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  2. BRCA mutation - Wikipedia

    en.wikipedia.org/wiki/BRCA_mutation

    BRCA 2 has the cytogenetic location 13q12.3 or the q arm of Chromosome 13 at position 12.3. Both genes produce proteins that help repair damaged DNA, keeping the genetic material of the cell stable. A damaged BRCA gene in either location can lead to increased risk of cancer, particularly breast or ovarian in women.

  3. BRCA1 - Wikipedia

    en.wikipedia.org/wiki/BRCA1

    BRCA1 is a human tumor suppressor gene [7] [8] (also known as a caretaker gene) and is responsible for repairing DNA. [ 9 ] BRCA1 and BRCA2 are unrelated proteins, [ 10 ] but both are normally expressed in the cells of breast and other tissue, where they help repair damaged DNA , or destroy cells if DNA cannot be repaired.

  4. File:BRCA Genes.svg - Wikipedia

    en.wikipedia.org/wiki/File:BRCA_Genes.svg

    BRCA 2 has the cytogenetic location 13q12.3 or the q arm of Chromosome 13 at position 12.3. Both genes produce proteins that help repair damaged DNA, keeping the genetic material of the cell stable. A damaged BRCA gene in either location can lead to increased risk of cancer, particularly breast or ovarian in women.

  5. Expert panel updates advice on BRCA cancer gene screening - AOL

    www.aol.com/news/expert-panel-updates-advice...

    Owens and his colleagues on the government-backed USPSTF reviewed all the available evidence before updating the panel's recommendations on risk assessment, genetic counseling, and genetic testing ...

  6. HRDetect - Wikipedia

    en.wikipedia.org/wiki/HRDetect

    As a result, with an application of a probabilistic cut-off 0.7, HRDetect was able to demonstrate a 98.7% sensitivity recognizing BRCA1/2- deficient cases. In contrast, germline mutations of BRCA1/2 are present in only 1~5% of breast cancer cases. Furthermore, these findings suggest that more breast cancer patients, as many as 1 in 5 (20%), may ...

  7. Ovarian cancer - Wikipedia

    en.wikipedia.org/wiki/Ovarian_cancer

    Women with hereditary nonpolyposis colon cancer (Lynch syndrome), and those with BRCA-1 and BRCA-2 genetic abnormalities are at increased risk. The major genetic risk factor for ovarian cancer is a mutation in BRCA1 or BRCA2 genes, or in DNA mismatch repair genes, which is present in 10% of ovarian cancer cases.