in conjunction with Nafion membrane on the surface of well oriented ZnO-NFs, resulting in a sensitive, selective, stable and reproducible uric acid sensor. Zinc Oxide 121-124 urate oxidase (pseudogene) Homo sapiens 11-18 22108293-3 2011 The as-synthesized SnO(2) nanoshuttles showed ultrahigh flexibility and strong toughness with a large elastic strain of ~ 6.2, which is much higher than reported for Si and ZnO nanowire as well as most crystalline metallic materials. Zinc Oxide 173-176 strawberry notch homolog 1 Homo sapiens 19-22 21656222-7 2011 Exposure of primary dendritic cells to ZnO nanoparticles upregulated expression of CD80 and CD86 (well-known markers of DC activation and maturation) and stimulated release of pro-inflammatory cytokines--IL-6 and TNF-alpha, thus pointing to the potential of ZnO nanoparticles in inducing inflammation. Zinc Oxide 39-42 CD86 molecule Homo sapiens 92-96 21656222-7 2011 Exposure of primary dendritic cells to ZnO nanoparticles upregulated expression of CD80 and CD86 (well-known markers of DC activation and maturation) and stimulated release of pro-inflammatory cytokines--IL-6 and TNF-alpha, thus pointing to the potential of ZnO nanoparticles in inducing inflammation. Zinc Oxide 39-42 tumor necrosis factor Homo sapiens 213-222 21664489-0 2011 ZnO nanorod-induced apoptosis in human alveolar adenocarcinoma cells via p53, survivin and bax/bcl-2 pathways: role of oxidative stress. Zinc Oxide 0-3 tumor protein p53 Homo sapiens 73-76 21664489-0 2011 ZnO nanorod-induced apoptosis in human alveolar adenocarcinoma cells via p53, survivin and bax/bcl-2 pathways: role of oxidative stress. Zinc Oxide 0-3 BCL2 associated X, apoptosis regulator Homo sapiens 91-94 21664489-0 2011 ZnO nanorod-induced apoptosis in human alveolar adenocarcinoma cells via p53, survivin and bax/bcl-2 pathways: role of oxidative stress. Zinc Oxide 0-3 BCL2 apoptosis regulator Homo sapiens 95-100 21664489-4 2011 ZnO nanorod was found to induce cytotoxicity, reactive oxygen species (ROS) generation, oxidative stress and activities of caspase-3 & caspase-9 in a dose- and time-dependent manner. Zinc Oxide 0-3 caspase 3 Homo sapiens 123-132 21664489-4 2011 ZnO nanorod was found to induce cytotoxicity, reactive oxygen species (ROS) generation, oxidative stress and activities of caspase-3 & caspase-9 in a dose- and time-dependent manner. Zinc Oxide 0-3 caspase 9 Homo sapiens 139-148 21664489-5 2011 Western blot results showed that ZnO nanorods induced the expression of heat shock protein 70, a first-tier marker of cell damage and a cell-cycle checkpoint protein p53. Zinc Oxide 33-36 tumor protein p53 Homo sapiens 166-169 21664489-6 2011 Moreover, pro-apoptotic protein bax was upregulated and the antiapoptotic proteins, survivin and bcl-2, were downregulated in ZnO nanorod exposed cells. Zinc Oxide 126-129 BCL2 associated X, apoptosis regulator Homo sapiens 32-35 21664489-6 2011 Moreover, pro-apoptotic protein bax was upregulated and the antiapoptotic proteins, survivin and bcl-2, were downregulated in ZnO nanorod exposed cells. Zinc Oxide 126-129 BCL2 apoptosis regulator Homo sapiens 97-102 21664489-7 2011 In conclusion, our data demonstrates that ZnO nanorod induced apoptosis in A549 cells through ROS and oxidative stress via p53, survivin, bax/bcl-2 and caspase pathways. Zinc Oxide 42-45 tumor protein p53 Homo sapiens 123-126 21664489-7 2011 In conclusion, our data demonstrates that ZnO nanorod induced apoptosis in A549 cells through ROS and oxidative stress via p53, survivin, bax/bcl-2 and caspase pathways. Zinc Oxide 42-45 BCL2 associated X, apoptosis regulator Homo sapiens 138-141 21664489-7 2011 In conclusion, our data demonstrates that ZnO nanorod induced apoptosis in A549 cells through ROS and oxidative stress via p53, survivin, bax/bcl-2 and caspase pathways. Zinc Oxide 42-45 BCL2 apoptosis regulator Homo sapiens 142-147 22413302-0 2011 Excitons emissions and Raman scattering of ZnO nanoparticles embedded in BaF2 matrices by reactive magnetron sputtering. Zinc Oxide 43-46 BANF family member 2 Homo sapiens 73-77 21903158-0 2011 ZnO nanoparticles induce apoptosis in human dermal fibroblasts via p53 and p38 pathways. Zinc Oxide 0-3 tumor protein p53 Homo sapiens 67-70 21903158-0 2011 ZnO nanoparticles induce apoptosis in human dermal fibroblasts via p53 and p38 pathways. Zinc Oxide 0-3 mitogen-activated protein kinase 14 Homo sapiens 75-78 21903158-3 2011 This study was designed to investigate the apoptosis induction by ZnO NPs via mitogen-activated protein kinase p38 and cell cycle checkpoint protein p53 pathways in human dermal fibroblasts. Zinc Oxide 66-69 mitogen-activated protein kinase 14 Homo sapiens 111-114 21903158-3 2011 This study was designed to investigate the apoptosis induction by ZnO NPs via mitogen-activated protein kinase p38 and cell cycle checkpoint protein p53 pathways in human dermal fibroblasts. Zinc Oxide 66-69 tumor protein p53 Homo sapiens 149-152 21903158-6 2011 Furthermore, in ZnO NP exposed cells, p53 protein was phosphorylated at Ser33 and Ser46 sites known to be phosphorylated by p38. Zinc Oxide 16-19 tumor protein p53 Homo sapiens 38-41 21903158-6 2011 Furthermore, in ZnO NP exposed cells, p53 protein was phosphorylated at Ser33 and Ser46 sites known to be phosphorylated by p38. Zinc Oxide 16-19 mitogen-activated protein kinase 14 Homo sapiens 124-127 21903158-7 2011 Our results suggest that ZnO NPs have the potential to induce apoptosis in human dermal fibroblasts via p53-p38 pathways. Zinc Oxide 25-28 tumor protein p53 Homo sapiens 104-107 21903158-7 2011 Our results suggest that ZnO NPs have the potential to induce apoptosis in human dermal fibroblasts via p53-p38 pathways. Zinc Oxide 25-28 mitogen-activated protein kinase 14 Homo sapiens 108-111 21974847-1 2011 Our previous studies found that zinc oxide (ZnO) particles induced expression of intercellular adhesion molecule-1 (ICAM-1) protein in vascular endothelial cells via NF-kappaB and that zinc ions dissolved from ZnO particles might play the major role in the process. Zinc Oxide 32-42 intercellular adhesion molecule 1 Homo sapiens 81-114 21974847-1 2011 Our previous studies found that zinc oxide (ZnO) particles induced expression of intercellular adhesion molecule-1 (ICAM-1) protein in vascular endothelial cells via NF-kappaB and that zinc ions dissolved from ZnO particles might play the major role in the process. Zinc Oxide 32-42 intercellular adhesion molecule 1 Homo sapiens 116-122 21974847-1 2011 Our previous studies found that zinc oxide (ZnO) particles induced expression of intercellular adhesion molecule-1 (ICAM-1) protein in vascular endothelial cells via NF-kappaB and that zinc ions dissolved from ZnO particles might play the major role in the process. Zinc Oxide 44-47 intercellular adhesion molecule 1 Homo sapiens 81-114 21974847-1 2011 Our previous studies found that zinc oxide (ZnO) particles induced expression of intercellular adhesion molecule-1 (ICAM-1) protein in vascular endothelial cells via NF-kappaB and that zinc ions dissolved from ZnO particles might play the major role in the process. Zinc Oxide 44-47 intercellular adhesion molecule 1 Homo sapiens 116-122 21974847-1 2011 Our previous studies found that zinc oxide (ZnO) particles induced expression of intercellular adhesion molecule-1 (ICAM-1) protein in vascular endothelial cells via NF-kappaB and that zinc ions dissolved from ZnO particles might play the major role in the process. Zinc Oxide 210-213 intercellular adhesion molecule 1 Homo sapiens 81-114 21974847-1 2011 Our previous studies found that zinc oxide (ZnO) particles induced expression of intercellular adhesion molecule-1 (ICAM-1) protein in vascular endothelial cells via NF-kappaB and that zinc ions dissolved from ZnO particles might play the major role in the process. Zinc Oxide 210-213 intercellular adhesion molecule 1 Homo sapiens 116-122 21807406-0 2011 The role of the tumor suppressor p53 pathway in the cellular DNA damage response to zinc oxide nanoparticles. Zinc Oxide 84-94 tumor protein p53 Homo sapiens 33-36 21807406-1 2011 In this paper, we explored how ZnO nanoparticles cross-interact with a critical tumor suppressive pathway centered around p53, which is one of the most important known tumor suppressors that protects cells from developing cancer phenotypes through its control over major pathways like apoptosis, senescence and cell cycle progression. Zinc Oxide 31-34 tumor protein p53 Homo sapiens 122-125 21807406-2 2011 We showed that the p53 pathway was activated in BJ cells (skin fibroblasts) upon ZnO nanoparticles treatment with a concomitant decrease in cell numbers. Zinc Oxide 81-84 tumor protein p53 Homo sapiens 19-22 21807406-3 2011 This suggests that cellular responses like apoptosis in the presence of ZnO nanoparticles require p53 as the molecular master switch towards programmed cell death. Zinc Oxide 72-75 tumor protein p53 Homo sapiens 98-101 21807406-6 2011 These p53 knocked down BJ cells became more resistant to ZnO nanoparticles induced cell death and increased cell progression. Zinc Oxide 57-60 tumor protein p53 Homo sapiens 6-9 22413302-1 2011 ZnO nanoparticles embedded in BaF2 matrix were fabricated by rf magnetic sputtering technology. Zinc Oxide 0-3 BANF family member 2 Homo sapiens 30-34 22413302-5 2011 The multiple-phonon Raman scattering spectrum showed that ZnO nanoparticles embedded in BaF2 matrix had a large deformation energy originated from lattice mismatch between ZnO and BaF2 matrix. Zinc Oxide 58-61 BANF family member 2 Homo sapiens 88-92 22413302-5 2011 The multiple-phonon Raman scattering spectrum showed that ZnO nanoparticles embedded in BaF2 matrix had a large deformation energy originated from lattice mismatch between ZnO and BaF2 matrix. Zinc Oxide 58-61 BANF family member 2 Homo sapiens 180-184 22413302-5 2011 The multiple-phonon Raman scattering spectrum showed that ZnO nanoparticles embedded in BaF2 matrix had a large deformation energy originated from lattice mismatch between ZnO and BaF2 matrix. Zinc Oxide 172-175 BANF family member 2 Homo sapiens 88-92 21803561-1 2011 A new zinc oxide nanoparticles/chitosan/carboxylated multiwall carbonnanotube/polyaniline (ZnO-NPs/CHIT/c-MWCNT/PANI) composite film has been synthesized on platinum (Pt) electrode using electrochemical techniques. Zinc Oxide 6-16 chitinase 1 Homo sapiens 99-103 22103098-1 2011 The enhancement of broadband optical absorption in zinc oxide (ZnO) nanotip (NT) arrays coated with evaporated gold (Au) on fluorine-doped SnO2 (FTO)/glass by a simple hydrothermal growth and subsequent Au evaporation is reported. Zinc Oxide 51-61 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 145-148 21851096-7 2011 While neither the embryos nor larvae demonstrated morphological abnormalities, high content fluorescence-based imaging demonstrated that CuO, ZnO, and NiO could induce increased expression of the heat shock protein 70:enhanced green fluorescence protein (hsp70:eGFP) in transgenic zebrafish larvae. Zinc Oxide 142-145 heat shock protein 8-like Danio rerio 255-260 22400217-5 2011 Next, we deposited the CdS nanoparticle-decorated TiO2 nanobelts onto a ZnO nanowire array forming an antireflective hybrid structure. Zinc Oxide 72-75 CDP-diacylglycerol synthase 1 Homo sapiens 23-26 22400340-5 2011 We have also been able to observe, for the first time by EPR spectroscopy, the formation of the ZnO phase and the nanocrystals size increase, which occur during annealing up to 500 degrees C, structural changes confirmed by XRD and TEM observations on the samples previously investigated by EPR. Zinc Oxide 96-99 MFT2 Homo sapiens 232-235 21823599-2 2011 Optical imaging of integrin alpha(v)beta(3) on U87MG human glioblastoma cells was achieved with RGD peptide-conjugated green fluorescent ZnO NWs, which opened up new avenues of research for investigating ZnO NW-based agents in tumor vasculature-targeted molecular imaging and drug delivery. Zinc Oxide 137-140 integrin subunit alpha V Homo sapiens 19-42 21823599-2 2011 Optical imaging of integrin alpha(v)beta(3) on U87MG human glioblastoma cells was achieved with RGD peptide-conjugated green fluorescent ZnO NWs, which opened up new avenues of research for investigating ZnO NW-based agents in tumor vasculature-targeted molecular imaging and drug delivery. Zinc Oxide 204-207 integrin subunit alpha V Homo sapiens 19-42 21553287-3 2011 Transferrin, the ligand targeting the cancer cells, was conjugated to the ZnO QDs. Zinc Oxide 74-77 transferrin Homo sapiens 0-11 22103098-1 2011 The enhancement of broadband optical absorption in zinc oxide (ZnO) nanotip (NT) arrays coated with evaporated gold (Au) on fluorine-doped SnO2 (FTO)/glass by a simple hydrothermal growth and subsequent Au evaporation is reported. Zinc Oxide 63-66 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 145-148 22103098-3 2011 For both FTO/glass and ZnO NT arrays on FTO/glass, the coating of Au improves the light absorption due to the antireflective geometry compared to the flat Au films and the absorptance is also enhanced by increasing the nominal thickness of Au with evaporation time. Zinc Oxide 23-26 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 40-43 22103098-4 2011 For the ZnO NT arrays with an Au evaporated for 600 s at 0.5 A/s, a high absorptance of >72% is achieved over the wavelength range of 250-2000 nm, indicating a significant increase due to the enhanced antireflection property as well as the increased surface area compared to the Au-coated FTO/glass without ZnO NT arrays. Zinc Oxide 8-11 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 292-295 21687894-1 2011 The ZnO(0001)-Zn terminated crystal face was studied after reduction at high temperatures by combination of STM, STS, XPS and TDS. Zinc Oxide 4-7 sulfotransferase family 1A member 3 Homo sapiens 108-111 21557612-0 2011 Enhancement of gas sensing properties of CdS nanowire/ZnO nanosphere composite materials at room temperature by visible-light activation. Zinc Oxide 54-57 CDP-diacylglycerol synthase 1 Homo sapiens 41-44 21777458-0 2011 Improved conversion efficiency of Ag2S quantum dot-sensitized solar cells based on TiO2 nanotubes with a ZnO recombination barrier layer. Zinc Oxide 105-108 angiotensin II receptor type 1 Homo sapiens 34-38 21777458-1 2011 We improve the conversion efficiency of Ag2S quantum dot (QD)-sensitized TiO2 nanotube-array electrodes by chemically depositing ZnO recombination barrier layer on plain TiO2 nanotube-array electrodes. Zinc Oxide 129-132 angiotensin II receptor type 1 Homo sapiens 40-44 21777458-4 2011 In addition, as compared to the Ag2S QD-sensitized TiO2 nanotube-array electrode without the ZnO layers, the conversion efficiency of the electrode with the ZnO layers increases significantly due to the formation of efficient recombination layer between the TiO2 nanotube array and electrolyte. Zinc Oxide 157-160 angiotensin II receptor type 1 Homo sapiens 32-36 21557612-1 2011 CdS nanowire/ZnO nanosphere materials (CdS/ZnO) with hierarchical structure were synthesized by a three-step solvothermal process. Zinc Oxide 13-16 CDP-diacylglycerol synthase 1 Homo sapiens 0-3 21557612-1 2011 CdS nanowire/ZnO nanosphere materials (CdS/ZnO) with hierarchical structure were synthesized by a three-step solvothermal process. Zinc Oxide 13-16 CDP-diacylglycerol synthase 1 Homo sapiens 39-42 21557612-1 2011 CdS nanowire/ZnO nanosphere materials (CdS/ZnO) with hierarchical structure were synthesized by a three-step solvothermal process. Zinc Oxide 43-46 CDP-diacylglycerol synthase 1 Homo sapiens 0-3 21634790-0 2011 Recyclable SERS substrates based on Au-coated ZnO nanorods. Zinc Oxide 46-49 seryl-tRNA synthetase 2, mitochondrial Homo sapiens 11-15 21557612-2 2011 XRD, FESEM and TEM analysis confirmed the growth of ZnO nanospheres on the surface of CdS nanowires (NWs). Zinc Oxide 52-55 CDP-diacylglycerol synthase 1 Homo sapiens 86-89 21634790-1 2011 Vertically aligned Au-coated ZnO nanorods (Au-ZnO NRs) were investigated as cheap, efficient and recyclable SERS-active substrates. Zinc Oxide 29-32 seryl-tRNA synthetase 2, mitochondrial Homo sapiens 108-112 21557612-3 2011 The transient photovoltage (TPV) measurements revealed that the interface between CdS and ZnO can inhibit the recombination of photogenerated excess carriers and prolong the lifetime of excess carriers in CdS/ZnO materials. Zinc Oxide 90-93 CDP-diacylglycerol synthase 1 Homo sapiens 82-85 21634790-1 2011 Vertically aligned Au-coated ZnO nanorods (Au-ZnO NRs) were investigated as cheap, efficient and recyclable SERS-active substrates. Zinc Oxide 46-49 seryl-tRNA synthetase 2, mitochondrial Homo sapiens 108-112 21557612-3 2011 The transient photovoltage (TPV) measurements revealed that the interface between CdS and ZnO can inhibit the recombination of photogenerated excess carriers and prolong the lifetime of excess carriers in CdS/ZnO materials. Zinc Oxide 90-93 CDP-diacylglycerol synthase 1 Homo sapiens 205-208 21557612-3 2011 The transient photovoltage (TPV) measurements revealed that the interface between CdS and ZnO can inhibit the recombination of photogenerated excess carriers and prolong the lifetime of excess carriers in CdS/ZnO materials. Zinc Oxide 209-212 CDP-diacylglycerol synthase 1 Homo sapiens 82-85 21557612-4 2011 Moreover, the CdS/ZnO materials exhibit a dramatic improvement in optoelectronic performance and visible-light-irradiation gas sensing activity, which gave 1 order of magnitude larger than that of CdS NWs in response to formaldehyde. Zinc Oxide 18-21 CDP-diacylglycerol synthase 1 Homo sapiens 14-17 21557612-4 2011 Moreover, the CdS/ZnO materials exhibit a dramatic improvement in optoelectronic performance and visible-light-irradiation gas sensing activity, which gave 1 order of magnitude larger than that of CdS NWs in response to formaldehyde. Zinc Oxide 18-21 CDP-diacylglycerol synthase 1 Homo sapiens 197-200 21608644-5 2011 The BET detection indicates that these ZnO mesoporous ellipsoids have high specific surface areas reaching to 136.57 m(2)/g, while their average BJH pore diameters are located at 8.8 nm. Zinc Oxide 39-42 delta/notch like EGF repeat containing Homo sapiens 4-7 21534629-4 2011 Both ZnO and grape-seed procyanidins significantly reduced urinary lactulose to mannitol ratios (P < 0.05) and enhanced the mRNA and protein expression of the intestinal mucosal tight junction proteins Ocln/ZO-1 (P < 0.05). Zinc Oxide 5-8 occludin Rattus norvegicus 205-209 21534629-4 2011 Both ZnO and grape-seed procyanidins significantly reduced urinary lactulose to mannitol ratios (P < 0.05) and enhanced the mRNA and protein expression of the intestinal mucosal tight junction proteins Ocln/ZO-1 (P < 0.05). Zinc Oxide 5-8 tight junction protein 1 Rattus norvegicus 210-214 21405183-1 2011 Electronic structures, magnetic properties, and spin-dependent electron transport characteristics of C-doped ZnO nanowires have been investigated via first-principles method based on density functional theory and nonequilibrium techniques of Green"s functions. Zinc Oxide 109-112 spindlin 1 Homo sapiens 48-52 22440169-5 2011 Both ZnO and outdoor rearing reduced ETEC excretion, and these effects were additive. Zinc Oxide 5-8 ETEC Sus scrofa 37-41 22440169-12 2011 The results indicate that the benefits of ZnO to the weaned pig extend beyond suppression of ETEC and appear mediated through altered development of the small intestine mucosa. Zinc Oxide 42-45 ETEC Sus scrofa 93-97 21354777-2 2011 A unique ZnO nanorods-grown substrate is developed here to not only immobilize a large amount of probe molecules, but also directly amplify the microarray fluorescent signals in detection of two important cancer biomarkers, carcinoembryonic antigen (CEA) and alpha-fetoprotein (AFP), achieving a detection limit of 1 pg mL(-1) in human serum, which is comparative to or lower than that of ELISA. Zinc Oxide 9-12 CEA cell adhesion molecule 3 Homo sapiens 224-248 21354777-2 2011 A unique ZnO nanorods-grown substrate is developed here to not only immobilize a large amount of probe molecules, but also directly amplify the microarray fluorescent signals in detection of two important cancer biomarkers, carcinoembryonic antigen (CEA) and alpha-fetoprotein (AFP), achieving a detection limit of 1 pg mL(-1) in human serum, which is comparative to or lower than that of ELISA. Zinc Oxide 9-12 CEA cell adhesion molecule 3 Homo sapiens 250-253 21354777-2 2011 A unique ZnO nanorods-grown substrate is developed here to not only immobilize a large amount of probe molecules, but also directly amplify the microarray fluorescent signals in detection of two important cancer biomarkers, carcinoembryonic antigen (CEA) and alpha-fetoprotein (AFP), achieving a detection limit of 1 pg mL(-1) in human serum, which is comparative to or lower than that of ELISA. Zinc Oxide 9-12 alpha fetoprotein Homo sapiens 259-276 21354777-2 2011 A unique ZnO nanorods-grown substrate is developed here to not only immobilize a large amount of probe molecules, but also directly amplify the microarray fluorescent signals in detection of two important cancer biomarkers, carcinoembryonic antigen (CEA) and alpha-fetoprotein (AFP), achieving a detection limit of 1 pg mL(-1) in human serum, which is comparative to or lower than that of ELISA. Zinc Oxide 9-12 alpha fetoprotein Homo sapiens 278-281 21339580-0 2011 Spin-polarized density functional investigation into ferromagnetism in C-doped (ZnO)n clusters; n = 1-12, 16. Zinc Oxide 80-83 spindlin 1 Homo sapiens 0-4 21770169-4 2011 In addition, we used a serum-containing medium to prevent the possible effects of IL-8 protein adsorption in the nano-ZnO and nano-TiO2. Zinc Oxide 118-121 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 21770169-8 2011 While only at 100 microg mL(-1) of nano-ZnO, an influence on the adsorption of IL-8 was observed. Zinc Oxide 40-43 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 21415474-1 2011 alpha-Fe(2)O(3)@ZnO core-shell nanospindles were synthesized via a two-step hydrothermal approach, and characterized by means of SEM/TEM/XRD/XPS. Zinc Oxide 16-19 MFT2 Homo sapiens 133-136 21292279-0 2011 Self-assembly of disk-like multiring ZnO-SnO2 colloidal nanoparticles. Zinc Oxide 37-40 strawberry notch homolog 1 Homo sapiens 41-44 21292279-1 2011 ZnO-SnO(2) colloidal nanoparticles have been successfully synthesized by using the composite of ZnCl(2) and Sn(OC(4)H(9))(4) as inorganic precursor and dodecylbenzenesulfonic acid (DBSA) as an organic template. Zinc Oxide 0-3 strawberry notch homolog 1 Homo sapiens 4-7 21292279-2 2011 The assembled nanostructures of ZnO-SnO(2) products have been carefully investigated by powder X-ray diffraction (XRD) and transmission electron microscopy (TEM). Zinc Oxide 32-35 strawberry notch homolog 1 Homo sapiens 36-39 21292279-3 2011 It is found that ZnO-SnO(2) colloidal nanoparticles take a disk-like multiring nanostructure. Zinc Oxide 17-20 strawberry notch homolog 1 Homo sapiens 21-24 21292279-4 2011 This interesting structure is predominantly determined by the tenacity for ZnO-SnO(2) mixtures to stabilize lamellae. Zinc Oxide 75-78 strawberry notch homolog 1 Homo sapiens 79-82 21395277-5 2011 Mesoporous ZnO films were prepared by doctor blading ethanolic pastes containing ZnO nanoparticles and ethyl cellulose onto FTO conductive glass substrate followed by calcination. Zinc Oxide 11-14 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 124-127 21371295-10 2011 Protein involved in oxidative stress such as NF-kappab was activated with ZnO and CdS nanoparticles. Zinc Oxide 74-77 nuclear factor kappa B subunit 1 Homo sapiens 45-54 21446523-6 2011 The average diameter of ZnO:V, which was calculated from BET result, was 11.7 nm when the molar ratio of V/Zn was 0.1. Zinc Oxide 24-27 delta/notch like EGF repeat containing Homo sapiens 57-60 21140179-0 2011 Fabrication and growth mechanism of ZnO nanostructures and their cytotoxic effect on human brain tumor U87, cervical cancer HeLa, and normal HEK cells. Zinc Oxide 36-39 small nucleolar RNA, C/D box 87 Homo sapiens 103-106 21140179-4 2011 Screening results from anticancer studies of the effects on human brain tumor U87, cervical cancer HeLa, and normal HEK cells of ZnO nanostructures of diverse shape were obtained and indicate promising activity that varies with changes in the structure and the size of the particles. Zinc Oxide 129-132 small nucleolar RNA, C/D box 87 Homo sapiens 78-81 21250674-5 2011 Analysis of the SPR signatures revealed two cluster groups corresponding to (i) sublethal pro-inflammatory responses to Al2O3, Au, Ag, SiO2 nanoparticles possibly related to ROS generation, and (ii) lethal genotoxic responses due to exposure to ZnO and Pt nanoparticles at a concentration range of 25-100 mug/mL at 12 h exposure. Zinc Oxide 245-248 sepiapterin reductase Mus musculus 16-19 21446559-2 2011 ZnO/M-FAU was prepared by exposing Er(3+)- or Ca(2+)-exchanged Na-FAU to Zn vapor and to air at 723 K. The ZnO formation in the M-FAU showed a change in intensity in the (220), (311) and (331) lines, but no indication of ZnO peaks. Zinc Oxide 107-110 FAU ubiquitin like and ribosomal protein S30 fusion Homo sapiens 66-69 21446559-1 2011 The photoluminescence of nano-sized ZnO in metal-ion-exchanged zeolite Y (ZnO/M-FAU, M = Na, Ca, Er) was investigated. Zinc Oxide 36-39 FAU ubiquitin like and ribosomal protein S30 fusion Homo sapiens 80-83 21446559-4 2011 In the photoluminescence spectra of all the ZnO/M-FAU samples, peaks were observed at around 380 nm (3.2 eV) and 530 nm (2.5 eV) of ZnO. Zinc Oxide 44-47 FAU ubiquitin like and ribosomal protein S30 fusion Homo sapiens 50-53 21446559-4 2011 In the photoluminescence spectra of all the ZnO/M-FAU samples, peaks were observed at around 380 nm (3.2 eV) and 530 nm (2.5 eV) of ZnO. Zinc Oxide 132-135 FAU ubiquitin like and ribosomal protein S30 fusion Homo sapiens 50-53 21446559-2 2011 ZnO/M-FAU was prepared by exposing Er(3+)- or Ca(2+)-exchanged Na-FAU to Zn vapor and to air at 723 K. The ZnO formation in the M-FAU showed a change in intensity in the (220), (311) and (331) lines, but no indication of ZnO peaks. Zinc Oxide 0-3 FAU ubiquitin like and ribosomal protein S30 fusion Homo sapiens 6-9 21446559-5 2011 In ZnO/ErNa-FAU sample, the reabsorption of Er3+ at 520 nm and its emission at 650 nm were observed at the 530 nm peak of ZnO, which can be explained in terms of the interaction of ZnO with Er3+ in the FAU. Zinc Oxide 3-6 FAU ubiquitin like and ribosomal protein S30 fusion Homo sapiens 12-15 21446559-2 2011 ZnO/M-FAU was prepared by exposing Er(3+)- or Ca(2+)-exchanged Na-FAU to Zn vapor and to air at 723 K. The ZnO formation in the M-FAU showed a change in intensity in the (220), (311) and (331) lines, but no indication of ZnO peaks. Zinc Oxide 0-3 FAU ubiquitin like and ribosomal protein S30 fusion Homo sapiens 66-69 21446559-5 2011 In ZnO/ErNa-FAU sample, the reabsorption of Er3+ at 520 nm and its emission at 650 nm were observed at the 530 nm peak of ZnO, which can be explained in terms of the interaction of ZnO with Er3+ in the FAU. Zinc Oxide 3-6 FAU ubiquitin like and ribosomal protein S30 fusion Homo sapiens 202-205 21446559-5 2011 In ZnO/ErNa-FAU sample, the reabsorption of Er3+ at 520 nm and its emission at 650 nm were observed at the 530 nm peak of ZnO, which can be explained in terms of the interaction of ZnO with Er3+ in the FAU. Zinc Oxide 122-125 FAU ubiquitin like and ribosomal protein S30 fusion Homo sapiens 12-15 21446559-5 2011 In ZnO/ErNa-FAU sample, the reabsorption of Er3+ at 520 nm and its emission at 650 nm were observed at the 530 nm peak of ZnO, which can be explained in terms of the interaction of ZnO with Er3+ in the FAU. Zinc Oxide 122-125 FAU ubiquitin like and ribosomal protein S30 fusion Homo sapiens 202-205 21446559-5 2011 In ZnO/ErNa-FAU sample, the reabsorption of Er3+ at 520 nm and its emission at 650 nm were observed at the 530 nm peak of ZnO, which can be explained in terms of the interaction of ZnO with Er3+ in the FAU. Zinc Oxide 122-125 FAU ubiquitin like and ribosomal protein S30 fusion Homo sapiens 12-15 21446559-2 2011 ZnO/M-FAU was prepared by exposing Er(3+)- or Ca(2+)-exchanged Na-FAU to Zn vapor and to air at 723 K. The ZnO formation in the M-FAU showed a change in intensity in the (220), (311) and (331) lines, but no indication of ZnO peaks. Zinc Oxide 0-3 FAU ubiquitin like and ribosomal protein S30 fusion Homo sapiens 66-69 21446559-2 2011 ZnO/M-FAU was prepared by exposing Er(3+)- or Ca(2+)-exchanged Na-FAU to Zn vapor and to air at 723 K. The ZnO formation in the M-FAU showed a change in intensity in the (220), (311) and (331) lines, but no indication of ZnO peaks. Zinc Oxide 107-110 FAU ubiquitin like and ribosomal protein S30 fusion Homo sapiens 6-9 21446559-2 2011 ZnO/M-FAU was prepared by exposing Er(3+)- or Ca(2+)-exchanged Na-FAU to Zn vapor and to air at 723 K. The ZnO formation in the M-FAU showed a change in intensity in the (220), (311) and (331) lines, but no indication of ZnO peaks. Zinc Oxide 107-110 FAU ubiquitin like and ribosomal protein S30 fusion Homo sapiens 66-69 21446559-2 2011 ZnO/M-FAU was prepared by exposing Er(3+)- or Ca(2+)-exchanged Na-FAU to Zn vapor and to air at 723 K. The ZnO formation in the M-FAU showed a change in intensity in the (220), (311) and (331) lines, but no indication of ZnO peaks. Zinc Oxide 107-110 FAU ubiquitin like and ribosomal protein S30 fusion Homo sapiens 66-69 21446559-2 2011 ZnO/M-FAU was prepared by exposing Er(3+)- or Ca(2+)-exchanged Na-FAU to Zn vapor and to air at 723 K. The ZnO formation in the M-FAU showed a change in intensity in the (220), (311) and (331) lines, but no indication of ZnO peaks. Zinc Oxide 107-110 FAU ubiquitin like and ribosomal protein S30 fusion Homo sapiens 6-9 21446559-2 2011 ZnO/M-FAU was prepared by exposing Er(3+)- or Ca(2+)-exchanged Na-FAU to Zn vapor and to air at 723 K. The ZnO formation in the M-FAU showed a change in intensity in the (220), (311) and (331) lines, but no indication of ZnO peaks. Zinc Oxide 107-110 FAU ubiquitin like and ribosomal protein S30 fusion Homo sapiens 66-69 21446559-5 2011 In ZnO/ErNa-FAU sample, the reabsorption of Er3+ at 520 nm and its emission at 650 nm were observed at the 530 nm peak of ZnO, which can be explained in terms of the interaction of ZnO with Er3+ in the FAU. Zinc Oxide 122-125 FAU ubiquitin like and ribosomal protein S30 fusion Homo sapiens 202-205 21067176-0 2010 Selective oxygen-plasma-etching technique for the formation of ZnO-FTO heterostructure nanotubes and their rectified photocatalytic properties. Zinc Oxide 63-66 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 67-70 21446559-6 2011 In the case of ZnO/CaNa-FAU, the peak at around 380 nm was broaden to a longer wavelength, which is supposed to have been caused by emission peak of (CaO)x(ZnO)y. Zinc Oxide 15-18 FAU ubiquitin like and ribosomal protein S30 fusion Homo sapiens 24-27 21446559-7 2011 In addition, there were some indications of interaction between Na+ ZnO in ZnO/Na-FAU and the ZnO that was doped with Na+. Zinc Oxide 68-71 FAU ubiquitin like and ribosomal protein S30 fusion Homo sapiens 82-85 21446559-7 2011 In addition, there were some indications of interaction between Na+ ZnO in ZnO/Na-FAU and the ZnO that was doped with Na+. Zinc Oxide 75-78 FAU ubiquitin like and ribosomal protein S30 fusion Homo sapiens 82-85 21067176-4 2010 An etching evolution mechanism of the ZnO-FTO nanotubes via oxygen plasma was tentatively proposed in this study. Zinc Oxide 38-41 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 42-45 21067176-1 2010 A novel ZnO-FTO heterostructure nanotube array was produced by combining a chemical solution process with oxygen-plasma etching. Zinc Oxide 8-11 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 12-15 21067176-2 2010 In this approach, presynthesized ZnO nanorod arrays act as templates, and FTO nanoparticles are deposited onto the ZnO nanorods by a simple spray pyrolysis method. Zinc Oxide 115-118 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 74-77 20851137-7 2010 The expression of pro-inflammatory cytokines IL-2, IL-6, IL-12p70 and TNF-alpha in plasma and peritoneal lavage was found to remain at low concentration in PLGA nanoparticles treated mice as well as ZnO nanoparticles during the 24 hour period. Zinc Oxide 199-202 interleukin 2 Mus musculus 45-49 20851137-7 2010 The expression of pro-inflammatory cytokines IL-2, IL-6, IL-12p70 and TNF-alpha in plasma and peritoneal lavage was found to remain at low concentration in PLGA nanoparticles treated mice as well as ZnO nanoparticles during the 24 hour period. Zinc Oxide 199-202 tumor necrosis factor Mus musculus 70-79 20829568-1 2010 High-density vertically aligned ZnO nanotube arrays were fabricated on FTO substrates by a simple and facile chemical etching process from electrodeposited ZnO nanorods. Zinc Oxide 32-35 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 71-74 20853387-0 2010 CdS-encapsulated TiO2 nanotube arrays lidded with ZnO nanorod layers and their photoelectrocatalytic applications. Zinc Oxide 50-53 CDP-diacylglycerol synthase 1 Homo sapiens 0-3 20853387-1 2010 A novel TiO(2) nanotube array/CdS nanoparticle/ZnO nanorod (TiO(2) NT/CdS/ZnO NR) photocatalyst was constructed which exhibited a wide-absorption (200-535 nm) response in the UV/Vis region and was applied for the photoelectrocatalytic (PEC) degradation of dye wastewater. Zinc Oxide 47-50 CDP-diacylglycerol synthase 1 Homo sapiens 30-33 20853387-1 2010 A novel TiO(2) nanotube array/CdS nanoparticle/ZnO nanorod (TiO(2) NT/CdS/ZnO NR) photocatalyst was constructed which exhibited a wide-absorption (200-535 nm) response in the UV/Vis region and was applied for the photoelectrocatalytic (PEC) degradation of dye wastewater. Zinc Oxide 47-50 CDP-diacylglycerol synthase 1 Homo sapiens 70-73 20674161-5 2010 Treatments with ZnO concentrations <=45 mug/ml were performed to determine the expression of intercellular adhesion molecule-1 (ICAM-1) protein, an indicator of vascular endothelium inflammation, revealing that ZnO particles induced a dose-dependent increase in ICAM-1 expression and marked increases in NF-kappaB reporter activity. Zinc Oxide 214-217 intercellular adhesion molecule 1 Homo sapiens 96-129 20674161-5 2010 Treatments with ZnO concentrations <=45 mug/ml were performed to determine the expression of intercellular adhesion molecule-1 (ICAM-1) protein, an indicator of vascular endothelium inflammation, revealing that ZnO particles induced a dose-dependent increase in ICAM-1 expression and marked increases in NF-kappaB reporter activity. Zinc Oxide 214-217 intercellular adhesion molecule 1 Homo sapiens 131-137 20674161-5 2010 Treatments with ZnO concentrations <=45 mug/ml were performed to determine the expression of intercellular adhesion molecule-1 (ICAM-1) protein, an indicator of vascular endothelium inflammation, revealing that ZnO particles induced a dose-dependent increase in ICAM-1 expression and marked increases in NF-kappaB reporter activity. Zinc Oxide 214-217 intercellular adhesion molecule 1 Homo sapiens 265-271 20674161-6 2010 Overexpression of IkappaBalpha completely inhibited ZnO-induced ICAM-1 expression, suggesting NF-kappaB plays a pivotal role in regulation of ZnO-induced inflammation in HUVECs. Zinc Oxide 52-55 NFKB inhibitor alpha Homo sapiens 18-30 20674161-6 2010 Overexpression of IkappaBalpha completely inhibited ZnO-induced ICAM-1 expression, suggesting NF-kappaB plays a pivotal role in regulation of ZnO-induced inflammation in HUVECs. Zinc Oxide 52-55 intercellular adhesion molecule 1 Homo sapiens 64-70 20674161-6 2010 Overexpression of IkappaBalpha completely inhibited ZnO-induced ICAM-1 expression, suggesting NF-kappaB plays a pivotal role in regulation of ZnO-induced inflammation in HUVECs. Zinc Oxide 142-145 NFKB inhibitor alpha Homo sapiens 18-30 20674161-7 2010 Additionally, TNF-alpha, a typical inflammatory cytokine, induced ICAM-1 expression in an NF-kappaB-dependent manner, and ZnO synergistically enhanced TNF-alpha-induced ICAM-1 expression. Zinc Oxide 122-125 tumor necrosis factor Homo sapiens 151-160 20674161-7 2010 Additionally, TNF-alpha, a typical inflammatory cytokine, induced ICAM-1 expression in an NF-kappaB-dependent manner, and ZnO synergistically enhanced TNF-alpha-induced ICAM-1 expression. Zinc Oxide 122-125 intercellular adhesion molecule 1 Homo sapiens 169-175 20878929-0 2010 Sintering, microstructure, mechanical, and antimicrobial properties of HAp-ZnO biocomposites. Zinc Oxide 75-78 hemaglutinin-associated protein Escherichia coli 71-74 20878929-2 2010 In our present work, we sintered Hydroxyapatite (HAp) with different concentrations of zinc oxide microrods (ZnO) at 1250 C to produce HAp-ZnO biocomposites. Zinc Oxide 87-97 hemaglutinin-associated protein Escherichia coli 49-52 20878929-2 2010 In our present work, we sintered Hydroxyapatite (HAp) with different concentrations of zinc oxide microrods (ZnO) at 1250 C to produce HAp-ZnO biocomposites. Zinc Oxide 109-112 hemaglutinin-associated protein Escherichia coli 135-138 20878929-2 2010 In our present work, we sintered Hydroxyapatite (HAp) with different concentrations of zinc oxide microrods (ZnO) at 1250 C to produce HAp-ZnO biocomposites. Zinc Oxide 139-142 hemaglutinin-associated protein Escherichia coli 49-52 20878929-2 2010 In our present work, we sintered Hydroxyapatite (HAp) with different concentrations of zinc oxide microrods (ZnO) at 1250 C to produce HAp-ZnO biocomposites. Zinc Oxide 139-142 hemaglutinin-associated protein Escherichia coli 135-138 20878929-3 2010 In vitro antimicrobial studies were carried out to understand how ZnO addition (up to 30 wt %) to HAp leads to the improvement in bacteria static/bactericidal property and thereby, can reduce bacterial infection on implant surface. Zinc Oxide 66-69 hemaglutinin-associated protein Escherichia coli 98-101 20878929-5 2010 After 4 h of incubation, it was observed that microbial activity on HAp-20 wt % and HAp-30 wt % ZnO are significantly reduced in comparison to control sample, independent of type of bacterial cells. Zinc Oxide 96-99 hemaglutinin-associated protein Escherichia coli 84-87 20878929-7 2010 A maximum up to 1.7 MPam(1/2) indentation fracture toughness and hardness of up to 6.8 GPa were measured in HAp-ZnO biocomposites. Zinc Oxide 112-115 hemaglutinin-associated protein Escherichia coli 108-111 20853387-1 2010 A novel TiO(2) nanotube array/CdS nanoparticle/ZnO nanorod (TiO(2) NT/CdS/ZnO NR) photocatalyst was constructed which exhibited a wide-absorption (200-535 nm) response in the UV/Vis region and was applied for the photoelectrocatalytic (PEC) degradation of dye wastewater. Zinc Oxide 74-77 CDP-diacylglycerol synthase 1 Homo sapiens 30-33 20853387-1 2010 A novel TiO(2) nanotube array/CdS nanoparticle/ZnO nanorod (TiO(2) NT/CdS/ZnO NR) photocatalyst was constructed which exhibited a wide-absorption (200-535 nm) response in the UV/Vis region and was applied for the photoelectrocatalytic (PEC) degradation of dye wastewater. Zinc Oxide 74-77 CDP-diacylglycerol synthase 1 Homo sapiens 70-73 20853387-7 2010 Photoelectric-property tests indicated that the TiO(2) NT/CdS/ZnO NR material maintained a very high PEC activity in both the ultraviolet (UV) and the visible region. Zinc Oxide 62-65 CDP-diacylglycerol synthase 1 Homo sapiens 58-61 20853387-8 2010 The maximum photoelectric conversion efficiencies of TiO(2) NT/CdS/ZnO NR were 31.8 and 5.98% under UV light (365 nm) and visible light (420-800 nm), respectively. Zinc Oxide 67-70 CDP-diacylglycerol synthase 1 Homo sapiens 63-66 20853387-9 2010 In the PEC oxidation, TiO(2) NT/CdS/ZnO NR exhibited a higher removal ability for methyl orange (MO) and a high stability. Zinc Oxide 36-39 CDP-diacylglycerol synthase 1 Homo sapiens 32-35 20716452-2 2010 With the assistance of polystyrene spheres monolayer template and morphology control agent, we succeeded in preparing a series of ordered ZnO microbowls with different sag height. Zinc Oxide 138-141 S-antigen visual arrestin Homo sapiens 168-171 20846902-0 2010 Spectroscopic investigation on assisted sonocatalytic damage of bovine serum albumin (BSA) by metronidazole (MTZ) under ultrasonic irradiation combined with nano-sized ZnO. Zinc Oxide 168-171 albumin Homo sapiens 71-84 20846902-1 2010 The previous work proved that the bovine serum albumin (BSA) could be damaged under the combined action of ultrasonic irradiation and ZnO. Zinc Oxide 134-137 albumin Homo sapiens 41-54 20714619-2 2010 The C@ZnO nanorod array-based sensor demonstrates a very high sensitivity of 9.4 muA muM(-1) cm(-2) and a low detection limit of 0.1 muM. Zinc Oxide 6-9 PWWP domain containing 3A, DNA repair factor Homo sapiens 85-91 20346586-3 2010 On degradation of nitrogen monoxide (NO) and formaldehyde (HCHO) at typical concentrations for indoor air quality, these nanocrystalline Zn(2)SnO(4) microcubes exhibited superior photocatalytic activity to the hydrothermally synthesized ZnO, SnO(2), and Degussa TiO(2) P25, as well as C doped TiO(2) under UV-vis light irradiation. Zinc Oxide 237-240 strawberry notch homolog 2 Homo sapiens 142-145 20876960-5 2010 The amounts of human fibrinogen (HFG) and human serum albumin (HSA) adsorbing on the ZnO films and reference samples were determined by using enzyme-linked immunosorbent assay (ELISA). Zinc Oxide 85-88 fibrinogen beta chain Homo sapiens 21-31 20876960-5 2010 The amounts of human fibrinogen (HFG) and human serum albumin (HSA) adsorbing on the ZnO films and reference samples were determined by using enzyme-linked immunosorbent assay (ELISA). Zinc Oxide 85-88 albumin Homo sapiens 48-61 20695623-2 2010 The SPV of the porous ZnO sensor can be remarkably reduced under visible light illumination after PCB adsorption, and the reduction of amplitude is proportional to the population of adsorbed PCB molecules. Zinc Oxide 22-25 pyruvate carboxylase Homo sapiens 98-101 20695623-2 2010 The SPV of the porous ZnO sensor can be remarkably reduced under visible light illumination after PCB adsorption, and the reduction of amplitude is proportional to the population of adsorbed PCB molecules. Zinc Oxide 22-25 pyruvate carboxylase Homo sapiens 191-194 20735115-3 2010 Glucose oxidase (GOx) was subsequently immobilized on the as-synthesized ZnO NWs, and the electrocatalytic properties of GOx-immobilized ZnO NWs were evaluated by amperometry. Zinc Oxide 73-76 hydroxyacid oxidase 1 Homo sapiens 0-15 20735115-3 2010 Glucose oxidase (GOx) was subsequently immobilized on the as-synthesized ZnO NWs, and the electrocatalytic properties of GOx-immobilized ZnO NWs were evaluated by amperometry. Zinc Oxide 73-76 hydroxyacid oxidase 1 Homo sapiens 17-20 20735115-3 2010 Glucose oxidase (GOx) was subsequently immobilized on the as-synthesized ZnO NWs, and the electrocatalytic properties of GOx-immobilized ZnO NWs were evaluated by amperometry. Zinc Oxide 137-140 hydroxyacid oxidase 1 Homo sapiens 0-15 20735115-3 2010 Glucose oxidase (GOx) was subsequently immobilized on the as-synthesized ZnO NWs, and the electrocatalytic properties of GOx-immobilized ZnO NWs were evaluated by amperometry. Zinc Oxide 137-140 hydroxyacid oxidase 1 Homo sapiens 17-20 20735115-3 2010 Glucose oxidase (GOx) was subsequently immobilized on the as-synthesized ZnO NWs, and the electrocatalytic properties of GOx-immobilized ZnO NWs were evaluated by amperometry. Zinc Oxide 137-140 hydroxyacid oxidase 1 Homo sapiens 121-124 20434478-8 2010 Treatment with ZnO (5mug/cm(2) corresponding to 11.5mug/ml) for 24h induced on LoVo cells a significant decrease of cell viability, H2O2/OH increase, O2(-) and GSH decrease, depolarization of inner mitochondrial membranes, apoptosis and IL-8 release. Zinc Oxide 15-18 immunoglobulin kappa variable 1D-39 Homo sapiens 150-155 20434478-8 2010 Treatment with ZnO (5mug/cm(2) corresponding to 11.5mug/ml) for 24h induced on LoVo cells a significant decrease of cell viability, H2O2/OH increase, O2(-) and GSH decrease, depolarization of inner mitochondrial membranes, apoptosis and IL-8 release. Zinc Oxide 15-18 C-X-C motif chemokine ligand 8 Homo sapiens 237-241 20875979-1 2010 This study describes the influence of relative humidity (RH) and reducing gases on the temperature coefficient of resonant frequency (TCF) of ZnO-based film bulk acoustic wave resonator (FBAR). Zinc Oxide 142-145 hepatocyte nuclear factor 4 alpha Homo sapiens 134-137 20875979-5 2010 Reducing gases, such as acetone, can reduce the density of ZnO through reaction with the adsorbed oxygen, leading to a lower TCF. Zinc Oxide 59-62 hepatocyte nuclear factor 4 alpha Homo sapiens 125-128 20515071-0 2010 Fabrication and SERS performance of silver-nanoparticle-decorated Si/ZnO nanotrees in ordered arrays. Zinc Oxide 69-72 seryl-tRNA synthetase 2, mitochondrial Homo sapiens 16-20 20515071-4 2010 In addition to the SERS application, such ordered Si/ZnO arrays might also find potential applications in light-emitting diodes and solar cells. Zinc Oxide 53-56 seryl-tRNA synthetase 2, mitochondrial Homo sapiens 19-23 21128395-0 2010 Immobilization of angiotensin II and bovine serum albumin on strip-patterned ZnO nanorod arrays. Zinc Oxide 77-80 angiotensinogen Homo sapiens 18-32 20194077-11 2010 Moreover, ZnO exposure also increased the binding of p65 to the IL-8 promoter and p65 phosphorylation at serines 276 and 536. Zinc Oxide 10-13 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 20194077-11 2010 Moreover, ZnO exposure also increased the binding of p65 to the IL-8 promoter and p65 phosphorylation at serines 276 and 536. Zinc Oxide 10-13 RELA proto-oncogene, NF-kB subunit Homo sapiens 82-85 20194077-12 2010 Overexpression of p65 constructs mutated at serines 276 or 536 significantly reduced ZnO-induced increase in IL-8 promoter reporter activity. Zinc Oxide 85-88 RELA proto-oncogene, NF-kB subunit Homo sapiens 18-21 20194077-12 2010 Overexpression of p65 constructs mutated at serines 276 or 536 significantly reduced ZnO-induced increase in IL-8 promoter reporter activity. Zinc Oxide 85-88 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 20194077-13 2010 CONCLUSION: p65 phosphorylation and IkappaBalpha phosphorylation and degradation are the primary mechanisms involved in ZnO nanoparticle-induced IL-8 expression in human bronchial epithelial cells. Zinc Oxide 120-123 RELA proto-oncogene, NF-kB subunit Homo sapiens 12-15 20194077-13 2010 CONCLUSION: p65 phosphorylation and IkappaBalpha phosphorylation and degradation are the primary mechanisms involved in ZnO nanoparticle-induced IL-8 expression in human bronchial epithelial cells. Zinc Oxide 120-123 NFKB inhibitor alpha Homo sapiens 36-48 20194077-13 2010 CONCLUSION: p65 phosphorylation and IkappaBalpha phosphorylation and degradation are the primary mechanisms involved in ZnO nanoparticle-induced IL-8 expression in human bronchial epithelial cells. Zinc Oxide 120-123 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 20630305-3 2010 The aim of this study was to investigate the effects of an epoxy resin-based sealer AH26, a zinc oxide-eugenol-based sealer Canals, and a paste sealer N2 on the expression of ALP in human osteoblastic cell line U2OS cells. Zinc Oxide 92-102 alkaline phosphatase, placental Homo sapiens 175-178 20194077-0 2010 Phosphorylation of p65 is required for zinc oxide nanoparticle-induced interleukin 8 expression in human bronchial epithelial cells. Zinc Oxide 39-49 RELA proto-oncogene, NF-kB subunit Homo sapiens 19-22 20194077-0 2010 Phosphorylation of p65 is required for zinc oxide nanoparticle-induced interleukin 8 expression in human bronchial epithelial cells. Zinc Oxide 39-49 C-X-C motif chemokine ligand 8 Homo sapiens 71-84 20194077-1 2010 BACKGROUND: Exposure to zinc oxide (ZnO) in environmental and occupational settings causes acute pulmonary responses through the induction of proinflammatory mediators such as interleukin-8 (IL-8). Zinc Oxide 24-34 C-X-C motif chemokine ligand 8 Homo sapiens 176-189 20194077-1 2010 BACKGROUND: Exposure to zinc oxide (ZnO) in environmental and occupational settings causes acute pulmonary responses through the induction of proinflammatory mediators such as interleukin-8 (IL-8). Zinc Oxide 24-34 C-X-C motif chemokine ligand 8 Homo sapiens 191-195 20194077-1 2010 BACKGROUND: Exposure to zinc oxide (ZnO) in environmental and occupational settings causes acute pulmonary responses through the induction of proinflammatory mediators such as interleukin-8 (IL-8). Zinc Oxide 36-39 C-X-C motif chemokine ligand 8 Homo sapiens 176-189 20194077-1 2010 BACKGROUND: Exposure to zinc oxide (ZnO) in environmental and occupational settings causes acute pulmonary responses through the induction of proinflammatory mediators such as interleukin-8 (IL-8). Zinc Oxide 36-39 C-X-C motif chemokine ligand 8 Homo sapiens 191-195 20194077-2 2010 OBJECTIVE: We investigated the effect of ZnO nanoparticles on IL-8 expression and the underlying mechanisms in human bronchial epithelial cells. Zinc Oxide 41-44 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 20194077-4 2010 Transcriptional activity of IL-8 promoter and nuclear factor kappa B (NFkappaB) in ZnO-treated BEAS-2B cells was measured using transient gene transfection of the luciferase reporter construct with or without p65 constructs. Zinc Oxide 83-86 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 20194077-4 2010 Transcriptional activity of IL-8 promoter and nuclear factor kappa B (NFkappaB) in ZnO-treated BEAS-2B cells was measured using transient gene transfection of the luciferase reporter construct with or without p65 constructs. Zinc Oxide 83-86 nuclear factor kappa B subunit 1 Homo sapiens 46-68 20194077-4 2010 Transcriptional activity of IL-8 promoter and nuclear factor kappa B (NFkappaB) in ZnO-treated BEAS-2B cells was measured using transient gene transfection of the luciferase reporter construct with or without p65 constructs. Zinc Oxide 83-86 nuclear factor kappa B subunit 1 Homo sapiens 70-78 20194077-4 2010 Transcriptional activity of IL-8 promoter and nuclear factor kappa B (NFkappaB) in ZnO-treated BEAS-2B cells was measured using transient gene transfection of the luciferase reporter construct with or without p65 constructs. Zinc Oxide 83-86 RELA proto-oncogene, NF-kB subunit Homo sapiens 209-212 20194077-7 2010 RESULTS: ZnO exposure (2-8 microg/mL) increased IL-8 mRNA and protein expression. Zinc Oxide 9-12 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 20194077-8 2010 Inhibition of transcription with actinomycin D blocked ZnO-induced IL-8 expression, which was consistent with the observation that ZnO exposure increased IL-8 promoter reporter activity. Zinc Oxide 55-58 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 20194077-8 2010 Inhibition of transcription with actinomycin D blocked ZnO-induced IL-8 expression, which was consistent with the observation that ZnO exposure increased IL-8 promoter reporter activity. Zinc Oxide 55-58 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 20194077-8 2010 Inhibition of transcription with actinomycin D blocked ZnO-induced IL-8 expression, which was consistent with the observation that ZnO exposure increased IL-8 promoter reporter activity. Zinc Oxide 131-134 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 20194077-8 2010 Inhibition of transcription with actinomycin D blocked ZnO-induced IL-8 expression, which was consistent with the observation that ZnO exposure increased IL-8 promoter reporter activity. Zinc Oxide 131-134 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 20194077-9 2010 Further study demonstrated that the kappaB-binding site in the IL-8 promoter was required for ZnO-induced IL-8 transcriptional activation. Zinc Oxide 94-97 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 20194077-9 2010 Further study demonstrated that the kappaB-binding site in the IL-8 promoter was required for ZnO-induced IL-8 transcriptional activation. Zinc Oxide 94-97 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 20194077-10 2010 ZnO stimulation modestly elevated IkappaBalpha phosphorylation and degradation. Zinc Oxide 0-3 NFKB inhibitor alpha Homo sapiens 34-46 20194077-11 2010 Moreover, ZnO exposure also increased the binding of p65 to the IL-8 promoter and p65 phosphorylation at serines 276 and 536. Zinc Oxide 10-13 RELA proto-oncogene, NF-kB subunit Homo sapiens 53-56 21128395-0 2010 Immobilization of angiotensin II and bovine serum albumin on strip-patterned ZnO nanorod arrays. Zinc Oxide 77-80 albumin Homo sapiens 44-57 21128395-1 2010 For an effective protein immobilization for highly sensitive biosensors, we determined the binding properties and characteristics of angiotensin II and bovine serum albumin on the surface of patterned ZnO nanorod arrays (NRAs) which were selectively grown on desired areas of Si substrates. Zinc Oxide 201-204 angiotensinogen Homo sapiens 133-147 21128395-1 2010 For an effective protein immobilization for highly sensitive biosensors, we determined the binding properties and characteristics of angiotensin II and bovine serum albumin on the surface of patterned ZnO nanorod arrays (NRAs) which were selectively grown on desired areas of Si substrates. Zinc Oxide 201-204 albumin Homo sapiens 159-172 21128395-2 2010 The surfaces of ZnO NRAs were modified by 3-aminopropyltriethoxysilane and gluteraldehyde, and the activated NRAs were then conjugated with angiotensin II protein and bovine serum albumin. Zinc Oxide 16-19 angiotensinogen Homo sapiens 140-154 21128395-2 2010 The surfaces of ZnO NRAs were modified by 3-aminopropyltriethoxysilane and gluteraldehyde, and the activated NRAs were then conjugated with angiotensin II protein and bovine serum albumin. Zinc Oxide 16-19 albumin Homo sapiens 174-187 21128477-2 2010 PA1 pore-array film consisting of the horizontal ZnO nanosheets