transcarbamylase love

transcarbamylase

Definitions

from Wiktionary, Creative Commons Attribution/Share-Alike License

  • n. Any transferase that catalyzes the transfer of a carbamyl group

Etymologies

Sorry, no etymologies found.

Examples

  • Aminoacidopathies (maple syrup urine disease; homocystinuria; cobalamin deficiencies; tyrosinemia; urea cycle defects (ornithine transcarbamylase, carbamyl phosphate synthase, citrullinemia, argininosuccinic aciduria, arginase deficiencies) and non-ketotic hyperglycinemia)

    Biochemical Genetics-Metabolic Disease

  • Klaus wanted me to analyze the active site of the enzyme aspartate transcarbamylase by chemically modifying different amino acids within it, and gave me a bench in a student lab.

    Martin Chalfie - Autobiography

  • These enzymes are similar in functional properties to aspartate transcarbamylase and its regulators (Section 10.1).

    Are Stereochemical Explanations Causally Sufficient?

  • This is a sign of a genetic disorder called OTC ornithine transcarbamylase deficiency.

    Telegraph.co.uk - Telegraph online, Daily Telegraph and Sunday Telegraph

  • The study includes infants, toddlers and children up to the age of five, who are suffering from the most severe forms of the following UCDs: ornithine transcarbamylase (OTC) deficiency, carbamoyl-phosphate synthetase I (CPS I) deficiency or argininosuccinate-synthetase (ASS) deficiency, also called citrullinemia.

    BioSpace.com Featured News and Stories

  • The most common of the disorders is called ornithine transcarbamylase deficiency (OTC), with a prevalence of around one in 30,000, said Dr. Mark Batshaw, principal investigator of the Urea Cycle Disorders Consortium, part of the NIH's Office of Rare Diseases Research Network.

    ABC News: Top Stories

  • Such issues include Jesse Gelsinger20 suffered from a rare genetic disorder called ornithine transcarbamylase de fi - exotic therapies versus cheaper more widely ciency, which, while requiring cumbersome treat - useful therapies; ment with diet and drugs, was not a life-threatening disorder for him.

    Recently Uploaded Slideshows

  • Ornithine transcarbamylase deficiency - A rare metabolic disorder, occurring in one out of every 80,000 births.

    House is Right

  • BUPHENYL is indicated as adjunctive therapy in the chronic management of patients with urea cycle disorders involving deficiencies of carbamylphosphate synthetase (CPS), ornithine transcarbamylase (OTC), or argininosuccinic acid synthetase (AS).

    Health News from Medical News Today

  • "I met a physician at a benefit in Los Angeles who pitched me a story about a rare genetic disease -- Ornithine transcarbamylase deficiency -- that he'd seen in a woman in his office, and that became the kernel of an episode.

    This Doctor Makes 'House' Calls

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