JAK2 V617F突变在骨髓增生异常/骨髓增殖性疾病中频繁出现，但在伴有纤维化的真性骨髓增生异常综合征中不存在。 - Suppr | 超能文献

The JAK2 V617F mutation occurs frequently in myelodysplastic/myeloproliferative diseases, but is absent in true myelodysplastic syndromes with fibrosis.

作者信息

Kremer M, Horn T, Dechow T, Tzankov A, Quintanilla-Martínez L, Fend F

出版信息

Leukemia. 2006 Jul;20(7):1315-6. doi: 10.1038/sj.leu.2404231. Epub 2006 Apr 13.

DOI:10.1038/sj.leu.2404231

Abstract

摘要

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The JAK2 V617F mutation occurs frequently in myelodysplastic/myeloproliferative diseases, but is absent in true myelodysplastic syndromes with fibrosis.JAK2 V617F突变在骨髓增生异常/骨髓增殖性疾病中频繁出现，但在伴有纤维化的真性骨髓增生异常综合征中不存在。

Leukemia. 2006 Jul;20(7):1315-6. doi: 10.1038/sj.leu.2404231. Epub 2006 Apr 13.

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Reply to Kremer M et al., the JAK2 V617F mutation occurs frequently in myelodysplastic/myeloproliferative diseases, but is absent in true myelodysplastic syndromes with fibrosis.对克雷默·M等人的回复：JAK2 V617F突变在骨髓增生异常/骨髓增殖性疾病中频繁出现，但在伴有纤维化的真性骨髓增生异常综合征中不存在。

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Prognostic impact of blast cell counts in dysplastic bone marrow disorders (MDS and CMML I) with concomitant fibrosis.伴有纤维化的发育异常性骨髓疾病（MDS 和 CMML I）中原始细胞计数对预后的影响。

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The implication of identifying JAK2 ( V617F ) in myeloproliferative neoplasms and myelodysplastic syndromes with bone marrow fibrosis.在骨髓增殖性肿瘤及伴有骨髓纤维化的骨髓增生异常综合征中鉴定JAK2（V617F）的意义。

J Hematop. 2008 Sep;1(2):111-7. doi: 10.1007/s12308-008-0014-8. Epub 2008 Aug 28.