PMID-sentid Pub_year Sent_text compound_name comp_offset prot_official_name organism prot_offset 30010332-0 2018 Synthesis, Crystal Structure, and Optical Gap of Two-Dimensional Halide Solid Solutions CsPb2(Cl1- xBr x)5. halide 65-71 adhesion G protein-coupled receptor L1 Homo sapiens 94-97 30010332-0 2018 Synthesis, Crystal Structure, and Optical Gap of Two-Dimensional Halide Solid Solutions CsPb2(Cl1- xBr x)5. halide 65-71 RE1 silencing transcription factor Homo sapiens 99-102 29283566-8 2018 Overall, the presently introduced orbital interaction model supports the view that with bacterial strain CBDB1, an inner-sphere electron transfer from the supernucleophile B12 Co(I) to the halogen substituent of the aromatic halide is likely to represent the rate-determining step of the reductive dehalogenation. halide 225-231 mitochondrially encoded cytochrome c oxidase I Homo sapiens 176-180 29969507-1 2018 The reaction of [RhCl(CS)(PPh3)2] with excess catecholborane affords the cumulenic carbido complex [Rh2(mu-C)Cl2(PPh3)4] which undergoes phosphine and halide substitution to afford a range of complexes in which the Rh[double bond, length as m-dash]C[double bond, length as m-dash]Rh spine remains intact. halide 151-157 protein phosphatase 4 catalytic subunit Homo sapiens 26-30 29969507-1 2018 The reaction of [RhCl(CS)(PPh3)2] with excess catecholborane affords the cumulenic carbido complex [Rh2(mu-C)Cl2(PPh3)4] which undergoes phosphine and halide substitution to afford a range of complexes in which the Rh[double bond, length as m-dash]C[double bond, length as m-dash]Rh spine remains intact. halide 151-157 protein phosphatase 4 catalytic subunit Homo sapiens 113-117 29779372-6 2018 The method was implemented using a 10 x 10 micropillar array (size = 3 x 3 mm) on CFTR-expressing epithelial cells, in which CFTR chloride channel function was measured from fluorescence in response to iodide addition using a genetically encoded cytoplasmic yellow fluorescent protein halide indicator. halide 285-291 CF transmembrane conductance regulator Homo sapiens 125-129 29719069-0 2018 Controlling Magnetic and Optical Properties of the van der Waals Crystal CrCl3-x Brx via Mixed Halide Chemistry. halide 95-101 cysteine rich hydrophobic domain 1 Homo sapiens 81-84 30046015-3 2018 Here, we identified slc26a3 inhibitors in a screen of 50,000 synthetic small molecules done in Fischer rat thyroid (FRT) cells coexpressing slc26a3 and a genetically encoded halide sensor. halide 174-180 solute carrier family 26 member 3 Rattus norvegicus 20-27 29797364-1 2018 The mixed cation lead mixed halide perovskite (MLMP) Csx FA1-x PbIy Br3-y is one of the most promising candidates for both single-junction and tandem solar cells due to its high efficiency and remarkable stability. halide 28-34 FA complementation group A Homo sapiens 57-60 29423483-4 2018 The presence of two halide or bifluoride HF2- (F-H-F-) anions forming anion-pi interactions, respectively above and below the ligand tetrazine ring, is the leitmotiv of the [(H2L2)X2] (X = HF2, Cl, Br, I) complexes in the solid state, while hydrogen bonding between the anions and protonated morpholine ligand groups contributes to strengthen the anion-ligand interaction, in particular in the case of Cl- and Br-. halide 20-26 complement factor H Homo sapiens 41-44 29423483-4 2018 The presence of two halide or bifluoride HF2- (F-H-F-) anions forming anion-pi interactions, respectively above and below the ligand tetrazine ring, is the leitmotiv of the [(H2L2)X2] (X = HF2, Cl, Br, I) complexes in the solid state, while hydrogen bonding between the anions and protonated morpholine ligand groups contributes to strengthen the anion-ligand interaction, in particular in the case of Cl- and Br-. halide 20-26 complement factor H Homo sapiens 189-192 29215774-3 2018 By exciting the host semiconductor with light that resonates with its electronic transition, we find that halide-containing aryl groups can covalently bond to the sp2 carbon lattice. halide 106-112 Sp2 transcription factor Homo sapiens 163-166 29360847-3 2018 This study assessed an alternative approach, using a small scale halide assay that can be adapted for a personalized high throughput setting to analyze CFTR function of pAEC. halide 65-71 CF transmembrane conductance regulator Homo sapiens 152-156 29360847-8 2018 The halide assay was able to discriminate functional restoration of CFTR in pAECCF treated with either WT-CFTR construct or the positive controls syntaxin 8 and B-cell receptor-associated protein 31 shRNAs. halide 4-10 CF transmembrane conductance regulator Homo sapiens 68-72 29360847-8 2018 The halide assay was able to discriminate functional restoration of CFTR in pAECCF treated with either WT-CFTR construct or the positive controls syntaxin 8 and B-cell receptor-associated protein 31 shRNAs. halide 4-10 CF transmembrane conductance regulator Homo sapiens 106-110 29360847-8 2018 The halide assay was able to discriminate functional restoration of CFTR in pAECCF treated with either WT-CFTR construct or the positive controls syntaxin 8 and B-cell receptor-associated protein 31 shRNAs. halide 4-10 syntaxin 8 Homo sapiens 146-156 29360847-8 2018 The halide assay was able to discriminate functional restoration of CFTR in pAECCF treated with either WT-CFTR construct or the positive controls syntaxin 8 and B-cell receptor-associated protein 31 shRNAs. halide 4-10 B cell receptor associated protein 31 Homo sapiens 161-198 29360847-9 2018 SIGNIFICANCE: The current study demonstrates that the halide assay can be adapted for pediatric pAECCF to evaluate restoration of CFTR function. halide 54-60 CF transmembrane conductance regulator Homo sapiens 130-134 29360847-10 2018 With the ongoing development of small molecules to modulate the folding and/or activity of various mutated CFTR proteins, this halide assay presents a small-scale personalized screening platform that could assess therapeutic potential of molecules across a broad range of CFTR mutations. halide 127-133 CF transmembrane conductance regulator Homo sapiens 107-111 29360847-10 2018 With the ongoing development of small molecules to modulate the folding and/or activity of various mutated CFTR proteins, this halide assay presents a small-scale personalized screening platform that could assess therapeutic potential of molecules across a broad range of CFTR mutations. halide 127-133 CF transmembrane conductance regulator Homo sapiens 272-276 29229814-0 2017 SE2 reaction in noncarbon system: Metal-halide catalysis for dehydrogenation of ammonia borane. halide 40-46 fucosyltransferase 2 Homo sapiens 0-3 29249848-5 2017 Analysis of the crystal structures suggests that their formation is influenced by steric interactions between the p-cym and AZBTZ-NMe2 ligands: in particular, larger monodentate halide ligands favor N,C-coordination. halide 178-184 NME/NM23 nucleoside diphosphate kinase 2 Homo sapiens 130-134 29111750-3 2017 Here, we report the first demonstration of self-catalyzed vapor-liquid-solid (VLS) growth of lead halide (PbX2; X = Cl, Br, or I) NWs and conversion to LHP. halide 98-104 PBX homeobox 2 Homo sapiens 106-110 29172645-0 2017 A Homogeneous Cell-Based Halide-Sensitive Yellow Fluorescence Protein Assay to Identify Modulators of the Cystic Fibrosis Transmembrane Conductance Regulator Ion Channel. halide 25-31 CF transmembrane conductance regulator Homo sapiens 106-157 29172645-7 2017 The assay utilizes a cystic fibrosis bronchial epithelial (CFBE41o-) cell line, which was engineered to report CFTR-mediated intracellular flux of iodide by a halide-sensitive yellow fluorescence protein (YFP) reporter. halide 159-165 CF transmembrane conductance regulator Homo sapiens 111-115 28902998-4 2017 These transformations highlight the special role of the high-valent transition metal halide in substrate activation and distinguish the reactivity of the TaCl5-PPh3 system from both non-metal- and late transition metal-based frustrated Lewis pairs. halide 85-91 protein phosphatase 4 catalytic subunit Homo sapiens 160-164 29166069-0 2017 Revealing the role of thiocyanate anion in layered hybrid halide perovskite (CH3NH3)2Pb(SCN)2I2. halide 58-64 sorcin Homo sapiens 88-91 28767258-1 2017 Quasi-two-dimensional lead halide perovskites, MAn-1PbnX3n+1, are quantum confined materials with an ever-developing range of optoelectronic device applications. halide 27-33 LEM domain containing 3 Homo sapiens 47-52 28773199-6 2017 We also successfully fabricated high-performance flexible mixed lead halide perovskite solar cells based on PEN substrates. halide 69-75 proprotein convertase subtilisin/kexin type 1 inhibitor Homo sapiens 108-111 29896377-2 2017 The approach involves a metathetical exchange of the niobium-centered nucleophile (NMe4)[Nb(CO)4(kappa2-tmps)] (1) (tmps = MeSi(CH2PMe2)3) with a suitable organotetrel(ii)halide. halide 171-177 NME/NM23 nucleoside diphosphate kinase 4 Homo sapiens 83-87 28715006-4 2017 Facile substitutions of the halide with L-type ligands such as MeCN, PR3 (R = C6H5, OEt, Me), pyridine and tBuNC afford diamagnetic cations of the type [(O[double bond, length as m-dash]CNHNpySMe)Fe(CO)2(L)]+ (2a-f). halide 28-34 proteinase 3 Homo sapiens 69-72 28585275-3 2017 Herein, a novel halide exchange-driven cation exchange (HEDCE) strategy is developed to prepare dually emitting Mn-doped CsPb(Cl/Br)3 NCs via postsynthetic replacement of partial Pb in preformed perovskite NCs. halide 16-22 granzyme B Homo sapiens 121-125 28631860-0 2017 ABi2 (IO3 )2 F5 (A=K, Rb, and Cs): A Combination of Halide and Oxide Anionic Units To Create a Large Second-Harmonic Generation Response with a Wide Bandgap. halide 52-58 abl interactor 2 Homo sapiens 0-4 28512770-0 2017 Role of Halide Ions in the Nature of the Magnetic Anisotropy in Tetrahedral CoII Complexes. halide 8-14 mitochondrially encoded cytochrome c oxidase II Homo sapiens 76-80 28621540-1 2017 Simple pairwise potentials for five alkali ions and four halide ions were developed by only fitting to ab initio MP2 forces with the adaptive force matching (AFM) method. halide 57-63 tryptase pseudogene 1 Homo sapiens 113-116 28561112-1 2017 Three penta-coordinate Co2+ complexes with halide substitutes were synthesized. halide 43-49 complement C2 Homo sapiens 23-26 29166069-5 2017 Our investigation suggests that doping SCN- ions into the perovskite materials could be a promising strategy to improve the stability and mechanical properties of organic-inorganic hybrid halide perovskite compounds. halide 188-194 sorcin Homo sapiens 39-42 28509561-0 2017 Lattice and Valence Electronic Structures of Crystalline Octahedral Molybdenum Halide Clusters-Based Compounds, Cs2[Mo6X14] (X = Cl, Br, I), Studied by Density Functional Theory Calculations. halide 79-85 chorionic somatomammotropin hormone 2 Homo sapiens 112-115 28405658-0 2017 Surface passivation of mixed-halide perovskite CsPb(BrxI1-x)3 nanocrystals by selective etching for improved stability. halide 29-35 granzyme B Homo sapiens 47-51 28405658-3 2017 Here faster degradation and PL quenching are observed at higher iodine content for mixed-halide perovskite CsPb(BrxI1-x)3 nanocrystals, and a simple yet effective method is reported to significantly enhance their stability. halide 89-95 granzyme B Homo sapiens 107-111 27918110-0 2017 Magnetodielectric Response from Spin-Orbital Interaction Occurring at Interface of Ferromagnetic Co and Organometal Halide Perovskite Layers via Rashba Effect. halide 116-122 spindlin 1 Homo sapiens 32-36 28970882-2 2017 The electronic band structure of thallium halides (TlX, where X = Br and I) show a strong resemblance to lead halide perovskites, where both Pb2+ and Tl+ exhibit a 6s2 inert pair of electrons and strong spin-orbit coupling. halide 42-48 CD46 molecule Homo sapiens 51-54 28161943-0 2017 Pd-Catalyzed Conjunctive Cross-Coupling between Grignard-Derived Boron "Ate" Complexes and C(sp2) Halides or Triflates: NaOTf as a Grignard Activator and Halide Scavenger. halide 98-104 Sp2 transcription factor Homo sapiens 91-96 28191552-6 2017 In each case, despite differences in binding in the CoII state, the reaction likely proceeds via formation of a [CoXR] adduct in the CoI state that weakens the breaking carbon-halide bond, suggesting this could be a general mechanism for cobalamin-dependent dehalogenation. halide 176-182 mitochondrially encoded cytochrome c oxidase I Homo sapiens 52-55 28174041-9 2017 The overwhelming majority of the total organic halide (TOX) content is still unknown in swimming pools. halide 47-53 thymocyte selection associated high mobility group box Homo sapiens 55-58 28383061-0 2017 Triple-cation mixed-halide perovskites: towards efficient, annealing-free and air-stable solar cells enabled by Pb(SCN)2 additive. halide 20-26 growth factor independent 1 transcriptional repressor Homo sapiens 112-120 28094839-4 2017 EXPERIMENTAL APPROACH: HEK293 cells expressing YFP-F508del-CFTR, in which halide sensitive YFP is tagged to the N-terminal of CFTR, were used to screen a small library of compounds based on the VX-770 scaffold. halide 74-80 CF transmembrane conductance regulator Homo sapiens 59-63 27918110-1 2017 The spin on a ferromagnetic Co surface can interact with the asymmetric orbital on an organometal halide perovskite surface, leading to an anisotropic magnetodielectric effect. halide 98-104 spindlin 1 Homo sapiens 4-8 27975092-0 2017 Guest-tuned spin crossover in flexible supramolecular assemblies templated by a halide (Cl-, Br- or I-). halide 80-86 spindlin 1 Homo sapiens 12-16 27470912-2 2016 The halide ligands can readily be replaced by other halides or organometallic ligands giving access to a novel family of technetium(i) compounds with the robust {Tc(NO)(Cp)(PPh3)}(+) core. halide 4-10 caveolin 1 Homo sapiens 173-177 28024369-9 2016 Full tunability of the NPl emission wavelength is achieved by varying the halide ion used (bromide, iodide). halide 74-80 N-acetylneuraminate pyruvate lyase Homo sapiens 23-26 27862759-3 2016 The nickel-catalytic system displays good chemoselectivity between the two C(sp2 )-halide coupling partners, thus demonstrating a mechanistic pathway distinct from other stepwise protocols. halide 83-89 Sp2 transcription factor Homo sapiens 75-80 27541364-11 2016 Notably, the ability of macrophages expressing mutant F508del CFTR to transport halide through their membranes is compromised and can be restored by downregulation of these inherently elevated Mirs, via restoration of autophagy. halide 80-86 CF transmembrane conductance regulator Homo sapiens 62-66 27437566-3 2016 Herein, we report facile solution growth of single-crystal NWs of inorganic perovskite CsPbX3 (X = Br, Cl) and their alloys [CsPb(Br,Cl)3] and a low-temperature vapor-phase halide exchange method to convert CsPbBr3 NWs into perovskite phase CsPb(Br,I)3 alloys and metastable CsPbI3 with well-preserved perovskite crystal lattice and NW morphology. halide 173-179 granzyme B Homo sapiens 87-91 27019333-1 2016 Mercury complex of 4-(2-pyridylazo)resorcinol (PAR-2Hg(2+)), a halide-ion chemosensor, was prepared and its efficiency as a tool for high-throughput screening (HTS) of transition-metal-catalyzed coupling reactions was investigated. halide 63-69 F2R like trypsin receptor 1 Homo sapiens 47-52 27087532-1 2016 Linear two-coordinate copper complexes of cyclic (alkyl)(amino)carbenes (CAAC)CuX (X = halide) show photoluminescence with solid-state quantum yields of up to 96%; in contrast to previously reported Cu photoemitters the emission is independent of temperature over the range T = 4-300 K and occurs very efficiently by prompt rather than delayed fluorescence, with lifetimes in the sub-nanosecond range. halide 87-93 cut like homeobox 1 Homo sapiens 78-81 26898502-1 2016 Myeloperoxidase (MPO) released at sites of inflammation catalyzes the formation of the oxidants hypochlorous acid (HOCl) and hypothiocyanous acid (HOSCN) from H2O2 and halide and pseudo-halide ions. halide 168-174 myeloperoxidase Homo sapiens 0-15 26898502-1 2016 Myeloperoxidase (MPO) released at sites of inflammation catalyzes the formation of the oxidants hypochlorous acid (HOCl) and hypothiocyanous acid (HOSCN) from H2O2 and halide and pseudo-halide ions. halide 168-174 myeloperoxidase Homo sapiens 17-20 26974872-1 2016 Single crystals of K8(K5F)U6Si8O40 were grown from a mixed alkali halide flux. halide 66-72 keratin 8 Homo sapiens 19-25 27007695-5 2016 When excess halide (X = Br(-) and I(-)) are present in the precursor solution (0.3 M PbX2 and 0.9 M CH3NH3X), the exclusive binding of Pb(2+) with Br(-) results in the formation of CH3NH3PbBr3 perovskites as opposed to mixed halide perovskite. halide 12-18 PBX homeobox 2 Homo sapiens 85-89 26607991-0 2016 An Experimental and Theoretical Investigation on Pentacoordinated Cobalt(III) Complexes with an Intermediate S=1 Spin State: How Halide Ligands Affect their Magnetic Anisotropy. halide 129-135 mitochondrially encoded cytochrome c oxidase III Homo sapiens 73-76 26866384-5 2016 Emission decay measurement and TD-DFT calculation suggested that the luminescence of Cu-X could be assigned to phosphorescence from the triplet metal-to-ligand charge-transfer ((3)MLCT) excited state, effectively mixed with the halide-to-ligand charge-transfer ((3)XLCT) excited state, at 77 K. The source of emission changed to thermally activated delayed fluorescence (TADF) with the same electronic transition nature at room temperature. halide 228-234 cut like homeobox 1 Homo sapiens 85-89 26607991-4 2016 In this context, we report a unique series of halide Co(III) complexes, [CoL(X)], with X=Cl, Br, I (CoX) and L=2,2"-(2,2"-bipyridine-6,6"-diyl)bis(1,1-diphenylethanethiolate), which possess a rare intermediate S=1 spin ground state. halide 46-52 mitochondrially encoded cytochrome c oxidase III Homo sapiens 53-60 26607991-7 2016 Their coordination sphere displays a distorted pentacoordinated square pyramidal geometry, with the halide located in the Co(III) axial position. halide 100-106 mitochondrially encoded cytochrome c oxidase III Homo sapiens 122-129 27064894-1 2015 The addition of AlCl3 to four-coordinate boranes of the general formula (C-N-chelate)BCl2 results in halide abstraction and formation of three-coordinate borenium cations of the general formula [(C-N-chelate)BCl]+. halide 101-107 BCL2 apoptosis regulator Homo sapiens 85-89 29861975-5 2016 The fluoride ligand of [TpBut,Me]MgF undergoes halide exchange with Me3SiX (X = Cl, Br, I) to afford [TpBut,Me]MgX and Me3SiF. halide 47-53 signal transducer and activator of transcription 5A Homo sapiens 33-36 26747811-1 2016 The ionic stochastic motions in the molten alkali halide NaF are investigated by quasielastic neutron scattering and first principles molecular dynamics simulation. halide 50-56 C-X-C motif chemokine ligand 8 Homo sapiens 57-60 26579678-3 2015 MPO is the antigen against which anti-MPO ANCAs are directed, the antigen to which pathogenic T cells that can induce antibody-independent AAV are directed, and MPO can induce glomerular injury directly by interacting with H2O2 and a halide to halogenate glomerular structures. halide 234-240 myeloperoxidase Homo sapiens 0-3 26233143-18 2015 In addition to the chemical potentials in solution used to obtain the activity coefficients, we also calculated the chemical potentials of salt crystals and used them to obtain the solubility of these alkali halide models in SPC/E water. halide 208-214 proline rich protein gene cluster Homo sapiens 225-228 26148842-2 2015 The binding is up to (3.6 +- 0.2) x 10(10) M(-1) in acetonitrile (for pentafoil knot [2 Cl](PF6)9), making these topologically complex host molecules some of the strongest synthetic noncovalent binders of halide anions measured to date, comparable in chloride ion affinity to silver salts. halide 205-211 sperm associated antigen 17 Homo sapiens 92-97 25647179-9 2015 Halide complexes [Re(X)(CO)3(bpy)] (X = Cl, Br, or I; bpy = 2,2"-bipyridine) exhibit complex electronic structure and large spin-orbit effects that do not correlate with the heavy atom effects. halide 0-6 spindlin 1 Homo sapiens 124-128 26049507-0 2015 Equations of state of anhydrous AlF3 and AlI3: Modeling of extreme condition halide chemistry. halide 77-83 adhesion molecule with Ig like domain 3 Homo sapiens 41-45 25747363-4 2015 Adsorbable organic halide (AOX) formation was significant when applying the UV/chlorine process in water that had not been previously chlorinated, while little additional formation was observed in prechlorinated water. halide 19-25 acyl-CoA oxidase 1 Homo sapiens 27-30 25637676-4 2015 Computational analysis of the interactions between the ligands and ERalpha-LBD demonstrated positive contribution of halide to binding properties. halide 117-123 estrogen receptor 1 Rattus norvegicus 67-74 25410496-2 2015 The bis-copper(I) chloride, bis-silver(I) chloride and bis-copper(I) bromide adducts of IMes PPh crystallize as halide ion bridged octanuclear molecules while the [IMes PPh](AuCl)2 adduct remains monomeric. halide 112-118 enolase 1 Homo sapiens 93-96 25531406-13 2015 The ratio of unknown total organic halide (UTOX) to TOX was substantially lower in the hot tap water as the THM to TOX ratio became correspondingly larger. halide 35-41 thymocyte selection associated high mobility group box Homo sapiens 44-47 25867140-5 2015 Here rapid methods are described for purification and functional reconstitution of the full-length CFTR protein into proteoliposomes of defined lipid composition that retains activity as a regulated halide channel. halide 199-205 CF transmembrane conductance regulator Homo sapiens 99-103 25531406-13 2015 The ratio of unknown total organic halide (UTOX) to TOX was substantially lower in the hot tap water as the THM to TOX ratio became correspondingly larger. halide 35-41 nuclear RNA export factor 1 Homo sapiens 91-94 25479082-1 2015 A direct and practical synthetic route to N-heterocyclic carbene copper complexes of [(NHC)CuX] (X = halide) and [(NHC)2Cu]PF6 types using commercially available copper powder is described. halide 101-107 cut like homeobox 1 Homo sapiens 91-94 25565062-8 2015 A discussion of the relevant analytical characteristics