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  2. Multiple endocrine neoplasia type 1 - Wikipedia

    en.wikipedia.org/wiki/Multiple_endocrine...

    About 3% of tumors secrete ACTH, producing Cushing's disease. Most of the remainder are nonfunctional. Local tumor expansion may cause visual disturbance, headache, and hypopituitarism. Pituitary tumors in MEN 1 patients appear to be larger and behave more aggressively than sporadic pituitary tumors.

  3. Multiple endocrine neoplasia - Wikipedia

    en.wikipedia.org/wiki/Multiple_endocrine_neoplasia

    Multiple endocrine neoplasia (abbreviated MEN) is a condition which encompasses several distinct syndromes featuring tumors of endocrine glands, each with its own characteristic pattern. In some cases, the tumors are malignant, in others, benign. Benign or malignant tumors of nonendocrine tissues occur as components of some of these tumor ...

  4. Multiple endocrine neoplasia type 2B - Wikipedia

    en.wikipedia.org/wiki/Multiple_endocrine...

    Multiple endocrine neoplasia type 2B (MEN 2B) is a genetic disease that causes multiple tumors on the mouth, eyes, and endocrine glands. It is the most severe type of multiple endocrine neoplasia , [ 2 ] differentiated by the presence of benign oral and submucosal tumors in addition to endocrine malignancies.

  5. Pituitary adenoma - Wikipedia

    en.wikipedia.org/wiki/Pituitary_adenoma

    Pituitary adenomas are tumors that occur in the pituitary gland. Most pituitary tumors are benign, approximately 35% are invasive and just 0.1% to 0.2% are carcinomas. [1] Pituitary adenomas represent from 10% to 25% of all intracranial neoplasms, with an estimated prevalence rate in the general population of approximately 17%. [1] [2]

  6. Ribosome-binding site - Wikipedia

    en.wikipedia.org/wiki/Ribosome-binding_site

    The RBS in prokaryotes is a region upstream of the start codon. This region of the mRNA has the consensus 5'-AGGAGG-3', also called the Shine-Dalgarno (SD) sequence. [1] The complementary sequence (CCUCCU), called the anti-Shine-Dalgarno (ASD) is contained in the 3’ end of the 16S region of the smaller (30S) ribosomal subunit.

  7. Prolactinoma - Wikipedia

    en.wikipedia.org/wiki/Prolactinoma

    A prolactinoma is a tumor of the pituitary gland that produces the hormone prolactin.It is the most common type of functioning pituitary tumor. [1] Symptoms of prolactinoma are due to abnormally high levels of prolactin in the blood (hyperprolactinemia), or due to pressure of the tumor on surrounding brain tissue and/or the optic nerves.

  8. Pituitary apoplexy - Wikipedia

    en.wikipedia.org/wiki/Pituitary_apoplexy

    After an episode of pituitary apoplexy, 80% of people develop hypopituitarism and require some form of hormone replacement therapy. [1] [2] The most common problem is growth hormone deficiency, which is often left untreated [1] [4] but may cause decreased muscle mass and strength, obesity and fatigue.

  9. Kozak consensus sequence - Wikipedia

    en.wikipedia.org/wiki/Kozak_consensus_sequence

    Variation within the Kozak sequence alters the "strength" thereof. Kozak sequence strength refers to the favorability of initiation, affecting how much protein is synthesized from a given mRNA. [4] [9] The A nucleotide of the "AUG" is delineated as +1 in mRNA sequences with the preceding base being labeled as −1, i.e. there is no 0 position ...