PMID-sentid Pub_year Sent_text compound_name comp_offset prot_official_name organism prot_offset 33776968-0 2021 Biotransformation of Methane and Carbon Dioxide Into High-Value Products by Methanotrophs: Current State of Art and Future Prospects. Methane 21-28 artemin Homo sapiens 108-111 18188238-0 1997 Precise frequency-difference measurement between the 1.66-mum transitions of methane. Methane 77-84 latexin Homo sapiens 58-61 21639359-5 1997 Tip diameters were down to 20 mum, enabling us to study methane distribution on a microscale. Methane 56-63 latexin Homo sapiens 30-33 8877703-2 1996 The results of a series of molecular dynamics simulations of methane in SPC/E water at different temperatures are reported. Methane 61-68 proline rich protein gene cluster Homo sapiens 72-75 15091518-4 1995 RP-HPLC analyses of aqueous samples show that the culture MM1 expresses the capability of C(11)LAS transformation in the presence or absence of methane. Methane 144-151 prefoldin subunit 5 Homo sapiens 58-61 15091518-7 1995 Comparable affinity of culture MM1 for both methane and C(11)LAS ( [Formula: see text], respectively), and more than four times higher maximum transformation rate for methane than for C(11)LAS ( [Formula: see text] (dry weight) cells day(-1), respectively), were determined. Methane 44-51 prefoldin subunit 5 Homo sapiens 31-34 24226516-1 1994 The transition state (TS) for loss of CH4 from protonated acetaldehyde has been located at the second-order Moller-Plesset (MP2)/6-31G(d, p) level of theory. Methane 38-41 tryptase pseudogene 1 Homo sapiens 124-127 1321105-4 1992 The detection limit for a 10,000 min counting time in a 10 mL counter containing the krypton (15 microL) and methane as counting gas corresponds to 25 mBq 85Kr per mL (STP) krypton or 2.5% of the mean atmospheric 85Kr activity concentration in the year 1990. Methane 109-116 thyroid hormone receptor interactor 10 Homo sapiens 168-171 11538398-9 1992 These studies show that acetylenic hydrocarbons formed by the photolysis of methane in the stratosphere of Jupiter may react with radicals formed by NH3 photolysis to give nonvolatile yellow-brown polymers, dialkylazines, alkylnitriles, and eventually HCN. Methane 76-83 metastasis associated lung adenocarcinoma transcript 1 Homo sapiens 252-255 33970624-0 2021 Spectroscopic Definition of a Highly Reactive Site in Cu-CHA for Selective Methane Oxidation: Tuning a Mono-mu-Oxo Dicopper(II) Active Site for Reactivity. Methane 75-82 transcription factor like 5 Homo sapiens 57-60 33970624-1 2021 Using UV-vis and resonance Raman spectroscopy, we identify a [Cu2O]2+ active site in O2 and N2O activated Cu-CHA that reacts with methane to form methanol at low temperature. Methane 130-137 transcription factor like 5 Homo sapiens 109-112 11667170-0 1996 The Role of Spin-Orbit Coupling and Symmetry in Oxadi-pi-methane Rearrangements and Some Related Photochemical Reactions. Methane 57-64 spindlin 1 Homo sapiens 12-16 8831906-1 1996 A new polymorphic form of glutathione S-transferase (GST), metabolising monohalogenated methanes, ethylene oxide and dichloromethane, has been purified from human erythrocytes and characterized. Methane 88-96 glutathione S-transferase kappa 1 Homo sapiens 26-51 8831906-1 1996 A new polymorphic form of glutathione S-transferase (GST), metabolising monohalogenated methanes, ethylene oxide and dichloromethane, has been purified from human erythrocytes and characterized. Methane 88-96 glutathione S-transferase kappa 1 Homo sapiens 53-56 21037787-1 1995 The effect of source (LED) noise on the sensitivity of fiber-optic methane sensors is discussed. Methane 67-74 small integral membrane protein 10 like 2A Homo sapiens 22-25 16534930-5 1995 Methane oxidation potentials were greatest where the vertical profiles of O(inf2) and CH(inf4) overlapped. Methane 0-7 inverted formin 2 Homo sapiens 76-80 8425445-7 1993 These data demonstrate that lactase-deficient children manifest significant increases in breath methane excretion following lactose ingestion and that enhanced methane production may be a consequence of several factors, including altered fecal pH and increased methanogenic substrates provided by colonic lactose fermentation. Methane 96-103 lactase Homo sapiens 28-35 2035644-2 1991 In the six CH4 producers, excess volumes of H2 excreted in breath were 73.4 +/- 11.9 and 35.1 +/- 14.1 (SE) ml/8 h (P less than 0.05) in response to right and left colonic infusion of mucin, respectively; excess volumes of CH4 were, respectively, 6.7 +/- 1.7 and 38.9 +/- 11.1 ml/8 h (P less than 0.05). Methane 11-14 LOC100508689 Homo sapiens 184-189 2001359-1 1991 In an earlier publication, we reported that corrinoids catalyze the sequential reduction of CCl4 to CHCl3, CH2Cl2, CH3Cl, and CH4 with titanium(III) citrate as electron donor [Krone, U. E., Thauer, R. K., & Hogenkamp, H. P. C. (1989) Biochemistry 28, 4908-4914]. Methane 126-129 C-C motif chemokine ligand 4 Homo sapiens 92-96 2178390-5 1990 With one exception, pasta meals that were completely absorbed were ingested by methane producers. Methane 79-86 solute carrier family 45 member 1 Homo sapiens 20-25 32797897-6 2020 Due to the synergistic effect between the functional groups of doped carbon dots, Sil-Glc-NCDs column showed enhanced separation selectivity compared with previous non-doped Sil-Glc-CDs column. Methane 69-80 STIL centriolar assembly protein Homo sapiens 82-85 33587606-4 2021 For production regions with few to no new wells being brought to production, and existing wells having reached a mature stage, as in the Barnett Shale production region in north central Texas, the methane emission intensity gradually increases, as natural gas production decreases faster than emissions decrease, following the general pattern exhibited by individual wells. Methane 197-204 gastrin Homo sapiens 256-259 33587606-0 2021 Projecting the Temporal Evolution of Methane Emissions from Oil and Gas Production Basins. Methane 37-44 gastrin Homo sapiens 68-71 33587606-1 2021 The methane emission intensity (methane emitted/gas produced or methane emitted/methane produced) of individual unconventional oil and gas production sites in the United States has a characteristic temporal behavior, exhibiting a brief period of decrease followed by a steady increase, with intensities after 10 years of production reaching levels that are 2-10 times the 10 year production-weighted average. Methane 4-11 gastrin Homo sapiens 48-51 33587606-1 2021 The methane emission intensity (methane emitted/gas produced or methane emitted/methane produced) of individual unconventional oil and gas production sites in the United States has a characteristic temporal behavior, exhibiting a brief period of decrease followed by a steady increase, with intensities after 10 years of production reaching levels that are 2-10 times the 10 year production-weighted average. Methane 4-11 gastrin Homo sapiens 135-138 32797897-6 2020 Due to the synergistic effect between the functional groups of doped carbon dots, Sil-Glc-NCDs column showed enhanced separation selectivity compared with previous non-doped Sil-Glc-CDs column. Methane 69-80 STIL centriolar assembly protein Homo sapiens 174-177 32797901-1 2020 We designed a simple, portable, low-cost and low-weight nondispersive infrared (NDIR) spectroscopy-based system for continuous remote sensing of atmospheric methane (CH4) with rapidly pulsed near-infrared light emitting diodes (NIR LED) at 1.65 mum. Methane 157-164 COP9 signalosome subunit 4 Drosophila melanogaster 166-169 34742147-4 2022 When the background gas is pure nitrogen and a mixture of nitrogen and carbon dioxide, the recovery effect of this method on methane is both close to the theoretical value when the background gas is air. Methane 125-132 gastrin Homo sapiens 20-23 31590051-0 2019 Multi-stimuli responsive mesoporous carbon nano-platform gated by human serum albumin for cancer thermo-chemotherapy. Methane 25-42 albumin Mus musculus 72-85 34627914-2 2022 CHOP(S) sites account for over 40% of all reported vented methane (CH4) from oil production in Alberta, and high rates of CH4 emissions have been confirmed in independent measurement studies. Methane 58-65 DNA damage inducible transcript 3 Homo sapiens 0-4 34627914-2 2022 CHOP(S) sites account for over 40% of all reported vented methane (CH4) from oil production in Alberta, and high rates of CH4 emissions have been confirmed in independent measurement studies. Methane 67-70 DNA damage inducible transcript 3 Homo sapiens 0-4 34627914-2 2022 CHOP(S) sites account for over 40% of all reported vented methane (CH4) from oil production in Alberta, and high rates of CH4 emissions have been confirmed in independent measurement studies. Methane 122-125 DNA damage inducible transcript 3 Homo sapiens 0-4 34627914-3 2022 In this study, we used truck-based surveys coupled with qualitative optical gas imaging (OGI) to quantify and characterize methane emission rates and sources at nearly 1350 and 940 well sites in two major CHOP(S) developments respectively in 2016 and 2018. Methane 123-130 DNA damage inducible transcript 3 Homo sapiens 205-209 34742147-4 2022 When the background gas is pure nitrogen and a mixture of nitrogen and carbon dioxide, the recovery effect of this method on methane is both close to the theoretical value when the background gas is air. Methane 125-132 gastrin Homo sapiens 192-195 34794579-2 2021 In this study, we describe the development of a reliable and novel fluorescent assay for ALP detection based on chitosan carbon dots (C-CDs, peak emission, 412 nm) and calcein (peak emission, 512 nm). Methane 121-132 alkaline phosphatase, placental Homo sapiens 89-92 34826564-1 2022 Syngas from pyrolysis/gasification process is a mixture of CO, CO2 and H2, which could be bio-converted to CH4, so called syngas biomethanation. Methane 107-110 complement C2 Homo sapiens 63-73 34962379-4 2022 TPA-DPA PPK is a metal-free catalyst for visible-light-driven CO2 photoreduction to CH4, which can be used as a solar fuel in the absence of any cocatalyst and sacrificial agent. Methane 84-87 kallikrein B1 Homo sapiens 8-11 34715343-3 2022 The results showed that the methane yields were increased by 11.54%~25.29% compared with the control group(CK), and the maximum cumulative methane production reached to 254.36 mL g-VS-1 when the H2-NBW addition was of 60%. Methane 28-35 cytidine/uridine monophosphate kinase 1 Homo sapiens 107-109 34715343-3 2022 The results showed that the methane yields were increased by 11.54%~25.29% compared with the control group(CK), and the maximum cumulative methane production reached to 254.36 mL g-VS-1 when the H2-NBW addition was of 60%. Methane 139-146 cytidine/uridine monophosphate kinase 1 Homo sapiens 107-109 34668284-3 2022 Among them, at -1.4 V, the L1.9C delivers the optimal activity (51.3 mA cm-2) and selectivity (41.5%) for C2+, comparable to or better than those of most reported Cu-based oxides, while the L1.7C exhibits the best activity (25.1 mA cm-2) and selectivity (22.1%) for CH4. Methane 266-269 immunoglobulin kappa variable 1-12 Homo sapiens 27-31 34798250-1 2022 To improve the efficiency of methane production from chicken manure (CM) anaerobic digestion, the mechanism of coal slime (CS) as an additive on methane production characteristics were investigated. Methane 29-36 citrate synthase Gallus gallus 123-125 34798250-1 2022 To improve the efficiency of methane production from chicken manure (CM) anaerobic digestion, the mechanism of coal slime (CS) as an additive on methane production characteristics were investigated. Methane 145-152 citrate synthase Gallus gallus 123-125 34798250-2 2022 The results showed that adding an appropriate amount of CS quickened the start of the fermentation and effectively increased the methane yield. Methane 129-136 citrate synthase Gallus gallus 56-58 34798250-6 2022 In addition, the reduction of CO2 was the main methanogenic pathway, and adding CS raised the abundance of genes for key enzymes in metabolic pathways during methane metabolism. Methane 158-165 citrate synthase Gallus gallus 80-82 34793119-2 2021 We herein report the use of microfluidically generated microgels containing VEGF-conjugated fluorescent carbon dots (CDs) (VEGF-CDs), a gelatin-phenol conjugate, and silk fibroin for imaging-monitored tracking of VEGF delivery to ischemic muscles. Methane 104-115 vascular endothelial growth factor A Gallus gallus 76-80 34793119-2 2021 We herein report the use of microfluidically generated microgels containing VEGF-conjugated fluorescent carbon dots (CDs) (VEGF-CDs), a gelatin-phenol conjugate, and silk fibroin for imaging-monitored tracking of VEGF delivery to ischemic muscles. Methane 104-115 vascular endothelial growth factor A Gallus gallus 123-127 34793119-2 2021 We herein report the use of microfluidically generated microgels containing VEGF-conjugated fluorescent carbon dots (CDs) (VEGF-CDs), a gelatin-phenol conjugate, and silk fibroin for imaging-monitored tracking of VEGF delivery to ischemic muscles. Methane 104-115 vascular endothelial growth factor A Gallus gallus 213-217 34783524-3 2021 Here, the chiral carbon dots (CDs)-glucose oxidase (GOx) nanoreactors named LGOx and DGOx were constructed by the coassembly of GOx with L/D-CDs, respectively. Methane 17-28 hydroxyacid oxidase 1 Homo sapiens 52-55 34945944-5 2021 The developed theory was used to explain the phenomenon of the self-acceleration of gas-dust outbursts in coal mines during the explosive opening of methane traps. Methane 149-156 gastrin Homo sapiens 84-87 34945944-6 2021 The results also explained the mechanisms of generating significant amounts of methane and the formation of coal nanoparticles in gas-dust outbursts. Methane 79-86 gastrin Homo sapiens 130-133 34783524-3 2021 Here, the chiral carbon dots (CDs)-glucose oxidase (GOx) nanoreactors named LGOx and DGOx were constructed by the coassembly of GOx with L/D-CDs, respectively. Methane 17-28 hydroxyacid oxidase 1 Homo sapiens 128-131 34926924-0 2021 Noncatalytic Oxidative Coupling of Methane (OCM): Gas-Phase Reactions in a Jet Stirred Reactor (JSR). Methane 35-42 PAXIP1 associated glutamate rich protein 1 Homo sapiens 50-53 34926924-6 2021 Simulations of different gas-phase models related to methane oxidation were implemented and compared against the experimental data. Methane 53-60 PAXIP1 associated glutamate rich protein 1 Homo sapiens 25-28 34946025-5 2021 Functional genes for methane-oxidation (prmAC, mimBD, adh, gfa, fdh) were identified. Methane 21-28 alcohol dehydrogenase 1A (class I), alpha polypeptide Homo sapiens 54-57 34946025-5 2021 Functional genes for methane-oxidation (prmAC, mimBD, adh, gfa, fdh) were identified. Methane 21-28 glutamine--fructose-6-phosphate transaminase 1 Homo sapiens 59-62 34946025-5 2021 Functional genes for methane-oxidation (prmAC, mimBD, adh, gfa, fdh) were identified. Methane 21-28 alcohol dehydrogenase 5 (class III), chi polypeptide Homo sapiens 64-67 34730482-8 2021 The inclusion of TR and TL decreased the production of methane. Methane 55-62 coagulation factor II thrombin receptor Homo sapiens 17-19 34388552-7 2021 In addition, using the strain LZ-G1 bioaugmented Cd2+-containing plant residues and cow manure mixed AD system, the system"s biogas and methane production significantly increased (98.97 % and 142.03 %, respectively). Methane 136-143 CD2 molecule Bos taurus 49-52 34775758-5 2021 ppb-Level Raman gas sensing at atmospheric pressure for several typical explosive gases and toxic gases in ambient air, including hydrogen (H2), methane (CH4), carbon monoxide (CO), hydrogen sulfide (H2S), and chlorine (Cl2), is achieved at 300 s exposure time. Methane 145-152 gastrin Homo sapiens 16-19 34775758-5 2021 ppb-Level Raman gas sensing at atmospheric pressure for several typical explosive gases and toxic gases in ambient air, including hydrogen (H2), methane (CH4), carbon monoxide (CO), hydrogen sulfide (H2S), and chlorine (Cl2), is achieved at 300 s exposure time. Methane 154-157 gastrin Homo sapiens 16-19 34841132-9 2021 The complexity of the pore surface, D 1, and specific surface area have a positive correlation, and with the increase of pore surface complexity, methane adsorption capacity could be significantly improved. Methane 146-153 leiomodin 1 Homo sapiens 36-39 34841132-10 2021 Therefore, D 1 may be used as a characterization parameter of CH4 adsorption capacity, which could provide some evidence to further clarify the adsorption mechanism of shale gas. Methane 62-65 leiomodin 1 Homo sapiens 11-14 34358988-4 2021 According to the results of the multiple linear regression analysis performed on the experimental data, the 79% variation of the soluble COD in the MS was the driving factor for the 38% increase of biogas and methane yields. Methane 209-216 small nuclear ribonucleoprotein polypeptides B and B1 Homo sapiens 137-140 34832062-8 2021 The model has been validated using literature data on mixed-gas separation of n-butane/methane and propylene/propane through polymeric membranes. Methane 87-94 gastrin Homo sapiens 60-63 34087019-10 2021 Among them, dimethylamine and isopropanol were strongly associated with methane and propanoate metabolism respectively in AD with FLG mutations (FDR-adjusted P < 0.01). Methane 72-79 filaggrin Homo sapiens 130-133 34658236-4 2021 We found that as the incident velocity of CH4 and CD4 increases, the sticking probabilities for both molecules on a CH4 condensed film decrease systematically, but that preferential sticking and condensation occur for CD4. Methane 42-45 CD4 molecule Homo sapiens 218-221 34658236-4 2021 We found that as the incident velocity of CH4 and CD4 increases, the sticking probabilities for both molecules on a CH4 condensed film decrease systematically, but that preferential sticking and condensation occur for CD4. Methane 116-119 CD4 molecule Homo sapiens 50-53 34658236-8 2021 We propose that enhanced multi-phonon interactions and inelastic cross sections between the incident CD4 projectile and the CH4 film allow for more efficacious gas-surface energy transfer. Methane 124-127 CD4 molecule Homo sapiens 101-104 34658236-8 2021 We propose that enhanced multi-phonon interactions and inelastic cross sections between the incident CD4 projectile and the CH4 film allow for more efficacious gas-surface energy transfer. Methane 124-127 gastrin Homo sapiens 160-163 34651161-6 2021 Temperature programmed reaction analysis shows that at temperatures higher than 530 K, a two-fold increase in the production of H2, CH4 and C2H6 is observed for Pt/beta-Mo2C as compared to beta-Mo2C, suggesting a higher catalytic activity for the Pt-containing carbide than for the pristine catalyst. Methane 132-135 pre T cell antigen receptor alpha Homo sapiens 161-168 34139563-2 2021 Results showed that compared with CK, the total methane emissions ofC, B1, B1C, B2, and B2C treatments declined by 16.4%, 25.2%, 45.4%, 7.8%, and 44.4%, respectively. Methane 48-55 membrane spanning 4-domains A1 Homo sapiens 71-82 34537657-1 2021 In order to make up for the deficiencies of traditional C18 column for separating strong polar compounds, combined with the good hydrophilicity of carbon dots (CDs), novel octadecylamine-derived CDs denoted as C18-CDs are designed, synthesized and applied in RPLC/HILIC mixed-mode chromatography with good separation performance towards both hydrophobic and hydrophilic compounds. Methane 147-158 Bardet-Biedl syndrome 9 Homo sapiens 210-213 34647205-0 2022 NO3- is an important driver of nitrite-dependent anaerobic methane oxidation bacteria and CH4 fluxes in the reservoir riparian zone. Methane 59-66 NBL1, DAN family BMP antagonist Homo sapiens 0-3 34647205-0 2022 NO3- is an important driver of nitrite-dependent anaerobic methane oxidation bacteria and CH4 fluxes in the reservoir riparian zone. Methane 90-93 NBL1, DAN family BMP antagonist Homo sapiens 0-3 34647205-7 2022 Under the influence of three different land use types, the increase in NO3- (grassland vs. woodland and sparse woods, + 132.81% and + 106.25%) caused structural changes in the composition of the N-DAMO bacterial community, increasing its abundance (- 9.58% and + 21.19%), thus promoting the oxidation of CH4 and reduced CH4 emissions (+ 4.78% and + 35.63%) from the riparian zone. Methane 304-307 NBL1, DAN family BMP antagonist Homo sapiens 71-74 34647205-7 2022 Under the influence of three different land use types, the increase in NO3- (grassland vs. woodland and sparse woods, + 132.81% and + 106.25%) caused structural changes in the composition of the N-DAMO bacterial community, increasing its abundance (- 9.58% and + 21.19%), thus promoting the oxidation of CH4 and reduced CH4 emissions (+ 4.78% and + 35.63%) from the riparian zone. Methane 320-323 NBL1, DAN family BMP antagonist Homo sapiens 71-74 34647205-8 2022 Appropriate NO3- input helps maintain the existing low methane emission fluxes in the riparian zone of the reservoir. Methane 55-62 NBL1, DAN family BMP antagonist Homo sapiens 12-15 34641573-0 2021 The Reactive Sites of Methane Activation: A Comparison of IrC3+ with PtC3. Methane 22-29 nuclear receptor coactivator 4 Homo sapiens 69-73 34087545-4 2021 In this study, through a combination of the advantages exhibited by ordered mesoporous carbon (OMC)@gold nanoparticles (AuNPs) composites and AuPt-methylene blue (AuPt-MB), a disposable ultrasensitive sandwich-configuration electrochemical immunosensor for determination of AFP was designed. Methane 76-93 alpha fetoprotein Homo sapiens 274-277 34274589-4 2021 The results showed that a 60% increase in the mixing rate of the system (from 50% to 80%) in the wastewater with concentration of 14,549 (mgl-1) increased the methane production rate by about 35% and increased the power consumption of the system by about 13 times. Methane 159-166 LLGL scribble cell polarity complex component 1 Homo sapiens 138-143 34500180-1 2021 Rivers and streams play a central role in global carbon budget, but our knowledge is limited on the magnitude and extent of urbanization influence on riverine methane (CH4) dynamics. Methane 159-166 COP9 signalosome subunit 4 Drosophila melanogaster 168-171 34695024-4 2021 The implementation of the depletion-time control was successful and reached a maximum methane production rate of 1.22 L CH4/d, showing an average productivity of 0.73 +- 0.3 L CH4/d. Methane 86-93 choline dehydrogenase Homo sapiens 120-125 34695024-4 2021 The implementation of the depletion-time control was successful and reached a maximum methane production rate of 1.22 L CH4/d, showing an average productivity of 0.73 +- 0.3 L CH4/d. Methane 86-93 choline dehydrogenase Homo sapiens 176-181 34683886-3 2021 Herein, a multiple targeted engineered exosomes nanoplatform was constructed through rare earth element Gd and Dy-doped and TAT peptide-modified carbon dots (CDs:Gd,Dy-TAT) encapsulated into RGD peptide engineered exosomes (Exo-RGD), which were used to enhance the effect of cancer imaging diagnosis and photothermal therapy. Methane 145-156 5'-3' exoribonuclease 1 Mus musculus 224-227 34146930-8 2021 Moreover, six different Fe concentrations (0, 40, 80, 120, 160 and 200 mgL-1) were tested, showing that the addition of 120 mgL-1 had the greatest effect for statistically improving the maximum methane production, with 33% improvement (0.12 +- 0.003 to 0.16 +- 0.012 LCH4 gCODadd-1) compared to no addition of Fe and the specific CH4 production to 0.040 +- 0.001 LCH4 gVS-1. Methane 194-201 LLGL scribble cell polarity complex component 1 Homo sapiens 71-76 34684974-7 2021 Furthermore, the graphene structures with slit-shaped pores were found to be very capable of adsorbing methane and separating methane from hydrogen in a mixture at reasonable working conditions (300 K and well below 15 atm). Methane 103-110 ATM serine/threonine kinase Homo sapiens 219-222 34684974-7 2021 Furthermore, the graphene structures with slit-shaped pores were found to be very capable of adsorbing methane and separating methane from hydrogen in a mixture at reasonable working conditions (300 K and well below 15 atm). Methane 126-133 ATM serine/threonine kinase Homo sapiens 219-222 34482874-2 2021 Here, a new strategy for simultaneous monitoring gamma-glutamyl transpeptidase (GGT) and alkaline phosphatase (ALP) activity has been fabricated based on dual-emission carbon dots (CDs). Methane 168-179 inactive glutathione hydrolase 2 Homo sapiens 49-78 34482874-2 2021 Here, a new strategy for simultaneous monitoring gamma-glutamyl transpeptidase (GGT) and alkaline phosphatase (ALP) activity has been fabricated based on dual-emission carbon dots (CDs). Methane 168-179 inactive glutathione hydrolase 2 Homo sapiens 80-83 34482874-2 2021 Here, a new strategy for simultaneous monitoring gamma-glutamyl transpeptidase (GGT) and alkaline phosphatase (ALP) activity has been fabricated based on dual-emission carbon dots (CDs). Methane 168-179 alkaline phosphatase, placental Homo sapiens 89-109 34482874-2 2021 Here, a new strategy for simultaneous monitoring gamma-glutamyl transpeptidase (GGT) and alkaline phosphatase (ALP) activity has been fabricated based on dual-emission carbon dots (CDs). Methane 168-179 alkaline phosphatase, placental Homo sapiens 111-114 34545073-4 2021 Here, we show direct evidence for the presence in basaltic magmas of methane, generated or remobilized from the host sedimentary sequence during the emplacement of this Large Igneous Province. Methane 69-76 presequence translocase associated motor 16 Homo sapiens 59-65 34146930-8 2021 Moreover, six different Fe concentrations (0, 40, 80, 120, 160 and 200 mgL-1) were tested, showing that the addition of 120 mgL-1 had the greatest effect for statistically improving the maximum methane production, with 33% improvement (0.12 +- 0.003 to 0.16 +- 0.012 LCH4 gCODadd-1) compared to no addition of Fe and the specific CH4 production to 0.040 +- 0.001 LCH4 gVS-1. Methane 194-201 LLGL scribble cell polarity complex component 1 Homo sapiens 124-129 34404041-13 2021 We illustrate the identification of unresponsive subspaces and ranked responsive directions for gas sensor arrays based on Co-MOF-74 and HKUST-1 aimed at quantitative sensing of CH4/N2/CO2/C2H6mixtures relevant to natural gas sensing. Methane 178-181 gastrin Homo sapiens 96-99 34612385-4 2021 The parent complexes isolated in a noble gas (Ng) matrix were obtained by deposition of the CH4/HCN/Ng gaseous mixture and characterized by comparison of experimental complexation-induced shifts of the HCN fundamentals with the results of the ab initio calculations. Methane 92-95 metastasis associated lung adenocarcinoma transcript 1 Homo sapiens 96-99 34404041-13 2021 We illustrate the identification of unresponsive subspaces and ranked responsive directions for gas sensor arrays based on Co-MOF-74 and HKUST-1 aimed at quantitative sensing of CH4/N2/CO2/C2H6mixtures relevant to natural gas sensing. Methane 178-181 gastrin Homo sapiens 222-225 34288668-3 2021 The complex cleaves the various sp2 and sp3 C-H bonds including those in hexane and methane as inferred from their H/D exchange reactions. Methane 84-91 Sp2 transcription factor Homo sapiens 32-35 34288668-3 2021 The complex cleaves the various sp2 and sp3 C-H bonds including those in hexane and methane as inferred from their H/D exchange reactions. Methane 84-91 Sp3 transcription factor Homo sapiens 40-43 34500553-1 2021 A highly water and thermally stable metal-organic framework (MOF) Zn2(Pydc)(Ata)2 (1, H2Pydc = 3,5-pyridinedicarboxylic acid; HAta = 3-amino-1,2,4-triazole) was synthesized on a large scale using inexpensive commercially available ligands for efficient separation of C2H2 from CH4 and CO2. Methane 277-280 solute carrier family 38 member 2 Homo sapiens 66-81 34260219-1 2021 Millions of abandoned oil and gas wells are scattered across the United States, causing methane emissions and other environmental hazards. Methane 88-95 gastrin Homo sapiens 30-33 34466287-10 2021 The greatest N2O emissions and CH4 sink were recorded under the highest rate of N fertilization (100 kg N ha-1). Methane 31-34 plasma membrane ATPase Triticum aestivum 106-110 34436392-7 2021 On the other hand, a significant enhancement of 45% in ideal CO2/CH4 selectivity was attained by MMMs incorporated with 2 wt% of zeolite NH2-RHO compared to a pristine PSf membrane. Methane 65-68 rhodopsin Homo sapiens 137-144 34436392-8 2021 Besides, all MMMs incorporated with zeolite NH2-RHO displayed higher ideal CO2/CH4 selectivity than that of the MMMs incorporated with zeolite RHO. Methane 79-82 rhodopsin Homo sapiens 44-51 34492971-1 2021 Ammonia stress changes microbial metabolism of anaerobic digestion and decreases methane yield, where proton pump overactivated by free ammonia suggested to be the centre of the metabolism changes in anaerobic digestion under ammonia stress. Methane 81-88 ATPase H+/K+ transporting subunit alpha Homo sapiens 102-113 34146930-8 2021 Moreover, six different Fe concentrations (0, 40, 80, 120, 160 and 200 mgL-1) were tested, showing that the addition of 120 mgL-1 had the greatest effect for statistically improving the maximum methane production, with 33% improvement (0.12 +- 0.003 to 0.16 +- 0.012 LCH4 gCODadd-1) compared to no addition of Fe and the specific CH4 production to 0.040 +- 0.001 LCH4 gVS-1. Methane 330-333 LLGL scribble cell polarity complex component 1 Homo sapiens 124-129 34347487-4 2021 Additionally, we report converged second order Moller-Plesset (MP2) CBS binding energies for the encapsulation of guests in the (H2O)20 cage of -4.3 +- 0.1 for CH4@(H2O)20, -6.6 +- 0.1 for CO2@(H2O)20, and -8.5 +- 0.1 kcal/mol for H2S@(H2O)20, respectively. Methane 160-163 tryptase pseudogene 1 Homo sapiens 63-66 34196493-3 2021 Herein, a biocompatible -Cu-O-Zn- bimetallic covalent doped carbon dots (CuZn-CDs) processing both catalase (CAT) and superoxide dismutase activities are reported, mainly because of their abundant electrons and the excellent electron transfer abilities. Methane 60-71 catalase Homo sapiens 99-107 34196493-3 2021 Herein, a biocompatible -Cu-O-Zn- bimetallic covalent doped carbon dots (CuZn-CDs) processing both catalase (CAT) and superoxide dismutase activities are reported, mainly because of their abundant electrons and the excellent electron transfer abilities. Methane 60-71 catalase Homo sapiens 109-112 34264090-3 2021 More specifically, our results from atomistic simulations on COF-5/methane systems show that, as the gas density increases, the cross-plane thermal conductivity along the direction of the laminar pores increases, whereas the in-plane thermal conductivity along the 2D sheets is monotonically decreased. Methane 67-74 gastrin Homo sapiens 101-104 34174729-5 2021 The CO2 concentrations in most sites and CH4 concentrations in all sites were supersaturated, with the average partial pressure of CO2 (pCO2) being 654+-34 muatm and the partial pressure of CH4 (pCH4) being 157+-37 muatm. Methane 190-193 tRNA splicing endonuclease subunit 54 Homo sapiens 195-199 34204768-7 2021 Methane is eliminated from the gas phase and stored in gas hydrates. Methane 0-7 gastrin Homo sapiens 31-34 34372218-0 2021 Development of Gas Sensor Array for Methane Reforming Process Monitoring. Methane 36-43 gastrin Homo sapiens 15-18 34308083-9 2021 The Langmuir model fits the adsorption curves of 80 and 100 C better, while the BET model is appropriate for 30 and 55 C. The adsorption affinity of CO2 is higher than CH4, with the value of alphaCO2/CH4 in the range of 2.47-12.16. Methane 170-173 aconitase 2 Homo sapiens 193-205 34278151-2 2021 Its thermal evolution and gas generation characteristics determined the grade of coalbed methane resources, especially the coal measure free gas resources in the basin. Methane 89-96 gastrin Homo sapiens 26-29 34278151-2 2021 Its thermal evolution and gas generation characteristics determined the grade of coalbed methane resources, especially the coal measure free gas resources in the basin. Methane 89-96 gastrin Homo sapiens 141-144 34201568-7 2021 The gas adsorption potential of the samples was probed with H2, CO2 and CH4, while the electrocatalytic properties were tested in an oxygen reduction reaction. Methane 72-75 gastrin Homo sapiens 4-7 34235331-4 2021 Furthermore, Fe/CM-CL with a particle size of 1.5-2.5 nm shows excellent catalytic performance, the conversion of carbon monoxide reaches 82.3%, and the selectivity of methane reaches 73.2%. Methane 168-175 general transcription factor IIE subunit 1 Homo sapiens 13-15 34368567-1 2021 It is still a great challenge to develop a new porous carbon adsorbent with excellent separation performance and to recover low-concentration CH4 in coal mine gas. Methane 142-145 gastrin Homo sapiens 159-162 34308083-3 2021 The preferential selection coefficient of CO2 for CH4 under different conditions was characterized by the absolute adsorption capacity (V abs) ratio of CO2 to CH4 (alphaCO2/CH4). Methane 50-53 aconitase 2 Homo sapiens 164-176 34308083-3 2021 The preferential selection coefficient of CO2 for CH4 under different conditions was characterized by the absolute adsorption capacity (V abs) ratio of CO2 to CH4 (alphaCO2/CH4). Methane 159-162 aconitase 2 Homo sapiens 164-176 34277569-0 2021 Methane Conversion Under Mild Conditions Using Semiconductors and Metal-Semiconductors as Heterogeneous Photocatalysts: State of the Art and Challenges. Methane 0-7 artemin Homo sapiens 133-136 34209036-1 2021 Recently, membrane contactors have gained more popularity in the field of CO2 removal; however, achieving high purity and competitive recovery for poor soluble gas (H2, N2, or CH4) remains elusive. Methane 176-179 gastrin Homo sapiens 160-163 34204768-7 2021 Methane is eliminated from the gas phase and stored in gas hydrates. Methane 0-7 gastrin Homo sapiens 55-58 35609752-3 2022 Conventional thermal pretreatment of sludge (~5% total solids, TS) produced 244 mL CH4/gTS, which could result in a positive energy balance of 2.6 kJ/kg TS. Methane 83-86 GTS Homo sapiens 87-90 34066547-0 2021 Catalytic Methane Decomposition to Carbon Nanostructures and COx-Free Hydrogen: A Mini-Review. Methane 10-17 cytochrome c oxidase subunit 8A Homo sapiens 61-64 34467296-5 2021 Moreover, at 150 C and 0.2 MPa, the hybrid membrane retains high separation performances with ideal selectivities higher than 200 and 30 for H2/CH4 and CO2/CH4, respectively, which are attractive for gas separation and purification of practical applications. Methane 145-148 gastrin Homo sapiens 201-204 34467296-5 2021 Moreover, at 150 C and 0.2 MPa, the hybrid membrane retains high separation performances with ideal selectivities higher than 200 and 30 for H2/CH4 and CO2/CH4, respectively, which are attractive for gas separation and purification of practical applications. Methane 157-160 gastrin Homo sapiens 201-204 35487006-2 2022 Here, we rationally designed a novel and vigorous chitosan grafted Fe-doped-carbon dots (CS@Fe/CDs) as an efficient artificial nanozyme to combat rigid bacterial biofilms through the selective activation of Fenton-like reaction-triggered peroxidase-like catalytic activity and the synergistic antibacterial activity of CS. Methane 76-87 AT695_RS02070 Staphylococcus aureus 238-248 34074750-5 2021 In contrast to and unlike OCM, the overoxidized CS2 by-product forms predominantly via CH4 oxidation, rather than from C2 products, through a series of C-H activation and S-addition steps at adsorbed sulfur sites on the FeS2 surface. Methane 87-90 chorionic somatomammotropin hormone 2 Homo sapiens 48-51 34074750-6 2021 The experimental rates for methane conversion are first order in both CH4 and S2, consistent with the involvement of two S sites in the rate-determining methane C-H activation step, with a CD4/CH4 kinetic isotope effect of 1.78. Methane 27-34 CD4 molecule Homo sapiens 189-192 34069713-1 2021 Natural gas hydrate occurrences contain predominantly methane; however, there are increasing reports of complex mixed gas hydrates and coexisting hydrate phases. Methane 54-61 gastrin Homo sapiens 8-11 35609752-4 2022 However, microwave pretreatment could generate only 178 mL CH4/gTS with a negative energy balance of -15.62 kJ/kg TS. Methane 59-62 GTS Homo sapiens 63-66 35358877-3 2022 The HPr/HAc ratios of 0.5 and 1.5 maintained efficient syntrophy among electroactive bacteria, hydrogenotrophic methanogens, and homoacetogens, leading to higher methane yields. Methane 162-169 haptoglobin-related protein Homo sapiens 4-7 35609177-7 2022 Small molecules like NH3 and CH4 are shown to be capable of expanding the interlayer spacing and of increasing the band gap and hole mobility in SnO and thus could potentially serve as the interlayer intercalants. Methane 29-32 strawberry notch homolog 2 Homo sapiens 145-148 35499189-0 2022 Sub-1 nm MoC Quantum Dots Decorating N-Doped Graphene as Advanced Electrocatalysts of Flexible Hybrid Alkali-Acid Zn-Quinone Battery. Methane 37-53 SUB1 regulator of transcription Homo sapiens 0-5 35538261-1 2022 An ultrasensitive fluorescence assay strategy on the basis of carbon dots (CDs) and cDNA-modified gold nanoparticles (AuNP-cDNA) was developed for the determination of microRNA-21 (miRNA-21) via internal filtering effect (IFE). Methane 62-73 microRNA 21 Homo sapiens 168-179 35452214-3 2022 To augment therapeutic efficacy and tumor selectivity, folic acid (FA)-functionalized carbon dots (CDs) embedded with GOx and paclitaxel (PTX) (FA-CD-(PTX-GOx)) was developed that showed the efficient killing of TNBC, MDA-MB-468 cells over noncancerous HEK 293 cells through synergistic effects of cancer starvation-induced oxidative stress and chemotherapy. Methane 86-97 FA complementation group D2 Homo sapiens 144-149 35452214-3 2022 To augment therapeutic efficacy and tumor selectivity, folic acid (FA)-functionalized carbon dots (CDs) embedded with GOx and paclitaxel (PTX) (FA-CD-(PTX-GOx)) was developed that showed the efficient killing of TNBC, MDA-MB-468 cells over noncancerous HEK 293 cells through synergistic effects of cancer starvation-induced oxidative stress and chemotherapy. Methane 86-97 hydroxyacid oxidase 1 Homo sapiens 155-158 35500109-3 2022 Here, we proposed a simple strategy for the preparation of a heterogeneous photocatalyst suitable for photo induced atom transfer radical polymerization (photoATRP) under full spectrum (from UV/vis light to NIR), by combining pyridine nitrogen doped carbon dots (N-CDs) and upconversion nanoparticles (UCNPs). Methane 250-261 NOC2 like nucleolar associated transcriptional repressor Homo sapiens 207-210 35611736-1 2022 In this study, voltage was used as a disturbance factor to investigate the relationship between microbial community and methane (CH4) production flux in a microbial electrolytic cell coupled anaerobic digestion (MEC-AD). Methane 120-127 C-C motif chemokine ligand 28 Homo sapiens 212-215 35611736-1 2022 In this study, voltage was used as a disturbance factor to investigate the relationship between microbial community and methane (CH4) production flux in a microbial electrolytic cell coupled anaerobic digestion (MEC-AD). Methane 129-132 C-C motif chemokine ligand 28 Homo sapiens 212-215 35629564-4 2022 After process optimization, the gas transport properties through the membranes were determined on the basis of pure gas permeation including CH4, CO2, O2, and N2 for two specific applications: biogas sweetening (CH4/CO2) and oxygen-enriched air (O2/N2). Methane 141-144 gastrin Homo sapiens 32-35 35629564-4 2022 After process optimization, the gas transport properties through the membranes were determined on the basis of pure gas permeation including CH4, CO2, O2, and N2 for two specific applications: biogas sweetening (CH4/CO2) and oxygen-enriched air (O2/N2). Methane 141-144 gastrin Homo sapiens 116-119 35629564-4 2022 After process optimization, the gas transport properties through the membranes were determined on the basis of pure gas permeation including CH4, CO2, O2, and N2 for two specific applications: biogas sweetening (CH4/CO2) and oxygen-enriched air (O2/N2). Methane 212-215 gastrin Homo sapiens 32-35 35629564-4 2022 After process optimization, the gas transport properties through the membranes were determined on the basis of pure gas permeation including CH4, CO2, O2, and N2 for two specific applications: biogas sweetening (CH4/CO2) and oxygen-enriched air (O2/N2). Methane 212-215 gastrin Homo sapiens 116-119 35562375-8 2022 The recognition of widespread gas-condensate migration adds to the complex history of internal hydrocarbon migration within the Montney tight-petroleum system including previously identified migration episodes of early oil and late-stage methane-rich gas. Methane 238-245 galactosamine (N-acetyl)-6-sulfatase Homo sapiens 251-254 35578731-6 2022 Different routes have been explored for the recovery of hydrogen from COG so far: i) separation/purification processes with pressure swing adsorption or membrane technology, ii) conversion routes that provide additional hydrogen from the chemical transformation of the methane contained in COG, and iii) direct use of COG as fuel for internal combustion engines or gas turbines with the aim of power generation. Methane 269-276 gastrin Homo sapiens 365-368 35538261-1 2022 An ultrasensitive fluorescence assay strategy on the basis of carbon dots (CDs) and cDNA-modified gold nanoparticles (AuNP-cDNA) was developed for the determination of microRNA-21 (miRNA-21) via internal filtering effect (IFE). Methane 62-73 microRNA 21 Homo sapiens 181-189 35615497-5 2022 However, substrate-amended incubations (with NO2 -, NO3 -, SO4 2-, Fe-, and Mn-oxides) revealed that none of the electron acceptors previously reported to support AOM enhanced methane turnover in Lake Sempach sediments under anoxic conditions. Methane 176-183 NBL1, DAN family BMP antagonist Homo sapiens 52-55 35615497-2 2022 Methane emissions are regulated to large parts by aerobic (MOx) and anaerobic (AOM) oxidation of methane, which are important CH4 sinks in lakes. Methane 0-7 monooxygenase DBH like 1 Homo sapiens 59-62 35615497-2 2022 Methane emissions are regulated to large parts by aerobic (MOx) and anaerobic (AOM) oxidation of methane, which are important CH4 sinks in lakes. Methane 97-104 monooxygenase DBH like 1 Homo sapiens 59-62 35615497-2 2022 Methane emissions are regulated to large parts by aerobic (MOx) and anaerobic (AOM) oxidation of methane, which are important CH4 sinks in lakes. Methane 126-129 monooxygenase DBH like 1 Homo sapiens 59-62 35565123-6 2022 With 70 days of incubation each, CH4 production decreased from 4.55 L g-1-chemical oxygen demand (COD) at 42 C with methanogen/total population (M TP-1) ratio of 0.041 to 1.52 L g-1 COD (M TP-1 ratio 0.027) and then to 0.94 L g-1 