was nearly superhydrophobic. Zinc Oxide 49-52 PAXIP1 associated glutamate rich protein 1 Homo sapiens 0-3 20155942-9 2010 Robust markers of apoptosis, Annexin V staining, loss of mitochondrial potential, and increased generation of superoxide were observed when cells were treated with ZnO particulate matter but not when treated with comparable concentration of a soluble Zn salt. Zinc Oxide 164-167 annexin A5 Homo sapiens 29-38 20516577-3 2010 Combined ZnO:SnO(2) nanowire arrays yield a desired emission color from (0.30, 0.31) to (0.35, 0.37) and a white luminescence of approximately 100 cd m(-2), whose reproducibility can be controlled accurately. Zinc Oxide 9-12 strawberry notch homolog 1 Homo sapiens 13-16 20303253-5 2010 The measured glucose concentration in human adipocytes or frog oocytes using our ZnO-nanorod sensor was consistent with values of glucose concentration reported in the literature; furthermore, the sensor was able to show that insulin increased the intracellular glucose concentration. Zinc Oxide 81-84 insulin Homo sapiens 226-233 20453289-1 2010 ZnO nanorods containing different hollow structures have been grown by a thermal evaporation-deposition method with a mixture of ZnS and SnO(2) powders as precursor. Zinc Oxide 0-3 strawberry notch homolog 1 Homo sapiens 137-140 20359021-3 2010 Typical DSSCs with ZnO nanosheets achieved moderately good conversion efficiency eta of approximately 2.12% with short-circuit current density J(SC) = 3.56 mA/cm2, open-circuit voltage V(OC) = 0.831 V, and fill factor FF = 71%. Zinc Oxide 19-22 endothelin receptor type A Homo sapiens 81-84 20359021-4 2010 The high J(SC) and eta are attributed to high dye absorption through high surface ZnO nanosheets, which increased the light harvesting. Zinc Oxide 82-85 endothelin receptor type A Homo sapiens 19-22 20000758-0 2010 Structure and activity of lysozyme on binding to ZnO nanoparticles. Zinc Oxide 49-52 lysozyme Homo sapiens 26-34 21389531-4 2010 Bond order calculations show that Zn preference for the Ca2 vacancy, near the OH channel and with greater structural flexibility, is associated with the formation of a four-fold (bulk) and nearly four-fold (surface) coordination, as in ZnO. Zinc Oxide 236-239 carbonic anhydrase 2 Homo sapiens 56-59 19957989-5 2010 An ultrathin layer of ZnO spontaneously shelled on SnO(2) nanoparticles is found to enhance V(oc) primarily by lifting the band edges rather than by suppressing recombination. Zinc Oxide 22-25 strawberry notch homolog 2 Homo sapiens 51-54 19957989-6 2010 Finally, by intensity modulated photocurrent/photovoltage spectroscopy (IMPS/IMVS), we have identified that recombination in SnO(2)/ZnO composite films is mainly determined by the ZnO shell condition on SnO(2), whereas electron transport is greatly influenced by the morphologies and sizes of the ZnO crystalline additives. Zinc Oxide 132-135 strawberry notch homolog 2 Homo sapiens 125-128 19957989-6 2010 Finally, by intensity modulated photocurrent/photovoltage spectroscopy (IMPS/IMVS), we have identified that recombination in SnO(2)/ZnO composite films is mainly determined by the ZnO shell condition on SnO(2), whereas electron transport is greatly influenced by the morphologies and sizes of the ZnO crystalline additives. Zinc Oxide 132-135 strawberry notch homolog 2 Homo sapiens 203-206 19957989-6 2010 Finally, by intensity modulated photocurrent/photovoltage spectroscopy (IMPS/IMVS), we have identified that recombination in SnO(2)/ZnO composite films is mainly determined by the ZnO shell condition on SnO(2), whereas electron transport is greatly influenced by the morphologies and sizes of the ZnO crystalline additives. Zinc Oxide 180-183 strawberry notch homolog 2 Homo sapiens 125-128 19957989-6 2010 Finally, by intensity modulated photocurrent/photovoltage spectroscopy (IMPS/IMVS), we have identified that recombination in SnO(2)/ZnO composite films is mainly determined by the ZnO shell condition on SnO(2), whereas electron transport is greatly influenced by the morphologies and sizes of the ZnO crystalline additives. Zinc Oxide 180-183 strawberry notch homolog 2 Homo sapiens 203-206 19957989-6 2010 Finally, by intensity modulated photocurrent/photovoltage spectroscopy (IMPS/IMVS), we have identified that recombination in SnO(2)/ZnO composite films is mainly determined by the ZnO shell condition on SnO(2), whereas electron transport is greatly influenced by the morphologies and sizes of the ZnO crystalline additives. Zinc Oxide 180-183 strawberry notch homolog 2 Homo sapiens 125-128 19957989-6 2010 Finally, by intensity modulated photocurrent/photovoltage spectroscopy (IMPS/IMVS), we have identified that recombination in SnO(2)/ZnO composite films is mainly determined by the ZnO shell condition on SnO(2), whereas electron transport is greatly influenced by the morphologies and sizes of the ZnO crystalline additives. Zinc Oxide 180-183 strawberry notch homolog 2 Homo sapiens 203-206 19957989-7 2010 In particular, ZnO nanotetrapods have proved to be superior in electron transport and therefore charge collection over ZnO particles additives in the SnO(2)/ZnO composite-based DSSCs. Zinc Oxide 15-18 strawberry notch homolog 2 Homo sapiens 150-153 20000758-1 2010 The interaction between ZnO nanoparticles (NPs) and lysozyme has been studied using calorimetric as well as spectrophotometric techniques, and interpreted in terms of the three-dimensional structure. Zinc Oxide 24-27 lysozyme Homo sapiens 52-60 20000758-3 2010 Glutaraldehyde cross-linking studies indicate that the monomeric form occurs to a greater extent than the dimer when lysozyme is conjugated with ZnO NPs. Zinc Oxide 145-148 lysozyme Homo sapiens 117-125 20000758-4 2010 The enthalpy-driven binding between lysozyme and ZnO possibly involves the region encompassing the active site in the molecule, which is also the site for the dimer formation in a homologous structure. Zinc Oxide 49-52 lysozyme Homo sapiens 36-44 20000758-6 2010 Compared to the free protein, lysozyme-ZnO conjugates are more stable in the presence of chaotropic agents (guanidine hydrochloride and urea) and also at elevated temperatures. Zinc Oxide 39-42 lysozyme Homo sapiens 30-38 20057029-3 2010 Then, ZnO quantum dots were in situ formed on the pore walls of the ordered PTh/SBA-15 composite. Zinc Oxide 6-9 parathyroid hormone Homo sapiens 76-79 19811107-0 2010 Adjuvant effect of zinc oxide on Th2 but not Th1 immune responses in mice. Zinc Oxide 19-29 heart and neural crest derivatives expressed 2 Mus musculus 33-36 19811107-1 2010 BACKGROUND AND AIM: We investigated the effect of zinc oxide (ZnO) on Th1 and Th2 immune responses in mice. Zinc Oxide 50-60 negative elongation factor complex member C/D, Th1l Mus musculus 70-73 19811107-1 2010 BACKGROUND AND AIM: We investigated the effect of zinc oxide (ZnO) on Th1 and Th2 immune responses in mice. Zinc Oxide 50-60 heart and neural crest derivatives expressed 2 Mus musculus 78-81 19811107-1 2010 BACKGROUND AND AIM: We investigated the effect of zinc oxide (ZnO) on Th1 and Th2 immune responses in mice. Zinc Oxide 62-65 negative elongation factor complex member C/D, Th1l Mus musculus 70-73 19811107-1 2010 BACKGROUND AND AIM: We investigated the effect of zinc oxide (ZnO) on Th1 and Th2 immune responses in mice. Zinc Oxide 62-65 heart and neural crest derivatives expressed 2 Mus musculus 78-81 19811107-5 2010 The production of anti-OVA IgG1 and IgE and secretion of IL-4 and IL-5 were markedly enhanced by ZnO. Zinc Oxide 97-100 LOC105243590 Mus musculus 27-31 19811107-5 2010 The production of anti-OVA IgG1 and IgE and secretion of IL-4 and IL-5 were markedly enhanced by ZnO. Zinc Oxide 97-100 interleukin 4 Mus musculus 57-61 19811107-5 2010 The production of anti-OVA IgG1 and IgE and secretion of IL-4 and IL-5 were markedly enhanced by ZnO. Zinc Oxide 97-100 interleukin 5 Mus musculus 66-70 19811107-6 2010 The enhancing effect of ZnO on these Th2 responses was as strong as aluminium hydroxide (Alum) that was widely used as an adjuvant. Zinc Oxide 24-27 heart and neural crest derivatives expressed 2 Mus musculus 37-40 19811107-8 2010 It was also observed that ZnO had a stimulating effect on the secretion of the proinflammatory cytokine IL-17 from a new lineage of effector Th cells. Zinc Oxide 26-29 interleukin 17A Mus musculus 104-109 19811107-9 2010 CONCLUSION: These results suggest that ZnO appears to have an adjuvant effect on the immune system, especially Th2 but not Th1 immune responses. Zinc Oxide 39-42 heart and neural crest derivatives expressed 2 Mus musculus 111-114 20355657-5 2010 A very thin layer of ZnO shells would form on CdO cores if the shell precursor was injected at a speed of 4 ml/h at temperature of 160 degrees C, and the shells had good crystal quality. Zinc Oxide 21-24 cell adhesion associated, oncogene regulated Homo sapiens 46-49 20113735-0 2010 AChE biosensor based on zinc oxide sol-gel for the detection of pesticides. Zinc Oxide 24-34 acetylcholinesterase (Cartwright blood group) Homo sapiens 0-4 20113735-1 2010 Zinc oxide has been used as a matrix for immobilization of acetylcholinesterase (AChE) and detection of the pesticide paraoxon. Zinc Oxide 0-10 acetylcholinesterase (Cartwright blood group) Homo sapiens 59-79 20113735-1 2010 Zinc oxide has been used as a matrix for immobilization of acetylcholinesterase (AChE) and detection of the pesticide paraoxon. Zinc Oxide 0-10 acetylcholinesterase (Cartwright blood group) Homo sapiens 81-85 20057029-1 2010 A modified ZnO quantum dot/polythiophene (ZnO/PTh) inorganic-organic hybrid architecture was fabricated by using ordered mesoporous silica (SBA-15) as the retaining template. Zinc Oxide 11-14 parathyroid hormone Homo sapiens 46-49 20499830-4 2010 Association of MnO and ZnO to three model biomedically important proteins (albumin, protamine and thrombin) has been characterized by ultra-violet and dynamic laser light spectroscopy, UVS and DLLS respectively. Zinc Oxide 23-26 coagulation factor II, thrombin Homo sapiens 98-106 19648064-1 2010 Nanostructured zinc oxide (Nano-ZnO) film has been deposited onto indium-tin-oxide (ITO) glass plate for co-immobilization of rabbit-immunoglubin antibodies (r-IgGs) and bovine serum albumin (BSA) for ochratoxin-A (OTA) detection. Zinc Oxide 15-25 albumin Homo sapiens 177-190 19648064-1 2010 Nanostructured zinc oxide (Nano-ZnO) film has been deposited onto indium-tin-oxide (ITO) glass plate for co-immobilization of rabbit-immunoglubin antibodies (r-IgGs) and bovine serum albumin (BSA) for ochratoxin-A (OTA) detection. Zinc Oxide 32-35 albumin Homo sapiens 177-190 19897006-6 2010 ZnO had the most drastic immunological effects leading to high expression of proinflammatory cytokine, IL-1beta, and enhanced production of neutrophil chemoattractant CXCL-9 on both cell types. Zinc Oxide 0-3 interleukin 1 beta Mus musculus 103-111 19755143-8 2010 Exposure to a sublethal concentration of ZnO increased the expression of four genes that are involved in apoptosis and oxidative stress responses BNIP, PRDX3, PRNP, and TXRND1, by at least 2.5-fold. Zinc Oxide 41-44 peroxiredoxin 3 Homo sapiens 152-157 19755143-8 2010 Exposure to a sublethal concentration of ZnO increased the expression of four genes that are involved in apoptosis and oxidative stress responses BNIP, PRDX3, PRNP, and TXRND1, by at least 2.5-fold. Zinc Oxide 41-44 prion protein Homo sapiens 159-163 19897006-6 2010 ZnO had the most drastic immunological effects leading to high expression of proinflammatory cytokine, IL-1beta, and enhanced production of neutrophil chemoattractant CXCL-9 on both cell types. Zinc Oxide 0-3 chemokine (C-X-C motif) ligand 9 Mus musculus 167-173 20038182-3 2010 The much higher photocataltyic activity of the microscale ZnO than P25 under UV-visible irradiation is attributed to the higher efficiency of generation, mobility, and separation of photoinduced electrons and holes. Zinc Oxide 58-61 tubulin polymerization promoting protein Homo sapiens 67-70 20038182-4 2010 The much higher visible photocataltyic activity of the microscale ZnO than P25 is due to the higher photosensitization efficiency of electron transfer from an excited dye to the conduction band of the microscale ZnO than that of P25. Zinc Oxide 66-69 tubulin polymerization promoting protein Homo sapiens 75-78 20038182-4 2010 The much higher visible photocataltyic activity of the microscale ZnO than P25 is due to the higher photosensitization efficiency of electron transfer from an excited dye to the conduction band of the microscale ZnO than that of P25. Zinc Oxide 66-69 tubulin polymerization promoting protein Homo sapiens 229-232 20038182-4 2010 The much higher visible photocataltyic activity of the microscale ZnO than P25 is due to the higher photosensitization efficiency of electron transfer from an excited dye to the conduction band of the microscale ZnO than that of P25. Zinc Oxide 212-215 tubulin polymerization promoting protein Homo sapiens 75-78 19908685-0 2009 Role of sp-d exchange interactions in room-temperature photoluminescence and ferromagnetism of CuCo Co-doped ZnO nanorods. Zinc Oxide 109-112 surfactant protein D Homo sapiens 8-12 21235170-2 2010 The ZrO(x)/ZnO was characterized by XPS, XRD, UV-Vis, BET and SEM techniques. Zinc Oxide 11-14 delta/notch like EGF repeat containing Homo sapiens 54-57 20015351-8 2009 Dose-response measurements with ZnO nanoparticles (0.3-8.5 mug/cm(2)) showed significant differences in mRNA expression of pro-inflammatory (IL-8) and oxidative stress (HO-1) markers when comparing submerged and air-liquid interface exposures. Zinc Oxide 32-35 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 19609684-8 2009 These findings indicate that ultrafine ZnO particles, with a small diameter and a large total surface area/mass, could release Zn2+ easily and increase intracellular Zn2+ concentration efficiently, thus decreasing FceRI-mediated mast cell degranulation through inhibitions of PI3K and protein tyrosine kinase activation. Zinc Oxide 39-42 membrane spanning 4-domains A2 Rattus norvegicus 214-219 19647266-6 2009 FTIR spectroscopy and TGA analysis confirmed the adsorption of PVME on the surface of ZnO nanostructures. Zinc Oxide 86-89 T-box transcription factor 1 Homo sapiens 22-25 19772329-0 2009 Hierarchical assembly of ZnO nanostructures on SnO(2) backbone nanowires: low-temperature hydrothermal preparation and optical properties. Zinc Oxide 25-28 strawberry notch homolog 1 Homo sapiens 47-50 18926680-12 2009 Dietary Zn supplementation increased plasma concentrations of ghrelin, IGF-I and cholecystokinin; IGF-I gene expression in the duodenum as well as food intake and piglet growth (Exp. Zinc Oxide 8-10 appetite-regulating hormone Sus scrofa 62-69 19772329-2 2009 The ZnO nanorods grow epitaxially on the SnO(2) nanowire side faces mainly with a four-fold symmetry. Zinc Oxide 4-7 strawberry notch homolog 1 Homo sapiens 41-44 19772329-5 2009 Such hybrid SnO(2)-ZnO nanostructures show an enhanced near-band gap emission compared with the primary SnO(2) nanowires. Zinc Oxide 19-22 strawberry notch homolog 1 Homo sapiens 12-15 19772329-5 2009 Such hybrid SnO(2)-ZnO nanostructures show an enhanced near-band gap emission compared with the primary SnO(2) nanowires. Zinc Oxide 19-22 strawberry notch homolog 1 Homo sapiens 104-107 19921917-10 2009 Alternatively, in vitro exposures to fine or nanoscale ZnO particles produced minor cytotoxic responses at 4 and 24 h, only in cocultures and at the highest (particle overload) dose with little detectable proinflammatory cytokine generation (MIP-2, and TNF-alpha). Zinc Oxide 55-58 C-X-C motif chemokine ligand 2 Rattus norvegicus 242-247 19921917-10 2009 Alternatively, in vitro exposures to fine or nanoscale ZnO particles produced minor cytotoxic responses at 4 and 24 h, only in cocultures and at the highest (particle overload) dose with little detectable proinflammatory cytokine generation (MIP-2, and TNF-alpha). Zinc Oxide 55-58 tumor necrosis factor Rattus norvegicus 253-262 18926680-0 2009 Dietary supplementation with zinc oxide stimulates ghrelin secretion from the stomach of young pigs. Zinc Oxide 29-39 appetite-regulating hormone Sus scrofa 51-58 18926680-12 2009 Dietary Zn supplementation increased plasma concentrations of ghrelin, IGF-I and cholecystokinin; IGF-I gene expression in the duodenum as well as food intake and piglet growth (Exp. Zinc Oxide 8-10 insulin like growth factor 1 Sus scrofa 71-76 18926680-12 2009 Dietary Zn supplementation increased plasma concentrations of ghrelin, IGF-I and cholecystokinin; IGF-I gene expression in the duodenum as well as food intake and piglet growth (Exp. Zinc Oxide 8-10 cholecystokinin Sus scrofa 81-96 18926680-14 2009 The effects of ZnO on plasma levels of ghrelin, intestinal IGF-I expression and piglet growth were independent of food intake. Zinc Oxide 15-18 appetite-regulating hormone Sus scrofa 39-46 18926680-14 2009 The effects of ZnO on plasma levels of ghrelin, intestinal IGF-I expression and piglet growth were independent of food intake. Zinc Oxide 15-18 insulin like growth factor 1 Sus scrofa 59-64 18926680-15 2009 Addition of ZnO to culture medium enhanced ghrelin production from gastric mucosal cells without affecting ghrelin mRNA levels. Zinc Oxide 12-15 appetite-regulating hormone Sus scrofa 43-50 18926680-16 2009 Collectively, our results indicate that ZnO stimulates ghrelin secretion from the stomach at the post-transcriptional level. Zinc Oxide 40-43 appetite-regulating hormone Sus scrofa 55-62 20652105-7 2009 In addition, ZnO nanoparticles induce the production of the proinflammatory cytokines, IFN-gamma, TNF-alpha, and IL-12, at concentrations below those causing appreciable cell death. Zinc Oxide 13-16 interferon gamma Homo sapiens 87-96 20652105-7 2009 In addition, ZnO nanoparticles induce the production of the proinflammatory cytokines, IFN-gamma, TNF-alpha, and IL-12, at concentrations below those causing appreciable cell death. Zinc Oxide 13-16 tumor necrosis factor Homo sapiens 98-107 19267955-7 2009 ZnO or TBZC significantly enhanced the mRNA and protein expression of occludin (P < 0.05) and zonula occludens protein-1 (ZO-1) (P < 0.05) in the ileal mucosa. Zinc Oxide 0-3 occludin Sus scrofa 70-78 19745534-0 2009 A tyrosinase biosensor based on ZnO nanorod clusters/nanocrystalline diamond electrodes for biosensing of phenolic compounds. Zinc Oxide 32-35 tyrosinase Homo sapiens 2-12 19745534-1 2009 An amperometric biosensor was constructed by using ZnO nanorod clusters as platforms for immobilizing tyrosinase on the nanocrystalline diamond (NCD) electrodes. Zinc Oxide 51-54 tyrosinase Homo sapiens 102-112 19267955-7 2009 ZnO or TBZC significantly enhanced the mRNA and protein expression of occludin (P < 0.05) and zonula occludens protein-1 (ZO-1) (P < 0.05) in the ileal mucosa. Zinc Oxide 0-3 zonula occludens 1 Sus scrofa 97-123 19267955-7 2009 ZnO or TBZC significantly enhanced the mRNA and protein expression of occludin (P < 0.05) and zonula occludens protein-1 (ZO-1) (P < 0.05) in the ileal mucosa. Zinc Oxide 0-3 zonula occludens 1 Sus scrofa 125-129 19377694-1 2009 A simple route for the synthesis of a novel mesoporous zinc oxide material having wurtzite like nanocrystalline pore walls by using Schiff-base amine as template is reported, which shows very high BET surface area (456 m(2) g(-1)) and remarkably enhanced photoconductivity and photoluminescence at room temperature under visible light irradiation vis-a-vis bulk ZnO material. Zinc Oxide 362-365 delta/notch like EGF repeat containing Homo sapiens 197-200 19745534-2 2009 The results showed that ZnO nanorod clusters provided an advantageous microenvironment due to their favorable isoelectric point (IEP) for tyrosinase loading; immobilized tyrosinase generally retained its activity. Zinc Oxide 24-27 tyrosinase Homo sapiens 138-148 19745534-3 2009 The tyrosinase/ZnO/NCD electrode showed a linear response range of 1-210 and sensitivity of 179.9 microA mmol(-1) cm(-2) for p-cresol. Zinc Oxide 15-18 tyrosinase Homo sapiens 4-14 19487805-3 2009 The microsized grains of the commercially available ZnO:Zn (P 15) were reduced to the nanometre scale by pulsed laser ablation at an oxygen ambient pressure of 10 kPa. Zinc Oxide 52-55 cyclin dependent kinase inhibitor 2B Homo sapiens 60-64 19394953-0 2009 Zinc oxide nanoparticles/glucose oxidase photoelectrochemical system for the fabrication of biosensor. Zinc Oxide 0-10 hydroxyacid oxidase 1 Homo sapiens 25-40 19394953-3 2009 UV-spectrum and circular dichroism (CD) results show that the structure of GOx is preserved after conjugation with ZnO nanoparticles. Zinc Oxide 115-118 hydroxyacid oxidase 1 Homo sapiens 75-78 19192952-6 2009 Zinc oxide nanoparticles induced transgene expression in the mtl-2::GFP transgenic C. elegans in a manner similar to that of ZnCl2, suggesting that intracellular biotransformation of the nanoparticles might have occurred or the nanoparticles have dissolved to Zn2+ to enact toxicity. Zinc Oxide 0-10 Metallothionein-2 Caenorhabditis elegans 61-66 19518886-3 2009 After thermal treatment of vapor phase grown ZnO samples in hydrogen atmosphere, most hydrogen forms shallow donors at the bond-centered site (HBC). Zinc Oxide 45-48 keratin 88, pseudogene Homo sapiens 143-146 20628464-0 2009 Synthesis and Characterization of ZnO Nanowire-CdO Composite Nanostructures. Zinc Oxide 34-37 cell adhesion associated, oncogene regulated Homo sapiens 47-50 20628464-1 2009 ZnO nanowire-CdO composite nanostructures were fabricated by a simple two-step process involving ammonia solution method and thermal evaporation. Zinc Oxide 0-3 cell adhesion associated, oncogene regulated Homo sapiens 13-16 20628464-2 2009 First, ZnO nanowires (NWs) were grown on Si substrate by aqueous ammonia solution method and then CdO was deposited on these ZnO NWs by thermal evaporation of cadmium chloride powder. Zinc Oxide 125-128 cell adhesion associated, oncogene regulated Homo sapiens 98-101 20628464-6 2009 The photocurrent measurements showed that ZnO NW-CdO composite structures have better photocurrent when compared with the bare ZnO NWs. Zinc Oxide 42-45 cell adhesion associated, oncogene regulated Homo sapiens 49-52 20628464-6 2009 The photocurrent measurements showed that ZnO NW-CdO composite structures have better photocurrent when compared with the bare ZnO NWs. Zinc Oxide 127-130 cell adhesion associated, oncogene regulated Homo sapiens 49-52 18930348-1 2009 In the present study, four explosives of NH(4)NO(3), mineral explosives (ME), picric acid (PA) and 2,6-dinitrotoluene (2,6-DNT) have been investigated by using ZnO-doped nanoparticle sensors with additives of Sb(2)O(3), TiO(2), V(2)O(5) and WO(3). Zinc Oxide 160-163 5', 3'-nucleotidase, cytosolic Homo sapiens 123-126 19230793-0 2009 A novel tyrosinase biosensor based on biofunctional ZnO nanorod microarrays on the nanocrystalline diamond electrode for detection of phenolic compounds. Zinc Oxide 52-55 tyrosinase Homo sapiens 8-18 19230793-1 2009 A novel tyrosinase biosensor based on biofuncational ZnO nanorod microarrays on the boron-doped nanocrystalline diamond (BDND) substrates was developed. Zinc Oxide 53-56 tyrosinase Homo sapiens 8-18 19230793-2 2009 The ZnO nanorod microarrays were firstly deposited on BDND thin film surfaces via a low-temperature solution method, and then ZnO nanorods were functionalized with the mixture of 3-aminopropyltriethoxysilane (APTES) and tetraethoxysilane (TEOS) by a co-condensation approach, then tyrosinase was immobilized to amino-modification ZnO nanorod surfaces by the covalent binding. Zinc Oxide 4-7 tyrosinase Homo sapiens 281-291 19146874-0 2009 Influences of nanoparticle zinc oxide on acutely isolated rat hippocampal CA3 pyramidal neurons. Zinc Oxide 27-37 carbonic anhydrase 3 Rattus norvegicus 74-77 19265384-6 2009 Modification of ZnO NCs with Co(II) resulted in the transfer of photoexcited electrons to the cobalt center where consequent nonradiative recombination, at energies lower than required for PC, was observed via a comparable decrease in both PL and PC activity. Zinc Oxide 16-19 mitochondrially encoded cytochrome c oxidase II Homo sapiens 29-35 19235945-1 2009 A network-structured SnO(2)/ZnO heterojunction nanocatalyst with high photocatalytic activity was successfully synthesized through a simple two-step solvothermal method. Zinc Oxide 28-31 strawberry notch homolog 2 Homo sapiens 21-24 19235945-5 2009 (2) The SnO(2)/ZnO sample might possess more surface reaction sites and adsorb and transport more dye molecules due to the higher BET surface area and many pore channels, also leading to higher photocatalytic activity. Zinc Oxide 15-18 strawberry notch homolog 2 Homo sapiens 8-11 19129007-2 2009 The apparent association constant for the association between ZnPcTyro and SnO(2)/ZnO is ranged from (3.7+/-0.2)x10(5)M(-1) to (6.7+/-0.2)x10(4)M(-1) with a degree of association ranged from 85% to 95%. Zinc Oxide 82-85 strawberry notch homolog 2 Homo sapiens 75-78 19129007-5 2009 Maximum incident photon-to-current conversion of 0.84-1% at 600 nm and photon-to-current conversion efficiency of around 37% and 43% was obtained for ZnPc-sensitized-SnO(2) and ZnPc-sensitized-ZnO. Zinc Oxide 193-196 strawberry notch homolog 2 Homo sapiens 166-169 19146874-2 2009 The results indicated that: (1) in the present of final concentration of 10(-4)g/ml nano-ZnO, the current-voltage curve of sodium current (I(Na)) was decreased, and the peak amplitudes of I(Na) were increased considerably from -50 to +20mV (p<0.05). Zinc Oxide 89-92 internexin neuronal intermediate filament protein, alpha Rattus norvegicus 139-144 19146874-2 2009 The results indicated that: (1) in the present of final concentration of 10(-4)g/ml nano-ZnO, the current-voltage curve of sodium current (I(Na)) was decreased, and the peak amplitudes of I(Na) were increased considerably from -50 to +20mV (p<0.05). Zinc Oxide 89-92 internexin neuronal intermediate filament protein, alpha Rattus norvegicus 188-193 19146874-3 2009 Meanwhile, the inactivation and the recovery from inactivation of I(Na) were also promoted by the nano-ZnO solution (10(-4)g/ml) (p<0.01). Zinc Oxide 103-106 internexin neuronal intermediate filament protein, alpha Rattus norvegicus 66-71 19146874-9 2009 These results suggested that 10(-4)g/ml nano-ZnO solution can lead to an enhancement in the current amplitudes of I(Na) and I(K) by increasing the opening number of sodium channels, delaying rectifier potassium channels, and enhancing the excitability of neurons, which lead to Na(+) influx and the accumulation of intracellular Na(+), as well as K(+) efflux plus the loss of cytoplasmic K(+). Zinc Oxide 45-48 internexin neuronal intermediate filament protein, alpha Rattus norvegicus 114-119 19067557-0 2009 Tyrosinase immobilization on ZnO nanorods for phenol detection. Zinc Oxide 29-32 tyrosinase Homo sapiens 0-10 19067557-2 2009 The gold wire was