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searching for bRIP1 7 found (15 total)

alternate case: BRIP1

Genetic heterogeneity (1,240 words) [view diff] exact match in snippet view article find links to article

associated with rare cancer syndromes. Mutations in CHECK2, ATM, NBS1, RAD50, BRIP1, and PALB2 can double the risk of breast cancer development. Biallelic mutations
ZNF350 (739 words) [view diff] exact match in snippet view article find links to article
2003). "Mutational analysis of the BRCA1-interacting genes ZNF350/ZBRK1 and BRIP1/BACH1 among BRCA1 and BRCA2-negative probands from breast-ovarian cancer
FANCI (996 words) [view diff] exact match in snippet view article find links to article
(also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group
Heterogeneous ribonucleoprotein particle (2,028 words) [view diff] exact match in snippet view article find links to article
the proper expression of other tumor suppressor genes including RAD51 and BRIP1 as well. Through these genes, hnRNP is necessary to induce cell-cycle arrest
Fanconi anemia (3,269 words) [view diff] exact match in snippet view article find links to article
FANCB, FANCC, FANCD1 (BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (BRIP1), FANCL, FANCM, FANCN (PALB2), FANCO (RAD51C), FANCP (SLX4), FANCQ (XPF)
Breast cancer (19,225 words) [view diff] exact match in snippet view article find links to article
PTEN (Cowden syndrome), and STK11 (Peutz–Jeghers syndrome), CHEK2, ATM, BRIP1, and PALB2. In 2012, researchers said that there are four genetically distinct
Kári Stefánsson (12,320 words) [view diff] exact match in snippet view article find links to article
Issue 20, ppages 5545–5557, 15 October 2014. T Rafnar et al., "Mutations in BRIP1 confer high risk of ovarian cancer," Nature Genetics (subscription required)