A high level of ornithine typically indicates a deficiency in the enzyme that breaks down ornithine, called ornithine transcarbamylase. This can lead to a condition called ornithine transcarbamylase deficiency, which results in the build-up of ammonia in the blood. This condition can be life-threatening and requires immediate medical attention.
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OTC usually stands for Over The Counter. It also stands for Ornithine transcarbamylase.
"OTC" stands for "over-the-counter," which in the US means that you can purchase that medication without a prescription.
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Ornithine decarboxylase is an enzyme that catalyzes the conversion of ornithine into putrescine in the polyamine biosynthesis pathway. It plays a crucial role in cell growth, proliferation, and differentiation. Inhibiting ornithine decarboxylase is a potential target for cancer therapy due to its involvement in promoting tumor growth.
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The metabolic product of arginine is ornithine and urea. The amino acid arginine is degraded by the enzyme arginase into ornithine and urea. The ornithine can be converted to glutamate that is oxidized to alpha ketoglutarate before it enters the kreb cycle.
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Nathan Hoskin has written:
'Polyamines and ornithine decarboxylase in carcinogenesis and neoplasia' -- subject(s): Abstracts, Carcinogens, Polyamines in the body, Ornithine decarboxylase
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The compound regenerated in the urea cycle is ornithine. This compound allows the cycle to continue by combining with carbamoyl phosphate to form citrulline, which is then further processed to produce urea.
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An arginase is an enzyme which catalyzes the hydrolysis of arginine to form urea and ornithine.
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The breakdown of amino acids, specifically arginine and ornithine, in the liver results in the formation of urea. This process is known as the urea cycle or ornithine cycle, and it plays a key role in removing toxic ammonia from the body.
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Arginine biosynthesis starts with glutamate as the precursor (the called "glutamate family") from where also proline and ornithine come from. The precursor of Arginine biosynthesis from glutamate - proline biosynthesis pathway is an intermediate compound, the glutamate-5-semialdehyde that is transaminated by the enzyme ornithine-delta-aminotransferase to form an ornithine molecule. On the other hand, glutamate can form ornithine through another way, first, the formation of N-Acetylglutamate (catalyzed by the enzyme N-acetylglutamate synthase) that is phosphorylated by ATP, catalyzed by the acetylglutamate kinase enzyme, to form N-Acetylglutamate-5-phosphate. This intermediate form N-Acetylglutamate-5-semialdehyde by the enzyme N-acetyl-gamma-glutamyl phosphate dehydrogenase in the presence of NAD(P)H. The next step is the formation of N-Acetylornithine catalyzed by the enzyme N-acetylornithine-delta-aminotransferase. Finally, ornithine is formed by the catalysis of the enzyme acetylornithine deacetylase. In both cases, an ornithine compound that goes to the urea cycle, that occurs partially in the mitochondrion and partially in the cytosol. In the urea cycle, ornithine is transported across the mitochondrial membrane by a specific transport system and converted to citrulline by an ornithine transcarbamoylase. Citrulline leaves the mitochondrion by a specific transport through the mitochondrial membrane and converted into Argininosuccinate by the enzyme argininosuccinate synthase. The latter compound is transformed into Arginineby the loss of fumarate molecule and catalyzed by the enzyme arginase.
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ODC is most commonly used as an acronym for: 1. ornithine decarboxylase or 2. open database connectivity.
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Non-essential amino acid for human development but is required intermediate in arginine biosynthesis. Found in virtually all vertebrate tissues as well as incorporated into proteins, such as tyrocidine. L-Ornithine hydrochloride is also a supplement that many athletes and bodybuilders use to gain an athletic edge. Supplement websites say that adding L-Ornithine hydrochloride powders to any workout routine increases tissue growth and leads to more lean muscle mass. However, scientific studies have not shown this to be true.
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morganella is positive for indole, urease, kcn, ornithine decarboxylase asnd phenylalanine deaminase
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I need the explanation of deficiency. I need the explanation of deficiency. I need the explanation of deficiency.
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Dwarfism is zinc deficiency.
hypothyroidism is iodine deficiency.
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Vitamin b 12 deficiency
Folate deficiency
Iron deficiency
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Thrombocytopenia is the medical term meaning deficiency of platelets. -penia is the combining form meaning deficiency.
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A deficiency of insulin causes diabetes mellitus.
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Thrombocytopenia is the medical term meaning a deficiency of clotting cells. -penia is the combining form meaning deficiency.
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Marasmus is caused by the deficiency of protein
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The prognosis for correcting riboflavin deficiency is excellent.
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Copper deficiency in children is associated with growth retardation. Zinc deficiency, Vitamin A deficiency and other nutritional deficiencies can also cause growth retardation.
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Anaemia is a deficiency of iron, night blindness is a deficiency if vitamin A and rickets is a deficiency of vitamin D.
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B) Goitre. Goitre is commonly caused by iodine deficiency, which is a mineral essential for the thyroid gland to produce thyroid hormones. Beriberi is caused by thiamine (vitamin B1) deficiency, scurvy is caused by vitamin C deficiency, and night blindness is caused by vitamin A deficiency.
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according to this website, NC does have an anti-deficiency provision.
http://www.helocbasics.com/list-of-non-recourse-mortgage-states-and-anti-deficiency-statutes/
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i guess so but then it would be called deficiency anemia because you are lacking nutrition
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There are quite a few deficiency diseases. Scurvy is caused by a vitamin C deficiency, Rickets is caused by a vitamin D deficiency, and Paresthesia is the from the lack of vitamin B5.
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wikipedia is a deficiency disease
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No, "deficiency" is not a suffix. It is a noun that refers to a lack or scarcity of something.
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what is your vitamins deficiency if you have boils
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A deficiency in the element Iodine in the diet.
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A deficiency in the early stages, before the outward signs have appeared.
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No, Pica is not a contagious condition. Pica is generally caused by a mineral deficiency, and someone with a mineral deficiency can't pass that deficiency on to others.
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A deficiency is a lack or shortage, therefore deficiency diseases are caused by a lack or shortage of necessary nutrients in the body. One example is scurvy, a disease associated with pirates that occurs when an individual suffers from a vitamin C deficiency.
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