Extensive loss of heterozygosity is suppressed during homologous repair of chromosomal breaks
about
Alternative-NHEJ is a mechanistically distinct pathway of mammalian chromosome break repairMechanisms of change in gene copy numberMeiotic versus mitotic recombination: two different routes for double-strand break repair: the different functions of meiotic versus mitotic DSB repair are reflected in different pathway usage and different outcomesRECQL5/Recql5 helicase regulates homologous recombination and suppresses tumor formation via disruption of Rad51 presynaptic filamentsYeast Mph1 helicase dissociates Rad51-made D-loops: implications for crossover control in mitotic recombination.Srs2 mediates PCNA-SUMO-dependent inhibition of DNA repair synthesis.Mitotic homologous recombination maintains genomic stability and suppresses tumorigenesisGenetic steps of mammalian homologous repair with distinct mutagenic consequencesMinding the gap: the underground functions of BRCA1 and BRCA2 at stalled replication forksSrs2 and Sgs1-Top3 suppress crossovers during double-strand break repair in yeastLimiting the persistence of a chromosome break diminishes its mutagenic potential.Human Fanconi anemia monoubiquitination pathway promotes homologous DNA repair.Mechanisms of recombination between diverged sequences in wild-type and BLM-deficient mouse and human cells.Mutagenic repair of DNA interstrand crosslinks.11q21.1-11q23.3 Is a site of intrinsic genomic instability triggered by irradiation.Mechanisms of double-strand break repair in somatic mammalian cells.Targeting abnormal DNA double strand break repair in cancerThe homologous chromosome is an effective template for the repair of mitotic DNA double-strand breaks in Drosophila.Changes in DNA repair during aging.Double-strand break repair by interchromosomal recombination: an in vivo repair mechanism utilized by multiple somatic tissues in mammals.Interhomolog recombination and loss of heterozygosity in wild-type and Bloom syndrome helicase (BLM)-deficient mammalian cells.Genetic evidence that synaptonemal complex axial elements govern recombination pathway choice in miceCorrect end use during end joining of multiple chromosomal double strand breaks is influenced by repair protein RAD50, DNA-dependent protein kinase DNA-PKcs, and transcription context.Inviting instability: Transposable elements, double-strand breaks, and the maintenance of genome integrity.Genomic Complexity Profiling Reveals That HORMAD1 Overexpression Contributes to Homologous Recombination Deficiency in Triple-Negative Breast Cancers.Interchromosomal crossover in human cells is associated with long gene conversion tracts.Defective break-induced replication leads to half-crossovers in Saccharomyces cerevisiae.Tetratricopeptide repeat factor XAB2 mediates the end resection step of homologous recombinationAberrant double-strand break repair resulting in half crossovers in mutants defective for Rad51 or the DNA polymerase delta complexXRCC2 and XRCC3 regulate the balance between short- and long-tract gene conversions between sister chromatids.Possible anti-recombinogenic role of Bloom's syndrome helicase in double-strand break processingRegulation of insulin synthesis and secretion and pancreatic Beta-cell dysfunction in diabetes.Collaboration and competition between DNA double-strand break repair pathways.Rad54, the motor of homologous recombination.Repair of DNA interstrand cross-links during S phase of the mammalian cell cycle.Differential regulation of short- and long-tract gene conversion between sister chromatids by Rad51C.Localized DNA cleavage secondary to genotoxic exposure adjacent to an Alu inverted repeat.Mammalian Fbh1 is important to restore normal mitotic progression following decatenation stress.Alternative pathways for the repair of RAG-induced DNA breaksConservative inheritance of newly synthesized DNA in double-strand break-induced gene conversion.
P2860
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P2860
Extensive loss of heterozygosity is suppressed during homologous repair of chromosomal breaks
description
2003 nî lūn-bûn
@nan
2003 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Extensive loss of heterozygosi ...... s repair of chromosomal breaks
@ast
Extensive loss of heterozygosi ...... s repair of chromosomal breaks
@en
Extensive loss of heterozygosi ...... s repair of chromosomal breaks
@nl
type
label
Extensive loss of heterozygosi ...... s repair of chromosomal breaks
@ast
Extensive loss of heterozygosi ...... s repair of chromosomal breaks
@en
Extensive loss of heterozygosi ...... s repair of chromosomal breaks
@nl
prefLabel
Extensive loss of heterozygosi ...... s repair of chromosomal breaks
@ast
Extensive loss of heterozygosi ...... s repair of chromosomal breaks
@en
Extensive loss of heterozygosi ...... s repair of chromosomal breaks
@nl
P2860
P1476
Extensive loss of heterozygosi ...... s repair of chromosomal breaks
@en
P2093
Jeremy M Stark
Maria Jasin
P2860
P304
P356
10.1128/MCB.23.2.733-743.2003
P407
P577
2003-01-01T00:00:00Z