| LAL | left axillary line; Limulus amebocyte lysate; low air loss; lysosomal acid lipase |
|---|---|
| AG | abdominal girth; agarose; aminoglutethimide; analytical grade; anion gap; antigen; antiglobulin; ant... |
| AGP | acid glycoprotein; agar gel precipitation; azurophil granule protein |
| BG | basal ganglion; basic gastrin; Bender Gestalt [test]; beta-galactosidase; beta-glucuronidase; bicolo... |
| CGAT | chromatin granule amine transformer |
| LAL | Lysosomal acid lipase |
|---|---|
| LAP | Lysosomal acid phosphatase |
| LSD | Lysosomal storage diseases |
| ML | mitochondrial lysosomal |
| CGC | Cerebellar granule cells |
| inborn lysosomal disease | Inherited disorder of one or more degradative enzymes normally located in lysosomes leading to accumulation (storage) of abnormal quantities of a substance, such as a glycosaminoglycan as in Hurler's syndrome or a lipopolysaccharide as in Gaucher's disease. (05 Mar 2000) |
|---|---|
| UDP-N-acetylglucosamine-lysosomal-enzyme-N-acetylglucosaminephosphotransferase | <enzyme> Fibroblasts from patients with i-cell (mucolipidosis II) and pseudo-hurler polydystrophy (mucolipidosis III) are deficient in above enzyme; for n-acetylglucosamine transferred to dolichyl phosphate see EC 2.7.8.15 Registry number: EC 2.7.8.17 Synonym: udpgnac gp gnac phosphotransferase, udpgnac phosphotransferase, uridine 5'-diphosphate-n-acetylglucosamine glycoprotein n-acetylglucosaminylphosphotransferase, n-acetylglucosamine-1-phosphotransferase, n-agapt, udp-n-acetylglucosamine-lysosomal glycoprotein n-acetylglucosaminylphosphotransferase, udp-acetylglucosamine-glycoprotein n-acetylglucosamine-1-phosphotransferase (26 Jun 1999) |
| UDP-N-acetylglucosamine:lysosomal enzyme N-acetylglucosaminyl-1-phosphotransferase | <enzyme> An enzyme that participates in the posttranslational modification of a number of lysosomal proteins; a deficiency or defect in this enzyme results in two forms of mucolipidoses, I-cell disease, and pseudo-Hurler polydystrophy. (05 Mar 2000) |
| lysosomal disease | A disease due to inadequate functioning of a lysosomal enzyme; most such disease's are associated with a storage disease. (05 Mar 2000) |
| lysosomal diseases | Diseases (also called storage diseases) in which a deficiency of a particular lysosomal enzyme leads to accumulation of the undigested substrate for that enzyme within cells. Not immediately fatal, but within a few years lead to serious neurological and skeletal disorders and eventually to death. See: the following conditions: Hurler sundrome, Hunter syndrome, San Fillipo, Gaucher's disease, Niemann-Pick, Pompe's disease, Tay Sachs disease. (18 Nov 1997) |
| lysosomal enzyme | <biochemistry> A range of degradative enzymes, most of which operate best at acid pH. The best known marker enzymes are acid phosphatase and glucuronidase, but many others are known. (18 Nov 1997) |
| lysosomal storage diseases | Inborn errors of metabolism characterised by defects in specific lysosomal hydrolases and resulting in intracellular accumulation of unmetabolised substrates. (12 Dec 1998) |
| acidophil granule | A granule that stains with an acid dye such as eosin. Synonym: oxyphil granule. (05 Mar 2000) |
| acrosomal granule | The single glycoprotein rich granule within an acrosomal vesicle, which results from the coalescence of proacrosomal granule's. (05 Mar 2000) |
| alpha granule | A granule of an alpha cell that was named as the first of several kinds or because it was acidophilic. (05 Mar 2000) |
| Altmann's granule | A granule that has an affinity for fuchsin. Synonym: Altmann's granule. (05 Mar 2000) |
| amphophil granule | A granule that stains with both acid and basic dyes. (05 Mar 2000) |
| atrial granule serine proteinase | <enzyme> Converts pro-atrial natriuretic factor to anf by cleaving the arg98-ser99 bond; n-terminal 26-residue amino acid sequence given in first source Registry number: EC 3.4.21.- (26 Jun 1999) |
| azurophil granule | <cell biology> Primary lysosomal granules found in neutrophil granulocytes, contain a wide range of hydrolytic enzymes. Sometimes referred to as primary granules to distinguish them from the specific or secondary granules. (02 Jan 1998) |
| Babes-Ernst granule | <microbiology> Metachromatic intracellular deposits of polyphosphate found in Corynebacterium diphtheriae when the bacteria are grown on sub optimal media. The granules stain reddish with methylene blue or toluidine blue. (02 Jan 1998) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|