Suchergebnisse - Hongjie Yuan

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  1. 1
    GRIN2D/GluN2D NMDA receptor: Unique features and its contribution to pediatric developmental and epileptic encephalopathy

    GRIN2D/GluN2D NMDA receptor: Unique features and its contribution to pediatric developmental and epileptic encephalopathy von Chad R. Camp, Hongjie Yuan

    Veröffentlicht 2019
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  2. 2
    De novo mutations and rare variants occurring in NMDA receptors

    De novo mutations and rare variants occurring in NMDA receptors von Wenshu XiangWei, Yuwu Jiang, Hongjie Yuan

    Veröffentlicht 2017
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  3. 3
    Conserved Structural and Functional Control of N-Methyl-d-aspartate Receptor Gating by Transmembrane Domain M3

    Conserved Structural and Functional Control of N-Methyl-d-aspartate Receptor Gating by Transmembrane Domain M3 von Hongjie Yuan, Kevin Erreger, Shashank M. Dravid, Stephen F. Traynelis

    Veröffentlicht 2005
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  4. 4
    Distinct Functional and Pharmacological Properties of Triheteromeric GluN1/GluN2A/GluN2B NMDA Receptors

    Distinct Functional and Pharmacological Properties of Triheteromeric GluN1/GluN2A/GluN2B NMDA Receptors von Kasper B. Hansen, Kevin K. Ogden, Hongjie Yuan, Stephen F. Traynelis

    Veröffentlicht 2014
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  5. 5
    Human GRIN2B variants in neurodevelopmental disorders

    Human GRIN2B variants in neurodevelopmental disorders von Chun Hu, Wenjuan Chen, Scott J. Myers, Hongjie Yuan, Stephen F. Traynelis

    Veröffentlicht 2016
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  6. 6
    Ionotropic GABA and Glutamate Receptor Mutations and Human Neurologic Diseases

    Ionotropic GABA and Glutamate Receptor Mutations and Human Neurologic Diseases von Hongjie Yuan, Chian‐Ming Low, Olivia A. Moody, Andrew Jenkins, Stephen F. Traynelis

    Veröffentlicht 2015
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  7. 7
    Control of NMDA Receptor Function by the NR2 Subunit Amino-Terminal Domain

    Control of NMDA Receptor Function by the NR2 Subunit Amino-Terminal Domain von Hongjie Yuan, Kasper B. Hansen, Katie M. Vance, Kevin K. Ogden, Stephen F. Traynelis

    Veröffentlicht 2009
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  8. 8
    Functional Evaluation of a De Novo <i>GRIN2A</i> Mutation Identified in a Patient with Profound Global Developmental Delay and Refractory Epilepsy

    Functional Evaluation of a De Novo <i>GRIN2A</i> Mutation Identified in a Patient with Profound Global Developmental Delay and Refractory Epilepsy von Wenjuan Chen, Anel Tankovic, Pieter B. Burger, Hirofumi Kusumoto, Stephen F. Traynelis, Hongjie Yuan

    Veröffentlicht 2017
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  9. 9
    Astrocytic control of synaptic NMDA receptors

    Astrocytic control of synaptic NMDA receptors von C. Justin Lee, Guido Mannaioni, Hongjie Yuan, Dong Ho Woo, Melissa B. Gingrich, Stephen F. Traynelis

    Veröffentlicht 2007
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  10. 10
    Distinct roles of GRIN2A and GRIN2B variants in neurological conditions

    Distinct roles of GRIN2A and GRIN2B variants in neurological conditions von Scott J. Myers, Hongjie Yuan, Jing‐Qiong Kang, Francis Chee Kuan Tan, Stephen F. Traynelis, Chian‐Ming Low

    Veröffentlicht 2019
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  11. 11
    Triheteromeric GluN1/GluN2A/GluN2C NMDARs with Unique Single-Channel Properties Are the Dominant Receptor Population in Cerebellar Granule Cells

    Triheteromeric GluN1/GluN2A/GluN2C NMDARs with Unique Single-Channel Properties Are the Dominant Receptor Population in Cerebellar Granule Cells von Subhrajit Bhattacharya, Alpa Khatri, Sharon A. Swanger, John O. DiRaddo, Feng Yi, Kasper B. Hansen, Hongjie Yuan, Stephen F. Traynelis

    Veröffentlicht 2018
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  12. 12
    Therapeutic potential of N-methyl-D-aspartate receptor modulators in psychiatry

