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The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). Additionally we are shipping Fanconi Anemia, Complementation Group B Proteins (4) and many more products for this protein.
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Loss-of-function FANCB (show BRCA2 Antibodies) mutations result in a recognizable, multiple malformation phenotype in hemizygous males for which we propose clinical criteria to aid diagnosis.
Inactivation of FancB (show BRCA2 Antibodies) may play a role in the pathogenesis of sporadic HNSCC.
Elevated serum FA-2 was associated with bony metastases from breast cancer.
the protein defective in individuals with Fanconi anemia (show PALB2 Antibodies) belonging to complementation group B is an essential component of the nuclear protein (show RDBP Antibodies) 'core complex' responsible for monoubiquitination of FANCD2 (show FANCD2 Antibodies)
summary of recent advances in the Fanconi anemia (show PALB2 Antibodies)-BRCA network with emphasis on the new discovery of FAAP95 as the true FANCB (show BRCA2 Antibodies) gene [review]
Mutations in FANCB (show BRCA2 Antibodies) are a cause of X linked VACTERL-H syndrome.
Mus81 (show MUS81 Antibodies) and FANCB (show BRCA2 Antibodies) have different roles in repair of DNA damage during replication in human cells
Our results rule out a major contribution of FANCB (show BRCA2 Antibodies) to hereditary breast cancer.
FANCB functions at critical stages of germ cell development and reveal a novel function of the FA pathway in the regulation of H3K9 methylation in the germline.
The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity\; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group B. Alternative splicing results in two transcript variants encoding the same protein.
Fanconi anemia group B protein
, Fanconi anemia-associated polypeptide of 95 kDa
, Fanconi anemia group B protein homolog