COD ( M TP-1 ratio 0.026) after the temperature was shifted to 45 C and 48 C, respectively. Methane 33-36 solute carrier family 40 member 1 Homo sapiens 146-152 35565123-6 2022 With 70 days of incubation each, CH4 production decreased from 4.55 L g-1-chemical oxygen demand (COD) at 42 C with methanogen/total population (M TP-1) ratio of 0.041 to 1.52 L g-1 COD (M TP-1 ratio 0.027) and then to 0.94 L g-1 COD ( M TP-1 ratio 0.026) after the temperature was shifted to 45 C and 48 C, respectively. Methane 33-36 solute carrier family 40 member 1 Homo sapiens 188-194 35565123-6 2022 With 70 days of incubation each, CH4 production decreased from 4.55 L g-1-chemical oxygen demand (COD) at 42 C with methanogen/total population (M TP-1) ratio of 0.041 to 1.52 L g-1 COD (M TP-1 ratio 0.027) and then to 0.94 L g-1 COD ( M TP-1 ratio 0.026) after the temperature was shifted to 45 C and 48 C, respectively. Methane 33-36 solute carrier family 40 member 1 Homo sapiens 237-243 35105960-1 2022 Gas hydrates deposited in subseafloor sediments are considered to primarily consist of biogenic methane. Methane 96-103 gastrin Homo sapiens 0-3 35500853-2 2022 In this paper, we constructed multicolor N-doped-carbon dots (mPD-CDs) by facile one-step hydrothermal carbonization of m-phenylenediamine (mPD). Methane 49-60 mevalonate (diphospho) decarboxylase Mus musculus 140-143 35591379-6 2022 Furthermore, because of good balance between CH4 dissociation and CO2 dissociation, NiP-2/Al2O3 catalyst exhibits best resistance of carbon deposition, few carbon depositions were formed after 50 h of dry methane reforming. Methane 45-48 BCL2 interacting protein 2 Homo sapiens 84-89 35275634-0 2022 Immunoregulatory Activity of Herbal Tea-Derived Carbon Dots. Methane 48-59 solute carrier family 7 (cationic amino acid transporter, y+ system), member 2 Mus musculus 36-39 35495656-7 2022 Co-occurrence analysis revealed that methane-metabolizing microbial communities were mainly associated with heterotrophic microorganisms, such as JS1, Bathy-1, and Bathy-15. Methane 37-44 carboxymethylenebutenolidase homolog Homo sapiens 146-149 35377591-0 2022 Optimizing the Microstructure of SnO2-CeO2 Binary Oxide Supported Palladium Catalysts for Efficient and Stable Methane Combustion. Methane 111-118 strawberry notch homolog 1 Homo sapiens 33-36 35212057-7 2022 Moreover, the adjacent Pd1 and PdNPs effectively stabilized intermediates such as *CHO, thereby favoring the pathway for CH4 production. Methane 121-124 programmed cell death 1 Homo sapiens 23-26 35601339-4 2022 Thermodynamically, methane is the most favorable product in a reaction system containing CO, CO2, and H2, as well as C1-4 alkanes, alkenes, and alcohols. Methane 19-26 heterogeneous nuclear ribonucleoprotein C Homo sapiens 117-121 35533487-4 2022 Herein, Sb is firstly captured by mesoporous carbon sphere (MCS) to form a composite of Sb/MCS, and then reduced graphene oxide (rGO) is adopted as an outer layer to wrap the Sb/MCS to obtain the dual-carbon confinement material (Sb/MCS@rGO). Methane 34-51 Miles-Carpenter X-linked mental retardation syndrome Homo sapiens 60-63 35533487-4 2022 Herein, Sb is firstly captured by mesoporous carbon sphere (MCS) to form a composite of Sb/MCS, and then reduced graphene oxide (rGO) is adopted as an outer layer to wrap the Sb/MCS to obtain the dual-carbon confinement material (Sb/MCS@rGO). Methane 34-51 Miles-Carpenter X-linked mental retardation syndrome Homo sapiens 91-94 35533487-4 2022 Herein, Sb is firstly captured by mesoporous carbon sphere (MCS) to form a composite of Sb/MCS, and then reduced graphene oxide (rGO) is adopted as an outer layer to wrap the Sb/MCS to obtain the dual-carbon confinement material (Sb/MCS@rGO). Methane 34-51 Miles-Carpenter X-linked mental retardation syndrome Homo sapiens 233-236 35148362-2 2022 The active Ni(I) species in MCR converts methyl-coenzyme M (CH3S-CoM) and coenzyme B (HS-CoB) to methane and heterodisulfide (CoM-S-S-CoB). Methane 97-104 metabolism of cobalamin associated B Homo sapiens 89-92 35066196-4 2022 The maximum methane yield was obtained from the digester amended with biochar (373.4 +- 6.0 ml g COD-1), followed by calcium hydroxide (350.1 +- 2.5 ml g COD-1). Methane 12-19 retinitis pigmentosa GTPase regulator Homo sapiens 97-102 35066196-4 2022 The maximum methane yield was obtained from the digester amended with biochar (373.4 +- 6.0 ml g COD-1), followed by calcium hydroxide (350.1 +- 2.5 ml g COD-1). Methane 12-19 retinitis pigmentosa GTPase regulator Homo sapiens 154-159 35135571-2 2022 RESULTS: We reported a strategy for the construction of a dual-emission fluorescent sensor using carbon dots (CDs) and confirmed their applications for ratiometric microRNA-21 sensing and bioimaging of cancer cells in a microfluidic device. Methane 97-108 microRNA 21 Homo sapiens 164-175 35207122-3 2022 The permeability of He, H2, N2, O2, CH4 and CO2 gases through these MMMs are analyzed as a function of the fraction of free volume (FFV) of the membrane and the kinetic diameter of the gas, allowing for the evaluation of the free volume. Methane 36-39 gastrin Homo sapiens 185-188 35239060-1 2022 An ultra-sensitive glyphosate nanosensor, based on carbon dots (CDs), was successfully developed with excellent long-wavelength emission (530 nm), a high quantum yield (41.3%), and an impressive detection limit (0.8 ng mL-1). Methane 51-62 L1 cell adhesion molecule Mus musculus 219-223 35268694-8 2022 In ultramicropores, the high concentration of CO2 (50-70%) is more conducive to CH4 desorption; however, when the CO2 concentration is greater than 70%, the corresponding CH4 adsorption amount is meager, and the selected adsorption coefficient SCO2/CH4 is small. Methane 80-83 synthesis of cytochrome C oxidase 2 Homo sapiens 244-248 35268694-8 2022 In ultramicropores, the high concentration of CO2 (50-70%) is more conducive to CH4 desorption; however, when the CO2 concentration is greater than 70%, the corresponding CH4 adsorption amount is meager, and the selected adsorption coefficient SCO2/CH4 is small. Methane 171-174 synthesis of cytochrome C oxidase 2 Homo sapiens 244-248 35201580-0 2022 Estimating the methane emissions and energy potential from Trichy and Thanjavur dumpsite by LandGEM model. Methane 15-22 GTP binding protein overexpressed in skeletal muscle Homo sapiens 92-99 35166550-0 2022 Gas-Phase Synthesis of Metal Olefins: Plasma-Assisted Methane Dehydrogenation and C C Bond Formation. Methane 54-61 gastrin Homo sapiens 0-3 35166550-2 2022 Utilizing a customized time of flight mass spectrometer combined with a magnetron sputtering (MagS) cluster source, here, we have conducted a study on the reactions of methane with small silver and copper clusters simply by introducing methane in argon as the working gas for sputtering. Methane 168-175 gastrin Homo sapiens 268-271 35166550-2 2022 Utilizing a customized time of flight mass spectrometer combined with a magnetron sputtering (MagS) cluster source, here, we have conducted a study on the reactions of methane with small silver and copper clusters simply by introducing methane in argon as the working gas for sputtering. Methane 236-243 gastrin Homo sapiens 268-271 34995071-3 2022 We investigate the reactivity of Cl and CCl3 radicals with methane on argon clusters using the pickup method. Methane 59-66 C-C motif chemokine ligand 3 Homo sapiens 40-44 35105091-4 2022 We test the robustness and accuracy of the method by computing the integral cross sections for the H/F + CH4/CHD3 reactions where the methane molecule is either initially in its vibrational ground or excited state (C-H stretch). Methane 134-141 chromodomain helicase DNA binding protein 3 Homo sapiens 109-113 35160533-0 2022 Molecular Simulation on Permeation Behavior of CH4/CO2/H2S Mixture Gas in PVDF at Service Conditions. Methane 47-50 gastrin Homo sapiens 67-70 35160533-4 2022 In order to clarify the permeation behavior and obtain the permeation mechanism of the mixture gas (CH4/CO2/H2S) in PVDF at the normal service conditions, molecular simulations were carried out by combining the Grand Canonical Monte Carlo (GCMC) method and the Molecular Dynamics (MD) method. Methane 100-103 gastrin Homo sapiens 95-98 35160533-10 2022 The diffusion belonged to Einstein diffusion and the diffusion coefficients of each gas followed the order of CH4 > CO2 > H2S. Methane 110-113 gastrin Homo sapiens 84-87 34995071-8 2022 It starts with the hydrogen abstraction from CH4 by a Cl radical resulting in HCl and CH3 followed by a halogenation step where CCl4 molecules react with the available CH3 radicals, yielding CH3Cl. Methane 45-48 C-C motif chemokine ligand 4 Homo sapiens 128-132 2538230-2 1989 During incubation of TNF sensitive mouse tumorigenic fibroblast L-M cells (2 X 10(7) cells) in the presence of rhTNF (100 U), hydroxyl radical production as detected by the evolution of methane gas from dimethyl sulfoxide increased gradually, at 18 h reaching 1.8 times that in the absence of rhTNF. Methane 186-193 tumor necrosis factor Mus musculus 21-24 34985901-2 2022 When methane (CH4) in the spatially homogeneous methane hydrate was replaced with deuterated methane (CD4), it showed a previously unrecognized strong anharmonic effect, identified by the Raman peak located at 1952.78 cm-1. Methane 5-12 CD4 molecule Homo sapiens 102-105 34985901-2 2022 When methane (CH4) in the spatially homogeneous methane hydrate was replaced with deuterated methane (CD4), it showed a previously unrecognized strong anharmonic effect, identified by the Raman peak located at 1952.78 cm-1. Methane 14-17 CD4 molecule Homo sapiens 102-105 35036704-2 2022 The research on gas production in such a manner is conducive to revealing mechanisms of coal and gas outburst and excess coalbed methane (CBM). Methane 129-136 gastrin Homo sapiens 16-19 35071178-1 2021 We determined the kinetic isotope effect on the serine hydroxymethyltransferase reaction (SHMT), which provides important C1 metabolites that are essential for the biosynthesis of DNA bases, O-methyl groups of lignin and methane. Methane 221-228 serine hydroxymethyltransferase 1 Sus scrofa 90-94 35071178-2 2021 An isotope effect on the SHMT reaction was suggested being responsible for the well-known isotopic depletion of methane. Methane 112-119 serine hydroxymethyltransferase 1 Sus scrofa 25-29 34672031-1 2022 The reactivity of the molybdenum oxide cluster anion (MoO3 )5 O- , bearing an unpaired electron at a bridging oxygen atom (Ob .- ), towards methane under thermal collision conditions has been studied by mass spectrometry and density functional theory calculations. Methane 140-147 cadherin 11 Homo sapiens 123-125 34672031-4 2022 This study not only makes up the blank of thermal methane activation by the Ob .- radical on negatively charged clusters but also yields new insights into methane activation by the atomic oxygen radical anions. Methane 50-57 cadherin 11 Homo sapiens 76-78 34672031-4 2022 This study not only makes up the blank of thermal methane activation by the Ob .- radical on negatively charged clusters but also yields new insights into methane activation by the atomic oxygen radical anions. Methane 155-162 cadherin 11 Homo sapiens 76-78 3721294-1 1986 This study determined the incidence and concentration of methane-producing bacteria in tap water enema samples of 130 individuals taken before sigmoidoscopy. Methane 57-64 nuclear RNA export factor 1 Homo sapiens 87-90 2845869-2 1988 During incubation of TNF sensitive mouse tumorigenic fibroblast L-M cells in the presence of rhTNF, hydroxyl radical production detected by the evolution of methane gas from dimethyl sulfoxide increased gradually, at 18 hours reached 1.8 times of that in the absence of rhTNF. Methane 157-164 tumor necrosis factor Mus musculus 21-24 3221192-5 1988 The effect of NO3- on methanogenesis was twofold: firstly, H2 accumulation decreased due to diversion of electrons towards NO3-/NO2- reduction, and as a result of H2 being used as an electron donor for NO3- reduction, resulting in the removal of the methanogenic substrate; secondly, there was direct inhibition of methane-producing bacteria by NO3- and NO2-. Methane 315-322 NBL1, DAN family BMP antagonist Homo sapiens 14-17 3103131-2 1987 For example, in a reconstituted system containing rabbit liver microsomal P-450 form 2, NADPH-cytochrome P-450 reductase, and NADPH, cumyl hydroperoxide yields acetophenone and methane, but no cumyl alcohol is formed. Methane 177-184 NADPH--cytochrome P450 reductase Oryctolagus cuniculus 88-120 2609348-7 1989 These results suggest that the reductive activation to free radicals, catalyzed by cytochrome P-450, and thus the induction of lipid peroxidation at low but physiological PO2 are characteristic not only of CCl4 but also of other polyhalogenated methanes, especially CBrCl3, CBr4, CHI3, CHBr3, and CHBr2Cl. Methane 245-253 cytochrome P450, family 2, subfamily g, polypeptide 1 Rattus norvegicus 83-99 2609348-7 1989 These results suggest that the reductive activation to free radicals, catalyzed by cytochrome P-450, and thus the induction of lipid peroxidation at low but physiological PO2 are characteristic not only of CCl4 but also of other polyhalogenated methanes, especially CBrCl3, CBr4, CHI3, CHBr3, and CHBr2Cl. Methane 245-253 C-C motif chemokine ligand 4 Rattus norvegicus 206-210 18581526-4 1987 At a loading rate of 16 kg COD/m(3) day the methane yield was 0.302 L CH(4) (STP)/g COD removed, and the observed cell yield was 0.112 g VSS/g COD removed. Methane 44-51 thyroid hormone receptor interactor 10 Homo sapiens 77-80 3576214-1 1987 Electrical coupling and dye coupling between pairs of rat hepatocytes were reversibly reduced by brief exposure to halogenated methanes (CBrCl3, CCl4, and CHCl3). Methane 127-135 C-C motif chemokine ligand 4 Rattus norvegicus 145-149 2819806-5 1987 CH4 mixtures give the highest yields of HCN while H2CO is most efficiently produced with the CO mixtures. Methane 0-3 metastasis associated lung adenocarcinoma transcript 1 Homo sapiens 40-43 16346563-4 1984 However, samples taken from the sediment-water interface contained as much as 3 muM methane and 50 CFU of methane-oxidizing bacteria per ml and showed significant rates of methane oxidation and incorporation. Methane 84-91 latexin Homo sapiens 80-83 3553530-5 1986 It is known that methylation of Hg2+ is mediated by a series of enzymatic reactions that are also responsible for the anaerobic evolution of methane. Methane 141-148 polycystin 1, transient receptor potential channel interacting pseudogene 2 Homo sapiens 32-35 18553828-10 1985 After adaptation, high loading and methane generation rates could be accommodated at satisfactory treatment efficiencies, namely, 86.4 kg COD/m(3) day and 26 m(3) CH(4)(STP)/m(3) day, respectively. Methane 35-42 thyroid hormone receptor interactor 10 Homo sapiens 169-172 3978755-4 1985 The characteristics of the reactions leading to the covalent binding of the N-methyl group of the azo derivative to microsomal protein and its metabolism to form the hydrocarbon, methane, possessed a number of similarities in the apparent kinetic parameters (Km and Vmax), induction, and inhibition patterns indicating a common pathway of metabolism to form a reactive intermediate and the involvement of cytochrome P-450. Methane 179-186 cytochrome P450 family 4 subfamily F member 3 Homo sapiens 405-421 16346563-6 1984 The concentration of methane increased with depth to a maximum of 150 to 325 muM at 2.5 cm, and significant rates of methane oxidation were found within the top 2.5 cm. Methane 21-28 latexin Homo sapiens 77-80 17738085-3 1979 For liquid methane superheated 50 K above its boiling point at 1 atmosphere, the energy of explosion is 2 to 3 percent of that of TNT. Methane 11-18 chromosome 16 open reading frame 82 Homo sapiens 130-133 7162801-2 1982 From their results, it appears that a variety of organic compounds, including unsaturated hydrocarbons and nitriles such as HCN, can be synthesized into noticeable amounts from CH4-N2 mixtures. Methane 177-180 metastasis associated lung adenocarcinoma transcript 1 Homo sapiens 124-127 17787481-1 1979 Methane concentrations as great as 30,000 nanoliters per liter were measured on two cruises in the northwest Caribbean Sea. Methane 0-7 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 119-122 6533090-6 1984 In addition, a higher proportion of methane producers was found amongst secretors of blood group substances (ABH antigen) than non-secretors. Methane 36-43 alkB homolog 1, histone H2A dioxygenase Homo sapiens 109-112 6087242-2 1984 Energy yields for the synthesis of HCN and H2CO from a spark discharge were determined for various mixtures of CH4, CO, CO2, H2, H2O, N2 and NH3. Methane 111-114 metastasis associated lung adenocarcinoma transcript 1 Homo sapiens 35-38 6087242-3 1984 The maximum yields of HCN and H2CO from CH4, CO, and CO2 as carbon sources are about 4 X 10(-8) moles cal-1. Methane 40-43 metastasis associated lung adenocarcinoma transcript 1 Homo sapiens 22-25 34045854-0 2021 Efficient Determination of PML/RARalpha Fusion Gene by the Electrochemical DNA Biosensor Based on Carbon Dots/Graphene Oxide Nanocomposites. Methane 98-109 PML nuclear body scaffold Homo sapiens 27-30 101517-2 1978 Suspensions of methane-grown cells of this organism oxidized C-1 compounds (methane, methanol, formaldehyde, formate); hydrocarbons (ethane, propane); primary alcohols (ethanol, propanol); primary aldehydes (acetaldehyde, propionaldehyde); alkenes (ethylene, propylene); dimethylether; and organic acids (acetate, malate, succinate, isocitrate). Methane 15-22 heterogeneous nuclear ribonucleoprotein C Homo sapiens 61-64 101517-8 1978 Extracts of methane-grown, but not succinate-grown, cells contained the key enzymes of the serine pathway, hydroxypyruvate reductase and malate lyase, indicating that the enzymes of C-1 assimilation are induced only during growth on C-1 compounds. Methane 12-19 heterogeneous nuclear ribonucleoprotein C Homo sapiens 182-185 101517-8 1978 Extracts of methane-grown, but not succinate-grown, cells contained the key enzymes of the serine pathway, hydroxypyruvate reductase and malate lyase, indicating that the enzymes of C-1 assimilation are induced only during growth on C-1 compounds. Methane 12-19 heterogeneous nuclear ribonucleoprotein C Homo sapiens 233-236 1024583-3 1976 It is demonstrated that CD4 is a competitive inhibitor of CH4 oxidation. Methane 58-61 CD4 molecule Homo sapiens 24-27 17771076-1 1974 Photochemically generated hot hydrogen atoms initiate reactions with simple molecular substrates including methane to produce organic alcohols, amines, acids, amino acids, and other compounds. Methane 107-114 alcohol dehydrogenase iron containing 1 Homo sapiens 1-4 6072276-0 1967 The effect of C18 unsaturated fatty acids of methane production in vitro by mixed rumen bacteria. Methane 45-52 Bardet-Biedl syndrome 9 Homo sapiens 14-17 17774061-2 1967 Methane shows by far the highest concentration, followed in order by the C(2), C(3), and C(4) fractions. Methane 0-7 complement C2 Homo sapiens 73-77 17774061-2 1967 Methane shows by far the highest concentration, followed in order by the C(2), C(3), and C(4) fractions. Methane 0-7 complement C3 Homo sapiens 79-83 17774061-2 1967 Methane shows by far the highest concentration, followed in order by the C(2), C(3), and C(4) fractions. Methane 0-7 complement C4A (Rodgers blood group) Homo sapiens 89-93 5927399-0 1966 Role of B12 compounds in methane formation. Methane 25-32 NADH:ubiquinone oxidoreductase subunit B3 Homo sapiens 8-11 33957451-1 2021 The present study is devoted to the creation of optical nanosensors for pH and temperature of liquid media based on carbon dots (CD) prepared via hydrothermal synthesis. Methane 116-127 phenylalanine hydroxylase Homo sapiens 72-74 33934792-3 2021 Herein, a fluorescence (FL)-infrared absorption (IRA) dual-mode nanoprobe was fabricated based on carbon dots (CDs)@SiO2 nanorod for CEA detection. Methane 98-109 CEA cell adhesion molecule 3 Homo sapiens 133-136 33933489-3 2021 The Pt-Au/R-TNTs with 0.33 wt% of SA metals, exhibited a maximum of 149 times higher photocatalytic performance than unmodified R-TNT and a total apparent quantum yield (AQY) of 17.9%, in which the yield of CH4 and C2H6 reached to 360.0 and 28.8 mumol g-1 h-1, respectively. Methane 207-210 chromosome 16 open reading frame 82 Homo sapiens 12-15 33714764-2 2021 In this study metformin derived carbon dots (Met-CDs) were synthesized using a microwave assisted method. Methane 32-43 MET proto-oncogene, receptor tyrosine kinase Danio rerio 45-48 16592182-0 1974 Diffusivity of Methane in a Mixture of CCl(4) and c-C(6)F(11)C(2)F(5) of the Critical Composition in the Region above the Temperature of Separation. Methane 15-22 C-C motif chemokine ligand 4 Homo sapiens 39-45 34058181-7 2021 A rapid response (34.5) for CdO-ZnO nanorices based formaldehyde gas sensor was observed as compared to other gases such as ammonia (12.3), methanol (16.5), ethanol (20), carbon monoxide (16.3) and methane (12.4), which confirm the high-selectivity towards formaldehyde gas. Methane 198-205 cell adhesion associated, oncogene regulated Homo sapiens 28-31 34048836-2 2021 Herein, BMP-2-conjugated carbon dots (CDs) was used as noninvasive detection platforms to deliver BMP-2 for therapeutic applications where osteogenesis and bioimaging are both required. Methane 25-36 bone morphogenetic protein 2 Homo sapiens 8-13 34048836-2 2021 Herein, BMP-2-conjugated carbon dots (CDs) was used as noninvasive detection platforms to deliver BMP-2 for therapeutic applications where osteogenesis and bioimaging are both required. Methane 25-36 bone morphogenetic protein 2 Homo sapiens 98-103 33961741-13 2021 In Ti+(CH4)4 and V+(CH4)4 all of the methanes have eta2 coordination. Methane 37-45 DNA polymerase iota Homo sapiens 51-55 34045854-0 2021 Efficient Determination of PML/RARalpha Fusion Gene by the Electrochemical DNA Biosensor Based on Carbon Dots/Graphene Oxide Nanocomposites. Methane 98-109 retinoic acid receptor alpha Homo sapiens 31-39 34008884-5 2021 In contrast, binding governed by orbital interactions results in a eta2 type coordination of methane. Methane 93-100 DNA polymerase iota Homo sapiens 67-71 34054564-0 2021 Methane Inhalation Protects Against Lung Ischemia-Reperfusion Injury in Rats by Regulating Pulmonary Surfactant via the Nrf2 Pathway. Methane 0-7 NFE2 like bZIP transcription factor 2 Rattus norvegicus 120-124 34038842-2 2021 The highest biogas and methane yield observed with the pretreated TR at HTP temperature of 140 C reached 288 and 207 L/Kg VS, 24 and 37% above than the raw TR (control), respectively, and the highest content of methane 72%. Methane 23-30 coagulation factor II thrombin receptor Homo sapiens 66-68 33735621-7 2021 High CH4 accumulation and subsequent emission in 2012 were preceded by CO2 and N2O consumption and under-saturation at the lake surface (uptakes at -30 mmol m-2 d-1 and -1.6 micromol m-2 d-1, respectively). Methane 5-8 leiomodin 1 Homo sapiens 161-171 33736232-7 2021 The highly agricultural river network acted as significant CO2 and CH4 sources with estimated emission fluxes of 409 +- 369 mmol m-2 d-1 for CO2 and 1.6 +- 1.2 mmol m-2 d-1 for CH4, and made a disproportionately large, relative to the area, contribution to the total aquatic carbon emission of the watershed. Methane 67-70 complement C2 Homo sapiens 141-152 34054564-8 2021 In conclusion, CH4 inhalation decreased oxidative stress injury, inflammatory response, and cell apoptosis, and improved lung function through Nrf2-mediated pulmonary surfactant regulation in rat lung I/R injury. Methane 15-18 NFE2 like bZIP transcription factor 2 Rattus norvegicus 143-147 33959811-3 2021 In this work, an electrochemical h-FABP immunosensor was developed based on Cd0.5Zn0.5S/d-Ti3C2Tx MXene (MXene: Transition metal carbide or nitride) composite as signal amplificator and core-shell high-crystalline graphitic carbon nitride@carbon dots (hc-g-C3N4@CDs) as electrochemical sensor platform. Methane 239-250 fatty acid binding protein 3 Homo sapiens 33-39 33460850-5 2021 Our results showed that the THCN exhibited the best CO2 conversion efficiency from CO2 to CH4 and CO fuels, compared with g-C3N4 (HCN) prepared by HCl-assisted hydrothermal stripping and g-C3N4 (TCN) prepared by thermal stripping/etching in air. Methane 90-93 metastasis associated lung adenocarcinoma transcript 1 Homo sapiens 29-32 33882562-6 2021 We estimate that every 10 cm of reduction in WTDe could reduce the net warming impact of CO2 and CH4 emissions (100-year Global Warming Potentials) by at least 3 t CO2e ha-1 yr-1, until WTDe is < 30 cm. Methane 97-100 Rho GTPase activating protein 45 Homo sapiens 169-178 33895952-5 2021 CP could enhance methane production from anaerobic co-digestion of PW and ES. Methane 17-24 ceruloplasmin Homo sapiens 0-2 33876814-2 2021 Methane hydrates, the most well-known gas hydrates, are considered a menace in flow assurance. Methane 0-7 gastrin Homo sapiens 38-41 33895952-6 2021 When the content of CP was 0.2 g/g (in terms of total suspended solids), the maximum methane production was 234.8 mL/g, about 1.4 times of the blank. Methane 85-92 ceruloplasmin Homo sapiens 20-22 33895952-8 2021 The presence of appropriate amount of CP promoted the activities of key enzymes in anaerobic fermentation process, and then increased the efficiency of methane production. Methane 152-159 ceruloplasmin Homo sapiens 38-40 33387767-3 2021 Therefore, the molecular rice breeding with a barley HvSUSIBA2 gene that confers elevated photosynthate flux to grains, is predicted to enhance rice yield and mitigate CH4 emissions in paddies. Methane 168-171 Sugar signaling in barley 2 Hordeum vulgare 53-62 33844496-0 2021 MOF-Mediated Interfacial Polymerization to Fabricate Polyamide Membranes with a Homogeneous Nanoscale Striped Turing Structure for CO2/CH4 Separation. Methane 135-138 lysine acetyltransferase 8 Homo sapiens 0-3 33881798-3 2021 The high-stability of these molecular sites in CHA is a key to intrinsic structure-performance descriptions of elemental steps such as O2 dissociation, and subsequent oxidation catalysis of industrial interest, such as the combustion of methane, propane, and CO. Methane 237-244 transcription factor like 5 Homo sapiens 47-50 33387767-4 2021 Here, in a series of field experiments with differences in growing season and rice variety, we show that SUSIBA2 rice reduced CH4 emissions from paddies. Methane 126-129 Sugar signaling in barley 2 Hordeum vulgare 105-112 33387767-7 2021 The reduction rates also varied between rice varieties, and SUSIBA2 japonica rice showed a more significant CH4 mitigation effect than SUSIBA2 indica rice. Methane 108-111 Sugar signaling in barley 2 Hordeum vulgare 60-67 33387767-9 2021 Compared with the wild type, SUSIBA2 rice significantly reduced soil organic carbon properties and the abundance of CH4-related microbes, and altered methanogenic and methanotrophic communities, indicating that SUSIBA2 rice released less carbon to the soil, which reduced CH4 production. Methane 116-119 Sugar signaling in barley 2 Hordeum vulgare 29-36 33387767-9 2021 Compared with the wild type, SUSIBA2 rice significantly reduced soil organic carbon properties and the abundance of CH4-related microbes, and altered methanogenic and methanotrophic communities, indicating that SUSIBA2 rice released less carbon to the soil, which reduced CH4 production. Methane 116-119 Sugar signaling in barley 2 Hordeum vulgare 211-218 33387767-9 2021 Compared with the wild type, SUSIBA2 rice significantly reduced soil organic carbon properties and the abundance of CH4-related microbes, and altered methanogenic and methanotrophic communities, indicating that SUSIBA2 rice released less carbon to the soil, which reduced CH4 production. Methane 272-275 Sugar signaling in barley 2 Hordeum vulgare 29-36 33387767-9 2021 Compared with the wild type, SUSIBA2 rice significantly reduced soil organic carbon properties and the abundance of CH4-related microbes, and altered methanogenic and methanotrophic communities, indicating that SUSIBA2 rice released less carbon to the soil, which reduced CH4 production. Methane 272-275 Sugar signaling in barley 2 Hordeum vulgare 211-218 33387767-11 2021 Thus, our results show that SUSIBA2 rice substantially reduces CH4 emissions and that SUSIBA2 can potentially mitigate the CH4 emissions of japonica and indica rice under distinct cultivation conditions. Methane 63-66 Sugar signaling in barley 2 Hordeum vulgare 28-35 33387767-11 2021 Thus, our results show that SUSIBA2 rice substantially reduces CH4 emissions and that SUSIBA2 can potentially mitigate the CH4 emissions of japonica and indica rice under distinct cultivation conditions. Methane 123-126 Sugar signaling in barley 2 Hordeum vulgare 86-93 33899409-3 2021 The CH4 concentration decreased from north to south, with the highest value in TAP station (1935.61 nmol mol-1) in Republic of Korea and RYO station (1907.19 nmol mol-1) in Japan. Methane 4-7 nuclear RNA export factor 1 Homo sapiens 79-82 33755454-8 2021 Then, we investigated the reactivities of the (mu-eta2:eta2-NO2)dicopper complex toward methane and benzene by considering the conversions of N2O to N2 in the presence and the absence of methane or benzene. Methane 88-95 DNA polymerase iota Homo sapiens 50-54 33755454-8 2021 Then, we investigated the reactivities of the (mu-eta2:eta2-NO2)dicopper complex toward methane and benzene by considering the conversions of N2O to N2 in the presence and the absence of methane or benzene. Methane 88-95 DNA polymerase iota Homo sapiens 55-59 33755454-8 2021 Then, we investigated the reactivities of the (mu-eta2:eta2-NO2)dicopper complex toward methane and benzene by considering the conversions of N2O to N2 in the presence and the absence of methane or benzene. Methane 187-194 DNA polymerase iota Homo sapiens 50-54 33755454-8 2021 Then, we investigated the reactivities of the (mu-eta2:eta2-NO2)dicopper complex toward methane and benzene by considering the conversions of N2O to N2 in the presence and the absence of methane or benzene. Methane 187-194 DNA polymerase iota Homo sapiens 55-59 33755454-10 2021 Thus, the (mu-eta2:eta2-NO2)dicopper complex prefers the reactions with methane and benzene to that with N2O. Methane 72-79 DNA polymerase iota Homo sapiens 14-18 33755454-10 2021 Thus, the (mu-eta2:eta2-NO2)dicopper complex prefers the reactions with methane and benzene to that with N2O. Methane 72-79 DNA polymerase iota Homo sapiens 19-23 33755454-11 2021 The reaction of the (mu-eta2:eta2-NO2)dicopper complex with methane or benzene generated the (mu-nitrosyl)dicopper complex. Methane 60-67 DNA polymerase iota Homo sapiens 24-28 33755454-11 2021 The reaction of the (mu-eta2:eta2-NO2)dicopper complex with methane or benzene generated the (mu-nitrosyl)dicopper complex. Methane 60-67 DNA polymerase iota Homo sapiens 29-33 33662768-8 2021 When spatial interpolators were applied to field data from the measurement system, the empirical Bayesian kriging demonstrated the best prediction of methane concentrations at unmeasured points. Methane 150-157 thymus, brain and testes associated Homo sapiens 5-12 33562386-2 2021 However, the arbitrary emissions or combustion of the associated gas, which mainly consists of CO2 and CH4, will cause the aggravation of the greenhouse effect and a huge waste of resources. Methane 103-106 gastrin Homo sapiens 65-68 33572312-3 2021 The largest (0.07%) loading of N-doped graphene derivatives impacted the morphology of the CS membrane significantly, reducing the crystallinity, tensile properties, and the KOH uptake, and increasing (by almost 10-fold) the ethanol permeability. Methane 31-47 citrate synthase Homo sapiens 91-93 33443520-5 2021 Most strikingly, the strong blue light emission by nitrogen and sulfur co-doped carbon dots (N,S-CDs) could be encapsulated in 1 to generate a dual-emission composite, namely, N,S-CDs@Eu-MOF, which shows solvent-dependent photoluminescence: N,S-CD-related blue luminescence in water and Eu-MOF-related red emission in organic solvents. Methane 80-91 lysine acetyltransferase 8 Homo sapiens 187-190 33443520-5 2021 Most strikingly, the strong blue light emission by nitrogen and sulfur co-doped carbon dots (N,S-CDs) could be encapsulated in 1 to generate a dual-emission composite, namely, N,S-CDs@Eu-MOF, which shows solvent-dependent photoluminescence: N,S-CD-related blue luminescence in water and Eu-MOF-related red emission in organic solvents. Methane 80-91 lysine acetyltransferase 8 Homo sapiens 290-293 33223238-2 2021 This work develops a label-free probe for Cyt c using the nitrogen and fluorine co-doped carbon dots (N, F-CDs) which were facile prepared through solvothermal method with 3, 4-difluorophenylhydrazine as precursor. Methane 89-100 cytochrome c, somatic Homo sapiens 42-47 33748605-1 2021 A type of carbon molecular sieve (CMS-3KT) was used as the adsorbent for the CH4 enrichment of a methane/oxygen/nitrogen (CH4/O2/N2) mixture using micro-positive pressure vacuum pressure swing adsorption (~120 kPa). Methane 77-80 immunoglobulin kappa variable 1D-39 Homo sapiens 122-131 33596059-0 2021 Correction to "Methane Emissions from Abandoned Oil and Gas Wells in Canada and the United States. Methane 15-22 gastrin Homo sapiens 56-59 33220246-5 2021 Although Fe(III)-citrate group also showed the fastest methane production rate, the efficiency of electron recovery in methane production was only 58-78%, which was evidently lower than that in both crystalline hematite (86-89%) and magnetite (93-97%) groups. Methane 55-62 general transcription factor IIE subunit 1 Homo sapiens 9-16 33127052-2 2021 Herein, we formed a heterostructure between Cu2O and SnS2/SnO2 nanocomposite using a solvothermal reactor, which reduced CO2 by H2O at ambient conditions to produce CO, H2, and CH4. Methane 177-180 sodium voltage-gated channel alpha subunit 11 Homo sapiens 53-57 33652868-3 2021 The permanent porosity of 1 was confirmed by N2, O2, CO, CO2, CH4 adsorption measurements at various temperatures (77 K, 273 K, 298 K), resulted in BET surface area 667 m2 g-1 and promising gas separation performance with selectivity factors up to 35.7 for CO2/N2, 45.4 for CO2/O2, 20.8 for CO2/CO, and 4.8 for CO2/CH4. Methane 62-65 delta/notch like EGF repeat containing Homo sapiens 148-151 33652869-6 2021 It was found that the confined methane hydrates dissociated into ultra viscous low-density liquid water (LDL) and methane gas. Methane 31-38 gastrin Homo sapiens 122-125 33652869-6 2021 It was found that the confined methane hydrates dissociated into ultra viscous low-density liquid water (LDL) and methane gas. Methane 114-121 gastrin Homo sapiens 122-125 33623088-0 2021 Dynamic and history of methane seepage in the SW Barents Sea: new insights from Leirdjupet Fault Complex. Methane 23-30 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 57-60 33623088-5 2021 Methane-derived authigenic carbonates precipitated due to local gas hydrate destabilization, in turn triggered by an increasing influx of warm Atlantic water and isostatic rebound linked to the retreat of the Barents Sea Ice Sheet. Methane 0-7 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 217-220 33562386-5 2021 The membrane exhibits high CO2 permeance of 3.451 x 10-7 mol m-2 s-1 Pa-1 and CO2/CH4 selectivity of 62 at 298 K and 0.15 MPa feed gas pressure. Methane 82-85 gastrin Homo sapiens 131-134 33540619-5 2021 For gas-sensing application, the sensor r-SnO2/GN showed good sensitivity (~13.8 under 500 ppm) and short response/recovering time toward methane gas. Methane 138-145 gastrin Homo sapiens 4-7 33540619-5 2021 For gas-sensing application, the sensor r-SnO2/GN showed good sensitivity (~13.8 under 500 ppm) and short response/recovering time toward methane gas. Methane 138-145 gastrin Homo sapiens 146-149 33135275-1 2021 Aerated topsoils are important sinks for atmospheric methane (CH4 ) via oxidation by CH4 -oxidizing bacteria (MOB). Methane 53-60 sphingomyelin synthase 1 Homo sapiens 110-113 33135275-1 2021 Aerated topsoils are important sinks for atmospheric methane (CH4 ) via oxidation by CH4 -oxidizing bacteria (MOB). Methane 62-65 sphingomyelin synthase 1 Homo sapiens 110-113 33525565-6 2021 As a result, both monensin and NEOH increased feed conversion efficiency of the feedlotting lambs (p < 0.01), suggesting that feed energy saved from CH4 production promoted the feed efficiency and ADG in the present study. Methane 149-152 ADG Ovis aries 197-200 33310598-3 2021 Results demonstrate that the ALK-2-CSTRs effectively promoted methane yield from the co-substrates via promoting hydrolysis, long chain fatty acids (LCFAs) degradation and protecting methanogens from exposure to high concentration of LCFAs directly. Methane 62-69 activin A receptor type 1 Homo sapiens 29-34 33463146-4 2021 The unique tubular channels lead to not only remarkable gas sorption capacity of C2H4, C2H2, and CO2, but also good selectivity for C2H2/CH4, C2H2/CH4, CO2/CH4, and C2H2/CO2, as demonstrated by single-component sorption isotherm results, ideal adsorbed solution theory calculations, and dynamic breakthrough curves. Methane 137-140 gastrin Homo sapiens 56-59 33439639-4 2021 Conveniently, methanol obtained from the gas phase could be easily isolated from the catalyst without contamination with CO, CH4, or formic acid (FA). Methane 125-128 gastrin Homo sapiens 41-44 33400502-6 2021 At the same time, the separation performance of H2/CH4 gas pair surpasses the 2008 upper bound and that of CO2/CH4 gas pair nearly approaches the 2008 upper bound. Methane 51-54 gastrin Homo sapiens 55-58 33443439-8 2021 The diffusion of gas molecules follows the order of CO2 > N2 (for CO2/N2) and CH4 > CO2 (for CO2/CH4) in the bulk and N2 > CO2 (for CO2/N2) and CH4 > CO2 (for CO2/CH4) at the interface of porous liquids. Methane 78-81 complement C2 Homo sapiens 93-100 33443439-8 2021 The diffusion of gas molecules follows the order of CO2 > N2 (for CO2/N2) and CH4 > CO2 (for CO2/CH4) in the bulk and N2 > CO2 (for CO2/N2) and CH4 > CO2 (for CO2/CH4) at the interface of porous liquids. Methane 78-81 complement C2 Homo sapiens 159-166 33400502-6 2021 At the same time, the separation performance of H2/CH4 gas pair surpasses the 2008 upper bound and that of CO2/CH4 gas pair nearly approaches the 2008 upper bound. Methane 111-114 gastrin Homo sapiens 115-118 32911412-3 2021 Such a chemical interaction made the optimized TC/PCN-2 with 2 wt% loading of Ti3C2 possess highest CH4 production (0.99 mumol h-1 g-1catalyst) under visible light (>420 nm), which was 14 times higher than that of pure PCN (0.07 micromol h-1 gcatalyst-1) at the same condition. Methane 100-103 potassium voltage-gated channel subfamily A member 4 Homo sapiens 50-55 33322902-1 2021 Abandoned oil and gas wells are one of the most uncertain sources of methane emissions into the atmosphere. Methane 69-76 gastrin Homo sapiens 18-21 33521461-0 2021 Synergetic Effect of Water, Temperature, and Pressure on Methane Adsorption in Shale Gas Reservoirs. Methane 57-64 gastrin Homo sapiens 85-88 31159681-5 2021 The methane percentage in biogas produced from digesters with INT and CON mixing were 63% and 62%, respectively, which were 4% and 5% higher than that from digesters with NO mixing (58%). Methane 4-11 inturned planar cell polarity protein Homo sapiens 62-65 33166885-0 2021 Corrigendum to "Construction of novel microbial consortia CS-5 and BC-4 valued for the degradation of catalpa sawdust and chlorophenols simultaneously with enhancing methane production" [Bioresource Technol. Methane 166-173 chorionic somatomammotropin hormone like 1 Homo sapiens 58-62 31159681-6 2021 The specific methane yield for digesters with NO, INT and CON mixing was 1.15, 1.15, and 1.49 m3-methane per kg-VS destroyed, however, those differences were not statistically significant (p > 0.05). Methane 13-20 inturned planar cell polarity protein Homo sapiens 50-53 33169990-0 2020 Eight-Year Estimates of Methane Emissions from Oil and Gas Operations in Western Canada Are Nearly Twice Those Reported in Inventories. Methane 24-31 gastrin Homo sapiens 55-58 33369565-9 2020 Gastrin levels were higher in GBT(H2)+ patients and lower in GBT(CH4)+ patients than those in GBT- patients. Methane 65-68 gastrin Homo sapiens 0-7 33307694-1 2020 Mass spectrometric analysis of the anionic products of interaction among Pt-, methane, and carbon dioxide shows that the methane activation complex, H3C-Pt-H-, reacts with CO2 to form [H3C-Pt-H(CO2)]-. Methane 78-85 parathyroid hormone Homo sapiens 153-157 33307694-1 2020 Mass spectrometric analysis of the anionic products of interaction among Pt-, methane, and carbon dioxide shows that the methane activation complex, H3C-Pt-H-, reacts with CO2 to form [H3C-Pt-H(CO2)]-. Methane 78-85 parathyroid hormone Homo sapiens 189-193 33307694-1 2020 Mass spectrometric analysis of the anionic products of interaction among Pt-, methane, and carbon dioxide shows that the methane activation complex, H3C-Pt-H-, reacts with CO2 to form [H3C-Pt-H(CO2)]-. Methane 121-128 parathyroid hormone Homo sapiens 153-157 33307694-1 2020 Mass spectrometric analysis of the anionic products of interaction among Pt-, methane, and carbon dioxide shows that the methane activation complex, H3C-Pt-H-, reacts with CO2 to form [H3C-Pt-H(CO2)]-. Methane 121-128 parathyroid hormone Homo sapiens 189-193 33307694-3 2020 Mechanistic study reveals that both CH4 and CO2 are activated by the anionic Pt atom and that the successive depletion of the negative charge on Pt drives the CO2 insertion into the Pt-H and Pt-C bonds of H3C-Pt-H-. Methane 36-39 parathyroid hormone Homo sapiens 182-186 33307694-3 2020 Mechanistic study reveals that both CH4 and CO2 are activated by the anionic Pt atom and that the successive depletion of the negative charge on Pt drives the CO2 insertion into the Pt-H and Pt-C bonds of H3C-Pt-H-. Methane 36-39 coiled-coil domain containing 6 Homo sapiens 191-195 33307694-3 2020 Mechanistic study reveals that both CH4 and CO2 are activated by the anionic Pt atom and that the successive depletion of the negative charge on Pt drives the CO2 insertion into the Pt-H and Pt-C bonds of H3C-Pt-H-. Methane 36-39 parathyroid hormone Homo sapiens 209-213 32966698-0 2020 Carbide Dihydrides: Carbonaceous Species Identified in Ta4+-Mediated Methane Dehydrogenation. Methane 69-76 trace amine associated receptor 6 Homo sapiens 55-58 33301703-6 2022 Next to this, gas production results show that the methane production was not affected by the ash addition, while the total gas release was reduced. Methane 51-58 gastrulation-defective Drosophila melanogaster 14-17 32743964-4 