IMP dehydrogenase mutants: cell culture model for hyperuricemia.

B. Ullman

Research output: Contribution to journalArticlepeer-review

5 Scopus citations


These studies with wild-type and mutant cells defective in IMP dehydrogenase and the previous data with the adenylosuccinate synthetase-deficient cell line suggest that among the clinical population with dominantly inherited hyperuricemia, patients with partial deficiencies in these enzymes exist. It is hoped that these pharmacogenetic cell culture models for overproduction hyperuricemia will lead to the initiation of a search for hyperuricemia patients with either of these deficiencies. If such patients are found it may be possible to design chemotherapeutic regimens by which effectors (inhibitors) of purine synthesis might ameliorate the overproduction of purines by the de novo pathway.

Original languageEnglish (US)
Pages (from-to)373-379
Number of pages7
JournalAdvances in experimental medicine and biology
Volume165 Pt A
StatePublished - 1984
Externally publishedYes

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)


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