| ¿µ¹® | polysaccharide | ÇÑ±Û | ´Ù´ç·ù |
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| IgM¥áHBc | IgM Antibody against Hepatitis B core Antigen |
|---|---|
| anti-HBc | antibody to hepatitis B core antigen |
| CBFB | core binding factor, beta |
| CCD | calibration curve data; central core disease; charge-coupled device; childhood celiac disease; cleid... |
| CORE | comprehensive assessment and referral evaluation |
| C-Ps | C polysaccharide |
|---|---|
| CP | Capsular polysaccharide |
| EPS | Extracellular polysaccharide |
| NSP | Nonstarch polysaccharide |
| O-PS | O polysaccharide |
| pneumococcal polysaccharide | A soluble type-specific polysaccharide produced during active growth of virulent pneumococci composing a large part of the capsule. Synonym: pneumococcal polysaccharide, soluble specific substance, specific soluble polysaccharide, specific soluble sugar. (05 Mar 2000) |
|---|---|
| polysaccharide | <biochemistry> Polymers of (arbitrarily) more than about ten monosaccharide residues linked glycosidically in branched or unbranched chains. (18 Nov 1997) |
| polysaccharide deacetylase | <enzyme> Involved in bacteriophage penetration of bacteria Registry number: EC 3.5.1.- (26 Jun 1999) |
| polysaccharide-lyases | <enzyme> A group of carbon-oxygen lyases. These enzymes catalyze the breakage of a carbon-oxygen bond in polysaccharides leading to an unsaturated product and the elimination of an alcohol. Registry number: EC 4.2.2. (12 Dec 1998) |
| polysaccharide pyruvyltransferase | <enzyme> Catalyses the pyruvylation of capsular polysaccharides; phosphoenolpyruvate is donor at the lipid-bound saccharide stage of various bacterial polysaccharides Registry number: EC 2.2.1.- Synonym: capsular polysaccharide pyruvyltransferase (26 Jun 1999) |
| polysaccharide sulfate esters | Sulfate esters of polysaccharides often found in cell walls. (05 Mar 2000) |
| C polysaccharide | <microbiology> Polysaccharide released by pneumococci which contains galactosamine 6 phosphate and phosphoryl choline. C-reactive protein is so called because it will precipitate this polysaccharide through an interaction with the phosphoryl choline. (18 Nov 1997) |
| specific soluble polysaccharide | A soluble type-specific polysaccharide produced during active growth of virulent pneumococci composing a large part of the capsule. Synonym: pneumococcal polysaccharide, soluble specific substance, specific soluble polysaccharide, specific soluble sugar. (05 Mar 2000) |
| atomic core | The nucleus plus the nonvalence electrons. (05 Mar 2000) |
| viral core proteins | Proteins found mainly in icosahedral DNA and RNA viruses. They consist of proteins directly associated with the nucleic acid inside the nucleocapsid. (12 Dec 1998) |
| central core disease | A congenital myopathy characterised by hypotonia, delay of motor development in infancy, and nonprogressive or slowly progressive muscle weakness; on biopsy the central core of muscle fibres stains abnormally, myofibrils are abnormally compact, and there is virtual absence of mitochondria and sarcoplasmic reticulum; histochemically, the cores are devoid of oxidative enzyme, phosphorylase, and ATPase activity; autosomal dominant inheritance, often subclinical. (05 Mar 2000) |
| central core disease of muscle | <neurology> One of the conditions that produces floppy baby syndrome. It causes hypotonia (floppiness) in the newborn baby, slowly progressive muscle weakness, and muscle cramps after exercise. Muscle biopsy shows a key diagnostic finding (absent mitochondria in the centre of many type I muscle fibres). The disease is inherited as a dominant trait. The CCD gene is on chromosome 19 (and involves ryanodine receptor-1). Inheritance: autosomal dominant. (12 Dec 1998) |
| central transactional core | The reticular activating system of the brain. (05 Mar 2000) |
| muscle, central core disease of | One of the conditions that produces 'floppy baby' syndrome. Ccd causes hypotonia (inadequately toned muscles characterised by floppiness) in the newborn baby, slowly progressive muscle weakness, and muscle cramps after exercise. Muscle biopsy shows a key diagnostic finding (absent mitochondria in the centre of many type i muscle fibres). Ccd is inherited as a dominant trait. The ccd gene is on chromosome 19 (and involves ryanodine receptor-1). (12 Dec 1998) |
| core | 1. The central mass of necrotic tissue in a boil. 2. A metal casting, usually with a post in the canal of a tooth root, designed to retain an artificial crown. 3. A sectional record, usually of plaster of Paris or one of its derivatives, of the relationships of parts, such as teeth, metallic restorations, or copings. Origin: L. Cor, heart 4. The pupil (of the eye). Origin: G. Kore, pupil (05 Mar 2000) |
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