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  2. Tyrosinemia type III - Wikipedia

    en.wikipedia.org/wiki/Tyrosinemia_type_III

    Tyrosinemia type III is a rare disorder caused by a deficiency of the enzyme 4-hydroxyphenylpyruvate dioxygenase (EC 1.13.11.27), encoded by the gene HPD. [2] This enzyme is abundant in the liver, and smaller amounts are found in the kidneys. It is one of a series of enzymes needed to break down tyrosine.

  3. Hawkinsinuria - Wikipedia

    en.wikipedia.org/wiki/Hawkinsinuria

    The gene affected is the HPD gene encoding 4-hydroxyphenylpyruvic acid dioxygenase, on chromosome 12q24. [4] It is unusual in that most other inborn errors of metabolism are caused by loss-of-function mutations, and hence have recessive inheritance (condition occurs only if both copies are mutated).

  4. 4-Hydroxyphenylpyruvate dioxygenase - Wikipedia

    en.wikipedia.org/wiki/4-Hydroxyphenylpyruvate_di...

    HPPD also catalyzes the conversion of phenylpyruvate to 2-hydroxyphenylacetate and the conversion of α-ketoisocaproate to β-hydroxy β-methylbutyrate. [2] [3] HPPD is an enzyme that is found in nearly all aerobic forms of life. [4] This reaction shows the conversion of 4-hydroxyphenylpyruvate into homogentisate by HPPD.

  5. Chemical Agents Warning Latency Initial Symptoms Properties ...

    images.huffingtonpost.com/2008-06-02-guide1.pdf

    and gasping for air Hydrogen chloride Gas: colorless, yellowish, or white Odor: strong, irritating Seconds to minutes Low does: eye and skin irritant High dose: rapid breathing, bluish discoloring of the skin, and fluid in the lungs Hydrogen cyanide Gas: colorless, or pale blue Odor: bitter almonds < 1 minute Hyperventilation, loss of

  6. Hospice Check - The Huffington Post

    projects.huffingtonpost.com/projects/hospice-inc/...

    The time period covers Jan. 2, 2004, to Oct. 16, 2014. The time since last inspection is calculated as of Oct. 24, 2014 — when the database was exported — using the most recent date of a certification inspection or private accreditation inspection.

  7. 4-Hydroxyphenylpyruvic acid - Wikipedia

    en.wikipedia.org/wiki/4-Hydroxyphenylpyruvic_acid

    4-Hydroxyphenylpyruvic acid (4-HPPA) is an intermediate in the metabolism of the amino acid phenylalanine. The aromatic side chain of phenylalanine is hydroxylated by the enzyme phenylalanine hydroxylase to form tyrosine. The conversion from tyrosine to 4-HPPA is in turn catalyzed by tyrosine aminotransferase. [2]

  8. AOL Mail - AOL Help

    help.aol.com/products/aol-webmail

    Get answers to your AOL Mail, login, Desktop Gold, AOL app, password and subscription questions. Find the support options to contact customer care by email, chat, or phone number.

  9. 4-hydroxyphenylpyruvate dioxygenase inhibitor - Wikipedia

    en.wikipedia.org/wiki/4-hydroxyphenylpyruvate_di...

    4-Hydroxyphenylpyruvate dioxygenase (HPPD) is an enzyme found in both plants and animals, which catalyzes the catabolism of the amino acid tyrosine. [4] Preventing the breakdown of tyrosine has three negative consequences: the excess of tyrosine stunts growth; the plant suffers oxidative damage due to lack of tocopherols (vitamin E); and ...