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  2. Oncogenomics - Wikipedia

    en.wikipedia.org/wiki/Oncogenomics

    Oncogenomics is a sub-field of genomics that characterizes cancer-associated genes.It focuses on genomic, epigenomic and transcript alterations in cancer. Cancer is a genetic disease caused by accumulation of DNA mutations and epigenetic alterations leading to unrestrained cell proliferation and neoplasm formation.

  3. Tumor suppressor gene - Wikipedia

    en.wikipedia.org/wiki/Tumor_suppressor_gene

    The cell cycle.Many tumor suppressors work to regulate the cycle at specific checkpoints in order to prevent damaged cells from replicating. A tumor suppressor gene (TSG), or anti-oncogene, is a gene that regulates a cell during cell division and replication. [1]

  4. Anticancer gene - Wikipedia

    en.wikipedia.org/wiki/Anticancer_gene

    TP-53 is a gene that encodes for the protein p53; this protein is a tumor suppressor. p53 was discovered in 1979 stemming from a study involving cancer immunology and the role of viruses in some cancers. The protein was so named because it was measured to have a weight of 53 kDa.

  5. Carcinogenesis - Wikipedia

    en.wikipedia.org/wiki/Carcinogenesis

    The central role of DNA damage and epigenetic defects in DNA repair genes in carcinogenesis. DNA damage is considered to be the primary cause of cancer. [17] More than 60,000 new naturally-occurring instances of DNA damage arise, on average, per human cell, per day, due to endogenous cellular processes (see article DNA damage (naturally occurring)).

  6. Gene expression profiling in cancer - Wikipedia

    en.wikipedia.org/wiki/Gene_expression_profiling...

    Gene expression profiling is a technique used in molecular biology to query the expression of thousands of genes simultaneously. While almost all cells in an organism contain the entire genome of the organism, only a small subset of those genes is expressed as messenger RNA (mRNA) at any given time, and their relative expression can be evaluated.

  7. Cancer genome sequencing - Wikipedia

    en.wikipedia.org/wiki/Cancer_genome_sequencing

    Cancer genome sequencing can be used to provide clinically relevant information in patients with rare or novel tumor types. Translating sequence information into a clinical treatment plan is highly complicated, requires experts of many different fields, and is not guaranteed to lead to an effective treatment plan. [21] [22]

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    mail.aol.com

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  9. G-quadruplex - Wikipedia

    en.wikipedia.org/wiki/G-quadruplex

    Identifying and predicting sequences which have the capacity to form quadruplexes is an important tool in further understanding their role. Generally, a simple pattern match is used for searching for possible intrastrand quadruplex forming sequences: d(G 3+ N 1-7 G 3+ N 1-7 G 3+ N 1-7 G 3+ ), where N is any nucleotide base (including guanine ...