Genome-wide RNA-mediated interference screen identifies miR-19 targets in Notch-induced T-cell acute lymphoblastic leukaemia

被引:0
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作者
Konstantinos J. Mavrakis
Andrew L. Wolfe
Elisa Oricchio
Teresa Palomero
Kim de Keersmaecker
Katherine McJunkin
Johannes Zuber
Taneisha James
Aly A. Khan
Christina S. Leslie
Joel S. Parker
Patrick J. Paddison
Wayne Tam
Adolfo Ferrando
Hans-Guido Wendel
机构
[1] Cancer Biology & Genetics Program,Department of Pathology
[2] Memorial Sloan-Kettering Cancer Center,Department of Pathology and Laboratory Medicine
[3] Weill Cornell Graduate School of Medical Science,undefined
[4] Columbia University,undefined
[5] Institute for Cancer Genetics,undefined
[6] Columbia University,undefined
[7] Cold Spring Harbor Laboratory,undefined
[8] Cold Spring Harbor,undefined
[9] Watson School of Biological Sciences,undefined
[10] Cold Spring Harbor Laboratory,undefined
[11] Cold Spring Harbor,undefined
[12] Computational Biology,undefined
[13] Memorial Sloan-Kettering Cancer Center,undefined
[14] Expression Analysis Inc.,undefined
[15] Fred Hutchinson Cancer Research Center,undefined
[16] Joan and Sanford I. Weill Medical College of Cornell University,undefined
[17] Present address: Department of Gene and Cell Medicine & Black Family Stem Cell Institute,undefined
[18] Mount Sinai School of Medicine,undefined
[19] New York,undefined
[20] New York 10029,undefined
[21] USA.,undefined
来源
Nature Cell Biology | 2010年 / 12卷
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摘要
The 17–92 miRNA cluster promotes tumourigenesis although the identity of the specific miRNA responsible for this effect has been unclear. MiR-19 is sufficient to promote Notch induced T-cell associated leukaemia in vivo and a shRNA screen for genes that phenocopy miR-19 effects identifies PI3-K regulators as miR-19 target genes.
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页码:372 / 379
页数:7
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