期刊文献+

JAK2基因突变与慢性骨髓增殖性疾病 被引量:7

原文传递
导出
摘要 慢性骨髓增殖性疾病(CMPD)是一类以一系或多系髓系细胞(包括红系、粒系和巨核系)增殖为主要特征的克隆性造血千细胞疾病。其特点是骨髓有核细胞增多,增殖的细胞可向终末分化成熟,多不伴发育异常。外周血一系或多系细胞增多,外周器官浸润,常伴有肝脾肿大。根据世界卫生组织(WHO)的恶性血液病分类方案,CMPD包括慢性粒细胞白血病(CML)、真性红细胞增多症(PV)、原发性血小板增多症(ET)、慢性特发性骨髓纤维化(CIMF)、慢性中性粒细胞白血病(CNL)、慢性嗜酸粒细胞白血病/高嗜酸粒细胞综合征(CEL/HES)及难分类的骨髓增殖性疾病(UMPD)。
出处 《中华血液学杂志》 CAS CSCD 北大核心 2006年第10期713-715,共3页 Chinese Journal of Hematology
  • 相关文献

参考文献15

  • 1Vardiman JW,Hams NL,Brunning RD.World Health Organization (WHO) classification of the myeloid neoplasms.Blood,2002,100:2292-2302.
  • 2Kralovics R,Passamonti F,Buser AS,et al.A gain-of-function mutation of JAK2 in myeloproliferative disorders.N Engl J Med,2005,352:1779-1790.
  • 3John MG,Junia VM.Chronic myeloid leukemia-advances in biology and new approaches to treatment.N Engl J Med,2003,349:1451-1464.
  • 4Levine RL,Wadleigh M.Activating mutation in the tyrosine kinase JAK2 in polycythemia vera,essential thrombocythemia,and myeloid metaplasia with myelofibrosis.Cancer Cell,2005,7:387-397.
  • 5Kaushansky K.On the molecular origins of the chronic myeloproliferative disorders:it all makes sense.Blood,2005,105:4187-4190.
  • 6Rawlings JS,Rosler KM,Harrison DA.The JAK/STAT signaling pathway.J Cell Sci,2004,117:1281-1283.
  • 7James C,Ugo V,le Couedic JP,et al.A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera.Nature,2005,434:1144-1148.
  • 8Baxter EJ,Scott LM,Campbell PJ,et al.Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders.Lancet,2005,365:1054-1061.
  • 9Zhao R,Xing S,Li ZJ,et al.Identification of an acquired JAK2 mutation in polycythemia vera.J Biol Chem,2005,280:22788-22792.
  • 10Jones AV,Kreil S,Zoi K,et al.Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders.Blood,2005,106:2162-2168.

同被引文献59

  • 1宋君红,李建勇,张苏江.骨髓增殖性疾病JAK2基因V617F点突变研究[J].中华血液学杂志,2006,27(9):632-633. 被引量:18
  • 2陆米则,李建勇,段丽敏,潘金兰,仇海荣,沈云峰,薛永权.原发性血小板增多症的细胞遗传学特征[J].实用临床医药杂志,2006,10(5):25-27. 被引量:3
  • 3段丽敏,李建勇,潘金兰,仇海荣,张苏江,吴亚芳,徐卫,薛永权.真性红细胞增多症的细胞遗传学研究[J].中国实验血液学杂志,2007,15(1):121-124. 被引量:10
  • 4李伟达,李建勇,张苏江,仇海荣,徐卫,王季石.特发性骨髓纤维化患者JAK2V617F突变研究[J].中国实验血液学杂志,2007,15(2):387-390. 被引量:10
  • 5Pikman Y, Lee BH, Mercher T, et al. MPLW515L is a novel somatic activating mutation in myelofibrosis with myeloid metaplasia. PLoS Med, 2006; 3:e270
  • 6Pardanani AD, Levine RL, Lasho T, et al. MPL515 mutations in myeloproliferative and other myeloid disorders: a study of 1182 patients. Blood, 2006 ; 108:3472 - 3476
  • 7Levine RL, Belisle C, Wadleigh M, et al. X-inactivation-based clonality analysis and quantitative JAK2V617F assessment reveal a strong association between clonality and JAK2V617F in PV but not ET/MMM, and identifies a subset of JAK2V617F-negative ET and MMM patients with clonal hematopoiesis. Blood, 2006; 107:4139 - 4141
  • 8Tefferi A, Lasho TL, Schwager SM, et al. The clinical phenotype of wild-type, heterozygous, and homozygous JAK2V617F in polycythemia vera. Cancer, 2006 ; 106:631 - 635
  • 9Hu WY, Zhao Y, Ishii T, et al. Haematopoietic cell lineage distribution of MPLW515L/K mutations in patients with idiopathic myelofibrosis. Br J Haematol, 2007; 137 : 374 -383
  • 10Lasho TL, Pardanani AD, McClure RF, et al. Concurrent MPLS15 and JAK2V617F mutations in myelofibrosis: chronology of clonal emergence and changes in mutant allele burden over time. Br J Haematol, 2006; 135 : 683 -687

引证文献7

二级引证文献49

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部