is presented herein, followed by a demonstration of halide assessment in water samples (sea, tap, river, and mineral waters) and food supplements enriched with iodide and chloride as early examples. halide 108-114 nuclear RNA export factor 1 Homo sapiens 149-152 25376759-10 2015 Halide abstraction afforded the dicationic bis-chelated octahedral Fe(II) complex [Fe(kappa(3)-P,N,P-PNP)2](2+) together with the free SNP ligand rather than [Fe(kappa(3)-P,N,P-PNP-nPr)(kappa(3)-S,P,N-PNS-nPr)](2+). halide 0-6 neuronal pentraxin receptor Homo sapiens 181-184 25376759-10 2015 Halide abstraction afforded the dicationic bis-chelated octahedral Fe(II) complex [Fe(kappa(3)-P,N,P-PNP)2](2+) together with the free SNP ligand rather than [Fe(kappa(3)-P,N,P-PNP-nPr)(kappa(3)-S,P,N-PNS-nPr)](2+). halide 0-6 neuronal pentraxin receptor Homo sapiens 205-208 25404061-5 2015 Treatment of [ClP(mu-NTer)2AsCl] with a halide-abstracting agent led to the novel cyclic cation [P(mu-NTer)2AsCl](+), while reduction with magnesium afforded the first arsaphosphadiazanediyl [P(mu-NTer)2As]. halide 40-46 calmodulin like 3 Homo sapiens 14-17 25265516-0 2014 Niobium(V) and tantalum(V) halide chalcogenoether complexes--towards single source CVD precursors for ME2 thin films. halide 27-33 malic enzyme 2 Homo sapiens 102-105 25459065-3 2015 Pd(PPh3)4 was demonstrated to be an effective catalyst for cross-coupling with on-DNA halide substrates under aqueous conditions. halide 86-92 caveolin 1 Homo sapiens 3-7 25294414-1 2014 The gas-phase structures of two halide-bound phenylalanine anions (PheX(-), X = Cl(-) or Br(-)) and five fluorinated derivatives have been identified using infrared multiple photon dissociation (IRMPD) spectroscopy. halide 32-38 phosphate regulating endopeptidase homolog X-linked Homo sapiens 67-71 26279325-4 2015 The microbicidal activity of MPO exists due to its capability to oxidize halide and pseudohalide ions (CI(-), Br(-), I(-) and SCN(-)) by H2O2, thereby producing respective hypohalous acids (HOX). halide 73-79 myeloperoxidase Homo sapiens 29-32 25347523-6 2014 The relevance of these results to the general question of the coordination geometry of MX2 and M(C5R5)2 (M = heavy alkaline earth and Ln(II), X = halide, and C5R5 = bulky persubstituted cyclopentadienyl) complexes and the importance of secondary H-bonding and nonbonding interactions on the structure are highlighted. halide 146-152 MX dynamin like GTPase 2 Homo sapiens 87-90 25315854-5 2014 By increasing the applied potential, halide ions present in the thin-layer sample (X(-)) are electrodeposited on the working electrode as AgX, while their respective counterions are transported across the perm-selective membrane to an outer solution. halide 37-43 UDP-N-acetylglucosamine pyrophosphorylase 1 Homo sapiens 138-141 25220078-7 2014 Chloride flux assays using halide-sensitive YFP revealed that TMEM16A is functionally involved in Ca(2+) -dependent Cl(-) secretion in NCL-SG3 cells. halide 27-33 anoctamin 1 Homo sapiens 62-69 25220078-7 2014 Chloride flux assays using halide-sensitive YFP revealed that TMEM16A is functionally involved in Ca(2+) -dependent Cl(-) secretion in NCL-SG3 cells. halide 27-33 nucleolin Homo sapiens 135-138 25316343-1 2014 The prospects of a control for a novel gallium nitride pseudo-halide vapor phase epitaxy (PHVPE) with HCN were thoroughly analyzed for hydrocarbons-NH3-Ga gas phase on the basis of quantum chemical investigation with DFT (B3LYP, B3LYP with D3 empirical correction on dispersion interaction) and ab-initio (CASSCF, coupled clusters, and multireference configuration interaction including MRCI+Q) methods. halide 62-68 metastasis associated lung adenocarcinoma transcript 1 Homo sapiens 102-105 25264809-5 2014 On the basis of these observations, a new class of Rh2 complexes, supported by CO ligands, has been prepared, allowing for the isolation and independent characterization of the proposed halide-bridged intermediates. halide 186-192 Rh associated glycoprotein Homo sapiens 51-54 24715057-1 2014 Net reductive elimination (RE) of MeX (X = halide or pseudo-halide: Cl(-), CF3CO2(-), HSO4(-), OH(-)) is an important step during Pt-catalyzed hydrocarbon functionalization. halide 43-49 zinc finger SWIM-type containing 2 Homo sapiens 34-37 24990084-1 2014 The [Pd(dppp)(OTf)2] complex acts as an efficient transporter of halide anions, in particular the biologically relevant chloride anion, across a phospholipid bilayer. halide 65-71 POU class 2 homeobox 2 Homo sapiens 14-19 26277971-4 2014 We also assess the role of spin-orbit coupling and show that it causes slight changes in lead-halide bonding that do not significantly affect the lattice parameters. halide 94-100 spindlin 1 Homo sapiens 27-31 25192004-3 2014 The solvated MeOH or EtOH molecules occupy vacant space, giving contacts with [1-4](2+), and connects to the Hal(-) ion through a hydrogen bridge via the H(1O)O(1S) H atom forming, by means of the Hal(-) HOR (Hal = Cl, Br) contact, the halide-alcohol cluster. halide 238-244 histidine ammonia-lyase Homo sapiens 109-112 25192004-3 2014 The solvated MeOH or EtOH molecules occupy vacant space, giving contacts with [1-4](2+), and connects to the Hal(-) ion through a hydrogen bridge via the H(1O)O(1S) H atom forming, by means of the Hal(-) HOR (Hal = Cl, Br) contact, the halide-alcohol cluster. halide 238-244 histidine ammonia-lyase Homo sapiens 197-200 25192004-3 2014 The solvated MeOH or EtOH molecules occupy vacant space, giving contacts with [1-4](2+), and connects to the Hal(-) ion through a hydrogen bridge via the H(1O)O(1S) H atom forming, by means of the Hal(-) HOR (Hal = Cl, Br) contact, the halide-alcohol cluster. halide 238-244 histidine ammonia-lyase Homo sapiens 197-200 25137532-5 2014 Herein, a new family of phosphazane-bridged Rh2 photocatalysts has been developed where the halide-bridged geometry is designed into the ground state. halide 92-98 Rh associated glycoprotein Homo sapiens 44-47 25137532-10 2014 H2 evolution from both HCl and HBr proceeds with a halide-bridged Rh2 hydride photoresting state. halide 51-57 Rh associated glycoprotein Homo sapiens 66-69 24715057-1 2014 Net reductive elimination (RE) of MeX (X = halide or pseudo-halide: Cl(-), CF3CO2(-), HSO4(-), OH(-)) is an important step during Pt-catalyzed hydrocarbon functionalization. halide 60-66 zinc finger SWIM-type containing 2 Homo sapiens 34-37 24450965-4 2014 Block-localized wave function (BLW) computations confirm that pi-conjugation lowers the net activation barriers of SN2 allyl (1t, coplanar), benzyl, propargyl, and acetonitrile halide identity exchange reactions, but does so to nearly the same extent. halide 177-183 solute carrier family 38 member 5 Homo sapiens 115-118 24813619-9 2014 Halide abstraction from 6 afforded the monocationic, tetranuclear complex [{Pd(dmba)}2(mu-L){Pd(dmba)}2(mu-Cl)]PF6 (7) in which the two Pd(dmba) moieties are connected by ligand L and a bridging chloride. halide 0-6 sperm associated antigen 17 Homo sapiens 111-114 24632382-1 2014 Myeloperoxidase is an important heme enzyme released by activated leukocytes that catalyzes the reaction of hydrogen peroxide with halide and pseudo-halide ions to form various hypohalous acids. halide 131-137 myeloperoxidase Homo sapiens 0-15 24880379-2 2014 We demonstrate that the simple method is effective for the samples from 100 mum to 16 mum in size using alkali halide crystals as a model system. halide 111-117 latexin Homo sapiens 76-79 24880379-2 2014 We demonstrate that the simple method is effective for the samples from 100 mum to 16 mum in size using alkali halide crystals as a model system. halide 111-117 latexin Homo sapiens 86-89 24519659-2 2014 Depending on the halide substituents, the double H-bond involved a nonconventional C H O interaction with either a H CXn (n=1-2, X=Cl, Br) or a H CAr bond (X=F), as shown in the solid-state crystal structures and by molecular modeling. halide 17-23 NHS actin remodeling regulator Homo sapiens 119-122 24878029-7 2014 Using higher energy resolution data we have also extracted the time-resolved spectra from excitons in an alkali halide, BaF2. halide 112-118 BANF family member 2 Homo sapiens 120-124 24598911-1 2014 A sparse-matrix screen for new crystallization conditions for the USP7 catalytic domain (USP7CD) led to the identification of a condition in which crystals grow reproducibly in 24-48 h. Variation of the halide metal, growth temperature and seed-stock concentration resulted in a shift in space group from P21 with two molecules in the asymmetric unit to C2 with one molecule in the asymmetric unit. halide 203-209 ubiquitin specific peptidase 7 Homo sapiens 66-70 24053146-4 2014 Although SCN(-) is the physiological substrate of LPO, the Duox/LPO/halide system can generate hypoiodous acid when the iodide (I(-)) concentration is elevated in ASL. halide 68-74 lactoperoxidase Homo sapiens 64-67 24393028-3 2014 For half a century, the halide chemistry of technetium has been defined by three compounds: TcF6, TcF5, and TcCl4. halide 24-30 transcription factor A, mitochondrial Homo sapiens 92-96 24393028-3 2014 For half a century, the halide chemistry of technetium has been defined by three compounds: TcF6, TcF5, and TcCl4. halide 24-30 CCAAT enhancer binding protein beta Homo sapiens 98-102 22810731-5 2014 Indeed, at the site of inflammation, taurine is known to react with and detoxify hypochlorous acid generated by the neutrophil myeloperoxidase (MPO)-halide system. halide 149-155 myeloperoxidase Homo sapiens 127-142 22810731-5 2014 Indeed, at the site of inflammation, taurine is known to react with and detoxify hypochlorous acid generated by the neutrophil myeloperoxidase (MPO)-halide system. halide 149-155 myeloperoxidase Homo sapiens 144-147 24194519-10 2013 HX1 was a mixed-type inhibitor of the halogenation activity of MPO with respect to both hydrogen peroxide and halide. halide 110-116 myeloperoxidase Homo sapiens 63-66 24504973-3 2014 The inhibition or the absence of the MPO-H2O2-halide system results in marked reduction in PMN killing of a variety of microbes, implicating its relative prominence in the hierarchy of PMN antimicrobial systems. halide 46-52 myeloperoxidase Homo sapiens 37-40 24113062-2 2013 Structure-activity data generated from both syn- and anti-aldol precursors provides significant insights into the requirements for enhanced potency, validating this novel ketone-to-aryl halide bioisostere hypothesis. halide 186-192 synemin Homo sapiens 44-47 24187915-1 2013 Halide-bridged rhombic dicopper(I) complexes, [Cu2(mu-X)2(DMSO)2(PPh3)2] (X = I(-), Br(-); DMSO = dimethyl sulfoxide; PPh3 = triphenylphosphine), were synthesized, the iodide complex of which exhibited interesting photochromic luminescence driven by photoirradiation and by exposure to DMSO vapor in the solid state. halide 0-6 caveolin 1 Homo sapiens 65-69 24187915-1 2013 Halide-bridged rhombic dicopper(I) complexes, [Cu2(mu-X)2(DMSO)2(PPh3)2] (X = I(-), Br(-); DMSO = dimethyl sulfoxide; PPh3 = triphenylphosphine), were synthesized, the iodide complex of which exhibited interesting photochromic luminescence driven by photoirradiation and by exposure to DMSO vapor in the solid state. halide 0-6 caveolin 1 Homo sapiens 118-122 23794083-10 2013 Our de novo LJP measurements of biionic combinations of the above undiluted salts, and NaI and NaF (with halide anions I- and F-), generally also gave excellent agreement with predicted values. halide 105-111 C-X-C motif chemokine ligand 8 Homo sapiens 95-98 24147984-5 2013 However, effect of F(-) or other halide ions on hERG channel properties has not been studied in detail. halide 33-39 ETS transcription factor ERG Homo sapiens 48-52 23802505-5 2013 The resulting aryl halide surfaces were activated using [Pd(PPh3)4] as a catalyst. halide 19-25 caveolin 1 Homo sapiens 60-64 23463616-2 2013 CFTR-dependent iodide transport measured by fluorescent quenching of ectopically expressed halide-sensitive yellow fluorescent protein (YFP) is widely being used to study CFTR function by microscopy or plate readers. halide 91-97 CF transmembrane conductance regulator Homo sapiens 0-4 23463616-2 2013 CFTR-dependent iodide transport measured by fluorescent quenching of ectopically expressed halide-sensitive yellow fluorescent protein (YFP) is widely being used to study CFTR function by microscopy or plate readers. halide 91-97 CF transmembrane conductance regulator Homo sapiens 171-175 23652950-2 2013 Taurine chloramine (Tau-Cl) is produced in polymorphonuclear leukocytes via the myeloperoxidase/halide system. halide 96-102 myeloperoxidase Mus musculus 80-95 22988949-3 2012 In the trinuclear complexes, the halide-bearing iron site sits in approximate trigonal-bipyramidal (tbp) geometry, formed by two ((Ph)L) anilides and an exogenous solvent molecule. halide 33-39 TATA-box binding protein Homo sapiens 100-103 23401229-2 2013 Key steps of the syntheses of the sulfanes are the photochemical trifluoromethylation of the thiols with CF3 Hal (Hal=halide) or substitution of alkoxyphosphinediamines with CF3 SSCF3 . halide 118-124 histidine ammonia-lyase Homo sapiens 114-117 23183829-13 2013 Taken together, it is likely that AQP6 permeates halide group anions as a Hg2+-sensitive anion channel in rat parotid secretory granules. halide 49-55 aquaporin 6 Rattus norvegicus 34-38 22890747-1 2013 MP2(full)/aug-cc-pVDZ(-PP) computations predict that new triangular bonding complexes CBr4...X-...H-C (where X- is a halide and H-C refers to a protic solvent molecule) consist of one halogen bond and two hydrogen bonds in the gas phase. halide 117-123 carbonyl reductase 4 Homo sapiens 86-90 22998521-0 2012 Halide ordering in reduced mixed halides, chlorides/iodides, of zirconium: syntheses and structures of Cs2[(Zr6B)(Cl,I)15] cluster compounds. halide 0-6 chorionic somatomammotropin hormone 2 Homo sapiens 103-106 23293095-3 2013 Halide abstraction from 1 a afforded [(kappa(3)-P,N,O-Mor-DalPhos)Pd(Ph)]OTf (5), bringing to light a potential stabilizing interaction that is offered by Mor-DalPhos. halide 0-6 opioid receptor mu 1 Homo sapiens 54-57 23293095-3 2013 Halide abstraction from 1 a afforded [(kappa(3)-P,N,O-Mor-DalPhos)Pd(Ph)]OTf (5), bringing to light a potential stabilizing interaction that is offered by Mor-DalPhos. halide 0-6 opioid receptor mu 1 Homo sapiens 155-158 23134573-4 2012 This sensing system exhibits a remarkably high selectivity toward halide ions over most of anions and cations and shows good linear ranges and lower detection limits: the linear ranges are 0.5-80 muM for Cl(-), 0.1-14 muM for Br(-), and 0.05-6 muM for I(-), respectively; the limits of detection for Cl(-), Br(-), and I(-), at a signal-to-noise ratio of 3, are estimated to be 200, 65, and 40 nM, respectively. halide 66-72 latexin Homo sapiens 196-199 23134573-4 2012 This sensing system exhibits a remarkably high selectivity toward halide ions over most of anions and cations and shows good linear ranges and lower detection limits: the linear ranges are 0.5-80 muM for Cl(-), 0.1-14 muM for Br(-), and 0.05-6 muM for I(-), respectively; the limits of detection for Cl(-), Br(-), and I(-), at a signal-to-noise ratio of 3, are estimated to be 200, 65, and 40 nM, respectively. halide 66-72 latexin Homo sapiens 218-221 23134573-4 2012 This sensing system exhibits a remarkably high selectivity toward halide ions over most of anions and cations and shows good linear ranges and lower detection limits: the linear ranges are 0.5-80 muM for Cl(-), 0.1-14 muM for Br(-), and 0.05-6 muM for I(-), respectively; the limits of detection for Cl(-), Br(-), and I(-), at a signal-to-noise ratio of 3, are estimated to be 200, 65, and 40 nM, respectively. halide 66-72 latexin Homo sapiens 218-221 22817529-3 2012 Spin-orbit excited-state calculations interpret their electronic absorption spectra as arising from a bunch of spin mixed states with a singlet component of only 50-90% (depending on the halide), and attribute the phosphorescence decay to thermal population of spin-mixed states with a substantial singlet character. halide 187-193 spindlin 1 Homo sapiens 0-4 22988949-5 2012 Zero-field, (57)Fe Mossbauer analysis reveals the diiron unit as the locus of oxidation, while the tbp site bearing the halide ligand remains divalent. halide 120-126 TATA-box binding protein Homo sapiens 99-102 22886133-0 2012 Substrate inhibition competes with halide inhibition in polyphenol oxidase. halide 35-41 protoporphyrinogen oxidase Homo sapiens 56-74 22886133-4 2012 Halides inhibit PPO activity in such a way that substrate inhibition is lessened when halide concentration is increased. halide 86-92 protoporphyrinogen oxidase Homo sapiens 16-19 22348603-2 2012 MPO is released by activated neutrophils, monocytes and some tissue macrophages, where it catalyses the conversion of hydrogen peroxide to hypohalous acids (HOX; X = Cl, Br, SCN) in the presence of halide and pseudo-halide ions. halide 198-204 myeloperoxidase Homo sapiens 0-3 22703526-6 2012 (1)H NMR and fluorescence spectroscopic titration experiments with a variety of anions in the competitive CD(3)OD/D(2)O (9:1) aqueous solvent mixture demonstrated the bromo- and syn iodo-imidazoliophane XB receptors to bind selectively iodide and bromide respectively, and sense these halide anions exclusively via a fluorescence response. halide 285-291 synemin Homo sapiens 178-181 22389542-1 2012 The most abundant geometries and relative stabilities of alkali halide clusters with a (XY)(n) (o) configuration (e.g., LiF, NaCl, KBr) are described. halide 64-70 LIF interleukin 6 family cytokine Homo sapiens 120-123 22252835-3 2012 For the halogenated cyclophane receptors 1 and 2, the halide ions are held by a bidentate array of halogen bonds (C-Br/C-I...X(-)), while multiple hydrogen-bonding interactions (C-H...X(-)) are present in the complexes of the nonhalogenated macrocyclic receptor 3. halide 54-60 cannabinoid receptor 1 Homo sapiens 114-118 21977976-0 2011 Luminescent copper(I) halide adducts of [Au(im(CH2py)2)2]PF6 exhibiting short Au(I) Cu(I) separations and unusual semibridging NHC ligands. halide 22-28 sperm associated antigen 17 Homo sapiens 57-60 21645494-5 2011 TMEM16A(0) expression is associated with Ca(2+)-activated Cl(-) channel activity as measured by three different functional assays based on the halide-sensitive yellow fluorescent protein, short-circuit current recordings, and patch-clamp technique. halide 143-149 anoctamin 1 Homo sapiens 0-7 22003826-2 2011 Hence, the total organic halide (TOX) measurement is used as a surrogate for toxic disinfection byproducts. halide 25-31 thymocyte selection associated high mobility group box Homo sapiens 33-36 21894921-0 2011 Nature of halide binding to the molybdenum site of sulfite oxidase. halide 10-16 sulfite oxidase Homo sapiens 51-66 21366549-9 2011 A cAMP-dependent increase in membrane permeability to halide was detected in resveratrol-treated CFPAC1 cells, and was inhibited by a selective inhibitor of CFTR. halide 54-60 CF transmembrane conductance regulator Homo sapiens 157-161 21276939-3 2011 Their mechanism for inhibition of TG2 is based on halide displacement, resulting in the formation of a stable imino thioether. halide 50-56 transglutaminase 2 Homo sapiens 34-37 21242622-0 2011 Growth of GaN nanotubes by halide vapor phase epitaxy. halide 27-33 gigaxonin Homo sapiens 10-13 21222447-4 2011 However, 1 readily reacts, with loss of its halide, in a selective, covalent, and irreversible manner with the active-site Cys249 of DDAH. halide 44-50 dimethylarginine dimethylaminohydrolase 1 Homo sapiens 133-137 21711888-4 2011 We proposed that the strong binding between Cd2+ and halide ions reduced the reactivity of the precursors, decreased the nuclei formed in the nucleation stage, and led to the high concentration of precursor in the growth stage, resulting in the increase of size and phase transformation of CdS nanocrystals. halide 53-59 CD2 molecule Homo sapiens 44-47 21141844-3 2011 Interestingly, the Cu(I) atoms within the Cu(3) units in 1-5 behave as coordinatively unsaturated pi-acid centers to contact soft halide/pseudohalide X atoms of CuX and Cu(2)X(2) motifs, which lead to novel sandwich substructures of [(Cu(3))(Cu(2)X(2))(Cu(3))] (X = Br, I, and SCN) in 2-4. halide 130-136 cut like homeobox 1 Homo sapiens 161-164 22039673-1 2011 Taurine chloramine (TauCl) is generated at the site of inflammation as a result of reaction of taurine with hypochlorous acid (HOCl), the product of myeloperoxidase-halide system of neutrophils. halide 165-171 myeloperoxidase Homo sapiens 149-164 22178883-6 2011 In HEK293 cells coexpressing TMEM16A and CFTR, whole cell currents activated by IMBX and forskolin were significantly reduced when compared with cells expressing CFTR only, while the halide permeability sequence of CFTR was not changed. halide 183-189 anoctamin 1 Homo sapiens 29-36 22178883-6 2011 In HEK293 cells coexpressing TMEM16A and CFTR, whole cell currents activated by IMBX and forskolin were significantly reduced when compared with cells expressing CFTR only, while the halide permeability sequence of CFTR was not changed. halide 183-189 CF transmembrane conductance regulator Homo sapiens 41-45 21594775-3 2011 A convenient assay for CFTR function is based on the halide sensitivity of the yellow fluorescent protein (YFP). halide 53-59 CF transmembrane conductance regulator Homo sapiens 23-27 20228064-3 2010 Exposure of SP-D to the complete MPO-H(2)O(2)-halide system caused loss of SP-D-dependent aggregating activity. halide 46-52 surfactant associated protein D Mus musculus 12-16 21049941-4 2010 Facile conversion of these precursors to halide-free spinodal form of Ta(5+)-doped TiO(2)-SnO(2) as a potential thermoelectric material is reported. halide 41-47 strawberry notch homolog 1 Homo sapiens 90-93 21050065-5 2010 With the adapted Fischer rat thyroid-yellow fluorescent protein halide flux assay to the combination high-throughput screening platform, we identified many interesting single agents as CFTR modulators from a library of approved drugs and mechanistic probe compounds, and combinations that synergistically modulate F508del-CFTR channel function in