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JAK2-mutant vascular niche contributes to JAK2 clonal expansion in myeloproliferative neoplasms.
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Activation of JAK/STAT Signaling in Megakaryocytes Sustains Myeloproliferation .
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Characterization of murine JAK2V617F-positive myeloproliferative disease.
Cancer Res. 2006 Dec 1;66(23):11156-65. doi: 10.1158/0008-5472.CAN-06-2210.
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Myeloproliferative neoplasms can be initiated from a single hematopoietic stem cell expressing JAK2-V617F.
J Exp Med. 2014 Oct 20;211(11):2213-30. doi: 10.1084/jem.20131371. Epub 2014 Oct 6.
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Deletion of Stat3 in hematopoietic cells enhances thrombocytosis and shortens survival in a JAK2-V617F mouse model of MPN.
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New insights into the generation and function of megakaryocytes in health and disease.
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Malignant JAK-signaling: at the interface of inflammation and malignant transformation.
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Proteomic screening identifies PF4/Cxcl4 as a critical driver of myelofibrosis.
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Editorial: Megakaryocytes as regulators of tumor microenvironments.
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Megakaryocytes as the Regulator of the Hematopoietic Vascular Niche.
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The CXCR1/CXCR2 Inhibitor Reparixin Alters the Development of Myelofibrosis in the Mice.
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JAK2 inhibitor persistence in MPN: uncovering a central role of ERK activation.
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本文引用的文献

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Deep imaging of bone marrow shows non-dividing stem cells are mainly perisinusoidal.
Nature. 2015 Oct 1;526(7571):126-30. doi: 10.1038/nature15250. Epub 2015 Sep 23.
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IL-33 signaling contributes to the pathogenesis of myeloproliferative neoplasms.
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Hematopoietic stem cell arrival triggers dynamic remodeling of the perivascular niche.
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The secret life of a megakaryocyte: emerging roles in bone marrow homeostasis control.
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The thrombopoietin receptor, MPL, is critical for development of a JAK2V617F-induced myeloproliferative neoplasm.
Blood. 2014 Dec 18;124(26):3956-63. doi: 10.1182/blood-2014-07-587238. Epub 2014 Oct 22.
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Megakaryocytes regulate hematopoietic stem cell quiescence through CXCL4 secretion.
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Neuropathy of haematopoietic stem cell niche is essential for myeloproliferative neoplasms.
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