2020 This work provides the first example of gas phase CO 2 photoreduction into methane without organic sacrificial agents on a MOF platform, thereby paving an avenue for developing MOF-based photocatalysts for applications in CO 2 photoreduction and other types of photoreactions. Methane 75-82 gastrin Homo sapiens 40-43 33314919-0 2021 Mobile Measurement System for the Rapid and Cost-Effective Surveillance of Methane and Volatile Organic Compound Emissions from Oil and Gas Production Sites. Methane 75-82 gastrin Homo sapiens 136-139 33344802-0 2020 Insight into the Adsorption of Methane on Gas Shales and the Induced Shale Swelling. Methane 31-38 gastrin Homo sapiens 42-45 33344802-4 2020 Adsorption and desorption of methane gas are some of the important physical and chemical processes involved in the accumulation, transport, and production of shale gas. Methane 29-36 gastrin Homo sapiens 37-40 33344802-4 2020 Adsorption and desorption of methane gas are some of the important physical and chemical processes involved in the accumulation, transport, and production of shale gas. Methane 29-36 gastrin Homo sapiens 164-167 33344802-5 2020 The shale matrix will shrink or swell due to the desorption or adsorption of methane gas, which will impact the recovery of shale gas reservoirs. Methane 77-84 gastrin Homo sapiens 85-88 33344802-5 2020 The shale matrix will shrink or swell due to the desorption or adsorption of methane gas, which will impact the recovery of shale gas reservoirs. Methane 77-84 gastrin Homo sapiens 130-133 33344802-6 2020 The main purpose of this investigation is to quantitatively ascertain how the adsorption of methane gas affects the volumetric changes of the shale matrix. Methane 92-99 gastrin Homo sapiens 100-103 33344802-7 2020 Based on the adsorption potential theory, a modified Dubinin-Astakhov (D-A) equation was employed to describe the adsorption of supercritical methane gas on shale. Methane 142-149 gastrin Homo sapiens 150-153 33169990-1 2020 The provinces of Alberta and Saskatchewan account for 70% of Canada"s methane emissions from the oil and gas sector. Methane 70-77 gastrin Homo sapiens 105-108 32758912-10 2020 We further conclude that increasing NO3- load can drive the DAMO process with more important implications on methane sink in estuarine ecosystems. Methane 109-116 NBL1, DAN family BMP antagonist Homo sapiens 36-39 33001080-1 2020 A novel expanded metal-organic framework (UTSA-111a) with functional pyrimidine sites exhibits simultaneously high gravimetric and volumetric methane storage working capacities of 309 cm3 (STP) g-1 and 183 cm3 (STP) cm-3 at 298 K and 5.8-65 bar. Methane 142-149 sulfotransferase family 1A member 1 Homo sapiens 189-192 33001080-1 2020 A novel expanded metal-organic framework (UTSA-111a) with functional pyrimidine sites exhibits simultaneously high gravimetric and volumetric methane storage working capacities of 309 cm3 (STP) g-1 and 183 cm3 (STP) cm-3 at 298 K and 5.8-65 bar. Methane 142-149 proline rich protein BstNI subfamily 3 Homo sapiens 194-209 33108865-0 2020 Projecting the Temporal Evolution of Methane Emissions from Oil and Gas Production Sites. Methane 37-44 gastrin Homo sapiens 68-71 33108865-1 2020 Many recent studies have reported methane emissions from oil and gas production regions, often reporting results as a methane emission intensity (methane emitted as a percentage of natural gas produced or methane produced). Methane 34-41 gastrin Homo sapiens 65-68 33108865-1 2020 Many recent studies have reported methane emissions from oil and gas production regions, often reporting results as a methane emission intensity (methane emitted as a percentage of natural gas produced or methane produced). Methane 118-125 gastrin Homo sapiens 65-68 33108865-1 2020 Many recent studies have reported methane emissions from oil and gas production regions, often reporting results as a methane emission intensity (methane emitted as a percentage of natural gas produced or methane produced). Methane 118-125 gastrin Homo sapiens 189-192 33108865-1 2020 Many recent studies have reported methane emissions from oil and gas production regions, often reporting results as a methane emission intensity (methane emitted as a percentage of natural gas produced or methane produced). Methane 118-125 gastrin Homo sapiens 65-68 33108865-1 2020 Many recent studies have reported methane emissions from oil and gas production regions, often reporting results as a methane emission intensity (methane emitted as a percentage of natural gas produced or methane produced). Methane 118-125 gastrin Homo sapiens 189-192 33108865-1 2020 Many recent studies have reported methane emissions from oil and gas production regions, often reporting results as a methane emission intensity (methane emitted as a percentage of natural gas produced or methane produced). Methane 118-125 gastrin Homo sapiens 65-68 33108865-1 2020 Many recent studies have reported methane emissions from oil and gas production regions, often reporting results as a methane emission intensity (methane emitted as a percentage of natural gas produced or methane produced). Methane 118-125 gastrin Homo sapiens 189-192 33121247-6 2020 In the current study, we created ascorbic acid-PEI carbon dots (CD), which were able to carry miR-2861, by the microwave-assisted pyrolysis method. Methane 51-62 microRNA 2861 Homo sapiens 94-102 33079552-9 2020 For CH4 dissociation, again embedded ASCI overestimates the dissociation barrier compared to emb-CASPT2 predictions. Methane 4-7 embigin Homo sapiens 28-31 33064815-7 2021 In regard to CH4, when the Q1 concentration was defined as the reference, the risks of gout were increased for participants exposed to the Q2, Q3 and Q4 concentrations (aHR, 1.16 with 95% CI, 1.06-1.26 in the Q2 concentration of CH4; aHR, 2.37 with 95% CI, 2.20-2.55 in the Q3 concentration of CH4; aHR, 8.73 with 95% CI, 8.16-9.34 in the Q4 concentration of CH4). Methane 13-16 aryl hydrocarbon receptor Homo sapiens 169-172 32604523-3 2020 To find the suitable rate, 25 sccm CH4, which is used as the source gas, was first injected into the chamber, and the characteristics were confirmed by changing the amount of H2 gas from 0 to 50 sccm. Methane 35-38 gastrin Homo sapiens 68-71 33063985-5 2020 As a result, the 6FDA-durene-DABA/CBMN MMMs exhibit improved separation performance for the CO2/CH4 and H2/CH4 gas pairs with H2/CH4 and CO2/CH4 selectivities up to 42.0 +- 4.0 and 33.6 +- 3.0, respectively. Methane 107-110 gastrin Homo sapiens 111-114 33063985-5 2020 As a result, the 6FDA-durene-DABA/CBMN MMMs exhibit improved separation performance for the CO2/CH4 and H2/CH4 gas pairs with H2/CH4 and CO2/CH4 selectivities up to 42.0 +- 4.0 and 33.6 +- 3.0, respectively. Methane 107-110 gastrin Homo sapiens 111-114 33063985-5 2020 As a result, the 6FDA-durene-DABA/CBMN MMMs exhibit improved separation performance for the CO2/CH4 and H2/CH4 gas pairs with H2/CH4 and CO2/CH4 selectivities up to 42.0 +- 4.0 and 33.6 +- 3.0, respectively. Methane 107-110 gastrin Homo sapiens 111-114 33063985-6 2020 The enhanced interfacial interaction leads to the comprehensive separation performance of CO2/CH4 and H2/CH4 gas pairs approaching or surpassing the 2008 Robeson upper bound. Methane 105-108 gastrin Homo sapiens 109-112 33063985-8 2020 When separating a mixed gas of CO2/CH4, the selectivity of CO2/CH4 remains stable at around 23 and the CO2 permeability keeps around 400 barrer during the long-term test. Methane 35-38 gastrin Homo sapiens 24-27 33063985-8 2020 When separating a mixed gas of CO2/CH4, the selectivity of CO2/CH4 remains stable at around 23 and the CO2 permeability keeps around 400 barrer during the long-term test. Methane 63-66 gastrin Homo sapiens 24-27 33064815-7 2021 In regard to CH4, when the Q1 concentration was defined as the reference, the risks of gout were increased for participants exposed to the Q2, Q3 and Q4 concentrations (aHR, 1.16 with 95% CI, 1.06-1.26 in the Q2 concentration of CH4; aHR, 2.37 with 95% CI, 2.20-2.55 in the Q3 concentration of CH4; aHR, 8.73 with 95% CI, 8.16-9.34 in the Q4 concentration of CH4). Methane 229-232 aryl hydrocarbon receptor Homo sapiens 169-172 33056993-0 2020 Plant species determine tidal wetland methane response to sea level rise. Methane 38-45 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 58-61 32643319-7 2020 We find a quasi-Mars-van-Krevelen (quasi-MvK) surface reaction mechanism involving extracting and refilling the surface carbon atoms for the nonoxidative conversion of methane on Fe 1 SiO 2 and this new surface process is identified to be more plausible than the alternative gas-phase reaction mechanism. Methane 168-175 mevalonate kinase Homo sapiens 41-44 32930574-3 2020 Herein, a kind of novel MXene/N-doped carbon foam (MXene/NCF) compressible composite with 3D hollow interconnected neuron-like architecture is directly prepared by one-step pyrolysis, and used for the freestanding, highly compressible supercapacitors. Methane 38-49 neutrophil cytosolic factor 4 Homo sapiens 57-60 32869639-0 2020 3D-Printed Miniature Fiber-Coupled Multi-pass Cell with Dense Spot Pattern for Ppb-level Methane Detection Using a Near-IR Diode Laser. Methane 89-96 histatin 1 Homo sapiens 79-82 32502870-10 2020 BC amendment to DM1, DM2 and IN significantly reduced cumulative CO2 emission by 16, 25.5 and 26.5%, CH4 emission by 184, 200 and 293% and N2O emission by 95, 86 and 93% respectively. Methane 101-104 DM1 protein kinase Homo sapiens 16-19 32502870-10 2020 BC amendment to DM1, DM2 and IN significantly reduced cumulative CO2 emission by 16, 25.5 and 26.5%, CH4 emission by 184, 200 and 293% and N2O emission by 95, 86 and 93% respectively. Methane 101-104 immunoglobulin heavy diversity 1-14 (non-functional) Homo sapiens 21-24 33455181-2 2020 In this study, amino phenylboronic acid-modified carbon dots (APBA-CDs) were introduced as a new nanoparticle-based on gp120 targeting that inhibits HIV-1 entry processes. Methane 49-60 inter-alpha-trypsin inhibitor heavy chain 4 Homo sapiens 119-124 32783833-0 2020 Methane concentrations in streams reveal gas leak discharges in regions of oil, gas, and coal development. Methane 0-7 gastrin Homo sapiens 41-44 32783833-0 2020 Methane concentrations in streams reveal gas leak discharges in regions of oil, gas, and coal development. Methane 0-7 gastrin Homo sapiens 80-83 32783833-1 2020 As natural gas has grown in importance as a global energy source, leakage of methane (CH4) from wells has sometimes been noted. Methane 77-84 gastrin Homo sapiens 11-14 32783833-11 2020 Instead, the median was statistically highest where dense coal mining was accompanied by conventional and unconventional oil and gas development, emphasizing the importance of CH4 contamination from coal mines into streams. Methane 176-179 gastrin Homo sapiens 129-132 32897698-0 2020 Enhancing Adsorption and Reaction Kinetics of Polysulfides by CoP Coated N-doped Mesoporous Carbon for High-Energy-Density Lithium-Sulfur Batteries. Methane 81-98 caspase recruitment domain family member 16 Homo sapiens 62-65 32894021-4 2020 Remarkably, photocatalytic CO2 reduction results indicate that COF-367-CoIII exhibits favorable activity and significantly enhanced selectivity to HCOOH, accordingly much reduced activ-ity and selectivity to CO and CH4, in sharp contrast to COF-367-CoII. Methane 215-218 mitochondrially encoded cytochrome c oxidase III Homo sapiens 71-76 32894021-4 2020 Remarkably, photocatalytic CO2 reduction results indicate that COF-367-CoIII exhibits favorable activity and significantly enhanced selectivity to HCOOH, accordingly much reduced activ-ity and selectivity to CO and CH4, in sharp contrast to COF-367-CoII. Methane 215-218 mitochondrially encoded cytochrome c oxidase II Homo sapiens 71-75 33003730-2 2020 The HO2 radical is formed in a microwave discharge flow tube reactor through a set of reactions initiated by F atoms in a CH4/O2/He gas mixture. Methane 122-125 heme oxygenase 2 Homo sapiens 4-7 33015485-7 2020 Furthermore, a self-promoting microcirculation reaction network is proposed to help analyze the chemical reactions involved in the multicomponent (CH4/CO/C2H6/H2) gas explosion. Methane 147-150 relaxin 2 Homo sapiens 154-161 32417581-4 2020 Meta-regression analyses, however, indicated a shift from a positive to a negative effect on soil CH4 uptake with increasing N additions both in boreal forests (threshold = 48 kg N ha-1 yr-1) and temperate forests (threshold = 27 kg N ha-1 yr-1), while no such shift was found in subtropical and tropical forests. Methane 98-101 solute carrier family 9 member B1 Homo sapiens 179-190 32879796-6 2020 The highest hydrogen and methane production of 8.7 m3 H2 ton-1 of high moisture MSW and 66.6 m3 CH4 ton-1 of high moisture MSW was achieved at organic loading of 43 gVS L-1 at IFA addition of 1% by two-stage AD process. Methane 25-32 COP9 signalosome subunit 4 Drosophila melanogaster 96-99 32922653-0 2020 Methane Ameliorates Lipopolysaccharide-Induced Acute Orchitis by Anti-inflammatory, Antioxidative, and Antiapoptotic Effects via Regulation of the PK2/PKR1 Pathway. Methane 0-7 prokineticin 2 Rattus norvegicus 147-150 32922653-0 2020 Methane Ameliorates Lipopolysaccharide-Induced Acute Orchitis by Anti-inflammatory, Antioxidative, and Antiapoptotic Effects via Regulation of the PK2/PKR1 Pathway. Methane 0-7 prokineticin receptor 1 Rattus norvegicus 151-155 32922653-12 2020 Furthermore, methane significantly increased SOD levels, decreased MDA levels, and decreased testicular expression of PK2 and PKR1. Methane 13-20 prokineticin 2 Rattus norvegicus 118-121 32922653-12 2020 Furthermore, methane significantly increased SOD levels, decreased MDA levels, and decreased testicular expression of PK2 and PKR1. Methane 13-20 prokineticin receptor 1 Rattus norvegicus 126-130 32644794-2 2020 In this study, the formation of protein coronas of fluorescent carbon dots (CDs) in roast beef with human serum albumin (HSA) and the corona effect on toxicity were reported. Methane 63-74 albumin Homo sapiens 106-119 32891383-2 2020 Herein, a coulometric signal readout is proposed instead of the potentiometric response for detection of NO3- based on an ordered mesoporous carbon (OMC)-based solid-contact ion-selective electrode (ISE). Methane 130-147 NBL1, DAN family BMP antagonist Homo sapiens 105-108 33102433-0 2020 Aerosol-Assisted Assembly of Mesoporous Carbon Spheres With Fast and Stable K-ion Storage. Methane 29-46 Fas activated serine/threonine kinase Homo sapiens 60-64 32803321-1 2020 A turn-on method for determining alpha-glucosidase activity is described using a chemical redox strategy in which the fluorescence of red fluorescent carbon dots (CDs) is modulated. Methane 150-161 sucrase-isomaltase Homo sapiens 33-50 32303014-1 2020 Dual targeted therapy in HER2-positive breast cancer cells with the combination of carbon dots/HER3 siRNA and Trastuzumab resulted in enhanced antitumor activity, which overcomes the resistance to Trastuzumab monotherapy. Methane 83-94 erb-b2 receptor tyrosine kinase 2 Homo sapiens 25-29 32662651-9 2020 The intra-atomic energy changes that occur in these systems are related to the hybridization of the heavy atoms in an analogous manner to the hybridization of C in CH4 from (2s)2(2p)2 to sp3 hybrid orbitals. Methane 164-167 Sp3 transcription factor Homo sapiens 187-190 32498160-6 2020 The highest and lowest CH4 emissions were from B45 and B15 in the first year, and B45 and B30 in the second year, respectively. Methane 23-26 NADH:ubiquinone oxidoreductase subunit B4 Homo sapiens 55-58 32498160-7 2020 Relative to the control, B15 and B30 reduced CH4 emission by 124% and 132% as averaged over 2-yr. With biochar amendments, total N2O emission was decreased by 71-110% and 39-47% in the first and second year. Methane 45-48 NADH:ubiquinone oxidoreductase subunit B4 Homo sapiens 25-28 32692922-3 2020 As a concrete example, we explore the gas separation of CO2 and CH4 by the two-layer membrane using a molecular dynamics simulation. Methane 64-67 gastrin Homo sapiens 38-41 32613831-7 2020 We also tested transfer learning across different gas species (i.e. from H2 to CH4), with predictive accuracy of CH4 adsorption being improved from 0.935 (direct training) to 0.980 (transfer learning). Methane 113-116 gastrin Homo sapiens 50-53 32775930-3 2020 Results show that with an increase of methane mole fraction in the hydrogen/methane system, the upper turning point (P 1-2, T 1-2) remains almost unchanged and the lower transition point (P 2-3, T 2-3) rotates counterclockwise around (P 1-2, T 1-2). Methane 38-45 DNA polymerase epsilon 4, accessory subunit Homo sapiens 117-129 32775930-3 2020 Results show that with an increase of methane mole fraction in the hydrogen/methane system, the upper turning point (P 1-2, T 1-2) remains almost unchanged and the lower transition point (P 2-3, T 2-3) rotates counterclockwise around (P 1-2, T 1-2). Methane 38-45 prostaglandin E synthase 3 Homo sapiens 188-200 32775930-3 2020 Results show that with an increase of methane mole fraction in the hydrogen/methane system, the upper turning point (P 1-2, T 1-2) remains almost unchanged and the lower transition point (P 2-3, T 2-3) rotates counterclockwise around (P 1-2, T 1-2). Methane 38-45 DNA polymerase epsilon 4, accessory subunit Homo sapiens 235-247 32775930-3 2020 Results show that with an increase of methane mole fraction in the hydrogen/methane system, the upper turning point (P 1-2, T 1-2) remains almost unchanged and the lower transition point (P 2-3, T 2-3) rotates counterclockwise around (P 1-2, T 1-2). Methane 76-83 DNA polymerase epsilon 4, accessory subunit Homo sapiens 117-129 32775930-3 2020 Results show that with an increase of methane mole fraction in the hydrogen/methane system, the upper turning point (P 1-2, T 1-2) remains almost unchanged and the lower transition point (P 2-3, T 2-3) rotates counterclockwise around (P 1-2, T 1-2). Methane 76-83 prostaglandin E synthase 3 Homo sapiens 188-200 32775930-3 2020 Results show that with an increase of methane mole fraction in the hydrogen/methane system, the upper turning point (P 1-2, T 1-2) remains almost unchanged and the lower transition point (P 2-3, T 2-3) rotates counterclockwise around (P 1-2, T 1-2). Methane 76-83 DNA polymerase epsilon 4, accessory subunit Homo sapiens 235-247 32519849-0 2020 A national estimate of methane leakage from pipeline mains in natural gas local distribution systems. Methane 23-30 gastrin Homo sapiens 70-73 32519849-1 2020 We estimate methane emissions from U.S. local distribution natural gas (NG) pipes using data collected from an advanced mobile leak detection (AMLD) platform. Methane 12-19 gastrin Homo sapiens 67-70 32441519-1 2020 This study investigated structural transformation, guest distributions, and the extent of replacement for CH4+C3H8 - flue gas replacement occurring in sII hydrates via gas chromatography, NMR spectroscopy, and powder X-ray diffraction (PXRD). Methane 106-109 transcription elongation factor A1 Homo sapiens 151-154 32452684-1 2020 Low temperature anaerobic methane conversion to methanol (MTM) using copper ion-exchanged mordenite (Cu-MOR) as the catalyst and water as the sole source of oxygen is promising for sustainable utilization of methane. Methane 26-33 opioid receptor mu 1 Homo sapiens 104-107 32452684-1 2020 Low temperature anaerobic methane conversion to methanol (MTM) using copper ion-exchanged mordenite (Cu-MOR) as the catalyst and water as the sole source of oxygen is promising for sustainable utilization of methane. Methane 208-215 opioid receptor mu 1 Homo sapiens 104-107 32556737-1 2020 A ratiometric fluorescent test pen filled with a mixing ink of blue carbon dots (CDs) and red CdTe quantum dots (CdTe QDs) is introduced for portable assay of silver ion (Ag(I)) on paper. Methane 68-79 proprotein convertase subtilisin/kexin type 1 inhibitor Homo sapiens 31-34 32441519-6 2020 CO2 and N2 were not complementary but competitive in replacing CH4 in the small (512) cages, which contributed to maintenance of the cage stability of the initial sII hydrate and, thus, resulted in a lower extent of replacement. Methane 63-66 transcription elongation factor A1 Homo sapiens 163-166 32679786-6 2020 At 270 K and methane adsorption value of ~8 mmol/g, the isosteric heat capacity of the methane-AC-4 system exceeded by ~45% that evaluated for the methane-AC-6 system. Methane 13-20 adenylate cyclase 4 Homo sapiens 95-99 32679786-6 2020 At 270 K and methane adsorption value of ~8 mmol/g, the isosteric heat capacity of the methane-AC-4 system exceeded by ~45% that evaluated for the methane-AC-6 system. Methane 87-94 adenylate cyclase 4 Homo sapiens 95-99 32679786-6 2020 At 270 K and methane adsorption value of ~8 mmol/g, the isosteric heat capacity of the methane-AC-4 system exceeded by ~45% that evaluated for the methane-AC-6 system. Methane 87-94 adenylate cyclase 6 Homo sapiens 155-159 32679786-6 2020 At 270 K and methane adsorption value of ~8 mmol/g, the isosteric heat capacity of the methane-AC-4 system exceeded by ~45% that evaluated for the methane-AC-6 system. Methane 87-94 adenylate cyclase 4 Homo sapiens 95-99 32679786-6 2020 At 270 K and methane adsorption value of ~8 mmol/g, the isosteric heat capacity of the methane-AC-4 system exceeded by ~45% that evaluated for the methane-AC-6 system. Methane 87-94 adenylate cyclase 6 Homo sapiens 155-159 32679786-7 2020 The higher micropore volume and structural heterogeneity of the more activated AC-6 compared to AC-4 determine its superior methane adsorption performance. Methane 124-131 adenylate cyclase 6 Homo sapiens 79-83 32679786-7 2020 The higher micropore volume and structural heterogeneity of the more activated AC-6 compared to AC-4 determine its superior methane adsorption performance. Methane 124-131 adenylate cyclase 4 Homo sapiens 96-100 32650459-0 2020 Antiresonant Hollow-Core Fiber-Based Dual Gas Sensor for Detection of Methane and Carbon Dioxide in the Near- and Mid-Infrared Regions. Methane 70-77 gastrin Homo sapiens 42-45 32610915-4 2020 Although microorganism-produced proteins and polypeptides, including marine methylotroph porin proteins, can accelerate methane hydrate formation under conditions simulating their natural occurrence at the seafloor, the role that particular peptide sequences play in biocatalytic hydrate kinetics enhancement is unclear, especially the underlying molecular-level mechanisms. Methane 120-127 voltage dependent anion channel 1 Homo sapiens 89-94 32291646-0 2020 Enhanced Pb(II) adsorption onto functionalized ordered mesoporous carbon (OMC) from aqueous solutions: the important role of surface property and adsorption mechanism. Methane 55-72 submaxillary gland androgen regulated protein 3B Homo sapiens 9-15 32291646-1 2020 Functionalized ordered mesoporous carbon (MOMC-NP) was synthesized by chemical modification using HNO3 and H3PO4 to enhance Pb(II) adsorption. Methane 23-40 submaxillary gland androgen regulated protein 3B Homo sapiens 124-130 32441519-2 2020 Simulated flue gas (CO2 (20%)+N2 (80%)) was injected into an sII CH4 (90%)+C3H8 (10%) hydrate for guest exchange. Methane 65-68 transcription elongation factor A1 Homo sapiens 61-64 32545838-1 2020 This research revealed the effect of carboxyl-functionalization on the mesoporous carbon (MC)-fixed glucose oxidase (GOx) for promoting the properties of bioelectrodes. Methane 71-88 hydroxyacid oxidase 1 Homo sapiens 117-120 32500859-0 2020 Methane Alleviates Inflammation and Apoptosis of Dextran Sulfate Sodium-Induced Inflammatory Bowel Diseases by Inhibiting Toll-Like Receptor 4 (TLR4)/Myeloid Differentiation Factor 88 (MyD88)/Nuclear Translocation of Nuclear Factor-kappaB (NF-kappaB) and Endoplasmic Reticulum Stress Pathways in Mice. Methane 0-7 toll-like receptor 4 Mus musculus 122-142 32401514-1 2020 Until now, reactions between methane photolysis products (CH3 , CH2) and active N atom or reactive NO radical are proposed as routes of HCN formation in prebiotic earth. Methane 29-36 metastasis associated lung adenocarcinoma transcript 1 Homo sapiens 136-139 32500859-0 2020 Methane Alleviates Inflammation and Apoptosis of Dextran Sulfate Sodium-Induced Inflammatory Bowel Diseases by Inhibiting Toll-Like Receptor 4 (TLR4)/Myeloid Differentiation Factor 88 (MyD88)/Nuclear Translocation of Nuclear Factor-kappaB (NF-kappaB) and Endoplasmic Reticulum Stress Pathways in Mice. Methane 0-7 toll-like receptor 4 Mus musculus 144-148 32500859-0 2020 Methane Alleviates Inflammation and Apoptosis of Dextran Sulfate Sodium-Induced Inflammatory Bowel Diseases by Inhibiting Toll-Like Receptor 4 (TLR4)/Myeloid Differentiation Factor 88 (MyD88)/Nuclear Translocation of Nuclear Factor-kappaB (NF-kappaB) and Endoplasmic Reticulum Stress Pathways in Mice. Methane 0-7 myeloid differentiation primary response gene 88 Mus musculus 185-190 32500859-0 2020 Methane Alleviates Inflammation and Apoptosis of Dextran Sulfate Sodium-Induced Inflammatory Bowel Diseases by Inhibiting Toll-Like Receptor 4 (TLR4)/Myeloid Differentiation Factor 88 (MyD88)/Nuclear Translocation of Nuclear Factor-kappaB (NF-kappaB) and Endoplasmic Reticulum Stress Pathways in Mice. Methane 0-7 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 Mus musculus 217-238 32500859-0 2020 Methane Alleviates Inflammation and Apoptosis of Dextran Sulfate Sodium-Induced Inflammatory Bowel Diseases by Inhibiting Toll-Like Receptor 4 (TLR4)/Myeloid Differentiation Factor 88 (MyD88)/Nuclear Translocation of Nuclear Factor-kappaB (NF-kappaB) and Endoplasmic Reticulum Stress Pathways in Mice. Methane 0-7 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 Mus musculus 240-249 32684189-3 2020 Starting with a systematic review of the terms "informatics, bioinformatics and big data" in animal health this special issue of AHRR illustrates some big-data applications with papers on how the use of various omics methods may be used to facilitate the development of improved diagnostics, therapeutics, and vaccines for foodborne pathogens in poultry and on how a better understanding of rumen microbiota could lead to improved feed absorption while minimizing methane production. Methane 464-471 aryl hydrocarbon receptor repressor Bos taurus 129-133 32079441-0 2020 Methane attenuates lung ischemia-reperfusion injury via regulating PI3K-AKT-NFkappaB signaling pathway. Methane 0-7 AKT serine/threonine kinase 1 Rattus norvegicus 72-75 32279166-3 2020 In this work, we developed a peptide-modified ratiometric fluorescent nanoprobe based on carbon dots (CDs) and gold nanoclusters (AuNCs) for the measurements of a pivotal biomarker S100B protein in the early diagnosis of mTBI. Methane 89-100 S100 calcium binding protein B Homo sapiens 181-186 32079441-8 2020 Methane suppressed the expression of the PI3K-AKT-NFkappaB signaling pathway during the lung IR injury, which inhibited the activation of NF-kB and decreased the level of inflammatory cytokines, such as TNF-alpha, IL-1beta, and IL-10. Methane 0-7 AKT serine/threonine kinase 1 Rattus norvegicus 46-49 32079441-8 2020 Methane suppressed the expression of the PI3K-AKT-NFkappaB signaling pathway during the lung IR injury, which inhibited the activation of NF-kB and decreased the level of inflammatory cytokines, such as TNF-alpha, IL-1beta, and IL-10. Methane 0-7 nuclear factor kappa B subunit 1 Rattus norvegicus 138-143 32079441-8 2020 Methane suppressed the expression of the PI3K-AKT-NFkappaB signaling pathway during the lung IR injury, which inhibited the activation of NF-kB and decreased the level of inflammatory cytokines, such as TNF-alpha, IL-1beta, and IL-10. Methane 0-7 tumor necrosis factor Rattus norvegicus 203-212 32079441-8 2020 Methane suppressed the expression of the PI3K-AKT-NFkappaB signaling pathway during the lung IR injury, which inhibited the activation of NF-kB and decreased the level of inflammatory cytokines, such as TNF-alpha, IL-1beta, and IL-10. Methane 0-7 interleukin 1 alpha Rattus norvegicus 214-222 32079441-8 2020 Methane suppressed the expression of the PI3K-AKT-NFkappaB signaling pathway during the lung IR injury, which inhibited the activation of NF-kB and decreased the level of inflammatory cytokines, such as TNF-alpha, IL-1beta, and IL-10. Methane 0-7 interleukin 10 Rattus norvegicus 228-233 32368914-3 2020 Besides, this study observes the structural coexistence of S-I and S-II methane hydrates as the large 51264 cages appear along with small 512 and large 51262 cages, in which, the low methane concentration favors the S-II structure. Methane 72-79 transcription elongation factor A1 Homo sapiens 67-71 32368914-3 2020 Besides, this study observes the structural coexistence of S-I and S-II methane hydrates as the large 51264 cages appear along with small 512 and large 51262 cages, in which, the low methane concentration favors the S-II structure. Methane 72-79 transcription elongation factor A1 Homo sapiens 216-220 32368914-3 2020 Besides, this study observes the structural coexistence of S-I and S-II methane hydrates as the large 51264 cages appear along with small 512 and large 51262 cages, in which, the low methane concentration favors the S-II structure. Methane 183-190 transcription elongation factor A1 Homo sapiens 67-71 32368914-3 2020 Besides, this study observes the structural coexistence of S-I and S-II methane hydrates as the large 51264 cages appear along with small 512 and large 51262 cages, in which, the low methane concentration favors the S-II structure. Methane 183-190 transcription elongation factor A1 Homo sapiens 216-220 32414061-5 2020 Attenuated total reflectance Fourier-transform infrared (ATR-FTIR) spectroscopy analysis showed that a triplet bond appeared after the implantation of methane ions (acceleration voltage: 80 keV), culminating in the creation of a more amorphous membrane structure. Methane 151-158 ATR serine/threonine kinase Homo sapiens 57-60 32477286-1 2020 Despite the recognition of streams and rivers as sources of methane (CH4) to the atmosphere, the role of CH4 oxidation (MOX) in these ecosystems remains poorly understood to date. Methane 105-108 monooxygenase DBH like 1 Homo sapiens 120-123 32477286-4 2020 Michealis-Menten kinetic parameter of MOX, maximum reaction velocity (V max ), and CH4 concentration at half V max (K S ) increased with CH4 supply. Methane 137-140 monooxygenase DBH like 1 Homo sapiens 38-41 32477286-5 2020 K S values in the micromolar range matched the CH4 concentrations measured in shallow stream sediments and indicate that MOX is mostly driven by low-affinity MOB. Methane 47-50 monooxygenase DBH like 1 Homo sapiens 121-124 32478270-1 2020 We presented a comprehensive thermodynamic study of the gas-phase chemical reaction mechanism of the AlN growth by high-temperature metal-organic chemical vapor deposition, investigating the addition reactions, pyrolysis reactions, and polymerization of amide DMANH2 and subsequent CH4 elimination reaction. Methane 282-285 gastrin Homo sapiens 56-59 32159384-10 2020 With 0-20 ppmv O2 in CH4/CO2/N2 mixtures, ions contain mostly organic nitrogen, with CNO- being the most intense ion peak. Methane 21-24 biogenesis of lysosomal organelles complex 1 subunit 4 Homo sapiens 85-88 32258867-4 2020 Results show that mixing 75 wt % of DMF with 25 wt % GBL enhanced the membrane gas permeability toward hydrogen, methane, helium, carbon dioxide, and nitrogen. Methane 113-120 gastrin Homo sapiens 79-82 31267121-2 2020 At RT and 65 bar, the total volumetric CH4 storage capacity of 212 cm3 (STP) cm-3 of FJU-101a is significantly higher than those of the isoreticular MFM-130a and UTSA-40a. Methane 39-42 thyroid hormone receptor interactor 10 Homo sapiens 72-75 32081186-3 2020 A turn-on ratiometric fluorescence bioassay based on the T7 exonuclease-mediated cyclic enzymatic amplification method was developed for miRNA-21 determination by using carbon dots (CDs) and FAM-labeled ssDNA as the signal source. Methane 169-180 microRNA 21 Homo sapiens 137-145 32174499-0 2020 Multiple factors dominate the distribution of methane and its sea-to-air flux in the Bohai Sea in summer and autumn of 2014. Methane 46-53 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 91-94 32174499-1 2020 The Bohai Sea is well-known as a source of atmospheric methane (CH4). Methane 64-67 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 10-13 31982753-5 2020 According to our estimates red deer and sheep populations across European heathlands produce 129.7 kt y-1 methane (se = 1.79) based on a hypothetical grass-ericaceous species mixed diet containing 30% of ericaceous species; this is 0.5% of total methane emissions from human activity across Europe (24,755 kt y-1), and a reduction in methane emissions of 63.8 kt y-1 against the same deer and sheep populations, if assumed to consume a grass-only diet. Methane 106-113 RNA, Ro60-associated Y1 Homo sapiens 102-105 31972063-7 2020 For the first time, a quantitative yield in methane is obtained at low magnetic field and mild conditions (25 mL min-1, 19 mT, 300 kHz, conversion 100%, methane selectivity 100%). Methane 44-51 CD59 molecule (CD59 blood group) Homo sapiens 113-118 31774616-1 2020 The first selective oxidation of methane to methanol is reported herein for zinc-exchanged MOR (Zn/MOR). Methane 33-40 opioid receptor mu 1 Homo sapiens 91-94 31774616-1 2020 The first selective oxidation of methane to methanol is reported herein for zinc-exchanged MOR (Zn/MOR). Methane 33-40 opioid receptor mu 1 Homo sapiens 99-102 32243481-6 2020 The results suggested that the best method was PstI RE-RRS analyzed with the reference-free approach, which accounted for 53.3+-5.9% of reads, and had repeatabilities of 0.49+-0.07 and 0.50+-0.07 for the first two principal components (PC1 and PC2), phenotypic correlations with methane yield of 0.43+-0.06 and 0.46+-0.06 for PC1 and PC2, and explained 41+-8% of the variation in methane yield. Methane 279-286 serine protease inhibitor Kazal-type 1 Ovis aries 47-51 32243481-6 2020 The results suggested that the best method was PstI RE-RRS analyzed with the reference-free approach, which accounted for 53.3+-5.9% of reads, and had repeatabilities of 0.49+-0.07 and 0.50+-0.07 for the first two principal components (PC1 and PC2), phenotypic correlations with methane yield of 0.43+-0.06 and 0.46+-0.06 for PC1 and PC2, and explained 41+-8% of the variation in methane yield. Methane 380-387 serine protease inhibitor Kazal-type 1 Ovis aries 47-51 32141284-1 2020 In this work, two types of mesoporous carbon particles with different morphology, size, and pore structure have been functionalized with a self-immolative polymer sensitive to changes in pH and tested as drug nanocarriers. Methane 27-44 phenylalanine hydroxylase Homo sapiens 187-189 31834467-3 2020 Hydrogen production increased as methane production decreased with decreasing HRT from 8 to 0.25 h. The maximum hydrogen yield of 3.2 +- 0.3 mL H2/g CODap (reported as mL H2 per gram of COD applied) and hydrogen production rate of 1951 +- 171 mL H2/day Lreactor were observed at the HRT of 0.25 h. The decrease in HRT from 8 to 0.25 h caused larger changes in the bacterial populations than the archaea populations. Methane 33-40 procollagen lysine, 2-oxoglutarate 5-dioxygenase 2 Mus musculus 141-146 31834467-3 2020 Hydrogen production increased as methane production decreased with decreasing HRT from 8 to 0.25 h. The maximum hydrogen yield of 3.2 +- 0.3 mL H2/g CODap (reported as mL H2 per gram of COD applied) and hydrogen production rate of 1951 +- 171 mL H2/day Lreactor were observed at the HRT of 0.25 h. The decrease in HRT from 8 to 0.25 h caused larger changes in the bacterial populations than the archaea populations. Methane 33-40 procollagen lysine, 2-oxoglutarate 5-dioxygenase 2 Mus musculus 168-173 31834467-3 2020 Hydrogen production increased as methane production decreased with decreasing HRT from 8 to 0.25 h. The maximum hydrogen yield of 3.2 +- 0.3 mL H2/g CODap (reported as mL H2 per gram of COD applied) and hydrogen production rate of 1951 +- 171 mL H2/day Lreactor were observed at the HRT of 0.25 h. The decrease in HRT from 8 to 0.25 h caused larger changes in the bacterial populations than the archaea populations. Methane 33-40 procollagen lysine, 2-oxoglutarate 5-dioxygenase 2 Mus musculus 168-173 31945685-0 2020 Construction of novel microbial consortia CS-5 and BC-4 valued for the degradation of catalpa sawdust and chlorophenols simultaneously with enhancing methane production. Methane 150-157 chorionic somatomammotropin hormone like 1 Homo sapiens 42-46 31945685-1 2020 This study might be the first to explore the novel constructed microbial consortia CS-5 and BC-4 for enhancing methane (CH4) production during anaerobic digestion (AD) with simultaneous degradation of catalpa sawdust and chlorophenols (CPs). Methane 111-118 chorionic somatomammotropin hormone like 1 Homo sapiens 83-87 31825639-7 2020 However, the SCGVB orbitals for methane, ethylene and acetylene differ markedly from the sp3, sp2 and sp hybrid orbitals traditionally associated with these molecules. Methane 32-39 Sp3 transcription factor Homo sapiens 89-92 32296263-7 2020 Specifically, we show that the poor compatibility between PIM-1 and ZIF-8, which manifests itself by the presence of nonselective void spaces at their interface, results in a decrease of the H2/CH4 permselectivity for the corresponding composite membrane as compared to the performances simulated for PIM-1 and ZIF-8 individually. Methane 194-197 Pim-1 proto-oncogene, serine/threonine kinase Homo sapiens 58-63 32296263-7 2020 Specifically, we show that the poor compatibility between PIM-1 and ZIF-8, which manifests itself by the presence of nonselective void spaces at their interface, results in a decrease of the H2/CH4 permselectivity for the corresponding composite membrane as compared to the performances simulated for PIM-1 and ZIF-8 individually. Methane 194-197 Pim-1 proto-oncogene, serine/threonine kinase Homo sapiens 301-306 32010098-1 2019 The flux of methane, a potent greenhouse gas, from the seabed is largely controlled by anaerobic oxidation of methane (AOM) coupled to sulfate reduction (S-AOM) in the sulfate methane transition (SMT). Methane 168-183 collagen type II alpha 1 chain Homo sapiens 156-159 32010098-2 2019 S-AOM is estimated to oxidize 90% of the methane produced in marine sediments and is mediated by a consortium of anaerobic methanotrophic archaea (ANME) and sulfate reducing bacteria. Methane 41-48 collagen type II alpha 1 chain Homo sapiens 2-5 32010098-3 2019 An additional methane sink, i.e., iron oxide coupled AOM (Fe-AOM), has been suggested to be active in the methanic zone of marine sediments. Methane 14-21 collagen type II alpha 1 chain Homo sapiens 53-56 32010098-3 2019 An additional methane sink, i.e., iron oxide coupled AOM (Fe-AOM), has been suggested to be active in the methanic zone of marine sediments. Methane 14-21 collagen type II alpha 1 chain Homo sapiens 58-64 32010098-9 2019 Methane oxidation rates of 0.095 +- 0.03 nmol cm-3 d-1 attributable to Fe-AOM were obtained in short-term radiotracer experiments. Methane 0-7 collagen type II alpha 1 chain Homo sapiens 71-77 32010098-11 2019 Thus, our findings prove that Fe-AOM occurs in methanic marine sediments containing mineral-bound ferric iron and is a previously overlooked but likely important component in the global methane budget. Methane 186-193 collagen type II alpha 1 chain Homo sapiens 30-36 32092961-8 2020 The sorption capacity of CH4 in R-HAL was 0.18 mmol/g, while in C-HAL 0.21 mmol/g. Methane 25-28 histidine ammonia-lyase Homo sapiens 34-37 32054937-5 2020 We quantitatively demonstrate that variations in sea level and organic carbon burial are the dominant controls on methane leakage since the Early Cretaceous. Methane 114-121 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 49-52 32054937-6 2020 Sea level controls methane seepage variations by imposing smooth trends on timescales in the order of tens of My. Methane 19-26 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 0-3 32083927-0 2020 Solving the CH_{4}^{-} Riddle: The Fundamental Role of Spin to Explain Metastable Anionic Methane. Methane 90-97 spindlin 1 Homo sapiens 55-59 31835146-4 2020 Methanogenesis tests showed that Air-NBW and CO2-NBW supplementation accelerated the utilization of crystalline cellulose, achieving methane yields of 264 and 246 mL CH4/g-VSreduced, increasing by 18% and 10% compared to deionized water addition (the control), respectively. Methane 133-140 complement C2 Homo sapiens 45-48 31816722-2 2020 Herein, a novel dual-colored carbon dots (CDs)-based ratiometric fluorescent sensor was constructed to accomplish high sensitive and accurate determination of ALP relyed on the difference of fluorescence resonance energy transfer (FRET) between blue light emitted CDs (B-CDs)-MnO2 nanohybrid and yellow light emitted CDs (Y-CDs)-MnO2 nanohybrid. Methane 29-40 alkaline phosphatase, placental Homo sapiens 159-162 31825639-7 2020 However, the SCGVB orbitals for methane, ethylene and acetylene differ markedly from the sp3, sp2 and sp hybrid orbitals traditionally associated with these molecules. Methane 32-39 Sp2 transcription factor Homo sapiens 94-97 31829361-6 2020 The ReacNetGenerator has been successfully used to analyze the reactive MD trajectories of the combustion of methane and 4-component surrogate fuel for rocket propellant 3 (RP-3), and it has great advantages in terms of efficiency and accuracy compared to traditional manual analysis. Methane 109-116 retinitis pigmentosa GTPase regulator Homo sapiens 152-177 32010098-1 2019 The flux of methane, a potent greenhouse gas, from the seabed is largely controlled by anaerobic oxidation of methane (AOM) coupled to sulfate reduction (S-AOM) in the sulfate methane transition (SMT). Methane 12-19 collagen type II alpha 1 chain Homo sapiens 119-122 32010098-1 2019 The flux of methane, a potent greenhouse gas, from the seabed is largely controlled by anaerobic oxidation of methane (AOM) coupled to sulfate reduction (S-AOM) in the sulfate methane transition (SMT). Methane 12-19 collagen type II alpha 1 chain Homo sapiens 156-159 32010098-1 2019 The flux of methane, a potent greenhouse gas, from the seabed is largely controlled by anaerobic oxidation of methane (AOM) coupled to sulfate reduction (S-AOM) in the sulfate methane transition (SMT). Methane 110-117 collagen type II alpha 1 chain Homo sapiens 119-122 31706145-3 2020 The CDs@YVO4: Dy3+ probe is constructed by the carbon dots (CDs) and YVO4: Dy3+ through a simple mixing method, in which the blue emission of CDs at 405 nm acts as the calibrated signal, the green emission of YVO4: Dy3+ at 574 nm decreased with the