熊偉

2001年畢業於北京大學生命科學學院，獲理學學士學位。

2006年畢業於北京大學生命科學學院，獲理學博士學位。

2006至2013年，在美國國立衞生研究院（NIH）酒精濫用與酒精中毒研究所（NIAAA）做博士後研究工作。

2013年3月加入中國科學技術大學生命科學學院。 ^[1] 

長期從事與藥物鎮痛、耐受和成癮有關的神經生物學研究，並運用多種先進的實驗技術對該問題從分子、細胞水平、到動物行為進行了完整的深入系統的研究，並取得了系列重要成果。研究工作發表在Nature Chemical Biology, Journal of Experimental Medicine, Journal of Neuroscience, Molecular Pharmacology等國際學術期刊上。文章被美國藥物依賴研究所（NIDA）評選為“FEATURED PAPER OF THE MONTH”。曾獲得2011年度美國國立衞生研究院頒發給優秀研究人員的獎項“Fellows Award for Research Excellence”。 ^[1] 

1、離子通道受體的調節機制及相關小分子藥物的設計與合成

2、質譜技術在神經科學中的應用

3、情緒認知調節感知覺的神經環路機制 ^[1] 

(1) Cannabinoid potentiation of glycine receptors contributes to cannabis-induced analgesia. - Nature Chemical Biology - 2011 -

(2) Cannabinoids suppress inflammatory and neuropathic pain by targeting α3 glycine receptors - Journal of Experimental Medicine - 2012 -

(3) A Common Molecular Basis for Exogenous and Endogenous Cannabinoid Potentiation of Glycine Receptors. - Journal of Neuroscience - 2012 -

(4) Anandamide Inhibition of 5-HT3A Receptors Varies with Receptor Density and Desensitization. - Molecular Pharmacology - 2008 -

(5) Loss of metabotropic glutamate receptor 2 escalates alcohol consumption - PNAS - 2013 -

(6) Psychotropic and nonpsychotropic cannabis derivatives inhibit human 5-HT3A receptors through a receptor desensitization-dependent mechanism. - Neuroscience - 2011 -

(7) Receptor trafficking induced by μ-opioid-receptor phosphorylation. - Neuroscience & Biobehavioral Review - 2009 -

(8) Mutations M287L and Q266I in the glycine receptor alpha1 subunit change sensitivity to volatile anesthetics in oocytes and neurons, but Not the minimal alveolar concentration in Knockin Mice. - Anesthesiology - 2012 -

(9) Characterization of Two Mutations, M287L and Q266I, in the α1 Glycine Receptor Subunit That Modify Sensitivity to Alcohols. - Journal of Pharmacology and Experimental Therapeutics - 2012 -

(10) Involvement of endogenous cholecystokinin in morphine tolerance in the nucleus accumbens of rats. - Behavioural Brain Research - 2006 -

(11) Involvements of mu- and kappa- opioid receptors in morphine-induced antinociception in the nucleus accumbens of rats. - Neuroscience Letters - 2006 - ^[1]