Primary defect of juvenile visceral steatosis (jvs) mouse with systemic carnitine deficiency is probably in renal carnitine transport system
- 1 April 1994
- journal article
- Published by Elsevier in Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
- Vol. 1226 (1) , 25-30
- https://doi.org/10.1016/0925-4439(94)90054-x
Abstract
No abstract availableKeywords
This publication has 39 references indexed in Scilit:
- Animal model of systemic carnitine deficiency: Analysis in C3H-H-2° strain of mouse associated with juvenile visceral steatosisBiochemical and Biophysical Research Communications, 1991
- Transport of carnitine into cells in hereditary carnitine deficiencyJournal of Inherited Metabolic Disease, 1989
- Medium-Chain Acyl-CoA Dehydrogenase DeficiencyNew England Journal of Medicine, 1988
- Primary Carnitine Deficiency Due to a Failure of Carnitine Transport in Kidney, Muscle, and FibroblastsNew England Journal of Medicine, 1988
- Neutral amino acid transport systems in animal cells: Potential targets of oncogene action and regulators of cellular growthThe Journal of Membrane Biology, 1988
- Renal handling of carnitine in children with carnitine deficiency and hyperammonemia associated with valproate therapyThe Journal of Pediatrics, 1986
- The regulation of neutral amino acid transport in mammalian cellsBiochimica et Biophysica Acta (BBA) - Reviews on Biomembranes, 1983
- Carnitine deficiency presenting as familial cardiomyopathy: A treatable defect in carnitine transportThe Journal of Pediatrics, 1982
- Systemic Carnitine Deficiency Presenting as Familial Endocardial FibroelastosisNew England Journal of Medicine, 1981
- Systemic Carnitine Deficiency — A Treatable Inherited Lipid-Storage Disease Presenting as Reye's SyndromeNew England Journal of Medicine, 1980