increasing targets ALP, and used as the output signal. Methane 47-58 alkaline phosphatase, placental Homo sapiens 268-271 32834906-9 2020 Therefore, it was suggested that TLR2, integrin, VSP, MMP1, and LRR-1 might be crucial molecules in the symbiosis between G. platifrons and methane oxidation bacteria by participating in symbiosis-related immune processes. Methane 140-147 toll like receptor 2 Homo sapiens 33-37 32342322-0 2020 First Discovery of Pogonophora (Annelida, Siboglinidae) in the Kara Sea Coincide with the Area of High Methane Concentration. Methane 103-110 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 68-71 32834906-9 2020 Therefore, it was suggested that TLR2, integrin, VSP, MMP1, and LRR-1 might be crucial molecules in the symbiosis between G. platifrons and methane oxidation bacteria by participating in symbiosis-related immune processes. Methane 140-147 matrix metallopeptidase 1 Homo sapiens 54-58 32834906-9 2020 Therefore, it was suggested that TLR2, integrin, VSP, MMP1, and LRR-1 might be crucial molecules in the symbiosis between G. platifrons and methane oxidation bacteria by participating in symbiosis-related immune processes. Methane 140-147 leucine rich repeat protein 1 Homo sapiens 64-69 31905761-0 2019 Enteric Methane Emissions of Dairy Cows Predicted from Fatty Acid Profiles of Milk, Cream, Cheese, Ricotta, Whey, and Scotta. Methane 8-15 Weaning weight-maternal milk Bos taurus 78-82 31905761-8 2019 Methane yield and intensity could be predicted from single milk samples with good accuracy (trueness and precision) with respect to those predicted from reference milk. Methane 0-7 Weaning weight-maternal milk Bos taurus 59-63 31905761-8 2019 Methane yield and intensity could be predicted from single milk samples with good accuracy (trueness and precision) with respect to those predicted from reference milk. Methane 0-7 Weaning weight-maternal milk Bos taurus 163-167 31546029-8 2019 Moreover, methane generation was almost completely inhibited from 25.3 +- 1.46 mg COD/L to 0.06 +- 0.04 mg COD/L. Methane 10-17 small nuclear ribonucleoprotein polypeptides B and B1 Homo sapiens 82-85 31546029-8 2019 Moreover, methane generation was almost completely inhibited from 25.3 +- 1.46 mg COD/L to 0.06 +- 0.04 mg COD/L. Methane 10-17 small nuclear ribonucleoprotein polypeptides B and B1 Homo sapiens 107-110 31039906-7 2019 The result showed that the NiO/Ce0.5Zr0.5O2-Sil-1 catalyst exhibited the best performance and its methane conversion efficiency reached up to 99.5%. Methane 98-105 SIL1 nucleotide exchange factor Homo sapiens 44-49 30601406-11 2019 Our data indicated that methane treatment prevented liver damage in sepsis via anti-inflammatory, anti-oxidative, and anti-apoptotic properties that involved the PPAR-gamma/ NF-kappaB signaling pathway. Methane 24-31 peroxisome proliferator activated receptor gamma Homo sapiens 162-172 30601406-11 2019 Our data indicated that methane treatment prevented liver damage in sepsis via anti-inflammatory, anti-oxidative, and anti-apoptotic properties that involved the PPAR-gamma/ NF-kappaB signaling pathway. Methane 24-31 nuclear factor kappa B subunit 1 Homo sapiens 174-183 31400653-4 2019 HRT 2 d resulted in (1) maximum removal efficiencies for COD, carbohydrate, lipid and protein contents with values of 58.5, 58.4, 62.6 and 79.1%, respectively; (2) peak hydrogen and methane production rates of 714 and 254 mL/L-d, respectively; and (3) biogas contents of hydrogen 8.6% and methane 48.0% in the produced gas. Methane 182-189 hes related family bHLH transcription factor with YRPW motif 2 Homo sapiens 0-5 31400653-4 2019 HRT 2 d resulted in (1) maximum removal efficiencies for COD, carbohydrate, lipid and protein contents with values of 58.5, 58.4, 62.6 and 79.1%, respectively; (2) peak hydrogen and methane production rates of 714 and 254 mL/L-d, respectively; and (3) biogas contents of hydrogen 8.6% and methane 48.0% in the produced gas. Methane 289-296 hes related family bHLH transcription factor with YRPW motif 2 Homo sapiens 0-5 31563113-0 2019 Effects of mixing time on methane production from anaerobic co-digestion of food waste and chicken manure: Experimental studies and CFD analysis. Methane 26-33 complement factor D Gallus gallus 132-135 31563113-3 2019 The simulated mixing time from CFD was selected as a reference for the first time to analyze the methane yield. Methane 97-104 complement factor D Gallus gallus 31-34 31323554-5 2019 The addition of GAC significantly shortened the lag phase (from 7 to 3 d), reduced accumulation of various volatile fatty acids (VFAs), and enhanced methane production rate (50-80% increase) compared to the control and magnetite-amended bioreactor. Methane 149-156 glutaminase Homo sapiens 16-19 31675572-3 2019 The present study showed that granular activated carbon (GAC) promoted the AD of HTLWW in continuous experiments, resulting in the higher methane yield (259 mL/g COD) compared to control experiment (202 mL/g COD). Methane 138-145 glutaminase Homo sapiens 57-60 31885797-12 2019 Methane also had a positive effect on the expression of the PGC-1alpha/SIRT3/SOD2 signaling pathway. Methane 0-7 PPARG coactivator 1 alpha Rattus norvegicus 60-70 31885797-12 2019 Methane also had a positive effect on the expression of the PGC-1alpha/SIRT3/SOD2 signaling pathway. Methane 0-7 sirtuin 3 Rattus norvegicus 71-76 31885797-12 2019 Methane also had a positive effect on the expression of the PGC-1alpha/SIRT3/SOD2 signaling pathway. Methane 0-7 superoxide dismutase 2 Rattus norvegicus 77-81 31827690-9 2019 Our data indicated that methane treatment prevented cholestatic liver injury via anti-inflammatory properties that involved the TLR4/NF-kappaB/NLRP3 signaling pathway. Methane 24-31 toll-like receptor 4 Rattus norvegicus 128-132 31827690-9 2019 Our data indicated that methane treatment prevented cholestatic liver injury via anti-inflammatory properties that involved the TLR4/NF-kappaB/NLRP3 signaling pathway. Methane 24-31 NLR family, pyrin domain containing 3 Rattus norvegicus 143-148 31326818-1 2019 Facilitating anaerobic degradation of long-chain fatty acids (LCFA) is key for tapping the high methane production potential of the fats, oil and grease (FOG) content of dairy wastewaters. Methane 96-103 chromosome 10 open reading frame 90 Homo sapiens 132-152 31781345-0 2019 Methane Alleviates Acetaminophen-Induced Liver Injury by Inhibiting Inflammation, Oxidative Stress, Endoplasmic Reticulum Stress, and Apoptosis through the Nrf2/HO-1/NQO1 Signaling Pathway. Methane 0-7 NFE2 like bZIP transcription factor 2 Homo sapiens 156-160 31781345-0 2019 Methane Alleviates Acetaminophen-Induced Liver Injury by Inhibiting Inflammation, Oxidative Stress, Endoplasmic Reticulum Stress, and Apoptosis through the Nrf2/HO-1/NQO1 Signaling Pathway. Methane 0-7 heme oxygenase 1 Homo sapiens 161-165 31781345-0 2019 Methane Alleviates Acetaminophen-Induced Liver Injury by Inhibiting Inflammation, Oxidative Stress, Endoplasmic Reticulum Stress, and Apoptosis through the Nrf2/HO-1/NQO1 Signaling Pathway. Methane 0-7 NAD(P)H quinone dehydrogenase 1 Homo sapiens 166-170 31781345-10 2019 We found that a methane-rich medium decreased the levels of reactive oxygen species (DHE fluorescent staining), inhibited apoptosis (cell flow test), and regulated the Nrf2/HO-1/NQO1 signaling pathway. Methane 16-23 NFE2 like bZIP transcription factor 2 Homo sapiens 168-172 31781345-10 2019 We found that a methane-rich medium decreased the levels of reactive oxygen species (DHE fluorescent staining), inhibited apoptosis (cell flow test), and regulated the Nrf2/HO-1/NQO1 signaling pathway. Methane 16-23 heme oxygenase 1 Homo sapiens 173-177 31781345-10 2019 We found that a methane-rich medium decreased the levels of reactive oxygen species (DHE fluorescent staining), inhibited apoptosis (cell flow test), and regulated the Nrf2/HO-1/NQO1 signaling pathway. Methane 16-23 NAD(P)H quinone dehydrogenase 1 Homo sapiens 178-182 31357360-3 2019 In this work, a fluorescence turn-off approach for the detection of ALP is designed on the basis of nitrogen doped carbon dots (N-CDs), which were synthesized by one-step hydrothermal method and applied as signal readout. Methane 115-126 alkaline phosphatase, placental Homo sapiens 68-71 31920221-1 2019 We present the design of a portable version of our miniaturized laser heterodyne radiometer (mini-LHR) that simultaneously measures methane (CH4) and carbon dioxide (CO2) in the atmospheric column. Methane 132-139 luteinizing hormone/choriogonadotropin receptor Homo sapiens 98-101 31339661-0 2019 MIL-53(Al) as a Versatile Platform for Ionic-Liquid/MOF Composites to Enhance CO2 Selectivity over CH4 and N2. Methane 99-102 lysine acetyltransferase 8 Homo sapiens 52-55 31339661-3 2019 Of the composite materials that were tested, [BMIM][PF6 ]/MIL-53(Al) exhibited the largest increase in CO2 /CH4 selectivity, 2.8-times higher than that of pristine MIL-53(Al), whilst [BMIM][MeSO4 ]/MIL-53(Al) exhibited the largest increase in CO2 /N2 selectivity, 3.3-times higher than that of pristine MIL-53(Al). Methane 108-111 sperm associated antigen 17 Homo sapiens 52-55 31339661-4 2019 A comparison of the CO2 separation potentials of the IL/MOF composites showed that the [BMIM][BF4 ]- and [BMIM][PF6 ]-incorporated MIL-53(Al) composites both showed enhanced CO2 /N2 and CO2 /CH4 selectivities at pressures of 1-5 bar compared to composites of CuBTC and ZIF-8 with the same ILs. Methane 191-194 sperm associated antigen 17 Homo sapiens 112-115 31268193-0 2019 A Reaction-Induced Localization of Spin Density Enables Thermal C-H Bond Activation of Methane by Pristine FeC4. Methane 87-94 spindlin 1 Homo sapiens 35-39 31323514-5 2019 The SCP yield on methane varied from 0.59 to 0.76 g cell dry weight (CDW)/g CH4. Methane 17-24 urocortin 3 Homo sapiens 4-7 31326650-2 2019 Compared with control group (T0), the maximum rate of biomethane production was significantly improved after the addition of biochar, especially, it has been improved by 40.6% in T1 (0.77 g/gTS sludge) with the methane production of 89.28 mL/gVS. Methane 57-64 GTS Homo sapiens 190-193 31228743-3 2019 Correlation analysis showed that methane production was significantly correlated with the activity of alpha-glucosidase at 0.01 level, and with protease activity, released polysaccharides and VFAs at 0.05 level. Methane 33-40 sucrase-isomaltase Homo sapiens 102-119 31313443-3 2019 By exploring methane adsorption on Pt1 substitutionally doped on many rutile-type oxides using hybrid density functional theory, we show that the occupancy of the Pt dz 2 orbital is the key to methane chemisorption. Methane 13-20 zinc finger protein 77 Homo sapiens 35-38 31026948-8 2019 In addition, it was revealed that the main crystal structure was changed from W2C to WC1-x by increasing W/CH4 composition ratio. Methane 107-110 ATPase copper transporting beta Homo sapiens 85-88 31216515-6 2019 The resultant membrane, the mica supported IL membrane (M-SILM), has about 80 GPU for CO2 permeance, and selectivity for CO2/H2, CO2/CH4 and CO2/N2 of 7.7, 28.6 and 87, respectively. Methane 133-136 MHC class I polypeptide-related sequence A Homo sapiens 28-32 31429561-4 2019 A new set of combination rules (DRS) for Morse-based FF has been proposed in our prior work and shown good performance in the simulation of CH4 adsorption isotherms in covalent organic frameworks. Methane 140-143 sushi repeat containing protein X-linked Homo sapiens 32-35 31505751-3 2019 We have developed a sensing platform by the conjugation of beta-galactosidase, a crucial enzyme, with lab-synthesized gel-like carbon dots (CDs) which have high luminescence, photostability, and easy surface functionalization. Methane 127-138 galactosidase beta 1 Homo sapiens 59-77 31482880-1 2019 We realized that tailoring the pore size/geometry and chemistry, by virtue of alkynyl or naphthalene replacing phenyl within a series of isomorphic MOFs, can optimize methane storage working capacities, affording an exceptionally high working capacity of 203 cm3 (STP) cm-3 at 298 K and 5-80 bar. Methane 167-174 thyroid hormone receptor interactor 10 Homo sapiens 264-267 31475262-2 2019 Aggregates are formed from surfactant molecules and act as methane concentrators, also trapping the catalyst (a silver-based complex) and the diazo reagent (ethyl diazoacetate, EDA), providing yields of ethyl propionate up to 14% (referred to as EDA). Methane 59-66 ectodysplasin A Homo sapiens 177-180 31475262-2 2019 Aggregates are formed from surfactant molecules and act as methane concentrators, also trapping the catalyst (a silver-based complex) and the diazo reagent (ethyl diazoacetate, EDA), providing yields of ethyl propionate up to 14% (referred to as EDA). Methane 59-66 ectodysplasin A Homo sapiens 246-249 33448841-2 2019 Therefore, we have built a multifunctional nanosystem based on sulforaphane-conjugated carbon dots (SFN-CDs) with thiourea skeleton and applied for EGFR-overexpressing cancer cells targeted imaging and inhibiting. Methane 87-98 epidermal growth factor receptor Homo sapiens 148-152 31313443-3 2019 By exploring methane adsorption on Pt1 substitutionally doped on many rutile-type oxides using hybrid density functional theory, we show that the occupancy of the Pt dz 2 orbital is the key to methane chemisorption. Methane 193-200 zinc finger protein 77 Homo sapiens 35-38 31195363-3 2019 The maximum methane production rate and accumulated CH4 production by the 6000 mg L-1 group increased by 90.7% and 156.0%, respectively. Methane 52-55 immunoglobulin kappa variable 1-16 Homo sapiens 82-85 31202647-11 2019 The positive genetic correlation between CH4 production and milk yield indicates that care needs to be taken when genetically selecting for lower CH4 production, to avoid a decrease in MY at the animal level. Methane 41-44 Weaning weight-maternal milk Bos taurus 60-64 31195363-3 2019 The maximum methane production rate and accumulated CH4 production by the 6000 mg L-1 group increased by 90.7% and 156.0%, respectively. Methane 12-19 immunoglobulin kappa variable 1-16 Homo sapiens 82-85 33448841-2 2019 Therefore, we have built a multifunctional nanosystem based on sulforaphane-conjugated carbon dots (SFN-CDs) with thiourea skeleton and applied for EGFR-overexpressing cancer cells targeted imaging and inhibiting. Methane 87-98 RNA exonuclease 2 Homo sapiens 100-103 30961746-4 2019 Consequently, the Ni/Zr-Sil-1 catalyst exhibited the best catalytic performance, with the CO selectivity in methane steam reforming drastically decreasing by 11.5%, H2 concentration in the reformed gas increasing by about 1.7%, and H2/CO molar ratio increasing by 0.8. Methane 108-115 SIL1 nucleotide exchange factor Homo sapiens 24-29 31467345-7 2019 Indeed, during the deglaciation and the accompanying sea-level rise, the thawing permafrost may have released important quantities of methane into the atmosphere that would have contributed to the Toarcian OAE rapid warming and its characteristic negative carbon isotope excursion. Methane 134-141 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 53-56 31440843-0 2019 Adsorption Behavior of CH4 Gas Molecule on the MoX2(S, Se, Te) Monolayer: The DFT Study. Methane 23-26 mesenchyme homeobox 2 Homo sapiens 47-51 31440843-1 2019 We predict the CH4-sensing performance of monolayer MoX2(S, Se, Te) with X-vacancy, Mo-vacancy, and divacancy by the density functional theory (DFT). Methane 15-18 mesenchyme homeobox 2 Homo sapiens 52-56 31440843-5 2019 The results are proposed to predict the CH4 gas molecule adsorption properties of MVD(MoTe2) and would help in guiding experimentalists to develop better materials based on MoX2 for efficient gas detection or sensing applications. Methane 40-43 mevalonate diphosphate decarboxylase Homo sapiens 82-85 31202647-11 2019 The positive genetic correlation between CH4 production and milk yield indicates that care needs to be taken when genetically selecting for lower CH4 production, to avoid a decrease in MY at the animal level. Methane 146-149 Weaning weight-maternal milk Bos taurus 60-64 31265225-3 2019 The 1P-PdPt/SnO2-A sensor obtained by self-assemblies of PdPt NPs exhibited temperature-dependent dual selectivity to CO at 100 C and CH4 at 320 C. Furthermore, the sensor possessed good long term stability and antihumidity interference. Methane 135-138 strawberry notch homolog 2 Homo sapiens 12-15 31348816-10 2019 In conclusion, crossbreeding may be an option to improve performance and reduce the CH4 per ADG in tropical climate conditions, resulting in lower methane emission per kg of meat produced. Methane 84-87 ADG Bos taurus 92-95 31403074-12 2019 Additionally, iso-MOF-4 also possesses efficient separation of C3H8/CH4 and C2H6/CH4, indicating its promising potential in storage/separation of light hydrocarbons in industry. Methane 68-71 lysine acetyltransferase 8 Homo sapiens 18-21 31403074-12 2019 Additionally, iso-MOF-4 also possesses efficient separation of C3H8/CH4 and C2H6/CH4, indicating its promising potential in storage/separation of light hydrocarbons in industry. Methane 81-84 lysine acetyltransferase 8 Homo sapiens 18-21 30590760-0 2019 Methane Control of Adventitious Rooting Requires gamma-Glutamyl Cysteine Synthetase-Mediated Glutathione Homeostasis. Methane 0-7 glutamate--cysteine ligase, chloroplastic Cucumis sativus 49-83 31115966-2 2019 To address this problem, we report a methane nano-trap that features oppositely adjacent open metal sites and dense alkyl groups in a metal-organic framework (MOF). Methane 37-44 lysine acetyltransferase 8 Homo sapiens 134-163 31120181-1 2019 The mechanisms of the thermal reactions of the two iconic magnesium oxide cations MgO.+ and Mg2 O2 .+ with methane have been re-evaluated at the CCSD(T)/CBS//CCSD/def2-TZVP level of theory. Methane 107-114 cystathionine beta-synthase Homo sapiens 153-156 31242854-2 2019 Cattle selected for low-RFI (feed efficient) have similar production levels but decreased feed intake, while also emitting less methane. Methane 128-135 RFI Bos taurus 24-27 30968506-1 2019 Mass spectrometric analysis of the anionic products of interaction between platinum atomic anions, Pt- , and methane, CH4 and CD4 , in a collision cell shows the preferred generation of [PtCH4 ]- and [PtCD4 ]- complexes and a low tendency toward dehydrogenation. Methane 109-116 CD4 molecule Homo sapiens 126-129 30590760-8 2019 Genetic evidence revealed that in the presence of CH4, Arabidopsis mutants cad2 (a gamma-ECS-defective mutant) exhibited, not only the decreased GSH content in vivo, but also the defects in adventitious root formation, both of which were rescued by GSH administration other than CH4. Methane 50-53 cinnamyl alcohol dehydrogenase homolog 2 Arabidopsis thaliana 75-79 30877874-0 2019 Methane ameliorates post-operative cognitive dysfunction by inhibiting microglia NF-kappaB/MAPKs pathway and promoting IL-10 expression in aged mice. Methane 0-7 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 Mus musculus 81-90 30877874-0 2019 Methane ameliorates post-operative cognitive dysfunction by inhibiting microglia NF-kappaB/MAPKs pathway and promoting IL-10 expression in aged mice. Methane 0-7 interleukin 10 Mus musculus 119-124 30877874-7 2019 Meanwhile, methane treatment suppressed lipopolysaccharide (LPS)-stimulated phosphorylation of MAPKs pathways and its downstream target TNF-alpha and IL-6 in BV2 cells. Methane 11-18 tumor necrosis factor Mus musculus 136-145 30877874-7 2019 Meanwhile, methane treatment suppressed lipopolysaccharide (LPS)-stimulated phosphorylation of MAPKs pathways and its downstream target TNF-alpha and IL-6 in BV2 cells. Methane 11-18 interleukin 6 Mus musculus 150-154 30877874-8 2019 Moreover, methane increased expression of IL-10 in the hippocampus 24 h after surgery, and blockade of IL-10 repressed the protective effect of methane on the cognitive impairments observed in MWM test, decreased microglial activation and the pro-inflammatory cytokine in plasma and hippocampal. Methane 10-17 interleukin 10 Mus musculus 42-47 30877874-8 2019 Moreover, methane increased expression of IL-10 in the hippocampus 24 h after surgery, and blockade of IL-10 repressed the protective effect of methane on the cognitive impairments observed in MWM test, decreased microglial activation and the pro-inflammatory cytokine in plasma and hippocampal. Methane 144-151 interleukin 10 Mus musculus 103-108 30877874-9 2019 Blockade of IL-10 abrogated the suppression effect of methane on the pro-inflammatory cytokine production and phosphorylation of NF-kappaB and p38MAPK both in hippocampus and in BV2 cells. Methane 54-61 interleukin 10 Mus musculus 12-17 30877874-9 2019 Blockade of IL-10 abrogated the suppression effect of methane on the pro-inflammatory cytokine production and phosphorylation of NF-kappaB and p38MAPK both in hippocampus and in BV2 cells. Methane 54-61 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 Mus musculus 129-138 30877874-9 2019 Blockade of IL-10 abrogated the suppression effect of methane on the pro-inflammatory cytokine production and phosphorylation of NF-kappaB and p38MAPK both in hippocampus and in BV2 cells. Methane 54-61 mitogen-activated protein kinase 14 Mus musculus 143-150 30744739-6 2019 So it is decisive to design effective catalyst system to increase C2-4 selectivity while decrease CH4 selectivity. Methane 98-101 complement C2 Homo sapiens 66-70 31067022-2 2019 Herein, we report the structural dependence of the Ce1- xFe xO2-delta catalysts for CH4 combustion and CO oxidation via changing lattice distortion degrees, surface Fe2O3 states, and oxygen vacancy concentrations. Methane 84-87 carboxylesterase 1 Homo sapiens 51-54 31100776-10 2019 The effect of Cu concentration on the sensing properties of SnO2 toward methane (CH4) gas was also investigated. Methane 81-84 strawberry notch homolog 2 Homo sapiens 60-63 31203933-1 2019 In practice, methane generation at U.S. landfills is typically predicted by using the EPA"s Landfill Gas Emissions Model (LandGEM), which includes two parameters, the methane production potential (L0, m3 CH4 Mg-1 wet waste) and the first-order decay rate constant (k, yr-1). Methane 13-20 GTP binding protein overexpressed in skeletal muscle Homo sapiens 122-129 31203933-1 2019 In practice, methane generation at U.S. landfills is typically predicted by using the EPA"s Landfill Gas Emissions Model (LandGEM), which includes two parameters, the methane production potential (L0, m3 CH4 Mg-1 wet waste) and the first-order decay rate constant (k, yr-1). Methane 167-174 GTP binding protein overexpressed in skeletal muscle Homo sapiens 122-129 31021087-0 2019 Synergy of Single-Atom Ni1 and Ru1 Sites on CeO2 for Dry Reforming of CH4. Methane 70-73 Scm like with four mbt domains 1 Homo sapiens 31-34 31021087-6 2019 Computational studies suggest a molecular mechanism for the observed synergy effects, which originate at (1) the different roles of Ni1 and Ru1 sites in terms of activations of CH4 to form CO on a Ni1 site and dissociation of CO2 to CO on a Ru1 site, respectively and (2) the sequential role in terms of first forming H atoms through activation of CH4 on a Ni1 site and then coupling of H atoms to form H2 on a Ru1 site. Methane 177-180 Scm like with four mbt domains 1 Homo sapiens 140-143 30828757-1 2019 In this work, a novel ratiometric fluorescent sensor, based on carbon dots (CDs) and gold nanoclusters (AuNCs), is developed for highly sensitive and selective visual colorimetric detection of Cu2+ and alkaline phosphatase (ALP). Methane 63-74 alkaline phosphatase, placental Homo sapiens 202-222 30997713-1 2019 OBJECTIVES: This study aimed at investigating cellular uptake pathways of carbon dots (CDs) in human adenoid cystic carcinoma cell line ACC-2. Methane 74-85 acetyl-CoA carboxylase beta Homo sapiens 136-141 32255127-4 2019 In particular, we have designed immunoadjuvant nanomedicine carriers on the basis of polydopamine (PDA) simultaneously loaded with resiquimod (R848)-a kind of toll-like receptor 7 (TLR7) agonist-and carbon dots (CDs)-a fluorescent agent. Methane 199-210 toll like receptor 7 Homo sapiens 181-185 30590760-4 2019 Further investigations showed that endogenous GSH content was rapidly increased by CH4 application, which was correlated with the increased CsGSH1 transcript and gamma-ECS activity. Methane 83-86 glutamate--cysteine ligase, chloroplastic Cucumis sativus 140-146 30931006-2 2019 Diversely substituted indoles (Ar1) react with quinoline aldehydes, quinolone aldehydes, chromone aldehydes, and fluorene aldehydes (Ar2CHO) and coumarins (Ar3) in 1:1:1 ratio to form the corresponding tris(heteroaryl)methanes (Ar1Ar2Ar3)CH along with (Ar1Ar1Ar2)CH triads. Methane 218-226 transcription factor 20 Homo sapiens 31-34 30709818-0 2019 Spatial-Temporal Pattern of Sulfate-Dependent Anaerobic Methane Oxidation in an Intertidal Zone of the East China Sea. Methane 56-63 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 114-117 30677902-6 2019 The variation of CO2/CH4 ratio also leaded to a noticeable changes on H2/CO ratio. Methane 21-24 relaxin 2 Homo sapiens 70-75 30801086-3 2019 The layered compounds demonstrate a permanent porosity with a BET surface area of up to 688 m2 g-1 with the possibility of selective gas adsorption (CO2 over N2 and CH4). Methane 165-168 delta/notch like EGF repeat containing Homo sapiens 62-65 30612804-12 2019 Similarly, methane production per unit of energy-corrected milk was not affected by fat source and averaged 15.5 +- 0.68 L/kg. Methane 11-18 Weaning weight-maternal milk Bos taurus 59-63 30845719-0 2019 Selective Detection of Hydrogen Sulfide and Methane by a Single MOX-Sensor. Methane 44-51 monooxygenase DBH like 1 Homo sapiens 64-67 30693766-3 2019 Graphene hydrogel (GH) was selected to fabricate a permeable electrode with the purpose of overcoming the steric hindrance of cells on electrode, which leads to errors in the detection of cell-surface receptors. Methane 0-17 gamma-glutamyl hydrolase Homo sapiens 19-21 30693766-4 2019 GLUT4 was labeled with carbon dots (CDs), which generate ECL emission at the interface between GH and cells, so about half the amount of GLUT4 expressed at the cell surface could be determined, which provided an accurate GLUT4 expression quantification. Methane 23-34 solute carrier family 2 member 4 Homo sapiens 0-5 30693766-4 2019 GLUT4 was labeled with carbon dots (CDs), which generate ECL emission at the interface between GH and cells, so about half the amount of GLUT4 expressed at the cell surface could be determined, which provided an accurate GLUT4 expression quantification. Methane 23-34 gamma-glutamyl hydrolase Homo sapiens 95-97 30693766-4 2019 GLUT4 was labeled with carbon dots (CDs), which generate ECL emission at the interface between GH and cells, so about half the amount of GLUT4 expressed at the cell surface could be determined, which provided an accurate GLUT4 expression quantification. Methane 23-34 solute carrier family 2 member 4 Homo sapiens 137-142 30693766-4 2019 GLUT4 was labeled with carbon dots (CDs), which generate ECL emission at the interface between GH and cells, so about half the amount of GLUT4 expressed at the cell surface could be determined, which provided an accurate GLUT4 expression quantification. Methane 23-34 solute carrier family 2 member 4 Homo sapiens 137-142 30747177-8 2019 This study increases the number of available rate coefficients for the reactions of NO3 with alkanes and sets significantly lower upper limits for reaction of NO3 with ethane and methane. Methane 179-186 NBL1, DAN family BMP antagonist Homo sapiens 84-87 30747177-8 2019 This study increases the number of available rate coefficients for the reactions of NO3 with alkanes and sets significantly lower upper limits for reaction of NO3 with ethane and methane. Methane 179-186 NBL1, DAN family BMP antagonist Homo sapiens 159-162 30696009-3 2019 In this work, the composition of biomarkers in the methane hydrate-bearing sediments in cores SH2B and SH7B from the Shenhu area, the South China Sea (SCS) were identified by gas chromatography-mass spectrometry (GC-MS) and comprehensive two-dimensional gas chromatography/time-of-flight mass spectrometry (GCxGC-TOFMS). Methane 51-58 SH2B adaptor protein 1 Homo sapiens 94-98 30691014-8 2019 Further research is essential for improving the performance of spherical SBA-15-based MOF materials and (in turn) the enrichment of CH4 from the CH4/N2 mixture. Methane 132-135 chimerin 2 Homo sapiens 145-151 30281847-6 2019 In methanotrophs, a Csp exported from the cytosol stores CuI for the active site of the ubiquitous enzyme that catalyses the oxidation of methane. Methane 138-145 DnaJ heat shock protein family (Hsp40) member C5 Homo sapiens 20-23 30457852-0 2019 Denitrifying Anaerobic Methane Oxidation: A Previously Overlooked Methane Sink in Intertidal Zone. Methane 23-30 tribbles pseudokinase 3 Homo sapiens 74-78 30457852-0 2019 Denitrifying Anaerobic Methane Oxidation: A Previously Overlooked Methane Sink in Intertidal Zone. Methane 66-73 tribbles pseudokinase 3 Homo sapiens 74-78 30457852-7 2019 The contribution rate of DAMO process to total anaerobic methane removal in the intertidal zone reached 65.6% ~ 100%, which indicates that DAMO process is an important methane sink in intertidal ecosystem. Methane 57-64 tribbles pseudokinase 3 Homo sapiens 176-180 30457852-7 2019 The contribution rate of DAMO process to total anaerobic methane removal in the intertidal zone reached 65.6% ~ 100%, which indicates that DAMO process is an important methane sink in intertidal ecosystem. Methane 168-175 tribbles pseudokinase 3 Homo sapiens 176-180 29911268-10 2019 The methane production reached values of 207 +- 2.2 mL CH4 g-1 COD at 10 g COD L-1. Methane 4-11 immunoglobulin kappa variable 1-16 Homo sapiens 79-82 30906697-2 2019 This study aimed to estimate the amounts of methane emissions from the municipal solid waste landfill in Yasuj city using LandGEM software. Methane 44-51 GTP binding protein overexpressed in skeletal muscle Homo sapiens 122-129 30906697-3 2019 The LandGEM model which is used for this aim is based on input data of open landfill year, land closure year, methane production rate, potential methane production capacity, and waste acceptance rate. Methane 110-117 GTP binding protein overexpressed in skeletal muscle Homo sapiens 4-11 30345599-6 2019 Thanks to the significantly enhanced redox abilities of the charge carriers in the direct Z-scheme system, the photocatalytic CO2 reduction performance of the optimized TiO2 /CdS is 3.5, 5.4, and 6.3 times higher than that of CdS, TiO2 , and commercial TiO2 (P25), respectively, in terms of methane production. Methane 291-298 CDP-diacylglycerol synthase 1 Homo sapiens 175-178 29141502-4 2019 The maximum methane production of 19 m3 CH4/m3 reactor/d was achieved at a H2/CO2 ratio of 4:1 and feeding rate of 24 m3 gas/m3 reactor/d. Methane 12-19 relaxin 2 Homo sapiens 75-94 29141502-4 2019 The maximum methane production of 19 m3 CH4/m3 reactor/d was achieved at a H2/CO2 ratio of 4:1 and feeding rate of 24 m3 gas/m3 reactor/d. Methane 40-43 relaxin 2 Homo sapiens 75-94 30623274-0 2019 L-Cysteine desulfhydrase-dependent hydrogen sulfide is required for methane-induced lateral root formation. Methane 68-75 L-cysteine desulfhydrase Solanum lycopersicum 0-24 30623274-1 2019 KEY MESSAGE: Methane-triggered lateral root formation is not only a universal event, but also dependent on L-cysteine desulfhydrase-dependent hydrogen sulfide signaling. Methane 13-20 L-cysteine desulfhydrase Solanum lycopersicum 107-131 30384210-0 2019 Acetoclastic methanogenesis led by Methanosarcina in anaerobic co-digestion of fats, oil and grease for enhanced production of methane. Methane 127-134 chromosome 10 open reading frame 90 Homo sapiens 79-83 30512947-4 2018 Importantly, the incorporation of Mg2+ and Co2+ ions in the framework of AlPO-ERI can greatly improve the adsorption selectivities of CO2 over CH4 and N2. Methane 143-146 complement C2 Homo sapiens 43-46 30553257-5 2018 Moreover, the effect of a so-called single atom alloy on the reactivity of methane is investigated by making predictions for CHD3 on Pt-Cu(111) and Pd-Cu(111). Methane 75-82 chromodomain helicase DNA binding protein 3 Homo sapiens 125-129 30444626-4 2018 The molecular rotation of methyl radicals isolated in the deuterated solid methane isotopomer, CD4, was investigated both by experimental and theoretical electron paramagnetic resonance (EPR) methods. Methane 75-82 CD4 molecule Homo sapiens 95-98 28871862-5 2018 The highest concentration of CH4 (75.1%) and yield of biogas (36.78 L d-1) were found using a packing material, the organic loading of which made 15.0 g L-1. Methane 29-32 immunoglobulin kappa variable 1-16 Homo sapiens 153-156 30129103-2 2018 Gas sorption results for these highly mesoporous materials show that alternately arranged fused benzene rings on one side of the ligand could serve as extra anchoring sites for CO2 molecules with pi-pi interactions, conspicuously enhancing CO2 uptake and CO2 /CH4 and CO2 /N2 selectivity; while more steric hindrance effect towards open CoII sites were imposed by ligands flanked with fused benzene rings on both sides, compromising such extra-sites enhancement. Methane 260-263 mitochondrially encoded cytochrome c oxidase II Homo sapiens 337-341 30410078-3 2018 To address this challenge, the concept of methane-carbon dioxide (CH4-CO2) swapping has appeared. Methane 42-49 complement C2 Homo sapiens 66-73 30099155-6 2018 In contrast, we observed a modest improvement on methane production (>10% compared to the control lacking GO) using 5 mg of GO L-1 in glucose-amended incubations. Methane 49-56 immunoglobulin kappa variable 1-16 Homo sapiens 130-133 30197132-16 2018 When pre-experimental RFI was used as a continuous variable, higher methane per kilogram of DMI was found for cows with negative RFI than positive RFI values, but not for methane per kilogram of ECM. Methane 68-75 RFI Bos taurus 22-25 30197132-16 2018 When pre-experimental RFI was used as a continuous variable, higher methane per kilogram of DMI was found for cows with negative RFI than positive RFI values, but not for methane per kilogram of ECM. Methane 68-75 RFI Bos taurus 129-132 30197132-16 2018 When pre-experimental RFI was used as a continuous variable, higher methane per kilogram of DMI was found for cows with negative RFI than positive RFI values, but not for methane per kilogram of ECM. Methane 68-75 RFI Bos taurus 129-132 30384725-3 2018 Here, we present results from a modified magnetic focusing apparatus and show that it can be used to separate the spin isomers of acetylene and methane. Methane 144-151 spindlin 1 Homo sapiens 114-118 29888540-1 2018 While pristine [TaO2 ]+ is rather inert in its thermal reactions with both methane and molecular hydrogen, the cluster oxide becomes reactive upon ligation with the closed-shell ligand CO2 . Methane 75-82 TAO kinase 2 Homo sapiens 16-20 30340381-9 2018 Consequently, the adsorbent of Na-Cp was suitable for nitrogen/methane mixture separation, which could make the concentration of methane concentrated from 19.7% to 30.72%. Methane 63-70 synuclein alpha Homo sapiens 31-36 30340381-9 2018 Consequently, the adsorbent of Na-Cp was suitable for nitrogen/methane mixture separation, which could make the concentration of methane concentrated from 19.7% to 30.72%. Methane 129-136 synuclein alpha Homo sapiens 31-36 30240204-3 2018 FJU-35 with coordinated solvent and formate in asymmetric mu3-eta1:eta2 coordination mode within the CdII-O-CdII chains is vulnerable to external attacks and is apt to collapse after activation, while FJU-36 with no coordinated solvent in the CdII-O-CdII chains but fully protected by the carboxylates from the ligands and the symmetric formate in the coordination mode mu3-eta2:eta2 is stable, and its activated sample shows efficient separation of C2H2/CH4 and C2H2/CO2 mixtures. Methane 455-458 DNA polymerase iota Homo sapiens 67-71 30316258-3 2018 In this article, we study the dynamics of methane, a small apolar solute, in the family of ILs 1-alkyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ( Im 1 , n + /NTf2 -), with n = 2, 4, 8 at temperatures that make the viscosity for each liquid similar and around 8 cP. Methane 42-49 nuclear transport factor 2 Homo sapiens 177-181 32254719-1 2018 A specific membrane and nucleus targeted fluorescence OFF-ON-OFF system, using the dodecane/sulfobetaine group of functionalized carbon dots (CD) with a copper ion (Cu2+-CD) based on the presence of pyrophosphate (PPi) molecules and alkaline phosphatase (ALP) activity, for cancer cell detection was designed. Methane 129-140 alkaline phosphatase, biomineralization associated Canis lupus familiaris 233-253 32254719-1 2018 A specific membrane and nucleus targeted fluorescence OFF-ON-OFF system, using the dodecane/sulfobetaine group of functionalized carbon dots (CD) with a copper ion (Cu2+-CD) based on the presence of pyrophosphate (PPi) molecules and alkaline phosphatase (ALP) activity, for cancer cell detection was designed. Methane 129-140 alkaline phosphatase, biomineralization associated Canis lupus familiaris 255-258 30255207-1 2018 The potential energy surface for the first step of the methane oxidation CH4 + O2 CH3 + HO2 was studied using the London-Eyring-Polanyi-Sato equation (LEPS) and the conventional transition-state theory (CTST). Methane 55-62 heme oxygenase 2 Homo sapiens 88-91 30255207-1 2018 The potential energy surface for the first step of the methane oxidation CH4 + O2 CH3 + HO2 was studied using the London-Eyring-Polanyi-Sato equation (LEPS) and the conventional transition-state theory (CTST). Methane 73-76 heme oxygenase 2 Homo sapiens 88-91 30195319-0 2018 Methane on a stepped surface: Dynamical insights on the dissociation of CHD3 on Pt(111) and Pt(211). Methane 0-7 chromodomain helicase DNA binding protein 3 Homo sapiens 72-76 30274243-1 2018 Ion-molecule reaction between atomic oxygen anion (O-) and methane (CH4) has been systematically investigated employing the on-the-fly ab initio molecular dynamics simulations. Methane 59-66 COP9 signalosome subunit 4 Drosophila melanogaster 68-71 29758502-0 2018 Dual element (CCl) isotope approach to distinguish abiotic reactions of chlorinated methanes by Fe(0) and by Fe(II) on iron minerals at neutral and alkaline pH. Methane 84-92 crystallin gamma E, pseudogene Homo sapiens 14-17 30188067-4 2018 Due to biological metabolism, the generation of methane in sewers was of 7.39 mg L-1; the decrease of nitrate and sulfate in sewage was 0.33 mg L-1 and 21.35 mg L-1, respectively. Methane 48-55 immunoglobulin kappa variable 1-16 Homo sapiens 81-84 30188067-5 2018 Based on our calculations, the consuming concentration of COD was 32.51 mg L-1for methane generation, 8.04 mg L-1 for denitrification, and 6.41 mg L-1for sulfate degradation by sulfate reducing bacteria. Methane 82-89 immunoglobulin kappa variable 1-16 Homo sapiens 75-78 29775905-2 2018 The bio-electrolysis reactor system (B-EL) yield more methane 148.5 ml/g COD in comparison to reactor system without bio-electrolysis (B-CONT) 125.1 ml/g COD. Methane 54-61 small nuclear ribonucleoprotein polypeptides B and B1 Homo sapiens 73-76 29775905-3 2018 Whereas bio-electrolysis reactor system (C-EL) Iron Scraps amended yield lesser methane (51.2 ml/g COD) in comparison to control bio-electrolysis reactor system without Iron scraps (C-CONT - 114.4 ml/g COD). Methane 80-87 carboxyl ester lipase Homo sapiens 41-45 29775905-3 2018 Whereas bio-electrolysis reactor system (C-EL) Iron Scraps amended yield lesser methane (51.2 ml/g COD) in comparison to control bio-electrolysis reactor system without Iron scraps (C-CONT - 114.4 ml/g COD). Methane 80-87 small nuclear ribonucleoprotein polypeptides B and B1 Homo sapiens 99-102 30134727-1 2018 Scandium monocarbide molecules, ScC, have been prepared by the reaction of 532 nm laser-ablated Sc metal with acetylene or methane under supersonic jet-cooled conditions. Methane 123-130 serpin family B member 3 Homo sapiens 32-35 29633220-1 2018 The present work explores the structures of species formed by dehydrogenation of methane (CH4) and perdeuterated methane (CD4) by the 5d transition metal cation osmium (Os+). Methane 113-120 CD4 molecule Homo sapiens 122-125 30211152-1 2018 Tin oxide SnO2-based gas sensors have been widely used for detecting typical fault characteristic gases extracted from power transformer oil, namely, H2, CO, CO2, CH4, C2H2, C2H4, and C2H6, due to the remarkable advantages of high sensitivity, fast response, long-term stability, and so on. Methane 163-166 strawberry notch homolog 2 Homo sapiens 10-13 30960837-4 2018 As expected, the PIL containing the TFSI- anion showed improved CO2 and CH4 permeabilities compared to its analogue containing the BF4-. Methane 72-75 serpin family A member 2 (gene/pseudogene) Homo sapiens 17-20 30128312-5 2018 23 cm3 min-1 with purity of 98-99% was successfully achieved, and remained stable over 120 h, with a methane conversion of 71-73% on the other side of perovskite membrane. Methane 101-108 CD59 molecule (CD59 blood group) Homo sapiens 7-12 31458983-6 2018 A high uptake of CO2 (up to 5.27 mmol/g at 0 C and 1 bar) and high CO2-over-N2 and CO2-over-CH4 selectivities were observed. Methane 93-96 solute carrier family 6 member 1 Homo sapiens 38-53 29973922-6 2018 The Fdx2- supplies electrons for reduction of the methyl group to methane. Methane 66-73 ferredoxin 2 Homo sapiens 4-8 30068164-14 2018 Methane elimination via nonadiabatic path leads to CH3CH(11A") + CH4(1 1A1), where both ethylidene and methane are in the ground electronic state. Methane 103-110 COP9 signalosome subunit 4 Drosophila melanogaster 65-68 29962172-5 2018 Because adaptive acclimation, more than 71% COD removal, which may have been converted to methane, was achieved. Methane 90-97 small nuclear ribonucleoprotein polypeptides B and B1 Homo sapiens 44-47 29962172-6 2018 Consequently, at COD/SO42-<=1.5, methane production was suppressed by 49% and 100% when the organics and SO42- removal rates were less than 17% and 5%, respectively. Methane 36-43 small nuclear ribonucleoprotein polypeptides B and B1 Homo sapiens 17-20 29962172-8 2018 In addition, the COD balance analysis revealed that less than 9.1% of the COD was converted to methane. Methane 95-102 small nuclear ribonucleoprotein polypeptides B and B1 Homo sapiens 17-20 29962172-8 2018 In addition, the COD balance analysis revealed that less than 9.1% of the COD was converted to methane. Methane 95-102 small nuclear ribonucleoprotein polypeptides B and B1 Homo sapiens 74-77 29738083-2 2018 Methane elimination occurred in the reactions with PPh2 H and SiPh2 H2 , this