Hyperexcitability in Cultured Cortical Neuron Networks from the G93A-SOD1 Amyotrophic Lateral Sclerosis Model Mouse and its Molecular Correlates

Autor: Marcuzzo, Stefania, Terragni, Benedetta, Bonanno, Silvia, Isaia, Davide, Cavalcante, Paola, Cappelletti, Cristina, Ciusani, Emilio, Rizzo, Ambra, Regalia, Giulia, Yoshimura, Natsue, Ugolini, Giovanni Stefano, Rasponi, Marco, Bechi, Giulia, Mantegazza, Massimo, Mantegazza, Renato, Bernasconi, Pia, Minati, Ludovico

Publikováno v: In Neuroscience 15 September 2019 416:88-99

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

Autor: Cestèle, Sandrine, Bechi, Giulia, Rusconi, Raffaella, Cestele, Sandrine, Striano, Pasquale, Franceschetti, Silvana, Mantegazza, Massimo

Publikováno v: Neurobiology of Disease
Neurobiology of Disease, 2015, 75, pp.100-114. ⟨10.1016/j.nbd.2014.12.028⟩
Neurobiology of Disease, Elsevier, 2015, 75, pp.100-114. ⟨10.1016/j.nbd.2014.12.028⟩
Neurobiology of Disease, Vol 75, Iss, Pp 100-114 (2015)

Mutations of the voltage gated Na(+) channel Na(V)1.1 (SCN1A) are important causes of different genetic epilepsies and can also cause familial hemiplegic migraine (FHM-III). In previous studies, some rescuable epileptogenic folding defective mutants

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d97686996c42a50406ea83dc0de68dce
https://hal.science/hal-02352057

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