Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
1
|
Mapping the genetic architecture of gene expression in human liver.
|
PLoS Biol
|
2008
|
19.44
|
2
|
Elucidating mechanisms of drug-induced toxicity.
|
Nat Rev Drug Discov
|
2005
|
2.06
|
3
|
Systematic genetic and genomic analysis of cytochrome P450 enzyme activities in human liver.
|
Genome Res
|
2010
|
2.06
|
4
|
DNA adduct bypass polymerization by Sulfolobus solfataricus DNA polymerase Dpo4: analysis and crystal structures of multiple base pair substitution and frameshift products with the adduct 1,N2-ethenoguanine.
|
J Biol Chem
|
2005
|
2.02
|
5
|
Complex reactions catalyzed by cytochrome P450 enzymes.
|
Biochim Biophys Acta
|
2006
|
1.76
|
6
|
Efficient and high fidelity incorporation of dCTP opposite 7,8-dihydro-8-oxodeoxyguanosine by Sulfolobus solfataricus DNA polymerase Dpo4.
|
J Biol Chem
|
2005
|
1.74
|
7
|
Kinetics and thermodynamics of ligand binding by cytochrome P450 3A4.
|
J Biol Chem
|
2006
|
1.63
|
8
|
Translesion synthesis across bulky N2-alkyl guanine DNA adducts by human DNA polymerase kappa.
|
J Biol Chem
|
2006
|
1.62
|
9
|
Binding of two flaviolin substrate molecules, oxidative coupling, and crystal structure of Streptomyces coelicolor A3(2) cytochrome P450 158A2.
|
J Biol Chem
|
2005
|
1.52
|
10
|
Roles of NADPH-P450 reductase and apo- and holo-cytochrome b5 on xenobiotic oxidations catalyzed by 12 recombinant human cytochrome P450s expressed in membranes of Escherichia coli.
|
Protein Expr Purif
|
2002
|
1.46
|
11
|
Cytochrome P450 activation of arylamines and heterocyclic amines.
|
Annu Rev Pharmacol Toxicol
|
2005
|
1.46
|
12
|
Translesion synthesis across O6-alkylguanine DNA adducts by recombinant human DNA polymerases.
|
J Biol Chem
|
2006
|
1.45
|
13
|
Hydrogen bonding of 7,8-dihydro-8-oxodeoxyguanosine with a charged residue in the little finger domain determines miscoding events in Sulfolobus solfataricus DNA polymerase Dpo4.
|
J Biol Chem
|
2007
|
1.38
|
14
|
Structural and functional elucidation of the mechanism promoting error-prone synthesis by human DNA polymerase kappa opposite the 7,8-dihydro-8-oxo-2'-deoxyguanosine adduct.
|
J Biol Chem
|
2009
|
1.31
|
15
|
Analysis of coumarin 7-hydroxylation activity of cytochrome P450 2A6 using random mutagenesis.
|
J Biol Chem
|
2005
|
1.29
|
16
|
Adduct size limits efficient and error-free bypass across bulky N2-guanine DNA lesions by human DNA polymerase eta.
|
J Mol Biol
|
2005
|
1.26
|
17
|
Recombinant enzymes overexpressed in bacteria show broad catalytic specificity of human cytochrome P450 2W1 and limited activity of human cytochrome P450 2S1.
|
Mol Pharmacol
|
2006
|
1.24
|
18
|
Sulfolobus solfataricus DNA polymerase Dpo4 is partially inhibited by "wobble" pairing between O6-methylguanine and cytosine, but accurate bypass is preferred.
|
J Biol Chem
|
2006
|
1.22
|
19
|
Inhibition of human cytochrome P450 1A1-, 1A2-, and 1B1-mediated activation of procarcinogens to genotoxic metabolites by polycyclic aromatic hydrocarbons.
|
Chem Res Toxicol
|
2006
|
1.20
|
20
|
1,N(2)-ethenoguanine, a mutagenic DNA adduct, is a primary substrate of Escherichia coli mismatch-specific uracil-DNA glycosylase and human alkylpurine-DNA-N-glycosylase.
|
J Biol Chem
|
2002
|
1.16
|
21
|
Structure and activity of Y-class DNA polymerase DPO4 from Sulfolobus solfataricus with templates containing the hydrophobic thymine analog 2,4-difluorotoluene.
|
J Biol Chem
|
2007
|
1.16
|
22
|
Expression of cytochromes P450 1A1 and 1B1 in human lung from smokers, non-smokers, and ex-smokers.
