Transport of carnitine into cells in hereditary carnitine deficiency
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01800711
Reference13 articles.
1. Akedo, H. and Chistensen, H. N. Nature of insulin action on amino acid uptake by the isolated diaphragm.J. Biol. Chem. 237 (1962) 118–122
2. Chapoy, P. R., Angelini, C., Brown, W. J., Stiff, J. E., Shug, A. L. and Cederbaum, S. D. Systemic carnitine deficiency — a treatable inherited lipid-storage disease presenting as Reye's syndrome.N Engl. J. Med. 303 (1980) 1389–1394
3. Carnicero, H. H., Englard, S. and Seifter, S. Carnitine uptake and fatty acid utilization by diploid cells aging in culture.Arch. Biochem. Biophys. 215 (1982) 78–88
4. Eriksson, B. O., Lindstedt, S. and Nordin, I. Hereditary defect in carnitine membrane transport is expressed in skin fibroblasts.Eur. J. Pediatr. 147 (1988) 662–663
5. Groth, U. and Rosenberg, L. E. Transport of dibasic amino acids, cystine, and tryptophan by cultured human fibroblasts: absence of a defect in cystinuria and Hartnup disease.J. Clin. Invest. 51 (1972) 2130–2142
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