scholarly article | Q13442814 |
P50 | author | Georgii A. Bazykin | Q54900881 |
P2093 | author name string | Ruslan A Soldatov | |
Vladimir B Seplyarskiy | |||
P2860 | cites work | 8.2% of the Human genome is constrained: variation in rates of turnover across functional element classes in the human lineage | Q21144867 |
Fundamental concepts in genetics: Effective population size and patterns of molecular evolution and variation | Q22122006 | ||
An integrated map of genetic variation from 1,092 human genomes | Q22122153 | ||
Initial sequence of the chimpanzee genome and comparison with the human genome | Q22122468 | ||
Initial sequencing and comparative analysis of the mouse genome | Q22122521 | ||
The accessible chromatin landscape of the human genome | Q24595581 | ||
REV1 and polymerase ζ facilitate homologous recombination repair | Q28118890 | ||
Exonuclease mutations in DNA polymerase epsilon reveal replication strand specific mutation patterns and human origins of replication | Q28248149 | ||
A new class of uracil-DNA glycosylases related to human thymine-DNA glycosylase | Q28294063 | ||
Widespread genomic signatures of natural selection in hominid evolution | Q28754708 | ||
The evolution of gene expression levels in mammalian organs | Q29617170 | ||
The fidelity of DNA synthesis by yeast DNA polymerase zeta alone and with accessory proteins. | Q33257520 | ||
Participation of DNA polymerase zeta in replication of undamaged DNA in Saccharomyces cerevisiae | Q33628462 | ||
Comparative analysis of DNA replication timing reveals conserved large-scale chromosomal architecture. | Q33628761 | ||
Impact of replication timing on non-CpG and CpG substitution rates in mammalian genomes | Q33762440 | ||
Correlated evolution of nearby residues in Drosophilid proteins | Q33839433 | ||
Evolutionarily conserved replication timing profiles predict long-range chromatin interactions and distinguish closely related cell types | Q33881351 | ||
Reduced local mutation density in regulatory DNA of cancer genomes is linked to DNA repair | Q33976821 | ||
Error-prone polymerase activity causes multinucleotide mutations in humans | Q34153783 | ||
Replication fork polarity gradients revealed by megabase-sized U-shaped replication timing domains in human cell lines | Q34229543 | ||
DNA methylation and the frequency of CpG in animal DNA. | Q34252001 | ||
Differential relationship of DNA replication timing to different forms of human mutation and variation | Q34313413 | ||
Understanding nucleotide excision repair and its roles in cancer and ageing. | Q34426055 | ||
Heterogeneous polymerase fidelity and mismatch repair bias genome variation and composition. | Q34439328 | ||
DNA replication timing and selection shape the landscape of nucleotide variation in cancer genomes | Q51553614 | ||
Levels of naturally occurring DNA polymorphism correlate with recombination rates in D. melanogaster | Q52443577 | ||
Disruption of mouse polymerase zeta (Rev3) leads to embryonic lethality and impairs blastocyst development in vitro | Q52541352 | ||
Major role of positive selection in the evolution of conservative segments ofDrosophilaproteins | Q52738682 | ||
A New and More Accurate Estimate of the Rate of Concurrent Tandem-Base Substitution Mutations in the Human Germline: ∼0.4% of the Single-Nucleotide Substitution Mutation Rate | Q57263625 | ||
Positive selection at sites of multiple amino acid replacements since rat–mouse divergence | Q59080389 | ||
Determinants of mutation rate variation in the human germline | Q35202583 | ||
Mutation Rates across Budding Yeast Chromosome VI Are Correlated with Replication Timing | Q35205793 | ||
Mutation rate distribution inferred from coincident SNPs and coincident substitutions | Q35211692 | ||
Whole genome RNAi screens reveal a critical role of REV3 in coping with replication stress | Q35223093 | ||
Replicative bypass of abasic site in Escherichia coli and human cells: similarities and differences | Q35255862 | ||
DNA polymerase ζ-dependent lesion bypass in Saccharomyces cerevisiae is accompanied by error-prone copying of long stretches of adjacent DNA. | Q35590948 | ||
