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- 2017
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Mark
Ligand Dependent Switch from RXR Homo- to RXR-NURR1 Heterodimerization
(
- Contribution to journal › Article
- 2016
-
Mark
Estrogen Receptor Beta Selective Agonists as Agents to Treat Chemotherapeutic-Induced Neuropathic Pain
(
- Contribution to journal › Article
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Mark
Chiral Dihydrobenzofuran Acids Show Potent Retinoid X Receptor-Nuclear Receptor Related 1 Protein Dimer Activation.
(
- Contribution to journal › Article
- 2014
-
Mark
Bexarotene prodrugs: Targeting through cleavage by NQO1 (DT-diaphorase).
(
- Contribution to journal › Article
- 2013
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Mark
Low Dose Bexarotene Treatment Rescues Dopamine Neurons and Restores Behavioral Function in Models of Parkinson's Disease
(
- Contribution to journal › Article
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Mark
Design of a Highly Selective and Potent Class of Non-planar Estrogen Receptor Agonists
(
- Contribution to journal › Article
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Mark
The A-CD analogue of 16 beta,17 alpha-estriol is a potent and highly selective estrogen receptor beta agonist
(
- Contribution to journal › Article
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Mark
AC-186, a Selective Nonsteroidal Estrogen Receptor beta Agonist, Shows Gender Specific Neuroprotection in a Parkinson's Disease Rat Model
(
- Contribution to journal › Article
- 2012
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Mark
Discovery of potential antipsychotic agents possessing pro-cognitive properties
(
- Contribution to journal › Article
- 2011
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Mark
Characterization of highly efficacious allosteric agonists of the human calcium-sensing receptor
(
- Contribution to journal › Article
- 2010
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Mark
Optimization of isochromanone based urotensin II receptor agonists
(
- Contribution to journal › Article
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Mark
Discovery of a class of calcium sensing receptor positive allosteric modulators; 1-(benzothiazol-2-yl)-1-phenylethanols
(
- Contribution to journal › Article
- 2009
-
Mark
Discovery of non-peptidergic MrgX1 and MrgX2 receptor agonists and exploration of an initial SAR using solid-phase synthesis
(
- Contribution to journal › Article
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Mark
Synthesis and evaluation of dibenzothiazepines : A novel class of selective cannabinoid-1 receptor inverse agonists
(
- Contribution to journal › Article
- 2008
-
Mark
Discovery of potent and selective small-molecule PAR-2 agonists
(
- Contribution to journal › Article