A human erythropoietin receptor gene mutant causing familial erythrocytosis is associated with deregulation of the rates of Jak2 and Stat5 inactivation-Reference-Cited by-同舟云学术

A human erythropoietin receptor gene mutant causing familial erythrocytosis is associated with deregulation of the rates of Jak2 and Stat5 inactivation

Published:1999-01 Issue:1 Volume:27 Page:63-74
ISSN:0301-472X
Container-title:Experimental Hematology
language:en
Short-container-title:Experimental Hematology

Author:

Arcasoy Murat O,Harris Kevin W,Forget Bernard G

Publisher

Elsevier BV

Subject

Cancer Research,Cell Biology,Genetics,Hematology,Molecular Biology

Reference60 articles.

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4. Activating mutations in cytokine receptors;Gonda;Blood,1997

5. Truncated erythropoietin receptor causes dominantly-inherited benign human erythrocytosis;de la Chapelle;Proc Natl Acad Sci USA,1993

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