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Expression data from Igf-1 -/- and Igf-1+/+ mouse cochleas
PubMed Full text in PMC Similar studies Analyze with GEO2R
Gene expression study of developing mammalian vestibular organ of wild type and Insulin-Like Growth Factor I deficient mice using Affymetrix whole transcript arrays
PubMed Similar studies Analyze with GEO2R
Expression data from E18.5 Igf1 -/- (homozygous mutant) and Igf1+/+ (normal wild type control) mouse lungs
Expression data from differentiating ventral otic Epithelial Cell line
UB/OC-1 differentiation
Cochlear hair cell line differentiation time course (Mu11K-B)
PubMed Full text in PMC Similar studies GEO Profiles Analyze DataSet
Cochlear hair cell line differentiation time course (Mu11K-A)
Temporal profiling of gene expression in cochleae of wild type and alpha9 null mice
Gene expression profiles along the tonotopic axis of the mouse cochlea during neonatal development
Expression data from cochlea isolated from N-myc mutant and wild-type mice at E15
Expression data of mice cochlea treated with L-methionine and valproic acid.
Epigenetic modifying reagents effect on a progressive hearing loss model: whole cochlea
Identification of microRNA targets in the mammalian inner ear using a comprehensive transcriptome and proteome integrated approach
Deafness Gene Expression Patterns in the Mouse Cochlea Found by Microarray Analysis
FoxM1 is essential for quiescence and maintenance of hematopoietic stem cell
Expression data from FoxM1 siRNA knock down Human aortic vascular smooth muscle cells
Global MEF2 target gene analysis in cardiac and skeletal muscle reveals novel regulation of DUSP6 by p38MAPKMEF2 signaling
PubMed Full text in PMC Similar studies
Global MEF2 target gene analysis in cardiac and skeletal muscle reveals novel regulation of DUSP6 by p38MAPKMEF2 signaling [RNA-seq]
PubMed Full text in PMC Similar studies SRA Run Selector
Global MEF2 target gene analysis in cardiac and skeletal muscle reveals novel regulation of DUSP6 by p38MAPKMEF2 signaling [ChIP-seq]
Skeletal muscle biopsies of patients with myotonic dystrophy (DM) and non-DM neuro-muscular disorders
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