| scholarly article | Q13442814 |
| review article | Q7318358 |
| P356 | DOI | 10.1021/BI00487A001 |
| P953 | full work available at URL | https://pubs.acs.org/doi/pdf/10.1021/bi00487a001 |
| P698 | PubMed publication ID | 1702019 |
| P50 | author | Thomas A Kunkel | Q62517517 |
| P433 | issue | 35 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | genetic model | Q67149661 |
| DNA replication | Q130996 | ||
| biochemistry | Q7094 | ||
| P304 | page(s) | 8003-8011 | |
| P577 | publication date | 1990-09-01 | |
| 1990-09-04 | |||
| P1433 | published in | Biochemistry | Q764876 |
| P1476 | title | Misalignment-mediated DNA synthesis errors | |
| P478 | volume | 29 |
| Q72012628 | 2–Aminofluorene modified DNA duplex exists in two interchangeable conformations |
| Q30453467 | 3'-Azido-3'-deoxythymidine (AZT) and AZT-resistant reverse transcriptase can increase the in vivo mutation rate of human immunodeficiency virus type 1. |
| Q34042634 | 8-Methoxypsoralen induced mutations are highly targeted at crosslinkable sites of photoaddition on the non-transcribed strand of a mammalian chromosomal gene |
| Q67482102 | A 22-bp deletion in the phenylalanine hydroxylase gene causing phenylketonuria in an Arab family |
| Q41973778 | A mechanism of nucleotide misincorporation during transcription due to template-strand misalignment |
| Q35753566 | A mismatch recognition defect in colon carcinoma confers DNA microsatellite instability and a mutator phenotype |
| Q42266867 | A molecular characterization of spontaneous frameshift mutagenesis within the trpA gene of Escherichia coli. |
| Q49119301 | A thumb subdomain mutant of the large fragment of Escherichia coli DNA polymerase I with reduced DNA binding affinity, processivity, and frameshift fidelity |
| Q64389525 | Analysis of spontaneous frameshift mutations in REV1 and rev1-1 strains of Saccharomyces cerevisiae |
| Q40696088 | Antigen diversity in the bacterium B. hermsii through "somatic" mutations in rearranged vmp genes |
| Q53768726 | Asymmetry of frameshift mutagenesis during leading and lagging-strand replication in Escherichia coli. |
| Q34443496 | Base composition of mononucleotide runs affects DNA polymerase slippage and removal of frameshift intermediates by mismatch repair in Saccharomyces cerevisiae |
| Q58074430 | Bi-directional Processing of DNA Loops by Mismatch Repair-dependent and -independent Pathways in Human Cells |
| Q33962585 | Complex frameshift mutations mediated by plasmid pKM101: mutational mechanisms deduced from 4-aminobiphenyl-induced mutation spectra in Salmonella. |
| Q57263791 | Complex gene rearrangements caused by serial replication slippage |
| Q33491775 | Complexity of the MSG gene family of Pneumocystis carinii |
| Q30424775 | Conditional reduction of human immunodeficiency virus type 1 replication by a gain-of-herpes simplex virus 1 thymidine kinase function |
| Q51906358 | CpG/CpNpG motifs in the coding region are preferred sites for mutagenesis in the breast cancer susceptibility genes. |
| Q43883867 | DNA end joining by the Klenow fragment of DNA polymerase I. |
| Q28277408 | DNA polymerase fidelity and the polymerase chain reaction |
| Q53105718 | DNA polymerase kappa microsatellite synthesis: two distinct mechanisms of slippage-mediated errors. |
| Q74164952 | DNA polymerases on the move |
| Q41264767 | DNA repair and colorectal cancer |
| Q35677447 | DNA replication fidelity |
| Q38332697 | DNA secondary structure effects on DNA synthesis catalyzed by HIV-1 reverse transcriptase |
| Q24548004 | DNA sequence analysis of spontaneous mutagenesis in Saccharomyces cerevisiae |
| Q33962568 | DNA sequence effects on single base deletions arising during DNA polymerization in vitro by Escherichia coli Klenow fragment polymerase |
| Q33692307 | DNA-directed mutations. Leading and lagging strand specificity |
| Q37263073 | Damage, repair, and mutagenesis in nuclear genes after mouse forebrain ischemia-reperfusion |
| Q34868968 | Database of p53 gene somatic mutations in human tumors and cell lines |
| Q54455718 | De novo mutations in familial adenomatous polyposis (FAP). |
| Q35975501 | Deletion between direct repeats in T7 DNA stimulated by double-strand breaks |
| Q34973894 | Deletion mutations caused by DNA strand slippage in Acinetobacter baylyi |
| Q50123699 | Deletogenic activity of 1,2:7,8-diepoxyoctane in the Salmonella typhimurium tester strain TA102. |
| Q33886145 | Determination of the site of first strand transfer during Moloney murine leukemia virus reverse transcription and identification of strand transfer-associated reverse transcriptase errors |
