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Integrative Genomic and Clinicopathologic Characterization of Pure Primary Ov...

Yoon(H),Kim(C),Lee(Y),Ahn(J),Jeong(M) Curr Oncol 2025-09-27

...BRCA2 frameshift mutation (c.7177dupA), an ATM nonsense mutation, and Tier II mutations in TP53 and PTEN. The tumor exhi...

Uterine leiomyosarcoma progression: A study of serial recurrences.

Sia(TY),Brown(DN),Miller(K),Curtin(C),Sele... Gynecol Oncol 2025-11-00

...BRCA2 (20 %), as well as clonal mutations affecting TP53 (30 %) and ATRX (10 %), were early events and present across su...

RAD51-mediated homologous recombination is a pro-tumour driver pathway.

Lopez(BS) Oncogene 2025-11-00

...BRCA2) in cancer result in the absence of RAD51 on damaged DNA, leaving access to alternative exclusively mutagenic repa...

Targeting RAD52 overcomes PARP inhibitor resistance in preclinical Brca2-defi...

Ota(Y),Gupta(V),Fashemi(BE),Akande(M),Babu... bioRxiv 2025-09-26

...Brca2-deficient mouse ovarian cancer models, ID8-OR and HGS2-OR. HGS2-OR cells had higher RAD52 expression than parental...

The Discovery of RP-2119: A Potent, Selective, and Orally Bioavailable Polθ A...

Mochirian(P),Papp(R),Mathieu(MC),Ferraro(G... J Med Chem 2025-09-25

...BRCA2 mutations. Here, we describe the discovery and preclinical development of RP-2119, a selective, potent, and bioava...

Reclassification of BRCA1 and BRCA2 Variants of Unknown Significance in a Tur...

Özer(L),Aktuna(S),Ünsal(E) Eur J Breast Health 2025-09-25

...BRCA2 variants. A total of 264 BRCA1/BRCA2 variants were detected. Of these, 130 (49.2%) were pathogenic variants (PV), ...

Molecular characterization of hereditary breast and ovarian cancer patients f...

Ribeiro(AAF),Queiroz Ladeira(T),Gonçalves ... Sci Rep 2025-09-29

...BRCA2 was the most frequently mutated gene contrasting with most reports from the country, in which BRCA1 predominates. ...

Recontact and follow-up for individuals with germline pathogenic variants in ...

Christopher(J),Edgerley(K),McIldowie(B),Je... J Med Genet 2025-10-01

...BRCA2, PALB2, ATM, CHEK2, BARD1, BRIP1, RAD51C, RAD51D and mismatch repair (MMR) genes (MLH1, MSH2, MSH6 and PMS2) to en...

Clinicopathological study of non-palpable familial breast cancer detected by ...

Saito(Motonobu),Matsuzaki(Masami),Sakuma(T... Breast Cancer 2016-04-11

...BRCA2 gene germ line mutation in three patients. IHC of BRCA was consistent with BRCA2 mutation status.,The family histo...

A case of familial breast cancer with double heterozygosity for BRCA1 and BRC...

Nomizu(Tadashi),Matsuzaki(Masami),Katagata... Breast Cancer 2016-06-02

...BRCA2 genes was transmitted to the paternal cousin, and the same BRCA2 mutation to the younger sister with bilateral bre...

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