HuGE Literature Finder
Records 1-6
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ASXL2 Mutations are Frequently Found in Pediatric AML Patients with t(8;21)/RUNX1-RUNX1T1 and Associated with a Better Prognosis.
Genes, chromosomes & cancer 2017 Jan . Yamato Genki, Shiba Norio, Yoshida Kenichi, Shiraishi Yuichi, Hara Yusuke, Ohki Kentaro, Okubo Jun, Okuno Haruna, Chiba Kenichi, Tanaka Hiroko, Kinoshita Akitoshi, Moritake Hiroshi, Kiyokawa Nobutaka, Tomizawa Daisuke, Park Myoung-Ja, Sotomatsu Manabu, Taga Takashi, Adachi Souichi, Tawa Akio, Horibe Keizo, Arakawa Hirokazu, Miyano Satoru, Ogawa Seishi, Hayashi Yasuhi |
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Genomewide meta-analysis identifies loci associated with IGF-I and IGFBP-3 levels with impact on age-related traits.
Aging cell 2016 Oct 15 (5): 811-24. Teumer Alexander, Qi Qibin, Nethander Maria, Aschard Hugues, Bandinelli Stefania, Beekman Marian, Berndt Sonja I, Bidlingmaier Martin, Broer Linda, , Cappola Anne, Ceda Gian Paolo, Chanock Stephen, Chen Ming-Huei, Chen Tai C, Chen Yii-Der Ida, Chung Jonathan, Del Greco Miglianico Fabiola, Eriksson Joel, Ferrucci Luigi, Friedrich Nele, Gnewuch Carsten, Goodarzi Mark O, Grarup Niels, Guo Tingwei, Hammer Elke, Hayes Richard B, Hicks Andrew A, Hofman Albert, Houwing-Duistermaat Jeanine J, Hu Frank, Hunter David J, Husemoen Lise L, Isaacs Aaron, Jacobs Kevin B, Janssen Joop A M J L, Jansson John-Olov, Jehmlich Nico, Johnson Simon, Juul Anders, Karlsson Magnus, Kilpelainen Tuomas O, Kovacs Peter, Kraft Peter, Li Chao, Linneberg Allan, Liu Yongmei, Loos Ruth J F, , Lorentzon Mattias, Lu Yingchang, Maggio Marcello, Magi Reedik, Meigs James, Mellström Dan, Nauck Matthias, Newman Anne B, Pollak Michael N, Pramstaller Peter P, Prokopenko Inga, Psaty Bruce M, Reincke Martin, Rimm Eric B, Rotter Jerome I, Saint Pierre Aude, Schurmann Claudia, Seshadri Sudha, Sjögren Klara, Slagboom P Eline, Strickler Howard D, Stumvoll Michael, Suh Yousin, Sun Qi, Zhang Cuilin, Svensson Johan, Tanaka Toshiko, Tare Archana, Tönjes Anke, Uh Hae-Won, van Duijn Cornelia M, van Heemst Diana, Vandenput Liesbeth, Vasan Ramachandran S, Völker Uwe, Willems Sara M, Ohlsson Claes, Wallaschofski Henri, Kaplan Robert |
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[Frequency and clinical features of ASXL2 gene mutation in acute myeloid leukemia patients with AML1- ETO fusion gene positive].
Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi 2016 Aug 37 (8): 676-81. Zhao J X, Chen X H, Li J L, Pan J, Tan Y H, Xu Z F, Ren F G, Zhang Y F, Xu J, Li M Q, Li J, Zhang N, Chang J M, Wang X J, Wang H |
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Whole-exome sequencing reveals the spectrum of gene mutations and the clonal evolution patterns in paediatric acute myeloid leukaemia.
British journal of haematology 2016 Jul . Shiba Norio, Yoshida Kenichi, Shiraishi Yuichi, Okuno Yusuke, Yamato Genki, Hara Yusuke, Nagata Yasunobu, Chiba Kenichi, Tanaka Hiroko, Terui Kiminori, Kato Motohiro, Park Myoung-Ja, Ohki Kentaro, Shimada Akira, Takita Junko, Tomizawa Daisuke, Kudo Kazuko, Arakawa Hirokazu, Adachi Souichi, Taga Takashi, Tawa Akio, Ito Etsuro, Horibe Keizo, Sanada Masashi, Miyano Satoru, Ogawa Seishi, Hayashi Yasuhi |
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DNMT3A R882 Mutation with FLT3-ITD Positivity Is an Extremely Poor Prognostic Factor in Patients with Normal-Karyotype Acute Myeloid Leukemia after Allogeneic Hematopoietic Cell Transplantation.
Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation 2015 Jul . Ahn Jae-Sook, Kim Hyeoung-Joon, Kim Yeo-Kyeoung, Lee Seun-Shin, Jung Sung-Hoon, Yang Deok-Hwan, Lee Je-Jung, Kim Nan Young, Choi Seung Hyun, Jung Chul Won, Jang Jun-Ho, Kim Hee Je, Moon Joon Ho, Sohn Sang Kyun, Won Jong-Ho, Kim Sung-Hyun, Kim Dennis Dong Hw |
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Mutations of polycomb-associated gene ASXL1 in myelodysplastic syndromes and chronic myelomonocytic leukaemia.
British journal of haematology 2009 Jun 145 (6): 788-800. Gelsi-Boyer Véronique, Trouplin Virginie, Adélaïde José, Bonansea Julien, Cervera Nathalie, Carbuccia Nadine, Lagarde Arnaud, Prebet Thomas, Nezri Meyer, Sainty Danielle, Olschwang Sylviane, Xerri Luc, Chaffanet Max, Mozziconacci Marie-Joëlle, Vey Norbert, Birnbaum Dani |
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- Page last updated:Dec 02, 2020
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