SH3TC2/KIAA1985 protein is required for proper myelination and the integrity of the node of Ranvier in the peripheral nervous system (Q24650643)

GOA release 2020-03-11

myelination

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Correction for Arnaud et al., SH3TC2/KIAA1985 protein is required for proper myelination and the integrity of the node of Ranvier in the peripheral nervous system

inferred from title

corrigendum / erratum

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author

Ueli Suter

11

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Nicolas Tricaud

7

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Claudia Stendel

4

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Estelle Arnaud

1

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Jennifer Zenker

2

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Jan Senderek

12

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Jean-Jacques Médard

6

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Roman Chrast

13

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Henning Kleine

object named as

Henning Kleine

8

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author name string

Anne-Sophie de Preux Charles

3

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Andreas Roos

5

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Bernhard Luscher

9

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Joachim Weis

Proceedings of the National Academy of Sciences of the United States of America

10

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language of work or name

English

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publication date

13 October 2009

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published in

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volume

106

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issue

41

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page(s)

17528-33

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cites work

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Mutations in a gene encoding a novel SH3/TPR domain protein cause autosomal recessive Charcot-Marie-Tooth type 4C neuropathy

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The local differentiation of myelinated axons at nodes of Ranvier

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Local regulation of fat metabolism in peripheral nerves

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Glial and neuronal isoforms of Neurofascin have distinct roles in the assembly of nodes of Ranvier in the central nervous system

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Neuron to glia signaling triggers myelin membrane exocytosis from endosomal storage sites

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Disruption of Mtmr2 produces CMT4B1-like neuropathy with myelin outfolding and impaired spermatogenesis

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Recycling endosomes can serve as intermediates during transport from the Golgi to the plasma membrane of MDCK cells

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Bral1, a brain-specific link protein, colocalizing with the versican V2 isoform at the nodes of Ranvier in developing and adult mouse central nervous systems

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Both laminin and Schwann cell dystroglycan are necessary for proper clustering of sodium channels at nodes of Ranvier.

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

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Founder SH3TC2 mutations are responsible for a CMT4C French-Canadians cluster

21 January 2018

1 reference

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Altered ion channels in an animal model of Charcot-Marie-Tooth disease type IA.

21 January 2018

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Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations

21 January 2018

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Nestin-Cre transgenic mouse line Nes-Cre1 mediates highly efficient Cre/loxP mediated recombination in the nervous system, kidney, and somite-derived tissues

21 January 2018

1 reference

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Distinct endocytic recycling of myelin proteins promotes oligodendroglial membrane remodeling

21 January 2018

1 reference

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Altered molecular architecture of peripheral nerves in mice lacking the peripheral myelin protein 22 or connexin32

28 November 2018

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12 December 2020

Pathological findings in the x-linked form of Charcot-Marie-Tooth disease: a morphometric and ultrastructural analysis

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12 December 2020

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

1 reference

12 December 2020

Clinical spectrum of CMT4C disease in patients homozygous for the p.Arg1109X mutation in SH3TC2

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.0905523106

1 reference

ADS bibcode

2009PNAS..10617528A

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1 reference

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PubMed publication ID

19805030

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