JAK2 mutation in a boy with polycythemia vera, but not in other pediatric hematologic Disorders
Author:
Publisher
Springer Science and Business Media LLC
Subject
Oncology,Cancer Research,Hematology
Link
http://www.nature.com/articles/2404259.pdf
Reference8 articles.
1. Baxter EJ, Scott LM, Campbell PJ, East C, Fourouclas N, Swanton S et al. Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders. Lancet 2005; 365: 1054–1061.
2. Kralovics R, Passamonti F, Buser AS, Teo SS, Tiedt R, Passweg JR et al. A gain-of-function mutation of JAK2 in myeloproliferative disorders. N Engl J Med 2005; 352: 1779–1790.
3. James C, Ugo V, Le Couedic JP, Staerk J, Delhommeau F, Lacout C et al. A unique clonal JAK2 mutation leading to constitutive signaling causes polycythaemia vera. Nature 2005; 434: 1144–1148.
4. Tono C, Xu G, Toki T, Takahashi Y, Sasaki S, Terui K et al. JAK2 Val617Phe activating tyrosine kinase mutation in juvenile myelomonocytic leukemia. Leukemia 2005; 19: 1843–1844.
5. Scott LM, Campbell PJ, Baxter EJ, Todd T, Stephens P, Edkins S et al. The V617F JAK2 mutation is uncommon in cancers and in myeloid malignancies other than the classic myeloproliferative disorders. Blood 2005; 106: 2920–2921.
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1. Characteristics and outcomes of patients with essential thrombocythemia or polycythemia vera diagnosed before 20 years of age: a systematic review;Haematologica;2019-01-24
2. JAK2V617F Mutation in a 9-Year-old Girl With Polycythemia Vera and Budd-Chiari Syndrome;Journal of Pediatric Hematology/Oncology;2012-04
3. A novelJAK2splicing mutation in neonatal myeloproliferative disorder accompanying congenital anomalies;British Journal of Haematology;2009-06
4. Clinical and hematological presentation of children and adolescents with polycythemia vera;Annals of Hematology;2009-05-26
5. Frequency and clinical features of the JAK2 V617F mutation in pediatric patients with sporadic essential thrombocythemia;Pediatric Blood & Cancer;2008-09-18
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