Progression of motor axon dysfunction and ectopic Nav1.8 expression in a mouse model of Charcot-Marie-Tooth disease 1B-Reference-Cited by-同舟云学术

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Progression of motor axon dysfunction and ectopic Nav1.8 expression in a mouse model of Charcot-Marie-Tooth disease 1B

Published:2016-09 Issue: Volume:93 Page:201-214
ISSN:0969-9961
Container-title:Neurobiology of Disease
language:en
Short-container-title:Neurobiology of Disease

Author:

Rosberg Mette R.,Alvarez Susana,Klein Dennis,Nielsen Finn Cilius,Martini Rudolf,Levinson S. Rock,Krarup Christian,Moldovan Mihai^ORCID

Funder

Lundbeck Foundation

Novo Nordisk Foundation

Danish Medical Research Council

Ludvig and Sara Elsass Foundation

Foundation for Research in Neurology

Jytte and Kaj Dahlboms Foundation

Publisher

Elsevier BV

Subject

Neurology

Reference83 articles.

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2. The tetrodotoxin-resistant sodium channel SNS has a specialized function in pain pathways;Akopian;Nat. Neurosci.,1999

3. Prolonged high frequency electrical stimulation is lethal to motor axons of mice heterozygously deficient for the myelin protein P(0) gene;Alvarez;Exp. Neurol.,2013

4. Effect of an R69C mutation in the myelin protein zero gene on myelination and ion channel subtypes;Bai;Arch. Neurol.,2006

5. Intracellular recording from vertebrate myelinated axons: mechanism of the depolarizing afterpotential;Barrett;J. Physiol.,1982

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1. Phenotypic spectrum of myelin protein zero-related neuropathies: a large cohort study from five mutation clusters across Italy;Journal of Neurology, Neurosurgery & Psychiatry;2024-06-05

2. Presymptomatic macrophage targeting has a long-lasting therapeutic effect on treatment termination in a mouse model of Charcot-Marie-Tooth 1;Experimental Neurology;2022-11

3. Challenges in Treating Charcot-Marie-Tooth Disease and Related Neuropathies: Current Management and Future Perspectives;Brain Sciences;2021-10-29

4. Therapeutic Development in Charcot Marie Tooth Type 1 Disease;International Journal of Molecular Sciences;2021-06-23

5. Myelin protein zero gene dose dependent axonal ion-channel dysfunction in a family with Charcot-Marie-Tooth disease;Clinical Neurophysiology;2020-10

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