being followed in the latter case by Si-H bond oxidative addition to give the hydride silylene derivative [Mo2 Cp2 H(mu-PtBu2 )(mu-SiPh2 )(CO)]. Methane 0-7 ceruloplasmin Homo sapiens 189-192 29973922-8 2018 The F420H2 donates electrons for reduction of the remaining methyl groups to methane requiring transfer of electrons from Fdx2- to F420. Methane 77-84 ferredoxin 2 Homo sapiens 122-126 29785845-2 2018 When the electron donor, CH4, was in ample supply, NO3- enhanced BrO3- reduction by stimulating the growth of denitrifying bacteria ( Meiothermus, Comamonadaceae, and Anaerolineaceae) able to reduce BrO3- and NO3- simultaneously. Methane 25-28 NBL1, DAN family BMP antagonist Homo sapiens 51-54 29785845-2 2018 When the electron donor, CH4, was in ample supply, NO3- enhanced BrO3- reduction by stimulating the growth of denitrifying bacteria ( Meiothermus, Comamonadaceae, and Anaerolineaceae) able to reduce BrO3- and NO3- simultaneously. Methane 25-28 NBL1, DAN family BMP antagonist Homo sapiens 209-212 29884064-1 2018 Replacing methane with carbon dioxide in gas hydrates has been suggested as a way of harvesting methane, while at the same time storing carbon dioxide. Methane 10-17 gastrin Homo sapiens 41-44 29884064-1 2018 Replacing methane with carbon dioxide in gas hydrates has been suggested as a way of harvesting methane, while at the same time storing carbon dioxide. Methane 96-103 gastrin Homo sapiens 41-44 29605331-11 2018 The MON and CIN tended to interact for increased methane production and bacterial N flow. Methane 49-56 pyridoxal phosphatase Homo sapiens 12-15 30068164-14 2018 Methane elimination via nonadiabatic path leads to CH3CH(11A") + CH4(1 1A1), where both ethylidene and methane are in the ground electronic state. Methane 0-7 COP9 signalosome subunit 4 Drosophila melanogaster 65-68 33442426-5 2018 Given its role as a potent greenhouse gas, new low-cost methods for detecting and monitoring methane may aid in protecting human and environmental health. Methane 93-100 activation induced cytidine deaminase Homo sapiens 105-108 29898526-5 2018 The results show that the concentrations of dissolved CH4 in groundwater had large spatial variability, ranging from 0 to 0.10 mg L-1 with a mean of 0.01 mg L-1 in Xilingol and from 0 to 8.99 mg L-1 with a mean of 1.44 mg L-1 in Xingan-Tongliao. Methane 54-57 immunoglobulin kappa variable 1-16 Homo sapiens 130-133 29898526-5 2018 The results show that the concentrations of dissolved CH4 in groundwater had large spatial variability, ranging from 0 to 0.10 mg L-1 with a mean of 0.01 mg L-1 in Xilingol and from 0 to 8.99 mg L-1 with a mean of 1.44 mg L-1 in Xingan-Tongliao. Methane 54-57 immunoglobulin kappa variable 1-16 Homo sapiens 157-160 29746104-2 2018 Ni/KCC-1 exhibits the highest catalyst performance with a CH4 formation rate of 33.02 x 10-2 molCH4 molmetal-1 s-1, 1.77 times higher than that of Co/KCC-1 followed by Zn/KCC-1 and finally the parent KCC-1. Methane 58-61 solute carrier family 12 member 4 Homo sapiens 3-8 29898526-5 2018 The results show that the concentrations of dissolved CH4 in groundwater had large spatial variability, ranging from 0 to 0.10 mg L-1 with a mean of 0.01 mg L-1 in Xilingol and from 0 to 8.99 mg L-1 with a mean of 1.44 mg L-1 in Xingan-Tongliao. Methane 54-57 immunoglobulin kappa variable 1-16 Homo sapiens 157-160 29898526-5 2018 The results show that the concentrations of dissolved CH4 in groundwater had large spatial variability, ranging from 0 to 0.10 mg L-1 with a mean of 0.01 mg L-1 in Xilingol and from 0 to 8.99 mg L-1 with a mean of 1.44 mg L-1 in Xingan-Tongliao. Methane 54-57 immunoglobulin kappa variable 1-16 Homo sapiens 157-160 29898526-6 2018 Substantial CH4 concentrations of about 2.5-5.5 mg L-1 were found in central areas of Xingan-Tongliao in the winter and the summer. Methane 12-15 immunoglobulin kappa variable 1-16 Homo sapiens 51-54 28231698-9 2018 During respiration chamber studies the methane production (L/kg DMI and L/kg digestible dry matter intake was significantly (p<0.001) lower in Group 2 and Group 3 as compared to control animals. Methane 39-46 DMI Bos taurus 64-67 29550332-0 2018 Reduction of nitrosative stress by methane: Neuroprotection through xanthine oxidoreductase inhibition in a rat model of mesenteric ischemia-reperfusion. Methane 35-42 xanthine dehydrogenase Rattus norvegicus 68-91 29550332-2 2018 We also tested the hypothesis that exogenous methane may modulate the evolution of nitroxidation by influencing xanthine oxidoreductase (XOR) activity. Methane 45-52 xanthine dehydrogenase Rattus norvegicus 112-135 29550332-2 2018 We also tested the hypothesis that exogenous methane may modulate the evolution of nitroxidation by influencing xanthine oxidoreductase (XOR) activity. Methane 45-52 xanthine dehydrogenase Rattus norvegicus 137-140 29550332-10 2018 These alterations were eliminated in methane-treated animals, XOR activity and nitrotyrosine formation decreased in all sites, and the duodenal nitrergic neuron ratio was re-established. Methane 37-44 xanthine dehydrogenase Rattus norvegicus 62-65 29550332-11 2018 The inhibitory effect of methane on XOR-linked nitrate reductase activity was also demonstrated in vitro. Methane 25-32 xanthine dehydrogenase Rattus norvegicus 36-39 29550332-13 2018 The XOR-inhibitory effect of methane can reduce nitroxidation and protects the nitrergic neuron population in such conditions. Methane 29-36 xanthine dehydrogenase Rattus norvegicus 4-7 29722776-5 2018 The procedure is demonstrated on the CH4, CD4, CH3D and CHD3 isotopologs of methane using three reduced-dimensional models, which were previously used in quantum reactive scattering studies of the CH4 + X CH3 + HX type reactions. Methane 76-83 chromodomain helicase DNA binding protein 3 Homo sapiens 56-60 29414361-3 2018 Multiple regression model analysis indicated that lysozyme levels exhibited a consistent negative association with methane (CH4: beta = -76.3, 95% CI -105 to -47.7) and sulfuretted hydrogen (H2S: beta = -11.7, 95% CI -20.2 to -3.19). Methane 115-122 lysozyme Homo sapiens 50-58 29414361-3 2018 Multiple regression model analysis indicated that lysozyme levels exhibited a consistent negative association with methane (CH4: beta = -76.3, 95% CI -105 to -47.7) and sulfuretted hydrogen (H2S: beta = -11.7, 95% CI -20.2 to -3.19). Methane 124-127 lysozyme Homo sapiens 50-58 30258639-5 2018 Results: With the addition of NO3 --N, VFAs were utilized during denitrification, after which methane production started. Methane 94-101 NBL1, DAN family BMP antagonist Homo sapiens 30-33 29797877-13 2018 The dissolved concentration and diffusion flux of CH4 ranged from 0 to 5.28 mumol L-1 and from -0.34 to 619.72 mug C m-2 h-1, respectively, with significant temporal and spatial variations. Methane 50-53 immunoglobulin kappa variable 1-16 Homo sapiens 82-85 29334088-1 2018 A hybrid QM:QM method that combines MP2 as high-level method on cluster models with density functional theory (PBE+D2) as low-level method on periodic models is applied to adsorption of methane and ethane on the MgO(001) surface for which reliable experimental desorption enthalpies are available. Methane 186-193 tryptase pseudogene 1 Homo sapiens 36-39 29900300-1 2018 This article describes initial and final configurations of methane hydrate structure I as PDB file at various cage occupancies and different temperatures. Methane 59-66 PDB1 Homo sapiens 90-93 29384499-3 2018 In this study, a new sensor based on carbon dots (CDs) linked with antibodies to specifically detect GFAP in human serum was developed. Methane 37-48 glial fibrillary acidic protein Homo sapiens 101-105 29411262-4 2018 reduced MA-induced mechanical allodynia and multiple methane treatments blocked activation of glial cells, decreased IL-1beta and TNF-alpha production and MMP-2 activity, and upregulated IL-10 expression in the spinal cord on day 10 post-MA. Methane 53-60 interleukin 1 beta Rattus norvegicus 117-125 29411262-4 2018 reduced MA-induced mechanical allodynia and multiple methane treatments blocked activation of glial cells, decreased IL-1beta and TNF-alpha production and MMP-2 activity, and upregulated IL-10 expression in the spinal cord on day 10 post-MA. Methane 53-60 tumor necrosis factor Rattus norvegicus 130-139 29411262-4 2018 reduced MA-induced mechanical allodynia and multiple methane treatments blocked activation of glial cells, decreased IL-1beta and TNF-alpha production and MMP-2 activity, and upregulated IL-10 expression in the spinal cord on day 10 post-MA. Methane 53-60 matrix metallopeptidase 2 Rattus norvegicus 155-160 29411262-4 2018 reduced MA-induced mechanical allodynia and multiple methane treatments blocked activation of glial cells, decreased IL-1beta and TNF-alpha production and MMP-2 activity, and upregulated IL-10 expression in the spinal cord on day 10 post-MA. Methane 53-60 interleukin 10 Rattus norvegicus 187-192 30258639-8 2018 Methane production was 0.02-0.03 L CH4/g VS higher with NO3 --N recirculation and feeding than that without feeding. Methane 0-7 NBL1, DAN family BMP antagonist Homo sapiens 56-59 29187296-5 2018 This work presents a concise appraisal of adsorption properties of MOFs and graphene-MOF hybrids toward CO2, volatile organic compounds, hydrogen and methane. Methane 150-157 lysine acetyltransferase 8 Homo sapiens 67-70 29965484-10 2018 The Pseudomonas and Thermomonas emerged when the nitrate concentration increased to 500 mg L-1, and the rate of methane conversion was increased by 34.7%. Methane 112-119 immunoglobulin kappa variable 1-16 Homo sapiens 91-94 29189040-4 2018 On planets with high fluxes of biogenic organic sulfur gases (CS2, OCS, CH3SH, and CH3SCH3), photochemistry involving these gases can drive haze formation at lower CH4/CO2 ratios than methane photochemistry alone. Methane 164-167 chorionic somatomammotropin hormone 2 Homo sapiens 62-65 29361159-4 2018 When added at 2 g L-1, decreases in not only ammonia production (-77%; P < 0.001), but also methane (-27%; P = 0.039) and total VFA production (-15%; P = 0.003) were observed. Methane 95-102 immunoglobulin kappa variable 1-16 Homo sapiens 18-21 29548403-9 2018 Activated membranes with high load capacity did not seem to have an influence on the methane oxidation process: MBP coupled with 220g/m2 and 360g/m2 membranes gave maximum MOR of 16.5gCH4/m2/hr and 17.4gCH4/m2/hr, respectively. Methane 85-92 myelin basic protein Homo sapiens 112-115 29448679-3 2018 The sp2/sp3 bonded carbon ratio in the grown films increased as the CH4 content increased up to 3 Vol% and then decreased beyond 4 Vol%. Methane 68-71 Sp2 transcription factor Homo sapiens 4-7 29448679-3 2018 The sp2/sp3 bonded carbon ratio in the grown films increased as the CH4 content increased up to 3 Vol% and then decreased beyond 4 Vol%. Methane 68-71 Sp3 transcription factor Homo sapiens 8-11 29249311-9 2018 A good agreement was observed between the average total CH4 generation rates determined by field measurements (147 kg CH4/h) and those estimated by the Afvalzorg model (154 kg CH4/h). Methane 56-59 RNA component of mitochondrial RNA processing endoribonuclease Homo sapiens 118-123 29137785-9 2018 The increase in the permeability of the gases was as follows: PCH4 (38%) <PN2 (58%) <PCO2 (88%) <PO2 (98%) Adding silica nanoparticles into the PE matrix, improved the separation performance of carbon dioxide/methane and carbon dioxide/nitrogen gases. Methane 218-225 tRNA splicing endonuclease subunit 54 Homo sapiens 62-66 29780471-6 2018 This variation in structure and redox leads to notably higher separation selectivity for C2H2/CH4 and C2H4/CH4 in MFM-300(VIII) than in MFM-300(VIV). Methane 94-97 cytochrome c oxidase subunit 8A Homo sapiens 122-126 28938186-4 2018 In this protocol, mesoporous carbon nanospheres were adopted to immobilize ECL reactant Ru(bpy)32+ and antibody via nafion to acquire the RET donor nanocomposites (MOCs/nafion/Ru(bpy)32+/antibody), which were tightly interconnected with epoxy group functionalized Fe3O4 nanoparticles. Methane 18-35 ret proto-oncogene Homo sapiens 138-141 28735588-1 2018 The objectives of this study were to determine the effect and mode of action of Saccharomyces cerevisiae (YST2) on enteric methane (CH4) mitigation in pigs. Methane 132-135 ribosomal 40S subunit protein S0B Saccharomyces cerevisiae S288C 106-110 28735588-4 2018 Results showed that S. cerevisiae YST2 decreased (P<0.05) the average daily enteric CH4 production by 25.3%, lowered the pH value from 6.99 to 6.69 in the rectum, and increased the Eh value in cecum and colon by up to -55 mV (P<0.05). Methane 87-90 ribosomal 40S subunit protein S0B Saccharomyces cerevisiae S288C 34-38 28735588-7 2018 Results of our study concluded that supplementation of S. cerevisiae YST2 at 3 g/kg substantially decreased enteric CH4 production in pigs. Methane 116-119 ribosomal 40S subunit protein S0B Saccharomyces cerevisiae S288C 69-73 29125685-4 2018 Ethane condition gives a growth rate about four times faster than methane, achieving about 420 microm min-1 for the growth of sub-centimeter graphene single crystals at temperature about 1000 C. In addition, the temperature threshold to obtain graphene using ethane can be reduced to 750 C, lower than the general growth temperature threshold (about 1000 C) with methane on copper foil. Methane 66-73 CD59 molecule (CD59 blood group) Homo sapiens 102-107 29073521-3 2018 Methanogens can consume H2 to produce CH4 in MECs, which has led to a drop of H2 production efficiency, H2 production rate (HPR) and also a low percentage of H2 in the produced biogas. Methane 38-41 haptoglobin-related protein Homo sapiens 104-122 29073521-3 2018 Methanogens can consume H2 to produce CH4 in MECs, which has led to a drop of H2 production efficiency, H2 production rate (HPR) and also a low percentage of H2 in the produced biogas. Methane 38-41 haptoglobin-related protein Homo sapiens 124-127 29161570-3 2018 The results demonstrated that after long term of acclimation to low pH, the digester could produce methane from propionate at pH 4.8-5.5 with 0.3-0.4 L g-1 propionic acid (HPr) d-1 of the volatile solids (VS) methane production. Methane 99-106 haptoglobin-related protein Homo sapiens 172-175 29161570-3 2018 The results demonstrated that after long term of acclimation to low pH, the digester could produce methane from propionate at pH 4.8-5.5 with 0.3-0.4 L g-1 propionic acid (HPr) d-1 of the volatile solids (VS) methane production. Methane 209-216 haptoglobin-related protein Homo sapiens 172-175 29136518-4 2018 Several independent lines of evidence obtained from microcosm experiments with the methanotrophic enrichment culture, tap water and bentazone at concentrations below 2 mg/L showed methanotrophic co-metabolic bentazone transformation: The culture removed 53% of the bentazone in 21 days in presence of 5 mg/L of methane, while only 31% was removed in absence of methane. Methane 311-318 nuclear RNA export factor 1 Homo sapiens 118-121 28950130-2 2018 In this study, the effects of the MEC on the rate of methane production from food waste were examined by comparing an AD reactor with an AD reactor combined with a MEC (AD+MEC). Methane 53-60 C-C motif chemokine ligand 28 Homo sapiens 34-37 28950130-3 2018 The use of the MEC accelerated methane production and stabilization via rapid organic oxidation and rapid methanogenesis. Methane 31-38 C-C motif chemokine ligand 28 Homo sapiens 15-18 28950130-6 2018 Based on these results, the MEC did not increase the methane yield over the theoretical value, but accelerated methane production and stabilization by bioelectrochemical reactions. Methane 111-118 C-C motif chemokine ligand 28 Homo sapiens 28-31 29091852-1 2018 Granular activated carbon (GAC) or magnetite could promote methane production from organic wastes, but their roles in enhancing anaerobic sludge digestion have not been clarified. Methane 59-66 glutaminase Homo sapiens 27-30 29091852-3 2018 Experimental results showed that average methane production increased by 7.3% for magnetite, 13.1% for GAC, and 20% for the combination of magnetite and GAC, and the effluent TCOD of the control, magnetite, GAC and magnetite-GAC digesters on day 56 were 53.2, 49.6, 48.0 and 46.6 g/L, respectively. Methane 41-48 glutaminase Homo sapiens 103-106 29091852-3 2018 Experimental results showed that average methane production increased by 7.3% for magnetite, 13.1% for GAC, and 20% for the combination of magnetite and GAC, and the effluent TCOD of the control, magnetite, GAC and magnetite-GAC digesters on day 56 were 53.2, 49.6, 48.0 and 46.6 g/L, respectively. Methane 41-48 glutaminase Homo sapiens 153-156 29091852-3 2018 Experimental results showed that average methane production increased by 7.3% for magnetite, 13.1% for GAC, and 20% for the combination of magnetite and GAC, and the effluent TCOD of the control, magnetite, GAC and magnetite-GAC digesters on day 56 were 53.2, 49.6, 48.0 and 46.6 g/L, respectively. Methane 41-48 glutaminase Homo sapiens 153-156 29091852-3 2018 Experimental results showed that average methane production increased by 7.3% for magnetite, 13.1% for GAC, and 20% for the combination of magnetite and GAC, and the effluent TCOD of the control, magnetite, GAC and magnetite-GAC digesters on day 56 were 53.2, 49.6, 48.0 and 46.6 g/L, respectively. Methane 41-48 glutaminase Homo sapiens 153-156 29136518-4 2018 Several independent lines of evidence obtained from microcosm experiments with the methanotrophic enrichment culture, tap water and bentazone at concentrations below 2 mg/L showed methanotrophic co-metabolic bentazone transformation: The culture removed 53% of the bentazone in 21 days in presence of 5 mg/L of methane, while only 31% was removed in absence of methane. Methane 361-368 nuclear RNA export factor 1 Homo sapiens 118-121 29220050-5 2018 The C2H2, CO2, and CH4 uptake capacities at 298 K and 1 atm are 120.2, 78.1, and 18.4 cm3 (STP) g-1 for ZJNU-77, and 122.0, 82.0, and 18.9 cm3 (STP) g-1 for ZJNU-78, respectively. Methane 19-22 sulfotransferase family 1A member 1 Homo sapiens 91-94 29220050-5 2018 The C2H2, CO2, and CH4 uptake capacities at 298 K and 1 atm are 120.2, 78.1, and 18.4 cm3 (STP) g-1 for ZJNU-77, and 122.0, 82.0, and 18.9 cm3 (STP) g-1 for ZJNU-78, respectively. Methane 19-22 sulfotransferase family 1A member 1 Homo sapiens 144-147 29965694-5 2018 In the anaerobic methane production test (BMP) that lasted for 22 days, compared with control group, the accumulated biogas production of the experiment group increased by 48%. Methane 17-24 bone morphogenetic protein 1 Homo sapiens 42-45 29125685-4 2018 Ethane condition gives a growth rate about four times faster than methane, achieving about 420 microm min-1 for the growth of sub-centimeter graphene single crystals at temperature about 1000 C. In addition, the temperature threshold to obtain graphene using ethane can be reduced to 750 C, lower than the general growth temperature threshold (about 1000 C) with methane on copper foil. Methane 366-373 CD59 molecule (CD59 blood group) Homo sapiens 102-107 28479085-12 2018 It could be thought that the high amount of non-biodegradable matters in leachate could be responsible for lower methane yield in leachate+sewage sludge+OFMSW (C1) reactor. Methane 113-120 complement C6 Homo sapiens 153-159 32264370-2 2017 The self-adaptive assembly of terbium ions (Tb3+), adenosine monophosphate (AMP), glucose oxidase (GOx), and carbon dots (CDs) leads to the formation of a GOx&CDs@AMP/Tb composite with catalytic and fluorescence properties. Methane 109-120 hydroxyacid oxidase 1 Homo sapiens 82-97 28926916-3 2017 All substrates had methane potentials close to the theoretical value except for bovine serum albumin (BSA) whose methane potential was lower, but the maximum methane potential reached the value during repeated methanization. Methane 113-120 albumin Homo sapiens 87-100 28926916-3 2017 All substrates had methane potentials close to the theoretical value except for bovine serum albumin (BSA) whose methane potential was lower, but the maximum methane potential reached the value during repeated methanization. Methane 113-120 albumin Homo sapiens 87-100 30815543-0 2018 A role for methanogens and methane in the regulation of GLP-1. Methane 27-34 glucagon Homo sapiens 56-61 30815543-8 2018 In addition, the direct effect of methane on GLP-1 secretion was assessed in two L-cell models (NCI-H716 and GLUTag). Methane 34-41 glucagon Homo sapiens 45-50 30815543-11 2018 In L cells, methane stimulated GLP-1 secretion and enhanced intracellular cAMP content. Methane 12-19 glucagon Homo sapiens 31-36 29170687-4 2017 In this paper, an extensive comparison and in-depth investigation of several force fields from literature is reported for the case of methane adsorption in the Zr-based Metal-Organic Frameworks UiO-66, UiO-67, DUT-52, NU-1000, and MOF-808. Methane 134-141 deoxyuridine triphosphatase Homo sapiens 210-213 27498752-11 2017 This was consistent with a sharp fall of methane productivity in those bioreactors in period 2. Methane 41-48 period circadian regulator 2 Homo sapiens 86-94 28525848-0 2017 An amplified comparative fluorescence resonance energy transfer immunosensing of CA125 tumor marker and ovarian cancer cells using green and economic carbon dots for bio-applications in labeling, imaging and sensing. Methane 150-161 mucin 16, cell surface associated Homo sapiens 81-86 28779660-4 2017 An S/X ratio of 0.5 showed the best hydrolysis efficiency (29%) reaching in a second stage process a methane yield of 193mL CH4g COD-1. Methane 101-108 component of oligomeric golgi complex 4 Homo sapiens 129-134 32264370-2 2017 The self-adaptive assembly of terbium ions (Tb3+), adenosine monophosphate (AMP), glucose oxidase (GOx), and carbon dots (CDs) leads to the formation of a GOx&CDs@AMP/Tb composite with catalytic and fluorescence properties. Methane 109-120 hydroxyacid oxidase 1 Homo sapiens 155-158 28426194-3 2017 It exhibits a high CO2 uptake of 180 mL(STP)/g at 1 bar, and 400 mL(STP)/g at 30 bar at 273 K. The uptakes of C2H2 and C2H4 reach 164 and 160 mL(STP)/g at 298 K and 1 bar, with good selectivity of C2H2 and C2H4 over CH4, both of which are among the highest levels of reported PCPs. Methane 216-219 sulfotransferase family 1A member 1 Homo sapiens 40-43 28426194-3 2017 It exhibits a high CO2 uptake of 180 mL(STP)/g at 1 bar, and 400 mL(STP)/g at 30 bar at 273 K. The uptakes of C2H2 and C2H4 reach 164 and 160 mL(STP)/g at 298 K and 1 bar, with good selectivity of C2H2 and C2H4 over CH4, both of which are among the highest levels of reported PCPs. Methane 216-219 sulfotransferase family 1A member 1 Homo sapiens 68-71 28426194-3 2017 It exhibits a high CO2 uptake of 180 mL(STP)/g at 1 bar, and 400 mL(STP)/g at 30 bar at 273 K. The uptakes of C2H2 and C2H4 reach 164 and 160 mL(STP)/g at 298 K and 1 bar, with good selectivity of C2H2 and C2H4 over CH4, both of which are among the highest levels of reported PCPs. Methane 216-219 sulfotransferase family 1A member 1 Homo sapiens 68-71 28913527-7 2017 This could give insight into the important catalytic process of the industrial scale synthesis of HCN from CH4 and NH3 over Pt. Methane 107-110 metastasis associated lung adenocarcinoma transcript 1 Homo sapiens 98-101 28597201-2 2017 Thus, we investigated the potential protective effects of methane-rich saline (MS) on CCl4-induced acute liver injury and explored the underlying mechanism. Methane 58-65 chemokine (C-C motif) ligand 4 Mus musculus 86-90 28815842-4 2017 The results of density functional calculations show a reduction in the methane activation barrier from 1.07 eV on Co(0001) to 0.87 eV on Co2+ /CeO2 (111), and to only 0.05 eV on Co0 /CeO2-x (111). Methane 71-78 complement C2 Homo sapiens 137-140 28691317-2 2017 The 6FDA-DAT1-OH polyimide is thermally stable up to 440 C, shows excellent solubility in polar solvents, and has moderately high Brunauer-Teller-Emmett (BET) surface area of 160 m2 g-1 , as determined by nitrogen adsorption at -196 C. Hydroxyl functionalization applied to the rigid 3D triptycene-based diamine building block results in a polyimide that exhibits moderate pure-gas CO2 permeability of 70 Barrer combined with high CO2 /CH4 selectivity of 50. Methane 438-441 solute carrier family 6 member 3 Homo sapiens 9-13 28691317-3 2017 Mixed-gas permeation studies demonstrate excellent plasticization resistance of 6FDA-DAT1-OH with impressive performance as potential membrane material for natural gas sweetening with a CO2 permeability of 50 Barrer and CO2 /CH4 selectivity of 40 at a typical natural gas well partial pressure of 10 atm. Methane 225-228 solute carrier family 6 member 3 Homo sapiens 85-89 28737377-1 2017 The fluorescence resonance energy transfer (FRET) mechanism has been established between carbon dots (CDs) and naphthalimide to monitor the activity of thioredoxin reductase (TrxR), which is often overexpressed in many cancer cells. Methane 89-100 peroxiredoxin 5 Homo sapiens 152-173 28737377-1 2017 The fluorescence resonance energy transfer (FRET) mechanism has been established between carbon dots (CDs) and naphthalimide to monitor the activity of thioredoxin reductase (TrxR), which is often overexpressed in many cancer cells. Methane 89-100 peroxiredoxin 5 Homo sapiens 175-179 29525064-0 2017 Inhaled Methane Protects Rats Against Neurological Dysfunction Induced by Cerebral Ischemia and Reperfusion Injury: PI3K/Akt/HO-1 Pathway Involved. Methane 8-15 AKT serine/threonine kinase 1 Rattus norvegicus 121-124 29525064-0 2017 Inhaled Methane Protects Rats Against Neurological Dysfunction Induced by Cerebral Ischemia and Reperfusion Injury: PI3K/Akt/HO-1 Pathway Involved. Methane 8-15 heme oxygenase 1 Rattus norvegicus 125-129 28601456-13 2017 Enteric CH4 emission per kilogram of energy-corrected milk was highest in the triticale silage diet, whereas CO2 emission was decreased by both wheat and triticale silage. Methane 8-11 Weaning weight-maternal milk Bos taurus 54-58 28597201-0 2017 Methane alleviates carbon tetrachloride induced liver injury in mice: anti-inflammatory action demonstrated by increased PI3K/Akt/GSK-3beta-mediated IL-10 expression. Methane 0-7 thymoma viral proto-oncogene 1 Mus musculus 126-129 28597201-0 2017 Methane alleviates carbon tetrachloride induced liver injury in mice: anti-inflammatory action demonstrated by increased PI3K/Akt/GSK-3beta-mediated IL-10 expression. Methane 0-7 glycogen synthase kinase 3 beta Mus musculus 130-139 28597201-0 2017 Methane alleviates carbon tetrachloride induced liver injury in mice: anti-inflammatory action demonstrated by increased PI3K/Akt/GSK-3beta-mediated IL-10 expression. Methane 0-7 interleukin 10 Mus musculus 149-154 28698659-8 2017 Conservative estimates amount to 5 kt of methane, equivalent to 67% of the annual release from the entire North Sea. Methane 41-48 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 112-115 28616938-1 2017 An all-solid-state Bi2WO6/Au/CdS Z-scheme system was constructed for the photocatalytic reduction of CO2 into methane in the presence of water vapor. Methane 110-117 CDP-diacylglycerol synthase 1 Homo sapiens 29-32 28376236-7 2017 River and lake CH4 emissions were 0.03 and 0.10 Tg C/yr, respectively. Methane 15-18 transglutaminase 2 Homo sapiens 48-52 28881075-0 2017 Formation of Methane versus Benzene in the Reactions of (C5 Me5 )2 Th(CH3 )2 with [CH3 PPh3 ]X (X=Cl, Br, I) Yielding Thorium-Carbene or Thorium-Ylide Complexes. Methane 13-20 protein phosphatase 4 catalytic subunit Homo sapiens 87-91 28323135-6 2017 Addition of 2% enrichment culture did not enhance methane production, whereas in Set-2 the methane yield was increased by 27%. Methane 91-98 SET domain containing 2, histone lysine methyltransferase Homo sapiens 81-86 29525064-12 2017 The HO-1 inhibitor ZnPP-IX, PI3K inhibitor LY294002 and Akt inhibitor triciribine all significantly abolished the effect of methane on neurological deficit. Methane 124-131 heme oxygenase 1 Rattus norvegicus 4-8 29525064-12 2017 The HO-1 inhibitor ZnPP-IX, PI3K inhibitor LY294002 and Akt inhibitor triciribine all significantly abolished the effect of methane on neurological deficit. Methane 124-131 AKT serine/threonine kinase 1 Rattus norvegicus 56-59 29051865-3 2017 Using large Pd nanocrystals, this study achieves CO and CH4 production rates as high as 0.75 and 0.11 mol h-1 gPd-1, respectively. Methane 56-59 glycerol-3-phosphate dehydrogenase 1 Homo sapiens 110-115 28724997-1 2017 In this report, a novel fluorescent sensing platform using nitrogen-doped carbon dots (N-CDs) as probes for fluorescence signal transmission has been designed for the detection of significant biomolecules pyrophosphate (PPi) and alkaline phosphatase (ALP). Methane 74-85 alkaline phosphatase, placental Homo sapiens 229-249 28724997-1 2017 In this report, a novel fluorescent sensing platform using nitrogen-doped carbon dots (N-CDs) as probes for fluorescence signal transmission has been designed for the detection of significant biomolecules pyrophosphate (PPi) and alkaline phosphatase (ALP). Methane 74-85 alkaline phosphatase, placental Homo sapiens 251-254 28266678-4 2017 Whilst not active for ammonia synthesis, the silicon nitride based materials were found to possess activity for the COx-free production of H2 from methane, which makes them candidates for applications in which the presence of low levels of CO in H2 feedstreams is detrimental. Methane 147-154 cytochrome c oxidase subunit 8A Homo sapiens 116-119 28502432-2 2017 In the present study, a facile and sensitive fluorescent assay based on enzyme activated inner filter effect (IFE) on nitrogen-doped carbon dots (CDs) was first developed for the detection of alpha-glucosidase. Methane 133-144 sucrase-isomaltase Homo sapiens 192-209 27815590-4 2017 We found that cysteine supplementation (100, 400, and 800 muM) accelerated CH4 production from propionate in paddy soil enrichments. Methane 75-78 latexin Homo sapiens 58-61 28336261-11 2017 Furthermore, methane treatment suppressed up-regulations of critical mitochondrial components (PGC-1alpha, NRF1 and TFAM) mRNA and mtDNA copy number, as well as improved the reduction of functional mitochondria markers, including citrate synthase activity and ATP content, in retinas with ONC. Methane 13-20 PPARG coactivator 1 alpha Rattus norvegicus 95-105 28336261-11 2017 Furthermore, methane treatment suppressed up-regulations of critical mitochondrial components (PGC-1alpha, NRF1 and TFAM) mRNA and mtDNA copy number, as well as improved the reduction of functional mitochondria markers, including citrate synthase activity and ATP content, in retinas with ONC. Methane 13-20 nuclear respiratory factor 1 Rattus norvegicus 107-111 28336261-11 2017 Furthermore, methane treatment suppressed up-regulations of critical mitochondrial components (PGC-1alpha, NRF1 and TFAM) mRNA and mtDNA copy number, as well as improved the reduction of functional mitochondria markers, including citrate synthase activity and ATP content, in retinas with ONC. Methane 13-20 transcription factor A, mitochondrial Rattus norvegicus 116-120 28336261-11 2017 Furthermore, methane treatment suppressed up-regulations of critical mitochondrial components (PGC-1alpha, NRF1 and TFAM) mRNA and mtDNA copy number, as well as improved the reduction of functional mitochondria markers, including citrate synthase activity and ATP content, in retinas with ONC. Methane 13-20 citrate synthase Rattus norvegicus 230-246 27815590-5 2017 Of the concentrations tested, 100 muM cysteine was the most effective at enhancing propionate degradation to CH4, and the rates of CH4 production and propionate degradation were increased by 109 and 79%, respectively, compared with the cysteine-free control incubations. Methane 109-112 latexin Homo sapiens 34-37 28453502-11 2017 Moreover, some GO terms (regulation of programmed cell death and regulation of cell death) and pathways (p53 signaling pathway, methane metabolism, and viral myocarditis) might be involved. Methane 128-135 tumor protein p53 Homo sapiens 105-108 28164345-4 2017 Furthermore, the effect of number, mass, and volume of POMs inserted in SPC on CO2 /CH4 (or CO2 /N2 ) selectivity over large pressure range was investigated in detail. Methane 84-87 proline rich protein gene cluster Homo sapiens 72-75 28430276-5 2017 Simulations indicate that CO2 and CH4 bind strongly in the MOF/GO interface region, resulting in synergistically enhanced adsorption properties. Methane 34-37 lysine acetyltransferase 8 Homo sapiens 59-65 28352256-3 2017 Therefore, the aim of this study was to understand the fate of [2H] when CH4 production in the rumen is inhibited by known methanogenesis inhibitors (nitrate, NIT; 3-nitrooxypropanol, NOP; anthraquinone, AQ) in comparison with a control treatment (CON) with the Rumen Simulation Technique (RUSITEC). Methane 73-76 prepronociceptin Homo sapiens 184-187 28230100-4 2017 Methane is almost exclusively produced when rhodium nanoparticles are mildly illuminated as hot electrons are injected into the anti-bonding orbital of a critical intermediate, while carbon monoxide and methane are equally produced without illumination. Methane 0-7 alcohol dehydrogenase iron containing 1 Homo sapiens 92-95 27166779-1 2017 Research was conducted, which aim was to evaluate the influence of mesophilic methane digestion on degradation of coplanar and indicator PCB in sewage sludge, and on dynamics of changes of these congeners during the process. Methane 78-85 pyruvate carboxylase Homo sapiens 137-140 28164345-2 2017 GCMC simulations showed this impregnation can enhance CO2 /CH4 (or CO2 /N2 ) selectivity almost 30 times compared to the bare SPC due to the strong interaction of CO2 with the nPOMs@SPC structures. Methane 59-62 proline rich protein gene cluster Homo sapiens 126-129 28164345-2 2017 GCMC simulations showed this impregnation can enhance CO2 /CH4 (or CO2 /N2 ) selectivity almost 30 times compared to the bare SPC due to the strong interaction of CO2 with the nPOMs@SPC structures. Methane 59-62 proline rich protein gene cluster Homo sapiens 182-185 27596480-1 2017 The feasibility of NO3- removal by the synergistic action of a prevailing denitrifying anoxic methane oxidising (DAMO), and nitrate-reducing and sulfide-oxidising bacterial (NR-SOB) consortium, using CH4 and H2 S from biogas as electron donors in a biotrickling filter was investigated. Methane 94-101 NBL1, DAN family BMP antagonist Homo sapiens 19-22 27596480-1 2017 The feasibility of NO3- removal by the synergistic action of a prevailing denitrifying anoxic methane oxidising (DAMO), and nitrate-reducing and sulfide-oxidising bacterial (NR-SOB) consortium, using CH4 and H2 S from biogas as electron donors in a biotrickling filter was investigated. Methane 200-203 NBL1, DAN family BMP antagonist Homo sapiens 19-22 27596480-3 2017 The results showed that NO3- was removed at rates up to 2.8 g mreactor-3 h-1 using CH4 as electron donor. Methane 84-87 NBL1, DAN family BMP antagonist Homo sapiens 24-27 30160411-3 2017 The main characteristic lines were assigned to CH, C2 and Halpha during the discharge process of CH4 at room temperature.The emission intensity of C2 at 516 nm is linear with the concentration of CH4 from 0.5% to 4.0% (phi), and the detection limit (S/N=3) is 0.19% (phi). Methane 97-100 complement C2 Homo sapiens 51-64 30160411-3 2017 The main characteristic lines were assigned to CH, C2 and Halpha during the discharge process of CH4 at room temperature.The emission intensity of C2 at 516 nm is linear with the concentration of CH4 from 0.5% to 4.0% (phi), and the detection limit (S/N=3) is 0.19% (phi). Methane 196-199 complement C2 Homo sapiens 51-64 28164345-6 2017 As a result, the proposed nPOMs@SPC structures are promising candidates for CO2 /N2 and CO2 /CH4 separations. Methane 93-96 proline rich protein gene cluster Homo sapiens 32-35 27846569-1 2016 Methyl-coenzyme M reductase (MCR) is the key enzyme of methanogenesis and anaerobic methane oxidation. Methane 84-91 coenzyme-B sulfoethylthiotransferase subunit beta Methanosarcina acetivorans C2A 0-27 28007572-0 2017 Methane ameliorates spinal cord ischemia-reperfusion injury in rats: Antioxidant, anti-inflammatory and anti-apoptotic activity mediated by Nrf2 activation. Methane 0-7 NFE2 like bZIP transcription factor 2 Rattus norvegicus 140-144 28007572-4 2017 MS treatment attenuated motor sensory deficits and produced high concentrations of methane in spinal cords during reperfusion, which increased Nrf2 expression and transcriptional activity in neurons, microglia and astrocytes in the ventral, intermediate and dorsal gray matter of lumbar segments. Methane 83-90 NFE2 like bZIP transcription factor 2 Rattus norvegicus 143-147 27692471-8 2017 Methane was always supersaturated (0.19 to 62.13muM), resulting from groundwater discharge and stream-bed methanogenesis. Methane 0-7 latexin Homo sapiens 48-51 27646453-1 2016 This study builds upon prior work showing that methane (CH4) could be utilized as the sole electron donor and carbon source in a membrane biofilm reactor (MBfR) for complete perchlorate (ClO4-) and nitrate (NO3-) removal. Methane 47-54 NBL1, DAN family BMP antagonist Homo sapiens 207-210 27646453-1 2016 This study builds upon prior work showing that methane (CH4) could be utilized as the sole electron donor and carbon source in a membrane biofilm reactor (MBfR) for complete perchlorate (ClO4-) and nitrate (NO3-) removal. Methane 56-59 NBL1, DAN family BMP antagonist Homo sapiens 207-210 27639056-4 2016 When the initial hydrogen partial pressure was 0.5 atm, the methane yield at high ammonia load (7 g NH4+-N L-1) was 41.0% and 22.3% lower than that at low ammonia load (1 g NH4+-N L-1) in mesophilic and thermophilic condition, respectively. Methane 60-67 immunoglobulin kappa variable 1-16 Homo sapiens 107-110 27639056-4 2016 When the initial hydrogen partial pressure was 0.5 atm, the methane yield at high ammonia load (7 g NH4+-N L-1) was 41.0% and 22.3% lower than that at low ammonia load (1 g NH4+-N L-1) in mesophilic and thermophilic condition, respectively. Methane 60-67 immunoglobulin kappa variable 1-16 Homo sapiens 180-183 31457169-0 2016 Hybrid Cu x O-TiO2 Heterostructured Composites for Photocatalytic CO2 Reduction into Methane Using Solar Irradiation: Sunlight into Fuel. Methane 85-92 cut like homeobox 1 Homo sapiens 7-11 27783615-12 2016 This theoretical investigation shows that thermodynamic control of PH2 on individual VFA produced and associated yield of hydrogen and methane cannot be explained without considering NADH oxidation. Methane 135-142 polyhomeotic homolog 2 Homo sapiens 67-70 27782458-3 2016 In particular, molecular dynamics simulations with accurate water potentials are used to study the energetics of the formation of structure I (sI) and II (sII) clathrate hydrates of methane, ethane, and propane. Methane 182-189 S-phase kinase associated protein 1 Homo sapiens 130-153 27782458-3 2016 In particular, molecular dynamics simulations with accurate water potentials are used to study the energetics of the formation of structure I (sI) and II (sII) clathrate hydrates of methane, ethane, and propane. Methane 182-189 transcription elongation factor A1 Homo sapiens 155-158 27782458-5 2016 The encapsulation energies of methane, ethane, and propane guests stabilize the small and large sI and sII hydrate cages, with the larger molecules giving larger encapsulation energies. Methane 30-37 transcription elongation factor A1 Homo sapiens 103-106 27474392-3 2016 In this study, a statistical experimental design method (Taguchi OA9) was implemented to investigate the effects of simultaneous variations of three parameters on methane production. Methane 163-170 OA9 Homo sapiens 65-68 27876764-3 2016 Here we show that cyclic sedimentation pulses related to the Indian monsoon in concert with authigenic precipitation of methane-derived aragonite gave rise to a well-laminated carbonate build-up within the oxygen minimum zone off Pakistan (northern Arabian Sea). Methane 120-127 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 257-260 27846569-1 2016 Methyl-coenzyme M reductase (MCR) is the key enzyme of methanogenesis and anaerobic methane oxidation. Methane 84-91 coenzyme-B sulfoethylthiotransferase subunit beta Methanosarcina acetivorans C2A 29-32 27717086-0 2016 Low-Temperature Transformation of Methane to Methanol on Pd1 O4 Single Sites Anchored on the Internal Surface of Microporous Silicate. Methane 34-41 programmed cell death 1 Homo sapiens 57-60 27690408-4 2016 Using a volumetric method, that is, measuring methane production over time, revealed that anaerobic digestion was stimulated by the addition of 5 mg L-1 nickel(II), and cobalt(II), and their mixture in day(s). Methane 46-53 immunoglobulin kappa variable 1-16 Homo sapiens 149-152 27590552-5 2016 In this letter, five important proteins, alpha1-antitrypsin, hemoglobin human, human serum albumin, human transferrin and r-globulin were chemically conjugated to two model drug carriers, namely carbon dots and polymer O-(2-carboxyethyl) polyethylene glycol. Methane 195-206 serpin family A member 1 Homo sapiens 41-59 27671638-5 2016 Our calculations demonstrate that anaerobic oxidation of CH4 coupled to SO42- reduction is a highly effective obstacle to CH4 accumulation in the atmosphere, possibly limiting atmospheric pCH4 to less than 10 ppm by volume for the second half of Earth history regardless of atmospheric pO2 If recent pO2 constraints from Cr isotopes are correct, we predict that reduced UV shielding by O3 should further limit pCH4 to very low levels similar to those seen today. Methane 57-60 tRNA splicing endonuclease subunit 54 Homo sapiens 188-192 27671638-5 2016 Our calculations demonstrate that anaerobic oxidation of CH4 coupled to SO42- reduction is a highly effective obstacle to CH4 accumulation in the atmosphere, possibly limiting atmospheric pCH4 to less than 10 ppm by volume for the second half of Earth history regardless of atmospheric pO2 If recent pO2 constraints from Cr isotopes are correct, we predict that reduced UV shielding by O3 should further limit pCH4 to very low levels similar to those seen today. Methane 57-60 tRNA splicing endonuclease subunit 54 Homo sapiens 410-414 27671638-5 2016 Our calculations demonstrate that anaerobic oxidation of CH4 coupled to SO42- reduction is a highly effective obstacle to CH4 accumulation in the atmosphere, possibly limiting atmospheric pCH4 to less than 10 ppm by volume for the second half of Earth history regardless of atmospheric pO2 If recent pO2 constraints from Cr isotopes are correct, we predict that reduced UV shielding by O3 should further limit pCH4 to very low levels similar to those seen