S. Periyasamy

发表

Design, synthesis, and neurochemical evaluation of 2-amino-5-(alkoxycarbonyl)-3,4,5,6-tetrahydropyridines and 2-amino-5-(alkoxycarbonyl)-1,4,5,6-tetrahydropyrimidines as M1 muscarinic receptor agonists.

D. A. Smith, P. Dunbar, G. J. Durant, 1994, Journal of medicinal chemistry.

Repression of transforming growth factor-β receptor type I promoter expression by Sp1 deficiency

M. Brattain, S. Periyasamy, S. Ammanamanchi, 2000, Oncogene.

Differential control of expression of type I and type II receptors of transforming growth factor‐β in colon carcinoma cells

Luzhe Sun, M. Brattain, S. Periyasamy, 1996 .

Reconstitution of TGF-beta sensitivity in the VACO-411 human colon carcinoma line by somatic cell fusion with MCF-7.

G. Casey, M. Brattain, S. Periyasamy, 2003, Journal of biomedical science.

Vanadate increases glucocorticoid receptor-mediated gene expression: a novel mechanism for potentiation of a steroid receptor

S. L. Calzi, E. R. Sánchez, S. Periyasamy, 2002, The Journal of Steroid Biochemistry and Molecular Biology.

Essential Role for Co-chaperone Fkbp52 but Not Fkbp51 in Androgen Receptor-mediated Signaling and Physiology*

M. Cohn, Weidong Yong, W. Shou, 2007, Journal of Biological Chemistry.

Synthesis, biochemical activity and behavioral effects of a series of 1,4,5,6-tetrahydropyrimidines as novel ligands for M1 receptors

W. Hoss, K. Ryan, P. Dunbar, 1992 .

Biochemical and behavioral responses of pilocarpine at muscarinic receptor subtypes in the CNS. Comparison with receptor binding and low-energy conformations

W. Hoss, S. Periyasamy, B. Ellerbrock, 1990, Brain Research.

Synthesis and biological characterization of 1,4,5,6-tetrahydropyrimidine and 2-amino-3,4,5,6-tetrahydropyridine derivatives as selective m1 agonists.

P. Dunbar, T. Rho, B. Ojo, 1997, Journal of medicinal chemistry.

Design, synthesis, and neurochemical evaluation of 5-(3-alkyl-1,2,4- oxadiazol-5-yl)-1,4,5,6-tetrahydropyrimidines as M1 muscarinic receptor agonists.

W. Hoss, P. Dunbar, G. J. Durant, 1993, Journal of Medicinal Chemistry.

Synthesis and biochemical activity of novel amidine derivatives as m1 muscarinic receptor agonists.

W. Hoss, P. Dunbar, G. J. Durant, 1996, Bioorganic & medicinal chemistry.

Inhibition of carbachol-stimulated phosphoinositide turnover by U-50,488H in rat hippocampus--involvement of GTP-binding protein.

W. Hoss, S. Periyasamy, 1991, European journal of pharmacology.

Kappa opioid receptors stimulate phosphoinositide turnover in rat brain.

W. Hoss, S. Periyasamy, Wayne Hoss, 1990, Life sciences.

FKBP51 and Cyp40 are Positive Regulators of Androgen-dependent Prostate Cancer Cell Growth and the Targets of FK506 and Cyclosporin A

W. Shou, T. Hinds, E. R. Sánchez, 2009, Oncogene.

1,2,5-Thiadiazole derivatives of arecoline stimulate M1 receptors coupled to phosphoinositide turnover

W. Hoss, S. Periyasamy, P. Sauerberg, 1995, Brain Research.

Targeted ablation reveals a novel role of FKBP52 in gene-specific regulation of glucocorticoid receptor transcriptional activity

Weidong Yong, W. Shou, T. Hinds, 2009, The Journal of Steroid Biochemistry and Molecular Biology.

FK506-binding protein 52 is essential to uterine reproductive physiology controlled by the progesterone receptor A isoform.

Jianming Xu, Weidong Yong, W. Shou, 2006, Molecular endocrinology.

Inhibition of heat shock transcription factor by GR.

E. R. Sánchez, S. Periyasamy, D. Li, 2001, Molecular endocrinology.

The immunophilin ligands cyclosporin A and FK506 suppress prostate cancer cell growth by androgen receptor-dependent and -independent mechanisms.

W. Shou, E. R. Sánchez, S. Periyasamy, 2007, Endocrinology.

Antagonism of glucocorticoid receptor transactivity and cell growth inhibition by transforming growth factor-beta through AP-1-mediated transcriptional repression.

E. R. Sánchez, S. Periyasamy, 2002, The international journal of biochemistry & cell biology.

Control of glucocorticoid and progesterone receptor subcellular localization by the ligand-binding domain is mediated by distinct interactions with tetratricopeptide repeat proteins.

Weidong Yong, W. Shou, T. Hinds, 2008, Biochemistry.

Enhancement of glucocorticoid receptor-mediated gene expression by constitutively active heat shock factor 1.

E. R. Sánchez, S. Periyasamy, S. Wadekar, 2004, Molecular endocrinology.

Regulation of the Phosphoinositide Cascade by Polyamines in Brain

W. Hoss, S. Periyasamy, Wayne Hoss, 1994, Journal of neurochemistry.

Binding of l-[3H]glutamate to repeatedly frozen-thawed rat brain membranes

T. Chiu, S. Periyasamy, Masatoshi Ito, 1987, Neurochemistry International.

Heat and Chemical Shock Potentiation of Glucocorticoid Receptor Transactivation Requires Heat Shock Factor (HSF) Activity

E. R. Sánchez, S. Periyasamy, T. Jones, 2000, The Journal of Biological Chemistry.

Reconstitution of TGF-β Sensitivity in the VACO-411 Human Colon Carcinoma Line by Somatic Cell Fusion with MCF-7

G. Casey, M. Brattain, S. Periyasamy, 2003, Journal of Biomedical Science.

Transforming Growth Factor β Isoform-specific Differences in Interactions with Type I and II Transforming Growth Factor β Receptors

K. M. Mulder, M. Brattain, G. L. Sechrist, 1995 .

Transforming growth factor beta isoform-specific differences in interactions with type I and II transforming growth factor beta receptors.

K. M. Mulder, M. Brattain, G. L. Sechrist, 1995, Cancer Research.

Targeted ablation reveals a novel role of FKBP52 in gene-specific regulation of glucocorticoid receptor transcriptional activity

Weidong Yong, W. Shou, T. Hinds, 2009, The Journal of Steroid Biochemistry and Molecular Biology.

Displaceable binding of [3H]l-glutamic acid to non-receptor materials.

T. Chiu, M. Ito, S. Periyasamy, 1986, Life sciences.

FK506-binding protein 52 is essential to uterine reproductive physiology controlled by the progesterone receptor A isoform.

Jianming Xu, Weidong Yong, W. Shou, 2006, Molecular endocrinology.