Nicole Gong, B.S.

Affiliations: 
Physiology Yale University School of Medicine, New Haven, CT 
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"Nicole Gong"
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Publications

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Xie D, Lu J, Xie J, et al. (2016) Discovery and analgesic evaluation of 8-chloro-1,4-dihydropyrido[2,3-b]pyrazine-2,3-dione as a novel potent d-amino acid oxidase inhibitor. European Journal of Medicinal Chemistry. 117: 19-32
Huang Q, Chen Y, Gong N, et al. (2016) Methylglyoxal mediates streptozotocin-induced diabetic neuropathic pain via activation of the peripheral TRPA1 and Nav1.8 channels. Metabolism: Clinical and Experimental. 65: 463-74
Jia Y, Gong N, Li TF, et al. (2015) Peptidic exenatide and herbal catalpol mediate neuroprotection via the hippocampal GLP-1 receptor/β-endorphin pathway. Pharmacological Research
Fan H, Li TF, Gong N, et al. (2015) Shanzhiside methylester, the principle effective iridoid glycoside from the analgesic herb Lamiophlomis rotata, reduces neuropathic pain by stimulating spinal microglial β-endorphin expression. Neuropharmacology
Ma S, Li XY, Gong N, et al. (2015) Contributions of spinal d-amino acid oxidase to chronic morphine-induced hyperalgesia. Journal of Pharmaceutical and Biomedical Analysis
Fan H, Gong N, Li TF, et al. (2015) The non-peptide GLP-1 receptor agonist WB4-24 blocks inflammatory nociception by stimulating β-endorphin release from spinal microglia. British Journal of Pharmacology. 172: 64-79
Zhu B, Gong N, Fan H, et al. (2014) Lamiophlomis rotata, an orally available Tibetan herbal painkiller, specifically reduces pain hypersensitivity states through the activation of spinal glucagon-like peptide-1 receptors. Anesthesiology. 121: 835-51
Gong N, Fan H, Ma AN, et al. (2014) Geniposide and its iridoid analogs exhibit antinociception by acting at the spinal GLP-1 receptors. Neuropharmacology. 84: 31-45
Wang YC, Lu JM, Jin HZ, et al. (2014) Beneficial effects of natural Jeju groundwaters on lipid metabolism in high-fat diet-induced hyperlipidemic rats. Nutrition Research and Practice. 8: 165-71
Gong N, Xiao Q, Zhu B, et al. (2014) Activation of spinal glucagon-like peptide-1 receptors specifically suppresses pain hypersensitivity. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 34: 5322-34
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