    Therapeutic potential of N-methyl-D-aspartate receptor modulators in psychiatry von Jesse E. Hanson, Hongjie Yuan, Riley E. Perszyk, Tue G. Banke, Hao Xing, Ming‐Chi Tsai, Frank S. Menniti, Stephen F. Traynelis

    Veröffentlicht 2023
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  13. 13
    A Rare Variant Identified Within the GluN2B C-Terminus in a Patient with Autism Affects NMDA Receptor Surface Expression and Spine Density

    A Rare Variant Identified Within the GluN2B C-Terminus in a Patient with Autism Affects NMDA Receptor Surface Expression and Spine Density von Shuxi Liu, Liang Zhou, Hongjie Yuan, Marta Vieira, Antonio Sanz-Clemente, John D. Badger, Wei Lü, Stephen F. Traynelis, Katherine W. Roche

    Veröffentlicht 2017
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  14. 14
    Clinical and therapeutic significance of genetic variation in the GRIN gene family encoding NMDARs

    Clinical and therapeutic significance of genetic variation in the GRIN gene family encoding NMDARs von Tim A. Benke, Kristen Park, Ilona Krey, Chad R. Camp, Rui Song, Amy J. Ramsey, Hongjie Yuan, Stephen F. Traynelis, Johannes R. Lemke

    Veröffentlicht 2021
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  15. 15
    A de novo loss-of-function GRIN2A mutation associated with childhood focal epilepsy and acquired epileptic aphasia

    A de novo loss-of-function GRIN2A mutation associated with childhood focal epilepsy and acquired epileptic aphasia von Kai Gao, Anel Tankovic, Yujia Zhang, Hirofumi Kusumoto, Jin Zhang, Wenjuan Chen, Wenshu XiangWei, Gil Shaulsky, Chun Hu, Stephen F. Traynelis, Hongjie Yuan, Yuwu Jiang

    Veröffentlicht 2017
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  16. 16
    Glutamate Receptor Ion Channels: Structure, Regulation, and Function

    Glutamate Receptor Ion Channels: Structure, Regulation, and Function von Stephen F. 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

    Veröffentlicht 2010
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  17. 17
    Mechanism for Noncompetitive Inhibition by Novel GluN2C/D <i>N</i>-Methyl-d-aspartate Receptor Subunit-Selective Modulators

    Mechanism for Noncompetitive Inhibition by Novel GluN2C/D <i>N</i>-Methyl-d-aspartate Receptor Subunit-Selective Modulators von Timothy M. Acker, Hongjie Yuan, Kasper B. Hansen, Katie M. Vance, Kevin K. Ogden, Henrik Jensen, Pieter B. Burger, Praseeda Mullasseril, James P. Snyder, Dennis C. Liotta, Stephen F. Traynelis

    Veröffentlicht 2011
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  18. 18
    GRIN1 mutation associated with intellectual disability alters NMDA receptor trafficking and function

    GRIN1 mutation associated with intellectual disability alters NMDA receptor trafficking and function von Wenjuan Chen, Christine Shieh, Sharon A. Swanger, Anel Tankovic, Margaret Au, Marianne McGuire, Michele Tagliati, John M. Graham, Suneeta Madan‐Khetarpal, Stephen F. Traynelis, Hongjie Yuan, Tyler Mark Pierson

    Veröffentlicht 2017
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  19. 19
    A subunit-selective potentiator of NR2C- and NR2D-containing NMDA receptors

    A subunit-selective potentiator of NR2C- and NR2D-containing NMDA receptors von Praseeda Mullasseril, Kasper B. Hansen, Katie M. Vance, Kevin K. Ogden, Hongjie Yuan, Natalie L. Kurtkaya, Rose Santangelo, Anna G. Orr, Phuong T. Le, Kimberly Vellano, Dennis C. Liotta, Stephen F. Traynelis

    Veröffentlicht 2010
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  20. 20
    Classification of missense variants in the <i>N</i>-methyl-<scp>d</scp>-aspartate receptor <i>GRIN</i> gene family as gain- or loss-of-function

    Classification of missense variants in the <i>N</i>-methyl-<scp>d</scp>-aspartate receptor <i>GRIN</i> gene family as gain- or loss-of-function von Scott J. Myers, Hongjie Yuan, Riley E. Perszyk, Jing Zhang, Sukhan Kim, Kelsey A. Nocilla, James P. Allen, Jennifer Bain, Johannes R. Lemke, Dennis Lal, Tim A. Benke, Stephen F. Traynelis

    Veröffentlicht 2023
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