|
Toxicol Appl Pharmacol
|
2004
|
1.16
|
23
|
Cytochrome P450 enzymes in drug metabolism and chemical toxicology: An introduction.
|
Biochem Mol Biol Educ
|
2006
|
1.16
|
24
|
Molecular basis of selectivity of nucleoside triphosphate incorporation opposite O6-benzylguanine by sulfolobus solfataricus DNA polymerase Dpo4: steady-state and pre-steady-state kinetics and x-ray crystallography of correct and incorrect pairing.
|
J Biol Chem
|
2007
|
1.16
|
25
|
Kinetic analysis of steps in the repair of damaged DNA by human O6-alkylguanine-DNA alkyltransferase.
|
J Biol Chem
|
2005
|
1.16
|
26
|
Kinetic evidence for inefficient and error-prone bypass across bulky N2-guanine DNA adducts by human DNA polymerase iota.
|
J Biol Chem
|
2006
|
1.15
|
27
|
Cytochrome P450 3A4-catalyzed testosterone 6beta-hydroxylation stereochemistry, kinetic deuterium isotope effects, and rate-limiting steps.
|
J Biol Chem
|
2005
|
1.15
|
28
|
Three-dimensional structure of steroid 21-hydroxylase (cytochrome P450 21A2) with two substrates reveals locations of disease-associated variants.
|
J Biol Chem
|
2012
|
1.13
|
29
|
Translesion synthesis across abasic lesions by human B-family and Y-family DNA polymerases α, δ, η, ι, κ, and REV1.
|
J Mol Biol
|
2010
|
1.12
|
30
|
Replication past the N5-methyl-formamidopyrimidine lesion of deoxyguanosine by DNA polymerases and an improved procedure for sequence analysis of in vitro bypass products by mass spectrometry.
|
Chem Res Toxicol
|
2009
|
1.11
|
31
|
Contributions of human enzymes in carcinogen metabolism.
|
Chem Res Toxicol
|
2012
|
1.11
|
32
|
Role of active site water molecules and substrate hydroxyl groups in oxygen activation by cytochrome P450 158A2: a new mechanism of proton transfer.
|
J Biol Chem
|
2005
|
1.10
|
33
|
Kinetic analysis of translesion synthesis opposite bulky N2- and O6-alkylguanine DNA adducts by human DNA polymerase REV1.
|
J Biol Chem
|
2008
|
1.10
|
34
|
Activation of bis-electrophiles to mutagenic conjugates by human O6-alkylguanine-DNA alkyltransferase.
|
Chem Res Toxicol
|
2004
|
1.10
|
35
|
Characterization of a mutagenic DNA adduct formed from 1,2-dibromoethane by O6-alkylguanine-DNA alkyltransferase.
|
J Biol Chem
|
2003
|
1.10
|
36
|
Cytochromes P450 and drug discovery.
|
Curr Opin Biotechnol
|
2007
|
1.10
|
37
|
Characterization of orphan human cytochromes P450.
|
Drug Metab Rev
|
2007
|
1.09
|
38
|
Effect of the O6 substituent on misincorporation kinetics catalyzed by DNA polymerases at O(6)-methylguanine and O(6)-benzylguanine.
|
Biochemistry
|
2002
|
1.09
|
39
|
Substrate binding to cytochromes P450.
|
Anal Bioanal Chem
|
2008
|
1.09
|
40
|
Selection of human cytochrome P450 1A2 mutants with enhanced catalytic activity for heterocyclic amine N-hydroxylation.
|
Biochemistry
|
2004
|
1.09
|
41
|
Misincorporation and stalling at O(6)-methylguanine and O(6)-benzylguanine: evidence for inactive polymerase complexes.
|
Biochemistry
|
2002
|
1.09
|
42
|
Mammalian cytochrome P450 enzymes catalyze the phenol-coupling step in endogenous morphine biosynthesis.
|
J Biol Chem
|
2009
|
1.08
|
43
|
Direct detection and mapping of sites of base modification in DNA fragments by tandem mass spectrometry.
|
Angew Chem Int Ed Engl
|
2008
|
1.08
|
44
|
Structure-function relationships of inhibition of human cytochromes P450 1A1, 1A2, 1B1, 2C9, and 3A4 by 33 flavonoid derivatives.
