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  2. BRCA1 - Wikipedia

    en.wikipedia.org/wiki/BRCA1

    High BRCA1 may protect cancer cells by acting in a pathway that removes the damages in DNA introduced by the platinum drugs. Thus the level of BRCA1 expression is a potentially important tool for tailoring chemotherapy in lung cancer management. [123] [124] Level of BRCA1 expression is also relevant

  3. BRCA mutation - Wikipedia

    en.wikipedia.org/wiki/BRCA_mutation

    Inheriting one BRCA1 mutation and one BRCA2 mutation has been reported occasionally; the child's risk for any given type of cancer is the higher risk of the two genes (e.g., the ovarian cancer risk from BRCA1 and the pancreatic cancer risk from BRCA2). Inheriting two BRCA2 mutations produces Fanconi anemia. [9]: 82–85

  4. Hereditary breast–ovarian cancer syndrome - Wikipedia

    en.wikipedia.org/wiki/Hereditary_breast–ovarian...

    Absolute risk of cancers in BRCA1 or BRCA2 mutation. [4]A number of genes are associated with HBOC. [5] The most common of the known causes of HBOC are: BRCA mutations: [5] Harmful mutations in the BRCA1 and BRCA2 genes can produce very high rates of breast and ovarian cancer, as well as increased rates of other cancers.

  5. I have the BRCA1 mutation, and so does 1 of my ... - AOL

    www.aol.com/news/brca1-mutation-does-1-daughters...

    After my sister was diagnosed with breast cancer, I tested positive for the BRCA1 gene mutation. Two of my daughters tested; one of them has it, too.

  6. This Breast Cancer Surgeon Discovered Her Own Cancer At ... - AOL

    www.aol.com/breast-cancer-surgeon-discovered-her...

    You’ve had genetic testing and have a known BRCA1 or BRCA2 gene mutation or have a first-degree relative (parent, brother, sister, or child) with a BRCA1 or BRCA2 gene mutation

  7. Does Medicare cover genetic testing? - AOL

    www.aol.com/lifestyle/does-medicare-cover...

    Limitations include once-in-a-lifetime testing for certain genetic mutations, such as those in the BRCA1 and BRCA2 genes. This means Medicare will not cover repeat tests, as the results of genetic ...

  8. Loss of heterozygosity - Wikipedia

    en.wikipedia.org/wiki/Loss_of_heterozygosity

    The individual does not develop cancer at this point because the remaining TSG allele on the other locus is still functioning normally. Second Hit: While the second hit is commonly assumed to be a deletion that results in loss of the remaining functioning TSG allele, the original published mechanism of RB1 LOH was mitotic recombination / gene ...

  9. Triple-negative breast cancer - Wikipedia

    en.wikipedia.org/wiki/Triple-negative_breast_cancer

    Triple-negative breast cancer comprises 15–20% of all breast cancer cases [3] and affects more young women or women with a mutation in the BRCA1 gene than other breast cancers. [4] Triple-negative breast cancers comprise a very heterogeneous group of cancers. TNBC is the most challenging breast cancer type to treat. [5]