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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 (4) 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
These results support the role of FANCM as a breast cancer susceptibility gene, particularly for triple-negative breast cancer.
FANCM is actively recruited to the alternative lengthening of telomeres that are experiencing replication stress.
we demonstrated that FANCM is a direct target of miR146a
This case-control study included 2047 BRCA1 and BRCA2 (Montrer BRCA2 Anticorps)-negative familial breast cancer cases and 2187 controls and revealed an association of FANCM mutations with breast cancer. More pronounced associations were identified for early-onset (before age 51 years) breast cancer and triple-negative breast cancer.
FANCM c.5101C > T nonsense mutation carriers have a reduced breast cancer survival but postoperative radiotherapy may diminish this survival disadvantage.
we provide evidence for the first time showing that the common p.Arg1931* loss-of-function variant in FANCM is a risk factor for familial breast cancer.
FANCM c.5101C>T mutation was not identified in Pakistani triple-negative breast cancer patients
MHF facilitates the processing of multiple types of branched DNAs by the DNA translocase FANCM. MHF complex recognizes branched DNA and stimulates FANCM activity at such a structure to promote genome maintenance.
FANCM is a breast cancer susceptibility gene, mutations in which confer a particularly strong predisposition for triple-negative breast cancer
The MHF complex, which is a heterotetramer that comprises two MHF1 (Montrer APITD1 Anticorps)-MHF2 heterodimers, is remodeled by FANCM to favor recognition of branched DNA over dsDNA.
Fancm(Delta2/Delta2) mice also showed unique features atypical for Fanconi anemia (Montrer PALB2 Anticorps) mice, including underrepresentation of female Fancm(Delta2/Delta2) mice and decreased overall and tumor-free survival.
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