Normal muscle CPT1 and CPT2 activities in hepatic presentation patients with CPT1 deficiency in fibroblasts
- 1 September 1989
- journal article
- research article
- Published by Elsevier in Journal of the Neurological Sciences
- Vol. 92 (2-3), 229-245
- https://doi.org/10.1016/0022-510x(89)90139-1
Abstract
No abstract availableKeywords
This publication has 55 references indexed in Scilit:
- Carnitine palmitoyltransferase: characterization of a labile detergent-extracted malonyl-CoA-sensitive enzyme from rat liver mitochondriaBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1987
- Regulatory properties of a mutant carnitine palmitoyltransferase in human skeletal muscleEuropean Journal of Biochemistry, 1985
- Selective carnitine palmitoyltransferase deficiency in fibroblasts from a patient with muscle CPT deficiencyAnnals of Neurology, 1981
- Fasting hypoglycemia resulting from hepatic carnitine palmitoyl transferase deficiencyThe Journal of Pediatrics, 1981
- Partial Deficiency of Muscle Carnitine Palmitoyltransferase with Normal Ketone ProductionNew England Journal of Medicine, 1978
- Biochemical and physiologic consequences of carnitine palmityltransferase deficiencyMuscle & Nerve, 1978
- A possible role for malonyl-CoA in the regulation of hepatic fatty acid oxidation and ketogenesis.Journal of Clinical Investigation, 1977
- Acyl group specificity of mitochondrial pools of carnitine acyltransferasesBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1974
- The effect of fasting on the acylation of carnitine and glycerophosphate in rat liver subcellular fractionsBiochimica et Biophysica Acta (BBA) - Bioenergetics, 1974
- Different carnitine acyltransferases in calf liverBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1972