Fischer rat thyroid cells, demonstrating the potential for combination therapeutics to address the defects that cause CF. halide 64-70 CF transmembrane conductance regulator Rattus norvegicus 185-189 21050066-4 2010 A functional assay with cells expressing F508del CFTR has been previously described by others using genetically engineered halide-sensitive yellow fluorescent protein to screen for CFTR modulators. halide 123-129 CF transmembrane conductance regulator Homo sapiens 49-53 21050066-4 2010 A functional assay with cells expressing F508del CFTR has been previously described by others using genetically engineered halide-sensitive yellow fluorescent protein to screen for CFTR modulators. halide 123-129 CF transmembrane conductance regulator Homo sapiens 181-185 20580059-2 2010 The formation of trihalomethanes (THMs), haloacetic acids (HAAs), and total organic halide (TOX) upon chlorination of untreated water, and after conventional treatment, granular activated carbon treatment, and nanofiltration were quantified using ANNs. halide 84-90 thymocyte selection associated high mobility group box Homo sapiens 92-95 20228064-3 2010 Exposure of SP-D to the complete MPO-H(2)O(2)-halide system caused loss of SP-D-dependent aggregating activity. halide 46-52 myeloperoxidase Mus musculus 33-36 20228064-3 2010 Exposure of SP-D to the complete MPO-H(2)O(2)-halide system caused loss of SP-D-dependent aggregating activity. halide 46-52 surfactant associated protein D Mus musculus 75-79 23710112-6 2010 Six of the reported analogues had low micromolar potency for increasing halide transport in DeltaF508-CFTR cells. halide 72-78 CF transmembrane conductance regulator Homo sapiens 102-106 19968966-1 2010 The heme peroxidase enzyme myeloperoxidase (MPO) is released by activated neutrophils and monocytes, where it uses hydrogen peroxide (H(2)O(2)) to catalyze the production of the potent oxidants hypochlorous acid (HOCl), hypobromous acid (HOBr) and hypothiocyanous acid (HOSCN) from halide and pseudohalide (SCN(-)) ions. halide 282-288 myeloperoxidase Homo sapiens 27-42 19968966-1 2010 The heme peroxidase enzyme myeloperoxidase (MPO) is released by activated neutrophils and monocytes, where it uses hydrogen peroxide (H(2)O(2)) to catalyze the production of the potent oxidants hypochlorous acid (HOCl), hypobromous acid (HOBr) and hypothiocyanous acid (HOSCN) from halide and pseudohalide (SCN(-)) ions. halide 282-288 myeloperoxidase Homo sapiens 44-47 19968966-3 2010 It is shown here that acetaminophen (paracetamol), a phenol-based drug with analgesic and antipyretic actions, is an efficient inhibitor of HOCl and HOBr generation by isolated MPO-H(2)O(2)-halide systems. halide 190-196 myeloperoxidase Homo sapiens 177-180 20089668-0 2010 CFTR-mediated halide transport in phagosomes of human neutrophils. halide 14-20 CF transmembrane conductance regulator Homo sapiens 0-4 20369749-4 2010 Oxidative stress (OS) is the main element in this modification and the most significant is the myeloperoxidase/H2O2/halide system. halide 116-122 myeloperoxidase Homo sapiens 95-110 21832347-3 2009 In contrast to the case for alkaline earth fluoride crystals with fluorite structure, the luminescence of the singlet STEs in MgF(2) shows smaller Stokes shift than that of the triplet STEs, which is similar to "typical" behavior observed for alkali halide crystals. halide 250-256 signal transducer and activator of transcription 5A Homo sapiens 126-129 19785436-2 2009 Screening of approximately 110000 small synthetic and natural compounds for inhibition of halide influx in CFTR-expressing epithelial cells yielded a new class of pyrimido-pyrrolo-quinoxalinedione (PPQ) CFTR inhibitors. halide 90-96 CF transmembrane conductance regulator Homo sapiens 107-111 19785436-2 2009 Screening of approximately 110000 small synthetic and natural compounds for inhibition of halide influx in CFTR-expressing epithelial cells yielded a new class of pyrimido-pyrrolo-quinoxalinedione (PPQ) CFTR inhibitors. halide 90-96 CF transmembrane conductance regulator Homo sapiens 203-207 19880323-4 2009 In particular, we evaluated the ability of novel DHPs to enhance the activity of the rescued DeltaF508-CFTR as measured with a functional assay based on the halide-sensitive yellow fluorescent protein. halide 157-163 CF transmembrane conductance regulator Homo sapiens 103-107 19809748-8 2009 The cation [Rh(CO)(PPh3){B(taz)3}]+ reacts with [NBu(n)(4)]I to give [Rh(PPh3)I{B(taz)3}], in which the halide is trans to the Rh-B bond, and a second species, possibly [Rh(CO)I{B(taz)3}]. halide 104-110 protein phosphatase 4 catalytic subunit Homo sapiens 19-23 19809748-8 2009 The cation [Rh(CO)(PPh3){B(taz)3}]+ reacts with [NBu(n)(4)]I to give [Rh(PPh3)I{B(taz)3}], in which the halide is trans to the Rh-B bond, and a second species, possibly [Rh(CO)I{B(taz)3}]. halide 104-110 protein phosphatase 4 catalytic subunit Homo sapiens 73-77 19099445-9 2009 Examination of the kinetics of halide release and decay of the 3-ketone intermediate catalyzed by wild-type and mutant LuxS enzymes revealed that Cys-84 is the general base responsible for proton abstraction in the three reaction steps, whereas Glu-57 likely facilitates substrate binding and proton transfer during catalysis. halide 31-37 Lutheran suppressor, X-linked Homo sapiens 119-123 19474308-8 2009 TMEM16B confers Ca(2+)-dependent chloride currents when overexpressed in mammalian cells as measured by halide sensitive fluorescent protein assays and whole-cell patch-clamp recordings. halide 104-110 anoctamin 2 Homo sapiens 0-7 19320492-6 2009 Except for methyliodosilane, halide substitution leads to an increase in the Si-C BDE in comparison to the Si-C BDE in methylsilane of 86.9 kcal/mol at 0 K. Unlike the methylhalosilanes, the halomethylsilanes all show a decrease in the Si-C BDE when compared to the Si-C BDE in methylsilane. halide 29-35 homeobox D13 Homo sapiens 82-85 19544505-3 2009 The presence of a cyano group leads in some cases to competitive reduction of the organic halide to the corresponding ArH compound. halide 90-96 low density lipoprotein receptor adaptor protein 1 Homo sapiens 118-121 19244346-5 2009 CFTR function assays performed on T84 cells expressing the Rab11a or Rab11b GDP-locked S25N mutants demonstrated that only the Rab11b mutant inhibited 80% of the cAMP-activated halide efflux and that only the constitutively active Rab11b-Q70L increased the rate constant for stimulated halide efflux. halide 177-183 CF transmembrane conductance regulator Homo sapiens 0-4 19244346-5 2009 CFTR function assays performed on T84 cells expressing the Rab11a or Rab11b GDP-locked S25N mutants demonstrated that only the Rab11b mutant inhibited 80% of the cAMP-activated halide efflux and that only the constitutively active Rab11b-Q70L increased the rate constant for stimulated halide efflux. halide 177-183 RAB11B, member RAS oncogene family Homo sapiens 127-133 19244346-5 2009 CFTR function assays performed on T84 cells expressing the Rab11a or Rab11b GDP-locked S25N mutants demonstrated that only the Rab11b mutant inhibited 80% of the cAMP-activated halide efflux and that only the constitutively active Rab11b-Q70L increased the rate constant for stimulated halide efflux. halide 177-183 cathelicidin antimicrobial peptide Homo sapiens 162-166 19244346-5 2009 CFTR function assays performed on T84 cells expressing the Rab11a or Rab11b GDP-locked S25N mutants demonstrated that only the Rab11b mutant inhibited 80% of the cAMP-activated halide efflux and that only the constitutively active Rab11b-Q70L increased the rate constant for stimulated halide efflux. halide 177-183 RAB11B, member RAS oncogene family Homo sapiens 127-133 19115824-4 2009 DFT was found to give significantly longer halide ion/carbon atom bond lengths for the ion-dipole complexes and central barrier transition state than MP2. halide 43-49 tryptase pseudogene 1 Homo sapiens 150-153 19166305-4 2009 When UCl4 is reacted with 1 equiv (PNP)K (6) in the presence of THF, trimethylphosphine oxide (TMPO), or triphenylphosphineoxide (TPPO), the tetravalent halide complexes (PNP)UCl3(THF) (9), (PNP)UCl3(TMPO)2 (10), and (PNP)UCl3(TPPO) (11), respectively, are formed in excellent yields. halide 153-159 thymopoietin Homo sapiens 200-204 19121944-6 2009 In particular, Arg312 in ALR1 (missing in ALR2) contributes favourably to the binding of DCL through an electrostatic interaction with the inhibitor"s electronegative halide atom and undergoes a conformational change upon Tolrestat binding. halide 167-173 aldo-keto reductase family 1 member B Homo sapiens 42-46 19128052-1 2009 The gas-liquid interface of halide-free 1,3-dialkylimidazolium alkyl sulfates [RMIM][R-OSO(3)] with R chain length from C(1)-C(4) and C(8) has been studied systematically using the surface-specific sum frequency generation (SFG) vibrational spectroscopy and surface tension measurements. halide 28-34 heterogeneous nuclear ribonucleoprotein C Homo sapiens 120-124 19128052-1 2009 The gas-liquid interface of halide-free 1,3-dialkylimidazolium alkyl sulfates [RMIM][R-OSO(3)] with R chain length from C(1)-C(4) and C(8) has been studied systematically using the surface-specific sum frequency generation (SFG) vibrational spectroscopy and surface tension measurements. halide 28-34 complement C4A (Rodgers blood group) Homo sapiens 125-129 19006284-0 2008 Ion partitioning at the liquid/vapor interface of a multicomponent alkali halide solution: a model for aqueous sea salt aerosols. halide 74-80 S13 erythroblastosis (avian) oncogene homolog Homo sapiens 111-114 19239179-2 2009 Taurine chloramine (TauCl) is the product of a reaction between cellular taurine and hypochlorous acid (HOCl/OCl-), the latter produced by the halide-dependent myeloperoxidase (MPO) system in inflammatory cells. halide 143-149 occludin Mus musculus 105-108 19239179-2 2009 Taurine chloramine (TauCl) is the product of a reaction between cellular taurine and hypochlorous acid (HOCl/OCl-), the latter produced by the halide-dependent myeloperoxidase (MPO) system in inflammatory cells. halide 143-149 myeloperoxidase Mus musculus 177-180 19378554-1 2009 Facile acetylide transfer reactions take place between gold(I) complexes Au(C[triple bond]CAr)(PPh3) (Ar = C6H5 or C6H4Me-4) and a variety of representative inorganic and organometallic complexes MXL, (M = metal, X = halide, L, = supporting ligands) featuring metals from groups 8-11, to afford the corresponding metal-alkynyl complexes M(C[triple bond]CR)Ln in modest to good yield. halide 217-223 protein phosphatase 4 catalytic subunit Homo sapiens 95-99 18652572-1 2008 Myeloperoxidase, released by activated phagocytes, forms reactive oxidants by catalysing the reaction of halide and pseudo-halide ions with H(2)O(2). halide 105-111 myeloperoxidase Homo sapiens 0-15 18652572-1 2008 Myeloperoxidase, released by activated phagocytes, forms reactive oxidants by catalysing the reaction of halide and pseudo-halide ions with H(2)O(2). halide 123-129 myeloperoxidase Homo sapiens 0-15 18652572-3 2008 With physiological levels of halide and pseudo-halide ions, similar amounts of HOCl (hypochlorous acid) and HOSCN (hypothiocyanous acid) are produced by myeloperoxidase. halide 29-35 myeloperoxidase Homo sapiens 153-168 18921987-1 2008 Photochemical properties of p-phenylphenacyl derivatives (PP-X) having C-halide, C-S, and C-O bonds in the lowest (T 1) and higher (T n ) triplet excited states were investigated in solution by using single-color and stepwise two-color two-laser flash photolysis techniques. halide 73-79 protein phosphatase 4 catalytic subunit Homo sapiens 58-62 18937477-6 2008 These labeling studies also imply that more favorable partitioning of the eta2-imine complex toward reaction with alkene versus regeneration of the starting bis-amido complex accounts for the higher reactivity of the mixed halide amido catalyst versus a homoleptic amido complex. halide 223-229 DNA polymerase iota Homo sapiens 74-78 18921987-7 2008 According to the relationship between the Phi dec and BDE values, it was shown that the decomposition of PP-X in the T n state is due to beta-cleavage of the corresponding C-X bond, and that the state energy of the reactive T n for the C-O bond cleavage differs from that for the C-halide and C-S bond cleavage. halide 282-288 protein phosphatase 4 catalytic subunit Homo sapiens 105-109 18829270-1 2008 Density functional calculations of (207)Pb NMR shielding in PbX(2) (X=F, Br, Cl and I) anionic fragments suggest that in solid PbX(2), the observed variation of chemical shift with halide is dominated by the paramagnetic contribution to the chemical shielding, with a lesser effect by the spin-orbit contribution. halide 181-187 PBX homeobox 2 Homo sapiens 60-66 18759427-3 2008 Combination of equimolar quantities of CNAr (Mes2) and CuX (X = Cl, Br and I) in tetrahydrofuran (THF) solution results in the formation of the bridging halide complexes (mu-X) 2[Cu(THF)(CNAr (Mes2))] 2. halide 153-159 cut like homeobox 1 Homo sapiens 55-58 18772398-5 2008 Transfection of epithelial cells with specific small interfering RNA against each of these proteins shows that TMEM16A, a member of a family of putative plasma membrane proteins with unknown function, is associated with calcium-dependent chloride current, as measured with halide-sensitive fluorescent proteins, short-circuit current, and patch-clamp techniques. halide 273-279 anoctamin 1 Homo sapiens 111-118 18829270-1 2008 Density functional calculations of (207)Pb NMR shielding in PbX(2) (X=F, Br, Cl and I) anionic fragments suggest that in solid PbX(2), the observed variation of chemical shift with halide is dominated by the paramagnetic contribution to the chemical shielding, with a lesser effect by the spin-orbit contribution. halide 181-187 PBX homeobox 2 Homo sapiens 127-133 18157587-1 2008 Taurine chloramine (TauCl) and taurine bromamine (TauBr), products of myeloperoxidase halide system, exert anti-inflammatory properties. halide 86-92 myeloperoxidase Mus musculus 70-85 18517193-3 2008 The reaction of 4 with EtO (-), followed by [MX 2(dcpe)] (X = halide), yields [(dcpe)Ni(S 2C 6H 2S 2)M(dcpe)] [M = Ni ( 5a), Pd ( 5b)]. halide 62-68 RUNX1 partner transcriptional co-repressor 1 Homo sapiens 23-26 18517193-3 2008 The reaction of 4 with EtO (-), followed by [MX 2(dcpe)] (X = halide), yields [(dcpe)Ni(S 2C 6H 2S 2)M(dcpe)] [M = Ni ( 5a), Pd ( 5b)]. halide 62-68 MX dynamin like GTPase 2 Homo sapiens 45-49 18005671-2 2008 HOCl and the myeloperoxidase-H(2)O(2)-halide system can modify both protein and lipid moieties of LDL and react with unsaturated phospholipids to form chlorohydrins. halide 38-44 myeloperoxidase Mus musculus 13-28 18424617-1 2008 The myeloperoxidase (MPO)-hydrogen peroxide-halide system is an efficient oxygen-dependent antimicrobial component of polymorphonuclear leukocyte (PMN)-mediated host defense. halide 44-50 myeloperoxidase Mus musculus 4-19 18424617-1 2008 The myeloperoxidase (MPO)-hydrogen peroxide-halide system is an efficient oxygen-dependent antimicrobial component of polymorphonuclear leukocyte (PMN)-mediated host defense. halide 44-50 myeloperoxidase Mus musculus 21-24 18290657-3 2008 The relative reactivities of the halides were a function of the azabicycle, the halide, and its bridge and the addition of Selectfluor or HgF(2) as a nucleofuge. halide 33-39 GINGF2 Homo sapiens 138-143 19122872-0 2008 Bi(OTf)(3)-Catalyzed 5-Exo-Trig Cyclization via Halide Activation. halide 48-54 POU class 5 homeobox 1 Homo sapiens 0-9 17719234-7 2007 Although the use of halogenated solvents could hinder efficient EC, dissociative EC, and proton transfer of negative ion-APPI due to their EC ability, the subsequently generated halide anions promoted halide attachment to compounds that otherwise could not be efficiently ionized. halide 178-184 amyloid beta precursor protein Homo sapiens 121-125 18022401-12 2007 Finally, using siRNA, we show that decreased ATF6 expression induces increased cAMP-dependent halide flux through DeltaF508-CFTR due to its increased membrane localization. halide 94-100 activating transcription factor 6 Homo sapiens 45-49 18022401-12 2007 Finally, using siRNA, we show that decreased ATF6 expression induces increased cAMP-dependent halide flux through DeltaF508-CFTR due to its increased membrane localization. halide 94-100 CF transmembrane conductance regulator Homo sapiens 124-128 18047295-1 2007 Hypohalous acids are generated from the oxidation of halide ions by myeloperoxidase and eosinophil peroxidase in the presence of H2O2. halide 53-59 myeloperoxidase Homo sapiens 68-83 18047295-1 2007 Hypohalous acids are generated from the oxidation of halide ions by myeloperoxidase and eosinophil peroxidase in the presence of H2O2. halide 53-59 eosinophil peroxidase Homo sapiens 88-109 17719234-7 2007 Although the use of halogenated solvents could hinder efficient EC, dissociative EC, and proton transfer of negative ion-APPI due to their EC ability, the subsequently generated halide anions promoted halide attachment to compounds that otherwise could not be efficiently ionized. halide 201-207 amyloid beta precursor protein Homo sapiens 121-125 17875773-11 2007 CONCLUSIONS: These results indicated that highly toxic ROS such as .OH generated via the hydrogen peroxide/MPO/halide system induce apoptosis and that ROS may be the direct mediators of EGCG-induced apoptosis in MPO-positive leukemic cells. halide 111-117 myeloperoxidase Homo sapiens 107-110 17875773-11 2007 CONCLUSIONS: These results indicated that highly toxic ROS such as .OH generated via the hydrogen peroxide/MPO/halide system induce apoptosis and that ROS may be the direct mediators of EGCG-induced apoptosis in MPO-positive leukemic cells. halide 111-117 myeloperoxidase Homo sapiens 212-215 17452108-2 2007 Thioetherification reaction of 4 or 5 with an organic halide catalyzed by indium or indium tribromide first affords appropriate sulfide 7 or 8, which is then converted into title compounds 9 or 10 by hydrogen peroxide oxidation catalyzed by ammonium molybdate in ionic liquid [bmim]PF6. halide 54-60 sperm associated antigen 17 Homo sapiens 282-285 17559270-1 2007 Arylation of both acyclic ketones and primary and secondary amines was achieved using a new, simple, stable, and easy-to-access nickel(II)-halide complex bearing mixed PPh3/N-heterocyclic carbene ligands as a catalyst precursor. halide 139-145 caveolin 1 Homo sapiens 168-172 17141727-0 2007 Differential effects of flavonols on inactivation of alpha1-antitrypsin induced by hypohalous acids and the myeloperoxidase-hydrogen peroxide-halide system. halide 142-148 serpin family A member 1 Homo sapiens 53-71 17335867-7 2007 Bench-scale tests with free chlorine showed O(3) is capable of reducing total organic halide (TOX) formation potential by at least 20%. halide 86-92 thymocyte selection associated high mobility group box Homo sapiens 94-97 17141727-0 2007 Differential effects of flavonols on inactivation of alpha1-antitrypsin induced by hypohalous acids and the myeloperoxidase-hydrogen peroxide-halide system. halide 142-148 myeloperoxidase Homo sapiens 108-123 16468798-3 2006 The stronger Lewis acids (TiX4 and BX3) favor the syn process that involves axial delivery of a halide ligand. halide 96-102 synemin Homo sapiens 50-53 17217282-2 2007 Monoarylations occur at the C-5 position preferentially, thus leaving the remaining C-3 halide free for further functionalization, to finally access differentially 3,5-disubstituted 2-pyridones. halide 88-94 complement C5 Homo sapiens 28-31 17217282-2 2007 Monoarylations occur at the C-5 position preferentially, thus leaving the remaining C-3 halide free for further functionalization, to finally access differentially 3,5-disubstituted 2-pyridones. halide 88-94 complement C3 Homo sapiens 84-87 17160175-3 2007 The dependence of both oxidation potential and nu(CO) for [MX(CO)(eta-RC[triple bond, length as m-dash]CR)Tp"] shows an inverse halide order which is consistent with an ionic component to the M-X bond; the small size of fluorine and its closeness to the metal centre leads to the highest energy HOMO and the lowest oxidation potential. halide 128-134 endothelin receptor type A Homo sapiens 66-69 16905147-4 2006 In addition to Cl- and Br-, two non-halide ions, NO3- and SCN-, are shown to be transported by CLC-ec1, but with reduced H+ counter-transport. halide 36-42 NBL1, DAN family BMP antagonist Homo sapiens 49-52 16905147-4 2006 In addition to Cl- and Br-, two non-halide ions, NO3- and SCN-, are shown to be transported by CLC-ec1, but with reduced H+ counter-transport. halide 36-42 Charcot-Leyden crystal galectin Homo sapiens 95-98 16791904-1 2006 Electronic origin for nonresonant enhancement of nonlinear optical response in the complexes formed from tetraalkylammonium halide and carbon tetrabromide is provided in view of electrostatic potentials of intermolecular donor (halide ion)-acceptor (CBr(4)). halide 124-130 carbonyl reductase 4 Homo sapiens 250-256 16468798-5 2006 The trends in syn vs anti selectivity, reactivity, and effects of different Lewis acidic metal halides are rationalized by competitive reaction pathways proceeding through syn carbocation-halide ion pairs and a higher order transition state that leads to inversion of configuration and formation of trans halohydrins, along with cyclic olefins arising from proton elimination. halide 95-101 synemin Homo sapiens 14-17 16468798-5 2006 The trends in syn vs anti selectivity, reactivity, and effects of different Lewis acidic metal halides are rationalized by competitive reaction pathways proceeding through syn carbocation-halide ion pairs and a higher order transition state that leads to inversion of configuration and formation of trans halohydrins, along with cyclic olefins arising from proton elimination. halide 95-101 synemin Homo sapiens 172-175 17209550-0 2007 Kinetic evidence supports the existence of two halide binding sites that have a distinct impact on the heme iron microenvironment in myeloperoxidase. halide 47-53 myeloperoxidase Homo sapiens 133-148 17209550-8 2007 Our results are consistent with two halide binding sites that could be populated by two