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Loss of Ezh2 cooperates with Jak2V617F in the development of myelofibrosis in a mouse model of myeloproliferative neoplasm

An activating JAK2V617F mutation has been found in ∼50% patients with myelofibrosis (MF). Inactivating mutations in histone methyltransferase enhancer of zeste homolog 2 (EZH2) also have been observed in patients with MF. Interestingly, inactivating EZH2 mutations are often associated with JAK2V617F...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:Blood
मुख्य लेखकों: Yang, Yue, Akada, Hajime, Nath, Dipmoy, Hutchison, Robert E., Mohi, Golam
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: American Society of Hematology 2016
विषय:
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC4929929/
https://ncbi.nlm.nih.gov/pubmed/27081096
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2015-11-679431
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