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Synthesis and Turnover of Purine Nucleoside Phosphorylase in Human Lymphocytes

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Book cover Purine and Pyrimidine Metabolism in Man V

Part of the book series: Advances in Experimental Medicine and Biology ((AEMB,volume 195B))

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Abstract

The inherited deficiency of purine nucleoside Phosphorylase results in severe T cell immunodeficiency disease1. We have studied the synthesis of purine nucleoside Phosphorylase during phytohumagglutinin induced T cell transformation and have examined the turnover of purine nucleoside Phosphorylase in the human lymphoblast WI-L2.

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References

  1. E.R. Giblett, A.J. Ammann, D.W. Wara, R. Sandman, and L.K. Diamond, Nucleoside Phosphorylase deficiency in a child with severely defective T cell immunity and normal B-cell immunity, Lancet, 1: 1010 (1975).

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© 1986 Plenum Press, New York

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Snyder, F.F., Neote, K., Kwan, E., Mably, E.R. (1986). Synthesis and Turnover of Purine Nucleoside Phosphorylase in Human Lymphocytes. In: Nyhan, W.L., Thompson, L.F., Watts, R.W.E. (eds) Purine and Pyrimidine Metabolism in Man V. Advances in Experimental Medicine and Biology, vol 195B. Springer, New York, NY. https://doi.org/10.1007/978-1-4684-1248-2_40

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  • DOI: https://doi.org/10.1007/978-1-4684-1248-2_40

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  • Publisher Name: Springer, New York, NY

  • Print ISBN: 978-1-4684-1250-5

  • Online ISBN: 978-1-4684-1248-2

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