نتایج جستجو برای: jak2v617f mutation

تعداد نتایج: 291772  

2009
Yongchao Wang Warren Fiskus Daniel G. Chong Kathleen M. Buckley Kavita Natarajan Rekha Rao Atul Joshi Ramesh Balusu Sanjay Koul Jianguang Chen Andrew Savoie Celalettin Ustun Anand P. Jillella Peter Atadja Ross L. Levine Kapil N. Bhalla

The mutant JAK2V617F tyrosine kinase (TK) is present in the majority of patients with BCR-ABL–negative myeloproliferative neoplasms (MPNs). JAK2V617F activates downstream signaling through the signal transducers and activators of transcription (STAT), RAS/mitogen-activated protein kinase (MAPK), and phosphatidylinositol 3 (PI3)/AKT pathways, conferring proliferative and survival advantages in t...

Journal: :Haematologica 2008
François Girodon Céline Schaeffer Cédric Cleyrat Morgane Mounier Ingrid Lafont Frédéric Dos Santos Aurélie Duval Marc Maynadié Sylvie Hermouet

We analyzed the effect of hydroxyurea on the JAK2V617F allelic ratio (%JAK2V617F), measured in purified blood granulocytes, of patients with polycythemia vera and essential thrombocythemia. Thirty-six patients were examined sequentially prior to and after start of hydroxy-urea therapy (8 polycythemia vera, 17 essential thrombocythemia), or while remaining untreated (2 polycythemia vera, 9 essen...

Journal: :Haematologica 2010
Michelle Ann Elliott Animesh Pardanani Terra L Lasho Susan M Schwager Ayalew Tefferi

In a retrospective analysis of 205 patients (median age 62 years) with primary myelofibrosis and known JAK2V617F mutational status, 13.2% experienced a vaso-occlusive event at or prior to their diagnosis. After a median follow up of 31 months, post-diagnosis thrombosis occurred in 22 patients (10.7%), including 9 (4.4%) and 16 (7.8%) patients with a total of 9 arterial and 24 venous events, res...

Journal: :Blood 2011
Paola Guglielmelli Flavia Biamonte Joannah Score Claire Hidalgo-Curtis Francisco Cervantes Margherita Maffioli Tiziana Fanelli Thomas Ernst Nils Winkelman Amy V Jones Katerina Zoi Andreas Reiter Andrew Duncombe Laura Villani Alberto Bosi Giovanni Barosi Nicholas C P Cross Alessandro M Vannucchi

We genotyped 370 subjects with primary myelofibrosis (PMF) and 148 with postpolycythemia vera/postessential thrombocythemia (PPV/PET) MF for mutations of EZH2. Mutational status at diagnosis was correlated with hematologic parameters, clinical manifestations, and outcome. A total of 25 different EZH2 mutations were detected in 5.9% of PMF, 1.2% of PPV-MF, and 9.4% of PET-MF patients; most were ...

Journal: :International Journal of Hematology and Oncology 2015

Journal: :Indian Journal of Hematology and Blood Transfusion 2016

2014
Wanke Zhao Kang Zou Taleah Farasyn Wanting Tina Ho Zhizhuang Joe Zhao

The JAK2V617F mutation is found in the majority of patients with myeloproliferative neoplasms (MPNs). Transgenic expression of the mutant gene causes MPN-like phenotypes in mice. We have produced JAK2V617F mice with p53 null background. Some of these mice developed acute erythroleukemia. From one of these mice, we derived a cell line designated J53Z1. J53Z1 cells were stained positive for surfa...

Journal: :Blood 2013
Ann Mullally Claudia Bruedigam Luke Poveromo Florian H Heidel Amy Purdon Therese Vu Rebecca Austin Dirk Heckl Lawrence J Breyfogle Catherine Paine Kuhn Demetrios Kalaitzidis Scott A Armstrong David A Williams Geoff R Hill Benjamin L Ebert Steven W Lane

Interferon-α (IFNα) is an effective treatment of patients with myeloproliferative neoplasms (MPNs). In addition to inducing hematological responses in most MPN patients, IFNα reduces the JAK2V617F allelic burden and can render the JAK2V617F mutant clone undetectable in some patients. The precise mechanism underlying these responses is incompletely understood and whether the molecular responses ...

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