Hematopoietic neoplasms with 9p24/JAK2 rearrangement: a multicenter study-Reference-Cited by-同舟云学术

Hematopoietic neoplasms with 9p24/JAK2 rearrangement: a multicenter study

Published:2018-11-06 Issue:4 Volume:32 Page:490-498
ISSN:0893-3952
Container-title:Modern Pathology
language:en
Short-container-title:Mod Pathol

Author:

Tang Guilin,Sydney Sir Philip John Kennedy,Weinberg Olga,Tam Wayne,Sadigh Sam,Lake Jonathan I.,Margolskee Elizabeth M.^ORCID,Rogers Heesun J.,Miranda Roberto N.,Bueso-Ramos C Carlos,Hsi Eric D.,Orazi Attilio,Hasserjian Robert P.,Arber Daniel A.,Bagg Adam,Wang Sa A.

Publisher

Springer Science and Business Media LLC

Subject

Pathology and Forensic Medicine

Link

http://www.nature.com/articles/s41379-018-0165-9.pdf

Reference26 articles.

1. Ihle JN, Gilliland DG. Jak2: normal function and role in hematopoietic disorders. Curr Opin Genet Dev. 2007;17:8–14.

2. Santos FP, Verstovsek S. JAK2 inhibitors: what’s the true therapeutic potential? Blood Rev. 2011;25:53–63.

3. Bain BJ, Ahmad S. Should myeloid and lymphoid neoplasms with PCM1-JAK2 and other rearrangements of JAK2 be recognized as specific entities? Br J Haematol. 2014;166:809–17.

4. Stewart K, Carstairs KC, Dube ID, Keating A. Neutrophilic myelofibrosis presenting as Philadelphia chromosome negative BCR non-rearranged chronic myeloid leukemia. Am J Hematol. 1990;34:59–63.

5. Reiter A, Walz C, Watmore A, et al. The t(8;9)(p22; p24) is a recurrent abnormality in chronic and acute leukemia that fuses PCM1 to JAK2. Cancer Res. 2005;65:2662–7.

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