Hongjie Yuan MD, PhD

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Works 1-10 of 29

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Article

Synthesis and Preliminary Evaluations of a Triazole-Cored Antagonist as a PET Imaging Probe ([F-18]N2B-0518) for GluN2B Subunit in the Brain

by Hualong Fu; Weiting Tang; Zhen Chen; Vasily V. Belov; Genwei Zhang; Tuo Shao; Xiaofei Zhang; Qingzhen Yu; Jian Rong; Xiaoyun Deng; Wei Han; Scott Myers; Pilar Giffenig; Lu Wang; Lee Josephson; Yihan Shao; April T. Davenport; James B. Daunais; Mikhail Papisov; Hongjie Yuan; Zijing Li; Stephen Traynelis; Steven H. Liang

2019

Article

De novo GRIN variants in NMDA receptor M2 channel pore-forming loop are associated with neurological diseases

by Jia Li; Jin Zhang; Weiting Tang; Ruth K. Mizu; Hirofumi Kusumoto; Wenshu XiangWei; Yuchen Xu; Wenjuan Chen; Johansen B. Amin; Eduardo Perozo; Chun Hu; Varun Kannan; Stephanie Keller; William Wilcox; Johannes R. Lemke; Scott Myers; Sharon A. Swanger; Lonnie P. Wollmuth; Slave Petrovski; Stephen Traynelis; Hongjie Yuan

2019

Article

Glutamate Receptor Ion Channels: Structure, Regulation, and Function

by Stephen Traynelis; Lonnie P. Wollmuth; Chris J. McBain; Frank S. Menniti; Katie M. Vance; Kevin K. Ogden; Kasper B. Hansen; Hongjie Yuan; Scott J. Myers; Raymond Dingledine

2010

Article

De novo mutations in GRIN1 cause extensive bilateral polymicrogyria

by Andrew E. Fry; Katherine A. Fawcett; Nathanel Zelnik; Hongjie Yuan; Belinda A.N. Thompson; Lilach Shemer-Meiri; Thomas D. Cushion; Hood Mugalaasi; David Sims; Neil Stoodley; Seo-Kyung Chung; Mark I. Rees; Chirag V. Patel; Louise A. Brueton; Valerie Layet; Fabienne Giuliano; Michael P. Kerr; Ehud Banne; Vardiella Meiner; Tally Lerman-Sagie; Katherine L. Helbig; Laura H. Kofman; Kristin M. Knight; Wenjuan Chen; Varun Kannan; Chun Hu; Hirofumi Kusumoto; Jin Zhang; Sharon A. Swanger; Gil H. Shaulsky; Ghadya M. Mirzaa; Alison M. Muir; Heather C. Mefford; William B. Dobyns; Amanda B. Mackenzie; Jonathan G.L> Mullins; Johannes R. Lemke; Nadia Bahi-Buisson; Stephen Traynelis; Heledd F. Iago; Daniela T. Pilz

2018

Article

Adenovo loss-of-function GRIN2A mutation associated with childhood focal epilepsy and acquired epileptic aphasia

by Kai Gao; Anel Tankovic; Yujia Zhang; Hirofumi Kusumoto; Jin Zhang; Wenjuan Chen; Wenshu Xiangwei; Gil H. Shaulsky; Chun Hu; Stephen Traynelis; Hongjie Yuan; Yuwu Jiang

2017

Article

A Novel Missense Mutation in GRIN2A Causes a Nonepileptic Neurodevelopmental Disorder

by Ana Fernandez-Marmiesse; Hirofumi Kusumoto; Saray Rekarte; Iria Roca; Jin Zhang; Scott J. Myers; Stephen Traynelis; Ma Luz Couce; Luis Gutierrez-Solana; Hongjie Yuan

2018

Article

Mechanism for Noncompetitive Inhibition by Novel GluN2C/D N-Methyl-d-aspartate Receptor Subunit-Selective Modulators

by Timothy M. Acker; Hongjie Yuan; Kasper B. Hansen; Katie M. Vance; Kevin K. Ogden; Henrik S. Jensen; Pieter B. Burger; Praseeda Mullasseril; James P Snyder; Dennis C Liotta; Stephen Traynelis

2011