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AMERICAN JOURNAL OF HUMAN GENETICS (2015)
ATR-Mediated Phosphorylation of FANCI Regulates Dormant Origin Firing in Response to Replication Stress
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Deficiency of UBE2T, the E2 Ubiquitin Ligase Necessary for FANCD2 and FANCI Ubiquitination, Causes FA-T Subtype of Fanconi Anemia
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Biallelic Mutations in BRCA1 Cause a New Fanconi Anemia Subtype
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The histone-fold complex MHF is remodeled by FANCM to recognize branched DNA and protect genome stability
David Fox et al.
CELL RESEARCH (2014)
DNA ligase III and DNA ligase IV carry out genetically distinct forms of end joining in human somatic cells
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BRCA1 Promotes Unloading of the CMG Helicase from a Stalled DNA Replication Fork
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MOLECULAR CELL (2014)
The Genetic and Biochemical Basis of FANCD2 Monoubiquitination
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MOLECULAR CELL (2014)
A selective USP1-UAF1 inhibitor links deubiquitination to DNA damage responses
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NATURE CHEMICAL BIOLOGY (2014)
Regulation of FANCD2 and FANCI monoubiquitination by their interaction and by DNA
Simonne Longerich et al.
NUCLEIC ACIDS RESEARCH (2014)
The MHF complex senses branched DNA by binding a pair of crossover DNA duplexes
Qi Zhao et al.
NATURE COMMUNICATIONS (2014)
Modularized Functions of the Fanconi Anemia Core Complex
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CELL REPORTS (2014)
Mutations in ERCC4, Encoding the DNA-Repair Endonuclease XPF, Cause Fanconi Anemia
Massimo Bogliolo et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2013)
ATR-Dependent Phosphorylation of FANCM at Serine 1045 Is Essential for FANCM Functions
Thiyam Ramsing Singh et al.
CANCER RESEARCH (2013)
RIF1 Counteracts BRCA1-mediated End Resection during DNA Repair
Lin Feng et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2013)
A Cell Cycle-Dependent Regulatory Circuit Composed of 53BP1-RIF1 and BRCA1-CtIP Controls DNA Repair Pathway Choice
Cristina Escribano-Diaz et al.
MOLECULAR CELL (2013)
FANCD2 regulates BLM complex functions independently of FANCI to promote replication fork recovery
Indrajit Chaudhury et al.
NUCLEIC ACIDS RESEARCH (2013)
53BP1 Regulates DSB Repair Using Rif1 to Control 5′ End Resection
Michal Zimmermann et al.
SCIENCE (2013)
Rif1 Prevents Resection of DNA Breaks and Promotes Immunoglobulin Class Switching
Michela Di Virgilio et al.
SCIENCE (2013)
Regulation of DNA cross-link repair by the Fanconi anemia/BRCA pathway
Hyungjin Kim et al.
GENES & DEVELOPMENT (2012)
Playing the End Game: DNA Double-Strand Break Repair Pathway Choice
J. Ross Chapman et al.
MOLECULAR CELL (2012)
A Ubiquitin-Binding Protein, FAAP20, Links RNF8-Mediated Ubiquitination to the Fanconi Anemia DNA Repair Network
Zhijiang Yan et al.
MOLECULAR CELL (2012)
Fanconi anemia proteins FANCD2 and FANCI exhibit different DNA damage responses during S-phase
Archana Sareen et al.
NUCLEIC ACIDS RESEARCH (2012)
Patient-derived C-terminal mutation of FANCI causes protein mislocalization and reveals putative EDGE motif function in DNA repair
Luca Colnaghi et al.
BLOOD (2011)
Origin, functional role, and clinical impact of Fanconi anemia FANCA mutations
Maria Castella et al.
BLOOD (2011)
Dynamics of DNA damage response proteins at DNA breaks: a focus on protein modifications
Sophie E. Polo et al.
GENES & DEVELOPMENT (2011)
MicroRNA-138 Modulates DNA Damage Response by Repressing Histone H2AX Expression
Yemin Wang et al.
MOLECULAR CANCER RESEARCH (2011)
Selective killing of ATM- or p53-deficient cancer cells through inhibition of ATR
Philip M. Reaper et al.
NATURE CHEMICAL BIOLOGY (2011)
Mutations of the SLX4 gene in Fanconi anemia
Yonghwan Kim et al.
NATURE GENETICS (2011)
53BP1 Inhibits Homologous Recombination in Brca1-Deficient Cells by Blocking Resection of DNA Breaks
Samuel F. Bunting et al.
CELL (2010)
Mutation of the RAD51C gene in a Fanconi anemia-like disorder
Fiona Vaz et al.
NATURE GENETICS (2010)
Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene
Alfons Meindl et al.
NATURE GENETICS (2010)
ATR-dependent phosphorylation of FANCA on serine 1449 after DNA damage is important for FA pathway function
Natalie B. Collins et al.
