网友 2 最佳答案 回答者:网友 3-hydroxyacyl-coa dehydrogenase 羟酰基辅酶A脱氢酶 双语对照 词典结果: 3-hydroxyacyl-CoA dehydrogenase [医]3-羟酰基-辅酶A脱氢酶; 以上结果来自金山词霸推荐: 丙二酸二乙酯 Cas No: 105-53-3 对溴苯酚 Cas No: 106-41-2 对氨基苯酚 Cas No: 123-30-8 肉桂酸 C...
词典结果：3-hydroxyacyl-CoA dehydrogenase [医]3-羟酰基-辅酶A脱氢酶;以上结果来自金山词霸
3-羟基辅酶A脱氢酶缺乏症是英文疾病名称3-hydroxyacyl-CoA dehydrogenase deficiency的中文翻译,又叫做3-α-羟基辅酶A脱氢酶缺乏症,HADH缺乏症。这种疾病是基因突变引起的遗传病,患者难以分解某些脂肪获得能量,尤其是在禁食、缺乏食物时,这种功能是非常重要的。
长链3-羟酰基辅酶A脱氢酶缺乏症的英文名字是Long Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency。基因解码表明:佳学基因通过基因解码发现:长链3-羟酰基辅酶A脱氢酶缺乏症是由基因突变引起的。这种疾病是由HADHA和HADHB基因中的突变引起的,这两个基因编码长链3-羟酰基辅酶A脱氢酶的亚单位。这种酶在脂肪酸代谢中起...
ERAB/HCD2 (Hydroxyacyl-Coenzyme A dehydrogenase) is a mitochondrial protein that catalyzes the oxidation of straight-chain 3-hydroxyacyl-CoAs as part of the beta-oxidation pathway. ERAB is characterized as a NAD+-dependent dehydrogenase that overexpres
Long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency is one of the recently discovered defects of mitochondrial fatty acid β-oxidation. As a group, the β-oxidation defects are among the most common inherited metabolic disorders, and LCHAD deficiency appears to be the most frequently diagn...
dehydrogenase; Medium and short-chain L-3-hydroxyacyl-coenzyme A dehydrogenase; MGC8392; mitochondrial; MSCHAD; OTTHUMP00000162626; OTTHUMP00000219688; SCHAD; Short chain 3 hydroxyacyl CoA dehydrogenase mitochondrial; short chain 3-hydroxyacyl-coa dehydrogenase; Short-chain 3-hydroxyacyl-CoA dehydrogenase....
【佳学基因检测】3-羟基酰基-CoA脱氢酶缺乏症基因检测3-hydroxyacyl-CoA dehydrogenase deficiency。遗传病罕见病基因检测导读:查询上海基因检测机构的基因检测项目列表,发现3-羟基酰基-CoA脱氢酶缺乏症是一个稳定高效的遗传病、罕见病基因检测项目。该项目有时双被称为3-α-羟基酰基辅酶 A 脱氢酶缺乏症新生儿筛查、3...
Summary Peroxisomal β-oxidation proceeds from enoyl-CoA through d-3-hydroxyacyl-CoA to 3-ketoacyl-CoA by the d-3-hydroxyacyl-CoA dehydratase/d-3-hydroxy-acyl-CoA dehydrogenase bifunctional protein (d-bifunctional protein), and the oxidation of bile-acid precursors also has been suggested as bein...