today. Methane 122-125 tRNA splicing endonuclease subunit 54 Homo sapiens 188-192 27671638-5 2016 Our calculations demonstrate that anaerobic oxidation of CH4 coupled to SO42- reduction is a highly effective obstacle to CH4 accumulation in the atmosphere, possibly limiting atmospheric pCH4 to less than 10 ppm by volume for the second half of Earth history regardless of atmospheric pO2 If recent pO2 constraints from Cr isotopes are correct, we predict that reduced UV shielding by O3 should further limit pCH4 to very low levels similar to those seen today. Methane 122-125 tRNA splicing endonuclease subunit 54 Homo sapiens 410-414 32263493-2 2016 Herein, etoposide (ETO) was loaded onto oxidized carbon nanohorns (oxCNHs), which were modified by polyethylene glycol (PEG) and further functionalized with the targeting ligand P-gp monoclonal antibody (PA) in an attempt to overcome MDR. Methane 49-65 ATP binding cassette subfamily B member 1 Homo sapiens 178-182 27607732-2 2016 Herein we demonstrate for the first time the liberation of CH4 and NH3 from a well-defined iron cyanide coordination complex, [SiP(iPr) 3 ]Fe(CN) (where [SiP(iPr) 3 ] represents a tris(phosphine)silyl ligand), on exposure to proton and electron equivalents. Methane 59-62 tumor protein p53 inducible nuclear protein 1 Homo sapiens 127-137 27607732-2 2016 Herein we demonstrate for the first time the liberation of CH4 and NH3 from a well-defined iron cyanide coordination complex, [SiP(iPr) 3 ]Fe(CN) (where [SiP(iPr) 3 ] represents a tris(phosphine)silyl ligand), on exposure to proton and electron equivalents. Methane 59-62 tumor protein p53 inducible nuclear protein 1 Homo sapiens 154-164 27607732-3 2016 [SiP(iPr) 3 ]Fe(CN) additionally serves as a useful entry point to rare examples of terminally-bound Fe(CNH) and Fe(CNH2 ) species that, in accord with preliminary mechanistic studies, are plausible intermediates of the cyanide reductive protonation to generate CH4 and NH3 . Methane 262-265 tumor protein p53 inducible nuclear protein 1 Homo sapiens 1-11 27208496-8 2016 Moreover, methane treatment significantly reduced the levels of oxidative stress biomarkers (8-OHdG, 4-HNE, MDA) and increased the antioxidant enzyme activities (SOD, CAT, GPx) in the retinas with IRI. Methane 10-17 catalase Rattus norvegicus 167-170 27208496-9 2016 Meanwhile, methane treatment significantly increased the anti-apoptotic gene (Bcl-2) expression and decreased the pro-apoptotic gene (Bax) expression, accompanied by the suppression of caspase-3 and caspase-9 activity. Methane 11-18 BCL2, apoptosis regulator Rattus norvegicus 78-83 27208496-9 2016 Meanwhile, methane treatment significantly increased the anti-apoptotic gene (Bcl-2) expression and decreased the pro-apoptotic gene (Bax) expression, accompanied by the suppression of caspase-3 and caspase-9 activity. Methane 11-18 BCL2 associated X, apoptosis regulator Rattus norvegicus 134-137 27208496-9 2016 Meanwhile, methane treatment significantly increased the anti-apoptotic gene (Bcl-2) expression and decreased the pro-apoptotic gene (Bax) expression, accompanied by the suppression of caspase-3 and caspase-9 activity. Methane 11-18 caspase 3 Rattus norvegicus 185-194 27208496-9 2016 Meanwhile, methane treatment significantly increased the anti-apoptotic gene (Bcl-2) expression and decreased the pro-apoptotic gene (Bax) expression, accompanied by the suppression of caspase-3 and caspase-9 activity. Methane 11-18 caspase 9 Rattus norvegicus 199-208 27438025-2 2016 Pt(+) cations are formed by laser ablation and exposed to controlled amounts of CH4/CD4 leading to [Pt,xC,(4x-2)H/D](+) dehydrogenation products. Methane 80-83 CD4 molecule Homo sapiens 84-87 27438025-6 2016 Thus, reaction of Pt(+) with methane occurs by C-H bond activation to form PtCH2(+), which reacts with an additional methane molecule by C-H bond activation to form the platinum dimethyl cation. Methane 29-36 patched 2 Homo sapiens 75-80 27438025-6 2016 Thus, reaction of Pt(+) with methane occurs by C-H bond activation to form PtCH2(+), which reacts with an additional methane molecule by C-H bond activation to form the platinum dimethyl cation. Methane 117-124 patched 2 Homo sapiens 75-80 27236758-7 2016 Methane production [L/kg of dry matter intake (DMI)] linearly decreased with increasing nitrate concentrations compared with the control, corresponding to a reduction of 6, 13, and 23% for the low, medium, and high diets, respectively. Methane 0-7 DMI Bos taurus 47-50 27236769-0 2016 Milk metabolome relates enteric methane emission to milk synthesis and energy metabolism pathways. Methane 32-39 Weaning weight-maternal milk Bos taurus 0-4 27236769-0 2016 Milk metabolome relates enteric methane emission to milk synthesis and energy metabolism pathways. Methane 32-39 Weaning weight-maternal milk Bos taurus 52-56 27107392-9 2016 Regarding the methane production after the extraction, it yielded 257 +- 8 and 180 +- 6 mLCH4/gVS from lipid-extracted P. tricornutum using hexane and methanol/hexane respectively. Methane 14-21 immunoregulatory 2 Mus musculus 88-93 27107392-10 2016 The methane production from the raw microalga was 258 +- 5 mLCH4/gVS in the same experiment. Methane 4-11 immunoregulatory 2 Mus musculus 59-64 27405597-0 2016 Methane limit LPS-induced NF-kappaB/MAPKs signal in macrophages and suppress immune response in mice by enhancing PI3K/AKT/GSK-3beta-mediated IL-10 expression. Methane 0-7 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 Mus musculus 26-35 27409586-6 2016 For RCP 2.6, 4.5 and 8.5 scenarios, the CH4 fluxes will increase by 5.7 g m-2 yr-1, 57.5 g m-2 yr-1 and 112.2 g m-2 yr-1. Methane 40-43 CGRP receptor component Homo sapiens 4-7 27405597-0 2016 Methane limit LPS-induced NF-kappaB/MAPKs signal in macrophages and suppress immune response in mice by enhancing PI3K/AKT/GSK-3beta-mediated IL-10 expression. Methane 0-7 thymoma viral proto-oncogene 1 Mus musculus 119-122 27405597-0 2016 Methane limit LPS-induced NF-kappaB/MAPKs signal in macrophages and suppress immune response in mice by enhancing PI3K/AKT/GSK-3beta-mediated IL-10 expression. Methane 0-7 glycogen synthase kinase 3 beta Mus musculus 123-132 27405597-0 2016 Methane limit LPS-induced NF-kappaB/MAPKs signal in macrophages and suppress immune response in mice by enhancing PI3K/AKT/GSK-3beta-mediated IL-10 expression. Methane 0-7 interleukin 10 Mus musculus 142-147 27405597-4 2016 Here we show that methane-rich saline (MS) ip treatment (16 ml/kg) alleviated endotoxin shock, bacteria-induced sepsis and dextran-sulfate-sodium-induced colitis in mice via decreased production of TNF-alpha and IL-6. Methane 18-25 tumor necrosis factor Mus musculus 198-207 27405597-4 2016 Here we show that methane-rich saline (MS) ip treatment (16 ml/kg) alleviated endotoxin shock, bacteria-induced sepsis and dextran-sulfate-sodium-induced colitis in mice via decreased production of TNF-alpha and IL-6. Methane 18-25 interleukin 6 Mus musculus 212-216 27551656-8 2016 This is the first time that such fidelity has been reached in modeling methane absorption in the investigated spectral region, fulfilling the accuracy requirements of the MERLIN mission. Methane 71-78 NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor Homo sapiens 171-177 26942576-11 2016 Furthermore, this research indicated that CH4 saline markedly increased the volume of T-AOC in plasma and alleviated the peak of TNF-alpha in both plasma and gastrocnemius. Methane 42-45 tumor necrosis factor Rattus norvegicus 129-138 27551656-0 2016 Precise methane absorption measurements in the 1.64 mum spectral region for the MERLIN mission. Methane 8-15 NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor Homo sapiens 80-86 27551656-2 2016 Accurate physical models of this absorption spectrum will be required by the Franco-German, Methane Remote Sensing LIDAR (MERLIN) space mission for retrievals of atmospheric methane. Methane 174-181 NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor Homo sapiens 122-128 27551656-7 2016 Comparison of the fitted model to the measured spectra reveals the ability to calculate the room-temperature, methane absorption coefficient to better than 0.1% at the on-line position of the MERLIN mission. Methane 110-117 NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor Homo sapiens 192-198 27283125-3 2016 We report intense methane emissions from the near-shore southern region of the North Sea characterized by the presence of extensive areas with gassy sediments. Methane 18-25 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 85-88 27177360-0 2016 Growth of Horizontal Semiconducting SWNT Arrays with Density Higher than 100 tubes/mum using Ethanol/Methane Chemical Vapor Deposition. Methane 101-108 latexin Homo sapiens 83-86 27177360-3 2016 We report herein a rational approach, using ethanol/methane chemical vapor deposition, to grow SWNT arrays with a s-SWNT ratio over 91% and a density higher than 100 tubes/mum. Methane 52-59 latexin Homo sapiens 172-175 27114238-3 2016 The best yield of methane (69 %) was achieved using 0.24 mol % ruthenium catalyst (in [omim][NTf2 ], 1-octyl-3-methylimidazolium bistrifluoromethanesulfonylimide, at 40 bar of hydrogen pressure plus 40 bar of CO2 pressure, and at 150 C. Methane 18-25 nuclear transport factor 2 Homo sapiens 93-97 27025361-3 2016 It is the first time for the MOF which contains phosphorus for selective separation of methane from natural gas and pyrolysis gas. Methane 87-94 lysine acetyltransferase 8 Homo sapiens 29-32 26871557-9 2016 Oxidation of CH4 was also detected during period 2 but, contrary to sulfide production, re-establishment of methanogenesis was not immediate after stopping nitrite dosing. Methane 13-16 period circadian regulator 2 Homo sapiens 42-50 27307988-10 2016 The increase of BRF/FS ratio enhanced GP and CH4 production (+7.7 and +3.3 mL/g DM per each class of increase, respectively). Methane 45-48 BRF1 RNA polymerase III transcription initiation factor subunit Homo sapiens 16-19 27062433-1 2016 High-level electronic structure calculations, in combination with Fourier transform ion cyclotron resonance (FT-ICR) mass spectrometric studies, permit the mechanism by which closed-shell, "naked" [TaO2 ](+) brings about C-H bond activation of methane to be revealed. Methane 244-251 TAO kinase 2 Homo sapiens 198-202 26841777-10 2016 We propose that aerobic methane oxidation coupled to denitrification and perchlorate reduction (AMO-D and AMO-PR) directly oxidized methane and reduced NO3 (-) to NO2 (-) or N2O under anoxic condition, producing organic matter for methanol-assimilating denitrification and perchlorate reduction (MA-D and MA-PR) to reduce NO3 (-). Methane 24-31 NBL1, DAN family BMP antagonist Homo sapiens 152-155 26841777-10 2016 We propose that aerobic methane oxidation coupled to denitrification and perchlorate reduction (AMO-D and AMO-PR) directly oxidized methane and reduced NO3 (-) to NO2 (-) or N2O under anoxic condition, producing organic matter for methanol-assimilating denitrification and perchlorate reduction (MA-D and MA-PR) to reduce NO3 (-). Methane 24-31 NBL1, DAN family BMP antagonist Homo sapiens 322-325 26841777-10 2016 We propose that aerobic methane oxidation coupled to denitrification and perchlorate reduction (AMO-D and AMO-PR) directly oxidized methane and reduced NO3 (-) to NO2 (-) or N2O under anoxic condition, producing organic matter for methanol-assimilating denitrification and perchlorate reduction (MA-D and MA-PR) to reduce NO3 (-). Methane 132-139 NBL1, DAN family BMP antagonist Homo sapiens 322-325 26841777-11 2016 Simultaneously, bacteria capable of anaerobic methane oxidation coupled to denitrification and perchlorate reduction (ANMO-D and ANMO-PR) used methane as the electron donor to respire NO3 (-) or ClO4 (-) directly. Methane 46-53 NBL1, DAN family BMP antagonist Homo sapiens 184-187 27028716-3 2016 Especially, 1-ims shows good adsorption selectivity of C3/C1 and C2/C1, and the selectivities of C3H8/CH4 are all over 100 at room temperature. Methane 102-105 complement C3 Homo sapiens 55-70 26578374-5 2016 Anaerobic methane oxidation coupled denitrification was estimated from the (13)C-labeled CO2 ((13)CO2) production during batch incubations with (13)CH4. Methane 10-17 complement C2 Homo sapiens 89-92 26632974-3 2015 Furthermore, the fused pentagon network shows an exceptionally high selectivity for H2/gas (CO, CH4, CO2, N2, et al.) Methane 96-99 relaxin 2 Homo sapiens 84-90 26711852-11 2016 In addition, methane significantly increased the superoxide dismutase (SOD) activity, lowered the CO-increased level of malondialdehyde (MDA) 3-nitrotyrosine (3-NT) and 8-hydroxy-2-deoxyguanosine (8-OHdG), inhibited levels of tumour necrosis factor-alpha (TNF-alpha), interleukin 1-beta (IL1-beta) and caspase-3 in the rat cerebral cortex and hippocampus but had no effect on IL-6 levels. Methane 13-20 tumor necrosis factor Rattus norvegicus 256-265 26711852-11 2016 In addition, methane significantly increased the superoxide dismutase (SOD) activity, lowered the CO-increased level of malondialdehyde (MDA) 3-nitrotyrosine (3-NT) and 8-hydroxy-2-deoxyguanosine (8-OHdG), inhibited levels of tumour necrosis factor-alpha (TNF-alpha), interleukin 1-beta (IL1-beta) and caspase-3 in the rat cerebral cortex and hippocampus but had no effect on IL-6 levels. Methane 13-20 interleukin 1 beta Rattus norvegicus 268-286 26711852-11 2016 In addition, methane significantly increased the superoxide dismutase (SOD) activity, lowered the CO-increased level of malondialdehyde (MDA) 3-nitrotyrosine (3-NT) and 8-hydroxy-2-deoxyguanosine (8-OHdG), inhibited levels of tumour necrosis factor-alpha (TNF-alpha), interleukin 1-beta (IL1-beta) and caspase-3 in the rat cerebral cortex and hippocampus but had no effect on IL-6 levels. Methane 13-20 interleukin 1 beta Rattus norvegicus 288-296 26711852-11 2016 In addition, methane significantly increased the superoxide dismutase (SOD) activity, lowered the CO-increased level of malondialdehyde (MDA) 3-nitrotyrosine (3-NT) and 8-hydroxy-2-deoxyguanosine (8-OHdG), inhibited levels of tumour necrosis factor-alpha (TNF-alpha), interleukin 1-beta (IL1-beta) and caspase-3 in the rat cerebral cortex and hippocampus but had no effect on IL-6 levels. Methane 13-20 caspase 3 Rattus norvegicus 302-311 26711852-11 2016 In addition, methane significantly increased the superoxide dismutase (SOD) activity, lowered the CO-increased level of malondialdehyde (MDA) 3-nitrotyrosine (3-NT) and 8-hydroxy-2-deoxyguanosine (8-OHdG), inhibited levels of tumour necrosis factor-alpha (TNF-alpha), interleukin 1-beta (IL1-beta) and caspase-3 in the rat cerebral cortex and hippocampus but had no effect on IL-6 levels. Methane 13-20 interleukin 6 Rattus norvegicus 376-380 26827223-3 2016 We focus here on the effect that the exchange-correlation functional has on the reactivity of methane on a metal surface, using CHD3 + Pt(111) as a test case. Methane 94-101 chromodomain helicase DNA binding protein 3 Homo sapiens 128-132 26781628-5 2016 The Pd/LSM-3 catalysts with 4.2wt% Pd loading exhibited the best performance for CH4 combustion that temperature for 10% and 90% of CH4 conversion is 315 and 520 C. Methane 81-84 LSM3 homolog, U6 small nuclear RNA and mRNA degradation associated Homo sapiens 7-12 26781628-5 2016 The Pd/LSM-3 catalysts with 4.2wt% Pd loading exhibited the best performance for CH4 combustion that temperature for 10% and 90% of CH4 conversion is 315 and 520 C. Methane 132-135 LSM3 homolog, U6 small nuclear RNA and mRNA degradation associated Homo sapiens 7-12 26597312-1 2016 Pyrolysis of chitosan films containing Au(3+) renders 1.1.1 oriented Au nanoplatelets (20 nm lateral size, 3-4 nm height) on a few layers of N-doped graphene (Au/fl-G), while the lateral sides were 0.0.1 oriented. Methane 141-157 filaggrin Homo sapiens 162-166 26745623-0 2016 High Coke-Resistance Pt/Mg1-xNixO Catalyst for Dry Reforming of Methane. Methane 64-71 mucin 5B, oligomeric mucus/gel-forming Homo sapiens 24-27 26745623-2 2016 The obtained Pt/Mg1-xNixO catalyst exhibited cubic structure nanocatalyst with a size of 50-80 nm and realized CH4 and CO2 conversions as high as 98% at 900 C with excellent stability in the dry reforming of methane. Methane 111-114 mucin 5B, oligomeric mucus/gel-forming Homo sapiens 16-19 27034707-9 2016 Moreover, candidate genes MMP1, CDC45, and CAT were, respectively, enriched in pathway in cancer, cell cycle, and methane metabolism. Methane 114-121 matrix metallopeptidase 1 Homo sapiens 26-30 27034707-9 2016 Moreover, candidate genes MMP1, CDC45, and CAT were, respectively, enriched in pathway in cancer, cell cycle, and methane metabolism. Methane 114-121 cell division cycle 45 Homo sapiens 32-37 27034707-9 2016 Moreover, candidate genes MMP1, CDC45, and CAT were, respectively, enriched in pathway in cancer, cell cycle, and methane metabolism. Methane 114-121 catalase Homo sapiens 43-46 32632338-2 2016 At the power plant, natural gas is a cleaner burning fuel than coal, but uncertainties exist in the amount of methane leakage occurring upstream in the extraction and production of natural gas. Methane 110-117 gastrin Homo sapiens 189-192 32632338-3 2016 At higher leakage levels, the additional methane emissions could offset the carbon dioxide emissions reduction benefit of switching from coal to natural gas. Methane 41-48 gastrin Homo sapiens 153-156 32632338-6 2016 While the system carbon dioxide emissions are reduced in most scenarios, total carbon dioxide equivalent emissions show an increase in scenarios in which natural gas prices remain low and, simultaneously, methane emissions from natural gas production are higher. Methane 205-212 gastrin Homo sapiens 236-239 26568372-1 2015 The size-controlled growth of nanocrystalline Fe-Fe2O3 particles (2-3 nm) and their concomitant dispersion on N-doped graphene (Fe-Fe2O3/NGr) could be attained when the mutually assisted redox reaction between NGr and Fe(3+) ions could be controlled within the aqueous droplets of a water-in-oil emulsion. Methane 110-126 reticulon 4 receptor Homo sapiens 137-140 26568372-1 2015 The size-controlled growth of nanocrystalline Fe-Fe2O3 particles (2-3 nm) and their concomitant dispersion on N-doped graphene (Fe-Fe2O3/NGr) could be attained when the mutually assisted redox reaction between NGr and Fe(3+) ions could be controlled within the aqueous droplets of a water-in-oil emulsion. Methane 110-126 reticulon 4 receptor Homo sapiens 210-213 26247542-7 2015 PHB contents varied between 2.5% and 8.5% independently of CH4/O2 ratios. Methane 59-62 prohibitin 1 Homo sapiens 0-3 26721437-6 2016 Furthermore, methane treatment obviously suppressed the secretion of proinflammatory cytokines including tumor necrosis factor-alpha (TNF-alpha), interferon-gamma (IFN-gamma), interleukin-6 (IL-6) and interleukin-1beta (IL-1beta) and increased anti-inflammatory cytokine interleukin-10 (IL-10). Methane 13-20 tumor necrosis factor Mus musculus 105-132 26721437-6 2016 Furthermore, methane treatment obviously suppressed the secretion of proinflammatory cytokines including tumor necrosis factor-alpha (TNF-alpha), interferon-gamma (IFN-gamma), interleukin-6 (IL-6) and interleukin-1beta (IL-1beta) and increased anti-inflammatory cytokine interleukin-10 (IL-10). Methane 13-20 tumor necrosis factor Mus musculus 134-143 26721437-6 2016 Furthermore, methane treatment obviously suppressed the secretion of proinflammatory cytokines including tumor necrosis factor-alpha (TNF-alpha), interferon-gamma (IFN-gamma), interleukin-6 (IL-6) and interleukin-1beta (IL-1beta) and increased anti-inflammatory cytokine interleukin-10 (IL-10). Methane 13-20 interferon gamma Mus musculus 146-162 26721437-6 2016 Furthermore, methane treatment obviously suppressed the secretion of proinflammatory cytokines including tumor necrosis factor-alpha (TNF-alpha), interferon-gamma (IFN-gamma), interleukin-6 (IL-6) and interleukin-1beta (IL-1beta) and increased anti-inflammatory cytokine interleukin-10 (IL-10). Methane 13-20 interferon gamma Mus musculus 164-173 26721437-6 2016 Furthermore, methane treatment obviously suppressed the secretion of proinflammatory cytokines including tumor necrosis factor-alpha (TNF-alpha), interferon-gamma (IFN-gamma), interleukin-6 (IL-6) and interleukin-1beta (IL-1beta) and increased anti-inflammatory cytokine interleukin-10 (IL-10). Methane 13-20 interleukin 6 Mus musculus 176-189 26721437-6 2016 Furthermore, methane treatment obviously suppressed the secretion of proinflammatory cytokines including tumor necrosis factor-alpha (TNF-alpha), interferon-gamma (IFN-gamma), interleukin-6 (IL-6) and interleukin-1beta (IL-1beta) and increased anti-inflammatory cytokine interleukin-10 (IL-10). Methane 13-20 interleukin 6 Mus musculus 191-195 26721437-6 2016 Furthermore, methane treatment obviously suppressed the secretion of proinflammatory cytokines including tumor necrosis factor-alpha (TNF-alpha), interferon-gamma (IFN-gamma), interleukin-6 (IL-6) and interleukin-1beta (IL-1beta) and increased anti-inflammatory cytokine interleukin-10 (IL-10). Methane 13-20 interleukin 1 beta Mus musculus 201-218 26721437-6 2016 Furthermore, methane treatment obviously suppressed the secretion of proinflammatory cytokines including tumor necrosis factor-alpha (TNF-alpha), interferon-gamma (IFN-gamma), interleukin-6 (IL-6) and interleukin-1beta (IL-1beta) and increased anti-inflammatory cytokine interleukin-10 (IL-10). Methane 13-20 interleukin 1 beta Mus musculus 220-228 26721437-6 2016 Furthermore, methane treatment obviously suppressed the secretion of proinflammatory cytokines including tumor necrosis factor-alpha (TNF-alpha), interferon-gamma (IFN-gamma), interleukin-6 (IL-6) and interleukin-1beta (IL-1beta) and increased anti-inflammatory cytokine interleukin-10 (IL-10). Methane 13-20 interleukin 10 Mus musculus 271-285 26721437-6 2016 Furthermore, methane treatment obviously suppressed the secretion of proinflammatory cytokines including tumor necrosis factor-alpha (TNF-alpha), interferon-gamma (IFN-gamma), interleukin-6 (IL-6) and interleukin-1beta (IL-1beta) and increased anti-inflammatory cytokine interleukin-10 (IL-10). Methane 13-20 interleukin 10 Mus musculus 287-292 26553610-0 2015 Methane excess in Arctic surface water-triggered by sea ice formation and melting. Methane 0-7 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 52-55 26143035-4 2015 The kinetic analysis revealed that the methane-oxidizing consortium showed a maximum methane oxidation rate (Vmax) of 3.7 mmol g-dry cell weight (DCW)(-1) h(-1) and a saturation constant (Km) of 184.1 muM. Methane 39-46 latexin Homo sapiens 201-204 26143035-4 2015 The kinetic analysis revealed that the methane-oxidizing consortium showed a maximum methane oxidation rate (Vmax) of 3.7 mmol g-dry cell weight (DCW)(-1) h(-1) and a saturation constant (Km) of 184.1 muM. Methane 85-92 latexin Homo sapiens 201-204 26143035-5 2015 MT and H2S show competitive inhibition on methane oxidation, with inhibition values (Ki) of 1504.8 and 359.8 muM, respectively. Methane 42-49 latexin Homo sapiens 109-112 26553610-2 2015 Indeed, recently observed enhanced atmospheric methane concentrations in Arctic regions with fractional sea-ice cover point to unexpected feedbacks in cycling of methane. Methane 47-54 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 104-107 26553610-2 2015 Indeed, recently observed enhanced atmospheric methane concentrations in Arctic regions with fractional sea-ice cover point to unexpected feedbacks in cycling of methane. Methane 162-169 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 104-107 26553610-3 2015 We report on methane excess in sea ice-influenced water masses in the interior Arctic Ocean and provide evidence that sea ice is a potential source. Methane 13-20 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 31-34 26553610-4 2015 We show that methane release from sea ice into the ocean occurs via brine drainage during freezing and melting i.e. in winter and spring. Methane 13-20 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 34-37 26009821-10 2015 Moreover, methane-rich saline reduced the amount of caspase-3 and the number of apoptotic cells. Methane 10-17 caspase 3 Rattus norvegicus 52-61 26688965-5 2015 Maximum biogas production rate was 383 l kg(-1) COD removed with 260 l of methane gas. Methane 74-81 small nuclear ribonucleoprotein polypeptides B and B1 Homo sapiens 48-51 26374390-2 2015 High pressure solution NMR, isotopic labeling studies, and kinetic analyses of the degenerate exchange of methane in the methyl complex [Tp(Me2)NbCH3(c-C3H5)(MeCCMe)] (1) are reported. Methane 106-113 malic enzyme 2 Homo sapiens 140-143 26374390-3 2015 Stoichiometric methane activation by the mesitylene complex [Tp(Me2)Nb(CH2-3,5-C6H3Me2)(c-C3H5) (MeCCMe)] (2) giving 1 is also realized. Methane 15-22 malic enzyme 2 Homo sapiens 64-67 26374390-4 2015 Evidence is provided that these reactions proceed via an intramolecular abstraction of a beta-H of the cyclopropyl group to form either methane or mesitylene from 1 or 2, respectively, yielding the transient unsaturated eta(2)-cyclopropene/metallabicyclobutane intermediate [Tp(Me2)Nb(eta(2)-c-C3H4) (MeCCMe)] A. Methane 136-143 malic enzyme 2 Homo sapiens 278-281 26258871-3 2015 At 298 K and 1 bar, a very high selectivity for separating CO2/N2 (41.7) and CO2/CH4 (6.8) gas mixture pairs was obtained on the O-doped carbon activated with KOH at 600 C. The excellent separation ability of the O-doped carbons was demonstrated in transient breakthrough simulations of CO2/CH4/N2 mixtures in a fixed bed adsorber. Methane 292-295 complement C2 Homo sapiens 59-65 26374005-6 2015 It is found that MP2 values for the methane binding energies and the cohesive energies of the water clusters without methane are in close agreement with the QMC benchmarks, but the agreement is aided by partial cancelation between 2-body and beyond-2-body errors of MP2. Methane 36-43 tryptase pseudogene 1 Homo sapiens 17-20 26374005-6 2015 It is found that MP2 values for the methane binding energies and the cohesive energies of the water clusters without methane are in close agreement with the QMC benchmarks, but the agreement is aided by partial cancelation between 2-body and beyond-2-body errors of MP2. Methane 117-124 tryptase pseudogene 1 Homo sapiens 17-20 26374005-7 2015 The embedding approach allows MP2 to be applied without loss of accuracy to the methane hydrate crystal, and it is shown that the resulting methane binding energy and the cohesive energy of the water lattice agree almost exactly with recently reported QMC values. Methane 140-147 tryptase pseudogene 1 Homo sapiens 30-33 26156457-2 2015 Here, we present potential mechanisms for the interconversions between sI and sH and sII and sH, as observed within molecular simulations of the cross-nucleation of different methane hydrate phases. Methane 175-182 transcription elongation factor A1 Homo sapiens 85-88 25815696-7 2015 In the case of methane, the CF2 radical promotes the formation of H via CF2 + CH3 CH2:CF2 + H, which then promotes the branching reaction H + O2 OH + O. Methane 15-22 ATPase H+ transporting accessory protein 1 Homo sapiens 28-31 25815696-7 2015 In the case of methane, the CF2 radical promotes the formation of H via CF2 + CH3 CH2:CF2 + H, which then promotes the branching reaction H + O2 OH + O. Methane 15-22 ATPase H+ transporting accessory protein 1 Homo sapiens 72-75 25815696-7 2015 In the case of methane, the CF2 radical promotes the formation of H via CF2 + CH3 CH2:CF2 + H, which then promotes the branching reaction H + O2 OH + O. Methane 15-22 ATPase H+ transporting accessory protein 1 Homo sapiens 72-75 26200336-10 2015 Three-year field trials in China demonstrated that the cultivation of SUSIBA2 rice was associated with a significant reduction in methane emissions and a decrease in rhizospheric methanogen levels. Methane 130-137 Sugar signaling in barley 2 Hordeum vulgare 70-77 26200336-12 2015 Approaches to increase rice productivity and reduce methane emissions as seen in SUSIBA2 rice may be particularly beneficial in a future climate with rising temperatures resulting in increased methane emissions from paddies. Methane 52-59 Sugar signaling in barley 2 Hordeum vulgare 81-88 26200336-12 2015 Approaches to increase rice productivity and reduce methane emissions as seen in SUSIBA2 rice may be particularly beneficial in a future climate with rising temperatures resulting in increased methane emissions from paddies. Methane 193-200 Sugar signaling in barley 2 Hordeum vulgare 81-88 26086090-2 2015 Reactions were carried out in a tubular flow reactor under pressures up to 42 bar at 830-910 C. Using a CH4 to steam to CO2 ratio of ~3:2:1 in the gas feed, the H2/CO ratio of 2:1 was achieved, which is desired for subsequent methanol synthesis. Methane 105-108 relaxin 2 Homo sapiens 162-180 26364485-0 2015 The effect of organic loading rate on VFA/COD ratio for methane production from an EGSB reactor. Methane 56-63 small nuclear ribonucleoprotein polypeptides B and B1 Homo sapiens 42-45 25819762-2 2015 The surface of the produced carbon foam had a well-developed open cell structure and the specific surface area according to the BET model was 458.59m(2)g(-1). Methane 28-39 delta/notch like EGF repeat containing Homo sapiens 128-131 26013160-4 2015 Significantly, the transmetalation of Co(II) or Ni(II) on the Zn(II) centers in 446-MOF can enhance the sorption capacities of CO2 and CH4 (16-21%), whereas the impregnation of Eu(III) and Tb(III) in the channels of 446-MOF will result in adjustable light-emitting behaviors. Methane 135-138 mitochondrially encoded cytochrome c oxidase II Homo sapiens 38-44 25500510-2 2015 The products of microbial utilization of methane and other hydrocarbons fuel rich chemosynthetic communities at these sites, with much higher respiration rates compared with the surrounding deep-sea floor. Methane 41-48 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 195-198 25959840-2 2015 This activated MOF exhibits high heat of absorption of CO2 and highly selective adsorption of CO2 over CH4. Methane 103-106 lysine acetyltransferase 8 Homo sapiens 15-18 24020504-3 2015 This review summarizes the current state of the art of bioprocess development for biological CH4 production (BMP) from pure cultures with pure gasses. Methane 93-96 bone morphogenetic protein 1 Homo sapiens 109-112 26601391-3 2015 We can retrieve the methane and carbon dioxide gas using thermal infrared satellite data AIRS, but it is rarely for the nitrous oxide retrieval. Methane 20-27 phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase Homo sapiens 89-93 32262068-1 2015 High-intensity fluorescent carbon dots (CDs) coupled with tyrosinase (TYR) yielded hybrids, as a fluorescent probe, which were efficient, fast, stable and sensitive in the detection of levodopa (l-DOPA). Methane 27-38 tyrosinase Homo sapiens 70-73 25976482-1 2015 UNLABELLED: Methane (CH4) generated from low-organic waste degradation at four Danish landfills was estimated by three first-order decay (FOD) landfill gas (LFG) generation models (LandGEM, IPCC, and Afvalzorg). Methane 12-19 GTP binding protein overexpressed in skeletal muscle Homo sapiens 181-188 25976482-1 2015 UNLABELLED: Methane (CH4) generated from low-organic waste degradation at four Danish landfills was estimated by three first-order decay (FOD) landfill gas (LFG) generation models (LandGEM, IPCC, and Afvalzorg). Methane 21-24 GTP binding protein overexpressed in skeletal muscle Homo sapiens 181-188 26016919-10 2015 By CCl4 extraction, methane at a concentration below 1.14 mmol/L has been detected by conventional Raman spectroscopy. Methane 20-27 C-C motif chemokine ligand 4 Homo sapiens 3-7 25773379-5 2015 Moreover, (13) C-depleted hopanoids diplopterol and 3beta-methylated C32 17beta(H),21beta(H)-hopanoic acid (both -40%) are preserved in lagoon sediments and are most likely derived from aerobic methanotrophic bacteria thriving in the methane-enriched water column. Methane 234-241 chemokine like factor Homo sapiens 69-72 25851127-8 2015 Noticeably, pek-MOF-1 showed excellent volumetric CO2 and CH4 uptakes at high pressures. Methane 58-61 eukaryotic translation initiation factor 2 alpha kinase 3 Homo sapiens 12-15 25825923-4 2015 The subsequent RE-1,4-NDC-fcu-MOF structural features, contracted windows/pores and high concentration of open metal sites combined with exceptional hydrothermal and chemical stabilities, yielded notable gas/solvent separation properties, driven mostly by adsorption kinetics as exemplified in this work for n-butane/methane, butanol/methanol, and butanol/water pair systems. Methane 317-324 lysine acetyltransferase 8 Homo sapiens 30-33 25768128-1 2015 The reaction of atomic thorium cations with CH4 (CD4) and the collision-induced dissociation (CID) of ThCH4(+) with Xe are studied using guided ion beam tandem mass spectrometry. Methane 44-47 CD4 molecule Homo sapiens 49-52 25983723-8 2015 Our data suggest that the interplay among JS1 bacteria, methanogenic archaea and Methanohalobium/ANME-3-related archaea may be important for iron reduction and methane cycling in deep methanic sediments of the Helgoland mud area and perhaps in other methane-rich depositional environments. Methane 160-167 carboxymethylenebutenolidase homolog Homo sapiens 42-45 25983723-8 2015 Our data suggest that the interplay among JS1 bacteria, methanogenic archaea and Methanohalobium/ANME-3-related archaea may be important for iron reduction and methane cycling in deep methanic sediments of the Helgoland mud area and perhaps in other methane-rich depositional environments. Methane 250-257 carboxymethylenebutenolidase homolog Homo sapiens 42-45 25503851-0 2015 Methane-rich water induces cucumber adventitious rooting through heme oxygenase1/carbon monoxide and Ca(2+) pathways. Methane 0-7 heme oxygenase 1, chloroplastic Cucumis sativus 65-80 25653109-1 2015 A doubly interpenetrated MOF was constructed using a new pyridyl carboxylate ligand with active pyridyl sites, which exhibits highly efficient luminescence sensing for Cu(2+) ions and sorption selectivities of CO2 over CH4 and N2. Methane 219-222 lysine acetyltransferase 8 Homo sapiens 25-28 25266683-2 2015 When normalizing the methane production to the daily feedstock characteristics, significantly greater methane was produced during two-phase mesophilic digestion compared to the single-stage operation (methane yield of 380 vs 446-L CH4 kg VS(-1); 359 vs 481-L CH4 kg COD(-1) removed for single vs two stage operation). Methane 102-109 component of oligomeric golgi complex 4 Homo sapiens 266-272 27682076-3 2015 C-1 compounds such as methane and methanol are important intermediates in the deep subsurface carbon cycle, and electron acceptors such as sulphate are critical components of oxidation processes. Methane 22-29 heterogeneous nuclear ribonucleoprotein C Homo sapiens 0-3 27682076-6 2015 Our results show that deep subsurface microbes exist in dormant states but rapidly reactivate their transcription and respiration systems in the presence of C-1 substrates, particularly methane. Methane 186-193 heterogeneous nuclear ribonucleoprotein C Homo sapiens 157-160 25266683-2 2015 When normalizing the methane production to the daily feedstock characteristics, significantly greater methane was produced during two-phase mesophilic digestion compared to the single-stage operation (methane yield of 380 vs 446-L CH4 kg VS(-1); 359 vs 481-L CH4 kg COD(-1) removed for single vs two stage operation). Methane 102-109 component of oligomeric golgi complex 4 Homo sapiens 266-272 25488307-4 2015 Most wells without plunger lifts unload less than 10 times per year with emissions averaging 21,000-35,000 scf methane (0.4-0.7 Mg) per event (95% confidence limits of 10,000-50,000 scf/event). Methane 111-118 KIT ligand Homo sapiens 107-110 25329687-3 2014 This photocatalytic behavior is completely different from that measured for Au/P25 (hydrogen evolution) and Cu/P25 (lower activity, but similar methane selectivity). Methane 144-151 tubulin polymerization promoting protein Homo sapiens 76-82 26177405-3 2015 The results show that the doses used produce a statistically significant increase of accumulated methane, giving values greater than 225 mL of CH4 per gram of volatile solids (VS) added, and 135% greater than that obtained in the control assay. Methane 97-104 COP9 signalosome subunit 4 Drosophila melanogaster 143-146 25336448-3 2014 Commercially available GaN powders with a wurtzite crystal structure showed superior stability and reactivity for converting light alkanes, including methane, propane, n-butane, n-hexane and cyclohexane into benzene at an elevated temperature with high selectivity. Methane 150-157 gigaxonin Homo sapiens 23-26 25423097-0 2014 Multifunctional anionic MOF material for dye enrichment and selective sorption of C2 hydrocarbons over methane via Ag(+)-exchange. Methane 103-110 lysine acetyltransferase 8 Homo sapiens 24-27 25462758-1 2015 Nitrate (NO3-) is commonly dosed in sewer systems to reduce sulfide (H2S) and methane (CH4) produced in anaerobic rising main pipes. Methane 78-85 NBL1, DAN family BMP antagonist Homo sapiens 9-12 25462758-1 2015 Nitrate (NO3-) is commonly dosed in sewer systems to reduce sulfide (H2S) and methane (CH4) produced in anaerobic rising main pipes. Methane 87-90 NBL1, DAN family BMP antagonist Homo sapiens 9-12 25039851-0 2014 Anaerobic oxidation of methane by sulfate in hypersaline groundwater of the Dead Sea aquifer. Methane 23-30 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 81-84 25039851-1 2014 Geochemical and microbial evidence points to anaerobic oxidation of methane (AOM) likely coupled with bacterial sulfate reduction in the hypersaline groundwater of the Dead Sea (DS) alluvial aquifer. Methane 68-75 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 173-176 25316343-2 2014 The computational screening of reactions for different hydrocarbons (CH4, C2H6, C3H8, C2H4, and C2H2) as readily available carbon precursors for HCN formation, potential chemical transport agents, and for controlled carbon doping of deposited GaN was carried out with the B3LYP method in conjunction with basis sets up to aug-cc-pVTZ. Methane 69-72 metastasis associated lung adenocarcinoma transcript 1 Homo sapiens 145-148 25044684-0 2014 Photothermal conversion of CO2 into CH4 with H2 over Group VIII nanocatalysts: an alternative approach for solar fuel production. Methane 36-39 cytochrome c oxidase subunit 8A Homo sapiens 59-63 25093213-3 2014 At a platinum electrode in bis(trifluoromethylsulfonyl)imide (NTf2)-based ILs, methane is electro-oxidized to produce CO2 and water when an oxygen reduction process is included. Methane 79-86 nuclear transport factor 2 Homo sapiens 62-66 25209573-5 2014 The M-ICOS method allowed for the determination of dissolved methane and carbon dioxide concentrations with a frequency of 1 Hz and with a method detection limit of 2.76 x 10(-10) mol L(-1) for methane and 1.5 x 10(-7) mol L(-1) for carbon dioxide. Methane 61-68 inducible T cell costimulator Homo sapiens 6-10 25111796-8 2014 The Au-H bond is relatively weak but, for interactions via an H atom that is bonded to a carbon atom (e.g., CH4), we find that there is large charge polarization of the Au-H-C moiety and partial activation of the inert C-H bond. Methane 108-111 AU RNA binding methylglutaconyl-CoA hydratase Homo sapiens 4-8 25111796-8 2014 The Au-H bond is relatively weak but, for interactions via an H atom that is bonded to a carbon atom (e.g., CH4), we find that there is large charge polarization of the Au-H-C moiety and partial activation of the inert C-H bond. Methane 108-111 AU RNA binding methylglutaconyl-CoA hydratase Homo sapiens 169-173 25209573-5 2014 The M-ICOS method allowed for the determination of dissolved methane and carbon dioxide concentrations with a frequency of 1 Hz and with a method detection limit of 2.76 x 10(-10) mol L(-1) for methane and 1.5 x 10(-7) mol L(-1) for carbon dioxide. Methane 194-201 inducible T cell costimulator Homo sapiens 6-10 24588097-0 2014 Temperature-dependent kinetics of charge transfer, hydrogen-atom transfer, and hydrogen-atom expulsion in the reaction of CO+ with CH4 and CD4. Methane 131-134 CD4 molecule Homo sapiens 139-142 24630651-7 2014 Feeding 3-nitrooxypropanol did not affect DMI; however, methane production was reduced from 17.8 to 7.18 g/kg of DMI. Methane 56-63 DMI Bos taurus 113-116 24685512-1 2014 Methane emission from landfill gas emission (LandGEM) model was validated through the results of laboratory scale biochemical methane potential assay. Methane 0-7 GTP binding protein overexpressed in skeletal muscle Homo sapiens 45-52 24685512-3 2014 Based on these findings, correction factors were developed to estimate CH4 emission using LandGEM model especially where the level of segregation is negligible or does not exist. Methane 71-74 GTP binding protein overexpressed in skeletal muscle Homo sapiens 90-97 25068305-4 2014 The aim of this paper was to evaluate the correlation of small intestinal bacterial overgrowth and gastrointestinal methane production with metabolic control and daily insulin requirements in patients with type 1 diabetes and. Methane 116-123 insulin Homo sapiens 168-175 25068977-7 2014 A hybrid membrane with 5 wt % SBMA@CNT exhibits the maximum CO2 permeability of 103 Barrer with a CO2/CH4 selectivity of 36. Methane 102-105 androgen receptor Homo sapiens 30-34 24531883-1 2014 The binding within the ethene-argon and formaldehyde-methane complexes in the ground and electronically excited states is studied with equation of motion coupled cluster theory (EOM-CCSD), second-order Moller-Plesset perturbation theory (MP2) and density functional theory with dispersion corrections (DFT-D). Methane 53-60 tryptase pseudogene 1 Homo sapiens 238-241 24755395-5 2014 For methane production, 11.77 or ~6m(3)STP/m(3)d of rate and 66-85% of content were observed with SPM or SCF, respectively. Methane 4-11 KIT ligand Homo sapiens 105-108 24450397-2 2014 However, soils can also represent a significant sink for methane through the activity of methane-oxidizing bacteria (MOB). Methane 57-64 sphingomyelin synthase 1 Homo sapiens 89-121 24450397-5 2014 The pmoA gene sequences related to two genotypes of uncultured MOB involved in atmospheric methane oxidation, the "upland soil cluster gamma" and the "upland soil cluster alpha", were detected in soils with near neutral and acidic pH, respectively. Methane 91-98 sphingomyelin synthase 1 Homo sapiens 63-66 24450397-7 2014 Overall, the results reported here showed that methane oxidation at both low and high methane concentrations occurs in high