Homocysteine/Related Articles: Difference between revisions
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Revision as of 18:39, 11 September 2009
- See also changes related to Homocysteine, or pages that link to Homocysteine or to this page or whose text contains "Homocysteine".
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Auto-populated based on Special:WhatLinksHere/Homocysteine. Needs checking by a human.
- Amino acid [r]: Biochemical with an amino group, a carboxyl group, a hydrogen atom, and a side chain bonded to a central carbon. [e]
- Coronary heart disease [r]: Disease of the heart that involves narrowing of the coronary arteries. [e]
- Cysteine [r]: One of the twenty common amino acids and one of two that contains a sulphur atom. [e]
- Genotype [r]: Genetic makeup, as distinguished from the physical appearance, of an organism or a group of organisms, based on a combination of alleles located on homologous chromosomes that determines a specific characteristic or trait. [e]
- Homocystinuria [r]: Hereditary disease characterized by a deficiency of the enzyme serine dehydratase, causing genetic defects. [e]
- List of organic compounds [r]: Add brief definition or description
- Methylenetetrahydrofolate reductase [r]: Enzyme (EC 1.5.1.20) that exists in the cytoplasm of cells, involved in the processing of amino acids, and for a chemical reaction involving forms of the vitamin folate. [e]
- Scoliosis [r]: Abnormal lateral curvature of the spine that occurs most often in the thoracic region. [e]
- Stroke [r]: A sudden loss of brain function due to interrupted blood supply. [e]
- Vascular disease [r]: Pathological processes involving any of the blood vessels in the cardiac or peripheral circulation. They include diseases of arteries; veins; and rest of the vasculature system in the body. [e]