Lamont Booker, PhD
Affiliations: | Department of Defense |
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"Lamont Booker"Mean distance: 15.98 (cluster 19) | S | N | B | C | P |
Parents
Sign in to add mentor| Aron H. Lichtman | grad student | 2006-2011 | VCU | |
| (Targeting the Endocannabinoid System to Reduce Nociception.) | ||||
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Publications
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| Schlosburg JE, Kinsey SG, Ignatowska-Jankowska B, et al. (2014) Prolonged monoacylglycerol lipase blockade causes equivalent cannabinoid receptor type 1 receptor-mediated adaptations in fatty acid amide hydrolase wild-type and knockout mice. The Journal of Pharmacology and Experimental Therapeutics. 350: 196-204 |
| Booker L, Kinsey SG, Abdullah RA, et al. (2012) The fatty acid amide hydrolase (FAAH) inhibitor PF-3845 acts in the nervous system to reverse LPS-induced tactile allodynia in mice. British Journal of Pharmacology. 165: 2485-96 |
| Schlosburg JE, Blankman JL, Long JZ, et al. (2010) Chronic monoacylglycerol lipase blockade causes functional antagonism of the endocannabinoid system. Nature Neuroscience. 13: 1113-9 |
| Long JZ, Nomura DK, Vann RE, et al. (2009) Dual blockade of FAAH and MAGL identifies behavioral processes regulated by endocannabinoid crosstalk in vivo. Proceedings of the National Academy of Sciences of the United States of America. 106: 20270-5 |
| Booker L, Naidu PS, Razdan RK, et al. (2009) Evaluation of prevalent phytocannabinoids in the acetic acid model of visceral nociception. Drug and Alcohol Dependence. 105: 42-7 |
| Naidu PS, Booker L, Cravatt BF, et al. (2009) Synergy between enzyme inhibitors of fatty acid amide hydrolase and cyclooxygenase in visceral nociception. The Journal of Pharmacology and Experimental Therapeutics. 329: 48-56 |
| Long JZ, Li W, Booker L, et al. (2009) Selective blockade of 2-arachidonoylglycerol hydrolysis produces cannabinoid behavioral effects. Nature Chemical Biology. 5: 37-44 |