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 enzyme acti
β¦ LIBER β¦
Induction of succinyl-coenzyme A:3-oxoacid coenzyme A-transferase during differentiation of 3T3-L1 cells
β Scribed by Mahrukh K. Ganapathi; Cindy Raefsky; Mulchand S. Patel
- Book ID
- 115706892
- Publisher
- Elsevier Science
- Year
- 1986
- Tongue
- English
- Weight
- 688 KB
- Volume
- 244
- Category
- Article
- ISSN
- 0003-9861
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## Abstract 3βHydroxy 3βmethylglutaryl Coenzyme A reductase (HMGβCoAR) and its endβproducts are crucial for insulinβinduced differentiation of fetal rat myoblasts (L6) both at early and terminal stages of development. Inhibition of HMGβCoAR activity and reduction of the enzyme levels impair the exp