Literature DB >> 19633776

Mutations in familial thrombocythemias.

Christof Dame.   

Abstract

Entities:  

Year:  2008        PMID： 19633776      PMCID： PMC2696733          DOI： 10.3238/arztebl.2008.0071c

Source DB:  PubMed          Journal:  Dtsch Arztebl Int        ISSN： 1866-0452            Impact factor:   5.594


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  3 in total

1.  An activating splice donor mutation in the thrombopoietin gene causes hereditary thrombocythaemia.

Authors:  A Wiestner; R J Schlemper; A P van der Maas; R C Skoda
Journal:  Nat Genet       Date:  1998-01       Impact factor: 38.330

2.  Mpl Baltimore: a thrombopoietin receptor polymorphism associated with thrombocytosis.

Authors:  Alison R Moliterno; Donna M Williams; Laura I Gutierrez-Alamillo; Roberto Salvatori; Roxann G Ingersoll; Jerry L Spivak
Journal:  Proc Natl Acad Sci U S A       Date:  2004-07-21       Impact factor: 11.205

3.  Familial essential thrombocythemia associated with a dominant-positive activating mutation of the c-MPL gene, which encodes for the receptor for thrombopoietin.

Authors:  Jianmin Ding; Hirokazu Komatsu; Atsushi Wakita; Miyuki Kato-Uranishi; Masato Ito; Atsushi Satoh; Kazuya Tsuboi; Masakazu Nitta; Hiroshi Miyazaki; Shinsuke Iida; Ryuzo Ueda
Journal:  Blood       Date:  2004-02-05       Impact factor: 22.113
  3 in total

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