The landscape of somatic mutations in infant MLL-rearranged acute lymphoblastic leukemias

被引:0
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作者
Anna K Andersson
Jing Ma
Jianmin Wang
Xiang Chen
Amanda Larson Gedman
Jinjun Dang
Joy Nakitandwe
Linda Holmfeldt
Matthew Parker
John Easton
Robert Huether
Richard Kriwacki
Michael Rusch
Gang Wu
Yongjin Li
Heather Mulder
Susana Raimondi
Stanley Pounds
Guolian Kang
Lei Shi
Jared Becksfort
Pankaj Gupta
Debbie Payne-Turner
Bhavin Vadodaria
Kristy Boggs
Donald Yergeau
Jayanthi Manne
Guangchun Song
Michael Edmonson
Panduka Nagahawatte
Lei Wei
Cheng Cheng
Deqing Pei
Rosemary Sutton
Nicola C Venn
Albert Chetcuti
Amanda Rush
Daniel Catchpoole
Jesper Heldrup
Thoas Fioretos
Charles Lu
Li Ding
Ching-Hon Pui
Sheila Shurtleff
Charles G Mullighan
Elaine R Mardis
Richard K Wilson
Tanja A Gruber
Jinghui Zhang
James R Downing
机构
[1] St. Jude Children's Research Hospital,Department of Pathology
[2] Lund University,Department of Clinical Genetics
[3] St. Jude Children's Research Hospital,Department of Computational Biology
[4] Pediatric Cancer Genome Project Laboratory,Department of Structural Biology
[5] St. Jude Children's Research Hospital,Department of Biostatistics
[6] St. Jude Children's Research Hospital,Department of Pediatrics
[7] St. Jude Children's Research Hospital,Department of Genetics
[8] Children's Cancer Institute Australia,Department of Oncology
[9] Lowy Cancer Research Centre,undefined
[10] University of New South Wales,undefined
[11] Tumor Bank,undefined
[12] Children's Cancer Research Unit,undefined
[13] Children's Hospital at Westmead,undefined
[14] Skåne University Hospital,undefined
[15] Washington University School of Medicine in St. Louis,undefined
[16] Genome Institute,undefined
[17] Washington University School of Medicine in St. Louis,undefined
[18] St. Jude Children's Research Hospital,undefined
来源
Nature Genetics | 2015年 / 47卷
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摘要
Anna Andersson, Tanja Gruber, James Downing and colleagues report a genomic analysis of infant acute lymphoblastic leukemias with MLL rearrangements. They identify recurrent activating mutations in tyrosine kinase, phosphatidylinositol 3-kinase and RAS pathway genes but find that these mutations were often present in minor subclones and lost at the time of relapse.
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页码:330 / 337
页数:7
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