review article | Q7318358 |
scholarly article | Q13442814 |
P356 | DOI | 10.1016/S0968-0004(99)01524-8 |
P698 | PubMed publication ID | 10664587 |
P2093 | author name string | Fuchs RP | |
Baynton K | |||
P2860 | cites work | hRAD30 mutations in the variant form of xeroderma pigmentosum | Q22010237 |
A human homolog of the Saccharomyces cerevisiae REV3 gene, which encodes the catalytic subunit of DNA polymerase zeta | Q24323043 | ||
Deoxycytidyl transferase activity of yeast REV1 protein | Q27931173 | ||
Efficient bypass of a thymine-thymine dimer by yeast DNA polymerase, Poleta | Q27935465 | ||
Thymine-thymine dimer bypass by yeast DNA polymerase zeta | Q27938043 | ||
The XPV (xeroderma pigmentosum variant) gene encodes human DNA polymerase eta | Q28115711 | ||
Efficient translesion replication in the absence of Escherichia coli Umu proteins and 3'-5' exonuclease proofreading function | Q33594697 | ||
Analysis of damage tolerance pathways in Saccharomyces cerevisiae: a requirement for Rev3 DNA polymerase in translesion synthesis | Q33771455 | ||
The T-T pyrimidine (6–4) pyrimidinone UV photoproduct is much less mutagenic in yeast than inEscherichia coli | Q34753798 | ||
UmuD'(2)C is an error-prone DNA polymerase, Escherichia coli pol V. | Q35588920 | ||
A model for a umuDC-dependent prokaryotic DNA damage checkpoint | Q35600001 | ||
Hydrogen bonding revisited: geometric selection as a principal determinant of DNA replication fidelity | Q36038818 | ||
The frequency and accuracy of replication past a thymine-thymine cyclobutane dimer are very different in Saccharomyces cerevisiae and Escherichia coli | Q36099447 | ||
Inactivation of DNA proofreading obviates the need for SOS induction in frameshift mutagenesis | Q36638036 | ||
Cellular strategies for accommodating replication-hindering adducts in DNA: control by the SOS response in Escherichia coli | Q37441805 | ||
Impaired translesion synthesis in xeroderma pigmentosum variant extracts | Q39444921 | ||
Mutagenesis induced by single UV photoproducts in E. coli and yeast | Q40486483 | ||
Structural and functional insights provided by crystal structures of DNA polymerases and their substrate complexes. | Q41728302 | ||
Identification of a DinB/UmuC homolog in the archeon Sulfolobus solfataricus | Q42641653 | ||
A RecA protein mutant deficient in its interaction with the UmuDC complex | Q43462173 | ||
DNA polymerase mutagenic bypass and proofreading of endogenous DNA lesions. | Q43518631 | ||
Use of single-turnover kinetics to study bulky adduct bypass by T7 DNA polymerase | Q44408924 | ||
DNA repair: getting past a lesion - at a cost. | Q53941431 | ||
Novel Mutagenic Properties of Abasic Sites inSaccharomyces cerevisiae | Q54606410 | ||
A umuDC-independent SOS pathway for frameshift mutagenesis | Q67965605 | ||
The dinB gene encodes a novel E. coli DNA polymerase, DNA pol IV, involved in mutagenesis | Q72994394 | ||
Mechanisms of frameshift mutations: insight from aromatic amines | Q73257198 | ||
The mutagenesis proteins UmuD' and UmuC prevent lethal frameshifts while increasing base substitution mutations | Q77231587 | ||
P433 | issue | 2 | |
P1104 | number of pages | 6 | |
P304 | page(s) | 74-79 | |
P577 | publication date | 2000-02-01 | |
P1433 | published in | Trends in Biochemical Sciences | Q1565711 |
P1476 | title | Lesions in DNA: hurdles for polymerases | |
P478 | volume | 25 |
Q43637756 | Abnormal kinetics of induction of UV-stimulated recombination in human DNA repair disorders |
Q47271432 | Aging and neurodegeneration are associated with increased mutations in single human neurons. |
Q41915115 | Cidofovir and (S)-9-[3-hydroxy-(2-phosphonomethoxy)propyl]adenine are highly effective inhibitors of vaccinia virus DNA polymerase when incorporated into the template strand |
Q47614597 | Constitutive and regulated expression of the mouse Dinb (Polkappa) gene encoding DNA polymerase kappa. |
Q42024376 | Contributions of ubiquitin- and PCNA-binding domains to the activity of Polymerase eta in Saccharomyces cerevisiae |
Q38324744 | 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. |
