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Evidence for restriction of ancient primate gammaretroviruses by APOBEC3 but not TRIM5alpha proteinsThe rate and molecular spectrum of spontaneous mutations in Arabidopsis thalianaPrebiotic cytosine synthesis: a critical analysis and implications for the origin of lifeMaking Sense of EpigeneticsDiversity of Endonuclease V: From DNA Repair to RNA EditingMismatch repair and the hereditary non-polyposis colorectal cancer syndrome (HNPCC)Structure of the gene for human uracil-DNA glycosylase and analysis of the promoter functionOxanine DNA glycosylase activity from Mammalian alkyladenine glycosylaseA sequence in the N-terminal region of human uracil-DNA glycosylase with homology to XPA interacts with the C-terminal part of the 34-kDa subunit of replication protein AVariation in the molecular clock of primatesBacterial niche-specific genome expansion is coupled with highly frequent gene disruptions in deep-sea sedimentsDNA methylation and genome evolution in honeybee: gene length, expression, functional enrichment covary with the evolutionary signature of DNA methylationCloning and Expression of Human G/T Mismatch-specific Thymine-DNA GlycosylaseProteome-wide analysis of arginine monomethylation reveals widespread occurrence in human cellsCorrelated Mutation in the Evolution of Catalysis in Uracil DNA Glycosylase SuperfamilyThe meta-epigenomic structure of purified human stem cell populations is defined at cis-regulatory sequencesTransposable Elements and DNA Methylation Create in Embryonic Stem Cells Human-Specific Regulatory Sequences Associated with Distal Enhancers and Noncoding RNAsModelling mutational landscapes of human cancers in vitro.Recent progress in the biology, chemistry and structural biology of DNA glycosylases.Evolution and control of imprinted FWA genes in the genus Arabidopsis.Recurrent V75M mutation within the Wiskott-Aldrich syndrome protein: description of a homozygous female patient.DNA methylome profiling of human tissues identifies global and tissue-specific methylation patterns.The parental non-equivalence of imprinting control regions during mammalian development and evolution.Short interspersed transposable elements (SINEs) are excluded from imprinted regions in the human genome.Features of recent codon evolution: a comparative polymorphism-fixation studyMBD4 cooperates with DNMT1 to mediate methyl-DNA repression and protects mammalian cells from oxidative stress.DNA modifications in the mammalian brainIdentification of RING finger protein 4 (RNF4) as a modulator of DNA demethylation through a functional genomics screenCytosine deamination is a major cause of baseline noise in next-generation sequencing.Base excision repair in a network of defence and tolerance.Development and characterisation of an expressed sequence tags (EST)-derived single nucleotide polymorphisms (SNPs) resource in rainbow troutNeighbor preferences of amino acids and context-dependent effects of amino acid substitutions in human, mouse, and dog.Molecular dissection of the domain architecture and catalytic activities of human PrimPol.Mutagenic consequences of cytosine alterations site-specifically embedded in the human genome.Comparative analysis of kabuli chickpea transcriptome with desi and wild chickpea provides a rich resource for development of functional markersComment on "genomic hypomethylation in the human germline associates with selective structural mutability in the human genome"RVD: a command-line program for ultrasensitive rare single nucleotide variant detection using targeted next-generation DNA resequencing.Methyl-CpG binding proteins and cancer: are MeCpGs more important than MBDs?Ultra-sensitive sequencing reveals an age-related increase in somatic mitochondrial mutations that are inconsistent with oxidative damageCodon usage in vertebrates is associated with a low risk of acquiring nonsense mutations.
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P2860
description
article publié dans la revue scientifique Nature
@fr
scientific article published in Nature
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована в Nature в жовтні 1980
@uk
name
Mutagenic deamination of cytosine residues in DNA
@en
Mutagenic deamination of cytosine residues in DNA
@nl
type
label
Mutagenic deamination of cytosine residues in DNA
@en
Mutagenic deamination of cytosine residues in DNA
@nl
prefLabel
Mutagenic deamination of cytosine residues in DNA
@en
Mutagenic deamination of cytosine residues in DNA
@nl
P356
P1433
P1476
Mutagenic deamination of cytosine residues in DNA
@en
P2093
B K Duncan
J H Miller
P2888
P304
P356
10.1038/287560A0
P407
P577
1980-10-01T00:00:00Z
P6179
1042867394