Hasil Pencarian - Robin N. Stringer

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  1. 1
    Pathophysiology of ion channels in amyotrophic lateral sclerosis

    Pathophysiology of ion channels in amyotrophic lateral sclerosis oleh Robin N. Stringer, Norbert Weiss

    Diterbitkan 2023-12-01
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  2. 2
    Electrophysiological characterization of a Cav3.2 calcium channel missense variant associated with epilepsy and hearing loss

    Electrophysiological characterization of a Cav3.2 calcium channel missense variant associated with epilepsy and hearing loss oleh Robin N. Stringer, Leos Cmarko, Gerald W. Zamponi, Michel De Waard, Norbert Weiss

    Diterbitkan 2023-09-01
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  3. 3
    Secretory carrier-associated membrane protein 2 (SCAMP2) regulates cell surface expression of T-type calcium channels

    Secretory carrier-associated membrane protein 2 (SCAMP2) regulates cell surface expression of T-type calcium channels oleh Leos Cmarko, Robin N. Stringer, Bohumila Jurkovicova-Tarabova, Tomas Vacik, Lubica Lacinova, Norbert Weiss

    Diterbitkan 2022-01-01
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  4. 4
    Electrophysiological and computational analysis of Cav3.2 channel variants associated with familial trigeminal neuralgia

    Electrophysiological and computational analysis of Cav3.2 channel variants associated with familial trigeminal neuralgia oleh Emilio R. Mustafá, Eder Gambeta, Robin N. Stringer, Ivana A. Souza, Gerald W. Zamponi, Norbert Weiss

    Diterbitkan 2022-11-01
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  5. 5
    Functional identification of potential non-canonical N-glycosylation sites within Cav3.2 T-type calcium channels

    Functional identification of potential non-canonical N-glycosylation sites within Cav3.2 T-type calcium channels oleh Vendula Ficelova, Ivana A. Souza, Leos Cmarko, Maria A. Gandini, Robin N. Stringer, Gerald W. Zamponi, Norbert Weiss

    Diterbitkan 2020-11-01
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  6. 6
    De novo SCN8A and inherited rare CACNA1H variants associated with severe developmental and epileptic encephalopathy

    De novo SCN8A and inherited rare CACNA1H variants associated with severe developmental and epileptic encephalopathy oleh Robin N. Stringer, Bohumila Jurkovicova-Tarabova, Ivana A. Souza, Judy Ibrahim, Tomas Vacik, Waseem Mahmoud Fathalla, Jozef Hertecant, Gerald W. Zamponi, Lubica Lacinova, Norbert Weiss

    Diterbitkan 2021-08-01
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  7. 7
    A rare CACNA1H variant associated with amyotrophic lateral sclerosis causes complete loss of Cav3.2 T-type channel activity

    A rare CACNA1H variant associated with amyotrophic lateral sclerosis causes complete loss of Cav3.2 T-type channel activity oleh Robin N. Stringer, Bohumila Jurkovicova-Tarabova, Sun Huang, Omid Haji-Ghassemi, Romane Idoux, Anna Liashenko, Ivana A. Souza, Yuriy Rzhepetskyy, Lubica Lacinova, Filip Van Petegem, Gerald W. Zamponi, Roger Pamphlett, Norbert Weiss

    Diterbitkan 2020-03-01
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