SH3TC2/KIAA1985 protein is required for proper myelination and the integrity of the node of Ranvier in the peripheral nervous system-Reference-Cited by-同舟云学术

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SH3TC2/KIAA1985 protein is required for proper myelination and the integrity of the node of Ranvier in the peripheral nervous system

Published:2009-09-29 Issue:41 Volume:106 Page:17528-17533
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Arnaud E.,Zenker J.,de Preux Charles A.-S.,Stendel C.,Roos A.,Medard J.-J.,Tricaud N.,Kleine H.,Luscher B.,Weis J.,Suter U.,Senderek J.,Chrast R.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference32 articles.

1. Genetic and clinical aspects of Charcot-Marie-Tooth's disease

2. Autosomal recessive form of hereditary motor and sensory neuropathy type I

3. A clinical, electrophysiologic, neuropathologic, and genetic study of two large Algerian families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease

4. Mutations in a Gene Encoding a Novel SH3/TPR Domain Protein Cause Autosomal Recessive Charcot-Marie-Tooth Type 4C Neuropathy

5. The phenotype of Charcot–Marie–Tooth disease type 4C due to SH3TC2 mutations and possible predisposition to an inflammatory neuropathy

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1. Quantitation of the physicochemical properties of myelin using Nile Red fluorescence spectroscopy;Journal of Neurochemistry;2024-08-17

2. Genetic Landscape of SH3TC2 variants in Russian patients with Charcot–Marie–Tooth disease;Frontiers in Genetics;2024-06-06

3. Postnatal persistence of hippocampal Cajal-Retzius cells has a crucial role in the establishment of the hippocampal circuit;Development;2024-01-01

4. Charcot-Marie-Tooth Disease;Reference Module in Neuroscience and Biobehavioral Psychology;2024

5. AAV9-mediated SH3TC2 gene replacement therapy targeted to Schwann cells for the treatment of CMT4C;Molecular Therapy;2023-11

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