PROBLEM TO BE SOLVED: To provide a DNA encoding a new enzyme mutant of β-ketothiolase, which produces a transformant having improved catalytic activity of β-ketothiolase in comparison with a wild type β-ketothiolase.MORIKAWA SOICHI守川 壮一...
网络酮硫解酶 网络释义 1. 酮硫解酶 中英文医... ... β受体, 肾上腺素能 beta-Blockers,Adrenergic β酮硫解酶beta-Ketothiolaseα-L-岩藻糖苷酶 alpha-L-Fucosidase ... www.5ibio.com|基于3个网页
Beta-ketothiolase deficiency (mitochondrial acetoacetyl-CoA thiolase, MAT or T2 deficiency) is a rare autosomal recessive disorder of isoleucine and ketone body metabolism due to acetyl-CoA acetyltransferase-1 (ACAT1) gene mutations. The disease is characterized by recurrent episodes of ketoasidosis ...
A. A thermostable beta- ketothiolase of polyhydroxyalkanoates (PHAs) in Thermus thermophilus: purification and biochemical properties. Molecular Cell Biochemistry, v. 269, p. 27-36, 2005.A.A. Pantazaki, A.K. Ioannou, D.A. Kyriakidis, A thermostable beta-ketothiolase of polyhydroxyalkanoate...
Sewell AC, Herwig J, Wiegratz I, Lehnert W, Niederhoff H, Song XQ, et al. Mitochondrial acetoacetyl-CoA thiolase (beta-ketothiolase) deficiency and pregnancy. J Inherit Metab Dis. 1998;21(4):441-2.A.C. Sewell, J. Herwig, I. Wiegratz, W. Lehnert, H. Niederhoff, X.Q. Song, ...
Challenges in the diagnosis of methylacetoacetyl-coenzymeAthiolase (beta-ketothiolase) deficiencyJ.O., SassS., ReichlL., BahrC., BritschgiK., BilicM., CukV., SarnavkaL., PalezacI., BaricK., Fumic
beta-ketoadipyl-coenzyme A thiolase| 基本信息 更多信息 中文名称: 中文同义词: 英文名称: beta-ketoadipyl-coenzyme A thiolase 英文同义词: beta-ketoadipyl-coenzyme A thiolase CAS号: 分子式: 分子量: 0 EINECS号: 信息错误报告 您的Email: 按国家浏览beta-ketoadipyl-coenzyme A thiolase国外...
Beta-ketothiolase (2-methylacetoacetyl-coenzyme A thiolase) deficiency: Identification of two patients in Israel. J Inherit Metab Dis 1996; 19:698–699. View ArticleGibson KM, Elpeleg ON, Bennett MJ (1996) ? –Ketothiolase (2–methylacetoacetyl–coenzyme A thiolase) deficiency: identification ...
Schutgens RBH, Middleton B, Blij JS et al (1982) Beta-ketothiolase deficiency in a family confirmed by in vitro enzymatic assays in fibroblasts. Eur J Pediatr 139 : 39–42.Schutgens RBH, Middleton B, Bliij JF, Oorthuys JWE, Veder HA, Vulsma T, Tegelaers WHH (1982) Beta-keto...
text>Beta-ketothiolase (BKT) deficiency is a rare inborn error of isoleucine and ketone body metabolism. Its clinical manifestations range from an asymptomatic course to severe life-threatening ketoacidotic attacks with coma and cardiomyopathy. Early diagnosis and proper management may save lives of ...