De novo CNV formation in mouse embryonic stem cells occurs in the absence of Xrcc4-dependent nonhomologous end joining.
about
Mechanisms underlying structural variant formation in genomic disordersStructural variation mutagenesis of the human genome: Impact on disease and evolution.Mutation spectrum of Drosophila CNVs revealed by breakpoint sequencing.Copy number variants are produced in response to low-dose ionizing radiation in cultured cells.Passage number is a major contributor to genomic structural variations in mouse iPSCs.Large transcription units unify copy number variants and common fragile sites arising under replication stressFactors Affecting the Radiosensitivity of Hexaploid Wheat to γ-Irradiation: Radiosensitivity of Hexaploid Wheat (Triticum aestivum L.) [Corrected].Translesion Polymerases Drive Microhomology-Mediated Break-Induced Replication Leading to Complex Chromosomal Rearrangements.Long Neural Genes Harbor Recurrent DNA Break Clusters in Neural Stem/Progenitor Cells.DNA repair pathway gene expression score correlates with repair proficiency and tumor sensitivity to chemotherapy.Enhancement of microhomology-mediated genomic rearrangements by transient loss of mouse Bloom syndrome helicaseReplicative mechanisms for CNV formation are error prone.The role of AUTS2 in neurodevelopment and human evolution.Chromothripsis and beyond: rapid genome evolution from complex chromosomal rearrangementsRepair of double-strand breaks by end joining.Quality control: Genome maintenance in pluripotent stem cells.Genomic instability: Crossing pathways at the origin of structural and numerical chromosome changes.Contrasting mechanisms of de novo copy number mutagenesis suggest the existence of different classes of environmental copy number mutagens.Achilles' heel of pluripotent stem cells: genetic, genomic and epigenetic variations during prolonged culture.Fragile sites in cancer: more than meets the eye.Elevated variant density around SV breakpoints in germline lineage lends support to error-prone replication hypothesis.Characterization of 26 deletion CNVs reveals the frequent occurrence of micro-mutations within the breakpoint-flanking regions and frequent repair of double-strand breaks by templated insertions derived from remote genomic regions.Diverse mechanisms of somatic structural variations in human cancer genomes.Signature of backward replication slippage at the copy number variation junction.Break induced replication in eukaryotes: mechanisms, functions, and consequences.An Organismal CNV Mutator Phenotype Restricted to Early Human Development.Small de novo CNVs as biomarkers of parental exposure to low doses of ionizing radiation of caesium-137.
P2860
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P2860
De novo CNV formation in mouse embryonic stem cells occurs in the absence of Xrcc4-dependent nonhomologous end joining.
description
2012 nî lūn-bûn
@nan
2012 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
De novo CNV formation in mouse ...... ent nonhomologous end joining.
@ast
De novo CNV formation in mouse ...... ent nonhomologous end joining.
@en
De novo CNV formation in mouse ...... ent nonhomologous end joining.
@nl
type
label
De novo CNV formation in mouse ...... ent nonhomologous end joining.
@ast
De novo CNV formation in mouse ...... ent nonhomologous end joining.
@en
De novo CNV formation in mouse ...... ent nonhomologous end joining.
@nl
prefLabel
De novo CNV formation in mouse ...... ent nonhomologous end joining.
@ast
De novo CNV formation in mouse ...... ent nonhomologous end joining.
@en
De novo CNV formation in mouse ...... ent nonhomologous end joining.
@nl
P2093
P2860
P1433
P1476
De novo CNV formation in mouse ...... ent nonhomologous end joining.
@en
P2093
Martin F Arlt
Shanda R Birkeland
Sountharia Rajendran
Thomas E Wilson
Thomas W Glover
P2860
P304
P356
10.1371/JOURNAL.PGEN.1002981
P577
2012-09-20T00:00:00Z