|
Chem Res Toxicol
|
2010
|
1.07
|
45
|
Analysis of the effect of bulk at N2-alkylguanine DNA adducts on catalytic efficiency and fidelity of the processive DNA polymerases bacteriophage T7 exonuclease- and HIV-1 reverse transcriptase.
|
J Biol Chem
|
2004
|
1.07
|
46
|
Conversion of 7-dehydrocholesterol to 7-ketocholesterol is catalyzed by human cytochrome P450 7A1 and occurs by direct oxidation without an epoxide intermediate.
|
J Biol Chem
|
2011
|
1.07
|
47
|
Translesion synthesis across 1,N2-ethenoguanine by human DNA polymerases.
|
Chem Res Toxicol
|
2006
|
1.06
|
48
|
Kinetic analysis of correct nucleotide insertion by a Y-family DNA polymerase reveals conformational changes both prior to and following phosphodiester bond formation as detected by tryptophan fluorescence.
|
J Biol Chem
|
2008
|
1.06
|
49
|
Site specific synthesis and polymerase bypass of oligonucleotides containing a 6-hydroxy-3,5,6,7-tetrahydro-9H-imidazo[1,2-a]purin-9-one base, an intermediate in the formation of 1,N2-etheno-2'-deoxyguanosine.
|
Chem Res Toxicol
|
2005
|
1.05
|
50
|
Different mechanisms for inhibition of human cytochromes P450 1A1, 1A2, and 1B1 by polycyclic aromatic inhibitors.
|
Chem Res Toxicol
|
2007
|
1.05
|
51
|
Different in vitro metabolism of paclitaxel and docetaxel in humans, rats, pigs, and minipigs.
|
Drug Metab Dispos
|
2004
|
1.05
|
52
|
Mitochondria-targeted cytochrome P450 2E1 induces oxidative damage and augments alcohol-mediated oxidative stress.
|
J Biol Chem
|
2010
|
1.05
|
53
|
Expansion of substrate specificity of cytochrome P450 2A6 by random and site-directed mutagenesis.
|
J Biol Chem
|
2005
|
1.04
|
54
|
Human liver microsomal cytochrome P450 3A enzymes involved in thalidomide 5-hydroxylation and formation of a glutathione conjugate.
|
Chem Res Toxicol
|
2010
|
1.04
|
55
|
Roles of the four DNA polymerases of the crenarchaeon Sulfolobus solfataricus and accessory proteins in DNA replication.
|
J Biol Chem
|
2011
|
1.04
|
56
|
Cytochrome P450 7A1 cholesterol 7alpha-hydroxylation: individual reaction steps in the catalytic cycle and rate-limiting ferric iron reduction.
|
J Biol Chem
|
2010
|
1.03
|
57
|
Kinetic analysis of oxidation of coumarins by human cytochrome P450 2A6.
|
J Biol Chem
|
2005
|
1.03
|
58
|
Paradoxical enhancement of the toxicity of 1,2-dibromoethane by O6-alkylguanine-DNA alkyltransferase.
|
J Biol Chem
|
2002
|
1.03
|
59
|
Versatility of Y-family Sulfolobus solfataricus DNA polymerase Dpo4 in translesion synthesis past bulky N2-alkylguanine adducts.
|
J Biol Chem
|
2008
|
1.03
|
60
|
Heterologous expression, purification, and properties of human cytochrome P450 27C1.
|
Arch Biochem Biophys
|
2005
|
1.03
|
61
|
Interactions of mammalian cytochrome P450, NADPH-cytochrome P450 reductase, and cytochrome b(5) enzymes.
|
Arch Biochem Biophys
|
2005
|
1.03
|
62
|
Electron transport pathway for a Streptomyces cytochrome P450: cytochrome P450 105D5-catalyzed fatty acid hydroxylation in Streptomyces coelicolor A3(2).
|
J Biol Chem
|
2007
|
1.02
|
63
|
Metabolism of heterocyclic aromatic amines by human hepatocytes and cytochrome P4501A2.
|
Mutat Res
|
2002
|
1.02
|
64
|
Search for an association between the human CYP1A2 genotype and CYP1A2 metabolic phenotype.
|
Pharmacogenet Genomics
|
2006
|
1.02
|
65
|
D-amino acid oxidase generates agonists of the aryl hydrocarbon receptor from D-tryptophan.
|
Chem Res Toxicol
|
2009
|
1.01
|
66
|
In vivo formation of a glutathione conjugate derived from thalidomide in humanized uPA-NOG mice.