skillfully treated to improve the nucleation for growth of ZnO nanostructures and to further improve the performance of the biosensor, which was construct by immobilizing tyrosinase (Tyr) on the ZnO nanorods for phenol detection. Zinc Oxide 213-216 tyrosinase Homo sapiens 189-199 19067557-2 2009 The gold wire was skillfully treated to improve the nucleation for growth of ZnO nanostructures and to further improve the performance of the biosensor, which was construct by immobilizing tyrosinase (Tyr) on the ZnO nanorods for phenol detection. Zinc Oxide 213-216 tyrosinase Homo sapiens 201-204 19067557-3 2009 Electrochemical measurement, Fourier transform infrared and scanning electron microscopic analyses demonstrated that the Tyr was stably adsorbed on the ZnO nanorods surface with bioactivity for phenol oxidization. Zinc Oxide 152-155 tyrosinase Homo sapiens 121-124 19441330-1 2009 Self-standing particle-binding ZnO film was fabricated by combination of crystallization in aqueous solution and annealing on FTO (SnO2:F) coated glass substrate. Zinc Oxide 31-34 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 126-129 19094028-1 2008 The effects of Bi(2)O(3) addition on the phase composition, microstructure and optical properties of ZnO-SnO(2) ceramics were investigated. Zinc Oxide 101-104 strawberry notch homolog 1 Homo sapiens 105-108 19123677-6 2008 Second, the two-photon action cross section of ZnO-nano [sigma(ZnO) ((TPEF)) approximately 0.26 GM; diameter, 18 nm] is high: approximately 500-fold of that inferred from its bulk third-order nonlinear susceptibility [Im chi(ZnO) ((3))], and is favorably compared to that of NAD[P]H and FAD. Zinc Oxide 47-50 transmembrane protein with EGF like and two follistatin like domains 2 Homo sapiens 70-74 19205211-6 2008 The interaction of NO with ZnO nanoparticles generates the dissolution of the particles and it is quite probable that NO3(-1), NOs(-2), N2O and N2 are formed; while its contact with SO2 probably yields SO4(-2), SO3(-2) and also the dissolution of the particles is observed. Zinc Oxide 27-30 nitric oxide synthase 2 Homo sapiens 127-133 18815691-0 2008 Type-II CdS nanoparticle-ZnO nanowire heterostructure arrays fabricated by a solution process: enhanced photocatalytic activity. Zinc Oxide 25-28 CDP-diacylglycerol synthase 1 Homo sapiens 8-11 18502114-0 2008 An interleukin-6 ZnO/SiO(2)/Si surface acoustic wave biosensor. Zinc Oxide 17-20 interleukin 6 Homo sapiens 3-16 18502114-1 2008 A novel high sensitivity ZnO/SiO(2)/Si Love mode surface acoustic wave (SAW) biosensor for the detection of interleukin-6 (IL-6), is reported. Zinc Oxide 25-28 interleukin 6 Homo sapiens 108-121 18502114-1 2008 A novel high sensitivity ZnO/SiO(2)/Si Love mode surface acoustic wave (SAW) biosensor for the detection of interleukin-6 (IL-6), is reported. Zinc Oxide 25-28 interleukin 6 Homo sapiens 123-127 18502114-2 2008 The biosensors operating at 747.7 MHz and 1.586 GHz were functionalized by immobilizing the monoclonal IL-6 antibody onto the ZnO biosensor surface both through direct surface adsorption and through covalent binding on gluteraldehyde. Zinc Oxide 126-129 interleukin 6 Homo sapiens 103-107 18815691-1 2008 We report a two-step, solution-based synthetic method to fabricate CdS nanoparticles-sensitized ZnO nanowire heterostructure arrays which showed enhanced photocatalytic activities in comparison with bare ZnO nanowire arrays. Zinc Oxide 96-99 CDP-diacylglycerol synthase 1 Homo sapiens 67-70 18815691-1 2008 We report a two-step, solution-based synthetic method to fabricate CdS nanoparticles-sensitized ZnO nanowire heterostructure arrays which showed enhanced photocatalytic activities in comparison with bare ZnO nanowire arrays. Zinc Oxide 204-207 CDP-diacylglycerol synthase 1 Homo sapiens 67-70 19049088-1 2008 Vertically well-aligned high quality ZnO nanowires were grown on GaN epilayer on c-plane sapphire via a vapor-liquid-solid (VLS) process by introducing an Au thin film (3 nm) as a catalyst. Zinc Oxide 37-40 gigaxonin Homo sapiens 65-68 18681455-2 2008 We demonstrate the use of zinc oxide nanorod (ZnO NR) arrays in a straightforward, reliable, and ultrasensitive detection of the cytokines interleukin-18 and tumor necrosis factor-alpha. Zinc Oxide 26-36 interleukin 18 Homo sapiens 139-185 18681455-2 2008 We demonstrate the use of zinc oxide nanorod (ZnO NR) arrays in a straightforward, reliable, and ultrasensitive detection of the cytokines interleukin-18 and tumor necrosis factor-alpha. Zinc Oxide 46-49 interleukin 18 Homo sapiens 139-185 18291278-4 2008 The aim of this study was to investigate the effects of epoxy resin-based root canal sealer AH26 and zinc oxide-eugenol-based root canal sealer Canals and one paste sealer N2 on the expression of MMPs and PAs in human osteoblastic cell line U2OS cells. Zinc Oxide 101-111 matrix metallopeptidase 2 Homo sapiens 196-200 19049196-4 2008 The X-ray diffraction analysis shows that the crystalline size of pure ZnO is 36 nm and it is 41 nm while doped with 0.8 mol% of GaN due to best stoichiometry between Zn and O. Photoluminescence studies reveal that intense deep level emissions have been observed for pure ZnO and it has been suppressed for the GaN doped ZnO structures. Zinc Oxide 71-74 gigaxonin Homo sapiens 129-132 19049196-4 2008 The X-ray diffraction analysis shows that the crystalline size of pure ZnO is 36 nm and it is 41 nm while doped with 0.8 mol% of GaN due to best stoichiometry between Zn and O. Photoluminescence studies reveal that intense deep level emissions have been observed for pure ZnO and it has been suppressed for the GaN doped ZnO structures. Zinc Oxide 71-74 gigaxonin Homo sapiens 311-314 19049196-4 2008 The X-ray diffraction analysis shows that the crystalline size of pure ZnO is 36 nm and it is 41 nm while doped with 0.8 mol% of GaN due to best stoichiometry between Zn and O. Photoluminescence studies reveal that intense deep level emissions have been observed for pure ZnO and it has been suppressed for the GaN doped ZnO structures. Zinc Oxide 272-275 gigaxonin Homo sapiens 129-132 19049196-4 2008 The X-ray diffraction analysis shows that the crystalline size of pure ZnO is 36 nm and it is 41 nm while doped with 0.8 mol% of GaN due to best stoichiometry between Zn and O. Photoluminescence studies reveal that intense deep level emissions have been observed for pure ZnO and it has been suppressed for the GaN doped ZnO structures. Zinc Oxide 272-275 gigaxonin Homo sapiens 129-132 19049196-5 2008 The images of atomic force microscope show that the rms surface roughness is 27 nm for pure ZnO and the morphology is improved with decrease in rms roughness, 18 nm with fine crystallines while doped with 1 mol% GaN. Zinc Oxide 92-95 gigaxonin Homo sapiens 212-215 19657381-0 2008 Photocatalytic Degradation of Reactive Brilliant Blue X-BR in Aqueous Solution Using Quantum-sized ZnO. Zinc Oxide 99-102 RE1 silencing transcription factor Homo sapiens 54-58 19657381-3 2008 The degradation rate of reactive brilliant blue X-BR in aqueous solution was used to evaluate the photocatalytic performance of the quantum-sized ZnO. Zinc Oxide 146-149 RE1 silencing transcription factor Homo sapiens 48-52 19657381-7 2008 The degradation rate of reactive brilliant blue X-BR could exceed 90% in 15 min at 35(o)C, when the concentration of the quantum-sized ZnO was 0.35 mg/L. Zinc Oxide 135-138 RE1 silencing transcription factor Homo sapiens 48-52 18844142-4 2008 Microstructure analysis by X-ray diffraction (XRD) showed that the sample consists of two phases, i. e. ZnO and YbF3, which verified that the ZnF2 was oxidized during the high temperatue sintering Composition analysis by scanning electron microscope (SEM) and spectroscopic measurements showed that the Er3+ and Yb3+ ons were successfully used in doping the lattice of ZnO, but most of Yb3+ ions were in the YbF3 phase. Zinc Oxide 104-107 zinc finger protein 2 Homo sapiens 142-146 18844142-4 2008 Microstructure analysis by X-ray diffraction (XRD) showed that the sample consists of two phases, i. e. ZnO and YbF3, which verified that the ZnF2 was oxidized during the high temperatue sintering Composition analysis by scanning electron microscope (SEM) and spectroscopic measurements showed that the Er3+ and Yb3+ ons were successfully used in doping the lattice of ZnO, but most of Yb3+ ions were in the YbF3 phase. Zinc Oxide 369-372 zinc finger protein 2 Homo sapiens 142-146 18512700-4 2008 ZnO nanostructures doped with Sn or Eu were grown by adding SnO(2) and Eu(2)O(3) powder, respectively, to the ZnO precursor powder. Zinc Oxide 0-3 strawberry notch homolog 1 Homo sapiens 60-63 17475461-0 2007 Dietary supplementation with zinc oxide decreases expression of the stem cell factor in the small intestine of weanling pigs. Zinc Oxide 29-39 KIT ligand Sus scrofa 68-84 18468116-2 2008 BaF2 is a wide-band gap material, and can confine carriers in the ZnO films. Zinc Oxide 66-69 BANF family member 2 Homo sapiens 0-4 18468116-12 2008 For comparison, ZnO films on BaF2 substrates were also fabricated by the magnetron sputtering method, and the same measurement methods were used. Zinc Oxide 16-19 BANF family member 2 Homo sapiens 29-33 18421853-2 2008 METHODS: MEF cells were treated with the suspension of carbon nanoparticles, zinc oxide nanoparticles and composite nanoparticles at the concentrations of 5, 10, 20, 50, 100 microg/ml. Zinc Oxide 77-87 E74-like factor 4 (ets domain transcription factor) Mus musculus 9-12 17475461-3 2007 The present study was conducted to test the novel hypothesis that supplementing ZnO to the diet for weanling piglets may inhibit SCF expression in the small intestine, thereby reducing the number of mast cells, histamine release, and diarrhea. Zinc Oxide 80-83 KIT ligand Sus scrofa 129-132 17475461-8 2007 Collectively, our results indicate that dietary supplementation with ZnO inhibits SCF expression in the small intestine, leading to reductions in the number of mast cells and histamine release. Zinc Oxide 69-72 KIT ligand Sus scrofa 82-85 17499919-2 2007 Prior to the reaction, the nanorods of zinc oxide were synthesized by the hydrothermal method and subsequently characterized by XRD, SEM, TG, N(2) BET, FT-IR. Zinc Oxide 39-49 delta/notch like EGF repeat containing Homo sapiens 147-150 17301066-18 2007 In addition, IL-6 secretion was measured in CS, AS, and nano-sized ZnO-exposed cocultures. Zinc Oxide 67-70 interleukin 6 Rattus norvegicus 13-17 16836118-2 2006 The photoluminescence efficiency of double layer sample PEDOT/MEH-PPV was enhanced by doping one-dimensional nanomaterials (TiO2 nanotube and ZnO nanorod) into PEDOT layer. Zinc Oxide 142-145 epoxide hydrolase 1 Homo sapiens 62-65 17294493-0 2007 ZnO-nanowire-inserted GaN/ZnO heterojunction light-emitting diodes. Zinc Oxide 0-3 gigaxonin Homo sapiens 22-25 16838348-4 2007 The aim of this study was to investigate the effects of zinc oxide-eugenol-based root canal sealer N2 and epoxy resin-based root canal sealer Topseal on the expression of HO-1 protein in cultured human gingival fibroblasts (HGFs). Zinc Oxide 56-66 heme oxygenase 1 Homo sapiens 171-175 17260759-1 2006 Ni-doped ZnO films were deposited on Si(100) by pulsed laser deposition(PLD) at room temperature. Zinc Oxide 9-12 glycosylphosphatidylinositol specific phospholipase D1 Homo sapiens 72-75 16765885-0 2006 Effect of ZnO addition on bioactive CaO-SiO2-P2O5-CaF2 glass-ceramics containing apatite and wollastonite. Zinc Oxide 10-13 CCR4-NOT transcription complex subunit 8 Homo sapiens 50-54 17676572-3 2007 The same approach was used to grow branched ZnO-SnO(2) heterojunction nanostructures. Zinc Oxide 44-47 strawberry notch homolog 1 Homo sapiens 48-51 16581242-0 2006 Morphological and binding properties of interleukin-6 on thin ZnO films grown on (100) silicon substrates for biosensor applications. Zinc Oxide 62-65 interleukin 6 Homo sapiens 40-53 16581242-2 2006 Interleukin-6 was immobilized in the range of 0.276-10 pg/ml on the surface of ZnO and SiO(2), and visualized at each stage, while protein-protein interactions were measured with the antigen/antibody immunoassay of solid-phase ELISA, which we modified for these types of substrates. Zinc Oxide 79-82 interleukin 6 Homo sapiens 0-13 16953504-6 2006 The important vulcanization accelerator mercaptobenzothiazole (C(7)H(5)NS(2), MBT) containing several donor sites reacts with the Zn(4)O(4) cluster with proton transfer from the NH group to one of the oxygen atoms of ZnO, and in addition the exocyclic thiono sulfur atom and the nitrogen atom coordinate to one and the same zinc atom, resulting in a binding energy of -247 kJ mol(-1). Zinc Oxide 217-220 proteinase 3 Homo sapiens 78-81 17041672-1 2006 ZnO/SnO nanocomposites have been designed to enhance the band edge emission and suppress the defect emission of ZnO nanorods simultaneously. Zinc Oxide 0-3 strawberry notch homolog 1 Homo sapiens 4-7 17041672-1 2006 ZnO/SnO nanocomposites have been designed to enhance the band edge emission and suppress the defect emission of ZnO nanorods simultaneously. Zinc Oxide 112-115 strawberry notch homolog 1 Homo sapiens 4-7 17041672-3 2006 The underlying mechanism is interpreted in terms of surface modification as well as carrier transfer from SnO nanoparticles to ZnO nanorods. Zinc Oxide 127-130 strawberry notch homolog 1 Homo sapiens 106-109 16772438-0 2006 Dietary supplementation with zinc oxide increases Igf-I and Igf-I receptor gene expression in the small intestine of weanling piglets. Zinc Oxide 29-39 insulin like growth factor 1 Sus scrofa 50-55 16772438-0 2006 Dietary supplementation with zinc oxide increases Igf-I and Igf-I receptor gene expression in the small intestine of weanling piglets. Zinc Oxide 29-39 insulin like growth factor 1 receptor Sus scrofa 60-74 16423360-1 2006 Zinc oxide was prepared by different methods by varying precipitating agents, the source of the salt precursors and the microwave irradiation time and was characterized by XRD, BET-surface area, surface acidity and crystallite sizes. Zinc Oxide 0-10 delta/notch like EGF repeat containing Homo sapiens 177-180 16430850-0 2006 Interfacing myoglobin to graphite electrode with an electrodeposited nanoporous ZnO film. Zinc Oxide 80-83 myoglobin Homo sapiens 12-21 16430850-5 2006 were used to characterize the nanoporous ZnO film and Mb-modified ZnO film. Zinc Oxide 66-69 myoglobin Homo sapiens 54-56 16035857-5 2005 For H2 on the zinc oxide corners, the MP2 binding energy using Zn4O(HCO2)6 molecule is 6.28 kJ/mol. Zinc Oxide 14-24 tryptase pseudogene 1 Homo sapiens 38-41 16384546-0 2006 A mediator-free phenol biosensor based on immobilizing tyrosinase to ZnO nanoparticles. Zinc Oxide 69-72 tyrosinase Homo sapiens 55-65 16384546-2 2006 The low-isoelectric point tyrosinase was adsorbed on the surface of high-isoelectric point ZnO nanoparticles (nano-ZnO) facilitated by the electrostatic interactions and then immobilized on the glassy carbon electrode via the film forming by chitosan. Zinc Oxide 91-94 tyrosinase Homo sapiens 26-36 16384546-2 2006 The low-isoelectric point tyrosinase was adsorbed on the surface of high-isoelectric point ZnO nanoparticles (nano-ZnO) facilitated by the electrostatic interactions and then immobilized on the glassy carbon electrode via the film forming by chitosan. Zinc Oxide 115-118 tyrosinase Homo sapiens 26-36 16384546-3 2006 It was found that the nano-ZnO matrix provided an advantageous microenvironment in terms of its favorable isoelectric point for tyrosinase loading and the immobilized tyrosinase retaining its activity to a large extent. Zinc Oxide 27-30 tyrosinase Homo sapiens 128-138 16384546-3 2006 It was found that the nano-ZnO matrix provided an advantageous microenvironment in terms of its favorable isoelectric point for tyrosinase loading and the immobilized tyrosinase retaining its activity to a large extent. Zinc Oxide 27-30 tyrosinase Homo sapiens 167-177 16123706-9 2005 Taken together, the activation of IL-6 and IL-8 mRNA gene expression may be one of the pathogenesis of zinc oxide-eugenol based and epoxy resin based root canal sealers-induced periapical inflammation. Zinc Oxide 103-113 interleukin 6 Homo sapiens 34-38 16123706-9 2005 Taken together, the activation of IL-6 and IL-8 mRNA gene expression may be one of the pathogenesis of zinc oxide-eugenol based and epoxy resin based root canal sealers-induced periapical inflammation. Zinc Oxide 103-113 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 16026622-12 2005 Wild-derived Tlr5-mutant MOLF/Ei mice were tolerant to BAL protein following repeated ZnO exposure. Zinc Oxide 86-89 toll-like receptor 5 Mus musculus 13-17 16486509-1 2006 Magnetic and EPR measurements, combined with crystal field theory, reveal that isolated Co2+ ions in ZnO possess a strong single ion anisotropy which leads to an "easy plane" ferromagnetic state when the ferromagnetic Co-Co interaction is considered. Zinc Oxide 101-104 complement C2 Homo sapiens 88-91 16853177-9 2005 Two strong Raman scattering peaks at 626 and 656 cm(-1) appeared in the micro-Raman spectrum of nc-ZnO/SnO(2) nanowires. Zinc Oxide 99-102 strawberry notch homolog 2 Homo sapiens 103-106 14664838-3 2004 Ultraviolet-visible spectra indicated that the N-containing MOx-ZnO powders absorbed not only ultraviolet light like pure ZnO powder, but also some visible-light. Zinc Oxide 64-67 monooxygenase DBH like 1 Homo sapiens 60-63 15760013-0 2004 [Electroluminescence property of MEH-PPV/ZnO nano-crystal structure]. Zinc Oxide 41-44 epoxide hydrolase 1 Homo sapiens 33-36 15760013-3 2004 And a new peak at 620 nm was found in the ITO/MEH-PPV/ZnO/Al structure"s electroluminescence spectrum, which should resulted from ZnO layer. Zinc Oxide 54-57 epoxide hydrolase 1 Homo sapiens 46-49 15760013-3 2004 And a new peak at 620 nm was found in the ITO/MEH-PPV/ZnO/Al structure"s electroluminescence spectrum, which should resulted from ZnO layer. Zinc Oxide 130-133 epoxide hydrolase 1 Homo sapiens 46-49 15760013-4 2004 In addition, the turning-on voltage of the two-layer structure decreased from 9 V of the single layer structure to 4 V. From the I-V curve, the authors concluded that the emitting area was around the interface of MEH-PPV/ZnO and the combination area could shift with changing the voltage. Zinc Oxide 221-224 epoxide hydrolase 1 Homo sapiens 213-216 15210026-0 2004 Inhibition of human pulpal gelatinases (MMP-2 and MMP-9) by zinc oxide cements. Zinc Oxide 60-70 matrix metallopeptidase 2 Homo sapiens 40-45 15210026-0 2004 Inhibition of human pulpal gelatinases (MMP-2 and MMP-9) by zinc oxide cements. Zinc Oxide 60-70 matrix metallopeptidase 9 Homo sapiens 50-55 15210026-3 2004 The aim of this work was to test the effect of zinc released from zinc oxide-eugenol (ZOE) cements, on the activity of the major pulpal gelatinolytic MMPs. Zinc Oxide 66-76 matrix metallopeptidase 2 Homo sapiens 150-154 15154797-20 2004 The rearrangement of trans-HCOH (carbon bound) to CH(2)O (oxygen bound) on ZnO(0001) was calculated to be the overall barrier of the MSR reaction. Zinc Oxide 75-78 5-methyltetrahydrofolate-homocysteine methyltransferase reductase Homo sapiens 133-136 15129976-5 2004 (2) Addition of zinc compounds was essential to diminish rapid insulin release and six-fold molar excess of ZnO to insulin was desirable. Zinc Oxide 108-111 insulin Homo sapiens 115-122 14664838-3 2004 Ultraviolet-visible spectra indicated that the N-containing MOx-ZnO powders absorbed not only ultraviolet light like pure ZnO powder, but also some visible-light. Zinc Oxide 122-125 monooxygenase DBH like 1 Homo sapiens 60-63 14664838-6 2004 This enhancement was ascribed to the MOx acting as a sink for photogenerated electrons in the UV case, and to a synergistic effect of N-doping and MOx-ZnO coupling in the case of visible-light. Zinc Oxide 151-154 monooxygenase DBH like 1 Homo sapiens 37-40 14664838-6 2004 This enhancement was ascribed to the MOx acting as a sink for photogenerated electrons in the UV case, and to a synergistic effect of N-doping and MOx-ZnO coupling in the case of visible-light. Zinc Oxide 151-154 monooxygenase DBH like 1 Homo sapiens 147-150 11801137-1 2002 Electron paramagnetic resonance and Hall measurements show consistently the presence of two donors ( D1 and D2) in state-of-the-art, nominally undoped ZnO single crystals. Zinc Oxide 151-154 leiomodin 1 Homo sapiens 101-110 12615477-0 2003 Induction of cyclooxygenase-2 mRNA and protein expression by epoxy resin and zinc oxide-eugenol based root canal sealers in human osteoblastic cells. Zinc Oxide 77-87 prostaglandin-endoperoxide synthase 2 Homo sapiens 13-29 12615477-5 2003 The aim of the present study was to investigate the effects of epoxy resin (AH26) and zinc oxide-eugenol based (Endomethansone and N2) root canal sealers on the expression of COX-2 mRNA gene and protein in cultured human osteoblastic cells. Zinc Oxide 86-96 prostaglandin-endoperoxide synthase 2 Homo sapiens 175-180 12586143-2 2003 The aim of this investigation was to trace back the alterations of the formation and the distribution behavior of PAH and PCDD/PCDF to the presence of CuO or a mixture of metal oxides (CdO, CuO, Fe(2)O(3), PbO, MoO(3), ZnO). Zinc Oxide 219-222 phenylalanine hydroxylase Homo sapiens 114-117 12527183-0 2003 Preparation of a copoly (dl-lactic/glycolic acid)-zinc oxide complex and its utilization to microcapsules containing recombinant human growth hormone. Zinc Oxide 50-60 growth hormone 1 Homo sapiens 135-149 9273875-0 1997 Metal fume fever: characterization of clinical and plasma IL-6 responses in controlled human exposures to zinc oxide fume at and below the threshold limit value. Zinc Oxide 106-116 interleukin 6 Homo sapiens 58-62 11401386-3 2001 Observation on dye-sensitizated photoelectrochemical cells made from SnO(2)/ZnO films sensitized with different dyes suggests that the electron transfer could occur in either direction, that is from semiconductor of high band position to the semiconductor of the low band position or vice versa, depending on which surface adsorbs the dye more strongly. Zinc Oxide 76-79 strawberry notch homolog 1 Homo sapiens 69-72 10391125-16 1999 ZnO induced NF-kappaB activation in JB6 cells through the generation of *OH resulting from light irradiation of ZnO which was measured by electron spin resonance. Zinc Oxide 0-3 nuclear factor kappa B subunit 1 Homo sapiens 12-21 10391125-16 1999 ZnO induced NF-kappaB activation in JB6 cells through the generation of *OH resulting from light irradiation of ZnO which was measured by electron spin resonance. Zinc Oxide 112-115 nuclear factor kappa B subunit 1 Homo sapiens 12-21 9506261-9 1998 Both Zn(2+)- and ZnO-induced CL was inhibited by manoalide, a phospholipase A2 inhibitor, with IC50 of 0.25 microM and 0.66 microM respectively. Zinc Oxide 17-20 phospholipase A2 group IB Homo sapiens 62-78 11736924-0 2001 Inhibition of human gelatinases (matrix metalloproteinase-2 and matrix metalloproteinase-9) activity by zinc oxide: a possible mechanism to enhance wound healing. Zinc Oxide 104-114 matrix metallopeptidase 2 Homo sapiens 33-90 11353230-0 2001 Hexagonal ammonium zinc phosphate, (NH4)ZnPO4, at 10 K. The title compound, (NH(4))ZnPO(4)-HEX, is built up from a three-dimensional network of ZnO(4) and PO(4) tetrahedra [d(av)(Zn-O) = 1.9400 (7) A and d(av)(P-O) = 1.5396 (7) A], fused together via Zn-O-P links [straight theta(av) = 133.47 (4) degrees ]. Zinc Oxide 144-147 hematopoietically expressed homeobox Homo sapiens 91-94 11094787-8 2000 The increase in IL-6 levels observed in the clinically responsive, and to a lesser extent, tolerant, states following zinc oxide inhalation is consistent with the dual role of IL-6 as a pyrogen and anti-inflammatory agent. Zinc Oxide 118-128 interleukin 6 Homo sapiens 16-20 11094787-8 2000 The increase in IL-6 levels observed in the clinically responsive, and to a lesser extent, tolerant, states following zinc oxide inhalation is consistent with the dual role of IL-6 as a pyrogen and anti-inflammatory agent. Zinc Oxide 118-128 interleukin 6 Homo sapiens 176-180 11272543-5 2000 [1]3+ was converted to an aza-capped Co4(III)Zn4(II) octanuclear complex, [Zn4O[Co(L)]4]6+ ([2]6+), by reaction with I- in the presence of Zn2+ and ZnO in water. Zinc Oxide 148-151 mitochondrially encoded cytochrome c oxidase III Homo sapiens 41-44 9604183-0 1998 Tumor necrosis factor-alpha and interleukin-8 release from U937 human mononuclear cells exposed to zinc oxide in vitro. Zinc Oxide 99-109 tumor necrosis factor Homo sapiens 0-27 9604183-0 1998 Tumor necrosis factor-alpha and interleukin-8 release from U937 human mononuclear cells exposed to zinc oxide in vitro. Zinc Oxide 99-109 C-X-C motif chemokine ligand 8 Homo sapiens 32-45 9604183-2 1998 Respiratory exposure to zinc oxide results in metal fume fever, a flu-like illness characterized by dose-dependent increases in pulmonary tumor necrosis factor-alpha (TNF) and interleukin-8 (IL-8). Zinc Oxide 24-34 tumor necrosis factor Homo sapiens 138-165 9604183-2 1998 Respiratory exposure to zinc oxide results in metal fume fever, a flu-like illness characterized by dose-dependent increases in pulmonary tumor necrosis factor-alpha (TNF) and interleukin-8 (IL-8). Zinc Oxide 24-34 tumor necrosis factor Homo sapiens 167-170 9604183-2 1998 Respiratory exposure to zinc oxide results in metal fume fever, a flu-like illness characterized by dose-dependent increases in pulmonary tumor necrosis factor-alpha (TNF) and interleukin-8 (IL-8). Zinc Oxide 24-34 C-X-C motif chemokine ligand 8 Homo sapiens 176-189 9604183-2 1998 Respiratory exposure to zinc oxide results in metal fume fever, a flu-like illness characterized by dose-dependent increases in pulmonary tumor necrosis factor-alpha (TNF) and interleukin-8 (IL-8). Zinc Oxide 24-34 C-X-C motif chemokine ligand 8 Homo sapiens 191-195 9604183-4 1998 Cell culture supernatant TNF and IL-8 was measured after 3, 8, and 24 hours of exposure to zinc oxide in varying concentrations. Zinc Oxide 91-101 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 9604183-5 1998 Zinc oxide exposure in vitro led to TNF release in a dose-dependent manner at 3, 8, and 24 hours (analysis of variance [ANOVA] P = 0.0001). Zinc Oxide 0-10 tumor necrosis factor Homo sapiens 36-39 9604183-8 1998 These data demonstrate that in vitro zinc oxide exposure stimulates U937 mononuclear cells to release TNF and IL-8 consistent with in vivo observations in metal fume fever. Zinc Oxide 37-47 tumor necrosis factor Homo sapiens 102-105 9604183-8 1998 These data demonstrate that in vitro zinc oxide exposure stimulates U937 mononuclear cells to release TNF and IL-8 consistent with in vivo observations in metal fume fever. Zinc Oxide 37-47 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 9356189-7 1997 Zinc oxide exposure was a statistically significant, dose-dependent predictor of increases in BAL TNF (mean exposure-sham difference +/- SE = 