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Discovery of the Potent and Selective M1 PAM-Agonist N-[(3R,4S)-3-Hydroxytetrahydro-2H-pyran-4-yl]-5-methyl-4-[4-(1,3-thiazol-4-yl)benzyl]pyridine-2-carboxamide (PF-06767832): Evaluation of Efficacy and Cholinergic Side Effects | Journal of Medicinal ...
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Inhibition of mutant RAS-RAF interaction by mimicking structural and dynamic properties of phosphorylated RAS | eLife
The CIC-ERF co-deletion underlies fusion-independent activation of ETS family member, ETV1, to drive prostate cancer progression | eLife
Development of M1 mAChR Allosteric and Bitopic Ligands: Prospective Therapeutics for the Treatment of Cognitive Deficits | ACS Chemical Neuroscience
Inhibition of mutant RAS-RAF interaction by mimicking structural and dynamic properties of phosphorylated RAS | eLife
Engineering SHP2 Phosphatase for Optical Control | Biochemistry
Hydrogenation and Redox Isomerization of Allylic Alcohols Catalyzed by a New Water-Soluble Pd–tetrahydrosalen Complex | Organometallics
Surface Probing by Fragment-Based Screening and Computational Methods Identifies Ligandable Pockets on the von Hippel–Lindau (VHL) E3 Ubiquitin Ligase | Journal of Medicinal Chemistry
Special Report: After the assassination 2008-2013 - DAWN.COM
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Recent Advances of SHP2 Inhibitors in Cancer Therapy: Current Development and Clinical Application | Journal of Medicinal Chemistry
World Development Report 2022 by World Bank Publications - Issuu
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