halides in which both display distinct effects on the MPO heme iron microenvironment. halide 36-42 myeloperoxidase Homo sapiens 142-145 18453132-3 2007 The inhibition or absence of the MPO-H2O2-halide system results in marked reduction in PMN killing of a variety of microbes, implicating its relative prominence in the hierarchy of PMN antimicrobial systems. halide 42-48 myeloperoxidase Homo sapiens 33-36 17076648-7 2006 Recently, we found that a highly toxic reactive oxygen species (ROS) generated via the hydrogen peroxide/myeloperoxidase [H(2)O(2)/MPO/halide] system by natural compounds induces apoptosis in MPO-positive leukemic cells. halide 135-141 myeloperoxidase Homo sapiens 105-120 17076648-7 2006 Recently, we found that a highly toxic reactive oxygen species (ROS) generated via the hydrogen peroxide/myeloperoxidase [H(2)O(2)/MPO/halide] system by natural compounds induces apoptosis in MPO-positive leukemic cells. halide 135-141 myeloperoxidase Homo sapiens 131-134 17076648-7 2006 Recently, we found that a highly toxic reactive oxygen species (ROS) generated via the hydrogen peroxide/myeloperoxidase [H(2)O(2)/MPO/halide] system by natural compounds induces apoptosis in MPO-positive leukemic cells. halide 135-141 myeloperoxidase Homo sapiens 192-195 16961375-7 2006 The halide ligand of (PyPO)Fe(III)Br coordinates on one of the two inequivalent faces of the macrocycle, leading to two distinct species: syn and anti. halide 4-10 synemin Homo sapiens 138-141 16526788-1 2006 Alkyl-substituted derivatives of 1,3-dipyrrolyl-1,3-propanedione BF2 complexes, the efficient receptors for halide and oxoanions with use of bridging CH as well as pyrrole NH, are reported. halide 108-114 forkhead box G1 Homo sapiens 65-68 16511313-0 2006 Crystallization and halide phasing of the C-terminal domain of human KIN17. halide 20-26 Kin17 DNA and RNA binding protein Homo sapiens 69-74 16489092-2 2006 We recently characterized NIS-specific cellular uptake of an alternative halide, radioastatine ((211)At), which emits high-energy alpha-particles. halide 73-79 solute carrier family 5 (sodium iodide symporter), member 5 Mus musculus 26-29 16435795-0 2006 Gas phase SN2 reactions of halide ions with trifluoromethyl halides: front- and back-side attack vs. complex formation. halide 27-33 solute carrier family 38 member 5 Homo sapiens 10-13 16111649-4 2006 The comparison of experimentally derived and calculated data revealed that Cl(2), Br(2), or BrCl will primarily be formed by the myeloperoxidase-H(2)O(2)-halide system. halide 154-160 myeloperoxidase Homo sapiens 129-144 16375846-7 2006 In contrast, LPO, a prototypical mammalian peroxidase, is protected from heme modification and its heme remains intact during the oxidation of halide ions. halide 143-149 lactoperoxidase Homo sapiens 13-16 16111649-5 2006 However, the eosinophil peroxidase-H(2)O(2)-halide system forms directly HOCl and HOBr. halide 44-50 eosinophil peroxidase Homo sapiens 13-34 15950531-0 2006 Structural and up-conversion luminescence properties in Tm3+/Yb3+-codoped heavy metal oxide-halide glasses. halide 92-98 tropomyosin 3 Homo sapiens 56-59 16787252-6 2006 High-throughput screening of small molecule collections utilizing a cell-based fluorescence assay of halide transport yielded thiazolidinone and glycine hydrazide CFTR inhibitors that block enterotoxin-mediated secretory diarrhea in rodent models, including a class of non-absorbable inhibitors that target the CFTR pore at its external entrance. halide 101-107 CF transmembrane conductance regulator Homo sapiens 163-167 16787252-6 2006 High-throughput screening of small molecule collections utilizing a cell-based fluorescence assay of halide transport yielded thiazolidinone and glycine hydrazide CFTR inhibitors that block enterotoxin-mediated secretory diarrhea in rodent models, including a class of non-absorbable inhibitors that target the CFTR pore at its external entrance. halide 101-107 CF transmembrane conductance regulator Homo sapiens 311-315 15950531-1 2006 Tm3+/Yb3+-codoped heavy metal oxide-halide glasses have been synthesized by conventional melting and quenching method. halide 36-42 tropomyosin 3 Homo sapiens 0-3 15950531-5 2006 With increasing halide content, the up-conversion luminescence intensity and blue luminescence lifetimes of Tm3+ ion increase notably. halide 16-22 tropomyosin 3 Homo sapiens 108-111 15614898-0 2004 Tri- and tetracarbanionic initiators by a lithium/halide exchange reaction: application to star-polymer synthesis. halide 50-56 tRNA-Ile (anticodon AAT) 9-1 Homo sapiens 0-3 16172643-3 2005 The EPR spectra of the complexes showed several superhyperfine structures that strongly indicated the presence of spin density on the halide ligands through the Cu-X bond. halide 134-140 cut like homeobox 1 Homo sapiens 161-165 16190711-1 2005 We have developed the first HNTf2-promoted 5-endo-dig cyclizations of 1-siloxy-1,5-diynes, which proceed with concomitant formation of C-Hal bonds as a result of halide abstraction from a halocarbon by the intermediate alkenyl cation. halide 162-168 histidine ammonia-lyase Homo sapiens 137-140 16127463-3 2005 To identify small-molecule correctors of defective cellular processing, we assayed iodide flux in DeltaF508-CFTR-transfected epithelial cells using a fluorescent halide indicator. halide 162-168 CF transmembrane conductance regulator Homo sapiens 108-112 16323941-5 2005 These complexes react with [Ag(OClO 3)PPh3] with displacement of the halide and formation of [NBu4][Pt4(mu-PPh2)4(mu-H)2(C6F5)3PPh3]. halide 69-75 caveolin 1 Homo sapiens 38-42 16035007-1 2005 1,3-Dipyrrolyl-1,3-propanediones, synthesized from pyrroles and malonyl chloride, form BF2 complexes, which represent a new class of naked-eye sensors for halide and oxoanions. halide 155-161 forkhead box G1 Homo sapiens 87-90 16144386-1 2005 Varying the steric bulk of either the phosphine or the halide in Au(PR3)2X complexes allows intuitive tuning of the phosphorescence energy to multiple visible colors, including the coveted blue for LED applications. halide 55-61 proteinase 3 Homo sapiens 68-71 15786498-1 2005 The use of microwave heating in lanthanide(II) halide (LnX2 = SmBr2, SmI2, and YbI2) mediated reduction and coupling reactions has been investigated for a variety of functional groups including alpha,beta-unsaturated esters, aldehydes, ketones, imines, and alkyl halides. halide 47-53 ligand of numb-protein X 2 Homo sapiens 55-59 15689384-5 2005 Among the antimicrobial systems formed in the phagosome is one consisting of myeloperoxidase (MPO), released into the phagosome during the degranulation process, hydrogen peroxide (H2O2), formed by the respiratory burst and a halide, particularly chloride. halide 226-232 myeloperoxidase Homo sapiens 77-92 15689384-5 2005 Among the antimicrobial systems formed in the phagosome is one consisting of myeloperoxidase (MPO), released into the phagosome during the degranulation process, hydrogen peroxide (H2O2), formed by the respiratory burst and a halide, particularly chloride. halide 226-232 myeloperoxidase Homo sapiens 94-97 15689384-8 2005 This review will consider the potential sources of H2O2 for the MPO-H2O2-halide system; the toxic products of the MPO system; the evidence for MPO involvement in the microbicidal activity of neutrophils; the involvement of MPO-independent antimicrobial systems; and the role of the MPO system in tissue injury. halide 73-79 myeloperoxidase Homo sapiens 64-67 15629108-1 2005 Lactoperoxidase (LPO) is found in mucosal surfaces and exocrine secretions including milk, tears, and saliva and has physiological significance in antimicrobial defense which involves (pseudo-)halide oxidation. halide 193-199 lactoperoxidase Homo sapiens 0-15 15629108-1 2005 Lactoperoxidase (LPO) is found in mucosal surfaces and exocrine secretions including milk, tears, and saliva and has physiological significance in antimicrobial defense which involves (pseudo-)halide oxidation. halide 193-199 lactoperoxidase Homo sapiens 17-20 15515069-7 2004 Because of fast isomerisation and high reactivity of the syn,cis complex, the major product formed upon alkylation is the linear product, especially for monosubstituted phenylallyl substrates in the presence of halide counterions. halide 211-217 synemin Homo sapiens 57-60 15366874-2 2004 The one-dimensional chains consist of Lambda2-configured pentagonal-bipyramidal cadmium complexes with metal-centered chirality bridged by [CdX4]2- tetrahedra via shared halide atoms. halide 170-176 caudal type homeobox 4 Homo sapiens 140-144 15163208-6 2004 Our structure-activity relationship studies demonstrated that (1) reactivity of the halide leaving group plays a weak role in GST inactivation by the haloenol lactones, (2) aromatic electron density may have some influence on the potency of GST inactivation, (3) high rigidity likely disfavors enzyme inhibition, (4) lipophilicity is inversely proportional to enzyme inactivation, and (5) an unsaturated system may be important for enzyme inhibition. halide 84-90 glutathione S-transferase kappa 1 Homo sapiens 126-129 15236560-0 2004 New halide-centered discrete Ag(I)(8) cubic clusters containing diselenophosphate ligands, [Ag(8)(X)[Se(2)P(OR)(2)](6)](PF(6)) (X = Cl, Br; R = Et, Pr, (i)Pr): syntheses, structures, and DFT calculations. halide 4-10 sperm associated antigen 17 Homo sapiens 120-126 15163208-6 2004 Our structure-activity relationship studies demonstrated that (1) reactivity of the halide leaving group plays a weak role in GST inactivation by the haloenol lactones, (2) aromatic electron density may have some influence on the potency of GST inactivation, (3) high rigidity likely disfavors enzyme inhibition, (4) lipophilicity is inversely proportional to enzyme inactivation, and (5) an unsaturated system may be important for enzyme inhibition. halide 84-90 glutathione S-transferase kappa 1 Homo sapiens 241-244 15252534-1 2004 Cationic nitrile complexes and neutral halide and cyanide complexes, with the general formula [MnL1L2(NO)(eta-C5H4Me)]z, undergo one-electron oxidation at a Pt electrode in CH2Cl2. halide 39-45 endothelin receptor type A Homo sapiens 106-109 15161651-1 2004 Inflammatory infiltrates can modify (lipo)proteins via hypochlorous acid/hypochlorite (HOCl/OCl(-)) an oxidant formed by the myeloperoxidase-H(2)O(2)-halide system. halide 150-156 myeloperoxidase Homo sapiens 125-140 15161651-9 2004 The demonstration of selective up-regulation of a subgroup of genes if proteinuria is accompanied by the presence of HOCl-modified (lipo)proteins support the potential pathophysiological role of the myeloperoxidase-H(2)O(2)-halide system and HOCl-LDL in renal disease. halide 224-230 myeloperoxidase Homo sapiens 199-214 14615977-10 2003 The results may be interpreted in the context of a model in which the halide order affects the rate of carbon-halogen bond cleavage of all such reactions catalyzed by the GSTs. halide 70-76 glutathione S-transferase theta 1 Rattus norvegicus 171-175 14599181-2 2003 These complexes can be obtained either via a halide metathesis reaction with AgF in dichloromethane or by reacting the corresponding dimethyl complexes with XeF2. halide 45-51 angiopoietin like 6 Homo sapiens 77-80 14615977-13 2003 With all of the GSTs, the halide order is seen in the enzyme efficiency, k(cat)/K(m), with C-Br cleavage approximately 10-fold faster than C-Cl cleavage. halide 26-32 glutathione S-transferase theta 1 Rattus norvegicus 16-20 12970574-7 2003 Progressive neutrophil accumulation and activation in the liver after MCT treatment were demonstrated by an increased activity of myeloperoxidase and pronounced staining for hypochlorite-modified proteins generated via the myeloperoxidase-hydrogen peroxide-halide system. halide 257-263 myeloperoxidase Rattus norvegicus 223-238 12930913-7 2003 A relation was also observed between MRP1 levels and presence of a cAMP-independent chloride conductive pathway, as determined by a halide-sensitive fluorescent assay. halide 132-138 ATP binding cassette subfamily C member 1 Homo sapiens 37-41 14556977-0 2003 Prostanoids and MPO-halide system products as a link between innate and adaptive immunity. halide 20-26 myeloperoxidase Homo sapiens 16-19 14556977-7 2003 In this paper we have focused on the role of taurine chloramine (TauCl), the physiological product of neutrophil MPO-halide system, in the regulation of immune system. halide 117-123 myeloperoxidase Homo sapiens 113-116 12269834-1 2002 Lactoperoxidase (LPO) is found in mucosal surfaces and exocrine secretions, including milk, tears, and saliva, and has physiological significance in antimicrobial defense which involves (pseudo-) halide oxidation. halide 196-202 lactoperoxidase Homo sapiens 0-15 12895099-2 2003 The isostructural Co(II) and the Ni(II) complexes show octahedral geometries around the metal ions with the coordination sites occupied by the pyridyl nitrogen atoms and the thioether sulfur atoms of the ligand and cis coordination of the halide ions. halide 239-245 mitochondrially encoded cytochrome c oxidase II Homo sapiens 18-24 12707270-9 2003 In contrast, previous studies have demonstrated that 5-bromouracil could be generated by either eosinophil peroxidase or myeloperoxidase, which preferentially brominates uracil at plasma concentrations of halide and under moderately acidic conditions. halide 205-211 myeloperoxidase Homo sapiens 121-136 12953846-1 2003 The microbicidal activity of the myeloperoxidase (MPO)-hydrogen peroxide-halide system has been implicated as the most efficient, oxygen-dependent antimicrobial component of neutrophil host defense. halide 73-79 myeloperoxidase Homo sapiens 33-48 12953846-1 2003 The microbicidal activity of the myeloperoxidase (MPO)-hydrogen peroxide-halide system has been implicated as the most efficient, oxygen-dependent antimicrobial component of neutrophil host defense. halide 73-79 myeloperoxidase Homo sapiens 50-53 12909089-5 2003 The halide contents were reduced to approximately 100 ppm Cl and 700 ppm F. The rest of these elements are in the form of CaF2. halide 4-10 CCR4-NOT transcription complex subunit 8 Homo sapiens 122-126 14582122-0 2003 Invesgations [correction investigations] on the influence of halide substituents on the estrogen receptor interaction of 2, 4, 5-tris(4-hydroxyphenyl)imidazoles. halide 61-67 estrogen receptor 1 Homo sapiens 88-105 12852954-3 2003 Utilizing a fluorescence cell-based assay of halide transport, the best compounds increased CFTR-dependent chloride transport with half-maximal stimulation at 20-50 microM. halide 45-51 CF transmembrane conductance regulator Homo sapiens 92-96 12732522-0 2003 Enhanced killing of Acanthamoeba cysts with a plant peroxidase-hydrogen peroxide-halide antimicrobial system. halide 81-87 peroxidase Glycine max 52-62 12506394-5 2002 All halide substituted imidazoles competed with estradiol for the binding site at the estrogen receptor. halide 4-10 estrogen receptor 1 Homo sapiens 86-103 12269834-1 2002 Lactoperoxidase (LPO) is found in mucosal surfaces and exocrine secretions, including milk, tears, and saliva, and has physiological significance in antimicrobial defense which involves (pseudo-) halide oxidation. halide 196-202 lactoperoxidase Homo sapiens 17-20 12060654-2 2002 One important pathway may involve the production of potent halogenating agents such as hypochlorous acid (HOCl) by the myeloperoxidase-hydrogen peroxide-halide system. halide 153-159 myeloperoxidase Homo sapiens 119-134 12208510-6 2002 In immortalized human CF cell lines expressing Delta F508 CFTR, a halide efflux assay showed that calnexin Delta 185-520 partially restored CFTR function. halide 66-72 CF transmembrane conductance regulator Homo sapiens 58-62 12208510-6 2002 In immortalized human CF cell lines expressing Delta F508 CFTR, a halide efflux assay showed that calnexin Delta 185-520 partially restored CFTR function. halide 66-72 calnexin Homo sapiens 98-106 12070141-8 2002 The colocalization of immunoreactive HOCl-modified epitopes with apolipoprotein A-I along with deposits of lipids in serial sections of human atheroma shown here indicates that the myeloperoxidase-H(2)O(2)-halide system contributes to oxidative damage of HDL in vivo. halide 206-212 apolipoprotein A1 Homo sapiens 65-83 12149031-3 2002 The halide in 2 can be replaced by reaction with TlBF(4) to produce Mo(2)(hpp)(4)(BF(4)), 3. halide 4-10 familial progressive hyperpigmentation 1 Homo sapiens 74-77 12163076-1 2002 Halorhodopsin, a light-driven halide pump, is the second archaeal rhodopsin involved in ion pumping to be studied at high resolution by X-ray crystallography. halide 30-36 rhodopsin Homo sapiens 4-13 12545199-13 2002 These data indicate that: 1) high concentrations of chlorides stimulate human PON1 activity toward paraoxon but not other substrates, 2) PON1 is inhibited by Cl(-) in other mammalian species, 3) the potency of human PON1 activation by halogene salts increases with decreasing atomic mass of the halide anion. halide 295-301 paraoxonase 1 Homo sapiens 137-141 12070141-8 2002 The colocalization of immunoreactive HOCl-modified epitopes with apolipoprotein A-I along with deposits of lipids in serial sections of human atheroma shown here indicates that the myeloperoxidase-H(2)O(2)-halide system contributes to oxidative damage of HDL in vivo. halide 206-212 myeloperoxidase Homo sapiens 181-196 12095332-1 2002 The class of compounds (RCp)2MX2, where M is a group IV metal, Cp is cyclopentadienyl, R is an alkyl, and X is a halide, has been of continuing interest as precursors for olefin coordination polymerization catalysts. halide 113-119 CGRP receptor component Homo sapiens 24-27 11991131-5 2002 This jibes with the high x-ray absorption provided by the 27%-higher x-ray attenuation coefficients (7.54 versus 6.07, at 60 KeV) that BaFI offers over BaF(Br(0.85),I(0.15)), a result of the high atomic number of BaFI"s exclusively iodine halide content. halide 239-245 BAF nuclear assembly factor 1 Homo sapiens 135-138 12545199-13 2002 These data indicate that: 1) high concentrations of chlorides stimulate human PON1 activity toward paraoxon but not other substrates, 2) PON1 is inhibited by Cl(-) in other mammalian species, 3) the potency of human PON1 activation by halogene salts increases with decreasing atomic mass of the halide anion. halide 295-301 paraoxonase 1 Homo sapiens 137-141 11796821-2 2002 Although the nature of the in vivo oxidants has not been clearly identified, increasing evidence suggested the myeloperoxidase (MPO)-H(2)O(2)-halide system to be responsible for the damage observed in leukocyte-dependent glomerulonephritis. halide 142-148 myeloperoxidase Homo sapiens 111-126 11741811-4 2002 Ado promoted arachidonic acid release from Calu-3 cells, and phospholipase A(2) (PLA(2)) inhibition blocked Ado-activated halide efflux in Calu-3 and COS-7 cells expressing CFTR. halide 122-128 phospholipase A2 group IB Homo sapiens 61-79 11741811-4 2002 Ado promoted arachidonic acid release from Calu-3 cells, and phospholipase A(2) (PLA(2)) inhibition blocked Ado-activated halide efflux in Calu-3 and COS-7 cells expressing CFTR. halide 122-128 phospholipase A2 group IB Homo sapiens 81-87 11741811-8 2002 In COS-7 cells transiently expressing DeltaF508 CFTR, Ado activated halide efflux. halide 68-74 CF transmembrane conductance regulator Homo sapiens 48-52 11741811-9 2002 Ado also activated G551D CFTR-dependent halide efflux when combined with arachidonic acid and phosphodiesterase inhibition. halide 40-46 CF transmembrane conductance regulator Homo sapiens 25-29 11796821-2 2002 Although the nature of the in vivo oxidants has not been clearly identified, increasing evidence suggested the myeloperoxidase (MPO)-H(2)O(2)-halide system to be responsible for the damage observed in leukocyte-dependent glomerulonephritis. halide 142-148 myeloperoxidase Homo sapiens 128-131 11796821-13 2002 The observed colocalization of HOCl-modified proteins and MPO in podocytes and adjacent basement membranes strengthens the assumption that the MPO-H(2)O(2)-halide system contributes to glomerular dysfunction in patients with membranous glomerulonephritis. halide 156-162 myeloperoxidase Homo sapiens 58-61 11796821-13 2002 The observed colocalization of HOCl-modified proteins and MPO in podocytes and adjacent basement membranes strengthens the assumption that the MPO-H(2)O(2)-halide system contributes to glomerular dysfunction in patients with membranous glomerulonephritis. halide 156-162 myeloperoxidase Homo sapiens 143-146 11600438-3 2001 We have developed a rapid, quantitative screening procedure for analysis of CFTR-mediated halide transport in cells with the use of a conventional fluorescence plate reader. halide 90-96 CF transmembrane conductance regulator Homo sapiens 76-80 11600438-7 2001 In cells cultured on 96-well plastic dishes, the assay gave reproducible halide permeabilities from well to well and could reliably detect a 2% activation of CFTR-dependent halide transport produced by low concentrations of forskolin. halide 73-79 CF transmembrane conductance regulator Homo sapiens 158-162 11600438-7 2001 In cells cultured on 96-well plastic dishes, the assay gave reproducible halide permeabilities from well to well and could reliably detect a 2% activation of CFTR-dependent halide transport produced by low concentrations of forskolin. halide 173-179 CF transmembrane conductance regulator Homo sapiens 158-162 11594511-1 2001 Optimal oxygen-dependent antimicrobial activity of circulating polymorphonuclear leukocytes reflects the synergistic effects of the myeloperoxidase (MPO)-hydrogen peroxide-halide system. halide 172-178 myeloperoxidase Homo sapiens 132-147 11606126-1 2001 Inhibition of the growth of the human ovarian cancer cell line A2780 by organometallic ruthenium(II) complexes of the type [(eta(6)-arene)Ru(X)(Y)(Z)], where arene is benzene or substituted benzene, X, Y, and Z are halide, acetonitrile, or isonicotinamide, or X,Y is ethylenediamine (en) or N-ethylethylenediamine, has been investigated. halide 215-221 endothelin receptor type A Homo sapiens 79-82 11511186-15 2001 The halide order appears most important in the dihalomethane conjugation