Glycine transport by cultured skin fibroblasts from a patient with isolated hyperglycinuria
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF02312539
Reference10 articles.
1. Bartsocas, C. S. and Erbe, R. W. Lowe's syndrome. Absence of amino acid transport defect in cultured fibroblasts.Acta Paediatr. Scand. 62 (1973) 615–616
2. Foster, D. O. and Pardee, A. B. Transport of amino acids by confluent and nonconfluent 3T3 and polyoma virus-transformed 3T3 cells growing on glass cover slips.J. Biol. Chem. 244 (1969) 2675–2681
3. Groth, U. and Rosenberg, L. E. Transport of dibasic amino acids, cystine, and tryptophan by cultured human fibroblasts: absence of a defect in cystinuría and Hartnup disease.J. Clin. Invest. 51 (1972) 2130–2142
4. Hillman, R. E. and Otto, E. F. Transport ofl-isoleucine by cultured human fibroblasts. Uptake by normal cell lines and isolation of a cell line lacking sodium-dependent uptake.J. Biol. Chem. 249 (1974) 3430–3435
5. Kelly, J. C., Otto, E. F. and Hillman, R. E. Glycine transport by human diploid fibroblasts. Absence of a defect in cells from patients with non-ketotic hyperglycinemia.Pediatr. Res. 13 (1979) 127–130
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1. Transport ofl-histidine by human diploid fibroblasts in culture;In Vitro;1983-07
2. Chapter 5. Prenatal Diagnosis of Inherited Metabolic Diseases: Principles, Pitfalls, and Prospects;Methods in Cell Biology;1982
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