「NBS1 I171V variant underlies individual differences in chromosomal radiosensitivity within human populations」の関連論文
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NBS1 I171V variant underlies individual differences in chromosomal radiosensitivity within human populations
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TDP2 suppresses genomic instability induced by androgen in the epithelial cells of prostate glands
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A novel motif of Rad51 serves as an interaction hub for recombination auxiliary factors.
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ATM suppresses c-Myc overexpression in the mammary epithelium in response to estrogen
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Phosphoregulation of DSB-1 mediates control of meiotic double-strand break activity
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Ubiquitination of DNA Damage-Stalled RNAPII Promotes Transcription-Coupled Repair
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The CST complex facilitates cell survival under oxidative genotoxic stress
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Fission yeast Srr1 and Skb1 promote isochromosome formation at the centromere
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Genetic Evidence for the Involvement of Mismatch Repair Proteins, PMS2 and MLH3, in a Late Step of Homologous Recombination
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Failure of DNA double-strand break repair by tau mediates Alzheimer's disease pathology in vitro
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The MRE11 nuclease promotes homologous recombination not only in DNA double-strand break resection but also in post-resection in human TK6 cells
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FIGNL1 AAA+ ATPase remodels RAD51 and DMC1 filaments in pre-meiotic DNA replication and meiotic recombination
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Lesion recognition by XPC, TFIIH and XPA in DNA excision repair
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Structure-based screening combined with computational and biochemical analyses identified the inhibitor targeting the binding of DNA Ligase 1 to UHRF1
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Mouse Slfn8 and Slfn9 genes complement human cells lacking SLFN11 during the replication stress response
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Analysis of disease model iPSCs derived from patients with a novel Fanconi anemia-like IBMFS ADH5/ALDH2 deficiency
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Fission yeast Stn1 maintains stability of repetitive DNA at subtelomere and ribosomal DNA regions