Hasil Pencarian - Sandrine Cestèle

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  1. 1
    Gain of Function for the SCN1A/hNav1.1-L1670W Mutation Responsible for Familial Hemiplegic Migraine

    Gain of Function for the SCN1A/hNav1.1-L1670W Mutation Responsible for Familial Hemiplegic Migraine oleh Sandra Dhifallah, Eric Lancaster, Shana Merrill, Nathalie Leroudier, Massimo Mantegazza, Sandrine Cestèle

    Diterbitkan 2018-07-01
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  2. 2
    Rescuable folding defective NaV1.1 (SCN1A) mutants in epilepsy: Properties, occurrence, and novel rescuing strategy with peptides targeted to the endoplasmic reticulum

    Rescuable folding defective NaV1.1 (SCN1A) mutants in epilepsy: Properties, occurrence, and novel rescuing strategy with peptides targeted to the endoplasmic reticulum oleh Giulia Bechi, Raffaella Rusconi, Sandrine Cestèle, Pasquale Striano, Silvana Franceschetti, Massimo Mantegazza

    Diterbitkan 2015-03-01
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  3. 3
    Structure-function relationship of new peptides activating human Nav1.1

    Structure-function relationship of new peptides activating human Nav1.1 oleh Ludivine Lopez, Stephan De Waard, Hervé Meudal, Cécile Caumes, Kuldip Khakh, Steve Peigneur, Barbara Oliveira-Mendes, Sophia Lin, Jolien De Waele, Jérôme Montnach, Sandrine Cestèle, Agnès Tessier, J.P. Johnson, Massimo Mantegazza, Jan Tytgat, Charles Cohen, Rémy Béroud, Frank Bosmans, Céline Landon, Michel De Waard

    Diterbitkan 2023-09-01
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