Hypoxia-Inducible mir-210 Regulates Normoxic Gene Expression Involved in Tumor Initiation
Top Cited Papers
- 1 September 2009
- journal article
- research article
- Published by Elsevier in Molecular Cell
- Vol. 35 (6), 856-867
- https://doi.org/10.1016/j.molcel.2009.09.006
Abstract
No abstract availableKeywords
Funding Information
- National Institutes of Health (1R01-CA118582, P01-CA06294, P01-CA67166)
This publication has 48 references indexed in Scilit:
- Four miRNAs associated with aggressiveness of lymph node-negative, estrogen receptor-positive human breast cancerProceedings of the National Academy of Sciences, 2008
- The impact of microRNAs on protein outputNature, 2008
- MicroRNA-210 Modulates Endothelial Cell Response to Hypoxia and Inhibits the Receptor Tyrosine Kinase Ligand Ephrin-A3Journal of Biological Chemistry, 2008
- A biochemical approach to identifying microRNA targetsProceedings of the National Academy of Sciences, 2007
- The role of site accessibility in microRNA target recognitionNature Genetics, 2007
- MicroRNA Targeting Specificity in Mammals: Determinants beyond Seed PairingMolecular Cell, 2007
- Hypoxia, gene expression, and metastasisCancer and Metastasis Reviews, 2007
- A signature pattern of stress-responsive microRNAs that can evoke cardiac hypertrophy and heart failureProceedings of the National Academy of Sciences, 2006
- Combinatorial microRNA target predictionsNature Genetics, 2005
- Conserved Seed Pairing, Often Flanked by Adenosines, Indicates that Thousands of Human Genes are MicroRNA TargetsCell, 2005