|
Chem Res Toxicol
|
2011
|
1.00
|
67
|
Exploiting Streptomyces coelicolor A3(2) P450s as a model for application in drug discovery.
|
Expert Opin Drug Metab Toxicol
|
2006
|
1.00
|
68
|
Development of oxidative stress by cytochrome P450 induction in rodents is selective for barbiturates and related to loss of pyridine nucleotide-dependent protective systems.
|
J Biol Chem
|
2008
|
0.99
|
69
|
Comparison of the in vitro replication of the 7-(2-oxoheptyl)-1,N2-etheno-2'-deoxyguanosine and 1,N2-etheno-2'-deoxyguanosine lesions by Sulfolobus solfataricus P2 DNA polymerase IV (Dpo4).
|
Chem Res Toxicol
|
2010
|
0.99
|
70
|
Enhancement of 7-methoxyresorufin O-demethylation activity of human cytochrome P450 1A2 by molecular breeding.
|
Arch Biochem Biophys
|
2004
|
0.99
|
71
|
Kinetic analysis of the three-step steroid aromatase reaction of human cytochrome P450 19A1.
|
J Biol Chem
|
2010
|
0.99
|
72
|
In vivo formation of dihydroxylated and glutathione conjugate metabolites derived from thalidomide and 5-Hydroxythalidomide in humanized TK-NOG mice.
|
Chem Res Toxicol
|
2012
|
0.99
|
73
|
Calcium is a cofactor of polymerization but inhibits pyrophosphorolysis by the Sulfolobus solfataricus DNA polymerase Dpo4.
|
Biochemistry
|
2006
|
0.98
|
74
|
The bis-electrophile diepoxybutane cross-links DNA to human histones but does not result in enhanced mutagenesis in recombinant systems.
|
Chem Res Toxicol
|
2009
|
0.98
|
75
|
Drug interactions of thalidomide with midazolam and cyclosporine A: heterotropic cooperativity of human cytochrome P450 3A5.
|
Drug Metab Dispos
|
2008
|
0.97
|
76
|
Cooperativity in oxidation reactions catalyzed by cytochrome P450 1A2: highly cooperative pyrene hydroxylation and multiphasic kinetics of ligand binding.
|
J Biol Chem
|
2008
|
0.97
|
77
|
Oxidation of N-Nitrosoalkylamines by human cytochrome P450 2A6: sequential oxidation to aldehydes and carboxylic acids and analysis of reaction steps.
|
J Biol Chem
|
2010
|
0.97
|
78
|
Rate-limiting steps in cytochrome P450 catalysis.
|
Biol Chem
|
2002
|
0.97
|
79
|
Cyclization of a cellular dipentaenone by Streptomyces coelicolor cytochrome P450 154A1 without oxidation/reduction.
|
J Am Chem Soc
|
2010
|
0.97
|
80
|
Conjugation of butadiene diepoxide with glutathione yields DNA adducts in vitro and in vivo.
|
Chem Res Toxicol
|
2012
|
0.96
|
81
|
Elucidation of functions of human cytochrome P450 enzymes: identification of endogenous substrates in tissue extracts using metabolomic and isotopic labeling approaches.
|
Anal Chem
|
2009
|
0.96
|
82
|
Aryl hydrocarbon receptor activation and cytochrome P450 1A induction by the mitogen-activated protein kinase inhibitor U0126 in hepatocytes.
|
Mol Pharmacol
|
2004
|
0.96
|
83
|
Exocyclic DNA lesions stimulate DNA cleavage mediated by human topoisomerase II alpha in vitro and in cultured cells.
|
Biochemistry
|
2005
|
0.96
|
84
|
Metabolic activation of polycyclic aromatic hydrocarbons and aryl and heterocyclic amines by human cytochromes P450 2A13 and 2A6.
|
Chem Res Toxicol
|
2013
|
0.95
|
85
|
Biochemical basis of genotoxicity of heterocyclic arylamine food mutagens: Human DNA polymerase eta selectively produces a two-base deletion in copying the N2-guanyl adduct of 2-amino-3-methylimidazo[4,5-f]quinoline but not the C8 adduct at the NarI G3 site.
|
J Biol Chem
|
2006
|
0.95
|
86
|
Bioactivation of fluorinated 2-aryl-benzothiazole antitumor molecules by human cytochrome P450s 1A1 and 2W1 and deactivation by cytochrome P450 2S1.
