JAK2V617Fmutation is associated with special alleles in essential thrombocythemia
Author:
Publisher
Informa UK Limited
Subject
Cancer Research,Oncology,Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/10428194.2010.542260
Reference17 articles.
1. Role of JAK2 in the pathogenesis and therapy of myeloproliferative disorders
2. JAK2Exon 12 Mutations in Polycythemia Vera and Idiopathic Erythrocytosis
3. MPLW515L Is a Novel Somatic Activating Mutation in Myelofibrosis with Myeloid Metaplasia
4. Increased risks of polycythemia vera, essential thrombocythemia, and myelofibrosis among 24 577 first-degree relatives of 11 039 patients with myeloproliferative neoplasms in Sweden
5. Germline and somatic JAK2 mutations and susceptibility to chronic myeloproliferative neoplasms
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. JAK2 rs10974944 is associated with both V617F‐positive and negative myeloproliferative neoplasms in a Vietnamese population: A potential genetic marker;Molecular Genetics & Genomic Medicine;2022-08-22
2. Genetic association between germline JAK2polymorphisms and myeloproliferative neoplasms in Hong Kong Chinese population: a case–control study;BMC Genetics;2014-12
3. The JAK2 46/1 haplotype (GGCC) in myeloproliferative neoplasms and splanchnic vein thrombosis: a pooled analysis of 26 observational studies;Annals of Hematology;2014-07-13
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