| Q35562130 | Differences in genome-wide repeat sequence instability conferred by proofreading and mismatch repair defects |
| Q35591486 | Differential DNA secondary structure-mediated deletion mutation in the leading and lagging strands |
| Q40393541 | Discordant expression and variable numbers of neighboring GGA- and GAA-rich triplet repeats in the 3' untranslated regions of two groups of messenger RNAs encoded by the rat polymeric immunoglobulin receptor gene |
| Q36754737 | Distinct mutational behaviors differentiate short tandem repeats from microsatellites in the human genome |
| Q33862468 | Does variation in genome sizes reflect adaptive or neutral processes? New clues from Passiflora |
| Q34310677 | EGNAS: an exhaustive DNA sequence design algorithm |
| Q43882514 | Effects of a guanine-derived formamidopyrimidine lesion on DNA replication: translesion DNA synthesis, nucleotide insertion, and extension kinetics |
| Q33807866 | Effects of amino acid substitutions at position 115 on the fidelity of human immunodeficiency virus type 1 reverse transcriptase |
| Q40393707 | Efficient extension of a misaligned tRNA-primer during replication of the HIV-1 retrovirus |
| Q33566378 | Energetic signatures of single base bulges: thermodynamic consequences and biological implications. |
| Q35598571 | Error-prone replication of repeated DNA sequences by T7 DNA polymerase in the absence of its processivity subunit |
| Q33994529 | Escherichia coli DNA polymerase IV mutator activity: genetic requirements and mutational specificity |
| Q38305884 | Examination of the long-range effects of aminofluorene-induced conformational heterogeneity and its relevance to the mechanism of translesional DNA synthesis |
| Q37593054 | Expression levels of DNA replication and repair genes predict regional somatic repeat instability in the brain but are not altered by polyglutamine disease protein expression or age. |
| Q71245633 | Fidelity and error specificity of the alpha catalytic subunit of Escherichia coli DNA polymerase III |
| Q35020670 | Fidelity and mutational spectrum of Pfu DNA polymerase on a human mitochondrial DNA sequence |
| Q24628707 | Fidelity of DNA synthesis catalyzed by human DNA polymerase alpha and HIV-1 reverse transcriptase: effect of reaction pH |
| Q88499445 | Forensic applicability of multi-allelic InDels with mononucleotide homopolymer structures |
| Q35748265 | Frameshift mutagenesis: the roles of primer-template misalignment and the nonhomologous end-joining pathway in Saccharomyces cerevisiae. |
| Q41182021 | Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environment |
| Q35588912 | Genetic evidence that both dNTP-stabilized and strand slippage mechanisms may dictate DNA polymerase errors within mononucleotide microsatellites |
| Q28264035 | Genetic instability in budding and fission yeast-sources and mechanisms |
| Q41886362 | Genetic instability within monotonous runs of CpG sequences in Escherichia coli |
| Q36627910 | Genome-wide analysis of the specificity and mechanisms of replication infidelity driven by imbalanced dNTP pools. |
| Q36621522 | High rates of frameshift mutations within homo-oligomeric runs during a single cycle of retroviral replication. |
| Q34467256 | High-frequency phenotypic reversion and pathogenicity of an acyclovir-resistant herpes simplex virus mutant |
| Q34964296 | Highly mutagenic replication by DNA polymerase V (UmuC) provides a mechanistic basis for SOS untargeted mutagenesis |
| Q73093633 | Homonucleotide tracts, short repeats and CpG/CpNpG motifs are frequent sites for heterogeneous mutations in the neurofibromatosis type 1 (NF1) tumour-suppressor gene |
| Q34055705 | Human base excision repair creates a bias toward -1 frameshift mutations |
| Q71937474 | Identification of a novel mutation causing aspartylglucosaminuria reveals a mutation hotspot region in the aspartylglucosaminidase gene |
| Q40988373 | In situ detection of frameshift mutations in mouse cells |
| Q45770163 | In vitro bypass replication of the cisplatin-d(GpG) lesion by calf thymus DNA polymerase beta and human immunodeficiency virus type I reverse transcriptase is highly mutagenic |
| Q37289159 | In vitro fidelity of the prototype primate foamy virus (PFV) RT compared to HIV-1 RT. |
| Q35824007 | In vitro molecular reconstitution of the respiratory burst in B lymphoblasts from p47-phox-deficient chronic granulomatous disease |
| Q33811519 | In vivo analysis of human T-cell leukemia virus type 1 reverse transcription accuracy |
| Q35847997 | Instability of (CTG)n•(CAG)n trinucleotide repeats and DNA synthesis |
