Cytogenetic studies at diagnosis in polycythemia vera: clinical and JAK2V617F allele burden correlates-Reference-Cited by-同舟云学术

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Cytogenetic studies at diagnosis in polycythemia vera: clinical and JAK2V617F allele burden correlates

Published:2008-03 Issue:3 Volume:80 Page:197-200
ISSN:0902-4441
Container-title:European Journal of Haematology
language:en
Short-container-title:Eur J Haematol

Author:

Gangat Naseema,Strand Jacob,Lasho Terra L.,Finke Christy M.,Knudson Ryan A.,Pardanani Animesh,Li Chin-Yang,Ketterling Rhett P.,Tefferi Ayalew

Publisher

Wiley

Subject

Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.2007.01003.x/fullpdf

Reference13 articles.

1. A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera

2. JAK2Exon 12 Mutations in Polycythemia Vera and Idiopathic Erythrocytosis

3. Evidence for a 15; 17 translocation in every patient with acute promyelocytic leukemia

4. The t(15;17) translocation of acute promyelocytic leukaemia fuses the retinoic acid receptor α gene to a novel transcribed locus

5. Lessons learned from the development of an Abl tyrosine kinase inhibitor for chronic myelogenous leukemia

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1. Association of JAK2V617F allele burden and clinical correlates in polycythemia vera: a systematic review and meta-analysis;Annals of Hematology;2024-04-23

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