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Fanconi Anemia Complementation Group D2 Protein

Known as: Fanconi Anemia Complementation Group D2 Protein [Chemical/Ingredient], FANCD2, Fanconi Anemia Group D2 Complementing Protein 
A Fanconi anemia complementation group protein that undergoes mono-ubiquitination by FANCL PROTEIN in response to DNA DAMAGE. Also, in response to… 
National Institutes of Health

Related topics

Related topics

15 relations
BARD1 PathwayCell Cycle ControlDNA RepairDNA Repair Gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
The Effect of Phototherapy on Cancer Predisposition Genes of Diabetic and Normal Human Skin Fibroblasts
The purpose of this study was to investigate whether LED light at different wavelengths affects the expression profile of 143… 
2011
2011
Patient-derived C-terminal mutation of FANCI causes protein mislocalization and reveals putative EDGE motif function in DNA repair.
Fanconi anemia (FA) is a rare familial genome instability syndrome caused by mutations in FA genes that results in defective DNA… 
2011
2011
Fanconi anemia D2 protein is an apoptotic target mediated by caspases
FANCD2, a key factor in the FANC‐BRCA1 pathway is monoubiquitinated and targeted to discrete nuclear foci following DNA damage… 
Review
2010
Review
2010
Role of ubiquitination in the DNA damage response: proteomic analysis to identify new DNA-damage-induced ubiquitinated proteins.
The DDR (DNA damage response) is a signalling transduction cascade utilizing many forms of post-translation modification of… 
2009
2009
FANCD2 Western blot as a diagnostic tool for Brazilian patients with Fanconi anemia.
Fanconi anemia is a rare hereditary disease showing genetic heterogeneity due to a variety of mutations in genes involved in DNA… 
2008
2008
FANCD2 monoubiquitination provides a link between the HHR6 and FA-BRCA pathways
Fanconi Anemia (FA) is a rare genetic disease characterized by chromosome instability mostly resulting from an improper… 
2007
2007
A novel Leu153Ser mutation of the Fanconi anemia FANCD2 gene is associated with severe chemotherapy toxicity in a pediatric T-cell acute lymphoblastic leukemia
Fanconi anemia (FA) is an autosomal recessive disease characterized by pancitopenia, congenital malformations, predisposition to… 
2007
2007
Developmental stage- and DNA damage-specific functions of C. elegans FANCD2
Highly Cited
2003
Highly Cited
2003
Fanconi anemia protein complex: mapping protein interactions in the yeast 2- and 3-hybrid systems.
Fanconi anemia (FA) is an autosomal recessive syndrome characterized by progressive bone marrow failure and cancer predisposition… 
2001
2001
Connecting Fanconi anemia to BRCA1
The genetic basis of Fanconi anemia (FA) is mysterious and complex, as none of the five genes previously associated with the… 
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