A novel germlineJAK2mutation in familial myeloproliferative neoplasms-Reference-Cited by-同舟云学术

A novel germlineJAK2mutation in familial myeloproliferative neoplasms

Published:2014-01 Issue:1 Volume:89 Page:117-118
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:Am. J. Hematol.

Author:

Rumi Elisa¹,Harutyunyan Ashot S.²,Casetti Ilaria¹,Pietra Daniela¹,Nivarthi Harini²,Moriggl Richard³,Cleary Ciara²,Bagienski Klaudia²,Astori Cesare¹,Bellini Marta¹,Berg Tiina²,Passamonti Francesco⁴,Kralovics Robert²⁵,Cazzola Mario¹

Affiliation:

1. Department of Hematology Oncology; Fondazione IRCCS Policlinico San Matteo, University of Pavia; Pavia Italy

2. CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences; Vienna Austria

3. Ludwig Boltzmann Institute of Cancer Research; Vienna Austria

4. Division of Hematology, Department Internal Medicine; A.O. Ospedale di Circolo e Fondazione Macchi; Varese Italy

5. Department of Internal Medicine I, Division of Hematology and Blood Coagulation; Medical University of Vienna; Vienna Austria

Funder

Associazione Italiana per la Ricerca sul Cancro, Special Program Molecular Clinical Oncology 5 per mille, Milan, Italy

Italian Ministry of Health for young researchers

Publisher

Wiley

Subject

Hematology

Reference10 articles.

1. Familial chronic myeloproliferative disorders: Clinical phenotype and evidence of disease anticipation;Rumi;J Clin Oncol,2007

2. Genetic and clinical implications of the Val617Phe JAK2 mutation in 72 families with myeloproliferative disorders;Bellanne-Chantelot;Blood,2006

3. The role of the JAK2 GGCC haplotype and the TET2 gene in familial myeloproliferative neoplasms;Olcaydu;Haematologica,2011

4. JAK2 (V617F) as an acquired somatic mutation and a secondary genetic event associated with disease progression in familial myeloproliferative disorders;Rumi;Cancer,2006

5. An activating splice donor mutation in the thrombopoietin gene causes hereditary thrombocythaemia;Wiestner;Nat Genet,1998

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