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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 FANCM Kits (2) et et beaucoup plus de produits pour cette protéine.
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Human Polyclonal FANCM Primary Antibody pour ELISA - ABIN4271349
Barroso, Pita, Arias, Menendez, Zamora, Blanco, Benitez, Ribas: The Fanconi anemia family of genes and its correlation with breast cancer susceptibility and breast cancer features. dans Breast cancer research and treatment 2009
Human Monoclonal FANCM Primary Antibody pour ICC, IF - ABIN4310526
Fouquet, Pawlikowska, Caburet, Guigon, Mäkinen, Tanner, Hietala, Urbanska, Bellutti, Legois, Bessieres, Gougeon, Benachi, Livera, Rosselli, Veitia, Misrahi: A homozygousFANCMmutation underlies a familial case of non-syndromic primary ovarian insufficiency. dans eLife 1970
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 M.
Fanconi anemia complementation group M
, fanconi anemia complementation group M
, ATP-dependent RNA helicase FANCM
, Fanconi anemia group M protein
, fanconi anemia-associated polypeptide of 250 kDa
, protein Hef ortholog
, Fanconi anemia group M protein homolog