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            <depositionDate>2023-01-14</depositionDate>
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        <title>D-cycloserine and glutamate bound human GluN1a-GluN2C NMDA receptor</title>
        <correspondingAuthor>
            <authorORCID>0000-0001-6154-6283</authorORCID>
            <firstName>Tsung Han</firstName>
            <lastName>Chou</lastName>
            <organization type="academic">Cold Spring Harbor Laboratory</organization>
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            <organization type="academic">Cold Spring Harbor Laboratory</organization>
            <street>1 Bungtown Rd</street>
            <townOrCity>Cold Spring Harbor</townOrCity>
            <stateOrProvince>NY</stateOrProvince>
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            <author authorORCID="0000-0001-6154-6283">Chou TH</author>
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                    <author authorORCID="0000-0001-6154-6283" order="1">Chou TH</author>
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                    <author order="3">Simorowski N</author>
                    <author authorORCID="0000-0002-3750-9615" order="4">Traynelis SF</author>
                    <author authorORCID="0000-0001-8296-8426" order="5">Furukawa H</author>
                    <title>Structural insights into assembly and function of GluN1-2C, GluN1-2A-2C, and GluN1-2D NMDARs</title>
                    <journal>Molecular Cell</journal>
                    <journalAbbreviation>Mol Cell</journalAbbreviation>
                    <country>United States</country>
                    <issue>23</issue>
                    <volume>82</volume>
                    <firstPage>4548</firstPage>
                    <lastPage>4563</lastPage>
                    <year>2022</year>
                    <language>English</language>
                    <externalReferences type="doi">10.1016/j.molcel.2022.10.008</externalReferences>
                    <externalReferences type="pubmed">36309015</externalReferences>
                    <details>Structural and functional analysis of human GluN2C- and GluN2D-containing N-methyl-D-aspartate receptors. The results reveal unique inter-subunit and domain arrangements of the GluN2C containing NMDARs. These features explain the mechanism of the binding of the GluN2C specific positive allosteric modulator, PYD-106.</details>
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