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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). De plus, nous expédions Fanconi Anemia, Complementation Group B Anticorps (43) et Fanconi Anemia, Complementation Group B Protéines (4) et beaucoup plus de produits pour cette protéine.
Loss-of-function FANCB (Montrer BRCA2 Kits ELISA) mutations result in a recognizable, multiple malformation phenotype in hemizygous males for which we propose clinical criteria to aid diagnosis.
Inactivation of FancB (Montrer BRCA2 Kits ELISA) 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 (Montrer PALB2 Kits ELISA) belonging to complementation group B is an essential component of the nuclear protein (Montrer RDBP Kits ELISA) 'core complex' responsible for monoubiquitination of FANCD2 (Montrer FANCD2 Kits ELISA)
summary of recent advances in the Fanconi anemia (Montrer PALB2 Kits ELISA)-BRCA network with emphasis on the new discovery of FAAP95 as the true FANCB (Montrer BRCA2 Kits ELISA) gene [review]
Mutations in FANCB (Montrer BRCA2 Kits ELISA) are a cause of X linked VACTERL-H syndrome.
Mus81 (Montrer MUS81 Kits ELISA) and FANCB (Montrer BRCA2 Kits ELISA) have different roles in repair of DNA damage during replication in human cells
Our results rule out a major contribution of FANCB (Montrer BRCA2 Kits ELISA) to hereditary breast cancer.
Data suggest that Fanconi anemia complementation group B protein (Montrer LEPREL2 Kits ELISA) Fancb(-/y) mouse model for studying the Fanconi anemia (Montrer PALB2 Kits ELISA) (FA) pathway not only in germ cell development but also in the maintenance of hematopoietic stem cell (HSC (Montrer FUT1 Kits ELISA)) function.
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