Metformin: treating the cause of Fanconi anemia?
Crossan, Gerry P.
; 128(24): 2748-2750, 2016 12 15.
Artigo em Inglês | MEDLINE | ID: mdl-27979864
FANCJ suppresses microsatellite instability and lymphomagenesis independent of the Fanconi anemia pathway.
The genetic and biochemical basis of FANCD2 monoubiquitination.
Ubiquitin-like protein UBL5 promotes the functional integrity of the Fanconi anemia pathway.
Massively parallel sequencing, aCGH, and RNA-Seq technologies provide a comprehensive molecular diagnosis of Fanconi anemia.
Common Variable Immunodeficiency Caused by FANC Mutations.
Patient-derived C-terminal mutation of FANCI causes protein mislocalization and reveals putative EDGE motif function in DNA repair.
FANCI Regulates Recruitment of the FA Core Complex at Sites of DNA Damage Independently of FANCD2.
The Fanconi anemia proteins FANCD2 and FANCJ interact and regulate each other's chromatin localization.
A ubiquitin-binding protein, FAAP20, links RNF8-mediated ubiquitination to the Fanconi anemia DNA repair network.
SnapShot: Fanconi anemia and associated proteins.