酰基辅酶A氧化酶I缺乏症的英文名字是Acyl-CoA Oxidase I Deficiency。基因解码表明:佳学基因通过基因解码发现:酰基辅酶A氧化酶I缺乏症是由基因突变引起的。这种疾病是由于ACOX1基因的突变导致酰基辅酶A氧化酶I的功能缺陷,从而影响脂肪酸的代谢。ACOX1基因位于人类染色体17号上,突变会导致酰基辅酶A氧化酶I的活性降低或...
Among several peroxisomal neurodegenerative disorders, the pseudoneonatal adrenoleukodystrophy (P-NALD) is characterized by the acyl-coenzyme A oxidase 1 (ACOX1) deficiency, which leads to the accumulation of very-long-chain fatty acids (VLCFA) and inflammatory demyelination. However, the components of...
Peroxisomal acyl-CoA-oxidase deficiency: two new cases. Am J Med Genet A. 2008;146A(13):1676-81.Carrozzo R, Bellini C, Lucioli S, Deodato F, Cassandrini D, Cassanello M, Caruso U, Rizzo C, Rizza T, Napolitano ML, et al. (2008) Peroxisomal acyl-CoA-oxidase deficiency: two new ...
Distinction between peroxisomal bifunctional enzyme and acyl-CoA oxidase deficiencies. Ann Neurol 1995; 38: 472–477Watkins PA, McGuinness MC, Raymond GV, Hicks BA, Sisk JM, Moser AB, Moser HW (1995) Distinction between per- oxisomal bifunctional enzyme and acyl-CoA oxidase defi- ciencies. ...
Acyl-CoA Oxidase 1Argan OilLPSPGC-1αPeroxisome ProliferationP-NALDPPARαPseudo-neonatal adrenoleukodystrophy (P-NALD) is a neurodegenerative disorder caused by acyl-CoA oxidase 1 (ACOX1) deficiency with subsequent impairment of peroxisomal fatty acid β-oxidation, accumulation of very long chain ...
The concentration of pristanic acid was measured in plasma from a patient with an isolated peroxisomal very long chain fatty acid (VLCFA) acyl-CoA oxidase deficiency, a defect in peroxisomal beta-oxidation resulting in accumulation of VLCFA in plasma and tissues. Although peroxisomes are believed ...
Related to acyl CoA dehydrogenase deficiency:Carnitine deficiency ac·yl (ăs′əl) n.Chemistry An organic group having the general formula RCO-, derived from an organic acid. [ac(id)+-yl.] American Heritage® Dictionary of the English Language, Fifth Edition. Copyright © 2016 by Hough...
英文名称:Acyl-CoA Oxidase/ Acyl-CoA:oxygen-2-oxidoreductase 保质期:长期个月 保存条件:-20℃ 品牌:百奥莱博 规格:500U 产地:国产|进口 编号:QN0378 CAS号:61116-22-1 储存条件:-20℃ 性状:黄色冻干粉 来源:微生物 比活:≥ 30U/mg protein ...
细胞长链脂酰辅酶A氧化酶(acyl-CoAoxidase)活性比色法定量检测试剂盒 产品规格: 20次 有效成分含量: 99 检测方法: 比色法 样本: 组织,细胞,线粒体,细菌等 保质期: 6个月 标记物: 血液 储存条件: 冷藏或-20℃ 用途范围: 仅用于科学实验研究使用 是否进口: 否 包装规格: 盒装 产地: 上海 ...
产品名称 组织中链脂酰辅酶A氧化酶(acyl-CoAoxidase)活性比色法定量检测试剂盒 产品规格 20次 有效成分含量 99% 是否进口 否 用途范围 仅用于科学实验研究使用 包装规格 盒装kg 检测方法 比色法 样本 组织,细胞,线粒体,细菌等 保质期 6个月 标记物 血液 储存条件 冷藏或-20℃ 运输 快递发货 ...