|
Chem Res Toxicol
|
2012
|
0.95
|
87
|
Cytochrome P450-dependent catabolism of vitamin K: ω-hydroxylation catalyzed by human CYP4F2 and CYP4F11.
|
Biochemistry
|
2013
|
0.94
|
88
|
Interaction of polycyclic aromatic hydrocarbons with human cytochrome P450 1B1 in inhibiting catalytic activity.
|
Chem Res Toxicol
|
2008
|
0.94
|
89
|
Structural basis for proficient incorporation of dTTP opposite O6-methylguanine by human DNA polymerase iota.
|
J Biol Chem
|
2010
|
0.94
|
90
|
Multiple sequential steps involved in the binding of inhibitors to cytochrome P450 3A4.
|
J Biol Chem
|
2007
|
0.94
|
91
|
Structure-function relationships in miscoding by Sulfolobus solfataricus DNA polymerase Dpo4: guanine N2,N2-dimethyl substitution produces inactive and miscoding polymerase complexes.
|
J Biol Chem
|
2009
|
0.93
|
92
|
Reverse type I binding spectra of human cytochrome P450 1B1 induced by flavonoid, stilbene, pyrene, naphthalene, phenanthrene, and biphenyl derivatives that inhibit catalytic activity: a structure-function relationship study.
|
Chem Res Toxicol
|
2009
|
0.93
|
93
|
Reactions of glyceraldehyde 3-phosphate dehydrogenase sulfhydryl groups with bis-electrophiles produce DNA-protein cross-links but not mutations.
|
Chem Res Toxicol
|
2007
|
0.93
|
94
|
In vitro bypass of the major malondialdehyde- and base propenal-derived DNA adduct by human Y-family DNA polymerases κ, ι, and Rev1.
|
Biochemistry
|
2010
|
0.92
|
95
|
Testosterone 1 beta-hydroxylation by human cytochrome P450 3A4.
|
Eur J Biochem
|
2004
|
0.92
|
96
|
Liquid chromatography-mass spectrometry analysis of DNA polymerase reaction products.
|
Curr Protoc Nucleic Acid Chem
|
2011
|
0.92
|
97
|
mRNA distribution and heterologous expression of orphan cytochrome P450 20A1.
|
Drug Metab Dispos
|
2008
|
0.92
|
98
|
Structural and functional analysis of Sulfolobus solfataricus Y-family DNA polymerase Dpo4-catalyzed bypass of the malondialdehyde-deoxyguanosine adduct.
|
Biochemistry
|
2009
|
0.92
|
99
|
Cytochromes P450 catalyze the reduction of α,β-unsaturated aldehydes.
|
Chem Res Toxicol
|
2011
|
0.91
|
100
|
7-Ketocholesterol induces P-glycoprotein through PI3K/mTOR signaling in hepatoma cells.
|
Biochem Pharmacol
|
2013
|
0.91
|
101
|
Decreased coumarin 7-hydroxylase activities and CYP2A6 expression levels in humans caused by genetic polymorphism in CYP2A6 promoter region (CYP2A6*9).
|
Pharmacogenetics
|
2003
|
0.91
|
102
|
Translesion synthesis past the C8- and N2-deoxyguanosine adducts of the dietary mutagen 2-Amino-3-methylimidazo[4,5-f]quinoline in the NarI recognition sequence by prokaryotic DNA polymerases.
|
Chem Res Toxicol
|
2006
|
0.91
|
103
|
High-throughput fluorescence assay of cytochrome P450 3A4.
|
Nat Protoc
|
2009
|
0.91
|
104
|
Untargeted analysis of mass spectrometry data for elucidation of metabolites and function of enzymes.
|
Anal Chem
|
2007
|
0.91
|
105
|
Biochemical analysis of six genetic variants of error-prone human DNA polymerase ι involved in translesion DNA synthesis.
|
Chem Res Toxicol
|
2014
|
0.90
|
106
|
Mechanism of the third oxidative step in the conversion of androgens to estrogens by cytochrome P450 19A1 steroid aromatase.
|
J Am Chem Soc
|
2014
|
0.90
|
107
|
Repair of O6-G-alkyl-O6-G interstrand cross-links by human O6-alkylguanine-DNA alkyltransferase.
|
Biochemistry
|
2008
|
0.90
|
108
|
Functional characterization of four allelic variants of human cytochrome P450 1A2.
