Human adenosine deaminase and chromosome 20
- 1 April 1978
- journal article
- research article
- Published by Springer Nature in Cellular and Molecular Life Sciences
- Vol. 34 (4), 531-532
- https://doi.org/10.1007/bf01935973
Abstract
In patients exhibiting in marrow cells deletion of the long arm of chromosome 20, the specific activities of adenosine deaminase in cells of the peripheral blood are normal. This suggests that the gene for adenosine deaminase is not localized to the distal segment of the long arm of this chromosome.Keywords
This publication has 15 references indexed in Scilit:
- A role for adenosine deaminase in human monocyte maturation.JCI Insight, 1976
- Characterization of residual enzyme activity in fibroblasts from patients with adenosine deaminase deficiency and combined immunodeficiency: evidence for a mutant enzyme.Proceedings of the National Academy of Sciences, 1976
- Conversion of human erythrocyte-adenosine deaminase activity to different tissue-specific isozymes. Evidence for a common catalytic unit.JCI Insight, 1975
- Molecular form of adenosine deaminase in severe combined immunodeficiencyBiochemical and Biophysical Research Communications, 1974
- Assignment of a Gene for Adenosine Deaminase to Human Chromosome 20Human Heredity, 1974
- Evidence for Control of Several Different Tissue-specific Isozymes of Adenosine Deaminase by a le Genetic LocusNature New Biology, 1973
- The 45, XO, Ph1 Subgroup of Chronic Granulocytic LeukaemiaScandinavian Journal of Haematology, 1972
- Adenosine deaminase isozymes in human tissuesAnnals of Human Genetics, 1971
- New Technique for Distinguishing between Human ChromosomesNature New Biology, 1971
- Adenosine deaminase polymorphism in manAnnals of Human Genetics, 1968