Post-translational dysfunctions in channelopathies of the nervous system-Reference-Cited by-同舟云学术

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Post-translational dysfunctions in channelopathies of the nervous system

Published:2018-04 Issue: Volume:132 Page:31-42
ISSN:0028-3908
Container-title:Neuropharmacology
language:en
Short-container-title:Neuropharmacology

Author:

Terragni Benedetta,Scalmani Paolo,Franceschetti Silvana,Cestèle Sandrine,Mantegazza Massimo^ORCID

Funder

European Union projects DESIRE

PROPANE study

Investissements d'Avenir-Laboratory of Excellence “Ion Channel Science and Therapeutics”

CNRS “International Project for Scientific Cooperation”

Italian Foundation for Research on Epilepsy

Publisher

Elsevier BV

Subject

Cellular and Molecular Neuroscience,Pharmacology

Reference123 articles.

1. FHF1 (FGF12) epileptic encephalopathy;Al-Mehmadi;Neurol. Genet.,2016

2. Two novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus;Annesi;Epilepsia,2003

3. Reciprocal changes in phosphorylation and methylation of mammalian brain sodium channels in response to seizures;Baek;J. Biol. Chem.,2014

4. Pure haploinsufficiency for Dravet syndrome Na(V)1.1 (SCN1A) sodium channel truncating mutations;Bechi;Epilepsia,2012

5. Rescuable folding defective NaV1.1 (SCN1A) mutants in epilepsy: properties, occurrence, and novel rescuing strategy with peptides targeted to the endoplasmic reticulum;Bechi;Neurobiol. Dis.,2015

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1. Voltage‐gated sodium channels in genetic epilepsy: up and down of excitability;Journal of Neurochemistry;2023-08-31

2. Perspective on the Effect of Membrane Mimetics on Dynamic Properties of Integral Membrane Proteins;The Journal of Physical Chemistry B;2023-04-20

3. SCN1A channelopathies: Navigating from genotype to neural circuit dysfunction;Frontiers in Neurology;2023-04-17

4. Gain of function SCN1A disease‐causing variants: Expanding the phenotypic spectrum and functional studies guiding the choice of effective antiseizure medication;Epilepsia;2023-01-26

5. Developmental and epileptic encephalopathies: from genetic heterogeneity to phenotypic continuum;Physiological Reviews;2023-01-01

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