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  2. Microsatellite instability - Wikipedia

    en.wikipedia.org/wiki/Microsatellite_instability

    MSI-H status raises the possibility of Lynch syndrome, but MSI-H can also occur in patients without Lynch Syndrome and confirmation of Lynch Syndrome requires testing germline DNA. Lynch syndrome is associated with MSI and increases the risk for colon, endometrium, ovary, stomach, small intestine, hepatobiliary tract, urinary tract, brain, and ...

  3. DNA mismatch repair - Wikipedia

    en.wikipedia.org/wiki/DNA_mismatch_repair

    DNA mismatch repair (MMR) is a system for recognizing and repairing erroneous insertion, deletion, and mis-incorporation of bases that can arise during DNA replication and recombination, as well as repairing some forms of DNA damage.

  4. Mismatch repair cancer syndrome - Wikipedia

    en.wikipedia.org/wiki/Mismatch_repair_cancer...

    Under the name constitutional mismatch repair-deficiency (CMMR-D), it has been mapped to MLH1, MSH2, MSH6 or PMS2. [2] Monoallelic mutations of these genes are observed in the condition known as Lynch syndrome or hereditary nonpolyposis colorectal cancer, while biallelic mutations are observed in CMMR-D. [3] People expressing the HNPCC (which itself is considered autosomal dominant) trait are ...

  5. Microsatellite - Wikipedia

    en.wikipedia.org/wiki/Microsatellite

    A microsatellite is a tract of tandemly repeated (i.e. adjacent) DNA motifs that range in length from one to six or up to ten nucleotides (the exact definition and delineation to the longer minisatellites varies from author to author), [1] [6] and are typically repeated 5–50 times.

  6. MLH1 - Wikipedia

    en.wikipedia.org/wiki/MLH1

    DNA mismatch repair protein Mlh1 or MutL protein homolog 1 is a protein that in humans is encoded by the MLH1 gene located on chromosome 3.The gene is commonly associated with hereditary nonpolyposis colorectal cancer.

  7. MSH2 - Wikipedia

    en.wikipedia.org/wiki/MSH2

    DNA mismatch repair protein Msh2 also known as MutS homolog 2 or MSH2 is a protein that in humans is encoded by the MSH2 gene, which is located on chromosome 2.MSH2 is a tumor suppressor gene and more specifically a caretaker gene that codes for a DNA mismatch repair (MMR) protein, MSH2, which forms a heterodimer with MSH6 to make the human MutSα mismatch repair complex.

  8. Scientists are testing mRNA vaccines to protect cows and ...

    www.aol.com/news/scientists-testing-mrna...

    The bird flu outbreak in U.S. dairy cows is prompting development of new, next-generation mRNA vaccines — akin to COVID-19 shots — that are being tested in both animals and people. Next month ...

  9. List of medical abbreviations: M - Wikipedia

    en.wikipedia.org/wiki/List_of_medical...

    MMR: measles, mumps, and rubella combined vaccination mismatch repair MMR-D: mismatch repair deficiency syndrome MMSE: mini-mental state examination: MMT: malignant mesenchymal tumor Mixed Mullerian Tumor MN: membranous nephropathy: MND: motor neurone disease, also known as amyotrophic lateral sclerosis (ALS), Lou Gehrig's disease or Charcot ...