Arctic soils and revealed that different groups of atmospheric MOB inhabit these soils. Methane 47-54 sphingomyelin synthase 1 Homo sapiens 187-190 24739053-1 2014 The interaction energy of a methane molecule encapsulated in a dodecahedral water cage is calculated using the MP2, MP2C, various dispersion-corrected DFT, and diffusion Monte Carlo (DMC) methods. Methane 28-35 tryptase pseudogene 1 Homo sapiens 111-114 24895840-7 2014 10 mL STP (i.e., 0.42 mmol) pure methane samples. Methane 33-40 sulfotransferase family 1A member 1 Homo sapiens 6-9 24827914-5 2014 The corresponding CH4 uptake was measured as 165 V(STP)/V (20 bar, 293 K) and 189 V(STP/V) (35 bar, 293 K) with a maximum CH4 uptake for NOTT-220a recorded at 20 bar and 195 K to be 287 V(STP)/V, while H2 uptake of NOTT-220a at 20 bar, 77 K is 42 g L(-1). Methane 18-21 sulfotransferase family 1A member 1 Homo sapiens 51-54 24826797-0 2014 Photoinduced conversion of methane into benzene over GaN nanowires. Methane 27-34 gigaxonin Homo sapiens 53-56 24826797-3 2014 Herein we demonstrate that Si-doped GaN nanowires (NWs) with a 97% rationally constructed m-plane can directly convert methane into benzene and molecular hydrogen under ultraviolet (UV) illumination at rt. Methane 119-126 gigaxonin Homo sapiens 36-39 24749673-0 2014 Theoretical kinetics study of the O(3P) + CH4/CD4 hydrogen abstraction reaction: the role of anharmonicity, recrossing effects, and quantum mechanical tunneling. Methane 42-45 CD4 molecule Homo sapiens 46-49 25055702-4 2014 The methanogens can use compounds such as acetic acid, hydrogen and CO2 athylamine as substrates for methane production. Methane 101-108 complement C2 Homo sapiens 68-71 24611507-6 2014 The porous MOM with the smallest PLD suitable for physisorption, dia-7i-1-Co, was thereby found to exhibit the highest Qst values for CO2 and CH4. Methane 142-145 glycosylphosphatidylinositol specific phospholipase D1 Homo sapiens 33-36 24602676-0 2014 Enhanced methane emissions from oil and gas exploration areas to the atmosphere--the central Bohai Sea. Methane 9-16 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 99-102 24602676-3 2014 The central Bohai Sea was thus a source of atmospheric methane during the survey periods. Methane 55-62 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 18-21 24602676-5 2014 This study demonstrated a method to detect seafloor CH4 leakages at the sea surface, which may have applicability in many shallow sea areas with oil and gas exploration activities around the world. Methane 52-55 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 43-46 24602676-5 2014 This study demonstrated a method to detect seafloor CH4 leakages at the sea surface, which may have applicability in many shallow sea areas with oil and gas exploration activities around the world. Methane 52-55 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 72-75 24661065-2 2014 Here we report the synthesis, crystal structure and methane adsorption properties of two new aluminum metal-organic frameworks, MOF-519 and MOF-520. Methane 52-59 lysine acetyltransferase 8 Homo sapiens 128-131 24661065-2 2014 Here we report the synthesis, crystal structure and methane adsorption properties of two new aluminum metal-organic frameworks, MOF-519 and MOF-520. Methane 52-59 lysine acetyltransferase 8 Homo sapiens 140-143 24661065-4 2014 Furthermore, MOF-519 exhibits an exceptional working capacity, being able to deliver a large amount of methane at pressures between 5 and 35 bar, 151 cm(3) cm(-3), and between 5 and 80 bar, 230 cm(3) cm(-3). Methane 103-110 lysine acetyltransferase 8 Homo sapiens 13-16 24568117-1 2014 The temperature dependences of the rate constants and product branching ratios for the reactions of FeO(+) with CH4 and CD4 have been measured from 123 to 700 K. The 300 K rate constants are 9.5 x 10(-11) and 5.1 x 10(-11) cm(3) s(-1) for the CH4 and CD4 reactions, respectively. Methane 112-115 CD4 molecule Homo sapiens 251-254 24568117-1 2014 The temperature dependences of the rate constants and product branching ratios for the reactions of FeO(+) with CH4 and CD4 have been measured from 123 to 700 K. The 300 K rate constants are 9.5 x 10(-11) and 5.1 x 10(-11) cm(3) s(-1) for the CH4 and CD4 reactions, respectively. Methane 243-246 CD4 molecule Homo sapiens 120-123 24164560-9 2014 The abundance and distribution of anammox bacterial gene markers indicate a potentially significant contribution of anammox bacteria to the marine N cycle in the deep-sea methane seep sediments. Methane 171-178 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 167-170 24827914-5 2014 The corresponding CH4 uptake was measured as 165 V(STP)/V (20 bar, 293 K) and 189 V(STP/V) (35 bar, 293 K) with a maximum CH4 uptake for NOTT-220a recorded at 20 bar and 195 K to be 287 V(STP)/V, while H2 uptake of NOTT-220a at 20 bar, 77 K is 42 g L(-1). Methane 18-21 sulfotransferase family 1A member 1 Homo sapiens 84-87 24827914-5 2014 The corresponding CH4 uptake was measured as 165 V(STP)/V (20 bar, 293 K) and 189 V(STP/V) (35 bar, 293 K) with a maximum CH4 uptake for NOTT-220a recorded at 20 bar and 195 K to be 287 V(STP)/V, while H2 uptake of NOTT-220a at 20 bar, 77 K is 42 g L(-1). Methane 18-21 sulfotransferase family 1A member 1 Homo sapiens 84-87 26269970-5 2014 The comparison suggests the use of the sudden approximation for treating the rotations even though CHD3 has large rotational constants and yields an estimated reaction barrier of 0.9 eV for CH4 + Pt(111). Methane 190-193 chromodomain helicase DNA binding protein 3 Homo sapiens 99-103 24619231-4 2014 With two exemplary cores we demonstrate that the dissolution of particulate Fe and Mn is coupled to the anaerobic oxidation of CH4 (AOM) either via the reduction of sulphate (SO4(2-)) and the subsequent generation of Fe(II) by S(-II) oxidation, or directly coupled to Fe reduction. Methane 127-130 transcription elongation factor A1 Homo sapiens 227-232 24651211-3 2014 Here, we report an in-situ low-temperature scanning tunneling microscopy (LT-STM) study of the elementary process of chemical vapor deposition (CVD) graphene growth via thermal decomposition of methane on Cu(110), including the formation of monodispersed carbon clusters at the initial stage, the graphene nucleation and the ripening of graphene islands to form continuous graphene film. Methane 194-201 sulfotransferase family 1A member 3 Homo sapiens 77-80 23820823-0 2014 Batch anaerobic co-digestion of cow manure and waste milk in two-stage process for hydrogen and methane productions. Methane 96-103 Weaning weight-maternal milk Bos taurus 53-57 24196659-4 2014 The two amine-modified MIL-101Cr-NH2 (4) and MIL-101Cr-pNH2 (5) showed the highest gas uptake capacities in the series with high ratios for the CO2 : N2 and CO2 : CH4 selectivities (up to 119 : 1 and 75 : 1, respectively, at 273 K). Methane 163-166 phosphatidylinositol glycan anchor biosynthesis class T Homo sapiens 55-59 25669355-3 2014 The method can reproduce the corrections to the MP2/cc-pVTZ energies of H2O, CH4, and C6H6 within a few mEh after several million MC steps. Methane 77-80 tryptase pseudogene 1 Homo sapiens 48-51 25156936-8 2014 Compared with Group High RFI, the CH4 emission of Group Low RFI was significantly lower (on the basis g/d and g/kg DMI by 11% and 19%, respectively). Methane 34-37 RFI Bos taurus 60-63 25156936-9 2014 Furthermore, the CH4 emission [g/d] was significantly correlated with RFI (r = 0.77). Methane 17-20 RFI Bos taurus 70-73 24649710-2 2014 A full-scale experiment was carried out to monitor the CH4 emission from anoxic/anaerobic/oxic process (A20) and sequencing batch reactor (SBR) wastewater treatment plants (WWTPs) for one year from May 2011 to April 2012. Methane 55-58 immunoglobulin kappa variable 1-27 Homo sapiens 104-107 24140486-6 2013 Several researchers have shown that specific methane yield (SMY) of anaerobic digestion of sludges from brackish/marine RAS is relatively low, mainly in the range of 0.001-0.184 m(3) CH4 (STP)/kg COD of sludge added. Methane 45-52 thyroid hormone receptor interactor 10 Homo sapiens 188-191 23947756-0 2013 Theoretical views on activation of methane catalyzed by Hf2+ and oxidation of CO (x(1)Sigma(+)) by N2O (x(1)Sigma(+)) Catalyzed by HfO2+ and TaO2+. Methane 35-42 TAO kinase 2 Homo sapiens 141-145 24283018-0 2013 What if we could tap vast deposits of methane-rich brine deep beneath the ocean and use the energy to cut carbon emissions? Methane 38-45 nuclear RNA export factor 1 Homo sapiens 17-20 23422220-6 2013 For terpenoids, the presence of 0.5% of car-3-ene, myrcene, and alpha-pinene reduced 95%, 75%, and 77% of methane production, respectively. Methane 106-113 carbonic anhydrase 3 Homo sapiens 40-45 24161402-3 2013 Here we discuss opportunities to use 1-aminocyclopropane-1-carboxylate deaminase to manage methane oxidation by regulating plant stress responses. Methane 91-98 unconventional SNARE in the ER 1 Homo sapiens 33-38 23746056-3 2013 Here, we link the anaerobic oxidation of methane (AOM) to the nitrogen cycle in microbial mats of the Black Sea by using stable isotope probing. Methane 41-48 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 108-111 23978308-5 2013 Methane activation by LiNH( ) and MgNH proceeds via hydrogen atom abstraction (HAA) and [2 + 2] transition states; only HAA pathways are isolated for NaNH and BeNH. Methane 0-7 neuraminidase 1 Homo sapiens 150-154 24027984-0 2013 [Distribution and air-sea fluxes of methane in the Yellow Sea and the East China Sea in the spring]. Methane 36-43 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 22-25 23812350-6 2013 From the collision energy dependence of the abstraction/insertion ratio, the barrier height for the abstraction pathway is estimated to be 0.7 +- 0.3 and 0.8 +- 0.1 kcal mol(-1) for O((1)D2) with CH4 and CD4, respectively. Methane 196-199 CD4 molecule Homo sapiens 204-207 23812350-7 2013 The insertion pathway of the O((1)D2) reaction with CH4 has a narrower angular width in the forward scattering and a larger insertion/abstraction ratio than the reaction with CD4, which indicates that the insertion reaction with CH4 has a larger cross section and a shorter reaction time than the reaction with CD4. Methane 52-55 CD4 molecule Homo sapiens 175-178 23812350-7 2013 The insertion pathway of the O((1)D2) reaction with CH4 has a narrower angular width in the forward scattering and a larger insertion/abstraction ratio than the reaction with CD4, which indicates that the insertion reaction with CH4 has a larger cross section and a shorter reaction time than the reaction with CD4. Methane 52-55 CD4 molecule Homo sapiens 311-314 23812350-7 2013 The insertion pathway of the O((1)D2) reaction with CH4 has a narrower angular width in the forward scattering and a larger insertion/abstraction ratio than the reaction with CD4, which indicates that the insertion reaction with CH4 has a larger cross section and a shorter reaction time than the reaction with CD4. Methane 229-232 CD4 molecule Homo sapiens 175-178 23812350-7 2013 The insertion pathway of the O((1)D2) reaction with CH4 has a narrower angular width in the forward scattering and a larger insertion/abstraction ratio than the reaction with CD4, which indicates that the insertion reaction with CH4 has a larger cross section and a shorter reaction time than the reaction with CD4. Methane 229-232 CD4 molecule Homo sapiens 311-314 23822884-3 2013 Microbial anaerobic oxidation of CH4 (AOM) is an important CH4 sink in marine sediments, but AOM has only recently been identified in a few nonmarine systems. Methane 33-36 collagen type II alpha 1 chain Homo sapiens 38-41 23822884-9 2013 Globally, we estimate that AOM could consume a large proportion of CH4 produced annually (1.6-49 Tg) and thereby constrain emissions and greenhouse gas forcing. Methane 67-70 collagen type II alpha 1 chain Homo sapiens 27-30 23811518-3 2013 In the present study, we cultivated iron-oxidizing bacteria (FeOB) and performed clone library analyses of functional genes related to carbon fixation and methane oxidization (cbbM and pmoA, respectively), in addition to bacterial and archaeal 16S rRNA genes, in freshwater iron-rich flocs at groundwater discharge points. Methane 155-162 opsin 1, medium wave sensitive Homo sapiens 176-180 23805867-15 2013 Methane adsorption isotherms for activated FMOF-1 attained volumetric adsorption capacities ranging from 67 V(STP)/V at 288 K and 31 bar to 133 V(STP)/V at 173 K and 5 bar, with an isosteric heat of adsorption of ca. Methane 0-7 sulfotransferase family 1A member 1 Homo sapiens 110-113 23805867-15 2013 Methane adsorption isotherms for activated FMOF-1 attained volumetric adsorption capacities ranging from 67 V(STP)/V at 288 K and 31 bar to 133 V(STP)/V at 173 K and 5 bar, with an isosteric heat of adsorption of ca. Methane 0-7 sulfotransferase family 1A member 1 Homo sapiens 146-149 23769353-10 2013 When adjusted for these 2 effects in the final mixed-effect model, monensin feeding (average 21 mg/kg of DMI) was associated with a 6+-3 g/d reduction in CH4 emissions in dairy cows. Methane 154-157 DMI Bos taurus 105-108 24027984-0 2013 [Distribution and air-sea fluxes of methane in the Yellow Sea and the East China Sea in the spring]. Methane 36-43 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 58-61 24027984-0 2013 [Distribution and air-sea fluxes of methane in the Yellow Sea and the East China Sea in the spring]. Methane 36-43 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 81-84 24027984-7 2013 Sea to air CH4 fluxes were (2.85 +/- 5.11) micromol x (m2 x d)(-1) (5.18 +/- 9.99) micromol x (m2 x d)(-1) respectively, calculated using the Liss and Merlivat (LM86), the Wanninkhof (W92) relationships and in situ wind speeds, and estimated emission rates of methane from the East China Sea and the Yellow Sea range from 7.05 x 10(-2) - 12.0 x 10(-2) Tg x a(-1) and 1.17 x 10(-2) - 2.20 x 10(-2) Tg x a(-1), respectively. Methane 11-14 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 0-3 24027984-7 2013 Sea to air CH4 fluxes were (2.85 +/- 5.11) micromol x (m2 x d)(-1) (5.18 +/- 9.99) micromol x (m2 x d)(-1) respectively, calculated using the Liss and Merlivat (LM86), the Wanninkhof (W92) relationships and in situ wind speeds, and estimated emission rates of methane from the East China Sea and the Yellow Sea range from 7.05 x 10(-2) - 12.0 x 10(-2) Tg x a(-1) and 1.17 x 10(-2) - 2.20 x 10(-2) Tg x a(-1), respectively. Methane 11-14 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 288-291 24027984-7 2013 Sea to air CH4 fluxes were (2.85 +/- 5.11) micromol x (m2 x d)(-1) (5.18 +/- 9.99) micromol x (m2 x d)(-1) respectively, calculated using the Liss and Merlivat (LM86), the Wanninkhof (W92) relationships and in situ wind speeds, and estimated emission rates of methane from the East China Sea and the Yellow Sea range from 7.05 x 10(-2) - 12.0 x 10(-2) Tg x a(-1) and 1.17 x 10(-2) - 2.20 x 10(-2) Tg x a(-1), respectively. Methane 11-14 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 288-291 24027984-7 2013 Sea to air CH4 fluxes were (2.85 +/- 5.11) micromol x (m2 x d)(-1) (5.18 +/- 9.99) micromol x (m2 x d)(-1) respectively, calculated using the Liss and Merlivat (LM86), the Wanninkhof (W92) relationships and in situ wind speeds, and estimated emission rates of methane from the East China Sea and the Yellow Sea range from 7.05 x 10(-2) - 12.0 x 10(-2) Tg x a(-1) and 1.17 x 10(-2) - 2.20 x 10(-2) Tg x a(-1), respectively. Methane 260-267 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 0-3 24027984-8 2013 The Yellow Sea and East China Sea are the net sources of atmospheric methane in the spring. Methane 69-76 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 11-14 24027984-8 2013 The Yellow Sea and East China Sea are the net sources of atmospheric methane in the spring. Methane 69-76 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 30-33 23675983-3 2013 Here, we use in situ low-temperature scanning tunneling microscopy (LT-STM) to reveal the graphene growth intermediates at different stages via thermal decomposition of methane on Cu(111). Methane 169-176 sulfotransferase family 1A member 3 Homo sapiens 71-74 23862497-1 2013 Steam CO2 reforming of methane was investigated over Ni-based perovskite catalyst to produce desired H2/CO ratio by adjusting the feed ratio of CH4, CO2 and H2O for floating GTL process application. Methane 23-30 relaxin 2 Homo sapiens 101-106 23947022-5 2013 The main gaseous products of CS2 decomposition with the addition of O2 in Ar gas were CO, CO2 COS and SO2, while, with the presence of H2 in Ar gas, the main products of CS2 decomposition were H2S and CH4. Methane 201-204 chorionic somatomammotropin hormone 2 Homo sapiens 170-173 23862497-1 2013 Steam CO2 reforming of methane was investigated over Ni-based perovskite catalyst to produce desired H2/CO ratio by adjusting the feed ratio of CH4, CO2 and H2O for floating GTL process application. Methane 144-147 relaxin 2 Homo sapiens 101-106 23274193-0 2013 Electrochemical immunosensor with N-doped graphene-modified electrode for label-free detection of the breast cancer biomarker CA 15-3. Methane 34-50 mucin 1, cell surface associated Homo sapiens 126-133 23274193-3 2013 This unique immunosensor, equipped with a highly conductive graphene (i.e., N-doped graphene sheets)-modified electrode, exhibited significantly increased electron transfer and high sensitivity toward CA 15-3. Methane 76-92 mucin 1, cell surface associated Homo sapiens 201-208 23095164-3 2013 Whereas the possible enzyme for methane activation (a variant of methyl-coenzyme M reductase, Mcr) was shown to be harboured by the archaea, enzymes for sulfate activation and reduction have not been localized so far. Methane 32-39 mast cell regulator Mus musculus 94-97 23480257-8 2013 Flooding with NO3- increased denitrification rate, net N2 O production and heterotrophic respiration, but a reduction in net CH4 production suggests inhibition of methanogenesis by NO3- or N2 O produced from denitrification. Methane 125-128 NBL1, DAN family BMP antagonist Homo sapiens 14-17 23459705-1 2013 We show that the MOF NU-111 exhibits equally high volumetric and gravimetric methane uptake values, both within 75% of the DOE targets at 300 K. Upon reducing the temperature to 270 K, the uptake increases to 0.5 g g(-1) and 284 cc(STP) per cc at 65 bar. Methane 77-84 lysine acetyltransferase 8 Homo sapiens 17-20 23429479-0 2013 Modulating methane storage in anionic nano-porous MOF materials via post-synthetic cation exchange process. Methane 11-18 lysine acetyltransferase 8 Homo sapiens 50-53 23469937-2 2013 Methane generation from U.S. landfills is usually estimated using the U.S. EPA"s Landfill Gas Emissions Model (LandGEM). Methane 0-7 GTP binding protein overexpressed in skeletal muscle Homo sapiens 111-118 23469937-3 2013 Default values for the two key parameters within LandGEM, the first-order decay rate (k) and the methane production potential (L0) are based on data collected in the 1990s. Methane 97-104 GTP binding protein overexpressed in skeletal muscle Homo sapiens 49-56 23469937-7 2013 The results suggest that the default k value assumed in LandGEM is likely too low, which implies that more methane is produced in the early years following waste burial when gas collection efficiencies tend to be lower. Methane 107-114 GTP binding protein overexpressed in skeletal muscle Homo sapiens 56-63 23398593-10 2013 The desolvated Co(II)(pybz)2 can absorb several gases such as CO2, N2, H2, and CH4 and also vapors of methanol, ethanol, benzene, and cyclohexane. Methane 79-82 mitochondrially encoded cytochrome c oxidase II Homo sapiens 15-21 23493710-2 2013 By drilling into 3.5-million-year-old subseafloor basalt, we demonstrated the presence of methane- and sulfur-cycling microbes on the eastern flank of the Juan de Fuca Ridge. Methane 90-97 alpha-L-fucosidase 1 Homo sapiens 163-167 23682310-0 2013 How Do Perfluorinated Alkanoic Acids Elicit Cytochrome P450 to Catalyze Methane Hydroxylation? Methane 72-79 cytochrome P450 family 4 subfamily F member 3 Homo sapiens 44-59 23312999-1 2013 Dietary coconut oil (CNO) can reduce dry matter intake (DMI), enteric methane (eCH(4)) emissions, and milk fat yield of lactating cows. Methane 70-77 biogenesis of lysosomal organelles complex 1 subunit 4 Bos taurus 21-24 23306128-0 2013 Effects of ultrasonic and thermo-chemical pre-treatments on methane production from fat, oil and grease (FOG) and synthetic kitchen waste (KW) in anaerobic co-digestion. Methane 60-67 FAT atypical cadherin 1 Homo sapiens 84-103 23425135-6 2013 Hypotaurine and other sulfinic acid analogs (methane and benzene sulfinic acids) showed very good inhibition for apple PPO at various concentrations with the highest inhibition occurring at 500 muM for hypotaurine (89%), methane sulfinic acid (100%), and benzene sulfinic acid (100%). Methane 45-52 polyphenol oxidase, chloroplastic Malus domestica 119-122 23054809-8 2013 The sheep receiving STA had shown a tendency (p = 0.15) to reduce methane emission when compared to the CON group. Methane 66-73 STA Ovis aries 20-23 23306128-1 2013 The effects of ultrasonic and thermo-chemical pre-treatments on the methane production potential of anaerobic co-digestion with synthetic kitchen waste (KW) or fat, oil and grease (FOG) were investigated. Methane 68-75 FAT atypical cadherin 1 Homo sapiens 160-179 23032298-1 2012 The hydrogen-methane compound (H(2))(4)CH(4)-or for short H4M-is one of the most promising hydrogen-storage materials. Methane 13-20 H4 clustered histone 9 Homo sapiens 58-61 23939301-4 2013 Moreover the methane storage ability of K-PAF-1-750 is among the best at 35 bars, and its low-pressure gas adsorption abilities are also comparable to the best porous materials in the world. Methane 13-20 PAF1 homolog, Paf1/RNA polymerase II complex component Homo sapiens 42-47 23026327-4 2012 High methane yield of 0.32 LCH(4) (STP)/g COD(removed) with compliance of the final treated effluent to the discharge limit were achieved. Methane 5-12 thyroid hormone receptor interactor 10 Homo sapiens 35-38 22928887-1 2013 Aerobic methane-oxidizing bacteria (MOB) play an important role in soils, mitigating emissions of the greenhouse gas methane (CH(4)) to the atmosphere. Methane 8-15 sphingomyelin synthase 1 Homo sapiens 36-39 23947712-4 2013 TCE and PCE were non-competitive inhibitors for methane oxidation, and their inhibition constants (Ki ) were 33.4 and 132.0 muM, respectively. Methane 48-55 latexin Homo sapiens 124-127 23032298-1 2012 The hydrogen-methane compound (H(2))(4)CH(4)-or for short H4M-is one of the most promising hydrogen-storage materials. Methane 39-44 H4 clustered histone 9 Homo sapiens 58-61 22655292-2 2012 High capacity methane storage (236 v(STP)/v) and a high selectivity to carbon dioxide adsorption were obtained in the nanomesh graphene with a high specific surface area (SSA) and a SSA-lossless tightly stacking manner. Methane 14-21 thyroid hormone receptor interactor 10 Homo sapiens 37-40 22950847-6 2012 Complex 5 is thermally unstable to methane loss, generating intermediate [PhBP(Ph)(3)]Fe(eta(2)-N(2)H(3)), which undergoes bimolecular coupling to produce {[PhBP(Ph)(3)]Fe}(2)(mu-eta(1):eta(1)-N(2)H(4))(mu-eta(2):eta(2)-N(2)H(2)). Methane 35-42 hyaluronan binding protein 2 Homo sapiens 74-78 23240211-6 2012 The average methane concentrations by volume in the surface air surrounding the landfill for SA1, SA2, SA3 and SA4 were 55.09, 118.29, 14.01 and 87.22 mgL(-1), respectively. Methane 12-19 stromal antigen 1 Homo sapiens 93-96 23240211-6 2012 The average methane concentrations by volume in the surface air surrounding the landfill for SA1, SA2, SA3 and SA4 were 55.09, 118.29, 14.01 and 87.22 mgL(-1), respectively. Methane 12-19 stromal antigen 2 Homo sapiens 98-101 23240211-6 2012 The average methane concentrations by volume in the surface air surrounding the landfill for SA1, SA2, SA3 and SA4 were 55.09, 118.29, 14.01 and 87.22 mgL(-1), respectively. Methane 12-19 LLGL scribble cell polarity complex component 1 Homo sapiens 151-157 23240414-0 2012 [The measurement of methane dissolved in water using raman spectroscopy assisted with CCl4 extraction]. Methane 20-27 C-C motif chemokine ligand 4 Homo sapiens 86-90 23240414-2 2012 In the present paper, a novel approach based on CCl4 extraction was introduced, and used in the measurement of methane dissolved in water using Raman spectroscopy under laboratory conditions. Methane 111-118 C-C motif chemokine ligand 4 Homo sapiens 48-52 23240414-3 2012 Saturated aqueous solution of CH4, CCl4 solution after extraction of CH4 from the saturated aqueous solution and the saturated CCl4 solution of CH4 were prepared, and the Raman spectra of three samples were obtained. Methane 69-72 C-C motif chemokine ligand 4 Homo sapiens 35-39 23240414-3 2012 Saturated aqueous solution of CH4, CCl4 solution after extraction of CH4 from the saturated aqueous solution and the saturated CCl4 solution of CH4 were prepared, and the Raman spectra of three samples were obtained. Methane 69-72 C-C motif chemokine ligand 4 Homo sapiens 35-39 23240414-4 2012 The obtained results show that the CH4 dissolved in saturated aqueous solution(the concentration of CH4 is about 1.14 mmol x L(-1)) can not been detected using Raman spectroscopy under laboratory conditions, but the CH4 Raman peak can be clearly seen in the spectra obtained for CCl4 solution after extraction. Methane 35-38 C-C motif chemokine ligand 4 Homo sapiens 279-283 23240414-4 2012 The obtained results show that the CH4 dissolved in saturated aqueous solution(the concentration of CH4 is about 1.14 mmol x L(-1)) can not been detected using Raman spectroscopy under laboratory conditions, but the CH4 Raman peak can be clearly seen in the spectra obtained for CCl4 solution after extraction. Methane 100-103 C-C motif chemokine ligand 4 Homo sapiens 279-283 22859731-6 2012 With hydrogen as the electron donor, strain B10(T) produced methane by reducing methanol. Methane 60-67 ectonucleotide pyrophosphatase/phosphodiesterase 3 Homo sapiens 44-47 23243839-2 2012 From 2009 to 2010, the diurnal cycle of hourly average CH4 concentration at LAN was found to be similar in all four seasons, with the highest level detected at 05:00 (Beijing Time) and the lowest at about 14:00. Methane 55-58 DiGeorge syndrome critical region gene 2 Homo sapiens 76-79 22405837-0 2012 Structure-dependent activation of NR4A2 (Nurr1) by 1,1-bis(3"-indolyl)-1-(aromatic)methane analogs in pancreatic cancer cells. Methane 82-90 nuclear receptor subfamily 4 group A member 2 Homo sapiens 34-39 22627268-0 2012 Identification of a mechanism of transformation of clathrate hydrate structures I to II or H. Binary mixed-gas hydrates including methane and other guest gases demonstrate a structural transition between the sI and sII phases. Methane 130-137 transcription elongation factor A1 Homo sapiens 215-218 22627268-1 2012 Under increasing pressure pure methane hydrate exhibits a phase transition first from sI to sII and then to sH. Methane 31-38 transcription elongation factor A1 Homo sapiens 92-95 22627268-3 2012 Recently, molecular dynamics simulations of methane hydrates suggest there may exist uncommon 15-hedral cages (51263), linking the sI and sII cages. Methane 44-51 transcription elongation factor A1 Homo sapiens 138-141 22405837-0 2012 Structure-dependent activation of NR4A2 (Nurr1) by 1,1-bis(3"-indolyl)-1-(aromatic)methane analogs in pancreatic cancer cells. Methane 82-90 nuclear receptor subfamily 4 group A member 2 Homo sapiens 41-46 22038990-7 2012 Selection for a decreased RFI phenotype can reduce feed intake, methane production, nutrient losses in manure, and visceral organ weights substantially in beef cattle. Methane 64-71 RFI Bos taurus 26-29 22524674-8 2012 The C-H bond can be readily activated by MH(+) (M = Os, Ir, and Pt) with a negligible barrier in the low-spin state; thus, OsH(+), IrH(+), and PtH(+) are likely to be excellent mediators for the activition of the C-H bond of methane. Methane 225-232 parathyroid hormone Homo sapiens 143-146 22301079-8 2012 Particularly for aerobic biostimulation, methane-amended microcosms degraded EDB, on average, at a first order rate eight times faster than unamended microcosms. Methane 41-48 vesicle associated membrane protein 8 Homo sapiens 77-80 22301079-10 2012 Residual methane concentrations and the emergence of methanotrophic bacteria, measured by culture independent bacterial analysis, provided strong indications that EDB degradation in aerobic methane-amended microcosms occurred via cometabolic degradation. Methane 9-16 vesicle associated membrane protein 8 Homo sapiens 163-166 22301079-10 2012 Residual methane concentrations and the emergence of methanotrophic bacteria, measured by culture independent bacterial analysis, provided strong indications that EDB degradation in aerobic methane-amended microcosms occurred via cometabolic degradation. Methane 190-197 vesicle associated membrane protein 8 Homo sapiens 163-166 22224587-6 2012 The developed methodology describes, for the first time, the fabrication of N-doped graphene using conducting polymers including heteroatoms in their structures as the carbonization precursor and demonstrates its use in a high-performance, flexible FET-type aptasensor to detect vascular endothelial growth factor as a cancer biomarker. Methane 76-92 vascular endothelial growth factor A Homo sapiens 279-313 21930516-8 2012 Throughout the experiment the average concentration of CH4 in ALR was higher than that in SLR (36.7 and 14.5%, respectively). Methane 55-58 growth factor, augmenter of liver regeneration Homo sapiens 62-65 22121022-0 2011 Structure of a methyl-coenzyme M reductase from Black Sea mats that oxidize methane anaerobically. Methane 76-83 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 54-57 22509597-5 2012 Distribution of methane in porewater is consistent with that of surface water, which decreases rapidly from B1, B2, B3 to B4 stations, from 2 212 micromol x L(-1) to 5 micromol x L(-1). Methane 16-23 immunoglobulin kappa variable 7-3 (pseudogene) Homo sapiens 108-124 22055104-4 2012 The maximum methane yield was 0.32 m3/kg CODremoved at an OLR of 9.27 kg COD/m3 d. Black matured granules of size between 2.5 and 5 mm were observed at the end of 225 d operation. Methane 12-19 small nuclear ribonucleoprotein polypeptides B and B1 Homo sapiens 41-44 22629685-0 2012 [Sulfate reduction, formation and oxidation of methane in Holocene era sediments of the Vyborg Bay, Baltic Sea]. Methane 47-54 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 107-110 22506700-5 2012 In contrast, HBP severely inhibited methanogens at 200 mg/L, but after acclimatisation it could be metabolised resulting in a 25% increase in methane production compared to the control. Methane 142-149 signal transducing adaptor molecule 2 Homo sapiens 13-16 21924895-0 2011 Dissolved methane oxidation and competition for oxygen in down-flow hanging sponge reactor for post-treatment of anaerobic wastewater treatment. Methane 10-17 solute carrier family 35 member G1 Homo sapiens 95-99 21913687-0 2011 Reaction mechanism for the thermal decomposition of BCl3/CH4/H2 gas mixtures. Methane 57-60 BCL3 transcription coactivator Homo sapiens 52-56 21318266-0 2011 Effects of composition of labile organic matter on biogenic production of methane in the coastal sediments of the Arabian Sea. Methane 74-81 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 122-125 21318266-6 2011 Proteins influenced methane production in the clayey sediments of shallow depths of the Arabian Sea (r = 0.933, p < 0.001) and mangrove estuary (r = 0.981, p < 0.001) but in the sandy beach sediments, carbohydrates (r = 0.924, p < 0.001) governed the net methane production. Methane 20-27 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 96-99 21890875-5 2011 Results showed that increasing OLR increased the amount of organic matter conversion and resulted in higher organic matter removal and volumetric methane (CH4) production (VMP) rates. Methane 146-153 neurensin 1 Homo sapiens 172-175 21890875-5 2011 Results showed that increasing OLR increased the amount of organic matter conversion and resulted in higher organic matter removal and volumetric methane (CH4) production (VMP) rates. Methane 155-158 neurensin 1 Homo sapiens 172-175 21494753-6 2011 Moreover, on increasing AVOL from 1.5 to 4.5 g COD L(-1) day(-1) methane production increased from 29.5 to 55.5 N mL CH(4) g COD(-1). Methane 65-72 retinitis pigmentosa GTPase regulator Homo sapiens 125-131 21924895-1 2011 Post-treatment of anaerobic wastewater was undertaken to biologically oxidize dissolved methane, with the aim of preventing methane emission. Methane 88-95 solute carrier family 35 member G1 Homo sapiens 0-4 21924895-1 2011 Post-treatment of anaerobic wastewater was undertaken to biologically oxidize dissolved methane, with the aim of preventing methane emission. Methane 124-131 solute carrier family 35 member G1 Homo sapiens 0-4 21392973-3 2011 The biochemical methane potential (BMP) of the liquid waste was reported and maximum cumulative methane production at the exit of the reactor is estimated to be 785 ml CH(4) (STP)/(gVSS added). Methane 16-23 thyroid hormone receptor interactor 10 Homo sapiens 175-178 21734907-5 2011 In the absence of sulfate, many SRB ferment organic acids and alcohols, producing hydrogen, acetate, and carbon dioxide, and may even rely on hydrogen- and acetate-scavenging methanogens to convert organic compounds to methane. Methane 219-226 chaperonin containing TCP1 subunit 4 Homo sapiens 32-35 21392199-0 2011 Bacterial enzymes for dissimilatory sulfate reduction in a marine microbial mat (Black Sea) mediating anaerobic oxidation of methane. Methane 125-132 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 87-90 21392199-3 2011 We collected microbial mats with high AOM activity from a methane seep in the Black Sea. Methane 58-65 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 84-87 21354776-0 2011 Bio-tarp alternative daily cover prototypes for methane oxidation atop open landfill cells. Methane 48-55 TCR gamma alternate reading frame protein Homo sapiens 4-8 21354776-3 2011 The methane oxidation capacity of methanotrophs embedded in a "bio-tarp" was investigated as a means to mitigate methane release from open landfill cells. Methane 4-11 TCR gamma alternate reading frame protein Homo sapiens 67-71 21354776-3 2011 The methane oxidation capacity of methanotrophs embedded in a "bio-tarp" was investigated as a means to mitigate methane release from open landfill cells. Methane 113-120 TCR gamma alternate reading frame protein Homo sapiens 67-71 21354776-7 2011 Multilayered bio-tarp prototypes consisting of alternating layers of the two geotextiles were found to remove 16% of the methane flowing through the bio-tarp. Methane 121-128 TCR gamma alternate reading frame protein Homo sapiens 17-21 21354776-7 2011 Multilayered bio-tarp prototypes consisting of alternating layers of the two geotextiles were found to remove 16% of the methane flowing through the bio-tarp. Methane 121-128 TCR gamma alternate reading frame protein Homo sapiens 153-157 21354776-8 2011 The addition of landfill cover soil, compost, or shale amendments to the bio-tarp increased the methane removal up to 32%. Methane 96-103 TCR gamma alternate reading frame protein Homo sapiens 77-81 21354776-10 2011 The multilayered bio-tarp and amended bio-tarp configurations were all found to decrease landfill methane flux; however, the performance efficacy of bio-tarps was not significantly different from controls without methanotrophs. Methane 98-105 TCR gamma alternate reading frame protein Homo sapiens 21-25 21354776-10 2011 The multilayered bio-tarp and amended bio-tarp configurations were all found to decrease landfill methane flux; however, the performance efficacy of bio-tarps was not significantly different from controls without methanotrophs. Methane 98-105 TCR gamma alternate reading frame protein Homo sapiens 42-46 21351767-3 2011 Among these functional PAFs, we found that tetrahydrofuran-like ether-functionalized PAF-1 shows higher adsorption capacity for CO(2) at 1 bar and 298 K (10 mol per kilogram of adsorbent) and also much higher selectivities for CO(2)/CH(4), CO(2)/N(2), and CO(2)/H(2) mixtures when compared with the amine functionality. Methane 233-238 PAF1 homolog, Paf1/RNA polymerase II complex component Homo sapiens 85-90 21240398-0 2011 Deuterium kinetic isotope effects on the gas-phase reactions of C2H with H2(D2) and CH4(CD4). Methane 84-87 CD4 molecule Homo sapiens 88-91 21079877-4 2011 It is shown that at high discharge power and lower CH4 concentrations, the sp3/sp2 fraction is higher. Methane 51-54 Sp3 transcription factor Homo sapiens 75-78 21036039-3 2011 The methane yield at each trial was 169, 201, 256 and 269 L(STP) CH(4)/kg COD(removed). Methane 4-11 thyroid hormone receptor interactor 10 Homo sapiens 60-63 21079877-4 2011 It is shown that at high discharge power and lower CH4 concentrations, the sp3/sp2 fraction is higher. Methane 51-54 Sp2 transcription factor Homo sapiens 79-82 21085725-2 2011 The reaction produces C(2)+ hydrocarbons and hydrogen in a single step at 1 atm in a continuous flow reactor at a nominal residence time of 60 s. The essentially complete conversion of methane appears to be due to protolytic activation of methane in the presence of H(+)AlBr(4)(-). Methane 185-192 ATM serine/threonine kinase Homo sapiens 76-79 21176945-9 2011 The strong positive correlation between K(m) and Sulfate Reduction Rates (SRR) and between K(d) and Methane Production Rates (MPR) supports the involvement of SRB in Hg methylation and MPA in MMHg demethylation in the sediments. Methane 100-107 chaperonin containing TCP1 subunit 4 Homo sapiens 159-162 21085725-2 2011 The reaction produces C(2)+ hydrocarbons and hydrogen in a single step at 1 atm in a continuous flow reactor at a nominal residence time of 60 s. The essentially complete conversion of methane appears to be due to protolytic activation of methane in the presence of H(+)AlBr(4)(-). Methane 239-246 ATM serine/threonine kinase Homo sapiens 76-79 20854329-4 2011 The dearth of NO3- and SO42- in Lake Matano waters suggests that anaerobic methane oxidation may be coupled to the reduction of Fe (and/or Mn) (hydr)oxides. Methane 75-82 NBL1, DAN family BMP antagonist Homo sapiens 14-17 20555363-2 2010 To investigate the role of methylotrophy in the cycling of carbon in this unusual environment, stable-isotope probing (SIP) was carried out using the one-carbon compounds methane, methanol and methylamine. Methane 171-178 tumor protein p53 inducible nuclear protein 1 Homo sapiens 95-123 21402221-1 2011 Coenzyme M (CoM) and coenzyme B (CoB) are essential for methane production by the euryarchaea that employ this specialized anaerobic metabolism. Methane 56-63 metabolism of cobalamin associated B Homo sapiens 21-31 19748937-5 2010 The maximum tolerated Na+ and K+ concentrations during active methane production were at least 4100 mg Na+ L-1 and 800 mg K+ L-1, respectively. Methane 62-69 immunoglobulin kappa variable 1-16 Homo sapiens 107-128 26616766-1 2010 Application to the CH4/CD3H/CD4 + CF3 Abstraction Reactions. Methane 19-22 CD247 molecule Homo sapiens 23-27 26616766-1 2010 Application to the CH4/CD3H/CD4 + CF3 Abstraction Reactions. Methane 19-22 CD4 molecule Homo sapiens 28-31 26616766-5 2010 The performance of this algorithm has been tested for the CH4/CD3H/CD4 + CF3 hydrogen abstraction reactions with encouraging results, i.e., when the fitting is performed using 13 points, the algorithm is about 30 times faster than the full calculation with deviations that are smaller than 5%. Methane 58-61 CD247 molecule Homo sapiens 62-66 26616766-5 2010 The performance of this algorithm has been tested for the CH4/CD3H/CD4 + CF3 hydrogen abstraction reactions with encouraging results, i.e., when the fitting is performed using 13 points, the algorithm is about 30 times faster than the full calculation with deviations that are smaller than 5%. Methane 58-61 CD4 molecule Homo sapiens 67-70 20400285-0 2010 Anaerobic co-digestion of the organic fraction of municipal solid waste with FOG waste from a sewage treatment plant: recovering a wasted methane potential and enhancing the biogas yield. Methane 138-145 zinc finger protein, FOG family member 1 Homo sapiens 77-80 20646941-1 2010 Clathrate hydrates formed from binary gas mixtures of methane and other small lipophilic molecules change from the sI phase to sII and back depending on the concentration of methane in the mixtures. Methane 54-61 transcription elongation factor A1 Homo sapiens 127-130 20646941-1 2010 Clathrate hydrates formed from binary gas mixtures of methane and other small lipophilic molecules change from the sI phase to sII and back depending on the concentration of methane in the mixtures. Methane 174-181 transcription elongation factor A1 Homo sapiens 127-130 20646941-2 2010 In contrast, pure methane hydrate under increasing pressure transforms first from sI to sII and then finally to sH. Methane 18-25 transcription elongation factor A1 Homo sapiens 88-91 19523879-8 2010 The slow deteriorating effect of calcium phosphate, and the production of methane show the importance of studying the combination of bioanode and biocathode in one electrochemical cell, and of studying long term performance of such an MEC. Methane 74-81 C-C motif chemokine ligand 28 Homo sapiens 235-238 20414304-7 2010 Because CH(4) is expected to be the dominant carbon-bearing species, disequilibrium processes such as vertical mixing and polymerization of methane into substances such as ethylene may be required to explain the hot Neptune"s small CH(4)-to-CO ratio, which is at least 10(5) times smaller than predicted. Methane 140-147 alcohol dehydrogenase iron containing 1 Homo sapiens 212-215 19716525-12 2009 Consequently, Methanosarcinales, which are acetate-utilizing methanogens, became the dominant archaea in the IAR, where high methane production was observed. Methane 125-132 protein tyrosine phosphatase receptor type N2 Homo sapiens 109-112 20030379-8 2010 Because of methane formation and biomass/SMP accumulation, the overall H(2) recovery was moderate at 1.8-2.0 mol of H(2)/mol of acetate in the MEC. Methane 11-18 C-C motif chemokine ligand 28 Homo sapiens 143-146 21302544-4 2010 By the same token, photochemical production of HCN is ineffective in Jupiter"s troposphere: CH4-NH3 coupling is inhibited by the physical separation of the CH4 photolysis region in the upper stratosphere from the NH3 photolysis and condensation region in the troposphere, and C2H2-NH3 coupling