HPRT and the Lesch?Nyhan syndrome-Reference-Cited by-同舟云学术

HPRT and the Lesch?Nyhan syndrome

Published:1985-01 Issue:1 Volume:2 Page:4-8
ISSN:0265-9247
Container-title:BioEssays
language:en
Short-container-title:Bioessays

Author:

Patel Pragna I.,Caskey C. Thomas

Publisher

Wiley

Subject

General Biochemistry, Genetics and Molecular Biology

Reference28 articles.

1. and (1983 ). Clinical syndromes associated with hypoxanthine-guanine phosphoribosyltransferase deficiency. In The Metabolic Basis of Inherited Disease. (ed. and ), 5th edition, pp. 1115-1143. McGraw-Hill, New York.

2. The rate of spontaneous mutation of a human gene

3. Human hypoxanthine-guanine phosphoribosyltransferase. Complete amino acid sequence of the erythrocyte enzyme.

4. Purification and Characterization of Human Hypoxanthine/Guanine Phosphoribosyltransferase

5. Regional Localization of the Gene for Human Phosphoribosylpyrophosphate Synthetase on the X Chromosome

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1. Alternative IMP Binding in Feedback Inhibition of Hypoxanthine–Guanine Phosphoribosyltransferase from Thermoanaerobacter tengcongensis;Journal of Molecular Biology;2005-05

2. Cloning, purification, and characterization of thermostable hypoxanthine–guanine phosphoribosyltransferase from Thermoanaerobacter tengcongensis;Protein Expression and Purification;2003-12

3. Protein preparation, crystallization and preliminary X-ray crystallographic studies of a thermostable hypoxanthine–guanine phosphoribosyltransferase fromThermoanaerobacter tengcongensis;Acta Crystallographica Section D Biological Crystallography;2003-09-19

4. Expression of active human hypoxanthine-guanine phosphoribosyltransferase in Escherichia coli and characterisation of the recombinant enzyme;Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression;1990-10

5. Characterization, evolutionary relationships, and chromosome location of processed mouse HPRT pseudogene;Somatic Cell and Molecular Genetics;1988-07