9.5 +/- 3.6 pg/mL, P = 0.02), IL-6 (mean exposure-sham difference +/- SE = 5.5 +/- 1.8 pg/mL, P = 0.009), and IL-8 (mean exposure-sham difference +/- SE = 64.1 +/- 23.9 pg/mL, P = 0.02). Zinc Oxide 0-10 tumor necrosis factor Homo sapiens 98-101 9356189-7 1997 Zinc oxide exposure was a statistically significant, dose-dependent predictor of increases in BAL TNF (mean exposure-sham difference +/- SE = 9.5 +/- 3.6 pg/mL, P = 0.02), IL-6 (mean exposure-sham difference +/- SE = 5.5 +/- 1.8 pg/mL, P = 0.009), and IL-8 (mean exposure-sham difference +/- SE = 64.1 +/- 23.9 pg/mL, P = 0.02). Zinc Oxide 0-10 interleukin 6 Homo sapiens 172-176 9356189-7 1997 Zinc oxide exposure was a statistically significant, dose-dependent predictor of increases in BAL TNF (mean exposure-sham difference +/- SE = 9.5 +/- 3.6 pg/mL, P = 0.02), IL-6 (mean exposure-sham difference +/- SE = 5.5 +/- 1.8 pg/mL, P = 0.009), and IL-8 (mean exposure-sham difference +/- SE = 64.1 +/- 23.9 pg/mL, P = 0.02). Zinc Oxide 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 252-256 9273875-7 1997 In a parallel fashion, plasma levels of interleukin 6 (IL-6), a pyrogen, were significantly elevated after exposure to 5 mg/m3 zinc oxide. Zinc Oxide 127-137 interleukin 6 Homo sapiens 40-53 9273875-7 1997 In a parallel fashion, plasma levels of interleukin 6 (IL-6), a pyrogen, were significantly elevated after exposure to 5 mg/m3 zinc oxide. Zinc Oxide 127-137 interleukin 6 Homo sapiens 55-59 9273875-12 1997 Inhalation of zinc oxide for 2 hours at the current TLV of 5 mg/m3 produces fever and symptoms along with elevation in plasma IL-6 levels. Zinc Oxide 14-24 interleukin 6 Homo sapiens 126-130 33971103-0 2021 Stabilization of Nrf2 leading to HO-1 activation protects against zinc oxide nanoparticles-induced endothelial cell death. Zinc Oxide 66-76 nuclear factor, erythroid derived 2, like 2 Mus musculus 17-21 8420406-9 1993 TNF, IL-6, and IL-8 in BAL fluid supernatant concentrations increased in a time and exposure-dependent fashion after zinc oxide welding fume exposure. Zinc Oxide 117-127 tumor necrosis factor Homo sapiens 0-3 8420406-9 1993 TNF, IL-6, and IL-8 in BAL fluid supernatant concentrations increased in a time and exposure-dependent fashion after zinc oxide welding fume exposure. Zinc Oxide 117-127 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 1432793-4 1992 The Temp Bond zinc oxide-eugenol luting agent exhibited a lower mean retentive strength than the IRM reinforced zinc oxide-eugenol and Life calcium hydroxide luting agents. Zinc Oxide 14-24 chromosome 1 open reading frame 210 Homo sapiens 4-8 1778627-2 1991 ZIN contained zinc oxide in the formulation. Zinc Oxide 14-24 striatin 4 Homo sapiens 0-3 16535188-6 1995 Specificity studies carried out with the fluorescence assay confirmed previous findings that Rhodococcus strain GIN-1 cells possess high affinities for TiO(inf2), ZnO, and coal fly ash and low affinities for other metal oxides. Zinc Oxide 163-166 gypsy retrotransposon integrase 1 Homo sapiens 112-117 33971103-0 2021 Stabilization of Nrf2 leading to HO-1 activation protects against zinc oxide nanoparticles-induced endothelial cell death. Zinc Oxide 66-76 heme oxygenase 1 Mus musculus 33-37 33825978-4 2021 The working resistance of AZO-ALD-MCP (Al2O3/ZnO atomic layer deposition microchannel plate) was measured for the first time by the MCP resistance test system. Zinc Oxide 45-48 CD46 molecule Homo sapiens 34-37 33779133-2 2021 We here report that noncytotoxic doses of silver nanoparticles coated with zinc oxide, Ag@ZnO, can stimulate proliferation and migration of human keratinocytes, HaCaT, with increased expression of Ki67 and vinculin at the leading edge of wounds. Zinc Oxide 75-85 vinculin Homo sapiens 206-214 33823299-0 2021 Inflammatory response in human alveolar epithelial cells after TiO2 NPs or ZnO NPs exposure: inhibition of surfactant protein A expression as an indicator for loss of lung function. Zinc Oxide 75-78 surfactant protein A1 Homo sapiens 107-127 33807340-2 2021 Information on the photoelectric and optical properties of nanocrystalline oxides SnO2, ZnO, In2O3, and WO3, which are the most widely used sensitive materials for semiconductor gas sensors, is presented. Zinc Oxide 88-91 gastrin Homo sapiens 178-181 33779133-2 2021 We here report that noncytotoxic doses of silver nanoparticles coated with zinc oxide, Ag@ZnO, can stimulate proliferation and migration of human keratinocytes, HaCaT, with increased expression of Ki67 and vinculin at the leading edge of wounds. Zinc Oxide 90-93 vinculin Homo sapiens 206-214 33775755-3 2021 The as-prepared CS/Zn fibers are then immersed into glutaraldehyde (GA) and sodium hydroxide solutions, respectively, and dried at T = 50 C. The resultant CS/ZnO/GA fibers of ca. Zinc Oxide 159-162 citrate synthase Homo sapiens 16-18 33802968-0 2021 Highly Sensitive Magnesium-Doped ZnO Nanorod pH Sensors Based on Electrolyte-Insulator-Semiconductor (EIS) Sensors. Zinc Oxide 33-36 phenylalanine hydroxylase Homo sapiens 45-47 33775755-5 2021 XRD and FE-SEM data confirm that the CS/ZnO/GA fibers consist of a large amount of hexagonal wurtzite ZnO nanorods up to 550 nm in length, and exhibit three-dimensional interconnected macroporous architecture. Zinc Oxide 40-43 citrate synthase Homo sapiens 37-39 33775755-5 2021 XRD and FE-SEM data confirm that the CS/ZnO/GA fibers consist of a large amount of hexagonal wurtzite ZnO nanorods up to 550 nm in length, and exhibit three-dimensional interconnected macroporous architecture. Zinc Oxide 102-105 citrate synthase Homo sapiens 37-39 33775755-6 2021 Photodegradation results clearly show that the CS/ZnO/GA fibers are effective for the removal of organic dyes upon UV irradiation and can be easily recovered and reused for at least 6 consecutive cycles. Zinc Oxide 50-53 citrate synthase Homo sapiens 47-49 33775755-7 2021 Unlike most reported CS/ZnO nanocomposites, the current CS/ZnO/GA fiber shows a higher adsorption of cationic MB rather than anionic MO, the mechanism of which is proposed. Zinc Oxide 24-27 citrate synthase Homo sapiens 56-58 33775755-7 2021 Unlike most reported CS/ZnO nanocomposites, the current CS/ZnO/GA fiber shows a higher adsorption of cationic MB rather than anionic MO, the mechanism of which is proposed. Zinc Oxide 59-62 citrate synthase Homo sapiens 21-23 33775755-7 2021 Unlike most reported CS/ZnO nanocomposites, the current CS/ZnO/GA fiber shows a higher adsorption of cationic MB rather than anionic MO, the mechanism of which is proposed. Zinc Oxide 59-62 citrate synthase Homo sapiens 56-58 33802968-3 2021 The results indicated that the ZnO nanorods doped with 3% Mg had a high hydrogen ion sensitivity (83.77 mV/pH), linearity (96.06%), hysteresis (3 mV), and drift (0.218 mV/h) due to the improved crystalline quality and the surface hydroxyl group role of ZnO. Zinc Oxide 31-34 phenylalanine hydroxylase Homo sapiens 107-109 33232271-5 2020 The viability for A549 cells showed a significant decrease in the ZnO NPs(Cp/Gem) group, respectively relative to Cp, Gem, the combination of Cp and Gem (Cp+Gem), and ZnO-NPs loaded with Cp (ZnO-NPs(Cp)) or Gem (ZnO-NPs(Gem)). Zinc Oxide 66-69 ceruloplasmin Homo sapiens 74-76 33589677-0 2021 Theory of the sp-d coupling of transition metal impurities with free carriers in ZnO. Zinc Oxide 81-84 surfactant protein D Homo sapiens 14-18 33232271-3 2020 In the present study, we developed ZnO-NPs loaded with both cisplatin (Cp) and gemcitabine (Gem) (ZnO-NPs(Cp/Gem)), then the morphologies and the size distribution of ZnO-NPs(Cp/Gem) particles were observed by transmission electron microscopy (TEM) and dynamic light scattering (DLS). Zinc Oxide 35-38 ceruloplasmin Homo sapiens 71-73 33232271-5 2020 The viability for A549 cells showed a significant decrease in the ZnO NPs(Cp/Gem) group, respectively relative to Cp, Gem, the combination of Cp and Gem (Cp+Gem), and ZnO-NPs loaded with Cp (ZnO-NPs(Cp)) or Gem (ZnO-NPs(Gem)). Zinc Oxide 66-69 GTP binding protein overexpressed in skeletal muscle Homo sapiens 77-80 33232271-3 2020 In the present study, we developed ZnO-NPs loaded with both cisplatin (Cp) and gemcitabine (Gem) (ZnO-NPs(Cp/Gem)), then the morphologies and the size distribution of ZnO-NPs(Cp/Gem) particles were observed by transmission electron microscopy (TEM) and dynamic light scattering (DLS). Zinc Oxide 35-38 GTP binding protein overexpressed in skeletal muscle Homo sapiens 92-95 33232271-3 2020 In the present study, we developed ZnO-NPs loaded with both cisplatin (Cp) and gemcitabine (Gem) (ZnO-NPs(Cp/Gem)), then the morphologies and the size distribution of ZnO-NPs(Cp/Gem) particles were observed by transmission electron microscopy (TEM) and dynamic light scattering (DLS). Zinc Oxide 35-38 ceruloplasmin Homo sapiens 106-108 33232271-6 2020 Furthermore, ZnO-NPs(Cp/Gem) remarkably enhanced the apoptosis-promoting effect of Cp and Gem in A549 cells. Zinc Oxide 13-16 ceruloplasmin Homo sapiens 21-23 33232271-3 2020 In the present study, we developed ZnO-NPs loaded with both cisplatin (Cp) and gemcitabine (Gem) (ZnO-NPs(Cp/Gem)), then the morphologies and the size distribution of ZnO-NPs(Cp/Gem) particles were observed by transmission electron microscopy (TEM) and dynamic light scattering (DLS). Zinc Oxide 35-38 ceruloplasmin Homo sapiens 106-108 33232271-6 2020 Furthermore, ZnO-NPs(Cp/Gem) remarkably enhanced the apoptosis-promoting effect of Cp and Gem in A549 cells. Zinc Oxide 13-16 GTP binding protein overexpressed in skeletal muscle Homo sapiens 24-27 33232271-6 2020 Furthermore, ZnO-NPs(Cp/Gem) remarkably enhanced the apoptosis-promoting effect of Cp and Gem in A549 cells. Zinc Oxide 13-16 ceruloplasmin Homo sapiens 83-85 33232271-6 2020 Furthermore, ZnO-NPs(Cp/Gem) remarkably enhanced the apoptosis-promoting effect of Cp and Gem in A549 cells. Zinc Oxide 13-16 GTP binding protein overexpressed in skeletal muscle Homo sapiens 90-93 34894563-0 2022 Influence of RE (Pr3+, Er3+, Nd3+) doping on structural, vibrational and enhanced persistent photocatalytic properties of ZnO nanostructures. Zinc Oxide 122-125 mitochondrially encoded NADH dehydrogenase 3 Homo sapiens 29-32 34717949-4 2022 Owing to the improved selectivity of ZnO, excellent conductivity of carbon fiber, promoted active site exposure and mass transfer of hollow structure, the free-standing membrane electrode shows superior 2e-WOR performances with high selectivity (83.8% at 2.8 V vs. RHE), H2O2 generation rate (19.7 mumol cm-2 min-1) and robust stability. Zinc Oxide 37-40 factor interacting with PAPOLA and CPSF1 Homo sapiens 265-268 33033627-2 2020 It is demonstrated that large negative and positive MOA and MPC effects can be tuned alternately in amorphous carbon ( a-C )/ZnO nanowires by controlling the sp2/sp3 ratio of a-C . Zinc Oxide 125-128 Sp2 transcription factor Homo sapiens 158-178 26146191-4 2015 Therefore, the present study was aimed to investigate the immunotoxic potential of ZnO NPs using human monocytic cell line (THP-1) as model to understand the underlying molecular mechanism. Zinc Oxide 83-86 GLI family zinc finger 2 Homo sapiens 124-129 26146191-8 2015 Our data demonstrated that ZnO NPs induce oxidative and nitrosative stress in human monocytes, leading to increased inflammatory response via activation of redox sensitive NF-kappaB and MAPK signalling pathways. Zinc Oxide 27-30 mitogen-activated protein kinase 3 Homo sapiens 186-190 34953261-0 2022 MOF-derived N-doped ZnO carbon skeleton@hierarchical Bi2MoO6 S-scheme heterojunction for photodegradation of SMX: Mechanism, pathways and DFT calculation. Zinc Oxide 20-23 lysine acetyltransferase 8 Homo sapiens 0-3 34600384-4 2022 ZnO and Cr3+ can form stable spinel-based phase, and TiO2 can suppress the formation of Cr6+. Zinc Oxide 0-3 teratocarcinoma-derived growth factor 1 pseudogene 6 Homo sapiens 88-91 34740155-4 2022 Growth inhibition, oxidative stress, apoptosis, and disturbance of growth hormone and insulin-like growth factor (GH/IGF) axis were induced by MPs and ZnO NPs alone, which were further aggravated by their co-exposure in F0 larvae. Zinc Oxide 151-154 growth hormone 1 Danio rerio 67-120 34740155-6 2022 Reduced growth and antioxidant capacity and down-regulated GH/IGF axis were merely observed in F1 larvae from F0 parents exposed to MPs + ZnO. Zinc Oxide 138-141 growth hormone 1 Danio rerio 59-61 34774314-0 2022 rGO decorated ZnO/CdO heterojunction as a photoanode for photoelectrochemical water splitting. Zinc Oxide 14-17 cell adhesion associated, oncogene regulated Homo sapiens 18-21 34774314-1 2022 A ternary photoanode of ZnO/CdO heterojunction decorated with reduced graphene oxide (rGO) was firstly fabricated by electrochemical deposition and thermal decomposition that is simple and effective compared with other method reported in literature. Zinc Oxide 24-27 cell adhesion associated, oncogene regulated Homo sapiens 28-31 34774314-3 2022 The photoanode expands the visible light absorption range to 428 nm, the photocurrent density reaches 1.15 mA cm-2 at 1.23 V (vs. RHE) that is 3 times and 1.85 times of pure ZnO (0.38 mA cm2) and ZnO/CdO (0.62 mA cm2) photoanodes. Zinc Oxide 196-199 cell adhesion associated, oncogene regulated Homo sapiens 200-203 34974288-8 2022 However, a higher concentration (160 microg/mL) of Cys-ZnO NPs led to apoptotic cell death marked by nuclear condensation, mitochondrial membrane depolarization, actin filament condensation, lysosomal damage LDH leakage, intracellular ROS production, blebbing, upregulation of Bax and downregulation of Bcl-2 gene expression. Zinc Oxide 55-58 BCL2 associated X, apoptosis regulator Homo sapiens 277-280 34626964-4 2022 Therefore, the resultant ZnO/Ag/beta-CD/PAN membrane displays splendid separation performance for oil/dye/water complex emulsions and high flux recovery (>90%). Zinc Oxide 25-28 ACD shelterin complex subunit and telomerase recruitment factor Homo sapiens 32-39 34426124-4 2022 ZnO-NGs@GO and ZnO-NGs@rGO modified MI-FETs sensor exhibited excellent responses towards Cr (III) and Cu (II) ions, which presented the remarkable sensitivities of ~49.28 mA muM-1. Zinc Oxide 0-3 PWWP domain containing 3A, DNA repair factor Homo sapiens 174-179 34450683-0 2022 Suspected hemolytic anemia secondary to acute zinc toxicity after ingestion of "max strength" (zinc oxide) diaper rash cream. Zinc Oxide 95-105 MYC associated factor X Canis lupus familiaris 80-83 34450683-3 2022 "Max Strength" zinc oxide cream had been applied to the patient daily for a week prior to presentation. Zinc Oxide 15-25 MYC associated factor X Canis lupus familiaris 1-4 34653855-0 2022 Orange peel extract influenced partial transformation of SnO2 to SnO in green 3D-ZnO/SnO2 system for chlorophenol degradation. Zinc Oxide 81-84 strawberry notch homolog 1 Homo sapiens 65-68 34755930-0 2022 Strong Structural and Electronic Binding of Bovine Serum Albumin to ZnO via Specific Amino Acid Residues and Zinc Atoms. Zinc Oxide 68-71 albumin Homo sapiens 51-64 34755930-1 2022 ZnO biointerfaces with serum albumin have attracted noticeable attention due to the increasing interest in developing ZnO-based materials for biomedical applications. Zinc Oxide 0-3 albumin Homo sapiens 23-36 34755930-1 2022 ZnO biointerfaces with serum albumin have attracted noticeable attention due to the increasing interest in developing ZnO-based materials for biomedical applications. Zinc Oxide 118-121 albumin Homo sapiens 23-36 34735834-4 2022 On the whole, NaCl, the coexisted metal cations (Cu2+, Zn2+ and Cr3+) and additional NH4Cl inhibited the biodegradation of PDM/ZnO. Zinc Oxide 127-130 teratocarcinoma-derived growth factor 1 pseudogene 3 Homo sapiens 64-67 34388437-3 2022 Accordingly, this study aims to optimize the conformation of nanocomposite prepared from a CdS/ZnO heterojunction on reduced graphene oxide (RGO) for boosting the photocatalytic removal of heavy metal contaminants of aqueous systems. Zinc Oxide 95-98 CDP-diacylglycerol synthase 1 Homo sapiens 91-94 34417700-0 2022 Green synthesis of zinc oxide nanoparticles loaded on activated carbon prepared from walnut peel extract for the removal of Eosin Y and Erythrosine B dyes from aqueous solution: experimental approaches, kinetics models, and thermodynamic studies. Zinc Oxide 19-29 estrogen receptor 2 Homo sapiens 136-149 34417700-2 2022 The present study investigate the green synthesis of zinc oxide nanoparticles (ZnO-NPs) doped on activated carbon (AC) prepared from walnut peel extract and to estimate its efficiency in the removal of Eosin Y (Eo-Y) and Erythrosine B (Er-B) from its aqueous solution. Zinc Oxide 53-63 estrogen receptor 2 Homo sapiens 221-234 34417700-2 2022 The present study investigate the green synthesis of zinc oxide nanoparticles (ZnO-NPs) doped on activated carbon (AC) prepared from walnut peel extract and to estimate its efficiency in the removal of Eosin Y (Eo-Y) and Erythrosine B (Er-B) from its aqueous solution. Zinc Oxide 53-63 estrogen receptor 2 Homo sapiens 236-240 34974288-8 2022 However, a higher concentration (160 microg/mL) of Cys-ZnO NPs led to apoptotic cell death marked by nuclear condensation, mitochondrial membrane depolarization, actin filament condensation, lysosomal damage LDH leakage, intracellular ROS production, blebbing, upregulation of Bax and downregulation of Bcl-2 gene expression. Zinc Oxide 55-58 BCL2 apoptosis regulator Homo sapiens 303-308 34216929-2 2021 Al doped ZnO nanoparticles were synthesized by the sol-gel method and validated by FTIR, XRD, TEM/EDS, TGA, BET, and particle size analysis. Zinc Oxide 9-12 delta/notch like EGF repeat containing Homo sapiens 108-111 34915775-9 2021 Our results indicate that the oxidative parameters are increased while the content of TAC, antioxidant enzymes activity, and gene expression of SOD, GPX, and CAT show a significant reduction in the liver of ZnO-treated rats compared to the control (p< 0.05). Zinc Oxide 207-210 catalase Rattus norvegicus 158-161 34947725-1 2021 The properties of H2S gas sensing were investigated using a ZnO nanostructure prepared with AZO (zinc oxide with aluminium) and Al surfaces which were developed on a MEMS (Micro Electromechanical System) device. Zinc Oxide 60-63 gastrin Homo sapiens 22-25 34947725-3 2021 To find the optimal conditions for H2S gas sensing, different ZnO growth times and different temperatures were considered and tested, and the results were analysed. Zinc Oxide 62-65 gastrin Homo sapiens 39-42 34947725-4 2021 At 250 C and 90 min growth time, a ZnO sensor prepared with AZO and 40 nm Al recorded an 8.5% H2S gas-sensing response at a 200 ppb gas concentration and a 14% sensing response at a gas concentration of 1000 ppb. Zinc Oxide 36-39 gastrin Homo sapiens 99-102 34947725-4 2021 At 250 C and 90 min growth time, a ZnO sensor prepared with AZO and 40 nm Al recorded an 8.5% H2S gas-sensing response at a 200 ppb gas concentration and a 14% sensing response at a gas concentration of 1000 ppb. Zinc Oxide 36-39 gastrin Homo sapiens 133-136 34947725-4 2021 At 250 C and 90 min growth time, a ZnO sensor prepared with AZO and 40 nm Al recorded an 8.5% H2S gas-sensing response at a 200 ppb gas concentration and a 14% sensing response at a gas concentration of 1000 ppb. Zinc Oxide 36-39 gastrin Homo sapiens 183-186 34216929-2 2021 Al doped ZnO nanoparticles were synthesized by the sol-gel method and validated by FTIR, XRD, TEM/EDS, TGA, BET, and particle size analysis. Zinc Oxide 9-12 T-box transcription factor 1 Homo sapiens 103-106 34921583-3 2022 Herein, the authors propose a chemical buffer layer coated on Zn metal (CBL@Zn) anode, in which ZnO nanorods are uniformly dispersed in graphene oxide (GO), to improve the reversibility of Zn ZnO electrochemical conversion process. Zinc Oxide 96-99 Cbl proto-oncogene Homo sapiens 72-75 34757758-1 2021 The dissociation of a single water molecule on a ZnO(1010) surface has been investigated at the atomic level by low temperature STM manipulation combined with DFT calculations. Zinc Oxide 49-52 sulfotransferase family 1A member 3 Homo sapiens 128-131 34553816-0 2021 Combined lead and zinc oxide-nanoparticles induced thyroid toxicity through 8-OHdG oxidative stress-mediated inflammation, apoptosis, and Nrf2 activation in rats. Zinc Oxide 18-28 NFE2 like bZIP transcription factor 2 Rattus norvegicus 138-142 34797187-12 2021 In addition, high concentration of ZnO NPs inhibited the proliferation of HGF-1 by regulating the expression of MDM2 and p53. Zinc Oxide 35-38 transformed mouse 3T3 cell double minute 2 Mus musculus 112-116 34797187-12 2021 In addition, high concentration of ZnO NPs inhibited the proliferation of HGF-1 by regulating the expression of MDM2 and p53. Zinc Oxide 35-38 transformation related protein 53, pseudogene Mus musculus 121-124 34857270-6 2021 In an anti-inflammatory assay, ZnO/DNA-HCl NGs significantly inhibited TNF-alpha, IL-6, iNOS and COX-2 expression in LPS-stimulated Raw264.7 cells. Zinc Oxide 31-34 tumor necrosis factor Mus musculus 71-80 34857270-6 2021 In an anti-inflammatory assay, ZnO/DNA-HCl NGs significantly inhibited TNF-alpha, IL-6, iNOS and COX-2 expression in LPS-stimulated Raw264.7 cells. Zinc Oxide 31-34 interleukin 6 Mus musculus 82-86 34857270-6 2021 In an anti-inflammatory assay, ZnO/DNA-HCl NGs significantly inhibited TNF-alpha, IL-6, iNOS and COX-2 expression in LPS-stimulated Raw264.7 cells. Zinc Oxide 31-34 nitric oxide synthase 2, inducible Mus musculus 88-92 34857270-6 2021 In an anti-inflammatory assay, ZnO/DNA-HCl NGs significantly inhibited TNF-alpha, IL-6, iNOS and COX-2 expression in LPS-stimulated Raw264.7 cells. Zinc Oxide 31-34 cytochrome c oxidase II, mitochondrial Mus musculus 97-102 34821210-0 2021 Monitoring the interactions between bovine serum albumin and ZnO/Ag nanoparticles by spectroscopic techniques. Zinc Oxide 61-64 albumin Homo sapiens 43-56 34821210-5 2021 In the present study, ZnO/Ag nanoparticles were synthesized and characterized by SEM and XRD techniques and the interaction between bovine serum albumin and ZnO/Ag nanoparticles was evaluated by employing ultra-violet, steady state fluorescence, circular dichroism and FTIR spectroscopic techniques. Zinc Oxide 22-25 albumin Homo sapiens 139-152 34821210-5 2021 In the present study, ZnO/Ag nanoparticles were synthesized and characterized by SEM and XRD techniques and the interaction between bovine serum albumin and ZnO/Ag nanoparticles was evaluated by employing ultra-violet, steady state fluorescence, circular dichroism and FTIR spectroscopic techniques. Zinc Oxide 157-160 albumin Homo sapiens 139-152 34821210-6 2021 Upon the excitation of bovine serum albumin, ZnO/Ag nanoparticles appreciably reduced the intrinsic fluorescence intensity of bovine serum albumin. Zinc Oxide 45-48 albumin Homo sapiens 30-43 34821210-6 2021 Upon the excitation of bovine serum albumin, ZnO/Ag nanoparticles appreciably reduced the intrinsic fluorescence intensity of bovine serum albumin. Zinc Oxide 45-48 albumin Homo sapiens 133-146 34961025-4 2021 The activity of alpha-amylase showed increase, while that of dehydrogenase decline, in response to ZnO NPs. Zinc Oxide 99-102 alpha-amylase Zea mays 16-29 34961025-7 2021 However, in response, antioxidant enzymes (superoxide dismutase, ascorbate peroxidase, guaiacol peroxidase, and catalase) showed increase up to lower concentrations (100 mg/L) of ZnO NPs but decline variably at higher levels (150-200 mg/L) in wheat and maize. Zinc Oxide 179-182 superoxide dismutase Zea mays 43-63 34961025-7 2021 However, in response, antioxidant enzymes (superoxide dismutase, ascorbate peroxidase, guaiacol peroxidase, and catalase) showed increase up to lower concentrations (100 mg/L) of ZnO NPs but decline variably at higher levels (150-200 mg/L) in wheat and maize. Zinc Oxide 179-182 peroxidase 1 Zea mays 75-85 34961025-7 2021 However, in response, antioxidant enzymes (superoxide dismutase, ascorbate peroxidase, guaiacol peroxidase, and catalase) showed increase up to lower concentrations (100 mg/L) of ZnO NPs but decline variably at higher levels (150-200 mg/L) in wheat and maize. Zinc Oxide 179-182 peroxidase 1 Zea mays 96-106 34832131-0 2021 Incorporation of Au Nanoparticles on ZnO/ZnS Core Shell Nanostructures for UV Light/Hydrogen Gas Dual Sensing Enhancement. Zinc Oxide 37-40 gastrin Homo sapiens 93-96 34832131-1 2021 ZnO/ZnS nanocomposite-based nanostructures exhibit dual light and gas sensing capabilities. Zinc Oxide 0-3 gastrin Homo sapiens 66-69 34735159-3 2021 In this work, we report the growth of crystalline ZnO on the surface of CsPb(Br/I)3 nanocrystals through a ligand-mediated in situ surface reaction route, which forms monodispersed CsPb(Br/I)3/ZnO heterostructure nanocrystals (PZNCs). Zinc Oxide 50-53 granzyme B Homo sapiens 72-76 34811457-1 2021 We report on morphology-controlled remote epitaxy via hydrothermal growth of ZnO micro- and nanostructure crystals on graphene-coated GaN substrate. Zinc Oxide 77-80 gigaxonin Homo sapiens 134-137 34811457-3 2021 Although the growth of ZnO is carried out on poly-domain graphene-coated GaN substrate, the direction of hexagonal sidewall facet of ZnO is homogeneous over the whole ZnO-grown area on graphene/GaN because of strong remote epitaxial relation between ZnO and GaN across graphene. Zinc Oxide 23-26 gigaxonin Homo sapiens 73-76 34811457-3 2021 Although the growth of ZnO is carried out on poly-domain graphene-coated GaN substrate, the direction of hexagonal sidewall facet of ZnO is homogeneous over the whole ZnO-grown area on graphene/GaN because of strong remote epitaxial relation between ZnO and GaN across graphene. Zinc Oxide 23-26 gigaxonin Homo sapiens 258-261 34811457-3 2021 Although the growth of ZnO is carried out on poly-domain graphene-coated GaN substrate, the direction of hexagonal sidewall facet of ZnO is homogeneous over the whole ZnO-grown area on graphene/GaN because of strong remote epitaxial relation between ZnO and GaN across graphene. Zinc Oxide 133-136 gigaxonin Homo sapiens 73-76 34811457-3 2021 Although the growth of ZnO is carried out on poly-domain graphene-coated GaN substrate, the direction of hexagonal sidewall facet of ZnO is homogeneous over the whole ZnO-grown area on graphene/GaN because of strong remote epitaxial relation between ZnO and GaN across graphene. Zinc Oxide 133-136 gigaxonin Homo sapiens 194-197 34811457-3 2021 Although the growth of ZnO is carried out on poly-domain graphene-coated GaN substrate, the direction of hexagonal sidewall facet of ZnO is homogeneous over the whole ZnO-grown area on graphene/GaN because of strong remote epitaxial relation between ZnO and GaN across graphene. Zinc Oxide 133-136 gigaxonin Homo sapiens 258-261 34811457-3 2021 Although the growth of ZnO is carried out on poly-domain graphene-coated GaN substrate, the direction of hexagonal sidewall facet of ZnO is homogeneous over the whole ZnO-grown area on graphene/GaN because of strong remote epitaxial relation between