The JAK2 exon 12 mutations: A comprehensive review-Reference-Cited by-同舟云学术

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The JAK2 exon 12 mutations: A comprehensive review

Published:2011-06-14 Issue:8 Volume:86 Page:668-676
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:Am. J. Hematol.

Author:

Scott Linda M.

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajh.22063/fullpdf

Reference99 articles.

1. Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders;Baxter;Lancet,2005

2. A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera;James;Nature,2005

3. A gain-of-function mutation of JAK2 in myeloproliferative disorders;Kralovics;N Engl J Med,2005

4. Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis;Levine;Cancer Cell,2005

5. JAK inhibitor therapy for myelofibrosis: Critical assessment of value and limitations;Pardanani;Leukemia,2011

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1. Screening for Janus kinase-2 exon 12 mutations among Janus kinase-2 V617F-negative polycythemia vera suspected Iraqi patients;Iraqi Journal of Hematology;2024-09-02

2. Inflammation as a cause of acute myocardial infarction in patients with myeloproliferative neoplasm;World Journal of Cardiology;2024-02-26

3. Sensitivity evaluation of methods for screening JAK2 exon 12 mutations based on heteroduplex and HRM analysis;Oncohematology;2024-01-27

4. Insights into the role of JAK2-I724T variant in myeloproliferative neoplasms from a unique cohort of New Zealand patients;Hematology;2024-01-10

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