reactions catalyzed by GST 5-5 and less so in GST T1 and DM11, probably due to changes in the rate-limiting steps. halide 4-10 glutathione S-transferase mu 3 Homo sapiens 96-103 11511186-15 2001 The halide order appears most important in the dihalomethane conjugation reactions catalyzed by GST 5-5 and less so in GST T1 and DM11, probably due to changes in the rate-limiting steps. halide 4-10 glutathione S-transferase theta 1 Homo sapiens 119-125 11594511-1 2001 Optimal oxygen-dependent antimicrobial activity of circulating polymorphonuclear leukocytes reflects the synergistic effects of the myeloperoxidase (MPO)-hydrogen peroxide-halide system. halide 172-178 myeloperoxidase Homo sapiens 149-152 11352159-7 2001 Neutrophil iodination activity (a measure of the myeloperoxidase/hydrogen peroxide/halide antibacterial system) is a very potent bactericidal mechanism of neutrophils and has previously been shown to be suppressed in periparturient cows. halide 83-89 myeloperoxidase Bos taurus 49-64 11262417-3 2001 The compounds were screened for their ability to activate CFTR at 50 microm concentration by measurement of the kinetics of iodide influx in Fisher rat thyroid cells expressing wild-type or G551D CFTR together with the green fluorescent protein-based halide indicator YFP-H148Q. halide 251-257 CF transmembrane conductance regulator Homo sapiens 58-62 11422382-3 2001 At plasma concentrations of halide ion, hypochlorous acid is a major product of the myeloperoxidase-hydrogen peroxide-chloride system. halide 28-34 myeloperoxidase Homo sapiens 84-99 11278358-1 2001 Hypochlorous acid/hypochlorite, generated by the myeloperoxidase/H(2)O(2)/halide system of activated phagocytes, has been shown to oxidize/modify low density lipoprotein (LDL) in vitro and may be involved in the formation of atherogenic lipoproteins in vivo. halide 74-80 myeloperoxidase Homo sapiens 49-64 10037693-7 1999 Co-expression of CFTR (but not of mutated DeltaF508-CFTR) with high levels of beta3-adrenoceptor produced an increased halide permeability under base-line conditions that was not further sensitive to cAMP or beta3-adrenoceptor stimulation. halide 119-125 CF transmembrane conductance regulator Homo sapiens 17-21 11013238-2 2001 Although the pseudohalide thiocyanate (SCN(-)) is the preferred substrate for eosinophil peroxidase (EPO) in fluids of physiologic halide composition, the product(s) of this reaction have not been directly identified, and mechanisms underlying their cytotoxic potential are poorly characterized. halide 19-25 eosinophil peroxidase Homo sapiens 78-99 11013238-2 2001 Although the pseudohalide thiocyanate (SCN(-)) is the preferred substrate for eosinophil peroxidase (EPO) in fluids of physiologic halide composition, the product(s) of this reaction have not been directly identified, and mechanisms underlying their cytotoxic potential are poorly characterized. halide 19-25 eosinophil peroxidase Homo sapiens 101-104 10880973-0 2000 Immunohistochemical evidence for the myeloperoxidase/H2O2/halide system in human atherosclerotic lesions: colocalization of myeloperoxidase and hypochlorite-modified proteins. halide 58-64 myeloperoxidase Homo sapiens 37-52 10880973-5 2000 The antibodies recognized a specific epitope present on various proteins after treatment with OCl- added as reagent or generated by the MPO/H2O2/halide system. halide 145-151 myeloperoxidase Homo sapiens 136-139 10880973-10 2000 The colocalization of immunoreactive MPO and HOCl-modified-epitopes in serial sections of human atheroma (type IV), fibroatheroma (type V) and complicated (type VI) lesions provides further convincing evidence for MPO/H2O2/halide system-mediated oxidation of (lipo)proteins under in vivo conditions. halide 223-229 myeloperoxidase Homo sapiens 37-40 10880973-10 2000 The colocalization of immunoreactive MPO and HOCl-modified-epitopes in serial sections of human atheroma (type IV), fibroatheroma (type V) and complicated (type VI) lesions provides further convincing evidence for MPO/H2O2/halide system-mediated oxidation of (lipo)proteins under in vivo conditions. halide 223-229 myeloperoxidase Homo sapiens 214-217 10532708-4 1999 Although glycoprotein hormones like hCG are mainly hormonogenic, their action in the latter process involves the efflux or conductance of halide ions. halide 138-144 hypertrichosis 2 (generalised, congenital) Homo sapiens 36-39 10913251-3 2000 We have studied the serpin, plasminogen activator inhibitor 1 (PAI-1), in both the active and the latent state and found that anionic halide ions may play a role in the active-to-latent structural transition. halide 134-140 serpin family E member 1 Homo sapiens 28-61 10913251-3 2000 We have studied the serpin, plasminogen activator inhibitor 1 (PAI-1), in both the active and the latent state and found that anionic halide ions may play a role in the active-to-latent structural transition. halide 134-140 serpin family E member 1 Homo sapiens 63-68 10913251-7 2000 Timecourse experiments measuring active PAI-1 stability in the presence of various halide ions showed a clear trend for stabilization of the active form with F(-) > Cl(-) > Br(-) >> I(-). halide 83-89 serpin family E member 1 Homo sapiens 40-45 10939618-1 2000 OBJECTIVE: HOCl, a major bactericidal product of neutrophil MPO-halide system reacts with taurine to form taurine chloramine (TauCl), a less toxic anti-inflammatory mediator. halide 64-70 myeloperoxidase Mus musculus 60-63 10939618-19 2000 Nevertheless, due to high concentration of taurine in PMN cytosol, formation of TauCl will be a major regulatory mechanism of MPO-halide-system. halide 130-136 myeloperoxidase Mus musculus 126-129 10766826-0 2000 X-ray crystal structure and characterization of halide-binding sites of human myeloperoxidase at 1.8 A resolution. halide 48-54 myeloperoxidase Homo sapiens 78-93 10766826-6 2000 The bromide-binding site in the distal cavity appears to be the halide-binding site responsible for shifts in the Soret band of the absorption spectrum of myeloperoxidase. halide 64-70 myeloperoxidase Homo sapiens 155-170 10699463-2 2000 Myeloperoxidase (MPO), a heme-containing glycoprotein located in the primary granules of polymorphonuclear leukocytes and monocytes, reacts with H(2)O(2) and halide ion and produces a more potent microbicidal oxidant, hypochlorous acid (HOCl). halide 158-164 myeloperoxidase Homo sapiens 0-15 10699463-2 2000 Myeloperoxidase (MPO), a heme-containing glycoprotein located in the primary granules of polymorphonuclear leukocytes and monocytes, reacts with H(2)O(2) and halide ion and produces a more potent microbicidal oxidant, hypochlorous acid (HOCl). halide 158-164 myeloperoxidase Homo sapiens 17-20 10587433-13 1999 Instead, bound halide is stabilized with hydrogen bonds to the N(eta)H of W118 and to N(delta)H of N52. halide 15-21 endothelin receptor type A Homo sapiens 65-68 10550245-5 1999 The cation had a large effect on the interfacial concentration of halide ions with HDPC micelles decreasing in the order Ca(2+) > Mg(2+) >> Li(+) > Na(+) > K(+) > Cs(+) > Rb(+) >> TMA(+). halide 66-72 decapping mRNA 2 Homo sapiens 83-87 10037693-7 1999 Co-expression of CFTR (but not of mutated DeltaF508-CFTR) with high levels of beta3-adrenoceptor produced an increased halide permeability under base-line conditions that was not further sensitive to cAMP or beta3-adrenoceptor stimulation. halide 119-125 adrenoceptor beta 3 Homo sapiens 78-96 10050002-11 1999 We also investigated the external halide dependence of WT ClC-2 using two-electrode voltage-clamp recording. halide 34-40 chloride voltage-gated channel 2 Homo sapiens 58-63 10050002-20 1999 The external halide dependence of hyperpolarization-activated gating of ClC-2 suggests that it is mediated or modulated by anions as in other ClC channels. halide 13-19 chloride voltage-gated channel 2 Homo sapiens 72-77 10050002-20 1999 The external halide dependence of hyperpolarization-activated gating of ClC-2 suggests that it is mediated or modulated by anions as in other ClC channels. halide 13-19 Charcot-Leyden crystal galectin Homo sapiens 72-75 10205803-5 1999 The biochemical properties of schistosome DPP I were similar to mammalian DPP I (= cathepsin C) in that schistosome DPP I was only slowly inhibited by the cysteine protease inhibitor trans-epoxysuccinyl-1-leucylamido (4-guanidino)-butane, partly inhibited by the blocked diazomethyl ketones Z-Phe-Ala-CHN2 and Z-Phe-Phe-CHN2, but enhanced by halide ions. halide 342-348 cathepsin C Homo sapiens 42-47 9950763-3 1999 In a simplified model using COS-7 cells, we demonstrate acquisition of an ATP-, ADP-, AMP-, and adenosine (ADO)-regulated halide permeability specifically following expression of wild-type (wt) cystic fibrosis transmembrane conductance regulator (CFTR). halide 122-128 CF transmembrane conductance regulator Homo sapiens 247-251 9754921-8 1998 The adverse effects may be due to scavenging of free oxygen radicals, or to interference with the interaction between luminol and the myeloperoxidase-H2O2-halide system. halide 155-161 myeloperoxidase Bos taurus 134-149 9766843-3 1998 During concomitant activation of the NADPH-dependent oxidase, the stimulated neutrophil also generates hydrogen peroxide, and in this way the MPO-hydrogen peroxide-halide system exerts its potent microbicidal activity. halide 164-170 myeloperoxidase Homo sapiens 142-145 10193578-1 1999 Dihydrolipoamide dehydrogenase (LADH) lipoamide reductase activity decreased whereas enzyme diaphorase activity increased after LADH treatment with myeloperoxidase (MPO) dependent systems (MPO/H2O2/halide, MPO/NADH/halide and MPO/H2O2/nitrite systems. halide 198-204 myeloperoxidase Equus caballus 148-163 10193578-1 1999 Dihydrolipoamide dehydrogenase (LADH) lipoamide reductase activity decreased whereas enzyme diaphorase activity increased after LADH treatment with myeloperoxidase (MPO) dependent systems (MPO/H2O2/halide, MPO/NADH/halide and MPO/H2O2/nitrite systems. halide 198-204 myeloperoxidase Equus caballus 165-168 10193578-1 1999 Dihydrolipoamide dehydrogenase (LADH) lipoamide reductase activity decreased whereas enzyme diaphorase activity increased after LADH treatment with myeloperoxidase (MPO) dependent systems (MPO/H2O2/halide, MPO/NADH/halide and MPO/H2O2/nitrite systems. halide 198-204 myeloperoxidase Equus caballus 189-192 10193578-1 1999 Dihydrolipoamide dehydrogenase (LADH) lipoamide reductase activity decreased whereas enzyme diaphorase activity increased after LADH treatment with myeloperoxidase (MPO) dependent systems (MPO/H2O2/halide, MPO/NADH/halide and MPO/H2O2/nitrite systems. halide 198-204 myeloperoxidase Equus caballus 189-192 10193578-1 1999 Dihydrolipoamide dehydrogenase (LADH) lipoamide reductase activity decreased whereas enzyme diaphorase activity increased after LADH treatment with myeloperoxidase (MPO) dependent systems (MPO/H2O2/halide, MPO/NADH/halide and MPO/H2O2/nitrite systems. halide 198-204 myeloperoxidase Equus caballus 189-192 10193578-1 1999 Dihydrolipoamide dehydrogenase (LADH) lipoamide reductase activity decreased whereas enzyme diaphorase activity increased after LADH treatment with myeloperoxidase (MPO) dependent systems (MPO/H2O2/halide, MPO/NADH/halide and MPO/H2O2/nitrite systems. halide 215-221 myeloperoxidase Equus caballus 148-163 10193578-1 1999 Dihydrolipoamide dehydrogenase (LADH) lipoamide reductase activity decreased whereas enzyme diaphorase activity increased after LADH treatment with myeloperoxidase (MPO) dependent systems (MPO/H2O2/halide, MPO/NADH/halide and MPO/H2O2/nitrite systems. halide 215-221 myeloperoxidase Equus caballus 165-168 10193578-1 1999 Dihydrolipoamide dehydrogenase (LADH) lipoamide reductase activity decreased whereas enzyme diaphorase activity increased after LADH treatment with myeloperoxidase (MPO) dependent systems (MPO/H2O2/halide, MPO/NADH/halide and MPO/H2O2/nitrite systems. halide 215-221 myeloperoxidase Equus caballus 189-192 10193578-1 1999 Dihydrolipoamide dehydrogenase (LADH) lipoamide reductase activity decreased whereas enzyme diaphorase activity increased after LADH treatment with myeloperoxidase (MPO) dependent systems (MPO/H2O2/halide, MPO/NADH/halide and MPO/H2O2/nitrite systems. halide 215-221 myeloperoxidase Equus caballus 189-192 10193578-1 1999 Dihydrolipoamide dehydrogenase (LADH) lipoamide reductase activity decreased whereas enzyme diaphorase activity increased after LADH treatment with myeloperoxidase (MPO) dependent systems (MPO/H2O2/halide, MPO/NADH/halide and MPO/H2O2/nitrite systems. halide 215-221 myeloperoxidase Equus caballus 189-192 10193578-6 1999 LADH inactivation by the MPO/NADH/halide systems was prevented by catalase and enhanced by superoxide dismutase, in close agreement with H2O2 production by the LADH/NADH system. halide 34-40 myeloperoxidase Equus caballus 25-28 9379167-0 1997 Halide permeation in wild-type and mutant cystic fibrosis transmembrane conductance regulator chloride channels. halide 0-6 cystic fibrosis transmembrane conductance regulator Cricetulus griseus 42-93 9486119-3 1998 With increasing numbers of microinjected pECE-CFTR copies, the baseline permeability to halide dose dependently increased, and the response to adenosine 3",5"-cyclic monophosphate (cAMP) stimulation decreased. halide 88-94 CF transmembrane conductance regulator Homo sapiens 46-50 9486119-4 1998 In cells hyperexpressing CFTR, the high level of halide permeability was reduced when a cell metabolism poisoning cocktail was applied to decrease intracellular ATP and, inversely, was increased by orthovanadate. halide 49-55 CF transmembrane conductance regulator Homo sapiens 25-29 9776476-2 1998 Taurine, the most abundant free amino acid in the cytosol of neutrophils, is chlorinated to form TauCl by the halide-dependent myeloperoxidase (MPO) system. halide 110-116 myeloperoxidase Mus musculus 144-147 9435272-7 1998 The halide permeability sequence was PCl > PF > PI > PBr indicating that permeation through the channel was dominated by ion binding sites with a high field strength. halide 4-10 translocator protein Homo sapiens 62-65 9706251-9 1998 The MPO/NADH/halide systems, where NADH replaced H2O2, also inactivated LADH. halide 13-19 myeloperoxidase Homo sapiens 4-7 9425735-3 1997 Here, Janusz Marcinkiewicz examines recent data indicating that chloramines, the neutrophil-specific products of the myeloperoxidase--hydrogen-peroxide--halide system, may provide a bridge between the afferent branches of the innate and acquired immune response. halide 153-159 myeloperoxidase Homo sapiens 117-132 9379167-1 1997 Permeation of cystic fibrosis transmembrane conductance regulator (CFTR) Cl channels by halide ions was studied in stably transfected Chinese hamster ovary cells by using the patch clamp technique. halide 88-94 cystic fibrosis transmembrane conductance regulator Cricetulus griseus 14-65 9379167-1 1997 Permeation of cystic fibrosis transmembrane conductance regulator (CFTR) Cl channels by halide ions was studied in stably transfected Chinese hamster ovary cells by using the patch clamp technique. halide 88-94 cystic fibrosis transmembrane conductance regulator Cricetulus griseus 67-71 9261850-11 1997 We conclude that proteinase-free myeloperoxidase, in the presence of non-toxic concentrations of its substrates, hydrogen peroxide and halide, produced increases in permeability to non-ionic molecules in the rat trachea within 15 minutes. halide 135-141 endogenous retrovirus group K member 25 Homo sapiens 17-27 9386357-3 1997 The PAM model suggested that TNF-alpha and GM-CSF could activate PAM to restrict the intracellular growth of the bacteria, probably not through the superoxide anion release, but through the myeloperoxidasae-halide system. halide 207-213 peptidylglycine alpha-amidating monooxygenase Homo sapiens 4-7 9386357-3 1997 The PAM model suggested that TNF-alpha and GM-CSF could activate PAM to restrict the intracellular growth of the bacteria, probably not through the superoxide anion release, but through the myeloperoxidasae-halide system. halide 207-213 tumor necrosis factor Homo sapiens 29-38 9386357-3 1997 The PAM model suggested that TNF-alpha and GM-CSF could activate PAM to restrict the intracellular growth of the bacteria, probably not through the superoxide anion release, but through the myeloperoxidasae-halide system. halide 207-213 colony stimulating factor 2 Homo sapiens 43-49 9386357-3 1997 The PAM model suggested that TNF-alpha and GM-CSF could activate PAM to restrict the intracellular growth of the bacteria, probably not through the superoxide anion release, but through the myeloperoxidasae-halide system. halide 207-213 peptidylglycine alpha-amidating monooxygenase Homo sapiens 65-68 9261850-11 1997 We conclude that proteinase-free myeloperoxidase, in the presence of non-toxic concentrations of its substrates, hydrogen peroxide and halide, produced increases in permeability to non-ionic molecules in the rat trachea within 15 minutes. halide 135-141 myeloperoxidase Homo sapiens 33-48 9151778-3 1997 Myeloperoxidase is the only human enzyme known to generate hypochlorous acid (HOCl), a potent oxidizing agent, at physiological halide concentrations. halide 128-134 myeloperoxidase Homo sapiens 0-15 9223231-9 1997 Interference with the MPO-H2O2-halide system was also observed with spiramycin, erythromycin and oxytetracycline, while the latter was also observed with penicillin. halide 31-37 myeloperoxidase Bos taurus 22-25 9033274-3 1997 Although the nature of the in vivo oxidants remains unknown, recent findings indicated that the myeloperoxidase (MPO)-H2O2-halide system could play an important role in modification of (lipo)proteins in human tissues. halide 123-129 myeloperoxidase Homo sapiens 96-111 9033274-3 1997 Although the nature of the in vivo oxidants remains unknown, recent findings indicated that the myeloperoxidase (MPO)-H2O2-halide system could play an important role in modification of (lipo)proteins in human tissues. halide 123-129 myeloperoxidase Homo sapiens 113-116 8886852-5 1996 The effects of taurine on O2- production was attributed to the in vitro formation of Tau-Cl catalyzed by PMN associated halide-dependent myeloperoxidase. halide 120-126 myeloperoxidase Mus musculus 137-152 9214581-8 1997 These findings suggest the involvement of an MPO-H2O2-halide system in the accelerated consumption of glutathione during the respiratory burst. halide 54-60 myeloperoxidase Rattus norvegicus 45-48 8849775-2 1996 5"-phosphorothioate-modified RNA (GMPS-RNA) sequences were selected from a randomized pool of oligoribonucleotides for their ability to accelerate a halide substitution reaction with N-bromoacetyl-bradykinin (BrBK). halide 149-155 guanine monophosphate synthase Homo sapiens 34-38 8960369-1 1996 Halide-dependent cytolysis of B-16 melanoma cells mediated by myeloperoxidase and lactoperoxidase systems was observed by turbidimetry. halide 0-6 myeloperoxidase Mus musculus 62-77 8849775-2 1996 5"-phosphorothioate-modified RNA (GMPS-RNA) sequences were selected from a randomized pool of oligoribonucleotides for their ability to accelerate a halide substitution reaction with N-bromoacetyl-bradykinin (BrBK). halide 149-155 kininogen 1 Homo sapiens 197-207 8842560-9 1996 CONCLUSION: Both granule basic proteins and reactive oxygen radical may be responsible for epithelial damage, probably via an EPO + H2O2 + halide system. halide 139-145 erythropoietin Cavia porcellus 126-129 7553790-8 1995 Halide efflux increases with P2U-purinoceptor stimulation which is consistent with the opening of a Ca(2+)-sensitive Cl- channel. halide 0-6 purinergic receptor P2Y2 Homo sapiens 29-32 8792002-10 1996 PA halide derivatives may have similar actions as tamoxifen because they show specificity for estrogen receptor-positive cells. halide 3-9 estrogen receptor 1 Homo sapiens 94-111 8825615-5 1996 The virucidal effect of eosinophils, PMA, and bromide under these conditions is inhibited by the peroxidase inhibitor azide and catalase, but not heated catalase or superoxide dismutase, implicating the EPO-H2O2-halide system. halide 212-218 catalase Homo sapiens 128-136 7573398-17 1995 The halide permeability sequence was PCl = PBr > PI. halide 4-10 resistance to Paracoccidioides brasiliensis Mus musculus 43-46 7653523-1 1995 External iodide (I-o) inhibits AE1 (band 3)-mediated anion exchange in human red blood cells by binding to a noncompetitive inhibitory site, the external halide modifier site. halide 154-160 solute carrier family 4 member 1 (Diego blood group) Homo sapiens 31-34 8037456-5 1994 The enzyme also resembles mammalian CA IV in its relative sensitivity to inhibition by sulfonamides and the resistance to inhibition by halide ions. halide 136-142 carbonic anhydrase 4 Homo sapiens 36-41 7530672-8 1995 Following infection with the adenovirus vector Ad2/CFTR2, a cAMP-induced halide efflux was observed for 31 days, although the number of responsive cells decreased with time. halide 73-79 apolipoprotein E Homo sapiens 47-50 7750983-0 1994 Oxidants generated by the myeloperoxidase-halide system activate the fifth component of human complement, C5. halide 42-48 myeloperoxidase Homo sapiens 26-41 7750983-7 1994 Since hypochlorite and T-NCl are biological products generated by the myeloperoxidase-halide system of stimulated leukocytes, the activation of C5 by these agents may be one way to complement activation during inflammation and tissue injury. halide 86-92 nucleolin Homo sapiens 25-28 7750983-7 1994 Since hypochlorite and T-NCl are biological products generated by the myeloperoxidase-halide system of stimulated leukocytes, the activation of C5 by these agents may be one way to complement activation during inflammation and tissue injury. halide 86-92 myeloperoxidase Homo sapiens 70-85 7861697-11 1994 Our results show that the hypohalous acid derived from that of H2O2-MPO-halide system is capable of increasing Palbumin. halide 72-78 myeloperoxidase Rattus norvegicus 68-71 7517633-3 1994 I/F also stimulated halide efflux from CFTR and delta F508 oocytes in the sequence Cl > Br > I. halide 20-26 cystic fibrosis transmembrane conductance regulator L homeolog Xenopus laevis 39-43 7814266-4 1994 The