|
Arch Biochem Biophys
|
2004
|
0.90
|
109
|
Cytochrome P450 2S1 is reduced by NADPH-cytochrome P450 reductase.
|
Drug Metab Dispos
|
2011
|
0.90
|
110
|
Kinetic analysis of base-pairing preference for nucleotide incorporation opposite template pyrimidines by human DNA polymerase iota.
|
J Mol Biol
|
2009
|
0.89
|
111
|
Steric and electrostatic effects at the C2 atom substituent influence replication and miscoding of the DNA deamination product deoxyxanthosine and analogs by DNA polymerases.
|
J Mol Biol
|
2009
|
0.89
|
112
|
Analysis of DNA adducts formed in vivo in rats and mice from 1,2-dibromoethane, 1,2-dichloroethane, dibromomethane, and dichloromethane using HPLC/accelerator mass spectrometry and relevance to risk estimates.
|
Chem Res Toxicol
|
2007
|
0.89
|
113
|
Tandem mass spectrometry-based detection of c4'-oxidized abasic sites at specific positions in DNA fragments.
|
Chem Res Toxicol
|
2009
|
0.89
|
114
|
Mitochondrial targeting of cytochrome P450 (CYP) 1B1 and its role in polycyclic aromatic hydrocarbon-induced mitochondrial dysfunction.
|
J Biol Chem
|
2014
|
0.89
|
115
|
Translesion synthesis across 1,N6-(2-hydroxy-3-hydroxymethylpropan-1,3-diyl)-2'-deoxyadenosine (1,N6-γ-HMHP-dA) adducts by human and archebacterial DNA polymerases.
|
J Biol Chem
|
2012
|
0.88
|
116
|
Spectral modification and catalytic inhibition of human cytochromes P450 1A1, 1A2, 1B1, 2A6, and 2A13 by four chemopreventive organoselenium compounds.
|
Chem Res Toxicol
|
2011
|
0.88
|
117
|
The alkaloid rutaecarpine is a selective inhibitor of cytochrome P450 1A in mouse and human liver microsomes.
|
Drug Metab Dispos
|
2002
|
0.88
|
118
|
Cytochromes P450 catalyze oxidation of alpha,beta-unsaturated aldehydes.
|
Arch Biochem Biophys
|
2007
|
0.88
|
119
|
Human liver mitochondrial cytochrome P450 2D6--individual variations and implications in drug metabolism.
|
FEBS J
|
2009
|
0.88
|
120
|
Human cytochrome P450 oxidation of 5-hydroxythalidomide and pomalidomide, an amino analogue of thalidomide.
|
Chem Res Toxicol
|
2013
|
0.88
|
121
|
Binding of diverse environmental chemicals with human cytochromes P450 2A13, 2A6, and 1B1 and enzyme inhibition.
|
Chem Res Toxicol
|
2013
|
0.87
|
122
|
CYP3A4 intron 6 C>T polymorphism (CYP3A4*22) is associated with reduced CYP3A4 protein level and function in human liver microsomes.
|
J Toxicol Sci
|
2013
|
0.87
|
123
|
Structure of the 1,N2-ethenodeoxyguanosine adduct opposite cytosine in duplex DNA: Hoogsteen base pairing at pH 5.2.
|
Chem Res Toxicol
|
2008
|
0.87
|
124
|
Structural identification of Diindole agonists of the aryl hydrocarbon receptor derived from degradation of indole-3-pyruvic acid.
|
Chem Res Toxicol
|
2009
|
0.87
|
125
|
Differential DNA recognition and cleavage by EcoRI dependent on the dynamic equilibrium between the two forms of the malondialdehyde-deoxyguanosine adduct.
|
Biochemistry
|
2005
|
0.87
|
126
|
In vivo oxidative damage in rats is associated with barbiturate response but not other cytochrome P450 inducers.
|
Mol Pharmacol
|
2007
|
0.87
|
127
|
Formation and reduction of aryl and heterocyclic nitroso compounds and significance in the flux of hydroxylamines.
|
Chem Res Toxicol
|
2004
|
0.86
|
128
|
Kinetics of nucleotide incorporation opposite polycyclic aromatic hydrocarbon-DNA adducts by processive bacteriophage T7 DNA polymerase.
|
Chem Res Toxicol
|
2005
|
0.86
|
129
|
Conformational changes during nucleotide selection by Sulfolobus solfataricus DNA polymerase Dpo4.
|
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