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JAK2V617F prevalence and allele burden in non-splanchnic venous thrombosis in the absence of overt myeloproliferative disorder.

作者信息

Pardanani A, Lasho T L, Schwager S, Finke C, Hussein K, Pruthi R K, Tefferi A

出版信息

Leukemia. 2007 Aug;21(8):1828-9. doi: 10.1038/sj.leu.2404710. Epub 2007 Apr 26.

DOI:10.1038/sj.leu.2404710
PMID:17460706
Abstract
摘要

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JAK2V617F prevalence and allele burden in non-splanchnic venous thrombosis in the absence of overt myeloproliferative disorder.无明显骨髓增殖性疾病情况下非内脏静脉血栓形成中JAK2V617F的患病率和等位基因负荷。
Leukemia. 2007 Aug;21(8):1828-9. doi: 10.1038/sj.leu.2404710. Epub 2007 Apr 26.
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Incidence of the JAK2 V617F mutation among patients with splanchnic or cerebral venous thrombosis and without overt chronic myeloproliferative disorders.内脏或脑静脉血栓形成且无明显慢性骨髓增殖性疾病患者中JAK2 V617F突变的发生率。
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Increased risk of lymphoid neoplasms in patients with Philadelphia chromosome-negative myeloproliferative neoplasms.费城染色体阴性骨髓增殖性肿瘤患者发生淋巴样肿瘤的风险增加。
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JAK2V617F mutation screening as part of the hypercoagulable work-up in the absence of splanchnic venous thrombosis or overt myeloproliferative neoplasm: assessment of value in a series of 664 consecutive patients.在无内脏静脉血栓形成或明显骨髓增殖性肿瘤的情况下,JAK2V617F突变筛查作为高凝检查的一部分:对664例连续患者的价值评估
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JAK2V617F mutation is ubiquitously present in splanchnic vein thrombosis accompanying myeloproliferative syndromes.JAK2V617F突变普遍存在于伴有骨髓增殖性综合征的内脏静脉血栓形成中。
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Absence of the JAK2 exon 12 mutations in patients with splanchnic venous thrombosis and without overt myeloproliferative neoplasms.内脏静脉血栓形成且无明显骨髓增殖性肿瘤患者中JAK2外显子12突变缺失。
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Inferior vena cava thrombosis and its relationship with the JAK2V617F mutation and chronic myeloproliferative disease.下腔静脉血栓形成及其与 JAK2V617F 突变和慢性骨髓增殖性疾病的关系。
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引用本文的文献

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JAK2V617F Mutation in Patient with Splanchnic Vein Thrombosis.内脏静脉血栓形成患者的JAK2V617F突变
Indian J Hematol Blood Transfus. 2020 Oct;36(4):700-704. doi: 10.1007/s12288-020-01292-x. Epub 2020 May 25.
2
The JAK2 V617F Allele Burden in Latent Myeloproliferative Neoplasms Presenting with Splanchnic Vein Thrombosis.伴有内脏静脉血栓形成的潜伏性骨髓增殖性肿瘤中的JAK2 V617F等位基因负荷
Pathol Oncol Res. 2016 Jan;22(1):229-30. doi: 10.1007/s12253-015-9994-8. Epub 2015 Oct 8.
3
Uses and abuses of JAK2 and MPL mutation tests in myeloproliferative neoplasms a paper from the 2010 William Beaumont hospital symposium on molecular pathology.
JAK2 和 MPL 基因突变检测在骨髓增殖性肿瘤中的应用与滥用——来自 2010 年威廉博蒙特医院分子病理学研讨会的论文。
J Mol Diagn. 2011 Sep;13(5):461-6. doi: 10.1016/j.jmoldx.2011.05.007. Epub 2011 Jun 30.
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Relevance of the JAK2V617F mutation in patients with deep vein thrombosis of the leg.下肢深静脉血栓形成患者 JAK2V617F 突变的相关性。
Ann Hematol. 2012 Jan;91(1):103-7. doi: 10.1007/s00277-011-1233-0. Epub 2011 Apr 12.
5
Early renal arterial stent thrombosis associated with the JAK2 V617F mutation.与JAK2 V617F突变相关的早期肾动脉支架血栓形成。
Leuk Res. 2009 Apr;33(4):573-4. doi: 10.1016/j.leukres.2008.06.016. Epub 2008 Jul 18.