ZnO and GaN across graphene. Zinc Oxide 167-170 gigaxonin Homo sapiens 194-197 34811457-3 2021 Although the growth of ZnO is carried out on poly-domain graphene-coated GaN substrate, the direction of hexagonal sidewall facet of ZnO is homogeneous over the whole ZnO-grown area on graphene/GaN because of strong remote epitaxial relation between ZnO and GaN across graphene. Zinc Oxide 167-170 gigaxonin Homo sapiens 258-261 34811457-3 2021 Although the growth of ZnO is carried out on poly-domain graphene-coated GaN substrate, the direction of hexagonal sidewall facet of ZnO is homogeneous over the whole ZnO-grown area on graphene/GaN because of strong remote epitaxial relation between ZnO and GaN across graphene. Zinc Oxide 250-253 gigaxonin Homo sapiens 73-76 34811457-3 2021 Although the growth of ZnO is carried out on poly-domain graphene-coated GaN substrate, the direction of hexagonal sidewall facet of ZnO is homogeneous over the whole ZnO-grown area on graphene/GaN because of strong remote epitaxial relation between ZnO and GaN across graphene. Zinc Oxide 250-253 gigaxonin Homo sapiens 194-197 34811457-3 2021 Although the growth of ZnO is carried out on poly-domain graphene-coated GaN substrate, the direction of hexagonal sidewall facet of ZnO is homogeneous over the whole ZnO-grown area on graphene/GaN because of strong remote epitaxial relation between ZnO and GaN across graphene. Zinc Oxide 250-253 gigaxonin Homo sapiens 258-261 34735159-3 2021 In this work, we report the growth of crystalline ZnO on the surface of CsPb(Br/I)3 nanocrystals through a ligand-mediated in situ surface reaction route, which forms monodispersed CsPb(Br/I)3/ZnO heterostructure nanocrystals (PZNCs). Zinc Oxide 50-53 granzyme B Homo sapiens 181-185 34197877-9 2021 Zinc oxide (ZnO), zinc nanoparticles, or ions can cause endothelial activation and increased levels of ICAM-1 and VCAM-1. Zinc Oxide 0-10 intercellular adhesion molecule 1 Homo sapiens 103-109 34766255-5 2021 Exposure to a non-cytotoxic concentration of ZnO NPs (16 mug/mL) increased the autophagy-marker proteins LC3B-II/I but decreased p62 accumulation, whereas a cytotoxic concentration of ZnO NPs (64 mug/mL) decreased LC3B-II/I proteins but did not affect p62 accumulation. Zinc Oxide 45-48 nucleoporin 62 Homo sapiens 129-132 33980385-3 2021 The results also suggest the possible role of oxygen vacancies or Ox- (defects) in the energy transfer from ZnO to the Er or Yb ions with a decrease of 3.18 eV and 3.19 eV in bandgap values to a red shift. Zinc Oxide 108-111 hypocretin neuropeptide precursor Homo sapiens 66-68 34869291-2 2021 Here, an ultrasensitive photoelectrochemical (PEC) sensor based on ZnO@polydopamine/Au nanocomposites was constructed for quantitative detection of Abeta. Zinc Oxide 67-70 amyloid beta precursor protein Homo sapiens 148-153 34834763-9 2021 The beneficial effects of ZnO-NPs were evident in the plants" defensive state, in which the concentration of ascorbic acid, free phenols, and the activity of superoxide dismutase, catalase, and ascorbate peroxidase were maintained at higher levels compared to NPs-untreated plants. Zinc Oxide 26-29 catalase isozyme 1 Solanum lycopersicum 180-188 34834763-10 2021 At severe drought conditions, 25 mg/L ZnO-NPs induced SOD, CAT, and APX activity by about 3.99-, 3.23-, and 2.82-fold of their corresponding controls, respectively. Zinc Oxide 38-41 cytosolic ascorbate peroxidase 2 Solanum lycopersicum 68-71 34197877-9 2021 Zinc oxide (ZnO), zinc nanoparticles, or ions can cause endothelial activation and increased levels of ICAM-1 and VCAM-1. Zinc Oxide 0-10 vascular cell adhesion molecule 1 Homo sapiens 114-120 34197877-9 2021 Zinc oxide (ZnO), zinc nanoparticles, or ions can cause endothelial activation and increased levels of ICAM-1 and VCAM-1. Zinc Oxide 12-15 intercellular adhesion molecule 1 Homo sapiens 103-109 34197877-9 2021 Zinc oxide (ZnO), zinc nanoparticles, or ions can cause endothelial activation and increased levels of ICAM-1 and VCAM-1. Zinc Oxide 12-15 vascular cell adhesion molecule 1 Homo sapiens 114-120 34197877-12 2021 Contrarily, endothelial activation and increased ICAM-1 and VCAM-1 levels can be caused by ZnO, zinc nanoparticles, or zinc ions. Zinc Oxide 91-94 intercellular adhesion molecule 1 Homo sapiens 49-55 34197877-12 2021 Contrarily, endothelial activation and increased ICAM-1 and VCAM-1 levels can be caused by ZnO, zinc nanoparticles, or zinc ions. Zinc Oxide 91-94 vascular cell adhesion molecule 1 Homo sapiens 60-66 34607338-3 2021 We have introduced aliovalent cations such as reducible Fe3+, stable Al3+ and oxidisable Cr3+ ions into ZnO and investigated its structural and optical properties. Zinc Oxide 104-107 teratocarcinoma-derived growth factor 1 pseudogene 3 Homo sapiens 89-92 34835685-0 2021 Interaction between ZnO Nanoparticles and Albumin and Its Effect on Cytotoxicity, Cellular Uptake, Intestinal Transport, Toxicokinetics, and Acute Oral Toxicity. Zinc Oxide 20-23 albumin Rattus norvegicus 42-49 34835685-3 2021 In this study, interactions between ZnO NPs and food proteins (albumin, casein, and zein) were evaluated by measuring changes in physicochemical property, fluorescence quenching ratios, and structural protein stability compared with ZnO interaction with glucose, the most interacted saccharide in our previous report. Zinc Oxide 36-39 albumin Rattus norvegicus 63-70 34835685-5 2021 The results demonstrate that interaction between ZnO and albumin reduced hydrodynamic diameters, but increased cytotoxicity, cellular uptake, and intestinal transport in a similar manner to ZnO interaction with glucose, without affecting primary structural protein stability and toxicokinetic behaviors. Zinc Oxide 49-52 albumin Rattus norvegicus 57-64 34636558-1 2021 It was demonstrated through a comparison between the spin-coated and inkjet-printed quantum-dot light-emitting diodes" (QLED) performance analysis outcomes that the annealing temperature of a zinc oxide nanoparticle (ZnO NP) electron transport layer (ETL) optimized for intense pulsed light (IPL) via a post-treatment differs depending on the film-formation method used. Zinc Oxide 192-202 spindlin 1 Homo sapiens 53-57 34590104-0 2021 Photoelectrochemical immunoassay of interleukin-6 based on covalent reaction-triggered photocurrent polarity switching of ZnO@fullerenol. Zinc Oxide 122-125 interleukin 6 Homo sapiens 36-49 34835545-0 2021 Atomic Layer Deposition of Ultrathin ZnO Films for Hybrid Window Layers for Cu(Inx,Ga1-x)Se2 Solar Cells. Zinc Oxide 37-40 fucosyltransferase 2 Homo sapiens 89-92 34590104-2 2021 The sensitive detection of interleukin-6 is achieved by using CA-encapsulated liposome as the label and COH-coated ZnO as the photoactive material, with a detection limit of 1.0 fg mL-1. Zinc Oxide 115-118 interleukin 6 Homo sapiens 27-40 34590104-2 2021 The sensitive detection of interleukin-6 is achieved by using CA-encapsulated liposome as the label and COH-coated ZnO as the photoactive material, with a detection limit of 1.0 fg mL-1. Zinc Oxide 115-118 L1 cell adhesion molecule Mus musculus 181-185 34685052-1 2021 This research work describes the synthesis of ZnO nanostructures doped with Ho3+ ions using a conventional sol-gel synthesis method. Zinc Oxide 46-49 histidyl-tRNA synthetase 2, mitochondrial Homo sapiens 76-79 34684721-4 2021 The synthesis and characterization of ZnO NPs were confirmed by UV-Vis spectrophotometry, Fourier Transform Infrared Spectroscopy (FTIR), X-ray Diffraction (XRD), Dynamic light scattering (DLS), Zeta potential, and Field Emission Scanning Electron Microscope (FESEM) techniques. Zinc Oxide 38-41 proteasome subunit alpha 5 Mus musculus 195-199 34620733-6 2021 Knockdown of TLNRD1 or CCNB1IP1 reduces ZnO NP-induced cytotoxicity. Zinc Oxide 40-43 talin rod domain containing 1 Homo sapiens 13-19 34620733-6 2021 Knockdown of TLNRD1 or CCNB1IP1 reduces ZnO NP-induced cytotoxicity. Zinc Oxide 40-43 cyclin B1 interacting protein 1 Homo sapiens 23-31 34721007-4 2021 This study demonstrated that angiogenesis and wound healing processes depend on pro-angiogenic factors as VEGF expression due to ZnO nanorods" exiting. Zinc Oxide 129-132 vascular endothelial growth factor A Homo sapiens 106-110 34546752-2 2021 Yet, it remains a great challenge to limit the thickness to the sub-1 nm scale and further combine with other components to obtain 2D hybrid zinc oxide (ZnO)-based sub-1 nm materials. Zinc Oxide 141-151 SUB1 regulator of transcription Homo sapiens 164-169 34546752-2 2021 Yet, it remains a great challenge to limit the thickness to the sub-1 nm scale and further combine with other components to obtain 2D hybrid zinc oxide (ZnO)-based sub-1 nm materials. Zinc Oxide 153-156 SUB1 regulator of transcription Homo sapiens 64-69 34546752-2 2021 Yet, it remains a great challenge to limit the thickness to the sub-1 nm scale and further combine with other components to obtain 2D hybrid zinc oxide (ZnO)-based sub-1 nm materials. Zinc Oxide 153-156 SUB1 regulator of transcription Homo sapiens 164-169 34546752-3 2021 Herein, a versatile strategy was successfully developed to realize the controllable preparation of ZnO-polyoxometalate (POM)-based 2D hybrid sub-1 nm nanosheet (HSNS) superstructures by incorporating three kinds of molybdenum-based POM clusters into the zinc oxide system. Zinc Oxide 254-264 SUB1 regulator of transcription Homo sapiens 141-146 34685052-6 2021 Finally, enhanced room temperature ferromagnetism (RT-FM) for Ho3+-doped ZnO (0.5 mol%) samples with a peak-to-peak line width of 452 G was detected and found to be highly correlated to the UV-VIS transmittance results. Zinc Oxide 73-76 histidyl-tRNA synthetase 2, mitochondrial Homo sapiens 62-65 34434272-11 2021 Zinc oxide reduced NF-kappaB p65, p-NF-kappaB p65, STAT1 and p-STAT1 expression. Zinc Oxide 0-10 synaptotagmin 1 Rattus norvegicus 29-32 34294308-4 2021 In this study, zinc oxide nanoparticles were homogeneously incorporated into the chitin hydrogel (ChT-1%ZnO) through one-step dissolution and regeneration method from alkaline/urea solution the first time. Zinc Oxide 15-25 solute carrier family 6 member 8 Rattus norvegicus 98-103 34294308-4 2021 In this study, zinc oxide nanoparticles were homogeneously incorporated into the chitin hydrogel (ChT-1%ZnO) through one-step dissolution and regeneration method from alkaline/urea solution the first time. Zinc Oxide 104-107 solute carrier family 6 member 8 Rattus norvegicus 98-103 34294308-5 2021 The remaining weights of ChT-1%ZnO in 150 mug/mL lysozyme solution was 52% after 5 weeks soaking. Zinc Oxide 31-34 solute carrier family 6 member 8 Rattus norvegicus 25-30 34294308-6 2021 ChT-1%ZnO showed statistical antibacterial activities for P. gingivalis and S. aureus at 6 h, 12 h, and 24 h. Moreover, ChT-1%ZnO exhibits osteogenesis promotion in vitro, and it was further evaluated with rat periodontal defect model in vivo. Zinc Oxide 6-9 solute carrier family 6 member 8 Rattus norvegicus 0-5 34294308-6 2021 ChT-1%ZnO showed statistical antibacterial activities for P. gingivalis and S. aureus at 6 h, 12 h, and 24 h. Moreover, ChT-1%ZnO exhibits osteogenesis promotion in vitro, and it was further evaluated with rat periodontal defect model in vivo. Zinc Oxide 6-9 solute carrier family 6 member 8 Rattus norvegicus 120-125 34294308-6 2021 ChT-1%ZnO showed statistical antibacterial activities for P. gingivalis and S. aureus at 6 h, 12 h, and 24 h. Moreover, ChT-1%ZnO exhibits osteogenesis promotion in vitro, and it was further evaluated with rat periodontal defect model in vivo. Zinc Oxide 126-129 solute carrier family 6 member 8 Rattus norvegicus 0-5 34294308-6 2021 ChT-1%ZnO showed statistical antibacterial activities for P. gingivalis and S. aureus at 6 h, 12 h, and 24 h. Moreover, ChT-1%ZnO exhibits osteogenesis promotion in vitro, and it was further evaluated with rat periodontal defect model in vivo. Zinc Oxide 126-129 solute carrier family 6 member 8 Rattus norvegicus 120-125 34294308-7 2021 The cemento-enamel junction value in ChT-1%ZnO group is 1.608 mm, presenting a statistical difference compared with no-membrane (1.825 mm) and ChT group (1.685 mm) after 8 weeks postoperatively. Zinc Oxide 43-46 solute carrier family 6 member 8 Rattus norvegicus 37-42 34339875-0 2021 NRF2 deficiency sensitizes human keratinocytes to zinc oxide nanoparticles-induced autophagy and cytotoxicity. Zinc Oxide 50-60 GA binding protein transcription factor subunit alpha Homo sapiens 0-4 34339875-5 2021 Knock-down of NRF2 (NRF2-KD) sensitized the cells to ZnO NPs-induced autophagy and cytotoxicity while an autophagy inhibitor, 3-methyladenine, protected the cells from ZnO NPs-induced cell death. Zinc Oxide 53-56 GA binding protein transcription factor subunit alpha Homo sapiens 14-18 34339875-5 2021 Knock-down of NRF2 (NRF2-KD) sensitized the cells to ZnO NPs-induced autophagy and cytotoxicity while an autophagy inhibitor, 3-methyladenine, protected the cells from ZnO NPs-induced cell death. Zinc Oxide 53-56 GA binding protein transcription factor subunit alpha Homo sapiens 20-27 34434272-11 2021 Zinc oxide reduced NF-kappaB p65, p-NF-kappaB p65, STAT1 and p-STAT1 expression. Zinc Oxide 0-10 signal transducer and activator of transcription 1 Rattus norvegicus 51-56 34434272-11 2021 Zinc oxide reduced NF-kappaB p65, p-NF-kappaB p65, STAT1 and p-STAT1 expression. Zinc Oxide 0-10 signal transducer and activator of transcription 1 Rattus norvegicus 63-68 34146667-8 2021 The results revealed that a decrease in BDNF and NGF mRNA expression, GSH concentration and GSH/GSSG ratio, increasing of GSSG and MDA levels, and neuronal loss in the CP-treated rats were reversed following the administration of different forms of ZnO, especially Gr ZnO NPs and ch ZnO NPs. Zinc Oxide 249-252 brain-derived neurotrophic factor Rattus norvegicus 40-44 34146667-8 2021 The results revealed that a decrease in BDNF and NGF mRNA expression, GSH concentration and GSH/GSSG ratio, increasing of GSSG and MDA levels, and neuronal loss in the CP-treated rats were reversed following the administration of different forms of ZnO, especially Gr ZnO NPs and ch ZnO NPs. Zinc Oxide 249-252 nerve growth factor Rattus norvegicus 49-52 34146667-9 2021 Co-administration of ZnO NPs to CP-treated rats restored the suppressive effects of CP on activities of antioxidant enzymes (SOD, GPX, CAT). Zinc Oxide 21-24 catalase Rattus norvegicus 135-138 34215060-3 2021 To solve the problems, we integrated the cosensitized structure of Ag2S/ZnO nanocomposities as photoelectrode with photogenerated hole-induced chemical redox cycling amplification (CRCA) strategy to develop a split-type PEC immunosensor for cardiac troponin I (cTnI) with high sensitivity. Zinc Oxide 72-75 troponin I3, cardiac type Homo sapiens 261-265 34217712-8 2021 Exposure of HTFs to ZnO nanoparticles can also induce the shifted peak, elevate the expression of Atg5, Atg12 and Becn1, enhance the autophagosome formation, and promote the LC3 expression, and thus activate autophagy signaling. Zinc Oxide 20-23 autophagy related 5 Homo sapiens 98-102 34500439-8 2021 FITC-Annexin V/propidium iodide double staining assay was used to analyze different apoptosis stages of B16F10 cells induced by ZnO NPs. Zinc Oxide 128-131 annexin A5 Mus musculus 5-14 34576552-5 2021 The structure and morphology of ZnO-CNT nanocomposites were analyzed by Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry-thermogravimetry (DSC-TG), X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), and transmission electron microscopy (TEM). Zinc Oxide 32-35 desmocollin 3 Homo sapiens 172-175 34576552-8 2021 DSC-TG analysis also reveals the formation of some physical bonds between ZnO and CNT, through the appearance of endothermic peaks which could be assigned to the decomposition of functional groups of the CNT chain and breaking of the ZnO-CNT bonds. Zinc Oxide 74-77 desmocollin 3 Homo sapiens 0-3 34612332-0 2021 Graphene-coated copper-doped ZnO quantum dots for sensitive photoelectrochemical bioanalysis of thrombin triggered by DNA nanoflowers. Zinc Oxide 29-32 coagulation factor II, thrombin Homo sapiens 96-104 34612332-1 2021 This work reports a photoelectrochemical (PEC) biosensing platform for the sensitive and specific screening of thrombin by using graphene oxide-coated copper-doped zinc oxide quantum dots (Cu0.3Zn0.7O-GO QDs) as the photoactive materials and glucose oxidase-encapsulated DNA nanoflowers (GOx-DFs) for signal amplification. Zinc Oxide 164-174 coagulation factor II, thrombin Homo sapiens 111-119 34514633-13 2021 Broiler breeder diet with ZnO enhance ZO-1, OC and mitigate TNF-alpha gene expression in jejunum maintenance of gut health in broiler breeders. Zinc Oxide 26-29 lipopolysaccharide induced TNF factor Gallus gallus 60-69 34217712-8 2021 Exposure of HTFs to ZnO nanoparticles can also induce the shifted peak, elevate the expression of Atg5, Atg12 and Becn1, enhance the autophagosome formation, and promote the LC3 expression, and thus activate autophagy signaling. Zinc Oxide 20-23 autophagy related 12 Homo sapiens 104-109 34217712-8 2021 Exposure of HTFs to ZnO nanoparticles can also induce the shifted peak, elevate the expression of Atg5, Atg12 and Becn1, enhance the autophagosome formation, and promote the LC3 expression, and thus activate autophagy signaling. Zinc Oxide 20-23 beclin 1 Homo sapiens 114-119 34217712-8 2021 Exposure of HTFs to ZnO nanoparticles can also induce the shifted peak, elevate the expression of Atg5, Atg12 and Becn1, enhance the autophagosome formation, and promote the LC3 expression, and thus activate autophagy signaling. Zinc Oxide 20-23 microtubule associated protein 1 light chain 3 alpha Homo sapiens 174-177 34495993-14 2021 ZnO NPs induced the activity of antioxidant enzymes, including peroxidase and catalase by averages of 48.3% and 41%, respectively. Zinc Oxide 0-3 peroxidase Glycine max 63-73 34495993-14 2021 ZnO NPs induced the activity of antioxidant enzymes, including peroxidase and catalase by averages of 48.3% and 41%, respectively. Zinc Oxide 0-3 catalase-3 Glycine max 78-86 34403579-4 2021 The densification of zinc oxide (ZnO) by CS using zinc acetylacetonate hydrate (Zn(acac)2 xH2O), a versatile ligand often used as a precursor for ZnO synthesis in wet chemistry, is reported. Zinc Oxide 21-31 citrate synthase Homo sapiens 41-43 34403579-4 2021 The densification of zinc oxide (ZnO) by CS using zinc acetylacetonate hydrate (Zn(acac)2 xH2O), a versatile ligand often used as a precursor for ZnO synthesis in wet chemistry, is reported. Zinc Oxide 33-36 citrate synthase Homo sapiens 41-43 34403579-5 2021 The successful densification of ZnO using H2O and Zn(acac)2 xH2O confirms the importance of speciation in CS, as ZnO has a very low solubility in pure H2O. Zinc Oxide 113-116 citrate synthase Homo sapiens 106-108 34403579-4 2021 The densification of zinc oxide (ZnO) by CS using zinc acetylacetonate hydrate (Zn(acac)2 xH2O), a versatile ligand often used as a precursor for ZnO synthesis in wet chemistry, is reported. Zinc Oxide 146-149 citrate synthase Homo sapiens 41-43 34403579-5 2021 The successful densification of ZnO using H2O and Zn(acac)2 xH2O confirms the importance of speciation in CS, as ZnO has a very low solubility in pure H2O. Zinc Oxide 32-35 citrate synthase Homo sapiens 106-108 34697744-0 2021 Evaluation of Induced Apoptosis by Biosynthesized Zinc Oxide Nanoparticles in MCF-7 Breast Cancer Cells Using Bak1 and Bclx Expression. Zinc Oxide 50-60 BCL2 antagonist/killer 1 Homo sapiens 110-114 34450010-3 2021 The effect of ZnO NW incorporation into PDMS on the sensing performance of pressure sensors is investigated, which results in a significantly enhanced sensitivity of 8.77 x 10-4 Pa-1 in low-pressure regions, compared to pristine PDMS (1.32 x 10-4 Pa-1). Zinc Oxide 14-17 PAXIP1 associated glutamate rich protein 1 Homo sapiens 178-182 34697744-0 2021 Evaluation of Induced Apoptosis by Biosynthesized Zinc Oxide Nanoparticles in MCF-7 Breast Cancer Cells Using Bak1 and Bclx Expression. Zinc Oxide 50-60 BCL2 like 1 Homo sapiens 119-123 34197967-0 2021 Synthesis and Characterization of Lysozyme-Conjugated Ag.ZnO@HA Nanocomposite: A Redox and pH-Responsive antimicrobial agent with photocatalytic activity. Zinc Oxide 57-60 lysozyme Homo sapiens 34-42 34688329-4 2021 In this work, further characterization studies were performed, which confirmed that the ZnO/Ag nanoparticles were physically embedded and evenly distributed in the ZnO/Ag/PVP/PCL nanofibers, enabling the sustained release of Ag and Zn. Zinc Oxide 88-91 PHD finger protein 1 Homo sapiens 175-178 34236500-4 2021 Our results displayed that ZnO NPs attenuated adjuvant-induced increased production of inflammatory mediators interleukin-1beta (IL-1beta), tumor necrosis factor alpha (TNF-alpha), interleukin-10 (IL-10), and total leukocyte count. Zinc Oxide 27-30 interleukin 1 beta Rattus norvegicus 110-127 34236500-4 2021 Our results displayed that ZnO NPs attenuated adjuvant-induced increased production of inflammatory mediators interleukin-1beta (IL-1beta), tumor necrosis factor alpha (TNF-alpha), interleukin-10 (IL-10), and total leukocyte count. Zinc Oxide 27-30 interleukin 1 alpha Rattus norvegicus 129-137 34236500-4 2021 Our results displayed that ZnO NPs attenuated adjuvant-induced increased production of inflammatory mediators interleukin-1beta (IL-1beta), tumor necrosis factor alpha (TNF-alpha), interleukin-10 (IL-10), and total leukocyte count. Zinc Oxide 27-30 tumor necrosis factor Rattus norvegicus 140-167 34236500-4 2021 Our results displayed that ZnO NPs attenuated adjuvant-induced increased production of inflammatory mediators interleukin-1beta (IL-1beta), tumor necrosis factor alpha (TNF-alpha), interleukin-10 (IL-10), and total leukocyte count. Zinc Oxide 27-30 tumor necrosis factor Rattus norvegicus 169-178 34236500-4 2021 Our results displayed that ZnO NPs attenuated adjuvant-induced increased production of inflammatory mediators interleukin-1beta (IL-1beta), tumor necrosis factor alpha (TNF-alpha), interleukin-10 (IL-10), and total leukocyte count. Zinc Oxide 27-30 interleukin 10 Rattus norvegicus 181-195 34236500-4 2021 Our results displayed that ZnO NPs attenuated adjuvant-induced increased production of inflammatory mediators interleukin-1beta (IL-1beta), tumor necrosis factor alpha (TNF-alpha), interleukin-10 (IL-10), and total leukocyte count. Zinc Oxide 27-30 interleukin 10 Rattus norvegicus 197-202 34688329-3 2021 In a previous study, we prepared and characterized electrospinning zinc oxide/silver/polyvinylpyrrolidone/polycaprolactone (ZnO/Ag/PVP/PCL) nanofibers using ZnO and Ag nanoparticles, and evaluated their antibacterial effect in vitro. Zinc Oxide 67-77 PHD finger protein 1 Homo sapiens 135-138 34688329-3 2021 In a previous study, we prepared and characterized electrospinning zinc oxide/silver/polyvinylpyrrolidone/polycaprolactone (ZnO/Ag/PVP/PCL) nanofibers using ZnO and Ag nanoparticles, and evaluated their antibacterial effect in vitro. Zinc Oxide 124-127 PHD finger protein 1 Homo sapiens 135-138 34688329-3 2021 In a previous study, we prepared and characterized electrospinning zinc oxide/silver/polyvinylpyrrolidone/polycaprolactone (ZnO/Ag/PVP/PCL) nanofibers using ZnO and Ag nanoparticles, and evaluated their antibacterial effect in vitro. Zinc Oxide 157-160 PHD finger protein 1 Homo sapiens 135-138 34688329-4 2021 In this work, further characterization studies were performed, which confirmed that the ZnO/Ag nanoparticles were physically embedded and evenly distributed in the ZnO/Ag/PVP/PCL nanofibers, enabling the sustained release of Ag and Zn. Zinc Oxide 164-167 PHD finger protein 1 Homo sapiens 175-178 34688329-7 2021 Therefore, ZnO/Ag/PVP/PCL bimetallic nanofibers may be a safe, efficient biomedical dressing for wound healing. Zinc Oxide 11-14 PHD finger protein 1 Homo sapiens 22-25 34323367-3 2021 The potentiostatic electrodeposition of zinc and lead starting directly from ZnO and PbO, which dissolve in (Hbet)(NTf2 ) in high concentrations is reported. Zinc Oxide 77-80 nuclear transport factor 2 Homo sapiens 115-119 34166973-0 2021 Evaluation of transcription factor and aquaporin gene expressions in response to Al2O3 and ZnO nanoparticles during barley germination. Zinc Oxide 91-94 HvPIP2;3 Hordeum vulgare 39-48 34323367-5 2021 The ionic conductivity of the solution of ZnO in (Hbet)(NTf2 ) is measured and the effect of various temperatures and potentials on the morphology of the deposited material is explored. Zinc Oxide 42-45 nuclear transport factor 2 Homo sapiens 56-60 34448982-8 2021 The results obtained from the study indicate that the ZnO nanoparticles of Solanum nigrum possess a dose-dependent cytotoxic effect against HeLa cell lines through the inhibition of beta-catenin and increasing the levels of p53, caspase-3, and caspase-9. Zinc Oxide 54-57 catenin beta 1 Homo sapiens 182-194 34448982-8 2021 The results obtained from the study indicate that the ZnO nanoparticles of Solanum nigrum possess a dose-dependent cytotoxic effect against HeLa cell lines through the inhibition of beta-catenin and increasing the levels of p53, caspase-3, and caspase-9. Zinc Oxide 54-57 tumor protein p53 Homo sapiens 224-227 34448982-8 2021 The results obtained from the study indicate that the ZnO nanoparticles of Solanum nigrum possess a dose-dependent cytotoxic effect against HeLa cell lines through the inhibition of beta-catenin and increasing the levels of p53, caspase-3, and caspase-9. Zinc Oxide 54-57 caspase 3 Homo sapiens 229-238 34448982-8 2021 The results obtained from the study indicate that the ZnO nanoparticles of Solanum nigrum possess a dose-dependent cytotoxic effect against HeLa cell lines through the inhibition of beta-catenin and increasing the levels of p53, caspase-3, and caspase-9. Zinc Oxide 54-57 caspase 9 Homo sapiens 244-253 34354203-6 2021 Experimental results demonstrate that the morphology of ZnO particles plays an important role in preserving the electrical characteristics of insulin. Zinc Oxide 56-59 insulin Homo sapiens 142-149 34157328-8 2021 In silico findings suggested CNC doped ZnO nanocomposites as possible inhibitors of beta-lactamase (Binding score: -7.936 kcal/mol), DHFR (Binding score: -5.691 kcal/mol) and FabI (Binding score: -8.673 kcal/mol). Zinc Oxide 39-42 dihydrofolate reductase Escherichia coli 133-137 34450944-5 2021 Then, we mainly focus on the recent progress in ZnO nanosensors according to the functional classification, including pressure sensor, gas sensor, photoelectric sensor, biosensor and temperature sensor. Zinc Oxide 48-51 gastrin Homo sapiens 135-138 34370102-7 2021 Quantitative PCR results revealed the significantly higher mRNA level of IL1B and CD69 in fresh NP-treated groups compared to that of aged ZnO NP- and zinc chloride-treated groups. Zinc Oxide 139-142 interleukin 1 beta Homo sapiens 73-77 34370102-7 2021 Quantitative PCR results