- 1. Aryepiglottic Muscle
- (UMLS (NCI) C0224177) =Body Part, Organ, or Organ Component
| - 8. arylsulfatase B deficiency
- [mucopolysaccharidosis with excessive chondroitin sulfate B in urine, characterized by dwarfism and deafness; caused by a deficiency of arylsulfatase B (N-acetylgalactosamine-4-sulfatase). ( CSP )] (UMLS (CSP) C0026709) =Disease or Syndrome ;
=Mucopolysaccharidoses;
enzyme deficiency |
- 2. aryl 4 monooxygenase
- [A large group of cytochrome P-450 (heme-thiolate) monooxygenases that complex with NAD(P)H-FLAVIN OXIDOREDUCTASE in numerous mixed-function oxidations of aromatic compounds. They catalyze hydroxylation of a broad spectrum of substrates and are important in the metabolism of steroids, drugs, and toxins such as PHENOBARBITAL, carcinogens, and insecticides. ( MSH )] (UMLS (CSP) C0003927) =Amino Acid, Peptide, or Protein; Enzyme
| - 9. aryltransferase
- [ ] (UMLS (CSP) C0525000) =Amino Acid, Peptide, or Protein; Enzyme
|
- 3. Aryl Hydrocarbon Hydroxylase
- [A polycyclic aromatic hydrocarbon-inducible cytochrome which is of significant clinical interest due to the large number of drug interactions associated with induction and inhibition of theophylline. Caffeine is considered to be a model substrate for this enzyme. It also metabolizes theophylline and antipyrene. Environmental factors including cigarette smoking, charbroiled meat, cruciferous vegetables, and a number of drugs including phenytoin, phenobarbital, and omeprazole produce increases in CYP1A2 activity. (Ann Pharmacother 1995;29:619-24) EC 1.-. ( NCI )] (UMLS (NCI) C0207509) =Amino Acid, Peptide, or Protein; Enzyme ;
=aryl 4 monooxygenase;
| - 10. Aryteno-Epiglottic Fold
- (UMLS (NCI) C1510944) =Body Part, Organ, or Organ Component; ;
|
- 4. Arylamine Acetylase
- [Wide specificity for aromatic amines, including serotonin; also catalyses acetyl-transfer between arylamines without CoA. [EC 2.3.1.5 created 1961] (from IUBMB) ( NCI )] (UMLS (NCI) C1261253) Arylamine N-Acetyltransferase 2;
EC 2.3.1.5;
N-Acetyltransferase;
NAT2;
Serotonin N-acetyltransferase =Amino Acid, Peptide, or Protein; Enzyme | - 11. Arytenoid Cartilage
- [One of a pair of small pyramidal cartilages that articulate with the lamina of the cricoid cartilage. The corresponding vocal ligament and several muscles are attached to it. ( MSH )] (UMLS (NCI) C0003943) =Body Part, Organ, or Organ Component ;
|
- 5. Aryldialkylphosphatase
- [Acts on organophosphorus compounds (such as paraoxon) including esters of phosphonic and phosphinic acids. Inhibited by chelating agents; requires divalent cations for activity. Previously regarded as identical with EC 3.1.1.2 Arylesterase [EC 3.1.8.1 created 1989] (from IUBMB Enzyme Nomenclature). ( NCI )] (UMLS (NCI) C0163401) =Amino Acid, Peptide, or Protein; Enzyme ;
| - 12. Arytenoid Muscle
- (UMLS (NCI) C1510945) =Tissue; ;
|
- 6. arylsulfatase
- [Enzymes that catalyze the hydrolysis of a phenol sulfate to yield a phenol and sulfate. Arylsulfatase A, B, and C have been separated. A deficiency of arylsulfatases is one of the causes of metachromatic leukodystrophy (LEUKODYSTROPHY, METACHROMATIC). EC 3.1.6.1. ( MSH )] (UMLS (CSP) C0003940) =Amino Acid, Peptide, or Protein; Enzyme
| - 13. arytenoideus
- [ ] (UMLS (CSP) C0598755) =Body Part, Organ, or Organ Component
|
- 7. arylsulfatase A deficiency
- [autosomal recessive lysosomal storage disease caused by a deficiency of cerebroside sulfatase leading to an accumulation of cerebroside sulfate in the nervous system and other organs. ( CSP )] (UMLS (CSP) C0023522) =Disease or Syndrome ;
=LEUKODYSTROPHY;
Sphingolipidoses;
inborn lysosomal enzyme disorder;
enzyme deficiency;
Hereditary Central Nervous System Demyelinating Diseases;
| |
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