Elizabeth M. Wilson

University of North Carolina at Chapel Hill — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

68h-index16.0kcitations195works0.02yr avg
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Research Topics

Estrogen and related hormone effects(73), Hormonal and reproductive studies(58), Prostate Cancer Treatment and Research(54), Sexual Differentiation and Disorders(29), Immunotherapy and Immune Responses(21)

Publications195 total

Data from 14-3-3η Amplifies Androgen Receptor Actions in Prostate Cancer
2023Open Access
Supplementary Data from 14-3-3η Amplifies Androgen Receptor Actions in Prostate Cancer
2023Open Access
Supplementary Data from 14-3-3η Amplifies Androgen Receptor Actions in Prostate Cancer
2023Open Access
Data from 14-3-3η Amplifies Androgen Receptor Actions in Prostate Cancer
2023Open Access
Activation Function 2 in the Human Androgen Receptor Ligand Binding Domain Mediates Interdomain Communication with the NH 2 -terminal Domain
UNC Libraries·2021· 20 citedOpen Access
An Androgen Receptor NH 2 -terminal Conserved Motif Interacts with the COOH Terminus of the Hsp70-interacting Protein (CHIP)
UNC Libraries·2021· 4 citedOpen Access
Evidence for an Anti-parallel Orientation of the Ligand-activated Human Androgen Receptor Dimer
UNC Libraries·2021· 3 citedOpen Access
Steroid requirement for androgen receptor dimerization and DNA binding. Modulation by intramolecular interactions between the NH2-terminal and steroid-binding domains.
UNC Libraries·2021Open Access
Liganded Androgen Receptor Interaction with β-Catenin: NUCLEAR CO-LOCALIZATION AND MODULATION OF TRANSCRIPTIONAL ACTIVITY IN NEURONAL CELLS
UNC Libraries·2021· 2 citedOpen Access
Dependence of Selective Gene Activation on the Androgen Receptor NH 2 - and COOH-terminal Interaction
UNC Libraries·2021· 12 citedOpen Access
Probing the Functional Link between Androgen Receptor Coactivator and Ligand-binding Sites in Prostate Cancer and Androgen Insensitivity
UNC Libraries·2021· 3 citedOpen Access
Androgen-induced NH 2 - and COOH-terminal Interaction Inhibits p160 Coactivator Recruitment by Activation Function 2
UNC Libraries·2021· 11 citedOpen Access
Transcriptional repression of the glycoprotein hormone alpha subunit gene by androgen may involve direct binding of androgen receptor to the proximal promoter.
UNC Libraries·2021Open Access
A ligand-dependent bipartite nuclear targeting signal in the human androgen receptor. Requirement for the DNA-binding domain and modulation by NH2-terminal and carboxyl-terminal sequences.
UNC Libraries·2021Open Access
Structural features discriminate androgen receptor N/C terminal and coactivator interactions
UNC Libraries·2021Open Access
Primate-specific Melanoma Antigen-A11 Regulates Isoform-specific Human Progesterone Receptor-B Transactivation
UNC Libraries·2020· 1 citedOpen Access
Gain in Transcriptional Activity by Primate-specific Coevolution of Melanoma Antigen-A11 and Its Interaction Site in Androgen Receptor
UNC Libraries·2020Open Access
Modulation of Androgen Receptor Activation Function 2 by Testosterone and Dihydrotestosterone
UNC Libraries·2020· 1 citedOpen Access
8-Alkylthio-6-thio-substituted theophylline analogues as selective noncompetitive progesterone receptor antagonists
UNC Libraries·2020Open Access
Melanoma Antigen Gene Protein-A11 (MAGE-11) F-box Links the Androgen Receptor NH 2 -terminal Transactivation Domain to p160 Coactivators
UNC Libraries·2020Open Access
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Frequent Co-authors

Frank S. French(12), Bin He(9), Dennis B. Lubahn(8), John T. Minges(5), Madhabananda Sar(4), Jon Kemppainen(4), Christopher W. Gregory(4), Peter Rotwein(4), F.S. French(3), D. Joseph(3), Zhongxiang Zhou(3), M. Sar(3), Suxia Bai(3), Jiann-an Tan(2), Henry N. Higgs(2), Thomas C. Spelsberg(2), T. R. Brown(2), Malcolm V. Lane(2), James L. Mohler(2), William Kelce(2)