Q34367279 | DNA damage recognition and repair pathway coordination revealed by the structural biochemistry of DNA repair enzymes. |
Q40437426 | DNA polymerase kappa is specifically required for recovery from the benzo[a]pyrene-dihydrodiol epoxide (BPDE)-induced S-phase checkpoint |
Q34311450 | DNA postreplication repair and mutagenesis in Saccharomyces cerevisiae |
Q40246661 | Effect of N-2-acetylaminofluorene and 2-aminofluorene adducts on DNA binding and synthesis by yeast DNA polymerase eta. |
Q34454503 | Error-prone translesion synthesis by human DNA polymerase eta on DNA-containing deoxyadenosine adducts of 7,8-dihydroxy-9,10-epoxy-7,8,9,10-tetrahydrobenzo[a]pyrene |
Q36023638 | Expression and possible functions of DNA lesion bypass proteins in spermatogenesis |
Q44556480 | Frameshift mutations induced by three classes of acridines in the lacZ reversion assay in Escherichia coli: potency of responses and relationship to slipped mispairing models |
Q34762160 | Genome stability and the processing of damaged replication forks by RecG. |
Q34983022 | Genotoxicity of 2-nitro-7-methoxy-naphtho[2,1-b]furan (R7000): a case study with some considerations on nitrofurantoin and nifuroxazide |
Q39535234 | Homologous recombination is essential for RAD51 up-regulation in Saccharomyces cerevisiae following DNA crosslinking damage |
Q28507940 | Involvement of mouse Rev3 in tolerance of endogenous and exogenous DNA damage |
Q27939810 | Lesion bypass in yeast cells: Pol eta participates in a multi-DNA polymerase process |
Q34919969 | Mutator phenotypes due to DNA replication infidelity. |
Q27938949 | Pol32, a subunit of Saccharomyces cerevisiae DNA polymerase delta, suppresses genomic deletions and is involved in the mutagenic bypass pathway |
Q28217047 | Preferential misincorporation of purine nucleotides by human DNA polymerase eta opposite benzo[a]pyrene 7,8-diol 9,10-epoxide deoxyguanosine adducts |
Q34025252 | Premature aging and cancer in nucleotide excision repair-disorders |
Q34020161 | Quantitative measurement of translesion replication in human cells: evidence for bypass of abasic sites by a replicative DNA polymerase |
Q33962242 | Recombinational repair and restart of damaged replication forks. |
Q89794767 | Regulation of the abundance of Y-family polymerases in the cell cycle of budding yeast in response to DNA damage |
Q28678572 | Replication of UV-damaged DNA: new insights into links between DNA polymerases, mutagenesis and human disease |
Q24535283 | Replication slippage involves DNA polymerase pausing and dissociation |
Q54637439 | Role of AtPolζ, AtRev1, and AtPolη in UV light-induced mutagenesis in Arabidopsis. |
Q44580538 | Sequence context-dependent replication of DNA templates containing UV-induced lesions by human DNA polymerase iota |
Q52138030 | Sez4 gene encoding an elongation subunit of DNA polymerase zeta is required for normal embryogenesis. |
Q27633013 | Solution structure of the 2-amino-1- methyl-6-phenylimidazo[4,5-b]pyridine C8-deoxyguanosine adduct in duplex DNA |
Q38350120 | The 3'-5' proofreading exonuclease of archaeal family-B DNA polymerase hinders the copying of template strand deaminated bases |
Q36249152 | The RAD6 pathway: control of DNA damage bypass and mutagenesis by ubiquitin and SUMO. |
Q36580706 | The effect of sequence context on spontaneous Polzeta-dependent mutagenesis in Saccharomyces cerevisiae |
Q34390593 | The major human abasic endonuclease: formation, consequences and repair of abasic lesions in DNA. |
Q36099918 | The many faces of DNA polymerases: strategies for mutagenesis and for mutational avoidance |
Q38339825 | The spacious active site of a Y-family DNA polymerase facilitates promiscuous nucleotide incorporation opposite a bulky carcinogen-DNA adduct: elucidating the structure-function relationship through experimental and computational approaches |
Q36457110 | Uracil recognition by replicative DNA polymerases is limited to the archaea, not occurring with bacteria and eukarya |
Q35013038 | poliota-dependent lesion bypass in vitro |
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