revealed the significantly higher mRNA level of IL1B and CD69 in fresh NP-treated groups compared to that of aged ZnO NP- and zinc chloride-treated groups. Zinc Oxide 139-142 CD69 molecule Homo sapiens 82-86 34578536-1 2021 We propose a hyperbolic metamaterial-based surface plasmon resonance (HMM-SPR) sensor by composing a few pairs of alternating silver (Ag) and zinc oxide (ZnO) layers. Zinc Oxide 142-152 sepiapterin reductase Homo sapiens 74-77 34578536-1 2021 We propose a hyperbolic metamaterial-based surface plasmon resonance (HMM-SPR) sensor by composing a few pairs of alternating silver (Ag) and zinc oxide (ZnO) layers. Zinc Oxide 154-157 sepiapterin reductase Homo sapiens 74-77 34443981-6 2021 Otherwise, the low concentration and the higher pH of GO suspension induce more lattice defects on the ZnO crystal structure. Zinc Oxide 103-106 phenylalanine hydroxylase Homo sapiens 48-50 34160494-2 2021 First, a two-step hydrothermal method was used to introduce ZnO and CdS onto an activated indium tin oxide (ITO) electrode to prepare a CdS/ZnO/ITO electrode. Zinc Oxide 60-63 CDP-diacylglycerol synthase 1 Homo sapiens 136-139 34361772-0 2021 Highly Sensitive and Selective Eco-Toxic 4-Nitrophenol Chemical Sensor Based on Ag-Doped ZnO Nanoflowers Decorated with Nanosheets. Zinc Oxide 89-92 ciliogenesis associated kinase 1 Homo sapiens 31-34 34259308-0 2021 In situ creation of ZnO@CdS nanoflowers on ITO electrodes for sensitive photoelectrochemical detection of copper ions in blood. Zinc Oxide 20-23 CDP-diacylglycerol synthase 1 Homo sapiens 24-27 34259308-1 2021 A highly selective and sensitive photoelectrochemical (PEC) detection method has been developed for the analysis of copper (Cu2+) ions using nanoflower-like ZnO@CdS heterojunctions, of which ZnO was first in situ grown onto the indium tin oxide electrodes by a hydrothermal method and then coated with CdS through the chemical bath deposition route. Zinc Oxide 157-160 CDP-diacylglycerol synthase 1 Homo sapiens 161-164 34259308-1 2021 A highly selective and sensitive photoelectrochemical (PEC) detection method has been developed for the analysis of copper (Cu2+) ions using nanoflower-like ZnO@CdS heterojunctions, of which ZnO was first in situ grown onto the indium tin oxide electrodes by a hydrothermal method and then coated with CdS through the chemical bath deposition route. Zinc Oxide 191-194 CDP-diacylglycerol synthase 1 Homo sapiens 161-164 34259308-2 2021 It was discovered that the ZnO@CdS heterojunction so formed could serve as a photosensitive catalyst with improved charge separation for visible-light-driven PEC responses. Zinc Oxide 27-30 CDP-diacylglycerol synthase 1 Homo sapiens 31-34 34259308-5 2021 A ZnO@CdS heterojunction-based PEC sensor was thereby developed for the detection of Cu2+ ions in blood in the linear concentrations ranging from 0.50 to 80 nM, with a limit of detection of 0.18 nM. Zinc Oxide 2-5 CDP-diacylglycerol synthase 1 Homo sapiens 6-9 34302391-9 2022 ZnO supplementation increased ADG and ADFI (p < 0.05) during the first period (D0-21) compared with pigs offered MP and MPD2 . Zinc Oxide 0-3 ADG Sus scrofa 30-33 34327239-0 2021 Reusable, Noninvasive, and Sensitive Fluorescence Enhanced ZnO-Nanorod-Based Microarrays for Quantitative Detection of AFP in Human Serum. Zinc Oxide 59-62 alpha fetoprotein Homo sapiens 119-122 34361202-0 2021 Magnetic and Highly Luminescent Heterostructures of Gd3+/ZnO Conjugated to GCIS/ZnS Quantum Dots for Multimodal Imaging. Zinc Oxide 57-60 GRDX Homo sapiens 52-55 34180924-0 2021 Ultrasensitive photoelectrochemical immunoassay for prostate-specific antigen based on silver nanoparticle-triggered ion-exchange reaction with ZnO/CdS nanorods. Zinc Oxide 144-147 kallikrein related peptidase 3 Homo sapiens 52-77 34180924-2 2021 Herein, we developed a new signal-amplified photoelectrochemical (PEC) immunosensing method for quantitative monitoring of the target PSA based on the ion-exchange reaction for the in situ formation of ZnO/CdS/Ag2S nanohybrids triggered by the as-released silver ions (Ag+) from silver nanolabels. Zinc Oxide 202-205 angiotensin II receptor type 1 Homo sapiens 210-214 34180924-5 2021 In this regard, an ion-exchange reaction occurred between the silver ions and ZnO/CdS nanorods on the photosensitive electrode, thus producing ZnO/CdS/Ag2S nanohybrids to generate a relatively strong photocurrent. Zinc Oxide 78-81 angiotensin II receptor type 1 Homo sapiens 151-155 34180924-5 2021 In this regard, an ion-exchange reaction occurred between the silver ions and ZnO/CdS nanorods on the photosensitive electrode, thus producing ZnO/CdS/Ag2S nanohybrids to generate a relatively strong photocurrent. Zinc Oxide 143-146 angiotensin II receptor type 1 Homo sapiens 151-155 34160494-3 2021 Then, AChE was immobilized on CdS/ZnO/ITO with chitosan to obtain an AChE/CdS/ZnO EGFET sensor. Zinc Oxide 78-81 acetylcholinesterase (Cartwright blood group) Homo sapiens 6-10 34160494-3 2021 Then, AChE was immobilized on CdS/ZnO/ITO with chitosan to obtain an AChE/CdS/ZnO EGFET sensor. Zinc Oxide 78-81 acetylcholinesterase (Cartwright blood group) Homo sapiens 69-73 34160494-3 2021 Then, AChE was immobilized on CdS/ZnO/ITO with chitosan to obtain an AChE/CdS/ZnO EGFET sensor. Zinc Oxide 78-81 CDP-diacylglycerol synthase 1 Homo sapiens 74-77 34160494-6 2021 The results show that the AChE/CdS/ZnO EGFET sensor has extremely high sensitivity and good selectivity. Zinc Oxide 35-38 acetylcholinesterase (Cartwright blood group) Homo sapiens 26-30 34160494-6 2021 The results show that the AChE/CdS/ZnO EGFET sensor has extremely high sensitivity and good selectivity. Zinc Oxide 35-38 CDP-diacylglycerol synthase 1 Homo sapiens 31-34 34160494-2 2021 First, a two-step hydrothermal method was used to introduce ZnO and CdS onto an activated indium tin oxide (ITO) electrode to prepare a CdS/ZnO/ITO electrode. Zinc Oxide 140-143 CDP-diacylglycerol synthase 1 Homo sapiens 68-71 34160494-2 2021 First, a two-step hydrothermal method was used to introduce ZnO and CdS onto an activated indium tin oxide (ITO) electrode to prepare a CdS/ZnO/ITO electrode. Zinc Oxide 140-143 CDP-diacylglycerol synthase 1 Homo sapiens 136-139 34160494-3 2021 Then, AChE was immobilized on CdS/ZnO/ITO with chitosan to obtain an AChE/CdS/ZnO EGFET sensor. Zinc Oxide 34-37 acetylcholinesterase (Cartwright blood group) Homo sapiens 6-10 34901589-10 2021 The improvement of the performances with the 3D architecture results from both of: (i) the enhancement of the ZnO/AL surface interface (1 mum2/mum2 for the 2D structure to 6.6 mum2/mum2 for the 3D architecture), (ii) the presence of ZnONWs inside the AL, which behave as numerous nanocollectors (~60 ZnONW/mum2) of electrons in the depth of the AL. Zinc Oxide 110-113 trafficking protein particle complex subunit 1 Homo sapiens 138-142 34241775-0 2022 The Prospective Ameliorative Role of Zinc Oxide Nanoparticles in STZ-Induced Diabetic Nephropathy in Rats: Mechanistic Targeting of Autophagy and Regulating Nrf2/TXNIP/NLRP3 Inflammasome Signaling. Zinc Oxide 37-47 NFE2 like bZIP transcription factor 2 Rattus norvegicus 157-161 34241775-0 2022 The Prospective Ameliorative Role of Zinc Oxide Nanoparticles in STZ-Induced Diabetic Nephropathy in Rats: Mechanistic Targeting of Autophagy and Regulating Nrf2/TXNIP/NLRP3 Inflammasome Signaling. Zinc Oxide 37-47 thioredoxin interacting protein Rattus norvegicus 162-167 34241775-0 2022 The Prospective Ameliorative Role of Zinc Oxide Nanoparticles in STZ-Induced Diabetic Nephropathy in Rats: Mechanistic Targeting of Autophagy and Regulating Nrf2/TXNIP/NLRP3 Inflammasome Signaling. Zinc Oxide 37-47 NLR family, pyrin domain containing 3 Rattus norvegicus 168-173 34241775-11 2022 Furthermore, ZnO NPs significantly increased Nrf2-DNA-binding activity and downregulated TXNIP gene expression leading to restoration of the redox status. Zinc Oxide 13-16 NFE2 like bZIP transcription factor 2 Rattus norvegicus 45-49 34241775-11 2022 Furthermore, ZnO NPs significantly increased Nrf2-DNA-binding activity and downregulated TXNIP gene expression leading to restoration of the redox status. Zinc Oxide 13-16 thioredoxin interacting protein Rattus norvegicus 89-94 34241775-13 2022 Based on our results, we concluded that ZnO NPs can be considered as a promising agent for slowing the progression of DN via interplay between autophagy and Nrf2/TXNIP/NLRP3 inflammasome signaling. Zinc Oxide 40-43 NFE2 like bZIP transcription factor 2 Rattus norvegicus 157-161 34241775-13 2022 Based on our results, we concluded that ZnO NPs can be considered as a promising agent for slowing the progression of DN via interplay between autophagy and Nrf2/TXNIP/NLRP3 inflammasome signaling. Zinc Oxide 40-43 thioredoxin interacting protein Rattus norvegicus 162-167 34241775-13 2022 Based on our results, we concluded that ZnO NPs can be considered as a promising agent for slowing the progression of DN via interplay between autophagy and Nrf2/TXNIP/NLRP3 inflammasome signaling. Zinc Oxide 40-43 NLR family, pyrin domain containing 3 Rattus norvegicus 168-173 33715695-0 2021 Efficiency Enhancement by Insertion of ZnO Recombination Barrier Layer in CdS Quantum Dot-Sensitized Solar Cells. Zinc Oxide 39-42 CDP-diacylglycerol synthase 1 Homo sapiens 74-77 33715695-1 2021 In this investigation we report the formation of thin ZnO recombination barrier layer at TiO2/CdS interface aimed for the improvement in performance of CdS sensitized solar cell. Zinc Oxide 54-57 CDP-diacylglycerol synthase 1 Homo sapiens 94-97 33715695-1 2021 In this investigation we report the formation of thin ZnO recombination barrier layer at TiO2/CdS interface aimed for the improvement in performance of CdS sensitized solar cell. Zinc Oxide 54-57 CDP-diacylglycerol synthase 1 Homo sapiens 152-155 33715695-4 2021 Moreover, the analysis of photovoltaic characteristics upon increasing the thickness of the ZnO film reveals that the ZnO recombination barrier layer with optimum thickness at porous TiO2/CdS interface proved to be an effective potential barrier for minimizing electron back recombination. Zinc Oxide 92-95 CDP-diacylglycerol synthase 1 Homo sapiens 188-191 33715695-4 2021 Moreover, the analysis of photovoltaic characteristics upon increasing the thickness of the ZnO film reveals that the ZnO recombination barrier layer with optimum thickness at porous TiO2/CdS interface proved to be an effective potential barrier for minimizing electron back recombination. Zinc Oxide 118-121 CDP-diacylglycerol synthase 1 Homo sapiens 188-191 34901589-10 2021 The improvement of the performances with the 3D architecture results from both of: (i) the enhancement of the ZnO/AL surface interface (1 mum2/mum2 for the 2D structure to 6.6 mum2/mum2 for the 3D architecture), (ii) the presence of ZnONWs inside the AL, which behave as numerous nanocollectors (~60 ZnONW/mum2) of electrons in the depth of the AL. Zinc Oxide 110-113 trafficking protein particle complex subunit 1 Homo sapiens 143-147 34901589-10 2021 The improvement of the performances with the 3D architecture results from both of: (i) the enhancement of the ZnO/AL surface interface (1 mum2/mum2 for the 2D structure to 6.6 mum2/mum2 for the 3D architecture), (ii) the presence of ZnONWs inside the AL, which behave as numerous nanocollectors (~60 ZnONW/mum2) of electrons in the depth of the AL. Zinc Oxide 110-113 trafficking protein particle complex subunit 1 Homo sapiens 176-180 34901589-10 2021 The improvement of the performances with the 3D architecture results from both of: (i) the enhancement of the ZnO/AL surface interface (1 mum2/mum2 for the 2D structure to 6.6 mum2/mum2 for the 3D architecture), (ii) the presence of ZnONWs inside the AL, which behave as numerous nanocollectors (~60 ZnONW/mum2) of electrons in the depth of the AL. Zinc Oxide 110-113 trafficking protein particle complex subunit 1 Homo sapiens 181-185 34901589-10 2021 The improvement of the performances with the 3D architecture results from both of: (i) the enhancement of the ZnO/AL surface interface (1 mum2/mum2 for the 2D structure to 6.6 mum2/mum2 for the 3D architecture), (ii) the presence of ZnONWs inside the AL, which behave as numerous nanocollectors (~60 ZnONW/mum2) of electrons in the depth of the AL. Zinc Oxide 110-113 trafficking protein particle complex subunit 1 Homo sapiens 306-310 34082750-12 2021 Tri-Z was prepared to concentration of 10 mg TMP and 1.8 mg Zn per ml, then serial dilutions were made. Zinc Oxide 60-62 tRNA-Ile (anticodon AAT) 9-1 Homo sapiens 0-3 34158559-3 2021 We performed the production of an FTO/ZnO/P3HT:PCBM/MoO3/Ag/MoO3 ST-OSC by integrating MoO3/Ag/MoO3 (10/(Formula: see text)/(Formula: see text) nm) instead of an Ag electrode in an opaque FTO/ZnO/P3HT:PCBM/MoO3/Ag (-/40/130/10/100 nm) OSC, after theoretically achieving optimal values of optical and electrical parameters depending on Ag layer thickness. Zinc Oxide 38-41 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 34-37 34257799-14 2021 The concentrations of IL-1beta, IL-6, and IL-8 in the plasma were all decreased upon ZnO administration. Zinc Oxide 85-88 interleukin 1 alpha Homo sapiens 22-30 34257799-14 2021 The concentrations of IL-1beta, IL-6, and IL-8 in the plasma were all decreased upon ZnO administration. Zinc Oxide 85-88 interleukin 6 Homo sapiens 32-36 34257799-14 2021 The concentrations of IL-1beta, IL-6, and IL-8 in the plasma were all decreased upon ZnO administration. Zinc Oxide 85-88 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 34235315-4 2021 In the research of barbed fiber fabrication and adsorption on bovine serum albumin (BSA), the effects of different chemical bath conditions on the growth of ZnO nanorods were discussed. Zinc Oxide 157-160 albumin Homo sapiens 69-82 34132526-1 2021 Herein, we propose the topotactic and self-templated fabrication of Zn1-xCdxSe porous nanobelt-ZnO nanorod (termed as ZnCdSe/ZnO) photoelectrode via the cadmium (Cd2+) ion-exchange process on zinc (Zn) foil. Zinc Oxide 95-98 CD2 molecule Homo sapiens 162-165 34132526-1 2021 Herein, we propose the topotactic and self-templated fabrication of Zn1-xCdxSe porous nanobelt-ZnO nanorod (termed as ZnCdSe/ZnO) photoelectrode via the cadmium (Cd2+) ion-exchange process on zinc (Zn) foil. Zinc Oxide 125-128 CD2 molecule Homo sapiens 162-165 34132526-4 2021 In particular Cd2+ ion temperature (140 C/18 h), the optimized ZnCdSe/ZnO-(F) photoelectrode shows an excellent photocurrent density of 14 mA cm-2 at 0 V vs Ag/AgCl with 219 mumol cm-2 hydrogen gas evolution for 3 h under 1 sun illumination. Zinc Oxide 71-74 CD2 molecule Homo sapiens 14-17 34204953-0 2021 Immunosensor Based on Zinc Oxide Nanocrystals Decorated with Copper for the Electrochemical Detection of Human Salivary Alpha-Amylase. Zinc Oxide 22-32 amylase alpha 1A Homo sapiens 111-133 34204953-2 2021 (2) Methods: Electrochemical immunodetection of human salivary alpha-amylase (HSA) used ZnO, CuO, and ZnO:xCu (x = 0.1, 0.4, 1.0, 4.0, and 12.0) NCs. Zinc Oxide 88-91 amylase alpha 1A Homo sapiens 54-76 34204953-4 2021 Graphite electrodes were used and the electrochemical signal increased by 40% when using ZnO:1Cu and 4Cu (0.25 mg mL-1), in an immunosensor (0.372 mg mL-1 of anti-alpha-amylase and 1% of casein). Zinc Oxide 89-92 L1 cell adhesion molecule Mus musculus 114-118 34082750-16 2021 Tri-Z, at ratio range of 0.15-0.2 (optimal ratio of 0.18) Zn/TMP, enabled embryos to survive influenza virus despite increasing viral load (> 80% survival at optimal ratio). Zinc Oxide 58-60 tRNA-Ile (anticodon AAT) 9-1 Homo sapiens 0-3 34064626-6 2021 Compared to the ZnO group, the chelate-ZnO group exhibited higher proportion of T-bet+ and FoxP3+ T cells and the nano-ZnO group had higher numbers of RORgt+ and GATA3+ T cells in the mesenteric lymph nodes. Zinc Oxide 16-19 T-box transcription factor 21 Sus scrofa 80-85 34064301-2 2021 We studied the properties of gel-like dispersions of ZnO NPs with immobilized terpenoids and their effects on the activity of LDH, GR, G6PDH, restoration of redox balance of co-enzyme pairs NAD+/NADH and NADP+/NADPH, as well as the activity of SOD, catalase, AlDH in erythrocytes in the treatment of burns in rats. Zinc Oxide 53-56 glutathione-disulfide reductase Rattus norvegicus 131-133 34064626-6 2021 Compared to the ZnO group, the chelate-ZnO group exhibited higher proportion of T-bet+ and FoxP3+ T cells and the nano-ZnO group had higher numbers of RORgt+ and GATA3+ T cells in the mesenteric lymph nodes. Zinc Oxide 16-19 forkhead box P3 Sus scrofa 91-96 34064626-6 2021 Compared to the ZnO group, the chelate-ZnO group exhibited higher proportion of T-bet+ and FoxP3+ T cells and the nano-ZnO group had higher numbers of RORgt+ and GATA3+ T cells in the mesenteric lymph nodes. Zinc Oxide 16-19 GATA binding protein 3 Sus scrofa 162-167 34065118-7 2021 This work suggests that ZnMgO has the potential to improve the performance of QLED, which consists of the ITO/ETL/InP QDs/TCTA/MoO3/Al, and Mg-doping strategy is an efficient route to directionally regulate ZnO conduction bands. Zinc Oxide 207-210 T cell leukemia translocation altered Homo sapiens 122-126 34064626-6 2021 Compared to the ZnO group, the chelate-ZnO group exhibited higher proportion of T-bet+ and FoxP3+ T cells and the nano-ZnO group had higher numbers of RORgt+ and GATA3+ T cells in the mesenteric lymph nodes. Zinc Oxide 39-42 T-box transcription factor 21 Sus scrofa 80-85 34064626-6 2021 Compared to the ZnO group, the chelate-ZnO group exhibited higher proportion of T-bet+ and FoxP3+ T cells and the nano-ZnO group had higher numbers of RORgt+ and GATA3+ T cells in the mesenteric lymph nodes. Zinc Oxide 39-42 forkhead box P3 Sus scrofa 91-96 34064626-6 2021 Compared to the ZnO group, the chelate-ZnO group exhibited higher proportion of T-bet+ and FoxP3+ T cells and the nano-ZnO group had higher numbers of RORgt+ and GATA3+ T cells in the mesenteric lymph nodes. Zinc Oxide 119-122 GATA binding protein 3 Sus scrofa 162-167 34064626-7 2021 ZnO group increased IL-6 and IL-8 levels in the colon tissues and these positive effects were observed in both chelate ZnO and nano-ZnO groups with lower level. Zinc Oxide 0-3 interleukin 6 Sus scrofa 20-24 34064626-7 2021 ZnO group increased IL-6 and IL-8 levels in the colon tissues and these positive effects were observed in both chelate ZnO and nano-ZnO groups with lower level. Zinc Oxide 0-3 C-X-C motif chemokine ligand 8 Sus scrofa 29-33 34064626-7 2021 ZnO group increased IL-6 and IL-8 levels in the colon tissues and these positive effects were observed in both chelate ZnO and nano-ZnO groups with lower level. Zinc Oxide 119-122 interleukin 6 Sus scrofa 20-24 34064626-7 2021 ZnO group increased IL-6 and IL-8 levels in the colon tissues and these positive effects were observed in both chelate ZnO and nano-ZnO groups with lower level. Zinc Oxide 119-122 C-X-C motif chemokine ligand 8 Sus scrofa 29-33 34064626-7 2021 ZnO group increased IL-6 and IL-8 levels in the colon tissues and these positive effects were observed in both chelate ZnO and nano-ZnO groups with lower level. Zinc Oxide 132-135 interleukin 6 Sus scrofa 20-24 34064626-7 2021 ZnO group increased IL-6 and IL-8 levels in the colon tissues and these positive effects were observed in both chelate ZnO and nano-ZnO groups with lower level. Zinc Oxide 132-135 C-X-C motif chemokine ligand 8 Sus scrofa 29-33 34318777-8 2021 The HRi composite presented a distinctive composition compared to other materials and was the only composite that showed a smaller percentage of SiO2, and also was the only composite that contained compounds, such as P2O5, ZnO, CaO, La2O3, and V2O5. Zinc Oxide 223-226 eukaryotic translation initiation factor 2 alpha kinase 1 Homo sapiens 4-7 35091950-4 2022 The formation of zinc oxide nanoparticles at different pH of the solution of coconut husk ash was confirmed through powder XRD, BET, SEM-EDX, UV-Vis, FTIR, and photoluminescence spectroscopy. Zinc Oxide 17-27 delta/notch like EGF repeat containing Homo sapiens 128-131 35272120-1 2022 In order to remove the organic pollution from water environment, Co2+-doped ZnO nanoarray photocatalyst was prepared through a hydrothermal process. Zinc Oxide 76-79 complement C2 Homo sapiens 65-68 35272120-2 2022 The influences of Co2+ doping amount and hydrothermal temperature on the nanostructure and photocatalytic performance of Co2+-doped ZnO nanoarray were discussed in detail. Zinc Oxide 132-135 complement C2 Homo sapiens 18-21 35272120-2 2022 The influences of Co2+ doping amount and hydrothermal temperature on the nanostructure and photocatalytic performance of Co2+-doped ZnO nanoarray were discussed in detail. Zinc Oxide 132-135 complement C2 Homo sapiens 121-124 35272120-3 2022 The standard ZnO structure and nanoarray morphology of Co2+-doped ZnO samples were achieved and the absorption of visible light was also realized through Co2+ doping. Zinc Oxide 13-16 complement C2 Homo sapiens 55-58 35272120-3 2022 The standard ZnO structure and nanoarray morphology of Co2+-doped ZnO samples were achieved and the absorption of visible light was also realized through Co2+ doping. Zinc Oxide 66-69 complement C2 Homo sapiens 55-58 35272120-3 2022 The standard ZnO structure and nanoarray morphology of Co2+-doped ZnO samples were achieved and the absorption of visible light was also realized through Co2+ doping. Zinc Oxide 66-69 complement C2 Homo sapiens 154-157 35272120-4 2022 The 2% Co2+-doped ZnO nanoarray prepared at 95 C exhibited excellent photocatalytic activity and could degrade 96% of methylene blue solution within 120 min under visible light. Zinc Oxide 18-21 complement C2 Homo sapiens 7-10 35107732-4 2022 Specifically, a high-efficiency photocatalyst carrier with a nanofiber structure (PAN/PU/beta-CD@Ag nanofiber membrane) was prepared by electrospinning and a simple silver plating process, and then ZnO NPs were synthesized in situ on the nanofiber membrane during the hydrothermal process. Zinc Oxide 198-201 ACD shelterin complex subunit and telomerase recruitment factor Homo sapiens 89-96 34121683-3 2021 Materials and Methods: ZnO nanoparticles were prepared by the solvothermal method and 10% bovine serum albumin was used as the dispersant. Zinc Oxide 23-26 albumin Homo sapiens 97-110 34138321-3 2021 The single-layer hollow ZHAs can not only reduce the reflection, but also widen the angle of the effective incident light and especially transfer the distribution of the optical field from the ZnO/FTO interface to the perovskite active layer confirmed by the 3D finite-difference time-domain simulation. Zinc Oxide 193-196 FTO alpha-ketoglutarate dependent dioxygenase Homo sapiens 197-200 35487015-2 2022 In this paper, we acquire a sensitive SPR biosensor based on ZnO@Au nanomaterial, and the classical sandwich strategy using biotin-streptavidin for secondary signal amplification system was used to detect human IgG (hIgG). Zinc Oxide 61-64 sepiapterin reductase Homo sapiens 38-41 35272120-5 2022 Furthermore, the as-prepared 2% Co2+-doped ZnO nanoarray still maintained 91% for removal rate after 3 cycles of photocatalytic degradation, showed good photocatalytic activity and recyclability. Zinc Oxide 43-46 complement C2 Homo sapiens 32-35 35272120-6 2022 All results indicate that ZnO nanoarray with Co2+ doping has a potential application in visible light photocatalysis for environmental protection and pollution control. Zinc Oxide 26-29 complement C2 Homo sapiens 45-48 35383422-6 2022 In contrast, the apoptotic level was significantly reduced after intervention of Drp-1 inhibitor, suggesting that ZnO NPs can induce the apoptosis of THP-1 cells by regulating mitochondrial division. Zinc Oxide 114-117 utrophin Homo sapiens 81-86 35248619-0 2022 Hierarchically porous biochar templated by in situ formed ZnO for rapid Pb2+ and Cd2+ adsorption in wastewater: Experiment and molecular dynamics study. Zinc Oxide 58-61 CD2 molecule Homo sapiens 81-84 35622663-7 2022 Moreover, analysis after triple staining (by annexin V-FITC, PI, and Hoechst) conducted at their respective IC50s revealed an apoptosis mode of cell death due to ZnO NPs, whereas CeO2-Zn nanocomposite induced a mechanism of cell death that was significantly different from apoptosis. Zinc Oxide 162-165 annexin A5 Homo sapiens 45-54 35304198-3 2022 The effect of chitosan-modified ZnO (CS-ZnO) nanoparticles content on the properties of WPU/CS-ZnO coatings and their films were systematically investigated. Zinc Oxide 32-35 citrate synthase Homo sapiens 37-39 35304198-3 2022 The effect of chitosan-modified ZnO (CS-ZnO) nanoparticles content on the properties of WPU/CS-ZnO coatings and their films were systematically investigated. Zinc Oxide 95-98 citrate synthase Homo sapiens 92-94 35304198-4 2022 The results indicated that WPU/CS-ZnO coatings displayed excellent storage stability and the particle sizes firstly decreased and then increased with CS-ZnO loading. Zinc Oxide 34-37 citrate synthase Homo sapiens 150-152 35304198-6 2022 CS-ZnO has a prominent reinforcement effect on the WPU/CS-ZnO matrix. Zinc Oxide 3-6 citrate synthase Homo sapiens 0-2 35304198-6 2022 CS-ZnO has a prominent reinforcement effect on the WPU/CS-ZnO matrix. Zinc Oxide 3-6 citrate synthase Homo sapiens 55-57 35304198-6 2022 CS-ZnO has a prominent reinforcement effect on the WPU/CS-ZnO matrix. Zinc Oxide 58-61 citrate synthase Homo sapiens 0-2 35304198-6 2022 CS-ZnO has a prominent reinforcement effect on the WPU/CS-ZnO matrix. Zinc Oxide 58-61 citrate synthase Homo sapiens 55-57 35304198-7 2022 With the addition of 2 wt% CS-ZnO, the tensile strength and Young"s modulus of the WPU/CS-ZnO2 film reached 13.4 and 112.1 MPa, 1.68 and 2.6 times over neat WPU film, respectively. Zinc Oxide 30-33 citrate synthase Homo sapiens 27-29 35304198-7 2022 With the addition of 2 wt% CS-ZnO, the tensile strength and Young"s modulus of the WPU/CS-ZnO2 film reached 13.4 and 112.1 MPa, 1.68 and 2.6 times over neat WPU film, respectively. Zinc Oxide 30-33 citrate synthase Homo sapiens 87-89 35304198-8 2022 TGA results showed that the thermal stability of WPU/CS-ZnO films improved with increased CS-ZnO content. Zinc Oxide 93-96 citrate synthase Homo sapiens 90-92 35594306-4 2022 Furthermore, we found that ZnO/MCB could influence the expression of miRNAs (miR-18a and miR-34a). Zinc Oxide 27-30 microRNA 18 Mus musculus 77-84 35594306-4 2022 Furthermore, we found that ZnO/MCB could influence the expression of miRNAs (miR-18a and miR-34a). Zinc Oxide 27-30 microRNA 34a Mus musculus 89-96 35600978-0 2023 Zinc oxide nanoparticles inhibit osteosarcoma metastasis by downregulating beta-catenin via HIF-1alpha/BNIP3/LC3B-mediated mitophagy pathway. Zinc Oxide 0-10 catenin beta 1 Homo sapiens 75-87 35600978-0 2023 Zinc oxide nanoparticles inhibit osteosarcoma metastasis by downregulating beta-catenin via HIF-1alpha/BNIP3/LC3B-mediated mitophagy pathway. Zinc Oxide 0-10 hypoxia inducible factor 1 