XRS2, a DNA repair gene of Saccharomyces cerevisiae, is needed for meiotic recombination.
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Human Rad50 is physically associated with human Mre11: identification of a conserved multiprotein complex implicated in recombinational DNA repairMultiple pathways of recombination induced by double-strand breaks in Saccharomyces cerevisiaeNbs1 potentiates ATP-driven DNA unwinding and endonuclease cleavage by the Mre11/Rad50 complexhMre11 and hRad50 nuclear foci are induced during the normal cellular response to DNA double-strand breaksCell cycle and genetic requirements of two pathways of nonhomologous end-joining repair of double-strand breaks in Saccharomyces cerevisiaeDNA end resection: many nucleases make light workXrs2p regulates Mre11p translocation to the nucleus and plays a role in telomere elongation and meiotic recombination.Distinct roles of two separable in vitro activities of yeast Mre11 in mitotic and meiotic recombination.Competing roles of DNA end resection and non-homologous end joining functions in the repair of replication-born double-strand breaks by sister-chromatid recombination.The yeast MER2 gene is required for chromosome synapsis and the initiation of meiotic recombination.RDH54, a RAD54 homologue in Saccharomyces cerevisiae, is required for mitotic diploid-specific recombination and repair and for meiosisFunctional differences and interactions among the putative RecA homologs Rad51, Rad55, and Rad57.Mutations in two Ku homologs define a DNA end-joining repair pathway in Saccharomyces cerevisiaeCoordination of the initiation of recombination and the reductional division in meiosis in Saccharomyces cerevisiaeThe nuclease activity of Mre11 is required for meiosis but not for mating type switching, end joining, or telomere maintenance.Interaction of Mre11 and Rad50: two proteins required for DNA repair and meiosis-specific double-strand break formation in Saccharomyces cerevisiae.RAD50 protein of S.cerevisiae exhibits ATP-dependent DNA binding.Exo1 roles for repair of DNA double-strand breaks and meiotic crossing over in Saccharomyces cerevisiaeRad50 is dispensable for the maintenance and viability of postmitotic tissuesConditional gene targeted deletion by Cre recombinase demonstrates the requirement for the double-strand break repair Mre11 protein in murine embryonic stem cellsThe location and structure of double-strand DNA breaks induced during yeast meiosis: evidence for a covalently linked DNA-protein intermediateMutations in the MRE11, RAD50, XRS2, and MRE2 genes alter chromatin configuration at meiotic DNA double-stranded break sites in premeiotic and meiotic cellsRole of RAD52 epistasis group genes in homologous recombination and double-strand break repairCharacterization of rec7, an early meiotic recombination gene in Schizosaccharomyces pombe.Post-replication repair suppresses duplication-mediated genome instabilityThe mammalian Mre11-Rad50-nbs1 protein complex: integration of functions in the cellular DNA-damage response.The rad52-Y66A allele alters the choice of donor template during spontaneous chromosomal recombinationSex and the single cell: meiosis in yeastDistribution of the Rad51 recombinase in human and mouse spermatocytes.The Mre11-Rad50-Xrs2 protein complex facilitates homologous recombination-based double-strand break repair in Saccharomyces cerevisiae.Heteroduplex DNA formation and homolog pairing in yeast meiotic mutantsGenetic requirements for RAD51- and RAD54-independent break-induced replication repair of a chromosomal double-strand breakMeiotic recombination initiated by a double-strand break in rad50 delta yeast cells otherwise unable to initiate meiotic recombination.Analysis of meiotic recombination pathways in the yeast Saccharomyces cerevisiaeMolecular and genetic analysis of REC103, an early meiotic recombination gene in yeast.Ku prevents Exo1 and Sgs1-dependent resection of DNA ends in the absence of a functional MRX complex or Sae2Multiple pathways promote short-sequence recombination in Saccharomyces cerevisiaeThe requirement for ATP hydrolysis by Saccharomyces cerevisiae Rad51 is bypassed by mating-type heterozygosity or RAD54 in high copyThe Coprinus cinereus adherin Rad9 functions in Mre11-dependent DNA repair, meiotic sister-chromatid cohesion, and meiotic homolog pairingAlteration of N-terminal phosphoesterase signature motifs inactivates Saccharomyces cerevisiae Mre11.
P2860
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P2860
XRS2, a DNA repair gene of Saccharomyces cerevisiae, is needed for meiotic recombination.
description
1992 nî lūn-bûn
@nan
1992 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
name
XRS2, a DNA repair gene of Saccharomyces cerevisiae, is needed for meiotic recombination.
@ast
XRS2, a DNA repair gene of Saccharomyces cerevisiae, is needed for meiotic recombination.
@en
type
label
XRS2, a DNA repair gene of Saccharomyces cerevisiae, is needed for meiotic recombination.
@ast
XRS2, a DNA repair gene of Saccharomyces cerevisiae, is needed for meiotic recombination.
@en
prefLabel
XRS2, a DNA repair gene of Saccharomyces cerevisiae, is needed for meiotic recombination.
@ast
XRS2, a DNA repair gene of Saccharomyces cerevisiae, is needed for meiotic recombination.
@en
P2093
P2860
P1433
P1476
XRS2, a DNA repair gene of Saccharomyces cerevisiae, is needed for meiotic recombination
@en
P2093
P2860
P304
P407
P577
1992-11-01T00:00:00Z