Galactose metabolism in transferase-deficient galactosaemic and normal long-term lymphoid cell lines
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01799977
Reference20 articles.
1. Beratis, N. G. and Hirschhorn, K. Establishment of long-term lymphoid cell lines.Mamm. Chromosomes Newsl. 14 (1973) 114–116
2. Cuatrecasas, P. and Segal, S. Galactose conversion toD-xylulose: an alternate route of galactose metabolism.Science 153 (1966) 549–551
3. Eggermont, E. and Hers, H. G. Une nouvelle méthode de détection de la galactosémia congenitale.Clin. Chim. Acta 7 (1962) 437–442
4. Friedman, T. B., Yarking, R. J. and Merril, C. R. Galactose and glucose metabolism in galactokinase deficient, galactose-1-P-uridyl transferase deficient and normal human fibroblasts.J. Cell. Physiol. 85 (1974) 569–578
5. Hayman, S., Lou, M. F., Merola, L. O. and Kinoshita, J. H. Aldose reductase activity in the lens and other tissues.Biochim. Biophys. Acta (1966) 474–482
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Oxidation of galactose by galactose-1-phosphate uridyltransferase-deficient lymphoblasts;Journal of Inherited Metabolic Disease;2001-07
2. Uridine Diphosphate Hexoses in Leukocytes and Fibroblasts of Classic Galactosemics and Patients with Other Metabolic Diseases;Pediatric Research;1994-11
3. Culture of galactosaemic fibroblasts in the presence of galactose: Effect of inosine;Journal of Inherited Metabolic Disease;1990-11
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