H2O2-MPO-halide system in phagocytosing cells was localized at the fine structural level by our development of 3,3"-diaminobenzidine (DAB) as a cytochemical probe for detecting peroxidase activities. halide 13-19 myeloperoxidase Homo sapiens 9-12 8027975-3 1994 The spectra are consistent with dissociation of the halide ligands to give Cp2-Ti2+(aq), which coordinates to nucleobase (N) and phosphate (O) binding sites. halide 52-58 ceruloplasmin Homo sapiens 75-78 8177196-4 1994 Measurement of O2- production capacity was used as a reflection of the activity of NADPH oxidase, and the activity of myeloperoxidase-H2O2-halide system was evaluated using luminol-dependent chemiluminescence. halide 139-145 myeloperoxidase Homo sapiens 118-133 8177196-8 1994 These results suggest that postoperative PMN signal transduction mechanisms, mediated by protein kinase C, may activate myeloperoxidase-H2-O2-halide system but suppress NADPH oxidase system dependently of the degree of surgical stress, revealing a differential effect of protein kinase C activation on PMN microbicidal activity. halide 142-148 myeloperoxidase Homo sapiens 120-135 7508815-6 1993 These results indicate that the CFTR-induced Cl- conductance in LTK- cells can be activated by either cyclic AMP or high intracellular halide concentrations. halide 135-141 CF transmembrane conductance regulator Homo sapiens 32-36 8145684-4 1993 As chemiluminogenic probes we have employed lucigenin and luminon that are know to be sensitive to the superoxide anion and the H2O2-myeloperoxidase-halide system of PMNs, respectively. halide 149-155 myeloperoxidase Homo sapiens 133-148 8145684-5 1993 Activated PMNs from children with trisomy 21 exhibited a low level of superoxide and a reduced activity of H2O2-myeloperoxidase-halide system compared to the control group. halide 128-134 myeloperoxidase Homo sapiens 112-127 7508815-6 1993 These results indicate that the CFTR-induced Cl- conductance in LTK- cells can be activated by either cyclic AMP or high intracellular halide concentrations. halide 135-141 leukocyte receptor tyrosine kinase Homo sapiens 64-67 7694154-2 1993 Mutations at Lys 335 and Arg 347 in the sixth predicted transmembrane helix of CFTR alter its halide selectivity in whole-cell studies and its single channel conductance, but the physical basis of these alterations is unknown and permeation in CFTR is poorly understood. halide 94-100 CF transmembrane conductance regulator Homo sapiens 79-83 8385432-3 1993 Hypohalous acids produced by the eosinophil peroxidase (EPO)-hydrogen peroxide (H2O2)-halide system are stable cytotoxic oxidants. halide 86-92 eosinophil peroxidase Rattus norvegicus 33-54 8385432-3 1993 Hypohalous acids produced by the eosinophil peroxidase (EPO)-hydrogen peroxide (H2O2)-halide system are stable cytotoxic oxidants. halide 86-92 eosinophil peroxidase Rattus norvegicus 56-59 8385432-9 1993 Thus, the acute changes in microvascular permeability were modulated by activity of the EPO-H2O2-Halide system, but the increased vascular and bronchial resistances were mediated through a different pathway. halide 97-103 eosinophil peroxidase Rattus norvegicus 88-91 1337069-6 1992 Both antimicrobial agents caused a dose-related stimulation of neutrophil migration which was associated with inhibition of leucoattractant-activated generation of superoxide and activity of the myeloperoxidase/H2O2/halide system. halide 216-222 myeloperoxidase Homo sapiens 195-210 1329616-4 1992 The antimicrobial agents also inhibited the generation of reactive oxidants by the MPO-H2O2-halide system during activation of both untreated and 1-hp-treated neutrophils by FMLP. halide 92-98 myeloperoxidase Homo sapiens 83-86 1319151-7 1992 Other halide ions are also found to inhibit the potato PPi-PFK: bromide is competitive like chloride, whereas fluoride and iodide have a mixed inhibition towards Fru 2,6-P2. halide 6-12 pyrophosphate--fructose 6-phosphate 1-phosphotransferase subunit alpha Solanum tuberosum 55-62 7522901-3 1993 To study the domains of CFTR involved in Cl- channel function, we expressed mutants lacking various domains and assayed cAMP-stimulated Cl- channel activity using the halide-sensitive fluorophore, 6-methoxy-N-(3"-sulfopropyl)-quinolinium. halide 167-173 CF transmembrane conductance regulator Homo sapiens 24-28 1662050-1 1991 The degranulation and myeloperoxidase-H2O2-halide activities of human polymorphonuclear leukocytes from healthy donors were tested after co-incubation with either Brucella melitensis 16M, Staphylococcus aureus or Staphylococcus aureus in presence of lipopolysaccharide, protein fraction, native hapten and soluble fractions released at 65 degrees C from smooth strain of Brucella melitensis 16M. halide 43-49 myeloperoxidase Homo sapiens 22-37 1715578-3 1991 Anion transport in CFTR transcript antisense-treated cells was then assessed with a halide-specific dye, 6-methoxy-N-(3-sulfopropyl)quinolinium, and fluorescent digital imaging microscopy to monitor halide influx and efflux from single sweat duct cells. halide 84-90 CF transmembrane conductance regulator Homo sapiens 19-23 1849170-7 1991 On the basis of above findings, we speculate that phagocytosis of CGD PMNs is increased because the H2O2-myeloperoxidase-halide system, which may modulate phagocytic activity of PMNs, fails to operate. halide 121-127 myeloperoxidase Homo sapiens 105-120 2002037-2 1991 The potent cytotoxic capacity of eosinophils for parasites and host tissue has in part been attributed to the catalytic action of eosinophil peroxidase (EPO), which preferentially oxidizes Br- to the powerful bleaching oxidant HOBr in buffers that mimic serum halide composition (100 mM Cl-, 20-100 microM Br-, less than 1 microM I-). halide 260-266 eosinophil peroxidase Rattus norvegicus 130-151 2002037-2 1991 The potent cytotoxic capacity of eosinophils for parasites and host tissue has in part been attributed to the catalytic action of eosinophil peroxidase (EPO), which preferentially oxidizes Br- to the powerful bleaching oxidant HOBr in buffers that mimic serum halide composition (100 mM Cl-, 20-100 microM Br-, less than 1 microM I-). halide 260-266 eosinophil peroxidase Rattus norvegicus 153-156 33588715-7 2021 Interestingly, Two PSAT structures from different organisms show halide binding near their active site. halide 65-71 phosphoserine aminotransferase 1 Homo sapiens 19-23 1650200-5 1991 formation (NBT reduction) and Myeloperoxidase (MPO) mediated oxidisable halide incorporation (131I incorporation) were found to be highly stimulated by SRBC in normal (CS) and tumour bearing counterparts (TS). halide 72-78 myeloperoxidase Mus musculus 30-45 1650200-5 1991 formation (NBT reduction) and Myeloperoxidase (MPO) mediated oxidisable halide incorporation (131I incorporation) were found to be highly stimulated by SRBC in normal (CS) and tumour bearing counterparts (TS). halide 72-78 myeloperoxidase Mus musculus 47-50 1985118-4 1991 Because EPO preferentially oxidizes Br- to hypobromous acid (HOBr) rather than Cl- to hypochlorous acid (HOCl) at physiologic halide concentrations, we characterized the Br(-)-dependent toxicity of both activated EOs and purified human EPO towards several types of endothelial cells and isolated working rat hearts. halide 126-132 eosinophil peroxidase Rattus norvegicus 8-11 34918929-0 2021 Twist-to-Untwist Evolution and Cation Polarization Behavior of Hybrid Halide Perovskite Nanoplatelets Revealed by Cryogenic Transmission Electron Microscopy. halide 70-76 twist family bHLH transcription factor 1 Homo sapiens 0-5 1847831-0 1991 Interaction of halides with the cyanide complex of myeloperoxidase: a model for substrate binding to compound I. EPR spectra of the low-spin cyanide complex of myeloperoxidase have been measured in the absence and presence of halide substrates; chloride, bromide and iodide. halide 15-21 myeloperoxidase Homo sapiens 51-66 1847831-0 1991 Interaction of halides with the cyanide complex of myeloperoxidase: a model for substrate binding to compound I. EPR spectra of the low-spin cyanide complex of myeloperoxidase have been measured in the absence and presence of halide substrates; chloride, bromide and iodide. halide 15-21 myeloperoxidase Homo sapiens 160-175 1801517-1 1991 Different from other proteases the halide- and thiol-dependent lysosomal dipeptidyl peptidase I (DPP I, cathepsin C, EC 3.4.14.1.) halide 35-41 cathepsin C Rattus norvegicus 73-95 1801517-1 1991 Different from other proteases the halide- and thiol-dependent lysosomal dipeptidyl peptidase I (DPP I, cathepsin C, EC 3.4.14.1.) halide 35-41 cathepsin C Rattus norvegicus 97-102 1801517-1 1991 Different from other proteases the halide- and thiol-dependent lysosomal dipeptidyl peptidase I (DPP I, cathepsin C, EC 3.4.14.1.) halide 35-41 cathepsin C Rattus norvegicus 104-115 2165113-3 1990 Further, both azide and catalase + superoxide dismutase inhibited the ability of normal neutrophils to damage hyphae, suggesting that this damage is mediated by products of the respiratory burst and by the MPO-halide system. halide 210-216 myeloperoxidase Homo sapiens 206-209 2111324-5 1990 CA IV resembles CA II in being a "high activity" isozyme, relatively resistant to inhibition by halide ions and sensitive to inhibition by sulfonamides. halide 96-102 carbonic anhydrase 4 Homo sapiens 0-5 33810499-4 2021 The predicted "homo-coupling" reaction of [PtBr(NCN-C(O)H-4)] led to the unexpected formation of 3,3",5,5"-tetra[(dimethylamino)methyl]-4,4"-bis(platinum halide)-benzophenone (halide = Br or Cl), referred to hereafter as the bispincer-benzophenone complex 13. halide 154-160 translocator protein Homo sapiens 43-47 33588715-8 2021 While the human PSAT1 shows a water molecule at this site with different interacting residues, suggesting the inability of halide binding in the human enzyme. halide 123-129 phosphoserine aminotransferase 1 Homo sapiens 16-21 35085411-3 2022 Here we disclose an efficient new nickel-catalyzed protocol for the C-N cross-coupling of amides and 2"-(pseudo)halide-substituted acetophenones, for the first time where the (pseudo)halide is chloride or sulfonate, which makes use of the commercial bisphosphine ligand PAd2-DalPhos ( L4 ) in combination with an organic amine base/halide scavenger, leading to 4-quinolones. halide 332-338 peptidyl arginine deiminase 2 Homo sapiens 270-274 34190377-6 2021 In fact, the whole series of non-radiative halide complexes (PPh4)((CF3)3AgX) (X = F to I) has been experimentally prepared and isolated in pure form. halide 43-49 potassium two pore domain channel subfamily K member 3 Homo sapiens 61-65 34160505-1 2021 The versatility of a bulky bis(imino)carbazolate ligand in lead(ii) chemistry is illustrated by the synthesis of a soluble, heteroleptic lead(ii) fluoride and several halide (Cl, Br and I), amide and hydrocarbyl congeners. halide 167-173 chromosome 12 open reading frame 73 Homo sapiens 179-187 35424921-0 2022 First-principles study on the elastic, electronic and optical properties of all-inorganic halide perovskite solid solutions of CsPb(Br1-x Cl x )3 within the virtual crystal approximation. halide 90-96 granzyme B Homo sapiens 127-131 35424921-0 2022 First-principles study on the elastic, electronic and optical properties of all-inorganic halide perovskite solid solutions of CsPb(Br1-x Cl x )3 within the virtual crystal approximation. halide 90-96 C-X-C motif chemokine ligand 11 Homo sapiens 132-135 35040632-3 2022 Furthermore, we illustrate reversible photochromism in halide perovskite by modulating the intermediate n phase in the FAn+2PbnBr3n+2 structure, enabling greater control of the optical band gap and luminescence of a (110) oriented mono-halide/cation perovskite. halide 55-61 neutral sphingomyelinase activation associated factor Homo sapiens 119-122 35113524-6 2022 The optimized Li2.6Er0.6Zr0.4Cl6 electrolyte exhibits both a high ionic conductivity of 1.13 mS cm-1 and a high oxidation voltage of 4.21 V. Furthermore, carbon additives are demonstrated to be beneficial for achieving high discharge capacity and better cycling stability and rate performance for halide-based ASSLIBs, which are completely different from the case of sulfide electrolytes. halide 297-303 ATP binding cassette subfamily A member 12 Homo sapiens 14-17 2560462-5 1989 Pretreatment with inhibitors of oxidative burst demonstrated that the yeast cell killing by MDP-stimulated PMN was not affected by SOD but was inhibited by sodium azide, indicating the involvement of myeloperoxidase (MPO)-halide system in fungicidal mechanisms induced by MDP. halide 222-228 myeloperoxidase Homo sapiens 217-220 35133160-3 2022 Herein, taking K+ and Cs+ co-incorporated mixed halide perovskites as a model, the impact of external ions on ion migration behavior has been interpreted via multiple dimensional characterization aspects. halide 48-54 citrate synthase Homo sapiens 22-24 2560462-7 1989 Inhibition by sodium azide and sodium benzoate indicated that these oxygen metabolites could be derived from the MPO-halide system but also from hydroxyl radical production. halide 117-123 myeloperoxidase Homo sapiens 113-116 2751158-9 1989 Catalase and azide significantly inhibited the lysis of these cells, suggesting the eosinophil peroxidase-catalyzed products of halide oxidation mediated this form of injury. halide 128-134 catalase Homo sapiens 0-8 2751158-9 1989 Catalase and azide significantly inhibited the lysis of these cells, suggesting the eosinophil peroxidase-catalyzed products of halide oxidation mediated this form of injury. halide 128-134 eosinophil peroxidase Homo sapiens 84-105 2751158-11 1989 We hypothesize that the eosinophil peroxidase-hydrogen peroxide-halide system and major basic protein may injure the nasal epithelium in inflammatory conditions such as allergic and nonallergic eosinophilic rhinitis. halide 64-70 eosinophil peroxidase Homo sapiens 24-45 2556228-1 1989 We have demonstrated that penicillamine (PSH) has the capacity to effect phagocytic cells by its interaction with the myeloperoxidase-halide system (MPOHS). halide 134-140 myeloperoxidase Homo sapiens 118-133 2556228-9 1989 In conclusion, PSH inhibits the myeloperoxidase-halide system at a cellular level by scavenging H2O2 rather than by oxidation of the myeloperoxidase enzyme. halide 48-54 myeloperoxidase Homo sapiens 32-47 2539694-2 1989 Activation of neutrophils in vitro with interferon-gamma resulted in enhanced production of O2- and myelopeoroxidase-H2O2-halide activity by neutrophils in the presence of B. abortus. halide 122-128 interferon gamma Bos taurus 40-56 2659666-0 1989 Comparative toxicity of the horse eosinophil peroxidase-H2O2-halide system and granule basic proteins. halide 61-67 eosinophil peroxidase Equus caballus 34-55 2659666-2 1989 EPO reacts with H2O2 formed by the respiratory burst and a halide to form cytotoxic oxidants. halide 59-65 eosinophil peroxidase Equus caballus 0-3 2659666-3 1989 The relative potency of the EPO-H2O2-halide system and the GBP is considered here. halide 37-43 eosinophil peroxidase Equus caballus 28-31 2659666-10 1989 Thus, under the conditions employed, the EPO-H2O2-halide system contributed to a considerably greater degree to the toxic activity of the granule components than did the GBP. halide 50-56 eosinophil peroxidase Equus caballus 41-44 2785522-4 1989 Ligand binding via this receptor is rapidly inactivated by products of the myeloperoxidase-hydrogen peroxide-halide system of PMN. halide 109-115 myeloperoxidase Homo sapiens 75-90 2831432-0 1988 Morphologic correlates of glomerular oxidant injury induced by the myeloperoxidase-hydrogen peroxide-halide system of the neutrophil. halide 101-107 myeloperoxidase Rattus norvegicus 67-82 2848083-1 1988 The neutrophil myeloperoxidase-H2O2-halide enzyme system produces hypochlorous acid and chlorinated amine compounds capable of killing a variety of target cells. halide 36-42 myeloperoxidase Homo sapiens 15-30 2979742-2 1988 There is a direct correlation between the nucleophilicity of the halide and increased total and individual isomeric propyl halide (PrX) products. halide 65-71 periaxin Homo sapiens 131-134 2822992-8 1987 These data indicate that this model of PMN-mediated IC GN is associated with activation of the MPO-H2O2-halide system, which may participate in mediating glomerular injury. halide 104-110 myeloperoxidase Rattus norvegicus 95-98 3311071-3 1987 The CD-spectral changes are strikingly similar to those brought about by halide ions which have been identified to reflect the 2 Zn----4 Zn insulin transition. halide 73-79 insulin Homo sapiens 140-147 3034783-17 1987 These findings suggest that cellular products generated by the H2O2-MPO-halide system down-regulate the rosette-forming and phagocytic activity of PMNs from normal healthy individuals, but not that from CGD and MPO-deficient patients. halide 72-78 myeloperoxidase Homo sapiens 68-71 3955002-0 1986 Ligand and halide binding properties of chloroperoxidase: peroxidase-type active site heme environment with cytochrome P-450 type endogenous axial ligand and spectroscopic properties. halide 11-17 cytochrome P450 family 4 subfamily F member 3 Homo sapiens 108-124 3032797-10 1987 Arginine, a scavenger of hypochlorite, significantly depressed the ability of sCM-treated neutrophils to kill amoebae and also prevented the amoebicidal properties of the MPO-H2O2-halide system. halide 180-186 myeloperoxidase Homo sapiens 171-174 3032797-11 1987 These results suggest that the MPO-H2O2-halide system is important in the killing of naegleriae by sCM-treated neutrophils and that hypochlorite may be the amoebicidal agent. halide 40-46 myeloperoxidase Homo sapiens 31-34 3009589-3 1986 The azurophilic granules supply enzymes for digestive and bactericidal functions and supply MPO to the MPO-halide-hydrogen peroxide bactericidal system. halide 107-113 myeloperoxidase Homo sapiens 92-95 3009589-3 1986 The azurophilic granules supply enzymes for digestive and bactericidal functions and supply MPO to the MPO-halide-hydrogen peroxide bactericidal system. halide 107-113 myeloperoxidase Homo sapiens 103-106 3033023-1 1987 Myeloperoxidase-hydrogen peroxide-halide system. halide 34-40 myeloperoxidase Rattus norvegicus 0-15 3033023-5 1987 We tested the hypothesis that the MPO-H2O2-halide system may induce glomerular injury by infusing MPO followed by H2O2 in a chloride-containing solution into the renal artery of rats. halide 43-49 myeloperoxidase Rattus norvegicus 34-37 3033023-5 1987 We tested the hypothesis that the MPO-H2O2-halide system may induce glomerular injury by infusing MPO followed by H2O2 in a chloride-containing solution into the renal artery of rats. halide 43-49 myeloperoxidase Rattus norvegicus 98-101 3033023-10 1987 The MPO-H2O2-halide system causes glomerular injury and may be important in neutrophil-mediated glomerulonephritis. halide 13-19 myeloperoxidase Rattus norvegicus 4-7 3029204-9 1987 Catalase and azide substantially inhibited the lysis produced by the EPO-H2O2-halide system, suggesting that EPO-catalyzed products of halide oxidation mediated this form of injury. halide 78-84 catalase Homo sapiens 0-8 3029204-9 1987 Catalase and azide substantially inhibited the lysis produced by the EPO-H2O2-halide system, suggesting that EPO-catalyzed products of halide oxidation mediated this form of injury. halide 78-84 eosinophil peroxidase Homo sapiens 69-72 3029204-9 1987 Catalase and azide substantially inhibited the lysis produced by the EPO-H2O2-halide system, suggesting that EPO-catalyzed products of halide oxidation mediated this form of injury. halide 78-84 eosinophil peroxidase Homo sapiens 109-112 3029204-9 1987 Catalase and azide substantially inhibited the lysis produced by the EPO-H2O2-halide system, suggesting that EPO-catalyzed products of halide oxidation mediated this form of injury. halide 135-141 catalase Homo sapiens 0-8 3029204-9 1987 Catalase and azide substantially inhibited the lysis produced by the EPO-H2O2-halide system, suggesting that EPO-catalyzed products of halide oxidation mediated this form of injury. halide 135-141 eosinophil peroxidase Homo sapiens 69-72 3029204-9 1987 Catalase and azide substantially inhibited the lysis produced by the EPO-H2O2-halide system, suggesting that EPO-catalyzed products of halide oxidation mediated this form of injury. halide 135-141 eosinophil peroxidase Homo sapiens 109-112 3029204-11 1987 We hypothesize that the EPO-H2O2-halide system may injure the lung in asthma and eosinophilic pulmonary syndromes. halide 33-39 eosinophil peroxidase Homo sapiens 24-27 2824603-3 1987 The intermediate and high levels of MPO activity detected in all the species studied except in pigeons suggest involvement of the MPO-H2O2-halide cytocidal system of PMNL in destroying Y. pestis. halide 139-145 myeloperoxidase Mus musculus 36-39 2824603-3 1987 The intermediate and high levels of MPO activity detected in all the species studied except in pigeons suggest involvement of the MPO-H2O2-halide cytocidal system of PMNL in destroying Y. pestis. halide 139-145 myeloperoxidase Mus musculus 130-133 3004333-8 1986 Results obtained in conjunction with these studies demonstrated that the thioredoxin m-linked activation of NADP-malate dehydrogenase in selectively enhanced by the presence of halide ions (e.g., chloride) and by an organic solvent (e.g., 2-propanol). halide 177-183 LOC101027257 Zea mays 73-84 3946895-2 1986 Of the neutrophil functions examined, the iodination reaction, which evaluates the activity of the myeloperoxidase-hydrogen peroxide-halide antibacterial system of the neutrophil, reflected the most marked differences among age groups. halide 133-139 myeloperoxidase Bos taurus 99-114 3002685-0 1985 Differentiated HL60 promyelocytic leukaemia cells have a deficient myeloperoxidase/halide killing system. halide 83-89 myeloperoxidase Homo sapiens 67-82 2991014-1 1985 We have previously studied purified human myeloperoxidase-hydrogen peroxide-halide ion systems as models of possible singlet oxygen production by granulocytes. halide 76-82 myeloperoxidase Homo sapiens 42-57 6696169-3 1984 The binding per se was not toxic to the organisms under our conditions, but