BLOOD (2009)
Inactivation of Murine Usp1 Results in Genomic Instability and a Fanconi Anemia Phenotype
Jung Min Kim et al.
DEVELOPMENTAL CELL (2009)
Cell cycle-dependent chromatin loading of the Fanconi anemia core complex by FANCM/FAAP24
Jung Min Kim et al.
BLOOD (2008)
Mutations to Ku reveal differences in human somatic cell lines
Kazi R. Fattah et al.
DNA REPAIR (2008)
FANCI phosphorylation functions as a molecular switch to turn on the Fanconi anemia pathway
Masamichi Ishiai et al.
NATURE STRUCTURAL & MOLECULAR BIOLOGY (2008)
FANCG promotes formation of a newly identified protein complex containing BRCA2, FANCD2 and XRCC3
J. B. Wilson et al.
ONCOGENE (2008)
RNF8 ubiquitylates histones at DNA double-strand breaks and promotes assembly of repair proteins
Niels Mailand et al.
CELL (2007)
Emergence of a DNA-damage response network consisting of Fanconi anaemia and BRCA proteins
Weidong Wang
NATURE REVIEWS GENETICS (2007)
Proteasome function is required for DNA damage response and Fanconi anemia pathway activation
Celine Jacquemont et al.
CANCER RESEARCH (2007)
FANCI is a second monoubiquitinated member of the Fanconi anemia pathway
Ashley E. Sims et al.
NATURE STRUCTURAL & MOLECULAR BIOLOGY (2007)
Identification of the FANCI protein, a monoubiquitinated FANCD2 paralog required for DNA repair
Agata Smogorzewska et al.
CELL (2007)
Identification of FAAP24, a Fanconi anemia core complex protein that interacts with FANCM
Alberto Ciccia et al.
MOLECULAR CELL (2007)
PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene
Nazneen Rahman et al.
NATURE GENETICS (2007)
Chk1-mediated phosphorylation of FANCE is required for the Fanconi anemia/BRCA pathway
XiaoZhe Wang et al.
MOLECULAR AND CELLULAR BIOLOGY (2007)
Evidence for subcomplexes in the Fanconi anemia pathway
Annette L. Medhurst et al.
BLOOD (2006)
Phosphorylation of FANCD2 on two novel sites is required for mitomycin C resistance
Gary P. H. Ho et al.
MOLECULAR AND CELLULAR BIOLOGY (2006)
Control of BRCA2 cellular and clinical functions by a nuclear partner, PALB2
Bing Xia et al.
MOLECULAR CELL (2006)
Regulation of monoubiquitinated PCNA by DUB autocleavage
TT Huang et al.
NATURE CELL BIOLOGY (2006)
A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M
AR Meetei et al.
NATURE GENETICS (2005)
The deubiquitinating enzyme USP1 regulates the Fanconi anemia pathway
SMB Nijman et al.
MOLECULAR CELL (2005)
The Fanconi anemia core complex associates with chromatin during S phase
J Mi et al.
BLOOD (2005)
ATR couples FANCD2 monoubiquitination to the DNA-damage response
PR Andreassen et al.
GENES & DEVELOPMENT (2004)
Facile methods for generating human somatic cell gene knockouts using recombinant adeno-associated viruses
M Kohli et al.
NUCLEIC ACIDS RESEARCH (2004)
A novel ubiquitin ligase is deficient in Fanconi anemia
AR Meetei et al.
NATURE GENETICS (2003)
Disruption of the Fanconi anemia-BRCA pathway in cisplatin-sensitive ovarian tumors
T Taniguchi et al.
NATURE MEDICINE (2003)
A splicing mutation affecting expression of ataxia-telangiectasia and Rad3-related protein (ATR) results in Seckel syndrome
M O'Driscoll et al.
NATURE GENETICS (2003)
Nonerythroid all spectrin is required for recruitment of FANCA and XPF to nuclear foci induced by DNA interstrand cross-links
D Sridharan et al.
JOURNAL OF CELL SCIENCE (2003)
Biallelic inactivation of BRCA2 in Fanconi anemia
NG Howlett et al.
SCIENCE (2002)
Function of the Fanconi anemia pathway in Fanconi anemia complementation group F and D1 cells
MA Siddique et al.
EXPERIMENTAL HEMATOLOGY (2001)
Functional analysis of patient-derived mutations in the Fanconi anemia gene, FANCG/XRCC9
K Nakanishi et al.
EXPERIMENTAL HEMATOLOGY (2001)
The emerging genetic and molecular basis of Fanconi anaemia
H Joenje et al.
NATURE REVIEWS GENETICS (2001)
Interaction of the fanconi anemia proteins and BRCA1 in a common pathway
I Garcia-Higuera et al.
MOLECULAR CELL (2001)