MicroRNA 17–92 expressed by a transposone-based vector changes expression level of cell-cycle-related genes
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Title
MicroRNA 17–92 expressed by a transposone-based vector changes expression level of cell-cycle-related genes
Authors
Keywords
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Journal
CELL BIOLOGY INTERNATIONAL
Volume 36, Issue 11, Pages 1005-1012
Publisher
Wiley
Online
2012-06-28
DOI
10.1042/cbi20110089
References
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Related references
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- CREB in the Pathophysiology of Cancer: Implications for Targeting Transcription Factors for Cancer Therapy
- (2009) K. M. Sakamoto et al. CLINICAL CANCER RESEARCH
- MicroRNA MiR-17 retards tissue growth and represses fibronectin expression
- (2009) Sze Wan Shan et al. NATURE CELL BIOLOGY
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- (2009) H Ebi et al. ONCOGENE
- ThemiR-17∼92cluster collaborates with the Sonic Hedgehog pathway in medulloblastoma
- (2009) Tamar Uziel et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- MicroRNA Profiling of Human-Induced Pluripotent Stem Cells
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- MicroRNAs in Cancer
- (2008) Yong Sun Lee et al. Annual Review of Pathology-Mechanisms of Disease
- MicroRNA-17-92 down-regulates expression of distinct targets in different B-cell lymphoma subtypes
- (2008) M. Inomata et al. BLOOD
- Identification of Hypoxia-Inducible Factor-1 as a Novel Target for miR-17-92 MicroRNA Cluster
- (2008) A. Taguchi et al. CANCER RESEARCH
- Lymphoproliferative disease and autoimmunity in mice with increased miR-17-92 expression in lymphocytes
- (2008) Changchun Xiao et al. NATURE IMMUNOLOGY
- MicroRNA regulation of a cancer network: Consequences of the feedback loops involving miR-17-92, E2F, and Myc
- (2008) B. D. Aguda et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
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