Pike, J. Wesley - Molecular and Cellular Pharmacology Training Program & Department of Biochemistry, University of Wisconsin at Madison

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Pike, J. Wesley - Molecular and Cellular Pharmacology Training Program & Department of Biochemistry, University of Wisconsin at Madison

Enhancers Located within Two Introns of the Vitamin D Receptor Gene Mediate Transcriptional
Molecular Structure of the Rat Vitamin D Receptor Ligand Binding Domain Complexed with 2-Carbon-Substituted Vitamin D3 Hormone Analogues and a
Distinct molecular mechanism for initiating TRAF6 signalling
1,25-Dihydroxyvitamin D3 Regulates the Expression of Low-Density Lipoprotein Receptor-Related Protein 5
Targeted Overexpression of Insulin-Like Growth Factor I to Osteoblasts of Transgenic Mice: Increased
1,25-Dihydroxyvitamin D3 Stimulates Cyclic Vitamin D Receptor/Retinoid X Receptor DNA-Binding, Co-activator
Androgens Suppress Osteoclast Formation Induced by RANKL and Macrophage-Colony Stimulating Factor
The Human Transient Receptor Potential Vanilloid Type 6 Distal Promoter Contains Multiple Vitamin D
Transcriptional Control of Receptor Activator of Nuclear Factor-B Ligand by the Protein Kinase A
Isolation and characterization of unsaturated fatty acids as natural ligands for the retinoid-X receptorq
2-Methylene-19-nor-(20S)-1,25-dihydroxyvitamin D3 Potently Stimulates Gene-specific DNA Binding of the
A potent analog of 1 ,25-dihydroxyvitamin D3 selectively induces bone formation
IL-4 inhibits osteoclast formation through a direct action on osteoclast precursors via peroxisome
Estrogens suppress RANK ligand-induced osteoclast differentiation via a stromal cell independent
Vitamin D Receptor as a Candidate Tumor-Suppressor Gene in Severe Hyperparathyroidism of Uremia*