Results 141 to 150 of about 44,727 (269)
Genes Involved in the Cisplatin Response of BRCA2 Cancers
Breast and ovarian cancers are two of the most prevalent types of cancer in women and kill over 55,000 people annually in the US alone. A number of these cases are deficient in BRCA1 or 2, tumor suppressor genes involved in DNA repair.
Rose, Juliana Mary
core
BRCA1 and BRCA2mutations in breast cancer patients from Venezuela
A sample of 58 familial breast cancer patients from Venezuela were screened for germline mutations in the coding sequences and exon-intron boundaries of BRCA1 (MIM no. 113705) and BRCA2 (MIM no.
Karlena Lara +3 more
doaj
Comparisons between HRM screening and sequencing of BRCA1 and BRCA2 genes.
Comparisons between HRM screening and sequencing of BRCA1 and BRCA2 genes.
Edmond Siu Kwan Ma (136398) +9 more
core +1 more source
Pharmacologic ascorbate (vitamin C) increases ROS, disrupts cellular metabolism, and induces DNA damage in CRPC cells. These effects sensitize tumors to PARP inhibition, producing synergistic growth suppression with olaparib in vitro and significantly delayed tumor progression in vivo. Pyruvate rescue confirms ROS‐dependent activity.
Nicolas Gordon +13 more
wiley +1 more source
This is the first genetic study of its kind in Brunei Darussalam. BRCA1 and BRCA2 genes are the most well-known and well described predictors of hereditary breast cancer due to their clinical importance.
Siti Nur Idayu Matusin +5 more
doaj +1 more source
BRCA1/2 mutation spectrum in Armenian patients with breast and ovarian cancers
The aim of the study was to compare the spectra of pathogenic BRCA1 and BRCA2 variants in patients with hereditary breast cancer (BC) and ovarian cancer (OC) from two groups of ethnic Armenians: Yerevan and cities of southern Russia.Material and Methods.
Y. V. Belysheva +9 more
doaj +1 more source
Single circulating tumor cells (sCTCs) from high‐grade serous ovarian cancer patients were enriched, imaged, and genomically profiled using WGA and NGS at different time points during treatment. sCTCs revealed enrichment of alterations in Chromosomes 2, 7, and 12 as well as persistent or emerging oncogenic CNAs, supporting sCTC identity.
Carolin Salmon +9 more
wiley +1 more source
BRCA2 as a Low-Penetrance Cancer Gene [PDF]
openaire +2 more sources
Background: In sporadic ovarian cancer, we have previously reported allele loss at D6S193 (62%) on chromosome 6q27, which suggested the presence of a putative tumour suppressor gene.
Liu, Y +35 more
core +1 more source