| Q34617609 | Is the rate of insertion and deletion mutation male biased?: Molecular evolutionary analysis of avian and primate sex chromosome sequences. |
| Q33401963 | Large-scale inference of the point mutational spectrum in human segmental duplications |
| Q40980167 | Lead and mercury mutagenesis: type of mutation dependent upon metal concentration |
| Q34385155 | Lesion bypass DNA polymerases replicate across non-DNA segments |
| Q29619994 | Lower in vivo mutation rate of human immunodeficiency virus type 1 than that predicted from the fidelity of purified reverse transcriptase |
| Q27659842 | Mechanism of error-free and semitargeted mutagenic bypass of an aromatic amine lesion by Y-family polymerase Dpo4 |
| Q42044589 | Mechanisms of dinucleotide repeat instability in Escherichia coli |
| Q30912512 | Mechanistic aspects of CoII(HAPP)(TFA)2 in DNA bulge-specific recognition. |
| Q45755067 | Methods for the detection of non-random base substitution in virus genes: models of synonymous nucleotide substitution in picornavirus genes |
| Q40022200 | Microsatellite instability in yeast: dependence on repeat unit size and DNA mismatch repair genes |
| Q43612705 | Mismatch repair and the regulation of phase variation in Neisseria meningitidis |
| Q41170340 | Mismatch repair defects in human carcinogenesis |
| Q27323040 | Molecular events during translocation and proofreading extracted from 200 static structures of DNA polymerase. |
| Q73457782 | Molecular mechanisms of mutagenesis by aromatic amines and amides |
| Q48076731 | Molecular nature of spontaneous mutations at the hypoxanthine-guanine phosphoribosyltransferase (hprt) locus in Chinese hamster ovary cells |
| Q36796836 | Mutagenesis by third-strand-directed psoralen adducts in repair-deficient human cells: high frequency and altered spectrum in a xeroderma pigmentosum variant |
| Q46447125 | Mutagenicity of a Model DNA-Peptide Cross-Link in Human Cells: Roles of Translesion Synthesis DNA Polymerases |
| Q39716050 | Mutation spectra of TA*, the major photoproduct of thymidylyl-(3'5')-deoxyadenosine, in Escherichia coli under SOS conditions |
| Q54583351 | Mutational and DNA binding specificity of the carcinogen 2-amino-3, 8-dimethylimidazo[4,5-f]quinoxaline. |
| Q72519717 | Mutational spectrum induced in Saccharomyces cerevisiae by the carcinogen N-2-acetylaminofluorene |
| Q41499457 | Mutational spectrum of ICR-191 at the hprt locus in human lymphoblastoid cells |
| Q73019259 | Mutations in the primer grip region of HIV reverse transcriptase can increase replication fidelity |
| Q33180107 | Mutations induced by some DNA minor groove binding alkylators in AS52 Chinese hamster cells |
| Q73687941 | Mutations of p53 gene in human colorectal cancer: distinct frameshifts among populations |
| Q54588472 | N-ethyl-N-nitrosourea-induced mutagenesis in Escherichia coli: Multiple roles for UmuC protein |
| Q34120857 | Nature, position, and frequency of mutations made in a single cycle of HIV-1 replication |
| Q44605177 | Nick-dependent and -independent processing of large DNA loops in human cells |
| Q48165910 | Nucleotide sequence analysis of human hypoxanthine phosphoribosyltransferase (HPRT) gene deletions |
| Q37191829 | On the origins of genetic variants |
| Q35226155 | On the sequence-directed nature of human gene mutation: the role of genomic architecture and the local DNA sequence environment in mediating gene mutations underlying human inherited disease |
| Q54642988 | Oxygen radical induced mutagenesis is DNA polymerase specific. |
| Q40637670 | Paradoxical homozygous expression from heterozygotes and heterozygous expression from homozygotes as a consequence of transcriptional infidelity through a polyadenine tract in the AP3B1 gene responsible for canine cyclic neutropenia. |
| Q48061099 | Poly(T) variation in heteroderid nematode mitochondrial genomes is predominantly an artefact of amplification |
| Q53766409 | Polymerase chain reaction-directed DNA sequencing of bleomycin-induced "nondeletion"-type, 6-thioguanine-resistant mutants in Chinese hamster ovary cell derivative AS52: effects of an inhibitor and a mimic of superoxide dismutase. |
| Q47951603 | Pooled analysis of p53 mutations in hematological malignancies |
| Q72679753 | Population screening of lactate dehydrogenase deficiencies in Fukuoka Prefecture in Japan and molecular characterization of three independent mutations in the lactate dehydrogenase-B(H) gene |
| Q46595699 | Purification and properties of wild-type and exonuclease-deficient DNA polymerase II from Escherichia coli |
