- Carnitine-Acylcarnitine Translocase
- Abbreviation: CAT
Универсальный русско-английский словарь. Академик.ру. 2011.
Carnitine-Acylcarnitine Translocase
Смотреть что такое "Carnitine-Acylcarnitine Translocase" в других словарях:
Carnitine-acylcarnitine translocase — protein Name=solute carrier family 25 (carnitine/acylcarnitine translocase), member 20 caption= width= HGNCid=1421 Symbol=SLC25A20 AltSymbols=CACT EntrezGene=788 OMIM=212138 RefSeq=NM 000387 UniProt=O43772 PDB= ECnumber= Chromosome=3 Arm=p… … Wikipedia
Carnitine-acylcarnitine translocase deficiency — DiseaseDisorder infobox Name = Carnitine acylcarnitine translocase deficiency ICD10 = ICD9 = ICD9|272.8 Carnitine acylcarnitine translocase deficiency is a rare, autosomal recessive metabolic disorder that prevents the body from converting long… … Wikipedia
Carnitine — Systematic (IUPAC) name 3 hydroxy 4 (trimethylazaniumyl)butanoate Clinical data AHFS/Drugs.com … Wikipedia
Carnitine palmitoyltransferase II deficiency — Classification and external resources Carnitine ICD 9 … Wikipedia
Translocase — is a general term for an enzyme that assists in moving another molecule, usually across a membrane.Translocases are most common secretion system in Gram positive bacteria.Examples include: * ornithine translocase (SLC25A15), associated with… … Wikipedia
Carnitine — Structure de la carnitine Général Nom IUPAC 3 hydroxy 4 triméthylammonio butanoate … Wikipédia en Français
carnitine — A trimethylammonium (betaine) derivative of γ amino β hydroxybutyric acid, formed from Nε,Nε,Nε trimethyllysine and from γ butyrobetaine; the l isomer is a thyroid inhibitor found in muscle, liver, and meat extracts; l c. is an acyl carrier with… … Medical dictionary
541-15-1 — Carnitine Carnitine Structure de la carnitine Général Nom IUPAC 3 hydroxy 4 triméthylammonio butanoate … Wikipédia en Français
C7H15NO3 — Carnitine Carnitine Structure de la carnitine Général Nom IUPAC 3 hydroxy 4 triméthylammonio butanoate … Wikipédia en Français
Inborn error of lipid metabolism — Classification and external resources Several fatty acid molecules ICD 10 E75 … Wikipedia
Inborn errors of lipid metabolism — ICD9|277.85 ICDO = OMIM = MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = D008052 Numerous genetic disorders are caused by errors in fatty acid metabolism. These disorders may be described as fatty oxidation disorders or as a lipid… … Wikipedia
