Chun Hu

2016- Pharmacology Yale University, New Haven, CT 
"Chun Hu"
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Evan P. Lebois research assistant 2012-2015 Emory
Joseph R. Manns research assistant 2012-2015 Emory
Stephen F. Traynelis research assistant 2015-2016 Emory
Minhong Yan research assistant 2017-2017 Genentech Inc.
Mark A. Lemmon grad student 2017- Yale (Chemistry Tree)
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Li J, Zhang J, Tang W, et al. (2019) De Novo GRIN Variants in NMDA Receptor M2 Channel Pore-Forming Loop Are Associated with Neurological Diseases. Human Mutation
Han M, Lyu L, Huang Y, et al. (2019) In situ generation and efficient activation of HO for pollutant degradation over CoMoS nanosphere-embedded rGO nanosheets and its interfacial reaction mechanism. Journal of Colloid and Interface Science. 543: 214-224
Fry AE, Fawcett KA, Zelnik N, et al. (2018) De novo mutations in GRIN1 cause extensive bilateral polymicrogyria. Brain : a Journal of Neurology
Hu C, Chen W, Myers SJ, et al. (2017) Corrigendum to "Human GRIN2B variants in neurodevelopmental disorders" [J Pharmacol Sci 132 (2) 115-121]. Journal of Pharmacological Sciences
Platzer K, Yuan H, Schütz H, et al. (2017) GRIN2B encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects. Journal of Medical Genetics
Gao K, Tankovic A, Zhang Y, et al. (2017) A de novo loss-of-function GRIN2A mutation associated with childhood focal epilepsy and acquired epileptic aphasia. Plos One. 12: e0170818
Ogden KK, Chen W, Swanger SA, et al. (2017) Molecular Mechanism of Disease-Associated Mutations in the Pre-M1 Helix of NMDA Receptors and Potential Rescue Pharmacology. Plos Genetics. 13: e1006536
Swanger SA, Chen W, Wells G, et al. (2016) Mechanistic Insight into NMDA Receptor Dysregulation by Rare Variants in the GluN2A and GluN2B Agonist Binding Domains. American Journal of Human Genetics
Hu C, Chen W, Myers SJ, et al. (2016) Human GRIN2B variants in neurodevelopmental disorders. Journal of Pharmacological Sciences
Li D, Yuan H, Ortiz-Gonzalez XR, et al. (2016) GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers. American Journal of Human Genetics
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