| Q36483459 | RETRACTED: In vivo and in vitro evidence for slipped mispairing in mammalian mitochondria |
| Q44920681 | Reduced frameshift fidelity and processivity of HIV-1 reverse transcriptase mutants containing alanine substitutions in helix H of the thumb subdomain. |
| Q39719038 | Replication bypass and mutagenic effect of alpha-deoxyadenosine site-specifically incorporated into single-stranded vectors |
| Q42660015 | Replication errors: cha(lle)nging the genome |
| Q73555611 | Replication of template-primers containing propanodeoxyguanosine by DNA polymerase beta. Induction of base pair substitution and frameshift mutations by template slippage and deoxynucleoside triphosphate stabilization |
| Q35468354 | Resistance of bulky DNA lesions to nucleotide excision repair can result from extensive aromatic lesion-base stacking interactions |
| Q34323549 | Ribosomal protein gene sequence changes in erythromycin-resistant mutants of Escherichia coli |
| Q74643959 | Screening for mutations of the APC gene in 66 Italian familial adenomatous polyposis patients: evidence for phenotypic differences in cases with and without identified mutation |
| Q41552163 | Selection for spontaneous null mutations in a chromosomally-integrated HSV-1 thymidine kinase gene yields deletions and a mutation caused by intragenic illegitimate recombination |
| Q42641512 | Sequence polymorphism in the E3 7.7K ORF of subspecies B1 human adenoviruses |
| Q24657452 | Sequence variation in the Fanconi anemia gene FAA |
| Q59070212 | Slippery DNA and diseases |
| Q34587260 | Somatic point mutations in the p53 gene of human tumors and cell lines: updated compilation |
| Q41540380 | Spectrum of spontaneous mutation in animal cells containing an aphidicolin-resistant DNA polymerase α |
| Q33952945 | Spontaneous microdeletions and microinsertions in a transgenic mouse mutation detection system: analysis of age, tissue, and sequence specificity |
| Q73606010 | Spontaneous mutation of the lacI transgene in rodents: absence of species, strain, and insertion-site influence |
| Q39718894 | Substitution and deletion mutations induced by 2-hydroxyadenine in Escherichia coli: effects of sequence contexts in leading and lagging strands |
| Q71921084 | Tandem sequence duplications functionally complement deletions in the D1 protein of photosystem II |
| Q77172508 | The base substitution and frameshift fidelity of Escherichia coli DNA polymerase III holoenzyme in vitro |
| Q72073105 | The effect of the 3′ → 5′ exonuclease of T7 DNA polymerase on frameshifts and deletions |
| Q35749719 | The gateway pDEST17 expression vector encodes a -1 ribosomal frameshifting sequence |
| Q33961004 | The influence of primary and secondary DNA structure in deletion and duplication between direct repeats in Escherichia coli |
| Q35757863 | The mode and tempo of genome size evolution in eukaryotes. |
| Q77231587 | The mutagenesis proteins UmuD' and UmuC prevent lethal frameshifts while increasing base substitution mutations |
| Q34551905 | The oxidized deoxynucleoside triphosphate pool is a significant contributor to genetic instability in mismatch repair-deficient cells |
| Q35902590 | The roles of Tyr391 and Tyr619 in RB69 DNA polymerase replication fidelity |
| Q47233090 | The size difference between leishmania major friedlin chromosome one homologues is localized to sub-telomeric repeats at one chromosomal end. |
| Q47356449 | The size distribution of insertions and deletions in human and rodent pseudogenes suggests the logarithmic gap penalty for sequence alignment |
| Q35773278 | Thermodynamic examination of 1- to 5-nt purine bulge loops in RNA and DNA constructs |
| Q72902049 | Transcribed heteroplasmic repeated sequences in the porcine mitochondrial DNA D-loop region |
| Q34570789 | Transmissible and nontransmissible mutations induced by irradiating Arabidopsis thaliana pollen with gamma-rays and carbon ions |
| Q37127515 | Unequal human immunodeficiency virus type 1 reverse transcriptase error rates with RNA and DNA templates |
| Q27935855 | Unique error signature of the four-subunit yeast DNA polymerase epsilon |
| Q36523157 | Variation of human papillomavirus type 6 (HPV-6) and HPV-11 genomes sampled throughout the world |
| Q34087170 | Visualizing sequence-governed nucleotide selectivities and mutagenic consequences through a replicative cycle: processing of a bulky carcinogen N2-dG lesion in a Y-family DNA polymerase |
| Q34131685 | What Is a Microsatellite: A Computational and Experimental Definition Based upon Repeat Mutational Behavior at A/T and GT/AC Repeats |
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