Patients Homozygous for the T435N Mutation of Succinyl-CoA:3-Ketoacid CoA Transferase (SCOT) Do Not Show Permanent Ketosis TOSHIYUKI FUKAO, HARUO SHINTAKU, RYOU KUSUBAE, GAI X. ZHANG, KOZUE NAKAMURA, MASASHI KONDO, AND NAOMI KONDO Department of Pediatrics [T.F., G.X.Z., K.N., M.K....
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Succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency is a rare disorder of ketone body catabolism. In the present study, we prenatally diagnosed SCOT deficiency in a fetus in a family of which the proband was the first patient with SCOT deficiency identified in Japan, by analysis of enzym...
英文名称: 3-ketoacid CoA-transferase 英文同义词: 3-ketoacid CoA-transferase;Succinyl-Coenzyme A Transferase from porcine heart;3-oxoacid CoA-transferase CAS号: 9027-43-4 分子式: 分子量: 0 EINECS号: 信息错误报告 您的Email: 按国家浏览3-ketoacid CoA-transferase国外供应商 中国供应商美国...
Metallothionein prevents diabetes-induced cardiac pathological changes, likely via the inhibition of succinyl-CoA: 3-ketoacid coenzyme A transferase-1 nitration ... W Cong,W Ma,T Zhao,... - 《Am J Physiol Endocrinol Metab》 被引量: 16发表: 2013年来源...
Single-base substitution at the last nucleotide of exon 6 (c.671GA), resulting in the skipping of exon 6, and exons 6 and 7 in human Succinyl-CoA 3-ketoacid CoA transferase (SCOT) gene 文档格式: .pdf 文档大小: 318.84K 文档页数: ...
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Maple syrup urine disease in man and cattle is an inborn metabolic error caused by the deficiency of the branched chain alpha-ketoacid dehydrogenase. We have studied the molecular basis of the disease in Polled Hereford calves. The E1 component of branched chain alpha-ketoacid dehydrogenase was vir...