HO : KMLE 의학 검색 엔진 - 의학사전, 의학용어, 의학약어, 의학논문, 약품/의약품 검색

MeSH(Medical Subject Headings) 맞춤 검색 (http://www.nlm.nih.gov) 결과 : 5 페이지: 9

Homocysteine S-Methyltransferase - 새창 An enzyme that catalyzes the demethylation of L-homocysteine to L-METHIONINE.
Synonyms : Homocysteine Methyltransferase, Homocysteine Transmethylase, S-Adenosylmethionine Homocysteine Methyltransferase, S-Methylmethionine Homocysteine Methyltransferase, Homocysteine Methyltransferase, S-Adenosylmethionine, Homocysteine S Methyltransferase
Homocystine - 새창
Synonyms :
Homocystinuria - 새창 An autosomal recessive inborn error of methionine metabolism usually caused by a deficiency of CYSTATHIONINE BETA-SYNTHASE and associated with elevations of homocysteine in plasma and urine. Clinical features include a tall, slender habitus, SCOLIOSIS, arachnodactyly, MUSCLE WEAKNESS, genu varis, thin blond hair, malar flush, lens dislocations, an increased incidence of MENTAL RETARDATION, and a tendency to develop fibrosis of arteries, frequently complicated by CEREBROVASCULAR ACCIDENTS and MYOCARDIAL INFARCTION. (From Adams et al., Principles of Neurology, 6th ed, p979)
Synonyms : Deficiency Disease, Cystathionine beta-Synthase, Cystathionine beta Synthase Deficiency Disease, Deficiency Disease, Cystathionine beta Synthase
Homogentisate 1,2-Dioxygenase - 새창 A mononuclear Fe(II)-dependent oxygenase, this enzyme catalyzes the conversion of homogentisate to 4-maleylacetoacetate, the third step in the pathway for the catabolism of TYROSINE. Deficiency in the enzyme causes ALKAPTONURIA, an autosomal recessive disorder, characterized by homogentisic aciduria, OCHRONOSIS and ARTHRITIS. This enzyme was formerly characterized as EC 1.13.1.5 and EC 1.99.2.5.
Synonyms : Homogentisate Dioxygenase, Homogentisate Oxidase, Homogentisate Oxygenase, Homogentisic Acid Oxidase, 1, 2-Dioxygenase, Homogentisate, Acid Oxidase, Homogentisic, Dioxygenase, Homogentisate, Homogentisate 1, 2 Dioxygenase, Oxidase, Homogentisate
Homogentisic Acid - 새창
Synonyms : Acid, Homogentisic