EPO-coated schistosomula were rapidly killed when H2O2 and halide were added, under conditions in which uncoated schistosomula were unaffected. halide 135-141 eosinophil peroxidase Homo sapiens 76-79 2990672-7 1985 The results suggest that hydrogen peroxide is also important for these cytotoxicities whereas, unlike the results with TAK, the H2O2:halide:myeloperoxidase system may partly participate in the cytotoxicities with some immunomodulators. halide 133-139 myeloperoxidase Mus musculus 140-155 2981925-3 1985 Neutrophils and other phagocytes can injure cells by means of oxygen-dependent mechanisms, particularly the myeloperoxidase (MPO)-H2O2-halide system. halide 135-141 myeloperoxidase Homo sapiens 108-123 2981925-3 1985 Neutrophils and other phagocytes can injure cells by means of oxygen-dependent mechanisms, particularly the myeloperoxidase (MPO)-H2O2-halide system. halide 135-141 myeloperoxidase Homo sapiens 125-128 2981586-3 1985 Recovery of B12 binding protein from neutrophils exposed to phorbol myristate acetate or opsonized zymosan was significantly enhanced on addition of heme enzyme inhibitors (azide, cyanide) or catalase or when halide-free medium was used. halide 209-215 NADH:ubiquinone oxidoreductase subunit B3 Homo sapiens 12-15 2981586-5 1985 These data indicate extracellular destruction of functional B12 binding protein by the halide-dependent heme enzyme myeloperoxidase and H2O2. halide 87-93 NADH:ubiquinone oxidoreductase subunit B3 Homo sapiens 60-63 2981586-5 1985 These data indicate extracellular destruction of functional B12 binding protein by the halide-dependent heme enzyme myeloperoxidase and H2O2. halide 87-93 myeloperoxidase Homo sapiens 116-131 2981586-7 1985 A cell-free extract of vitamin B12 binding protein was readily inactivated on exposure to purified myeloperoxidase, H2O2, and a halide. halide 128-134 NADH:ubiquinone oxidoreductase subunit B3 Homo sapiens 31-34 6095920-1 1984 The effect of myeloperoxidase, hydrogen peroxide (H2O2) and a halide (Cl) on the opsonizing molecules in immunoglobulin G (IgG) and complement factor C3b was assayed. halide 62-68 complement C3 Homo sapiens 150-153 6095920-7 1984 Since the myeloperoxidase-H2O2-halide system also affects chemotactic factors, leukotrienes, proteinases and membrane receptors, the system may in several ways affect the development of the inflammatory response. halide 31-37 myeloperoxidase Homo sapiens 10-25 6487320-1 1984 A method for investigating the cellular response of polymorphonuclear leukocytes to various stimuli was introduced using simultaneously native (luminol-independent) and luminol dependent luminescence as an indicator for myeloperoxidase (MPO)-H2O2-halide and O2- mediated reactions. halide 247-253 myeloperoxidase Homo sapiens 220-235 6487320-1 1984 A method for investigating the cellular response of polymorphonuclear leukocytes to various stimuli was introduced using simultaneously native (luminol-independent) and luminol dependent luminescence as an indicator for myeloperoxidase (MPO)-H2O2-halide and O2- mediated reactions. halide 247-253 myeloperoxidase Homo sapiens 237-240 6487320-3 1984 Consequently the MPO-H2O2-halide system could be distinguished from the O2- dependent system by interpreting the recorded temporal traces of the emitted light. halide 26-32 myeloperoxidase Homo sapiens 17-20 6432048-1 1984 The effect of halide ions on frog epidermis tyrosinase has been characterized with the trypsin-activated enzyme. halide 14-20 tyrosinase Homo sapiens 44-54 6321554-10 1984 These data indicate that, apart from being a potent antimicrobial system, the oxidizing activity of the MPO-H2O2-halide system may modulate the inflammatory response by impairing certain receptor-mediated recognition mechanisms of phagocytic cells, which otherwise could elicit inflammatory reactions and tissue injury. halide 113-119 myeloperoxidase Homo sapiens 104-107 6322510-8 1984 In addition, the MPO deficiency impairs the H2O2-halide-MPO system, which is of particular importance for fungal killing, e.g. of C. albicans, which has also been reported to be deficient in DS. halide 49-55 myeloperoxidase Homo sapiens 17-20 6090506-1 1984 The myeloperoxidase (MPO)-hydrogen peroxide (H2O2)-halide systems were found to produce chemiluminescence at 1,268 nm, a characteristic emission band for singlet oxygen (1O2). halide 51-57 myeloperoxidase Homo sapiens 4-19 6090506-1 1984 The myeloperoxidase (MPO)-hydrogen peroxide (H2O2)-halide systems were found to produce chemiluminescence at 1,268 nm, a characteristic emission band for singlet oxygen (1O2). halide 51-57 myeloperoxidase Homo sapiens 21-24 6090506-12 1984 While the MPO-H2O2-halide systems can efficiently produce 1O2, the conditions required are not physiologic, which suggests that the chemiluminescence of the stimulated neutrophil does not derive from 1O2 generated by a MPO mechanism. halide 19-25 myeloperoxidase Homo sapiens 10-13 6311062-2 1983 The exposure of alpha 1-protease inhibitor to the myeloperoxidase-hydrogen peroxide-halide system resulted in a nearly complete loss of its ability to bind and inactivate purified human neutrophil elastase. halide 84-90 serpin family A member 1 Homo sapiens 16-42 6315700-2 1983 We report here that both the myeloperoxidase-H2O2-halide system and OH released in this way can degrade the leukotrienes (LT) formed by neutrophils. halide 50-56 myeloperoxidase Homo sapiens 29-44 6315700-6 1983 LTC4 degradation by the cell-free myeloperoxidase-H2O2-halide system and the OH -generating acetaldehyde-xanthine oxidase-Fe2+ system had inhibitor profiles comparable to normal and myeloperoxidase-deficient neutrophils, respectively. halide 55-61 myeloperoxidase Homo sapiens 34-49 6311062-2 1983 The exposure of alpha 1-protease inhibitor to the myeloperoxidase-hydrogen peroxide-halide system resulted in a nearly complete loss of its ability to bind and inactivate purified human neutrophil elastase. halide 84-90 myeloperoxidase Homo sapiens 50-65 6311062-2 1983 The exposure of alpha 1-protease inhibitor to the myeloperoxidase-hydrogen peroxide-halide system resulted in a nearly complete loss of its ability to bind and inactivate purified human neutrophil elastase. halide 84-90 elastase, neutrophil expressed Homo sapiens 186-205 6311062-3 1983 A similar loss of binding to and inactivation of human neutrophil elastase was observed on exposure of alpha 1-protease inhibitor to human neutrophils in the presence of a halide and the neutrophil-activating agent, phorbol myristate acetate. halide 172-178 elastase, neutrophil expressed Homo sapiens 55-74 6311062-3 1983 A similar loss of binding to and inactivation of human neutrophil elastase was observed on exposure of alpha 1-protease inhibitor to human neutrophils in the presence of a halide and the neutrophil-activating agent, phorbol myristate acetate. halide 172-178 serpin family A member 1 Homo sapiens 103-129 6307386-2 1983 The process of inactivation is impeded by the addition of inhibitors of myeloperoxidase (KCN, NaN3), of catalase, of methionine but not by the addition of superoxide dismutase, indicating that the mechanism of inactivation is the oxidation of methionine residue by myeloperoxidase-H2O2-halide system. halide 286-292 myeloperoxidase Homo sapiens 72-87 6312841-2 1983 MPO is found in polymorphonuclear leukocytes and is important as a bactericidal agent in the presence of H2O2 and halide ions. halide 114-120 myeloperoxidase Homo sapiens 0-3 6300255-2 1983 Inhibition by anaerobiosis, azide, cyanide, halide-free conditions, catalase, histidine, and tryptophan suggested mediation of hyphal damage primarily through the myeloperoxidase system. halide 44-50 myeloperoxidase Homo sapiens 163-178 6882464-4 1983 During benzyl halide reduction, cytochrome P-450 complexes, which are very unstable to O2 and characterized by a Soret peak at 478 nm, are formed in steady-state concentrations. halide 14-20 cytochrome P450, family 2, subfamily g, polypeptide 1 Rattus norvegicus 32-48 6186607-4 1983 In the present investigation we show that the MPO-H2O2-halide system can degranulate isolated mast cells with release of histamine and 3H-serotonin. halide 55-61 myeloperoxidase Homo sapiens 46-49 6292103-6 1982 Both A. fumigatus and R. oryzae hyphae were damaged by the myeloperoxidase-hydrogen peroxide-halide system either with reagent hydrogen peroxide or enzymatic systems for generating hydrogen peroxide (glucose oxidase with glucose, or xanthine oxidase with either hypoxanthine or acetaldehyde). halide 93-99 myeloperoxidase Homo sapiens 59-74 6295926-9 1983 Our results suggest that Raji target cell destruction by PMA-activated neutrophils depends on the myeloperoxidase-hydrogen peroxide-halide system. halide 132-138 myeloperoxidase Homo sapiens 98-113 6292313-11 1982 These evidences suggest that the inactivation of lysosomal enzymes is mainly due to MPO-H2O2-halide system, resulting in inhibition of lysosomal enzyme release from PMN during phagocytosis. halide 93-99 myeloperoxidase Homo sapiens 84-87 6288561-4 1982 Both chlamydial biotypes were also rapidly inactivated by the cell-free myeloperoxidase-H2O2-halide system. halide 93-99 myeloperoxidase Homo sapiens 72-87 6281334-1 1982 The slow-reacting substance (SRS) bioactivity of leukotrienes C4 (LTC4) and D4 (LTD4) was rapidly decreased by incubation with eosinophil peroxidase (EPO), H2O2, and iodide, bromide, or to a lesser degree, chloride, LTB4 chemotactic activity was also decreased by the EPO-H2-H2-halide system, although at a slower rate. halide 278-284 eosinophil peroxidase Equus caballus 127-148 6802924-1 1982 Eosinophil peroxidase (EPO), a cationic protein purified from horse blood, adhered to four different types of tumor cells, markedly potentiating their lysis by preformed or enzymatically generated H(2)0(2) (up to 76-fold, as assayed in serum-containing tissue culture medium without supplemental halide). halide 296-302 eosinophil peroxidase Equus caballus 0-21 6802924-1 1982 Eosinophil peroxidase (EPO), a cationic protein purified from horse blood, adhered to four different types of tumor cells, markedly potentiating their lysis by preformed or enzymatically generated H(2)0(2) (up to 76-fold, as assayed in serum-containing tissue culture medium without supplemental halide). halide 296-302 eosinophil peroxidase Equus caballus 23-26 6286969-4 1982 The MPO-mediated oxidation of GSH required the simultaneous presence of MPO, H2O2, and a halide ion. halide 89-95 myeloperoxidase Homo sapiens 4-7 7068574-0 1982 Effects of halide ions on porcine kidney catalase. halide 11-17 catalase Homo sapiens 41-49 6282274-5 1982 Preincubation experiments indicated suppression of the myeloperoxidase-halide system. halide 71-77 myeloperoxidase Homo sapiens 55-70 6276480-6 1982 This suggests that the oxidation of met5-enkephalin by phagocytosing PMN was, at least in part, dependent on the MPO system (MPO-H2O2-halide). halide 134-140 myeloperoxidase Homo sapiens 113-116 6276480-6 1982 This suggests that the oxidation of met5-enkephalin by phagocytosing PMN was, at least in part, dependent on the MPO system (MPO-H2O2-halide). halide 134-140 myeloperoxidase Homo sapiens 125-128 7068574-1 1982 The inactivating effects of halide ions on porcine kidney catalase were investigated. halide 28-34 catalase Homo sapiens 58-66 7068574-4 1982 Additions of halide ions to catalase solution caused subtle but evident alterations in the absorption and CD spectra. halide 13-19 catalase Homo sapiens 28-36 225353-0 1979 Chemotactic factor inactivation by the myeloperoxidase-hydrogen peroxide-halide system. halide 73-79 myeloperoxidase Homo sapiens 39-54 7068574-7 1982 From these changes and also changes in CD spectra, we deduced that fluoride, chloride, and bromide ions can bind with heme iron of the catalase molecule as ligands to form stable catalase-halide complexes, but iodide ions showed a different reactivity with catalase from other halides and may cause gross alteration in the structure or conformation of catalase. halide 188-194 catalase Homo sapiens 135-143 7068574-7 1982 From these changes and also changes in CD spectra, we deduced that fluoride, chloride, and bromide ions can bind with heme iron of the catalase molecule as ligands to form stable catalase-halide complexes, but iodide ions showed a different reactivity with catalase from other halides and may cause gross alteration in the structure or conformation of catalase. halide 188-194 catalase Homo sapiens 179-187 7068574-7 1982 From these changes and also changes in CD spectra, we deduced that fluoride, chloride, and bromide ions can bind with heme iron of the catalase molecule as ligands to form stable catalase-halide complexes, but iodide ions showed a different reactivity with catalase from other halides and may cause gross alteration in the structure or conformation of catalase. halide 188-194 catalase Homo sapiens 179-187 7068574-7 1982 From these changes and also changes in CD spectra, we deduced that fluoride, chloride, and bromide ions can bind with heme iron of the catalase molecule as ligands to form stable catalase-halide complexes, but iodide ions showed a different reactivity with catalase from other halides and may cause gross alteration in the structure or conformation of catalase. halide 188-194 catalase Homo sapiens 179-187 6264686-0 1981 Inhibition of the neuraminidase of paramyxoviruses by halide ions: a possible means of modulating the two activities of the HN protein. halide 54-60 neuraminidase 1 Homo sapiens 18-31 6420461-1 1984 It has been previously demonstrated that eosinophil peroxidase (EPO) when supplemented with hydrogen peroxide and a halide induces noncytotoxic mast cell degranulation. halide 116-122 eosinophil peroxidase Homo sapiens 41-62 6420461-1 1984 It has been previously demonstrated that eosinophil peroxidase (EPO) when supplemented with hydrogen peroxide and a halide induces noncytotoxic mast cell degranulation. halide 116-122 eosinophil peroxidase Homo sapiens 64-67 6811483-2 1982 Stimulation of neutrophil migration and lymphocyte transformation following a single intravenous injection of 1 g of ascorbate was associated with inhibition of the MPO/H2O2/halide system. halide 174-180 myeloperoxidase Homo sapiens 165-168 6267057-5 1981 In a cell-free system, the fluorescence of 3,3"-dipropylthiodicarbocyanine, but not that of 3,3"-dipentyloxadicarbocyanine, was rapidly eliminated by myeloperoxidase in the presence of hydrogen peroxide and a halide; this loss of fluorescence was inhibited by azide, cyanide, or catalase. halide 209-215 myeloperoxidase Homo sapiens 150-165 6162845-1 1981 We have examined the effect of the myeloperoxidase-hydrogen peroxide-halide system and of activated human neutrophils on the ability of serum alpha 1-protease inhibitor (alpha 1-PI) to bind and inhibit porcine pancreatic elastase. halide 69-75 serpin family A member 1 Homo sapiens 142-168 6162845-1 1981 We have examined the effect of the myeloperoxidase-hydrogen peroxide-halide system and of activated human neutrophils on the ability of serum alpha 1-protease inhibitor (alpha 1-PI) to bind and inhibit porcine pancreatic elastase. halide 69-75 serpin family A member 1 Homo sapiens 170-180 6162845-8 1981 Thus, stimulated neutrophils secrete myeloperoxidase and H2O2 which combine with a halide to inactivate alpha 1-PI. halide 83-89 serpin family A member 1 Homo sapiens 104-114 6156983-1 1980 Eosinophil peroxidase (EPO) at relatively low levels (4-30 mU), when supplemented with H2O2 and a halide, induced mast cell degranulation. halide 98-104 eosinophil peroxidase Homo sapiens 0-21 6156983-1 1980 Eosinophil peroxidase (EPO) at relatively low levels (4-30 mU), when supplemented with H2O2 and a halide, induced mast cell degranulation. halide 98-104 eosinophil peroxidase Homo sapiens 23-26 6156983-10 1980 The stimulation of mast cell mediator release by the EPO-H2O2-halide system and the formation of MCG/EPO complexes with augmented cytotoxic activity may influence the adjacent inflammatory response. halide 62-68 eosinophil peroxidase Homo sapiens 53-56 6255998-0 1980 The halide complexes of myeloperoxidase and the mechanism of the halogenation reactions. halide 4-10 myeloperoxidase Homo sapiens 24-39 6255998-1 1980 The spectral changes caused by the addition of halides to myeloperoxidase (donor:hydrogen-peroxide oxidoreductase, EC 1.11.1.7) have been investigated and the dissociation constants of the enzyme-halide complexes have been determined. halide 47-53 myeloperoxidase Homo sapiens 58-73 6255998-2 1980 The pH dependence of the dissociation constants suggests that halide binding is associated with a protonation step in myeloperoxidase. halide 62-68 myeloperoxidase Homo sapiens 118-133 6987309-2 1980 The EPO-H2O2-halide bactericidal system had an acid pH optimum and was inhibited by the proteins albumin and gelatin and by the hemeprotein inhibitors azide, cyanide, and aminotriazole. halide 13-19 erythropoietin Cavia porcellus 4-7 6259027-5 1980 It has been suggested that observed intracellular deficiencies of selected enzymes within the neutrophils are of importance with regard to lowered antitumor activity of that cells operating mainly through the myeloperoxidase-H2O2-halide system. halide 230-236 myeloperoxidase Homo sapiens 209-224 6259068-6 1980 It is suggested that enhanced neutrophil motility is not related to beta-receptor blockade but rather to restricting the availability of hydrogen peroxide and reactive products of the MPO/H2O2/halide system. halide 193-199 myeloperoxidase Homo sapiens 184-187 510429-0 1979 Halide control of color of the chicken cone pigment iodopsin. halide 0-6 opsin 1 (cone pigments), long-wave-sensitive (color blindness, protan) Gallus gallus 52-60 225353-2 1979 The ability of the myeloperoxidase-H(2)O(2)-halide system of the neutrophil to inactivate chemoattractants was examined using both a radioassay and a morphologic assay of chemotaxis. halide 44-50 myeloperoxidase Homo sapiens 19-34 396794-5 1979 Optimal killing requires the translocation of granule myeloperoxidase into the phagocytic vacuole containing the bacteria and a suitable halide ion. halide 137-143 myeloperoxidase Homo sapiens 54-69 225268-1 1979 Estradiol 17 beta prevented the fall in the microbicidal activity of the myeloperoxidase-H2O2-halide system induced by high H2O2 concentrations. halide 94-100 myeloperoxidase Homo sapiens 73-88 225268-2 1979 In contrast, when the H2O2 (and halide) concentrations were low the myeloperoxidase-H2O2-halide antimicrobial system was inhibited by estradiol. halide 32-38 myeloperoxidase Homo sapiens 68-83 225268-2 1979 In contrast, when the H2O2 (and halide) concentrations were low the myeloperoxidase-H2O2-halide antimicrobial system was inhibited by estradiol. halide 89-95 myeloperoxidase Homo sapiens 68-83 6987309-3 1980 When the EPO concentration of the reaction mixture was lowered, the bactericidal effect at pH 7.0 was lost first with chloride, then with bromide, and finally with iodide as the halide. halide 178-184 erythropoietin Cavia porcellus 9-12 6987310-4 1980 The MCG/EPO complex retained the capacity of the isolated EPO to catalyze the iodination reaction when supplemented with iodide, H2O2, and a protein acceptor and to kill microorganisms when supplemented with H2O2 and a halide (iodide, chloride). halide 219-225 eosinophil peroxidase Homo sapiens 8-11 6987310-4 1980 The MCG/EPO complex retained the capacity of the isolated EPO to catalyze the iodination reaction when supplemented with iodide, H2O2, and a protein acceptor and to kill microorganisms when supplemented with H2O2 and a halide (iodide, chloride). halide 219-225 eosinophil peroxidase Homo sapiens 58-61 225142-2 1978 After phagocytosis, MPO is released into the phagosome from adjacent granules where it interacts with H2O2 generated either by leukocytic or microbial metabolism and a halide such as chloride or iodide to form agents toxic to the ingested organisms. halide 168-174 myeloperoxidase Homo sapiens 20-23 207742-6 1978 Using dapsone concentrations (1-30 mug/ml) comparable with those found after therapeutic doses, we have found that the drug interferes primarily with the myeloperoxidase (MPO)-H(2)O(2)-halide-mediated cytotoxic system in the PMNL. halide 185-191 myeloperoxidase Homo sapiens 154-169 207742-6 1978 Using dapsone concentrations (1-30 mug/ml) comparable with those found after therapeutic doses, we have found that the drug interferes primarily with the myeloperoxidase (MPO)-H(2)O(2)-halide-mediated cytotoxic system in the PMNL. halide 185-191 myeloperoxidase Homo sapiens 171-174 207742-10 1978 Because the MPO-H(2)O(2)-halide system not only fulfills the antimicrobial activity but is suggested to be a modulator of the inflammatory reaction as well, the action of dapsone in dermatitis herpetiformis may in part be explained by its effect on this system. halide 25-31 myeloperoxidase Homo sapiens 12-15 225142-15 1978 Both the xanthine oxidase system and the MPO-H2O2-halide system convert diphenylfuran into cis-dibenzoylethylene, an effect which is compatible with, although not proof of, the formation of 1O2 by these systems. halide 50-56 myeloperoxidase Homo sapiens 41-44 19435-0 1977 Effect of halide anions on the binding of FAD to D-amino acid oxidase and the tryptophanyl fluorescence of the apoenzyme. halide 10-16 D-amino acid oxidase Homo sapiens 49-69 886447-4 1977 Exclusive formation of the 6-isomer in these reactions is explained by halide-ion-catalyzed isomerization of the 6-halo opiate to the 8-halo isomer followed by a normal SN2" displacement of the halogen. halide 71-77 solute carrier family 38 member 5 Homo sapiens 169-172 1131257-0 1975 Halide dependence of the myeloperoxidase-mediated antimicrobial system of the polymorphonuclear leukocyte in the phenomenon of electronic excitation. halide 0-6 myeloperoxidase Homo sapiens 25-40 1148208-0 1975 Anion binding properties of human serum albumin from halide ion quadrupole relaxation. halide 53-59 albumin Homo sapiens 34-47 1148208-1 1975 The nuclear magnetic quadrupole relaxation enhancement of 35Cl-, 81Br-, and 12I- anions on binding to human serum albumin has been studied