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Long-term safety and anti-tumour activity of olaparib monotherapy after combi...

van der Noll(Ruud),Marchetti(Serena),Steeg... Br J Cancer 2015-10-14

...BRCA2). TRAEs were mostly haematological and most prominent shortly after switching from combination to monotherapy, pro...

A phase II evaluation of the potent, highly selective PARP inhibitor velipari...

Coleman(Robert L),Sill(Michael W),Bell-McG... Gynecol Oncol 2015-09-01

...BRCA2. We studied the clinical activity and toxicity of veliparib in ovarian cancer patients carrying a germline BRCA1 o...

Skin-sparing mastectomy.

González(Eduardo G),Rancati(Alberto O) Gland Surg 2015-12-08

...BRCA2 mutations, and also due to new staging standards and use of nuclear magnetic resonance. This increase in the indic...

Novel high-grade serous epithelial ovarian cancer cell lines that reflect the...

Fleury(Hubert),Communal(Laudine),Carmona(E... Genes Cancer 2015-12-01

...BRCA2 nonsense mutation, both of germline origin. The novel BRCA1 mutation induced abnormal splicing, mRNA instability, ...

[Infrared fluorescent markers for microarray DNA analysis on biological micro...

Spitsyn(M A),Shershov(V E),Kuznetsova(V E)... Mol Biol (Mosk) 2015-11-24

...BRCA2 and CHECK2 genes associated with breast cancer. The fluorescent label was introduced to the analyzed DNA during PC...

DNA-Repair Defects and Olaparib in Metastatic Prostate Cancer.

Mateo(Joaquin),Carreira(Suzanne),Sandhu(Sh... N Engl J Med 2015-11-06

...BRCA2 loss (4 with biallelic somatic loss, and 3 with germline mutations) and 4 of 5 with ATM aberrations. The specifici...

Prolonged Survival in a Patient with a Pancreatic Acinar Cell Carcinoma.

Ploquin(Anne),Baldini(Capucine),Vuagnat(Pe... Case Rep Oncol 2015-11-25

...BRCA2 mutation. None of the precedent case reports describe a chemosensibility to the GEMOX regimen. In spite of the lac...

Double Heterozygosity of BRCA2 and STK11 in Familial Breast Cancer Detected b...

Ataei-Kachouei(Mojgan),Nadaf(Javad),Akbari... Iran J Public Health 2015-11-20

...BRCA2) can be involved in pathogenesis of hereditary breast cancer which can be explained by incomplete penetrance of BR...

The frequency of BRCA1 founder mutation c.5266dupC (5382insC) in breast cance...

Gorodetska(Ielizaveta),Serga(Svitlana),Lev... Hered Cancer Clin Pract 2015-10-15

...BRCA2, are known to increase the risk of breast cancer. These heritable mutations are unequally represented among popula...

Rare coding variants and breast cancer risk: evaluation of susceptibility Loc...

Zhang(Yanfeng),Long(Jirong),Lu(Wei),Shu(Xi... Cancer Epidemiol Biomarkers... 2015-01-21

...BRCA2 gene was associated with 16.5-fold elevated risk (95% CI, 2.2-124.5; P = 2.2 × 10(-4)). Gene-based analyses sugges...

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