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Molecular Neurobiology|January 1, 1990
Molecular mechanisms of cAMP-regulated gene expressionK M Walton, R P RehfussThe Journal of Biological Chemistry|July 26, 1996
Identification and characterization of a novel transcriptional activation domain in the CREB-binding proteinS Bisotto, S Minorgan, R P RehfussProceedings of the National Academy of Sciences of the United States of America|October 1, 1993
Engineered leucine zippers show that hemiphosphorylated CREB complexes are transcriptionally activeM M Loriaux, R P Rehfuss, R G Brennan, et al.The Journal of Biological Chemistry|October 5, 1991
The cAMP-regulated enhancer-binding protein ATF-1 activates transcription in response to cAMP-dependent protein kinase AR P Rehfuss, K M Walton, M M Loriaux, et al.Metabolism: Clinical and Experimental|September 1, 1990
Somatostatin gene regulation: an overviewR H Goodman, R P Rehfuss, M Verhave, et al.Nucleic Acids Research|January 26, 1987
Actinomycin D facilitates transition of AT domains in molecules of sequence (AT)nAGCT(AT)n to a DNAse I detectable alternating structureM J Lane, S Laplante, R P Rehfuss, et al.Molecular Endocrinology (Baltimore, Md.)|October 1, 1992
3',5'-cyclic adenosine monophosphate-regulated enhancer binding (CREB) activity is required for normal growth and differentiated phenotype in the FRTL5 thyroid follicular cell lineP I Woloshin, K M Walton, R P Rehfuss, et al.Molecular Endocrinology (Baltimore, Md.)|April 1, 1992
A dominant repressor of cyclic adenosine 3',5'-monophosphate (cAMP)-regulated enhancer-binding protein activity inhibits the cAMP-mediated induction of the somatostatin promoter in vivoK M Walton, R P Rehfuss, J C Chrivia, et al.Nucleic Acids Research|December 9, 1988
Actinomycin D induced DNase I cleavage enhancement caused by sequence specific propagation of an altered DNA structureY Q Huang, R P Rehfuss, S R LaPlante, et al.Endocrinology|March 10, 1998
Analysis of molecular mechanisms controlling neuroendocrine cell specific transcription of the chromogranin A geneL Canaff, S Bevan, D G Wheeler, et al.Pageof 1