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Letter to the Editor

CALR and ASXL1 mutation analysis in 190 patients with essential thrombocythemia

, , , , , , , , & show all
Pages 820-822 | Received 03 Mar 2014, Accepted 22 Jun 2014, Published online: 13 Aug 2014

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Juliana Alvarez Argote & Constantin A. Dasanu. (2018) ASXL1 mutations in myeloid neoplasms: pathogenetic considerations, impact on clinical outcomes and survival. Current Medical Research and Opinion 34:5, pages 757-763.
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Articles from other publishers (12)

Diletta Fontana, Ilaria Crespiatico, Valentina Crippa, Federica Malighetti, Matteo Villa, Fabrizio Angaroni, Luca De Sano, Andrea Aroldi, Marco Antoniotti, Giulio Caravagna, Rocco Piazza, Alex Graudenzi, Luca Mologni & Daniele Ramazzotti. (2023) Evolutionary signatures of human cancers revealed via genomic analysis of over 35,000 patients. Nature Communications 14:1.
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Yan‑Bo Nie, Meng Sun, Colin He, Man‑Kai Ju, Fu‑Ling Zhou, San‑Yun Wu, Yi Zhou, Li Liu, Hui Shen, Ting‑Ting Huang, Pan Liu, Ying Xu, Liang Shao & Xue‑Lan Zuo. (2018) ASXL1 mutations in Chinese patients with essential thrombocythemia. Experimental and Therapeutic Medicine.
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L Falchi, H M Kantarjian & S Verstovsek. (2017) Assessing the thrombotic risk of patients with essential thrombocythemia in the genomic era. Leukemia 31:9, pages 1845-1854.
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Sarah Martin, Casey M. Wright & Linda M. Scott. (2017) Progenitor genotyping reveals a complex clonal architecture in a subset of CALR- mutated myeloproliferative neoplasms . British Journal of Haematology 177:1, pages 55-66.
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Yu-Qing Pei, Yue Wu, Fei Wang & Wei Cui. (2016) Prognostic value of CALR vs. JAK2V617F mutations on splenomegaly, leukemic transformation, thrombosis, and overall survival in patients with primary fibrosis: a meta-analysis. Annals of Hematology 95:9, pages 1391-1398.
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Yonggoo Kim, Joonhong Park, Irene Jo, Gun Dong Lee, Jiyeon Kim, Ahlm Kwon, Hayoung Choi, Woori Jang, Hyojin Chae, Kyungja Han, Ki-Seong Eom, Byung-Sik Cho, Sung-Eun Lee, Jinyoung Yang, Seung-Hwan Shin, Hyunjung Kim, Yoon Ho Ko, Haeil Park, Jong Youl Jin, Seungok Lee, Dong Wook Jekarl, Seung-Ah Yahng & Myungshin Kim. (2016) Genetic–pathologic characterization of myeloproliferative neoplasms. Experimental & Molecular Medicine 48:7, pages e247-e247.
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Kolsoum Saeidi. (2016) Myeloproliferative neoplasms: Current molecular biology and genetics. Critical Reviews in Oncology/Hematology 98, pages 375-389.
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Hao Kong, Yancheng Liu, Sai Luo, Qiaoqiao Li & Qinglu Wang. (2016) Frequency of Calreticulin (CALR) Mutation and Its Clinical Prognostic Significance in Essential Thrombocythemia and Primary Myelofibrosis: A Meta-analysis. Internal Medicine 55:15, pages 1977-1984.
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Haixiu Guo, Xiuhua Chen, Ruiyuan Tian, Jianmei Chang, Jianlan Li, Yanhong Tan, Zhifang Xu, Fanggang Ren, Junxia Zhao, Jie Pan, Na Zhang, Xiaojuan Wang, Jianxia He, Wanfang Yang & Hongwei Wang. (2015) Frequencies, Laboratory Features, and Granulocyte Activation in Chinese Patients with CALR-Mutated Myeloproliferative Neoplasms. PLOS ONE 10:9, pages e0138250.
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Yining Yang, Xiaorui Wang, Chun Wang & Youwen Qin. (2014) A meta-analysis comparing clinical characteristics and outcomes in CALR-mutated and JAK2V617F essential thrombocythaemia. International Journal of Hematology 101:2, pages 165-172.
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Bo Hyun Kim, Young-Uk Cho, Mi-Hyun Bae, Seongsoo Jang, Eul-Ju Seo, Hyun-Sook Chi, Yunsuk Choi, Dae-Young Kim, Jung-Hee Lee, Je-Hwan Lee, Kyoo-Hyung Lee, Young-Mi Park, Jong-Keuk Lee & Chan-Jeoung Park. (2015) JAK2 V617F, MPL , and CALR Mutations in Korean Patients with Essential Thrombocythemia and Primary Myelofibrosis . Journal of Korean Medical Science 30:7, pages 882.
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Sang Hyuk ParkShine Young KimSun Min LeeJongyoun YiIn-Suk KimHyung Hoi KimChulhun Ludgerus ChangEun Yup LeeMoo-Kon SongHo-Jin ShinJoo Seop Chung. (2015) Incidence, Clinical Features, and Prognostic Impact of CALR Exon 9 Mutations in Essential Thrombocythemia and Primary Myelofibrosis: An Experience of a Single Tertiary Hospital in Korea . Annals of Laboratory Medicine 35:2, pages 233.
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