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Cox, Marc B.

One or more keywords matched the following items that are connected to Cox, Marc B.

Item Type	Name
Academic Article	Targeting the regulation of androgen receptor signaling by the heat shock protein 90 cochaperone FKBP52 in prostate cancer cells.
Academic Article	Inactivation of ID4 promotes a CRPC phenotype with constitutive AR activation through FKBP52.
Concept	Receptors, Androgen
Academic Article	Regulation of steroid hormone receptor function by the 52-kDa FK506-binding protein (FKBP52).
Academic Article	Physiological role for the cochaperone FKBP52 in androgen receptor signaling.
Academic Article	Yeast-based reporter assays for the functional characterization of cochaperone interactions with steroid hormone receptors.
Academic Article	Androgen receptor splice variants are resistant to inhibitors of Hsp90 and FKBP52, which alter androgen receptor activity and expression.
Academic Article	The FKBP52 Cochaperone Acts in Synergy with ?-Catenin to Potentiate Androgen Receptor Signaling.
Academic Article	Similarities and Distinctions in Actions of Surface-Directed and Classic Androgen Receptor Antagonists.
Academic Article	Coregulator control of androgen receptor action by a novel nuclear receptor-binding motif.
Academic Article	The cochaperone SGTA (small glutamine-rich tetratricopeptide repeat-containing protein alpha) demonstrates regulatory specificity for the androgen, glucocorticoid, and progesterone receptors.
Academic Article	Therapeutic Targeting of the FKBP52 Co-Chaperone in Steroid Hormone Receptor-Regulated Physiology and Disease.
Academic Article	Functional Comparison of Human and Zebra Fish FKBP52 Confirms the Importance of the Proline-Rich Loop for Regulation of Steroid Hormone Receptor Activity.

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Receptors Androgen

RCMI CC is supported by the National Institute on Minority Health and Health Disparities, National Institutes of Health (NIH), through Grant Number U24MD015970. The contents of this site are solely the responsibility of the authors and do not necessarily represent the official views of the NIH

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