Genome-wide patterns and properties of de novo mutations in humans | Q35798123 | ||
SOD1 aggregation in ALS mice shows simplistic test tube behavior | Q35961208 | ||
DNA polymerase ζ generates tandem mutations in immunoglobulin variable regions | Q36021801 | ||
DNA polymerase zeta is required for proliferation of normal mammalian cells | Q36044873 | ||
Transcription-associated mutagenesis in yeast is directly proportional to the level of gene expression and influenced by the direction of DNA replication | Q36083014 | ||
Mutator alleles of yeast DNA polymerase zeta. | Q36247787 | ||
Genomic evidence for elevated mutation rates in highly expressed genes | Q36440506 | ||
Pervasive Multinucleotide Mutational Events in Eukaryotes | Q36553453 | ||
The enigmatic thymine DNA glycosylase | Q36658394 | ||
Transcription induces strand-specific mutations at the 5' end of human genes | Q36804846 | ||
DNA polymerase zeta generates clustered mutations during bypass of endogenous DNA lesions in Saccharomyces cerevisiae. | Q36918652 | ||
Rates and Genomic Consequences of Spontaneous Mutational Events inDrosophila melanogaster | Q37063145 | ||
The choice of nucleotide inserted opposite abasic sites formed within chromosomal DNA reveals the polymerase activities participating in translesion DNA synthesis | Q37302944 | ||
Contributions of intrinsic mutation rate and selfish selection to levels of de novo HRAS mutations in the paternal germline | Q37395153 | ||
DNA polymerases ζ and Rev1 mediate error-prone bypass of non-B DNA structures | Q37416977 | ||
Modulation of mutagenesis in eukaryotes by DNA replication fork dynamics and quality of nucleotide pools | Q37483304 | ||
Human Pol ζ purified with accessory subunits is active in translesion DNA synthesis and complements Pol η in cisplatin bypass | Q37612640 | ||
The UCSC Genome Browser database: 2014 update | Q37661736 | ||
A novel codon4 mutation (A4F) in the SOD1gene in familial amyotrophic lateral sclerosis. | Q37865738 | ||
Variation in the mutation rate across mammalian genomes | Q37942062 | ||
Differential DNA mismatch repair underlies mutation rate variation across the human genome | Q38906828 | ||
Replication-Associated Mutational Asymmetry in the Human Genome | Q39582800 | ||
Prevalence of multinucleotide replacements in evolution of primates and Drosophila. | Q40577986 | ||
A sensitive genetic assay for the detection of cytosine deamination: determination of rate constants and the activation energy | Q41203605 | ||
Developmental control of cell cycle regulators: a fly's perspective | Q41239581 | ||
Human mutation rate associated with DNA replication timing | Q42085559 | ||
Patterns and mutational signatures of tandem base substitutions causing human inherited disease | Q43584644 | ||
Heterogeneity of the transition/transversion ratio in Drosophila and Hominidae genomes. | Q43721710 | ||
Late-replicating domains have higher divergence and diversity in Drosophila melanogaster | Q43847740 | ||
A novel SOD1 gene mutation in a Korean family with amyotrophic lateral sclerosis | Q44247546 | ||
Transcription-associated mutational asymmetry in mammalian evolution | Q44337576 | ||
Induction of invasive mouse skin carcinomas in transgenic mice with mutations in both H-ras and p53. | Q46778165 | ||
P433 | issue | 12 | |
P304 | page(s) | 3158-3172 | |
P577 | publication date | 2015-09-15 | |
P1433 | published in | Molecular Biology and Evolution | Q1992656 |
P1476 | title | Polymerase ζ Activity Is Linked to Replication Timing in Humans: Evidence from Mutational Signatures | |
P478 | volume | 32 |
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Q52720551 | In-depth characterization of the cisplatin mutational signature in human cell lines and in esophageal and liver tumors |
Q92756188 | Insights into the Link between the Organization of DNA Replication and the Mutational Landscape |
Q36192609 | Multi-nucleotide de novo Mutations in Humans |
Q64907663 | Multinucleotide mutations cause false inferences of lineage-specific positive selection. |
Q50021424 | Reading the genome like a history book |
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