is inhibited by the low tropospheric abundance of C2H2. Methane 92-95 metastasis associated lung adenocarcinoma transcript 1 Homo sapiens 47-50 21302544-4 2010 By the same token, photochemical production of HCN is ineffective in Jupiter"s troposphere: CH4-NH3 coupling is inhibited by the physical separation of the CH4 photolysis region in the upper stratosphere from the NH3 photolysis and condensation region in the troposphere, and C2H2-NH3 coupling is inhibited by the low tropospheric abundance of C2H2. Methane 156-159 metastasis associated lung adenocarcinoma transcript 1 Homo sapiens 47-50 19849830-5 2009 CO/CH4 and NH3/NH4+ in fluids distilled out of layer silicates and zeolites in the subducting plate at an early stage of subduction will react upon heating and form HCN, which is then available for further organic reactions to, for instance, carbohydrates, nucleosides or even nucleotides, under alkaline conditions in hydrated mantle rocks of the overriding plate. Methane 3-6 metastasis associated lung adenocarcinoma transcript 1 Homo sapiens 165-168 19090563-2 2009 The full potential curves of the methane dimer at 12 symmetric conformations were calculated by the supermolecule counterpoise-corrected second-order Moller-Plesset (MP2) perturbation theory. Methane 33-40 tryptase pseudogene 1 Homo sapiens 166-169 21255289-4 2009 Per mole of methane produced this is 27-35 kJ mol(-1), indicating that PAH-based methanogenesis is exergonic. Methane 12-19 phenylalanine hydroxylase Homo sapiens 71-74 19354304-10 2009 The final persistence of a small portion of sII hydrate points to a miscibility gap between CH(4)-rich sI and C(2)H(6)-rich sII hydrates. Methane 92-97 transcription elongation factor A1 Homo sapiens 44-47 19480947-13 2009 The concept of an energy supply system that provides more than two forms of energy is met by (1) upgrading obtained ethanol to fuel-grade quality and providing methane to CHP plants for the production of (2) electric energy and (3) utility steam that in turn can be used to operate distillation columns in the ethanol production process. Methane 160-167 CHP Triticum aestivum 171-174 19321185-3 2009 During period 2 (day 379-745), the methane yield at 25 degrees C decreased by 45% when total ammonium-N and ammonia-N were increased in two of the four ASBRs to levels >4000 mg NH(4)(+)-N/L and >80 mg NH(3)-N/L, respectively. Methane 35-42 period circadian regulator 2 Homo sapiens 7-15 19509004-10 2009 A BC501-A liquid scintillation spectrometer provided the fluence values for energies beyond 1.2 MeV, a methane-filled SP2 counter from 800 keV to 1.4 MeV and an H(2)-filled SP2 counter from 144 to 800 keV. Methane 103-110 Sp2 transcription factor Homo sapiens 118-121 19275154-2 2009 By adsorbing one CH(4) molecule per open metal, these sites alone can generate very large methane storage capacities, 160-174 cm(3)(STP)/cm(3), approaching the DOE target of 180 cm(3)(STP)/cm(3) for material-based methane storage at room temperature. Methane 90-97 thyroid hormone receptor interactor 10 Homo sapiens 132-135 19275154-2 2009 By adsorbing one CH(4) molecule per open metal, these sites alone can generate very large methane storage capacities, 160-174 cm(3)(STP)/cm(3), approaching the DOE target of 180 cm(3)(STP)/cm(3) for material-based methane storage at room temperature. Methane 90-97 thyroid hormone receptor interactor 10 Homo sapiens 184-187 19275154-3 2009 Our adsorption isotherm measurements at 298 K and 35 bar for the five M(2)(dhtp) compounds yield excess methane adsorption capacities ranging from 149 to 190 cm(3)(STP)/cm(3) (derived using their crystal densities), indeed roughly equal to the predicted, maximal adsorption capacities of the open metals (within +/-10%) in these MOFs. Methane 104-111 thyroid hormone receptor interactor 10 Homo sapiens 164-167 19050859-3 2009 As a result, the current production increased from 66 +/- 2 to 156 +/- 1 A m(-3) MEC by removing the membrane with an applied voltage of -0.8 V. Methane was the main energetic product despite continuous operation under carbonate-limited and slightly acidified conditions (pH 6.1-6.2). Methane 145-152 C-C motif chemokine ligand 28 Homo sapiens 81-84 19209919-3 2009 The observed faster structural conversion rate in the higher methane concentration atmosphere can be explained in terms of the differences in driving force (difference in chemical potential of water in sI and sII hydrates) and kinetics (mass transfer of gas and water rearrangement). Methane 61-68 transcription elongation factor A1 Homo sapiens 209-212 19209919-4 2009 The kinetic hydrate inhibitor increased the conversion rate at 65% methane in ethane (sI is thermodynamically stable) but retards the rate at 93% methane in ethane (sII is thermodynamically stable), implying there is a complex interaction between the polymer, water, and hydrate guests at crystal surfaces. Methane 146-153 transcription elongation factor A1 Homo sapiens 165-168 18939576-5 2008 Greater methane conversion was observed by increasing the percentage of metals added to the zeolite even though the BET surface area of the zeolite consequently decreased. Methane 8-15 bet Drosophila melanogaster 116-119 18823644-6 2008 Overall, the results show that MBT residual is a suitable support medium for methane oxidation in landfill covers in field conditions in a boreal climate. Methane 77-84 proteinase 3 Homo sapiens 31-34 19199493-5 2009 The MH(+) (M = Ru, Rh, and Pd) complexes are expected from the general energy profiles of the reaction pathways to efficiently convert methane to metal methyl, thus RuH(+), RhH(+), and PdH(+) are likely to be excellent mediators for the activity of methane. Methane 135-142 pyruvate dehydrogenase phosphatase catalytic subunit 1 Homo sapiens 185-188 19708115-4 2009 Electroreduction of CCl4 in RTIL through outer sphere electron transfer would be a promising pathway for its direct conversion to methane. Methane 130-137 C-C motif chemokine ligand 4 Homo sapiens 20-24 18680385-1 2008 Data on the adsorption behavior of CO 2, CH 4, and N 2 on coal are needed to develop enhanced coalbed methane (ECBM) recovery processes, a technology where the recovery of CH 4 is enhanced by injection of a gas stream consisting of either pure CO 2, pure N 2, or a mixture of both. Methane 102-109 complement C2 Homo sapiens 35-39 18609141-9 2008 A weak correlation between hydrogen excretion and PYY levels was demonstrated in non-producers of methane. Methane 98-105 peptide YY Homo sapiens 50-53 18218032-5 2008 Our comparative study explored the coupling of AOM with sulfate reduction (SR) and methane generation (MOG) in microbial communities from Gulf of Mexico cold seep sediments that were naturally enriched with methane and other hydrocarbons. Methane 83-90 myelin oligodendrocyte glycoprotein Homo sapiens 103-106 18218032-9 2008 Anaerobic oxidation of methane, MOG and SR rates decreased significantly with decreasing concentration of methane, and in the presence of the SR inhibitor molybdate, but reacted differently to the MOG inhibitor 2-bromoethanesulfonate (BES). Methane 106-113 myelin oligodendrocyte glycoprotein Homo sapiens 32-35 18318514-0 2008 Theoretical study of the reaction mechanism of HCN+ and CH4 of relevance to Titan"s ion chemistry. Methane 56-59 metastasis associated lung adenocarcinoma transcript 1 Homo sapiens 47-50 18318514-5 2008 The initial association of HCN+ with CH4 is found to be a prereaction complex 1 (HCNHCH3(+)) without barrier. Methane 37-40 metastasis associated lung adenocarcinoma transcript 1 Homo sapiens 27-30 18247598-0 2008 Heterogeneous crystal growth of methane hydrate on its sII [001] crystallographic face. Methane 32-39 transcription elongation factor A1 Homo sapiens 55-58 18247598-1 2008 This paper presents a systematic molecular simulation study of the heterogeneous crystal growth of methane hydrate sII from supersaturated aqueous methane solutions. Methane 99-106 transcription elongation factor A1 Homo sapiens 115-118 18247598-1 2008 This paper presents a systematic molecular simulation study of the heterogeneous crystal growth of methane hydrate sII from supersaturated aqueous methane solutions. Methane 147-154 transcription elongation factor A1 Homo sapiens 115-118 18247598-5 2008 We show that the growth of a [001] face of sII hydrate can produce an sI crystalline structure, confirming that cross-nucleation of methane hydrate structures is possible. Methane 132-139 transcription elongation factor A1 Homo sapiens 43-46 18754511-6 2008 The subsequent reactions involving Br, methane, and CBrF3 play a major role in the observed enhanced yield of CH2=CF2. Methane 39-46 ATPase H+ transporting accessory protein 1 Homo sapiens 110-117 18697520-7 2008 In addition, a methane production enzyme coding gene, i.e. MCR, in a J1 bore immediately bordering the sources in the J site showed the greatest concentration, but it was precipitously decreased in the downgradient direction toward the outer boundary of landfill. Methane 15-22 nuclear receptor subfamily 3 group C member 2 Homo sapiens 59-62 18323114-9 2008 The highest levels of EDB removal occurred in microcosms that produced the highest amounts of methane. Methane 94-101 vesicle associated membrane protein 8 Homo sapiens 22-25 19551051-2 2007 In this paper, we demonstrate methane sensing with a 1670-nm band HC-PBF. Methane 30-37 PTTG1 interacting protein Homo sapiens 69-72 18059498-7 2007 This is the first report on fungal communities from methane hydrate-bearing deep-sea marine sediments in South China Sea. Methane 52-59 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 81-84 18167585-4 2007 For the methane dimer, errors for SCS(N)-(L)MP2/CBS remain in the 0.2-0.3 kcal mol(-1) range, corresponding to a larger relative error of 40-50%. Methane 8-15 cystathionine beta-synthase Homo sapiens 48-51 18059498-7 2007 This is the first report on fungal communities from methane hydrate-bearing deep-sea marine sediments in South China Sea. Methane 52-59 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 117-120 17685497-0 2007 Hydrogen migration and vinylidene pathway for formation of methane in the 193 nm photodissociation of propene: CH3CH=CH2 and CD3CD=CD2. Methane 59-66 CD2 molecule Homo sapiens 131-134 18069330-3 2007 The methane content in the water column of the Chukchi sea varied from 8 nmol CH4 l(-1) in the eastern part of the sea to 31 nmol CH4 l(-1) in the northern part of the Herald Canyon. Methane 4-11 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 55-58 18069330-3 2007 The methane content in the water column of the Chukchi sea varied from 8 nmol CH4 l(-1) in the eastern part of the sea to 31 nmol CH4 l(-1) in the northern part of the Herald Canyon. Methane 4-11 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 115-118 17315920-3 2007 A detailed electronic structure analysis leads to the presumption that the properties of the FeV=O bond can be modified by introducing substituents to the aromatic rings of TPA and thus the reactivity of HO-(TPA)FeV=O for the hydrogen atom abstraction of methane hydroxylation can be tuned on the quartet potential energy surface. Methane 255-262 plasminogen activator, tissue type Homo sapiens 173-176 17315920-3 2007 A detailed electronic structure analysis leads to the presumption that the properties of the FeV=O bond can be modified by introducing substituents to the aromatic rings of TPA and thus the reactivity of HO-(TPA)FeV=O for the hydrogen atom abstraction of methane hydroxylation can be tuned on the quartet potential energy surface. Methane 255-262 plasminogen activator, tissue type Homo sapiens 208-211 16722672-8 2006 A simplified reaction scheme was delineated: NO + HO2 --> NO2 + OH followed by OH + CH4 --> CH3 + H2O and OH + C2H6 --> C2H5 + H2O. Methane 87-90 heme oxygenase 2 Homo sapiens 50-53 17030134-7 2007 Calculations are also reported for the isotopic methane (CD4, 13CH4) hydrates. Methane 48-55 CD4 molecule Homo sapiens 57-60 17287000-7 2007 In the absence of any inhibition, the methane yield varied from 0.76 to 0.98 L methane at STP per g volatile solids added. Methane 38-45 thyroid hormone receptor interactor 10 Homo sapiens 90-93 17287000-7 2007 In the absence of any inhibition, the methane yield varied from 0.76 to 0.98 L methane at STP per g volatile solids added. Methane 79-86 thyroid hormone receptor interactor 10 Homo sapiens 90-93 17249765-1 2007 High-resolution electron spin resonance (ESR) spectra of radical pairs of a hydrogen atom that coupled with a methyl radical (H...CH3, H...CHD2, D...CH2D, and D...CD3) were observed for X-ray irradiated solid argon containing selectively deuterium-labeled methanes, CH4, CH2D2, and CD4, at 4.2 K. The double-quartet 1H-hyperfine (hf) splittings of ca. Methane 256-264 CD4 molecule Homo sapiens 282-285 17249765-1 2007 High-resolution electron spin resonance (ESR) spectra of radical pairs of a hydrogen atom that coupled with a methyl radical (H...CH3, H...CHD2, D...CH2D, and D...CD3) were observed for X-ray irradiated solid argon containing selectively deuterium-labeled methanes, CH4, CH2D2, and CD4, at 4.2 K. The double-quartet 1H-hyperfine (hf) splittings of ca. Methane 266-269 CD4 molecule Homo sapiens 282-285 17227418-0 2007 Diversity and abundance of sulfate-reducing microorganisms in the sulfate and methane zones of a marine sediment, Black Sea. Methane 78-85 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 120-123 17165710-1 2006 The intermolecular C-H bond activation of benzene occurs under very mild conditions (room temperature) via a rare stereospecific 1,3-H addition on an unsaturated eta2-cyclopropene intermediate generated by a beta-H abstraction of CH4 from TpMe2NbMe(c-C3H5)(MeCCMe) to give TpMe2NbPh(c-C3H5)(MeCCMe). Methane 230-233 DNA polymerase iota Homo sapiens 162-166 17112259-2 2006 Efficient electron transfer (>19%) is observed with CS2, NH3, C6F6, NO2, NO*, and C6H6, molecular addition occurs with D2O, CH4, CH3F, CH3Cl, and OCS, and SF6, CO, CO2, N2O, and O2 showed no measurable reactivity with Hg*+. Methane 127-130 chorionic somatomammotropin hormone 2 Homo sapiens 55-58 17029440-3 2006 Au+ (1S0) reacts with methane by endothermic dehydrogenation to form AuCH2+ as well as C-H bond cleavage to yield AuH+ and AuCH3+. Methane 22-29 AU RNA binding methylglutaconyl-CoA hydratase Homo sapiens 114-117 17007140-2 2006 The motivation behind the study is that reaction of CHF3 with CH4 provides a possible route for synthesis of CH2=CF2 (C2H2F2). Methane 62-65 ATPase H+ transporting accessory protein 1 Homo sapiens 113-116 17269229-2 2007 This study uses a radio frequency (rf) discharge to consider the effect of added CH4 and CO to simulated NO/N2/O2/H2O mixtures on the elevation of NO conversion and the reduction of NO into N2. Methane 81-84 immunoglobulin kappa variable 1D-39 Homo sapiens 111-117 17002291-5 2006 Further study of this complex has led here to the proposal that the pMMO-R is in fact methanol dehydrogenase, the subsequent enzyme in the methane oxidation pathway by methanotrophs. Methane 139-146 malate dehydrogenase 2 Homo sapiens 86-108 17002291-8 2006 These studies of pMMO-MDH complexes have provided further understanding of the structural basis for the particular functions of the enzymes in this system which might also be of relevance to the complete process of methane oxidation by methanotrophs under high copper concentration in the environment. Methane 215-222 malate dehydrogenase 2 Homo sapiens 22-25 16965085-1 2006 We have calculated the intermolecular interaction potentials of the methane dimer at the minimum-energy D(3d) conformation using the Hartree-Fock (HF) self-consistent theory, the correlation-corrected second-order Moller-Plesset (MP2) perturbation theory, and the density functional theory (DFT) with the Perdew-Wang (PW91) functional as the exchange or the correlation part. Methane 68-75 tryptase pseudogene 1 Homo sapiens 230-233 16460197-3 2006 Different intramolecular modes of the three methane isotopologues under study--CH(4), CD(4), and CD(3)H--are excited; the degenerate deformation mode nu(4) is observed for CH(4) and CD(4) at 7.69 and 10.11 microm, respectively, as well as the nu(2) and nu(4) modes of CD(3)H at 7.79, 9.75, and 9.98 microm. Methane 44-51 CD247 molecule Homo sapiens 97-103 16555885-5 2006 The estimated MP2 interaction energies of methane, ethane, and propane dimers at the basis set limit [EMP2(limit)] by the method of Helgaker et al. Methane 42-49 tryptase pseudogene 1 Homo sapiens 14-17 16555885-21 2006 The estimated EMP2(limit) values of the ten dimers were fitted to the form m0+m1X (X is 1 for methane, 2 for ethane, etc.). Methane 94-101 epithelial membrane protein 2 Homo sapiens 14-18 16483211-1 2006 Full-dimensional ab initio potential-energy surface (PES) and dipole moment surface are constructed for a methane molecule at the CCSD(T)/cc-pVTZ and MP2/cc-pVTZ levels of theory, respectively, by the modified Shepard interpolation method based on the fourth-order Taylor expansion [MSI(4th)]. Methane 106-113 tryptase pseudogene 1 Homo sapiens 150-153 16460197-3 2006 Different intramolecular modes of the three methane isotopologues under study--CH(4), CD(4), and CD(3)H--are excited; the degenerate deformation mode nu(4) is observed for CH(4) and CD(4) at 7.69 and 10.11 microm, respectively, as well as the nu(2) and nu(4) modes of CD(3)H at 7.79, 9.75, and 9.98 microm. Methane 44-51 CD247 molecule Homo sapiens 268-274 16599113-1 2006 An on-line method for measurement of the 13C/12C ratio of methane by a gas chromatography/high-temperature conversion/ isotope ratio mass spectrometry (GC/C/MS) technique was developed. Methane 58-65 guanylate cyclase 2C Homo sapiens 152-156 16332791-1 2005 In the northwestern Black Sea, methane oxidation rates reveal that above shallow and deep gas seeps methane is removed from the water column as efficiently as it is at sites located off seeps. Methane 31-38 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 26-29 16332791-1 2005 In the northwestern Black Sea, methane oxidation rates reveal that above shallow and deep gas seeps methane is removed from the water column as efficiently as it is at sites located off seeps. Methane 100-107 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 26-29 15962992-0 2005 Reactions of methane with titanium atoms: CH3TiH, CH2=TiH2, agostic bonding, and (CH3)2TiH2. Methane 13-20 RuvB like AAA ATPase 2 Homo sapiens 54-58 16834244-2 2005 Accompanying ab initio calculations at the MP2/6-311++G(2df,2p) level for the n = 1-3 clusters suggest that methane molecules prefer to attach to the chloride anion by single linear H-bonds and sit adjacent to one another. Methane 108-115 tryptase pseudogene 1 Homo sapiens 43-46 16853246-2 2005 The surface chemistry of carbon-nitrogen coupling is of fundamental importance to catalytic processes such as the industrial-scale synthesis of HCN from CH4 and NH3 over Pt. Methane 153-156 metastasis associated lung adenocarcinoma transcript 1 Homo sapiens 144-147 16190251-8 2005 The mixture obtained (71% H2: 23% CH4) could be used as a hydrogen source to obtain pure hydrogen or hydrogen-natural gas mixtures to fuel a captive fleet of public urban vehicles powered by fuel cells or dedicated ICE, respectively. Methane 34-37 carboxylesterase 2 Homo sapiens 215-218 15962992-0 2005 Reactions of methane with titanium atoms: CH3TiH, CH2=TiH2, agostic bonding, and (CH3)2TiH2. Methane 13-20 RuvB like AAA ATPase 2 Homo sapiens 87-91 15962992-1 2005 Laser-ablated titanium atoms react with methane to form the insertion product CH3TiH, which undergoes a reversible photochemical alpha-H transfer to give the methylidene complex CH2=TiH2. Methane 40-47 RuvB like AAA ATPase 2 Homo sapiens 182-186 15740154-13 2005 The involvement of metastable trans-2 in the gas phase oxidation of methane and isobutane is firmly established to take place on the unrestricted [UB3LYP/6-311+G(d,p)] potential energy surface (PES) with classical activations barriers for the hydrogen abstraction step that are 15.7 and 5.9 kcal/mol lower than the corresponding activation energies for producing products methanol and tert-butyl alcohol formed on the restricted PES. Methane 68-75 protein tyrosine phosphatase non-receptor type 22 Homo sapiens 150-153 15997700-8 2005 The presented findings indicate that the metabolic diversity of the Black Sea mat is wider than currently known and that probably other bacteria than those of the methane-oxidizing consortia contribute to aromatic degradation in this anoxic habitat. Methane 163-170 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 74-77 15876569-6 2005 This suggests that, although extant methanogens produce methane from various substrates (CO(2), formate, acetate, methylated C-1 compounds), these archaea have a core of conserved enzymes that have undergone little evolutionary change. Methane 56-63 heterogeneous nuclear ribonucleoprotein C Homo sapiens 125-128 16119857-0 2005 [Anaerobic methane oxidation and sulfate reduction in bacterial mats of coral-like carbonate structures in the Black Sea]. Methane 11-18 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 117-120 16833628-4 2005 A survey of four other polybrominated methanes, CH2Br2, CHClBr2, CF2Br2, and CBr4, shows that they all generate secondary Br atoms when photolyzed at 266 nm in the presence of O2 and NO, suggesting that their reaction sequences are similar to that of bromoform. Methane 38-46 immunoglobulin kappa variable 1D-39 Homo sapiens 176-185 19787985-4 2005 There has been a controversial discussion about an experiment which seemed to indicate that deuteron transfer from CD4+ to CH4 can create stable isotopomers with chemically distinguishable hydrogen atoms, CH3-HD+. Methane 123-126 CD4 molecule Homo sapiens 115-118 19787985-6 2005 In collisions of CH4+ with CH4 or CD4, there is significant scrambling and one would need to use differential scattering selection for getting ions produced exclusively via a specific mechanism. Methane 17-21 CD4 molecule Homo sapiens 34-37 19787985-6 2005 In collisions of CH4+ with CH4 or CD4, there is significant scrambling and one would need to use differential scattering selection for getting ions produced exclusively via a specific mechanism. Methane 17-20 CD4 molecule Homo sapiens 34-37 15926547-7 2005 It has been found that the reaction steps involving CF2 are responsible for the formation of CH4. Methane 93-96 ATPase H+ transporting accessory protein 1 Homo sapiens 52-55 15755164-3 2005 Further reactions of 5 with Cp2ZrMe2 (8) and Cp2ZrHCl in toluene lead to the intermolecular elimination of CH4 and H2 and the formation of mu-O-bridged dinuclear aluminum and zirconium complexes [LAlMe(mu-O)ZrMeCp2] (6) and [LAlMe(mu-O)ZrClCp2] (7), respectively, in high yields. Methane 107-110 ceruloplasmin Homo sapiens 28-31 15614369-0 2005 A crystalline organic substrate absorbs methane under STP conditions. Methane 40-47 thyroid hormone receptor interactor 10 Homo sapiens 54-57 19785141-9 2005 These activation protocols led to VCx-ZSM5 catalysts about three times more active than those activated in pure CH4 reactants. Methane 112-115 variable charge X-linked Homo sapiens 34-37 15315423-3 2004 The presence of the polyoxometalate is presumed to allow the facile oxidation of a Pt(II) intermediate to a Pt(IV) intermediate and to aid in the addition of methane to the Pt catalytic center. Methane 158-165 activation induced cytidine deaminase Homo sapiens 135-138 16313004-0 2005 Preliminary studies on methane flux from the ornithogenic soils on Xi-sha atoll, South China Sea. Methane 23-30 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 93-96 16313004-1 2005 Methane flux from the ornithogenic soils was preliminarily measured by closed chamber method on Xi-sha atoll, South China Sea during March 10 to April 11, 2003 for the first time. Methane 0-7 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 122-125 15601617-9 2004 In the C6H6/H2/Ar system, besides C2H2, CH4, C2H4 and C2H6 were also detected, and their yields increased with increasing H2/C6H6 ratio. Methane 40-43 H2A clustered histone 19 Homo sapiens 7-17 15267839-3 2004 For isotopomers containing CH4, 13CH4, and CD4, two sets of transitions with K = 0 and one with K = 1 were recorded, correlating to the j = 0, 1, and 2 rotational levels of free methane, respectively (j is the rotational angular momentum quantum number of the methane monomer). Methane 178-185 CD4 molecule Homo sapiens 43-46 15276161-2 2004 The results of a study of the ion-molecule reactions of N(+), N(2)(+), and HCN(+) with methane, acetylene, and ethylene are reported. Methane 87-94 metastasis associated lung adenocarcinoma transcript 1 Homo sapiens 75-78 15250698-0 2004 High-temperature electrocatalysis using thermophilic P450 CYP119: dehalogenation of CCl4 to CH4. Methane 92-95 C-C motif chemokine ligand 4 Homo sapiens 84-88 15250698-5 2004 The yield of methane from the CYP119-catalyzed reduction of CCl4 is increased 35-fold from 25 degrees C to 55 degrees C. In combination with the lack of C2 products, the facility of an overall eight-electron reductive dehalogenation suggests that the substrate is constrained within the protein during electrocatalytic turnover. Methane 13-20 C-C motif chemokine ligand 4 Homo sapiens 60-64 15250683-1 2004 We present an ab initio direct dynamics trajectory study of the hydrogen abstraction reaction: H2CO+ + CD4 --> H2COD+ + CD3, with methane excited in two different distortion modes (nu4 and nu2). Methane 133-140 CD4 molecule Homo sapiens 103-106 15521181-0 2004 [The biogeochemical cycle of methane in the coastal zone and littoral of the Kandalaksha Bay of the White Sea]. Methane 29-36 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 106-109 15249000-1 2004 The structures, stability and vibrational spectra of the binary complexes CH4...HONO-trans and CH4...HONO-cis have been investigated using ab initio calculations at the SCF and MP2 levels with 6-311++G(d,p) basis set and B3LYP calculations with 6-31G(d,p) and 6-31+G(d,p) basis sets. Methane 74-77 KIT ligand Homo sapiens 169-172 15249000-1 2004 The structures, stability and vibrational spectra of the binary complexes CH4...HONO-trans and CH4...HONO-cis have been investigated using ab initio calculations at the SCF and MP2 levels with 6-311++G(d,p) basis set and B3LYP calculations with 6-31G(d,p) and 6-31+G(d,p) basis sets. Methane 74-77 tryptase pseudogene 1 Homo sapiens 177-180 15249000-1 2004 The structures, stability and vibrational spectra of the binary complexes CH4...HONO-trans and CH4...HONO-cis have been investigated using ab initio calculations at the SCF and MP2 levels with 6-311++G(d,p) basis set and B3LYP calculations with 6-31G(d,p) and 6-31+G(d,p) basis sets. Methane 95-98 KIT ligand Homo sapiens 169-172 15249000-1 2004 The structures, stability and vibrational spectra of the binary complexes CH4...HONO-trans and CH4...HONO-cis have been investigated using ab initio calculations at the SCF and MP2 levels with 6-311++G(d,p) basis set and B3LYP calculations with 6-31G(d,p) and 6-31+G(d,p) basis sets. Methane 95-98 tryptase pseudogene 1 Homo sapiens 177-180 15323515-1 2004 We have measured the adsorption of methane and ethane to high pressure on SBA-2, a structured mesoporous silica composed of spheres connected by narrow channels. Methane 35-42 WD repeat and SOCS box containing 2 Homo sapiens 74-79 15267839-4 2004 For isotopomers containing CH3D and CHD3, two K = 0 components were recorded, correlating to the j(k) = 0(0) and 1(1) rotational levels of free methane (k corresponds to the projection of j onto the C3 axis of CH3D and CHD3). Methane 144-151 chromodomain helicase DNA binding protein 3 Homo sapiens 36-40 15267839-4 2004 For isotopomers containing CH3D and CHD3, two K = 0 components were recorded, correlating to the j(k) = 0(0) and 1(1) rotational levels of free methane (k corresponds to the projection of j onto the C3 axis of CH3D and CHD3). Methane 144-151 chromodomain helicase DNA binding protein 3 Homo sapiens 219-223 15268303-0 2004 Energy transfer in Li(4p) + (Ar,H2,CH4) collisions. Methane 35-38 lipase family member N Homo sapiens 19-24 14973610-1 2004 We demonstrate here an alternative scheme for C(1) coupling by way of methane bromination, followed by concurrent bromomethane condensation and quantitative HBr neutralization; regeneration of the metal oxide with O(2) with recovery of Br(2) completes the cycle. Methane 70-77 heterogeneous nuclear ribonucleoprotein C Homo sapiens 46-50 19474906-3 2004 As an example we show how the largest absorption coefficient exhibited by methane at 3057.7cm(-1) can be accessed (amongst others) and gas plumes imaged in concentrations as low as 30ppm.m using a parametric oscillator based on periodically-poled RbTiOAsO(4) (PP-RTA). Methane 74-81 MAS related GPR family member F Homo sapiens 263-266 15198039-0 2004 [Methane content in bottom sediments and water mass of the Black Sea]. Methane 1-8 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 65-68 15198039-1 2004 The methane content in bottom sediments and water column of the Black Sea was determined using various methods of desorption and analysis of gases and various methods of calculating their concentrations. Methane 4-11 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 70-73 15198039-6 2004 In certain deep-sea regions, peaks of methane content in the 1000-1200 m horizons of the water column were revealed, which were most probably due to local influx of abyssal waters enriched with this gas. Methane 38-45 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 16-19 15198040-0 2004 [Intensities of microbial production and oxidation of methane in bottom sediments and water mass of the Black Sea]. Methane 54-61 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 110-113 15198040-1 2004 Intensities of biogeochemical (microbial) processes of methane production and methane oxidation were determined in bottom sediments and water column of the Black Sea. Methane 55-62 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 162-165 15198040-1 2004 Intensities of biogeochemical (microbial) processes of methane production and methane oxidation were determined in bottom sediments and water column of the Black Sea. Methane 78-85 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 162-165 15267276-6 2004 In agreement with previous observations, only 4% of the energy available to the products of the reaction of Cl atoms with methane was channeled into CH3 radical internal energy, and 1% into HCl rotation, with 92% ending up as translational energy. Methane 122-129 COP9 signalosome subunit 3 Drosophila melanogaster 149-152 14597150-5 2004 Furthermore, the inhibition of COX enzyme by Ch-4 was selective for COX-2 over COX-1. Methane 45-49 prostaglandin-endoperoxide synthase 2 Mus musculus 68-73 14597150-5 2004 Furthermore, the inhibition of COX enzyme by Ch-4 was selective for COX-2 over COX-1. Methane 45-49 cytochrome c oxidase I, mitochondrial Mus musculus 79-84 12728361-3 2003 The methyl radical, concomitantly released by methyl-coenzyme M (CoM), is rapidly quenched by hydrogen atom transfer from the coenzyme B (CoB) thiol group, yielding methane as the first product of the reaction. Methane 165-172 metabolism of cobalamin associated B Homo sapiens 126-136 15137422-7 2004 Methane production and content in the system were 0.3 L CH4/g VS(fed) (0.67 L CH4/g VS destroyed) and 80%, respectively, corresponding to 0.23 L CH4/g COD removal (@STP). Methane 0-7 thyroid hormone receptor interactor 10 Homo sapiens 165-168 14674778-1 2003 The mechanism and kinetics of the gas-phase selective oxidation of methane to formaldehyde (MPO) are revised in the general context of catalytic oxidations. Methane 67-74 myeloperoxidase Homo sapiens 92-95 14674778-2 2003 In agreement with ab initio calculations of the energy barrier for the activation of methane on transition metal oxide complexes, a formal Langmuir-Hinshelwood kinetic model is proposed which accounts for the "steady-state" conditions and activity-selectivity pattern of MPO catalysts, providing an original support to process design and catalyst development. Methane 85-92 myeloperoxidase Homo sapiens 271-274 18968911-2 2003 The method involves the multiphoton dissociation of methane under the influence of the high power pulsed ultraviolet laser radiation at 355 nm wavelength at room temperature (293 K) and standard pressure (1 atm). Methane 52-59 ATM serine/threonine kinase Homo sapiens 207-210 14509706-3 2003 In situ circulation of vitamin B12 and a chemical reductant has also been field tested for treatment of chlorinated methanes, ethanes, and ethenes. Methane 116-124 NADH:ubiquinone oxidoreductase subunit B3 Homo sapiens 31-34 12783540-3 2003 The temperature dependence of the EIE for oxidative addition of CH4 and CD4 differs significantly from that for coordination, with the EIE being normal at all temperatures and approaching infinity at 0 K. In contrast to oxidative addition of methane which is normal at all temperatures, the EIE for oxidative addition of H2 and D2 exhibits a transition from inverse to normal upon raising the temperature. Methane 242-249 CD4 molecule Homo sapiens 72-75 12961851-1 2003 In this paper, we determined the ratio of C13/C12 of methane in slurry gas from oil wells by the method of laser frequency modulation absorption spectroscopy that has many advantages such as high precision, high spectroscopic resolution and rapidly and simply dealing with samples. Methane 53-60 homeobox C13 Homo sapiens 42-45 12600379-3 2003 HPr was then fully degraded to methane and carbon dioxide via acetate. Methane 31-38 haptoglobin-related protein Homo sapiens 0-3 12530828-2 2003 The H1-e Pd films were shown to have high surface areas (approximately 28 m2 g(-1)) and to act as effective and stable catalysts for the detection of methane in air on heating to 500 degrees C. The response of the H1-e Pd-coated planar pellistors was found to be linearly proportional to the concentration of methane between 0 and 2.5% in air with a detection limit below 0.125%. Methane 150-157 H1.4 linker histone, cluster member Homo sapiens 4-8 12530828-2 2003 The H1-e Pd films were shown to have high surface areas (approximately 28 m2 g(-1)) and to act as effective and stable catalysts for the detection of methane in air on heating to 500 degrees C. The response of the H1-e Pd-coated planar pellistors was found to be linearly proportional to the concentration of methane between 0 and 2.5% in air with a detection limit below 0.125%. Methane 150-157 H1.4 linker histone, cluster member Homo sapiens 214-218 12530828-2 2003 The H1-e Pd films were shown to have high surface areas (approximately 28 m2 g(-1)) and to act as effective and stable catalysts for the detection of methane in air on heating to 500 degrees C. The response of the H1-e Pd-coated planar pellistors was found to be linearly proportional to the concentration of methane between 0 and 2.5% in air with a detection limit below 0.125%. Methane 309-316 H1.4 linker histone, cluster member Homo sapiens 4-8 12530828-2 2003 The H1-e Pd films were shown to have high surface areas (approximately 28 m2 g(-1)) and to act as effective and stable catalysts for the detection of methane in air on heating to 500 degrees C. The response of the H1-e Pd-coated planar pellistors was found to be linearly proportional to the concentration of methane between 0 and 2.5% in air with a detection limit below 0.125%. Methane 309-316 H1.4 linker histone, cluster member Homo sapiens 214-218 14621157-6 2003 PO4(3-) and NH4+ content significantly enhanced, and NO2- and NO3- content inhibited, both N2O and CH4 fluxes. Methane 99-102 NBL1, DAN family BMP antagonist Homo sapiens 62-65 12169733-0 2002 Microbial reefs in the Black Sea fueled by anaerobic oxidation of methane. Methane 66-73 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 29-32 12244729-0 2002 [Biogeochemical cycle of methane in the northwestern shelf of the Black Sea]. Methane 25-32 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 72-75 12244729-5 2002 The delta 13C values of methane ranged from -70.7 to -81.8@1000, demonstrating its microbial origin and contradicting the concept of the migration of methane from cold seeps or from the oil fields located at the Black Sea shelf. Methane 24-31 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 218-221 11910813-1 2002 The aragonite constructions of the Black Sea are formed in a stable anaerobic zone and are a perfect object to study the natural mechanism of anaerobic methane oxidation. Methane 152-159 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 41-44 11965370-0 2002 The mechanism of the irreversible inhibition of estrone sulfatase (ES) through the consideration of a range of methane- and amino-sulfonate-based compounds. Methane 111-118 steroid sulfatase Homo sapiens 48-65 11965370-0 2002 The mechanism of the irreversible inhibition of estrone sulfatase (ES) through the consideration of a range of methane- and amino-sulfonate-based compounds. Methane 111-118 steroid sulfatase Homo sapiens 67-69 11942842-7 2002 The resulting methyl radical is rapidly quenched by hydrogen-atom transfer from the CoB thiol group, yielding the methane molecule and the CoB radical. Methane 114-121 metabolism of cobalamin associated B Homo sapiens 84-87 10864164-6 2000 CCl4 and CH3CCl3 in the presence of a stoichiometric deficiency of sodium produced only CH4 and CH3CH3 and recovered CCl4 or CH3CCl3, respectively. Methane 88-91 C-C motif chemokine ligand 4 Homo sapiens 0-4 11800686-0 2002 Rotational motion of methane within the confines of zeolite NaCa A: molecular dynamics and ab initio calculations. Methane 21-28 nascent polypeptide associated complex subunit alpha Homo sapiens 60-64 12188534-3 2002 A maximum methane production rate of 152+/-21 mlCH4(STP)/gVS.day was obtained for the suspended sludge taken on day 70, when oleate at a concentration of 2 g COD/l was fed with a co-substrate (50% COD). Methane 10-17 sulfotransferase family 1A member 1 Homo sapiens 52-55 12188534-4 2002 The maximum plateau achieved in the methane production curve was 1145+/-307 mlCH4(STP)/gVS, obtained for the suspended sludge taken on day 162, when oleate was fed as the sole carbon source at 6 g COD/I. Methane 36-43 sulfotransferase family 1A member 1 Homo sapiens 82-85 11169041-3 2001 Methane release and methanogenic counts were suppressed by the fatty acids C12 : 0, C14 : 0 and C18 : 2 whereas C8 : 0, C10 : 0, C16 : 0 and C18 : 0 showed no corresponding effects. Methane 0-7 Bardet-Biedl syndrome 9 Homo sapiens 96-99 11233156-6 2000 Finally, phylogenetic studies indicate that only specific groups of Archaea and SRB are involved in methane oxidation. Methane 100-107 chaperonin containing TCP1 subunit 4 Homo sapiens 80-83 11605974-3 2001 Strong reagent ion signals were observed when the ionization energies of the reagents (1,3-C4H6, CS2, CH3Cl) were lower than the recombination energy (approximately 11.5 eV) of the excited state benzene ion, while the signals were negligible for reagents (CH3F,CH4) with higher ionization energy. Methane 261-264 chorionic somatomammotropin hormone 2 Homo sapiens 97-100 11720266-0 2001 Inhibition of methane oxidation by volatile sulfur compounds (CH3SH and CS2) in landfill cover soils. Methane 14-21 chorionic somatomammotropin hormone 2 Homo sapiens 72-75 11427068-2 2001 An initial model compound was constructed from a structure obtained by 300-ps molecular dynamics simulation of compound I-formed P-450cam under physiologic conditions, and it consisted of porphine for protoporphyrin IX, S(-)-CH(3) for the side chain of Cys357 of the fifth ligand of heme, a methane molecule for the substrate, a heme iron, and an oxygen atom of the sixth ligand of heme. Methane 291-298 cytochrome P450 family 4 subfamily F member 3 Homo sapiens 111-121 11389640-5 2001 The observation of a PtH(2)(+) product provides evidence that methane activation proceeds via a (H)(2)PtCH(2)(+) intermediate. Methane 62-69 parathyroid hormone Homo sapiens 21-24 11140963-2 2000 Intermolecular cyclocondensation of 1 at 110 degrees C in toluene leads, under liberation of methane, to the distorted hexameric-prismatic (AlP)6 cluster 2 in 98% yield. Methane 93-100 ATHS Homo sapiens 140-143 10458116-0 1999 Bioremediation of trichloroethylene and cis-1,2-dichloroethylene-contaminated groundwater by methane-utilizing bacteria. Methane 93-100 cytokine inducible SH2 containing protein Homo sapiens 40-45 11543516-2 2000 The results show the formation of a band at 2080 cm-1 in binary mixtures, NH3:CH4 and N2:CH4, which we attribute to HCN embedded in the organic residue formed by ion irradiation. Methane 78-81 metastasis associated lung adenocarcinoma transcript 1 Homo sapiens 116-119 11543516-2 2000 The results show the formation of a band at 2080 cm-1 in binary mixtures, NH3:CH4 and N2:CH4, which we attribute to HCN embedded in the organic residue formed by ion irradiation. Methane 89-92 metastasis associated lung adenocarcinoma transcript 1 Homo sapiens 116-119 11271989-1 2000 We have measured the sticking probability of methane excited to v = 1 of the v3 antisymmetric C-H stretching vibration on a clean Ni(100) surface as a function of rotational state (J = 0, 1, 2 and 3) and have investigated the effect of Coriolis-mixing on reactivity. Methane 45-52 immunoglobulin kappa variable 1-5 Homo sapiens 64-69 11386301-4 2000 Within 27 days of incubation, up to 0.55 to 0.67 m3 of methane (STP)/kg VS added was produced under the studied conditions. Methane 55-62 thyroid hormone receptor interactor 10 Homo sapiens 64-67 10638751-2 2000 For example, catalytic methane combustion, which generates power with reduced greenhouse-gas and nitrogen-oxide emissions, is limited by the availability of catalysts that are sufficiently active at low temperatures for start-up and are then able to sustain activity and mechanical integrity at flame temperatures as high as 1,300 degrees C. Here we use sol-gel processing in reverse microemulsions to produce discrete barium hexa-aluminate nanoparticles that display excellent methane combustion activity, owing to their high surface area, high thermal stability and the ultrahigh dispersion of cerium oxide on the their surfaces. Methane 23-30 hexosaminidase subunit alpha Homo sapiens 426-430 9750275-2 1998 When growing in shake flasks, under various methane and oxygen tensions, culture MM1 revealed the capability of a stable association consisting of one obligate methanotroph with type II intracytoplasmic membranes as the dominant strain, and four or five heterotrophs of different morphological, physiological and metabolic characteristics. Methane 44-51 prefoldin subunit 5 Homo sapiens 81-84