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32199 publications found in the database

*2012 (1980)

*Starting in 2010, coverage has been refocused on core journals.

2012 Publications

Myocardial transcriptome analysis of human arrhythmogenic right ventricular cardiomyopathy
Gaertner, A. et al. Physiological Genomics 44(1), 99-109, 2012, Human Genome U133 Plus 2.0 Array  PubMed

Profiling CCK-mediated pancreatic growth: the dynamic genetic program and the role of STATs as potential regulators
Gurda, G. T. et al. Physiological Genomics 44(1), 14-24, 2012, Mouse Expression Set 430  PubMed

Hyaluronan Synthase HAS2 Promotes Tumor Progression in Bone by Stimulating the Interaction of Breast Cancer Stem-Like Cells with Macrophages and Stromal Cells
Okuda, H. et al. Cancer Research 72(2), 537-47, 2012, Human Gene 1.0 ST Array  PubMed

Energy-sensing Factors Coactivator Peroxisome Proliferator-activated Receptor gamma Coactivator 1-alpha (PGC-alpha) and AMP-activated Protein Kinase Control Expression of Inflammatory Mediators in Liver: INDUCTION OF INTERLEUKIN 1 RECEPTOR ANTAGONIST
Buler, M. et al. Journal of Biological Chemistry 287(3), 1847-60, 2012, Mouse Genome 430 2.0 Array  PubMed

Histone Deacetylase Inhibitors Induce Growth Arrest and Differentiation in Uveal Melanoma
Landreville, S. et al. Clinical Cancer Research 18(2), 408-16, 2012, Human Genome U133 Set  PubMed

Duplication of the ZIC2 Gene is not Associated With Holoprosencephaly
Jobanputra, V. et al. American Journal of Medical Genetics Part a 158A(1), 103-8, 2012, Genome-Wide Human SNP Array 6.0  PubMed

Androgen Deprivation Causes Epithelial-Mesenchymal Transition in the Prostate: Implications for Androgen-Deprivation Therapy
Sun, Y. T. et al. Cancer Research 72(2), 527-36, 2012, Human Genome U133 Plus 2.0 Array  PubMed

Transcriptomic Concentration-Response Evaluation of Valproic Acid, Cyproconazole, and Hexaconazole in the Neural Embryonic Stem Cell Test (ESTn)
Theunissen, P. T. et al. Toxicological Sciences 125(2), 430-8, 2012, Mouse Genome 430 2.0 Array  PubMed

Chromosomal Loss of 3q26.3-3q26.32, Involving a Partial Neuroligin 1 Deletion, Identified by Genomic Microarray in a Child With Microcephaly, Seizure Disorder, and Severe Intellectual Disability
Millson, A. et al. American Journal of Medical Genetics Part a 158A(1), 159-65, 2012  PubMed

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