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Publications by Erin M. Rock
A Comparison of Novel, Selective Fatty Acid Amide Hydrolase (FAAH), Monoacyglycerol Lipase (MAGL) or Dual FAAH/MAGL Inhibitors to Suppress Acute and Anticipatory Nausea in Rat Models
Psychopharmacology
Pharmacology
Related publications
FAAH, but Not MAGL, Inhibition Modulates Acute TLR3-induced Neuroimmune Signaling in the Rat, Independent of Sex
Journal of Neuroscience Research
Molecular Neuroscience
Cellular
Progesterone Activates Fatty Acid Amide Hydrolase (FAAH) Promoter in Human T Lymphocytes Through the Transcription Factor Ikaros
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Discovery of 1,5-Diphenylpyrazole-3-Carboxamide Derivatives as Potent, Reversible, and Selective Monoacylglycerol Lipase (MAGL) Inhibitors
Journal of Medicinal Chemistry
Drug Discovery
Molecular Medicine
Rational Development of MAGL Inhibitors
Methods in Molecular Biology
Genetics
Molecular Biology
Discovery of 1,5-Diphenylpyrazole-3-Carboxamide Derivatives as Potent, Reversible, and Selective Monoacylglycerol Lipase (MAGL) Inhibitors
Elevated Anandamide, Enhanced Recall of Fear Extinction, and Attenuated Stress Responses Following Inhibition of Fatty Acid Amide Hydrolase (FAAH): A Randomized, Controlled Experimental Medicine Trial
Biological Psychiatry
Biological Psychiatry
Fatty Acid Amide Hydrolase (FAAH) Inhibitor PF-3845 Reduces Viability, Migration and Invasiveness of Human Colon Adenocarcinoma Colo-205 Cell Line: An in Vitro Study
Acta Biochimica Polonica
Biochemistry
Genetics
Molecular Biology
Exploration of a Fundamental Substituent Effect of Α-Ketoheterocycle Enzyme Inhibitors: Potent and Selective Inhibitors of Fatty Acid Amide Hydrolase
Bioorganic and Medicinal Chemistry Letters
Organic Chemistry
Molecular Medicine
Molecular Biology
Biochemistry
Clinical Biochemistry
Pharmaceutical Science
Drug Discovery
Optimization of a Benzoylpiperidine Class Identifies a Highly Potent and Selective Reversible Monoacylglycerol Lipase (MAGL) Inhibitor