Functional Characterization of the Carnitine Transporter Defective in Primary Carnitine Deficiency
- 1 April 1999
- journal article
- Published by Elsevier in Archives of Biochemistry and Biophysics
- Vol. 364 (1) , 99-106
- https://doi.org/10.1006/abbi.1999.1118
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- Defective urinary carnitine transport in heterozygotes for primary carnitine deficiencyGenetics in Medicine, 1998
- Transport of Carnitine in Neuroblastoma NB-2a CellsArchives of Biochemistry and Biophysics, 1995
- l-Carnitine uptake in differentiating human cultured muscleBiochimica et Biophysica Acta (BBA) - Molecular Cell Research, 1991
- Transport of carnitine into cells in hereditary carnitine deficiencyJournal of Inherited Metabolic Disease, 1989
- Uptake of acetyl-l-carnitine in the brainNeurochemical Research, 1989
- Primary Carnitine Deficiency Due to a Failure of Carnitine Transport in Kidney, Muscle, and FibroblastsNew England Journal of Medicine, 1988
- Enhanced uptake of carnitine by perfused rat liver following starvationBiochimica et Biophysica Acta (BBA) - Biomembranes, 1987
- Carnitine transport in cultured muscle cells and skin fibroblasts from patients with primary systemic carnitine deficiencyIn Vitro Cellular & Developmental Biology - Plant, 1982
- Carnitine uptake into human heart cells in cultureBiochimica et Biophysica Acta (BBA) - Biomembranes, 1977
- Active transport of butyrobetaine and carnitine into isolated liver cellsBiochimica et Biophysica Acta (BBA) - Biomembranes, 1976