How To Use Ornithine In A Sentence
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A complete postorbital bar is seen elsewhere in Mesozoic birds: confuciusornithids and the enantiornithine
ScienceBlogs Channel : Life Science
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Green tea catechins have been shown to inhibit the actions of 5-alpha-reductase and ornithine decarboxylase, two enzymes considered important in the development of prostate cancer.
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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
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When your body doesn't digest protein completely, gut bacteria convert two of the amino acids in protein, arginine and ornithine, to compounds called polyamines.
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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
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Objective To examine the function of ornithine decarboxylase antizyme inhibitor ( Oazin ) gene in the mouse development.
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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
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It stimulates your release of growth hormone and ornithine decarboxylase enzymes.
Diary
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Bird bones are thin, small and hollow and do not fossilize well; but we are gradually accumulating a good many enantiornithine - and perhaps even archaeornithine - fossils.
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Poly - L - Ornithine can change electric charge on the surface of protoplasts or foreign DNA.
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This may occur in part as a result of pathologically elevated activity of arginase, an enzyme that hydrolyzes arginine to ornithine and urea.
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Polyamines are associated with cell growth and cancer development, and previous research has shown that a polyamine-inhibiting regimen of difluoromethylornithine (DFMO) plus sulindac
Medlogs - Recent stories
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About 50-percent of ingested arginine is rapidly converted in the body to ornithine, primarily by the enzyme arginase.
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Ornidyl can no longer be bought for love or money but Aventis, and later, Bristol-Myers Squibb, began to market eflornithine to the West as Vaniqa, a prescription-only facial depilatory.
Harriet A. Washington: Gene Patenting Produces Profits, Not Cures
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The trial was investigating a treatment for a genetic liver condition, where a gene for a liver enzyme, ornithine trans-carbamylase, is either missing or defective.
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It stimulates your release of growth hormone and ornithine decarboxylase enzymes.
Diary
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Several clinical trials are in progress for therapeutic application of genetic diseases, such as hemophilia, cystic fibrosis, ornithine transcarbamylase deficiencies.
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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
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Alvarenga & Höfling (2003) grouped phorusrhacids into five subgroups; the small, gracile psilopterines, known from the Palaeocene to the Pliocene and including the oldest of all phorusrhacids; the mid-sized, shallow-skulled, gracile-legged mesembriornithines of the Miocene-Pliocene; the mid-sized patagornithines of the Oligocene, Miocene and Pliocene; the gigantic, robust brontornithines of the Oligocene and Miocene; and the mostly large, gracile-legged phorusrhacines of the Miocene, Pliocene and Pleistocene.
Archive 2006-10-01
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The major immune system and human growth hormone stimulants are the amino acids lysine, arginine, and ornithine.
The New Super-Nutrition
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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
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Paleogene fossils also document diverse extinct branches of the neornithine tree, ranging from large pseudotoothed seabirds to giant flightless land birds to small zygodactyl perching birds.
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He was undergoing treatment for ornithine transcarbamylase deficiency, a disorder that prevents the liver from effectively processing ammonia, a toxin produced in the breakdown of proteins.
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Several clinical trials are in progress for therapeutic application of genetic diseases, such as hemophilia, cystic fibrosis, ornithine transcarbamylase deficiencies.
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Jesse was participating in a gene therapy trial for ornithine transcarboxylase deficiency (OTCD).
Gene Therapy Novel Therapeutic Branch of Modern Medicine
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D. Dakin he investigated arginase, the ferment which hydrolyses arginine into urea and ornithine, and later he discovered agmatine in herring roe and devised a method for preparing it.
Albrecht Kossel - Biography
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DFMO is an inhibitor that specifically targets a key protein called ornithine decarboxylase
Medlogs - Recent stories
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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
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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
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Objective To examine the function of ornithine decarboxylase antizyme inhibitor ( Oazin ) gene in the mouse development.
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Ultimately, House deduces that the patient has OTD (ornithine transcarbamylase deficiency).