subunit alpha Homo sapiens 92-102 35600978-0 2023 Zinc oxide nanoparticles inhibit osteosarcoma metastasis by downregulating beta-catenin via HIF-1alpha/BNIP3/LC3B-mediated mitophagy pathway. Zinc Oxide 0-10 BCL2 interacting protein 3 Homo sapiens 103-108 35600978-0 2023 Zinc oxide nanoparticles inhibit osteosarcoma metastasis by downregulating beta-catenin via HIF-1alpha/BNIP3/LC3B-mediated mitophagy pathway. Zinc Oxide 0-10 microtubule associated protein 1 light chain 3 beta Homo sapiens 109-113 35600978-6 2023 We further proved that Zn2+ released from ZnO NPs induced downregulation of beta-catenin expression via HIF-1alpha/BNIP3/LC3B-mediated mitophagy pathway. Zinc Oxide 42-45 catenin beta 1 Homo sapiens 76-88 35570560-7 2022 ZnO nanoparticles also reduced thrombin production and protein-coated GMNP nanoparticles prevented unwanted leakage of factor VIII through blood vessels. Zinc Oxide 0-3 coagulation factor II, thrombin Homo sapiens 31-39 35600978-6 2023 We further proved that Zn2+ released from ZnO NPs induced downregulation of beta-catenin expression via HIF-1alpha/BNIP3/LC3B-mediated mitophagy pathway. Zinc Oxide 42-45 hypoxia inducible factor 1 subunit alpha Homo sapiens 104-114 35600978-6 2023 We further proved that Zn2+ released from ZnO NPs induced downregulation of beta-catenin expression via HIF-1alpha/BNIP3/LC3B-mediated mitophagy pathway. Zinc Oxide 42-45 BCL2 interacting protein 3 Homo sapiens 115-120 35600978-6 2023 We further proved that Zn2+ released from ZnO NPs induced downregulation of beta-catenin expression via HIF-1alpha/BNIP3/LC3B-mediated mitophagy pathway. Zinc Oxide 42-45 microtubule associated protein 1 light chain 3 beta Homo sapiens 121-125 35600978-7 2023 ZnO NPs combined with ICG-001, a beta-catenin inhibitor, showed a synergistic inhibitory effect on OS lung metastasis and a longer survival time. Zinc Oxide 0-3 catenin beta 1 Homo sapiens 33-45 35600978-9 2023 In summary, our current study not only proved that ZnO NPs can inhibit OS metastasis by degrading beta-catenin in HIF-1alpha/BNIP3/LC3B-mediated mitophagy pathway, but also provided a far-reaching potential of ZnO NPs in clinical OS treatment with metastasis. Zinc Oxide 51-54 catenin beta 1 Homo sapiens 98-110 35600978-9 2023 In summary, our current study not only proved that ZnO NPs can inhibit OS metastasis by degrading beta-catenin in HIF-1alpha/BNIP3/LC3B-mediated mitophagy pathway, but also provided a far-reaching potential of ZnO NPs in clinical OS treatment with metastasis. Zinc Oxide 51-54 hypoxia inducible factor 1 subunit alpha Homo sapiens 114-124 35600978-9 2023 In summary, our current study not only proved that ZnO NPs can inhibit OS metastasis by degrading beta-catenin in HIF-1alpha/BNIP3/LC3B-mediated mitophagy pathway, but also provided a far-reaching potential of ZnO NPs in clinical OS treatment with metastasis. Zinc Oxide 51-54 BCL2 interacting protein 3 Homo sapiens 125-130 35600978-9 2023 In summary, our current study not only proved that ZnO NPs can inhibit OS metastasis by degrading beta-catenin in HIF-1alpha/BNIP3/LC3B-mediated mitophagy pathway, but also provided a far-reaching potential of ZnO NPs in clinical OS treatment with metastasis. Zinc Oxide 51-54 microtubule associated protein 1 light chain 3 beta Homo sapiens 131-135 35600978-9 2023 In summary, our current study not only proved that ZnO NPs can inhibit OS metastasis by degrading beta-catenin in HIF-1alpha/BNIP3/LC3B-mediated mitophagy pathway, but also provided a far-reaching potential of ZnO NPs in clinical OS treatment with metastasis. Zinc Oxide 210-213 catenin beta 1 Homo sapiens 98-110 35600978-9 2023 In summary, our current study not only proved that ZnO NPs can inhibit OS metastasis by degrading beta-catenin in HIF-1alpha/BNIP3/LC3B-mediated mitophagy pathway, but also provided a far-reaching potential of ZnO NPs in clinical OS treatment with metastasis. Zinc Oxide 210-213 hypoxia inducible factor 1 subunit alpha Homo sapiens 114-124 35600978-9 2023 In summary, our current study not only proved that ZnO NPs can inhibit OS metastasis by degrading beta-catenin in HIF-1alpha/BNIP3/LC3B-mediated mitophagy pathway, but also provided a far-reaching potential of ZnO NPs in clinical OS treatment with metastasis. Zinc Oxide 210-213 microtubule associated protein 1 light chain 3 beta Homo sapiens 131-135 35591741-0 2022 Polypyrrole Decorated Flower-like and Rod-like ZnO Composites with Improved Microwave Absorption Performance. Zinc Oxide 47-50 kinetochore associated 1 Homo sapiens 38-41 35538896-4 2022 Despite the improvement of bacterial load, WBS, Qol and NRS was evident in all 3 groups, the analysis of our results demonstrates that the application of zinc oxide bandage, directly in contact with the wound bed and/or the perilesional skin, resulted in a higher improvement and a significant reduction of WBS and bacterial load. Zinc Oxide 154-164 sphingolipid transporter 1 (putative) Homo sapiens 56-59 35586688-1 2022 Objective: To investigate the clinical effect of minocycline plus zinc oxide eugenol cement in the treatment of acute pulpitis and its effect on the levels of HIF-1alpha, Bcl-2, and tumor necrosis factor alpha. Zinc Oxide 66-76 hypoxia inducible factor 1 subunit alpha Homo sapiens 159-169 35586688-1 2022 Objective: To investigate the clinical effect of minocycline plus zinc oxide eugenol cement in the treatment of acute pulpitis and its effect on the levels of HIF-1alpha, Bcl-2, and tumor necrosis factor alpha. Zinc Oxide 66-76 BCL2 apoptosis regulator Homo sapiens 171-176 35586688-1 2022 Objective: To investigate the clinical effect of minocycline plus zinc oxide eugenol cement in the treatment of acute pulpitis and its effect on the levels of HIF-1alpha, Bcl-2, and tumor necrosis factor alpha. Zinc Oxide 66-76 tumor necrosis factor Homo sapiens 182-209 35586688-6 2022 Minocycline plus zinc oxide eugenol cement was associated with significantly lower positive rates of HIF-1alpha and Bcl-2 and lower levels of TNF-alpha versus minocycline alone (p < 0.05). Zinc Oxide 17-27 hypoxia inducible factor 1 subunit alpha Homo sapiens 101-111 35586688-6 2022 Minocycline plus zinc oxide eugenol cement was associated with significantly lower positive rates of HIF-1alpha and Bcl-2 and lower levels of TNF-alpha versus minocycline alone (p < 0.05). Zinc Oxide 17-27 BCL2 apoptosis regulator Homo sapiens 116-121 35586688-6 2022 Minocycline plus zinc oxide eugenol cement was associated with significantly lower positive rates of HIF-1alpha and Bcl-2 and lower levels of TNF-alpha versus minocycline alone (p < 0.05). Zinc Oxide 17-27 tumor necrosis factor Homo sapiens 142-151 35586688-8 2022 Conclusion: Minocycline plus zinc oxide eugenol cement offers a viable alternative for acute pulpitis as it mitigates the pain of patients, alleviates inflammatory responses, and lowers the positive rate of HIF-1alpha and Bcl-2, so it is worthy of clinical promotion. Zinc Oxide 29-39 hypoxia inducible factor 1 subunit alpha Homo sapiens 207-217 35586688-8 2022 Conclusion: Minocycline plus zinc oxide eugenol cement offers a viable alternative for acute pulpitis as it mitigates the pain of patients, alleviates inflammatory responses, and lowers the positive rate of HIF-1alpha and Bcl-2, so it is worthy of clinical promotion. Zinc Oxide 29-39 BCL2 apoptosis regulator Homo sapiens 222-227 35631863-4 2022 The effect of GO and ZnO on the morphology, hierarchical structure, and hydrophilicity of fabricated membranes was studied using a scanning electron microscope (SEM), small and ultra-small angle neutron scattering (USANS and SANS), contact angle, zeta potential, and BET (Brunauer, Emmett and Teller) surface area analysis. Zinc Oxide 21-24 USH1 protein network component sans Homo sapiens 225-229 35631863-4 2022 The effect of GO and ZnO on the morphology, hierarchical structure, and hydrophilicity of fabricated membranes was studied using a scanning electron microscope (SEM), small and ultra-small angle neutron scattering (USANS and SANS), contact angle, zeta potential, and BET (Brunauer, Emmett and Teller) surface area analysis. Zinc Oxide 21-24 delta/notch like EGF repeat containing Homo sapiens 267-270 35591741-1 2022 In this study, zinc oxide (ZnO)/polypyrrole (PPy) composites with flower- and rod-like structures were successfully fabricated by in situ polymerization and the hydrothermal method and used as microwave absorption (MWA) materials. Zinc Oxide 15-25 kinetochore associated 1 Homo sapiens 78-81 35591741-1 2022 In this study, zinc oxide (ZnO)/polypyrrole (PPy) composites with flower- and rod-like structures were successfully fabricated by in situ polymerization and the hydrothermal method and used as microwave absorption (MWA) materials. Zinc Oxide 27-30 kinetochore associated 1 Homo sapiens 78-81 35591741-4 2022 The MWA ability of flower- and rod-like ZnO/PPy composites is significantly enhanced after introduction of PPy. Zinc Oxide 40-43 kinetochore associated 1 Homo sapiens 31-34 35591741-7 2022 PPy addition and stacked structure of rod-like ZnO/PPy composites can effectively improve the dielectric properties, form multiple reflections of incident electromagnetic waves, and generate an interfacial polarization effect, resulting in improved MWA properties of composite materials. Zinc Oxide 47-50 kinetochore associated 1 Homo sapiens 38-41 35487772-1 2022 To imitate the composition of natural bone and further improve the biological property of the materials, ZnO/hydroxyapatite/chitosan-polyethylene oxide@gelatin (ZnO/HAP/CS-PEO@GEL) composite scaffolds were developed. Zinc Oxide 105-108 citrate synthase Homo sapiens 169-171 35591210-5 2022 The biosensors were fabricated by immobilizing the acetylcholinesterase (AChE) enzyme on ZnO, which is directly grown on the flexible substrates. Zinc Oxide 89-92 acetylcholinesterase (Cartwright blood group) Homo sapiens 51-71 35591210-5 2022 The biosensors were fabricated by immobilizing the acetylcholinesterase (AChE) enzyme on ZnO, which is directly grown on the flexible substrates. Zinc Oxide 89-92 acetylcholinesterase (Cartwright blood group) Homo sapiens 73-77 35352424-6 2022 Meanwhile, through in/ex-situ tests, the formation of ZnO layer on the metallic Zn surface inhibits the hydrogen evolution reactions (1.8 mmol h-1 cm-2 ) and passivation during cycling. Zinc Oxide 54-57 H1.5 linker histone, cluster member Homo sapiens 143-151 35571515-0 2022 Development of Morphologically engineered Flower-like Hafnium-Doped ZnO with Experimental and DFT Validation for Low-Temperature and Ultrasensitive Detection of NOX Gas. Zinc Oxide 68-71 gastrin Homo sapiens 165-168 35571515-3 2022 Herein, hafnium (Hf)-doped ZnO (Hf-ZnO) nanostructures are developed by the hydrothermal method for high selectivity of hazardous NOX gas in the atmosphere, substantially portraying the role of doping concentration on the enhancement of structural, optical, and sensing behavior. Zinc Oxide 27-30 gastrin Homo sapiens 134-137 35571515-4 2022 ZnO microspheres with 5% Hf doping showed excellent sensing and detected 22 parts per billion (ppb) NOX gas in the atmosphere, within 24 s, which is much faster than ZnO (90 s), and rendered superior sensing ability (S = 67) at a low temperature (100 C) compared to ZnO (S = 40). Zinc Oxide 0-3 gastrin Homo sapiens 104-107 35571515-4 2022 ZnO microspheres with 5% Hf doping showed excellent sensing and detected 22 parts per billion (ppb) NOX gas in the atmosphere, within 24 s, which is much faster than ZnO (90 s), and rendered superior sensing ability (S = 67) at a low temperature (100 C) compared to ZnO (S = 40). Zinc Oxide 267-270 gastrin Homo sapiens 104-107 35350348-4 2022 The UV-vis spectra displayed a strong absorption band spreading over a wide wavelength range, encompassing UV and visible light, with a band gap of 2.69 eV for CP1 and 2.56 eV for CP2, both of which are smaller than that of ZnO. Zinc Oxide 224-227 ceruloplasmin Homo sapiens 160-169 35533486-5 2022 The prepared ZnO/PCMT exhibits higher specific surface area (1076m2g-1) and excellent microwave absorption performance. Zinc Oxide 13-16 isoprenylcysteine carboxyl methyltransferase Homo sapiens 17-21 35533486-6 2022 With a filler loading of only 6.7wt.%, the ZnO/PCMT achieved a great electromagnetic wave absorbing performance. Zinc Oxide 43-46 isoprenylcysteine carboxyl methyltransferase Homo sapiens 47-51 35531425-0 2022 ZnO nanoparticles attenuate polymer-wear-particle induced inflammatory osteolysis by regulating the MEK-ERK-COX-2 axis. Zinc Oxide 0-3 midkine Mus musculus 100-103 35531425-0 2022 ZnO nanoparticles attenuate polymer-wear-particle induced inflammatory osteolysis by regulating the MEK-ERK-COX-2 axis. Zinc Oxide 0-3 mitogen-activated protein kinase 1 Mus musculus 104-107 35531425-0 2022 ZnO nanoparticles attenuate polymer-wear-particle induced inflammatory osteolysis by regulating the MEK-ERK-COX-2 axis. Zinc Oxide 0-3 cytochrome c oxidase II, mitochondrial Mus musculus 108-113 35531425-9 2022 Results: ZnO NPs (<=50 nm, 5 mug/mL) showed no obvious cytotoxicity and attenuated PEEK or PE particle-induced inflammation and inflammatory osteolysis by reducing MEK and ERK phosphorylation and decreasing COX-2 expression. Zinc Oxide 9-12 midkine Mus musculus 164-167 35531425-9 2022 Results: ZnO NPs (<=50 nm, 5 mug/mL) showed no obvious cytotoxicity and attenuated PEEK or PE particle-induced inflammation and inflammatory osteolysis by reducing MEK and ERK phosphorylation and decreasing COX-2 expression. Zinc Oxide 9-12 mitogen-activated protein kinase 1 Mus musculus 172-175 35531425-9 2022 Results: ZnO NPs (<=50 nm, 5 mug/mL) showed no obvious cytotoxicity and attenuated PEEK or PE particle-induced inflammation and inflammatory osteolysis by reducing MEK and ERK phosphorylation and decreasing COX-2 expression. Zinc Oxide 9-12 cytochrome c oxidase II, mitochondrial Mus musculus 207-212 35531425-10 2022 Conclusion: ZnO NPs (<=50 nm, 5 mug/mL) attenuated polymer wear particle-induced inflammation via regulation of the MEK-ERK-COX-2 axis. Zinc Oxide 12-15 midkine Mus musculus 116-119 35531425-10 2022 Conclusion: ZnO NPs (<=50 nm, 5 mug/mL) attenuated polymer wear particle-induced inflammation via regulation of the MEK-ERK-COX-2 axis. Zinc Oxide 12-15 mitogen-activated protein kinase 1 Mus musculus 120-123 35531425-10 2022 Conclusion: ZnO NPs (<=50 nm, 5 mug/mL) attenuated polymer wear particle-induced inflammation via regulation of the MEK-ERK-COX-2 axis. Zinc Oxide 12-15 cytochrome c oxidase II, mitochondrial Mus musculus 124-129 35364806-9 2022 Furthermore, the findings implied that the elevated level of TNF-alpha may link with ZnO NPs-mediated apoptosis in the liver of rats. Zinc Oxide 85-88 tumor necrosis factor Rattus norvegicus 61-70 35368896-0 2022 Zinc Oxide Nanoparticle Inhibits Tumorigenesis of Renal Cell Carcinoma by Modulating Lipid Metabolism Targeting miR-454-3p to Repressing Metabolism Enzyme ACSL4. Zinc Oxide 0-10 acyl-CoA synthetase long chain family member 4 Homo sapiens 155-160 35230806-5 2022 In particular, AZO/PAP(P1.0D0.5) possesses an average HT of over 11% at the wavelength range of 600-850 nm and an angular intensity distribution of over 1.5% at an azimuthal angle of around 55 , indicating stronger far-field scattering than the conventional pyramid-textured B-doped ZnO (BZO/F). Zinc Oxide 283-286 poly(A) polymerase alpha Homo sapiens 15-22 35458329-4 2022 This surface functionalization of zinc oxide nanoparticles (ZnO-NPs-GPTMS) was experimentally confirmed by infrared spectroscopy (FT-IR), TGA, and XRD, and its morphological characterization was performed with SEM. Zinc Oxide 34-44 T-box transcription factor 1 Homo sapiens 138-141 35331238-6 2022 The experiments showed that ZnO/Ag nanoparticles could exhibit a self-therapeutic effect that was attributed to reducing innate cytokine profiles by inactivating p65 in proinflammatory macrophages and abrogating secretion of adaptive cytokines in KCs by downregulating ROS-mediated STAT3-cyclin D1 signaling. Zinc Oxide 28-31 v-rel reticuloendotheliosis viral oncogene homolog A (avian) Mus musculus 162-165 35331238-6 2022 The experiments showed that ZnO/Ag nanoparticles could exhibit a self-therapeutic effect that was attributed to reducing innate cytokine profiles by inactivating p65 in proinflammatory macrophages and abrogating secretion of adaptive cytokines in KCs by downregulating ROS-mediated STAT3-cyclin D1 signaling. Zinc Oxide 28-31 signal transducer and activator of transcription 3 Mus musculus 282-287 35331238-6 2022 The experiments showed that ZnO/Ag nanoparticles could exhibit a self-therapeutic effect that was attributed to reducing innate cytokine profiles by inactivating p65 in proinflammatory macrophages and abrogating secretion of adaptive cytokines in KCs by downregulating ROS-mediated STAT3-cyclin D1 signaling. Zinc Oxide 28-31 cyclin D1 Mus musculus 288-297 35230806-2 2022 This paper studies the effect of the interface morphology of the hole array pattern (HAP) and the pillar array pattern (PAP) on the far-field scattering properties of OR-PF substrates fabricated by spin-coating Al-doped ZnO (AZO) on nanoimprint-patterned glasses for improving the performance of superstrate-type thin-film solar cells. Zinc Oxide 220-223 poly(A) polymerase alpha Homo sapiens 120-123 35350348-4 2022 The UV-vis spectra displayed a strong absorption band spreading over a wide wavelength range, encompassing UV and visible light, with a band gap of 2.69 eV for CP1 and 2.56 eV for CP2, both of which are smaller than that of ZnO. Zinc Oxide 224-227 ceruloplasmin Homo sapiens 180-183 35269073-5 2022 The results showed that the sample doped with zinc oxide (ZnO) recorded the highest density (rhoglass), molar polarizability (alpham), molar refraction (Rm), refractive index (n), and third-order nonlinear optical susceptibility (chi3) and the lowest optical energy gap (Eopt) among the samples under investigation. Zinc Oxide 46-56 chitinase 1 Homo sapiens 230-234 35108020-0 2022 Coherent Spin Preparation of Indium Donor Qubits in Single ZnO Nanowires. Zinc Oxide 59-62 spindlin 1 Homo sapiens 9-13 35108020-2 2022 Utilizing the indium donor, we show that favorable donor-bound exciton optical and electron spin properties are retained in isolated ZnO nanowires. Zinc Oxide 133-136 spindlin 1 Homo sapiens 92-96 35323440-0 2022 Reverse Electrochemical Sensing of FLT3-ITD Mutations in Acute Myeloid Leukemia Using Gold Sputtered ZnO-Nanorod Configured DNA Biosensors. Zinc Oxide 101-104 fms related receptor tyrosine kinase 3 Homo sapiens 35-39 35269073-5 2022 The results showed that the sample doped with zinc oxide (ZnO) recorded the highest density (rhoglass), molar polarizability (alpham), molar refraction (Rm), refractive index (n), and third-order nonlinear optical susceptibility (chi3) and the lowest optical energy gap (Eopt) among the samples under investigation. Zinc Oxide 58-61 chitinase 1 Homo sapiens 230-234 35218495-4 2022 Here, six hybrids of functionalized bio-silica and ZnO were synthesized and characterized by FT-IR, XRD, SEM/EDX, BET/BJH, and UV-Vis spectroscopy. Zinc Oxide 51-54 delta/notch like EGF repeat containing Homo sapiens 114-117 35064776-4 2022 RESULTS: In the Vit B6 group, a decrease in feed intake (FI), egg production (EP), albumin, Zn, Fe and Mg, and an increase in triglyceride and insulin in HSC were observed, in addition to a decrease in cholesterol and an increase in egg weight (EW) in NC. Zinc Oxide 92-94 vitrin Gallus gallus 16-19 35064776-8 2022 Increased insulin and decreased glutathione peroxidase activity were detected with the Vit B6+Zn compared to feeding either Vit B6 or Zn in HSC. Zinc Oxide 94-96 insulin Gallus gallus 10-17 35064776-8 2022 Increased insulin and decreased glutathione peroxidase activity were detected with the Vit B6+Zn compared to feeding either Vit B6 or Zn in HSC. Zinc Oxide 94-96 vitrin Gallus gallus 87-90 35147029-4 2022 The lateral synaptic diode is based on a p-n junction of an organic semiconductor (OSC) and amorphous In-Ga-Zn-O, in which the upper OSC layer can directly interact with the gas molecules in the atmosphere. Zinc Oxide 108-112 gastrin Homo sapiens 174-177 35044769-3 2022 We, herein, demonstrated an extremely simple but extraordinary effective strategy to boost PEC water splitting in a three-dimensional (3D) network structure (Ni foam, i.e., NF)-supported ZnO nanowire (NW)/CdS nanoparticle (NP) (NF/ZnO/CdS) photoelectrode. Zinc Oxide 187-190 neurofascin Homo sapiens 173-175 35371543-3 2022 In one mol-ecule, the metal atom is in a distorted trigonal-bipyramidal ZnN2O3 environment (tau5 = 0.192) with a long bond to an ether O donor atom (Zn-O = 2.727 (6) A). Zinc Oxide 149-153 microtubule associated protein tau Homo sapiens 92-95 35044769-3 2022 We, herein, demonstrated an extremely simple but extraordinary effective strategy to boost PEC water splitting in a three-dimensional (3D) network structure (Ni foam, i.e., NF)-supported ZnO nanowire (NW)/CdS nanoparticle (NP) (NF/ZnO/CdS) photoelectrode. Zinc Oxide 187-190 neurofascin Homo sapiens 228-230 35044769-3 2022 We, herein, demonstrated an extremely simple but extraordinary effective strategy to boost PEC water splitting in a three-dimensional (3D) network structure (Ni foam, i.e., NF)-supported ZnO nanowire (NW)/CdS nanoparticle (NP) (NF/ZnO/CdS) photoelectrode. Zinc Oxide 231-234 neurofascin Homo sapiens 173-175 35044769-3 2022 We, herein, demonstrated an extremely simple but extraordinary effective strategy to boost PEC water splitting in a three-dimensional (3D) network structure (Ni foam, i.e., NF)-supported ZnO nanowire (NW)/CdS nanoparticle (NP) (NF/ZnO/CdS) photoelectrode. Zinc Oxide 231-234 neurofascin Homo sapiens 228-230 35044769-6 2022 This real-time self-built PE polarization, assisted by the heteroband junction, enables the NF/ZnO/CdS photoanode system to obtain an improved photocurrent density by 12.2-fold compared with pure ZnO (at 1.23 V vs RHE). Zinc Oxide 95-98 neurofascin Homo sapiens 92-94 35044769-6 2022 This real-time self-built PE polarization, assisted by the heteroband junction, enables the NF/ZnO/CdS photoanode system to obtain an improved photocurrent density by 12.2-fold compared with pure ZnO (at 1.23 V vs RHE). Zinc Oxide 196-199 neurofascin Homo sapiens 92-94 35160376-8 2022 Based on the results of the investigated organic catalytic reactions, the prepared CS/ZnO nanocomposite film (20 wt.%) could be a viable an effective, recyclable, and heterogeneous base catalyst in the synthesis of thiazoles. Zinc Oxide 86-89 citrate synthase Homo sapiens 83-85 35207032-8 2022 ZnO/PVDF membrane recorded excellent bovine serum albumin (BSA) rejection at 93.4% +- 0.4 with flux recovery rate at 70.9% +- 2.1. Zinc Oxide 0-3 albumin Homo sapiens 44-57 34959229-1 2022 In this work, a novel antibacterial nanocomposite system was developed using mesoporous silica (MSN) as an effective nanocarrier, and the resultant nanocomposites demonstrated remarkable antibacterial performance due to the synergistic effect among nano zinc oxides, silver nanoparticles, and polydopamine (PDA). Zinc Oxide 254-265 moesin Homo sapiens 96-99 34959229-2 2022 The successful synthesis of MSN/ZnO@PDA/Ag nanocomposites was confirmed. Zinc Oxide 32-35 moesin Homo sapiens 28-31 35425191-4 2022 Albumin-grafted, polycaprolactone-coated, zinc oxide-loaded cloxacillin (APCL-CLOX-ZnO) nanoparticles with a diameter of 85-110 nm were obtained via a coaxial electrospray technique. Zinc Oxide 42-52 APC regulator of WNT signaling pathway 2 Homo sapiens 73-77 35425191-4 2022 Albumin-grafted, polycaprolactone-coated, zinc oxide-loaded cloxacillin (APCL-CLOX-ZnO) nanoparticles with a diameter of 85-110 nm were obtained via a coaxial electrospray technique. Zinc Oxide 42-52 cut like homeobox 1 Homo sapiens 78-82 35527148-6 2022 Western blotting assay analysis showed that ZnO-EGCG@H downregulated trauma inflammatory factors (TNF-alpha, IL-6) by 46.9% and 57%, respectively, while upregulating 1.7-fold VEGF and 2-fold EGF, accelerating wound healing by reducing inflammatory response and promoting proliferation of vascular endothelial cells and skin epidermal cells. Zinc Oxide 44-47 tumor necrosis factor Rattus norvegicus 98-107 34983566-0 2022 Skin damage induced by zinc oxide nanoparticles combined with UVB is mediated by activating cell pyroptosis via the NLRP3 inflammasome-autophagy-exosomal pathway. Zinc Oxide 23-33 NLR family pyrin domain containing 3 Homo sapiens 116-121 35527148-6 2022 Western blotting assay analysis showed that ZnO-EGCG@H downregulated trauma inflammatory factors (TNF-alpha, IL-6) by 46.9% and 57%, respectively, while upregulating 1.7-fold VEGF and 2-fold EGF, accelerating wound healing by reducing inflammatory response and promoting proliferation of vascular endothelial cells and skin epidermal cells. Zinc Oxide 44-47 interleukin 6 Rattus norvegicus 109-113 35527148-6 2022 Western blotting assay analysis showed that ZnO-EGCG@H downregulated trauma inflammatory factors (TNF-alpha, IL-6) by 46.9% and 57%, respectively, while upregulating 1.7-fold VEGF and 2-fold EGF, accelerating wound healing by reducing inflammatory response and promoting proliferation of vascular endothelial cells and skin epidermal cells. Zinc Oxide 44-47 vascular endothelial growth factor A Rattus norvegicus 175-185 34762320-3 2022 Here, a binary blend is employed of CQDs and ZnO nanocrystals in order to passivate the in-gap trap states of PbS-CQD gain medium. Zinc Oxide 45-48 TRAP Homo sapiens 95-99 34419959-9 2022 Results also showed a marked inhibition of the JAK/STAT pathway by ZnO nanoparticles; confirmed by downregulation of Mcl-1 and Bcl-XL expression. Zinc Oxide 67-70 Janus kinase 2 Homo sapiens 47-50 34419959-9 2022 Results also showed a marked inhibition of the JAK/STAT pathway by ZnO nanoparticles; confirmed by downregulation of Mcl-1 and Bcl-XL expression. Zinc Oxide 67-70 BCL2 like 1 Homo sapiens 127-133 34419959-10 2022 The present data demonstrated that ZnO nanofluids could combat breast CSCs via decreasing stemness markers, stimulating apoptosis, and suppressing JAK/STAT activity. Zinc Oxide 35-38 Janus kinase 2 Homo sapiens 147-150 35099326-12 2022 In addition, high concentration of ZnO NPs inhibited the proliferation of HGF-1 by regulating the expression of MDM2 and p53. Zinc Oxide 35-38 transformed mouse 3T3 cell double minute 2 Mus musculus 112-116 35099326-12 2022 In addition, high concentration of ZnO NPs inhibited the proliferation of HGF-1 by regulating the expression of MDM2 and p53. Zinc Oxide 35-38 transformation related protein 53, pseudogene Mus musculus 121-124 35104992-3 2022 This paper presents the development and the first neutron imaging results of a neutron flat-panel detector (nFPD) based on an In-Ga-Zn-O (IGZO) thin-film transistor (TFT)/photodiode array coupled with a LiF/ZnS scintillator sheet. Zinc Oxide 132-136 LIF interleukin 6 family cytokine Homo sapiens 203-206