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  2. Double minute - Wikipedia

    en.wikipedia.org/wiki/Double_minute

    An extensive cancer database search found that about 1.4% of all cases are positive for DMs, and out of cancer types, neuroblastoma has the highest frequency of DMs at 31.7%. [10] The amplification of specific genes that support the growth of tumor cells, such as oncogenes or drug-resistant genes, is critical to the cell adoption of malignancy ...

  3. Gene amplification - Wikipedia

    en.wikipedia.org/wiki/Gene_amplification

    Common sources of gene duplications include ectopic recombination, retrotransposition event, aneuploidy, polyploidy, and replication slippage. [ 4 ] A piece of DNA or RNA that is the source and/or product of either natural or artificial amplification or replication events is called an amplicon .

  4. Myc - Wikipedia

    en.wikipedia.org/wiki/Myc

    Hence inhibitors of SUMOylation may be a possible treatment for cancer. [21] Amplification of the MYC gene was found in a significant number of epithelial ovarian cancer cases. [22] In TCGA datasets, the amplification of Myc occurs in several cancer types, including breast, colorectal, pancreatic, gastric, and uterine cancers. [23]

  5. Gene duplication - Wikipedia

    en.wikipedia.org/wiki/Gene_duplication

    Gene duplication (or chromosomal duplication or gene amplification) is a major mechanism through which new genetic material is generated during molecular evolution. It can be defined as any duplication of a region of DNA that contains a gene .

  6. Amplicon - Wikipedia

    en.wikipedia.org/wiki/Amplicon

    In this context the term amplicon can refer both to a section of chromosomal DNA that has been excised, amplified, and reinserted elsewhere in the genome, and to a fragment of extrachromosomal DNA known as a double minute, each of which can be composed of one or more genes. Amplification of the genes encoded by these amplicons generally ...

  7. Homogeneously staining region - Wikipedia

    en.wikipedia.org/wiki/Homogeneously_staining_region

    An HSR is one type of change in a chromosome's structure which is frequently observed in the nucleus of human cancer cells. In the region of a chromosome where an HSR occurs, a segment of the chromosome, which presumably contains a gene or genes that give selective advantage to the progression of the cancer, is amplified or duplicated many times.