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Germline TP53 mutational spectrum in French Canadians with breast cancer.

Arcand(Suzanna L),Akbari(Mohammed R),Mes-M... BMC Med Genet 2015-06-30

Specific germline mutations in the hereditary breast-ovarian cancer susceptibility (HBC/HBOC) genes, BRCA1, BRCA2 and PA...

RAD51, XRCC3, and XRCC2 mutation screening in Finnish breast cancer families.

Pelttari(Liisa M),Kiiski(Johanna I),Ranta(... Springerplus 2015-04-28

...BRCA2 are specifically involved in the homologous recombination repair (HRR) of DNA double-strand breaks. A central play...

Brca2 deficiency leads to T cell loss and immune dysfunction.

Jeong(Jun-Hyeon),Jo(Areum),Park(Pilgu),Lee... Mol Cells 2015-12-14

...BRCA2, we used T cell-specific conditional Brca2 knockout mice, which were previously shown to develop thymic lymphoma a...

Prevalence of BRCA1 and BRCA2 germline mutations in patients with triple-nega...

Wong-Brown(Michelle W),Meldrum(Cliff J),Ca... Breast Cancer Res Treat 2015-11-20

...BRCA2 were amplified and sequenced by next-generation sequencing. We identified a BRCA1 or BRCA2 mutation in 74 of 774 (...

Characterization of three alternative transcripts of the BRCA1 gene in patien...

Gambino(Gaetana),Tancredi(Mariella),Falasc... Int J Mol Med 2015-12-01

...BRCA2 genes. Total RNA was analyzed for the presence of BRCA1 and BRCA2 naturally occurring and pathological transcripts...

Treatment with the PARP inhibitor, niraparib, sensitizes colorectal cancer ce...

Genther Williams(Sybil M),Kuznicki(Apryle ... Cancer Cell Int 2015-02-16

...BRCA2 genes, are sensitive to PARP inhibition. Microsatellite instability (MSI) accounts for 10-15% of colorectal cancer...

Breast cancer risks and risk prediction models.

Engel(Christoph),Fischer(Christine) Breast Care (Basel) 2015-05-11

...BRCA2 mutation carriers. For ovarian cancer, the risk estimates are in the range of 22-65% for BRCA1 and 10-35% for BRCA...

Genotype/Phenotype correlations in patients with hereditary breast cancer.

Wittersheim(Maike),Büttner(Reinhard),Marki... Breast Care (Basel) 2015-05-11

...BRCA2 account for about 25-28% of these cases. For the remainder, several genes of moderate and low penetrance have been...

CDH1 germ-line missense mutation identified by multigene sequencing in a fami...

Lajus(Tirzah Braz Petta),Sales(Roberto Mag... Gene 2015-08-21

...BRCA2 single nucleotide polymorphism in homozygosis. In this family, the mutation c.1849G>A in the CDH1 gene is not rela...

TP53 mutations, tetraploidy and homologous recombination repair defects in ea...

Chien(Jeremy),Sicotte(Hugues),Fan(Jian-Bin... Nucleic Acids Res 2015-11-24

...BRCA2 mutations were observed in two tumors, with nine showing evidence of a homologous recombination (HR) defect. Combi...

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