Hypoxanthine-Guanine Phosphoribosyltransferase (HGPRT) Deficiency: Immunologic Studies on the Mutant Enzyme-Reference-Cited by-同舟云学术

Hypoxanthine-Guanine Phosphoribosyltransferase (HGPRT) Deficiency: Immunologic Studies on the Mutant Enzyme

Published:1974 Issue: Volume: Page:177-185
ISSN:0065-2598
Container-title:Advances in Experimental Medicine and Biology
language:
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Author:

Arnold W. J.,Kelley W. N.

Publisher

Springer US

Link

http://link.springer.com/content/pdf/10.1007/978-1-4684-3294-7_21

Reference9 articles.

1. Arnold, W. J., Meade, J. C. and Kelley, W. N. 1972. Hypoxanthine-guanine phosphoribosyltransferase: Characteristics of the mutant enzyme in erythrocytes from patients with the Lesch-Nyhan syndrome. J. Clin. Invest. 51: 1805–1812.

2. Kelley, W. N. and Meade, J. C. 1971. Studies on hypoxanthineguanine phosphoribosyltransferase in fibroblasts from patients with the Lesch-Nyhan syndrome. Evidence for genetic heterogeneity. J. Biol. Chem. 246: 2953–2958.

3. Kelley, W.N. and Arnold, W.J. Human hypoxanthine-guanine phosphoribosyltransferase: Studies on the normal and mutant forms of the enzyme. Fed. Proc. (in press).

4. Lesch, M. and Nyhan, W. L. 1964. A familial disorder of uric acid metabolism and central nervous system function. Amer. J. Med. 36: 561–570.

5. Mizuno, T., Segawa, M., Kurumada, T., Maruyama, H. and Onisawa, J. 1970. Clinical and therapeutic aspects of the Lesch-Nyhan syndrome in Japanese children. Neuropaediatrie. 2: 38–52.

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1. The potentiation of adenine toxicity to Chinese hamster cells by coformycin: Suppression in mutants with altered regulation of purine biosynthesis or increased adenylate-deaminase activity;Journal of Cellular Physiology;1981-01

2. Reaction of antibody to normal human hypoxanthine phosphoribosyltransferase with products of mutant genes;Archives of Biochemistry and Biophysics;1976-12

3. Disorders of Purine and Pyrimidine Metabolism;The Year in Metabolism 1975–1976;1976

4. Inherited Deficiency of Hypoxanthine-Guanine Phosphoribosyltransferase in X-Linked Uric Aciduria (the Lesch-Nyhan Syndrome and Its Variants);Advances in Human Genetics 6;1976