Skip to main content
NCBI home page
Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1968 Jun;60(2):545–552. doi: 10.1073/pnas.60.2.545

Single-allele expression at an X-linked hyperuricemia locus in heterozygous human cells.

J Salzmann, R DeMars, P Benke
PMCID: PMC225082  PMID: 5248811

Full text

PDF
545

Images in this article

547Image
on p.547
547Image
on p.547
547Image
on p.547
549Image
on p.549

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Barr M. L. The significance of the sex chromatin. Int Rev Cytol. 1966;19:35–95. doi: 10.1016/s0074-7696(08)60564-1. [DOI] [PubMed] [Google Scholar]
  2. DAVIDSON R. G., NITOWSKY H. M., CHILDS B. DEMONSTRATION OF TWO POPULATIONS OF CELLS IN THE HUMAN FEMALE HETEROZYGOUS FOR GLUCOSE-6-PHOSPHATE DEHYDROGENASE VARIANTS. Proc Natl Acad Sci U S A. 1963 Sep;50:481–485. doi: 10.1073/pnas.50.3.481. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Danes B. S., Bearn A. G. Hurler's syndrome: a genetic study of clones in cell culture with particular reference to the Lyon hypothesis. J Exp Med. 1967 Sep 1;126(3):509–522. doi: 10.1084/jem.126.3.509. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. DeMars R. The single-active-X: functional differentiation at the chromosome level. Natl Cancer Inst Monogr. 1967 Sep;26:327–351. [PubMed] [Google Scholar]
  5. Grüneberg H. Sex-linked genes in man and Lyon hypothesis. Ann Hum Genet. 1967 Jan;30(3):239–257. doi: 10.1111/j.1469-1809.1967.tb00025.x. [DOI] [PubMed] [Google Scholar]
  6. HOEFNAGEL D., ANDREW E. D., MIREAULT N. G., BERNDT W. O. HEREDITARY CHOREOATHETOSIS, SELF-MUTILATION AND HYPERURICEMIA IN YOUNG MALES. N Engl J Med. 1965 Jul 15;273:130–135. doi: 10.1056/NEJM196507152730303. [DOI] [PubMed] [Google Scholar]
  7. Kelley W. N., Rosenbloom F. M., Henderson J. F., Seegmiller J. E. A specific enzyme defect in gout associated with overproduction of uric acid. Proc Natl Acad Sci U S A. 1967 Jun;57(6):1735–1739. doi: 10.1073/pnas.57.6.1735. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. LESCH M., NYHAN W. L. A FAMILIAL DISORDER OF URIC ACID METABOLISM AND CENTRAL NERVOUS SYSTEM FUNCTION. Am J Med. 1964 Apr;36:561–570. doi: 10.1016/0002-9343(64)90104-4. [DOI] [PubMed] [Google Scholar]
  9. LYON M. F. Gene action in the X-chromosome of the mouse (Mus musculus L.). Nature. 1961 Apr 22;190:372–373. doi: 10.1038/190372a0. [DOI] [PubMed] [Google Scholar]
  10. NANCE W. E. GENETIC TESTS WITH A SEX-LINKED MARKER: GLUCOSE-6-PHOSPHATE DEHYDROGENASE. Cold Spring Harb Symp Quant Biol. 1964;29:415–425. doi: 10.1101/sqb.1964.029.01.043. [DOI] [PubMed] [Google Scholar]
  11. RUSSELL L. B. Mammalian X-chromosome action: inactivation limited in spread and region of origin. Science. 1963 May 31;140(3570):976–978. doi: 10.1126/science.140.3570.976. [DOI] [PubMed] [Google Scholar]
  12. Seegmiller J. E., Rosenbloom F. M., Kelley W. N. Enzyme defect associated with a sex-linked human neurological disorder and excessive purine synthesis. Science. 1967 Mar 31;155(3770):1682–1684. doi: 10.1126/science.155.3770.1682. [DOI] [PubMed] [Google Scholar]
  13. Shapiro S. L., Sheppard G. L., Jr, Dreifuss F. E., Newcombe D. S. X-linked recessive inheritance of a syndrome of mental retardation with hyperuricemia. Proc Soc Exp Biol Med. 1966 Jun;122(2):609–611. doi: 10.3181/00379727-122-31204. [DOI] [PubMed] [Google Scholar]
  14. Wajntal A., DeMars R. A tetrazolium method for distinguishing between cultured human fibroblasts having eiter normal or deficient levels of glucose-6-phosphate dehydrogenase. Biochem Genet. 1967 Jun;1(1):61–64. doi: 10.1007/BF00487737. [DOI] [PubMed] [Google Scholar]

Articles from Proceedings of the National Academy of Sciences of the United States of America are provided here courtesy of National Academy of Sciences

RESOURCES