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

MeSH(Medical Subject Headings) 맞춤 검색 (http://www.nlm.nih.gov) 결과 : 2 페이지: 1

Cytochrome-c Oxidase Deficiency - 새창 A disease that results from a congenital defect in ELECTRON TRANSPORT COMPLEX IV. Defects in ELECTRON TRANSPORT COMPLEX IV can be caused by mutations in the SURF1, SCO2, COX10, or SCO1 genes. ELECTRON TRANSPORT COMPLEX IV deficiency caused by mutation in SURF1 manifests itself as LEIGH DISEASE; that caused by mutation in SCO2 as fatal infantile cardioencephalomyopathy; that caused by mutation in COX10 as tubulopathy and leukodystrophy; and that caused by mutation in SCO1 as early-onset hepatic failure and neurologic disorder. (from Online Mendelian Inheritance in Man, http://www.ncbi.nlm.nih.gov/Omim, MIM#220110, May 17, 2001)
Synonyms : Cytochrome Oxidase Deficiency, Deficiency, Cytochrome-c Oxidase, Cytochrome Oxidase Deficiencies, Cytochrome c Oxidase Deficiency, Cytochrome-c Oxidase Deficiencies, Deficiencies, Cytochrome Oxidase, Deficiencies, Cytochrome-c Oxidase
Cytochrome-c Peroxidase - 새창 A hemeprotein which catalyzes the oxidation of ferrocytochrome c to ferricytochrome c in the presence of hydrogen peroxide. EC 1.11.1.5.
Synonyms : Cytochrome Peroxidase, Cytochrome c-551 Peroxidase, Cytochrome c 551 Peroxidase, Cytochrome c Peroxidase, Peroxidase, Cytochrome, Peroxidase, Cytochrome c-551, Peroxidase, Cytochrome-c