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Prevalence of BRCA1 and BRCA2 founder mutations in Ashkenazi Jewish (AJ) fami...

Marcotrigiano(M C),Wadsworth(E),Balistreri... J Clin Oncol 0000-00-00

...BRCA2 6174delT).,57 families met the above criteria. BRCA1 or BRCA2 mutations were identified in 25 of 57 families (43.9...

Pancreatic cancer and BRCA mutation in familial breast cancer families.

Hall(M),Olopade(O) J Clin Oncol 0000-00-00

...BRCA2 mutations was performed in 31(47%) probands or close relatives. 8BRCA1 and 9BRCA2 mutations were found, as well as...

Association of personal and family history with decision to undergo risk-redu...

Kauff(N D),Wadsworth(E),Goldfrank(D J),Rob... J Clin Oncol 0000-00-00

...BRCA2 mutation identified between 6/1995 and 12/2003 with ovarian tissue at risk and enrolled on one of two prospective ...

ERCC2 polymorphism Asp711Asp is associated with risk of young-onset pancreati...

McWilliams(R R),Cunningham(J),Bamlet(W),Ra... J Clin Oncol 0000-00-00

...BRCA2 have been studied in pancreatic cancer, common polymorphisms of the more than 100 other DNA repair genes have not ...

Germline TP53 mutations in women with very early onset breast cancer (BR).

Masciari(S),Harris(L),Branda(K),Petkovska(... J Clin Oncol 0000-00-00

...BRCA2 mutations.,The prevalence of germline TP53 mutations among women diagnosed with BR age ≤33 years was assessed. DNA...

Four-year follow-up of outcomes following risk-reducing salpingo-oophorectomy...

Kemel(Y),Kauff(N D),Robson(M E),Goldfrank(... J Clin Oncol 0000-00-00

...BRCA2. (Kauff ND, et al. NEJM 2002) Limitations of that report included a relatively short mean follow-up of 24.2 months...

Parathyroid carcinoma: A rare case with mandible brown tumor.

Samareh Pahlavan(P) J Clin Oncol 0000-00-00

...BRCA2 were recognized. Clinical manifestations are mainly due to hypercalcemia per se. Diagnosis is based on lymph node ...

Factors that influence genetic testing outcomes in high-risk breast/ovarian f...

Herold(C I),Goldfeder(K L),Tigges(J),Stopf... J Clin Oncol 0000-00-00

...BRCA2 (BRCA1/2). As effective interventions exist to prevent OV and BC in women with BRCA1/2 mutations, genetic testing ...

The Slavic NBN Founder Mutation: A Role for Reproductive Fitness?

Seemanova(Eva),Varon(Raymonda),Vejvalka(Ja... PLoS One 0000-00-00

...BRCA2.

Molecular alterations in triple-negative breast cancer-the road to new treatm...

Denkert(Carsten),Liedtke(Cornelia),Tutt(An... Lancet 0000-00-00

...BRCA2 function. A minority of triple-negative tumours express luminal markers, such as androgen receptors, and have a lo...

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