Evaluation of rare variants in the new fanconi anemia gene ERCC4 (FANCQ) as familial breast/ovarian cancer susceptibility alleles.
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Mechanisms of interstrand DNA crosslink repair and human disordersFanconi anemia pathway defects in inherited and sporadic cancersThe GADD45A (1506T>C) Polymorphism Is Associated with Ovarian Cancer Susceptibility and PrognosisMutation analysis of the ERCC4/FANCQ gene in hereditary breast cancer.The carboxyl terminus of FANCE recruits FANCD2 to the Fanconi Anemia (FA) E3 ligase complex to promote the FA DNA repair pathway.Current insights into inherited bone marrow failure syndromesRecruitment and positioning determine the specific role of the XPF-ERCC1 endonuclease in interstrand crosslink repair.CRISPR/Cas9 Targeted Gene Editing and Cellular Engineering in Fanconi Anemia.Inhibition of non-homologous end joining in Fanconi Anemia cells results in rescue of survival after interstrand crosslinks but sensitization to replication associated double-strand breaks.Repair protein persistence at DNA lesions characterizes XPF defect with Cockayne syndrome features
P2860
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P2860
Evaluation of rare variants in the new fanconi anemia gene ERCC4 (FANCQ) as familial breast/ovarian cancer susceptibility alleles.
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Evaluation of rare variants in ...... cancer susceptibility alleles.
@en
Evaluation of rare variants in the new fanconi anemia gene ERCC4
@nl
type
label
Evaluation of rare variants in ...... cancer susceptibility alleles.
@en
Evaluation of rare variants in the new fanconi anemia gene ERCC4
@nl
prefLabel
Evaluation of rare variants in ...... cancer susceptibility alleles.
@en
Evaluation of rare variants in the new fanconi anemia gene ERCC4
@nl
P2093
P2860
P50
P356
P1433
P1476
Evaluation of rare variants in ...... cancer susceptibility alleles
@en
P2093
Alicia Barroso
Conxi Lázaro
Daniel Fernández
Francisco Quiles
Javier Benítez
José Fernández Piqueras
Maria Marín
Marta Santamariña
Rogelio González-Sarmiento
P2860
P304
P356
10.1002/HUMU.22438
P577
2013-10-07T00:00:00Z