Stress and DNA repair biology of the Fanconi anemia pathway
about
Genetic causes of cancer predisposition in children and adolescentsBRCA Mutations, DNA Repair Deficiency, and Ovarian AgingClose encounters for the first time: Helicase interactions with DNA damageThe Fanconi Anemia C Protein Binds to and Regulates Stathmin-1 PhosphorylationDrugging the Cancers Addicted to DNA Repair.CRISPR/Cas9-Mediated Correction of the FANCD1 Gene in Primary Patient CellsRibosomopathies and the paradox of cellular hypo- to hyperproliferation.Human FAN1 promotes strand incision in 5'-flapped DNA complexed with RPA.Replication Protein A (RPA) deficiency activates the Fanconi anemia DNA repair pathway.Fancb deficiency impairs hematopoietic stem cell function.Differential regulation of the anti-crossover and replication fork regression activities of Mph1 by Mte1.Anemia of Central Origin.Common Chemical Inductors of Replication Stress: Focus on Cell-Based Studies.Promotion of RAD51-Mediated Homologous DNA Pairing by the RAD51AP1-UAF1 Complex.FANCI-FANCD2 stabilizes the RAD51-DNA complex by binding RAD51 and protects the 5'-DNA end.Upregulated LINE-1 Activity in the Fanconi Anemia Cancer Susceptibility Syndrome Leads to Spontaneous Pro-inflammatory Cytokine Production.Strategic role of the ubiquitin-dependent segregase p97 (VCP or Cdc48) in DNA replication.Abundance of the Fanconi anaemia core complex is regulated by the RuvBL1 and RuvBL2 AAA+ ATPases.Aplastic anemia and clonal evolution: germ line and somatic genetics.SNM1B/Apollo in the DNA damage response and telomere maintenancep53 downregulates the Fanconi anaemia DNA repair pathway.The Fanconi anemia pathway is required for efficient repair of stress-induced DNA damage in haematopoietic stem cellsComplementation of hypersensitivity to DNA interstrand crosslinking agents demonstrates that XRCC2 is a Fanconi anaemia gene.Human RAD52 - a novel player in DNA repair in cancer and immunodeficiencyHypomorphic FANCA mutations correlate with mild mitochondrial and clinical phenotype in Fanconi anemia.Clinical utility of next-generation sequencing for inherited bone marrow failure syndromes.Coordination of the recruitment of the FANCD2 and PALB2 Fanconi anemia proteins by an ubiquitin signaling network.The Guardian of the Genome Revisited: p53 Downregulates Genes Required for Telomere Maintenance, DNA Repair, and Centromere Structure.
P2860
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P2860
Stress and DNA repair biology of the Fanconi anemia pathway
description
2014 nî lūn-bûn
@nan
2014年の論文
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2014年学术文章
@wuu
2014年学术文章
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2014年学术文章
@zh-hans
2014年学术文章
@zh-my
2014年学术文章
@zh-sg
2014年學術文章
@yue
2014年學術文章
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2014年學術文章
@zh-hant
name
Stress and DNA repair biology of the Fanconi anemia pathway
@en
type
label
Stress and DNA repair biology of the Fanconi anemia pathway
@en
prefLabel
Stress and DNA repair biology of the Fanconi anemia pathway
@en
P2093
P2860
P1433
P1476
Stress and DNA repair biology of the Fanconi anemia pathway
@en
P2093
Gary M Kupfer
Patrick Sung
Simonne Longerich
Yong Xiong
P2860
P304
P356
10.1182/BLOOD-2014-04-526293
P407
P577
2014-09-18T00:00:00Z