under conditions of variable protein and anion concentration and also in the presence of simple inorganic, amphiphilic, and complex anions which compete with the halide ions for the protein anion binding sites. halide 301-307 albumin Homo sapiens 108-121 165258-4 1975 The findings support a mechanism involving the phagocytosis-induced extracellular release of MPO and H2O2 and their reation with a halide cofactor to damage the target cells. halide 131-137 myeloperoxidase Homo sapiens 93-96 194641-0 1977 Myeloperoxidase--H2O2--halide system: cytotoxic effect on human blood leukocytes. halide 23-29 myeloperoxidase Homo sapiens 0-15 966110-1 1976 C15 halide, C5 hydroxy sulfone approach. halide 4-10 placenta associated 8 Homo sapiens 0-3 33470489-0 2021 Efficient Luminescent Halide Quadruple-Perovskite Nanocrystals via Trap-Engineering for Highly Sensitive Photodetectors. halide 22-28 TRAP Homo sapiens 67-71 19873131-5 1939 Since the halide concentration of the sap at the end of the experiment is (within the limits of natural variation) the same as in the intact cell, we conclude that electrolyte also enters the sap about 10 times as fast as in the intact cell. halide 10-16 SH2 domain containing 1A Homo sapiens 38-41 33826216-4 2021 In contrast, it can cleave C-X bonds (X = F, Cl) of hard organic Lewis bases with a high tendency to form SiX4 (X = F, Cl) after halide/triflate exchange. halide 129-135 SIX homeobox 4 Homo sapiens 106-110 33652850-8 2021 Thirty-five compounds were tested using the functional assay based on the halide-sensitive yellow fluorescent protein (HS-YFP) that measured CFTR activity. halide 74-80 CF transmembrane conductance regulator Homo sapiens 141-145 1120184-4 1975 Myeloperoxidase was effective with either chloride or iodide as the halide, while lastoperoxidase was effective with iodide but not chloride. halide 68-74 myeloperoxidase Homo sapiens 0-15 4970226-0 1968 Myeloperoxidase-halide-hydrogen peroxide antibacterial system. halide 16-22 myeloperoxidase Cavia porcellus 0-15 4970226-4 1968 Lactoperoxidase was considerably less effective than was myeloperoxidase when chloride was the halide employed. halide 95-101 myeloperoxidase Cavia porcellus 57-72 33040403-7 2021 Compared to the peptide agonist fMLF, RE-04-001 is more resistant to inactivation by the MPO-H2 O2 -halide system. halide 100-106 myeloperoxidase Homo sapiens 89-92 33247485-3 2021 We show that the optical properties and spin-orbit coupling (SOC) behaviour can be tuned through changing the A cation and the halide. halide 127-133 spindlin 1 Homo sapiens 40-44 33538737-0 2021 Unravelling halide-dependent charge carrier dynamics in CsPb(Br/Cl)3 perovskite nanocrystals. halide 12-18 granzyme B Homo sapiens 56-60 33507187-2 2021 Here, we investigated the structure and electronic properties of halide perovskite CsPbX3 (X = I, Br, Cl) by particle swarm optimization and first principles methods at hydrostatic pressure. halide 65-71 chromosome 12 open reading frame 73 Homo sapiens 98-100 32134102-2 2020 A stepwise halogen exchange, leading to a mixed-halide Cl-B-F intermediate, is implicated in the conversion of F-aza-BODIPYs to Cl-aza-BODIPYs upon treatment with BCl3. halide 48-54 BCL3 transcription coactivator Homo sapiens 163-167 33405901-0 2021 Halide-Enhanced Spin-Orbit Coupling and the Phosphorescence Rate in Ir(III) Complexes. halide 0-6 spindlin 1 Homo sapiens 16-20 33210903-5 2020 We found that the Nd3+ cation incorporated into the NCs more effectively suppressed nonradiative recombination compared with common halide anion exchange from temperature dependence of optical properties. halide 132-138 mitochondrially encoded NADH dehydrogenase 3 Homo sapiens 18-21 32969214-2 2020 In the solid state, 2 assembles into a stable halide-metal-organic material (Hal-MOM-2), which catalyzes H2O oxidation under photo- and electrocatalytic conditions, operating with a maximum TON = 78 and TOF = 1.26 s-1. halide 46-52 ATP synthase F1 subunit alpha Homo sapiens 81-86 32926491-4 2021 The halide ions are coordinated by one or two donor groups ( mu 1 - and mu 2 -coordinations), to stabilize a discrete monomer or dimer motifs to 1D supramolecular zig-zag chains. halide 4-10 glutathione S-transferase mu 1 Homo sapiens 61-76 33011567-9 2020 For a pre-oxidation with Mn(VII), ClO2 and Fe(VI), similar correlations between the EDC abatement and the chlorine demand or the adsorbable organic halide (AOX) formation were obtained. halide 148-154 acyl-CoA oxidase 1 Homo sapiens 156-159 33206507-6 2020 Reactions of [Re(NCCH3)6]2+ with a halide mixture consisting of NaX and AgX (X = Cl, I) result in the formation of the corresponding ReIII complexes [trans-ReX2(NCCH3)4]+. halide 35-41 RNA exonuclease 2 Homo sapiens 156-160 33153239-1 2020 The effect of halide composition on the structural, electronic, and optical properties of CsPb(Br1-xClx)3 perovskite was investigated in this study. halide 14-20 granzyme B Homo sapiens 90-94 33153239-1 2020 The effect of halide composition on the structural, electronic, and optical properties of CsPb(Br1-xClx)3 perovskite was investigated in this study. halide 14-20 C-X-C motif chemokine ligand 11 Homo sapiens 95-98 33126636-1 2020 The geometry, energy and electron density properties of the 1:1, 1:2 and 1:3 complexes between cyclic (Py-M)3 (M = Au, Ag and Cu) and halide ions (F-, Cl- and Br-) were studied using Moller Plesset (MP2) computational methods. halide 134-140 PYM homolog 1, exon junction complex associated factor Homo sapiens 103-109 32787199-0 2020 Intramolecular Band Alignment and Spin-Orbit Coupling in Two-Dimensional Halide Perovskites. halide 73-79 spindlin 1 Homo sapiens 34-38 32489095-1 2020 The silicon atom in LSiCl or LSiMes (L = PhC(NtBu)2, Mes = 2,4,6-Me3C6H2) inserts into the B-X bond of RBX2 (R = Ph, Mes, N(SiMe3)2; X = Cl, Br), which is followed by the migration of the amidinate ligand and the halide atom. halide 213-219 ring finger protein 7 Homo sapiens 103-107 32493948-5 2020 The results indicated that Pb(II) was immobilized as lead oxalate outside the fungal cell, bound with phosphate, nitro, halide, hydroxyl, amino, and carboxyl groups on the cell wall, precipitated as pyromorphite [Pb5(PO4)3Cl] on the cell wall, and reduced to Pb(0) inside the cell. halide 120-126 submaxillary gland androgen regulated protein 3B Homo sapiens 27-33 32130744-5 2020 Interlocked analogues were also prepared, and preliminary luminescent chloride anion spectrometric titrations with 12 Ru (PF 6 ) 2 demonstrate a marked increase in halide binding affinity due to the complementary chloride binding pocket of the [2]rotaxane. halide 164-170 sperm associated antigen 17 Homo sapiens 122-126 31807686-4 2019 This broad survey provided a number of insights into FDH activity, including halide specificity and substrate preference, that were not apparent from the more focused studies reported to date. halide 77-83 alcohol dehydrogenase 5 (class III), chi polypeptide Homo sapiens 53-56 32134656-1 2020 With the objective to establish a correlation between the spacer distance and halide dependence on the structural features of coordination polymers (CPs) assembled by the reaction between CuX salts (X = Cl, Br, I) and dithioether ligands BzS(CH2)nSBz (n = 1-9; Bz = benzyl), a series of 26 compounds have been prepared and structurally investigated. halide 78-84 cut like homeobox 1 Homo sapiens 188-191 32201633-5 2020 The small organic salt, NMe4OC(CF3)3, added as a halide abstractor, enables the use of a catalytic amount of Ag, reversing the rapid precipitation of AgBr. halide 49-55 NME/NM23 nucleoside diphosphate kinase 4 Homo sapiens 24-28 31424363-4 2020 At the time we demonstrated protein chlorination by HOCl, the major product of neutrophil MPO-halide system enhances protein immunogenicity. halide 94-100 myeloperoxidase Homo sapiens 90-93 31796835-2 2019 In this work, we reported a 286% improvement in current efficiency (CE) of PLEDs by using double-layered alkali halide electron injection layer (EIL) NaCl/LiF instead of LiF. halide 112-118 LIF interleukin 6 family cytokine Homo sapiens 155-158 31592571-2 2019 In this work, a new doping strategy is developed for P3HT as the HTL in triple-cation/double-halide ((FA1-x-y MAx Csy )Pb(I1-x Brx )3 ) mesoscopic PSCs. halide 93-99 FA complementation group A Homo sapiens 102-105 31034237-4 2019 In this work, we present a facile wet chemistry approach to yield well-defined cuprous halide (CuX, X = Cl, Br or I) microcrystals with different degrees of truncations at edges/vertices, which can be ascribed to the oxidative etching mechanism of halide ions. halide 87-93 cut like homeobox 1 Homo sapiens 95-98 31531905-0 2019 Lead-Free Halide Rb2 CuBr3 as Sensitive X-Ray Scintillator. halide 10-16 RB transcriptional corepressor like 2 Homo sapiens 17-20 31531905-4 2019 A novel lead-free halide is presented, namely Rb2 CuBr3 , as a scintillator with exceptionally high light yield. halide 18-24 RB transcriptional corepressor like 2 Homo sapiens 46-49 31173035-6 2019 Afterwards a halide mediated ligand exchange (LE) was carried out in order to remove insulating oleic acid residues from the PbS NPL surface and to form stable dispersions in polar organic solvents enabling thin-film fabrication. halide 13-19 N-acetylneuraminate pyruvate lyase Homo sapiens 129-132 31349038-3 2019 We demonstrate that the conversion of OH to carbonate and halogen radicals via reactions with serum-relevant carbonate and halide concentrations fundamentally alters the targeting of amino acids and loss of enzymatic activity in catalase, albumin and carbonic anhydrase, three important blood proteins. halide 124-130 catalase Homo sapiens 230-238 31349038-3 2019 We demonstrate that the conversion of OH to carbonate and halogen radicals via reactions with serum-relevant carbonate and halide concentrations fundamentally alters the targeting of amino acids and loss of enzymatic activity in catalase, albumin and carbonic anhydrase, three important blood proteins. halide 124-130 albumin Homo sapiens 240-247 31378058-2 2019 Herein, an intriguing halide perovskite (PVK) and metal dichalcogenide (MD) heterojunction, i.e., a lead-free Cs2SnI6 perovskite nanocrystal/SnS2 nanosheet hybrid, was fabricated in situ for the first time. halide 22-28 sodium voltage-gated channel alpha subunit 11 Homo sapiens 141-145 31085160-6 2019 In fact, Act-389949 was found to be as potent as the prototype FPR2 peptide agonist WKYMVM and had the advantage of being resistant to oxidation by MPO-H2O2-halide derived oxidants, as compared to the sensitive WKYMVM. halide 157-163 myeloperoxidase Homo sapiens 148-151 31276320-3 2019 Furthermore, due to the continuous chelating reaction with the oxalate ion, chloride anions from the mixed-halide CsPb(Cl/Br)3 perovskite NCs could be extracted, and green emitting CsPbBr3 NCs with PL QY of 85% at 511 nm emission are obtained. halide 107-113 granzyme B Homo sapiens 114-118 31259546-4 2019 The weakening of the Pb-I bond following the hole trapping (oxidation of the iodide site) and its expulsion from the lattice in the form of iodine provided further insight into the photoinduced segregation of halide ions in mixed halide perovskite films. halide 209-215 apolipoprotein B mRNA editing enzyme catalytic subunit 3C Homo sapiens 21-25 30974025-3 2019 In addition to the classical B2 X4 L2 diborane(4) bis-adducts, certain more sterically demanding carbene ligands induce a halide displacement which led to the first halide-bridged monocationic diboron species, [B2 X3 L2 ]A (A=BCl4 , Br, I). halide 122-128 BCL3 transcription coactivator Homo sapiens 226-230 30974025-3 2019 In addition to the classical B2 X4 L2 diborane(4) bis-adducts, certain more sterically demanding carbene ligands induce a halide displacement which led to the first halide-bridged monocationic diboron species, [B2 X3 L2 ]A (A=BCl4 , Br, I). halide 165-171 BCL3 transcription coactivator Homo sapiens 226-230 31206857-1 2019 Perovskite solar cells increasingly feature mixed-halide mixed-cation compounds (FA1- x - y MAx Csy PbI3- z Brz ) as photovoltaic absorbers, as they enable easier processing and improved stability. halide 50-56 FA complementation group A Homo sapiens 81-84 31241070-2 2019 Calculations at the MP2/aug-cc-pVTZ level reveal that the multiple nucleophilic sites of multivalent halide monomers can promote the formation of various types of halogen bonds, among which the most stable ones are At-halogen bond complexes with multivalent astatine as a Lewis acid center, followed by the pi-halogen bond dimers, and the weakest ones are the X-halogen bonds. halide 101-107 tryptase pseudogene 1 Homo sapiens 20-23 31034237-4 2019 In this work, we present a facile wet chemistry approach to yield well-defined cuprous halide (CuX, X = Cl, Br or I) microcrystals with different degrees of truncations at edges/vertices, which can be ascribed to the oxidative etching mechanism of halide ions. halide 248-254 cut like homeobox 1 Homo sapiens 95-98 31020291-0 2019 PbX2(OOCMMIm) (X = Cl, Br): photoluminescent organic-inorganic hybrid lead halide compounds with high proton conductivity. halide 75-81 PBX homeobox 2 Homo sapiens 0-4 31080112-3 2019 The introduction of a halide-sensitive YFP variant enabled automated quantitative measurement of Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) function in iPSC-derived intestinal epithelia. halide 22-28 CF transmembrane conductance regulator Homo sapiens 97-148 31080112-3 2019 The introduction of a halide-sensitive YFP variant enabled automated quantitative measurement of Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) function in iPSC-derived intestinal epithelia. halide 22-28 CF transmembrane conductance regulator Homo sapiens 150-154 31020291-1 2019 Differences in the electronegativity and hydrophilicity of halogens lead to differences in proton-conducting and photoluminescence properties in hybrid organic-inorganic lead halide compounds of [PbX2(OOCMMIm)]n (X = Cl (1), Br (2), HOOCMMIm = 1-carboxymethyl-3-methylimidazolium). halide 175-181 PBX homeobox 2 Homo sapiens 196-200 30929427-1 2019 All inorganic mixed-halide perovskite, CsPb(Br xI1- x)3 (0 <= x <= 1), nanocrystals possess tunable photoluminescence with high quantum yield in the visible window. halide 20-26 granzyme B Homo sapiens 39-43 31002525-4 2019 That is, a polar organic solution of lead halide (PbX2) was impregnated into the MOF pores to give PbX2@MIL-101, which was then subjected to a perovskite-formation reaction with cesium halide (CsX) dissolved in methanol. halide 42-48 PBX homeobox 2 Homo sapiens 50-54 31002525-4 2019 That is, a polar organic solution of lead halide (PbX2) was impregnated into the MOF pores to give PbX2@MIL-101, which was then subjected to a perovskite-formation reaction with cesium halide (CsX) dissolved in methanol. halide 42-48 PBX homeobox 2 Homo sapiens 99-103 31002525-4 2019 That is, a polar organic solution of lead halide (PbX2) was impregnated into the MOF pores to give PbX2@MIL-101, which was then subjected to a perovskite-formation reaction with cesium halide (CsX) dissolved in methanol. halide 42-48 NK2 homeobox 5 Homo sapiens 193-196 30268081-2 2019 This work hypothesises that the nanostructure of a PIL can be altered via halide addition, directly affecting the solvation of PEO. halide 74-80 serpin family A member 2 (gene/pseudogene) Homo sapiens 51-54 30687859-1 2019 Electrochemically driven interfacial halogen bonding between redox-active SAMs and halide anions was quantitatively studied for the first time. halide 83-89 methionine adenosyltransferase 1A Homo sapiens 74-78 30962670-4 2019 In contrast, addition of HBPin, (Pin = pinacolato) B2Pin2 and aryl halides resulted in the formation of net one-electron oxidation products: cationic Co(II)-boryl and Co(II)-halide/aryl complexes, respectively. halide 67-73 mitochondrially encoded cytochrome c oxidase II Homo sapiens 150-156 30962670-4 2019 In contrast, addition of HBPin, (Pin = pinacolato) B2Pin2 and aryl halides resulted in the formation of net one-electron oxidation products: cationic Co(II)-boryl and Co(II)-halide/aryl complexes, respectively. halide 67-73 mitochondrially encoded cytochrome c oxidase II Homo sapiens 167-173 30724309-5 2019 Furthermore, we confirm that mixing these NCs with the same halide but different structures will induce halide diffusion from Cs4PbX6 NCs and CsX NCs to CsPbX3 NCs. halide 60-66 NK2 homeobox 5 Homo sapiens 142-145 30724309-6 2019 This feature can be explored to utilize the Cs4PbX6 NCs and CsX NCs as a halide source to improve the photoluminescence efficiency and colloidal stability of CsPbX3 NCs. halide 73-79 NK2 homeobox 5 Homo sapiens 60-63 30643909-1 2019 Here, we show a two-liquid interfacial 3D plasmonic array for SERS examination on direct photoreduction of p-nitrothiophenol (4-NTP) to p-aminothiophenol (4-ATP) without the need for traditional catalysts and reductants, revealing the mechanism of halide-assisted activation of atomic hydrogen and the balance between the enhancing effect from etching of the Ag surface and the weakening effect from the reduction of the 4-NTP molecules, which provides insights into the light-to-energy conversion schemes on noble metal surfaces. halide 248-254 seryl-tRNA synthetase 2, mitochondrial Homo sapiens 62-66 30375695-0 2019 Retardation of Trap-Assisted Recombination in Lead Halide Perovskite Solar Cells by a Dimethylbiguanide Anchor Layer. halide 51-57 TRAP Homo sapiens 15-19 30259748-0 2018 Roles of SnX2 (X = F, Cl, Br) Additives in Tin-Based Halide Perovskites toward Highly Efficient and Stable Lead-Free Perovskite Solar Cells. halide 53-59 sorting nexin 2 Homo sapiens 9-13 30303005-0 2018 C-F Bond Activation of P(C6F5)3 by Ruthenium Dihydride Complexes: Isolation and Reactivity of the "Missing" Ru(PPh3)3H(halide) Complex, Ru(PPh3)3HF. halide 119-125 protein phosphatase 4 catalytic subunit Homo sapiens 111-115 30303005-0 2018 C-F Bond Activation of P(C6F5)3 by Ruthenium Dihydride Complexes: Isolation and Reactivity of the "Missing" Ru(PPh3)3H(halide) Complex, Ru(PPh3)3HF. halide 119-125 protein phosphatase 4 catalytic subunit Homo sapiens 139-143 30501174-0 2018 Design Principles for Trap-Free CsPbX3 Nanocrystals: Enumerating and Eliminating Surface Halide Vacancies with Softer Lewis Bases. halide 89-95 TRAP Homo sapiens 22-26 30500170-3 2018 Metalation of B2P2 with CuX (X = Cl, Br, I) results in the formation of bimetallic complexes of the formula (B2P2)Cu2X2 of two different structure types, depending on the halide. halide 171-177 cut like homeobox 1 Homo sapiens 24-27 30433792-0 2018 Halide Ion-Mediated Synthesis of L10-FePt Nanoparticles with Tunable Magnetic Properties. halide 0-6 immunoglobulin kappa variable 3-7 (non-functional) Homo sapiens 33-36 30433792-2 2018 Here, we present a facile control route for synthesis of hard magnetic L10-FePt NPs in which halide ions (Cl-, Br-, or I-) were added to the synthetic process to promote the phase transformation. halide 93-99 immunoglobulin kappa variable 3-7 (non-functional) Homo sapiens 71-74 30433792-3 2018 It is confirmed that the strong ionic binding force between halide ions and Fe3+ or Pt2+ ions could facilitate the formation of L10-FePt phase due to favoring growth of FePt NPs in a more thermodynamically stable way, which enables the formation of an ordered structure. halide 60-66 immunoglobulin kappa variable 3-7 (non-functional) Homo sapiens 128-131 30433792-4 2018 L10-FePt NPs with the highest coercivity of 8.64 kOe and saturation magnetization of 64.21 emu/g at room temperature can be directly obtained by controlling the amount of the halide ions. halide 175-181 immunoglobulin kappa variable 3-7 (non-functional) Homo sapiens 0-3 30252954-8 2018 I- influx assays using halide-sensitive YFP showed that LRRC8A is crucially important for mediating VRAC activity in HaCaTs and NHEKs. halide 23-29 leucine rich repeat containing 8 VRAC subunit A Homo sapiens 56-62 30281312-0 2018 Spin-optotronic Properties of Organometal Halide Perovskites. halide 42-48 spindlin 1 Homo sapiens 0-4 30211918-5 2018 Using the climbing-image nudged elastic band method, these double perovskites are found with different barriers for halide ion migrations around Ag- and BIII-octahedrons due to different migration bottleneck radii and B-X bond characters. halide 116-122 calcium voltage-gated channel subunit alpha1 B Homo sapiens 153-157 30169031-0 2018 Two-Dimensional Halide Perovskites Incorporating Straight Chain Symmetric Diammonium Ions, (NH3C mH2 mNH3)(CH3NH3) n-1Pb nI3 n+1 ( m = 4-9; n = 1-4). halide 16-22 histocompatibility-2, MHC Mus musculus 97-100 30170492-4 2018 Interestingly, we observed that the ligands, which help in the formation of a uniform SnO2 QD thin film, spontaneously exchange for halide through a perovskite solution, and finally we form a suitable SnO2 QD-halide junction for high-performance HPSCs. halide 132-138 strawberry notch homolog 2 Homo sapiens 86-89 30627411-4 2018 Consequently, the quantum yield (Phi P), lifetime (tau) and color of RTP can be tuned by changing the fluorophore and halide in the perovskites, as well as their solid morphology. halide 118-124 pleckstrin homology domain interacting protein Homo sapiens 33-38 30170492-4 2018 Interestingly, we observed that the ligands, which help in the formation of a uniform SnO2 QD thin film, spontaneously exchange for halide through a perovskite solution, and finally we form a suitable SnO2 QD-halide junction for high-performance HPSCs. halide 209-215 strawberry notch homolog 2 Homo sapiens 86-89 30157629-1 2018 In this work, the spatially dependent recombination kinetics of mixed-halide hybrid perovskite CH3NH3Pb(Br1- xCl x)3 (0 <= x <= 0.19) single crystals are investigated using time-resolved photoluminescence spectroscopy with one- and two-photon femtosecond laser excitation. halide 70-76 C-X-C motif chemokine ligand 11 Homo sapiens 104-107 29553256-6 2018 We also report the reaction of the LPh ligand with both AlBr3 and AlI3 and demonstrate a different reactivity profile for the heavier halide relative to the lighter members of the group. halide 134-140 adhesion molecule with Ig like domain 3 Homo sapiens 66-70