(Q73382747)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9169515%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

title

Structural abnormalities and deficient maintenance of peripheral nerve myelin in mice lacking the gap junction protein connexin 32 (English)

1 reference

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3 November 2019

author name string

P Anzini

1

1 reference

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3 November 2019

D H Neuberg

2

1 reference

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3 November 2019

E Nelles

4

1 reference

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3 November 2019

K Willecke

5

1 reference

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3 November 2019

J Zielasek

6

1 reference

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3 November 2019

K V Toyka

7

1 reference

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3 November 2019

U Suter

8

1 reference

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3 November 2019

publication date

1 June 1997

1 reference

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3 November 2019

published in

Journal of Neuroscience

1 reference

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3 November 2019

volume

17

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3 November 2019

issue

12

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3 November 2019

page(s)

4545-4551

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Cardiac malformation in neonatal mice lacking connexin43.

3 November 2019

cites work

1 reference

12 December 2020

Connexin43 is another gap junction protein in the peripheral nervous system.

1 reference

12 December 2020

Charcot-Marie-Tooth disease and related inherited neuropathies

1 reference

12 December 2020

Biology and Genetics of Hereditary Motor and Sensory Neuropathies

1 reference

12 December 2020

Correlation between connexin 32 gene mutations and clinical phenotype in X-linked dominant Charcot-Marie-Tooth neuropathy

1 reference

12 December 2020

A study of degeneration and regeneration in the divided rat sciatic nerve based on electron microscopy. II. The development of the "regenerating unit"

1 reference

12 December 2020

New functions for gap junctions

1 reference

12 December 2020

A connexin-32 mutation associated with Charcot-Marie-Tooth disease does not affect channel formation in oocytes.

1 reference

12 December 2020

Mice doubly deficient in the genes for P0 and myelin basic protein show that both proteins contribute to the formation of the major dense line in peripheral nerve myelin

1 reference

12 December 2020

Absence of the myelin-associated glycoprotein (MAG) and the neural cell adhesion molecule (N-CAM) interferes with the maintenance, but not with the formation of peripheral myelin

1 reference

12 December 2020

Connexin mutations in X-linked Charcot-Marie-Tooth disease

1 reference

12 December 2020

Molecular basis of common hereditary motor and sensory neuropathies in humans and in mouse models

1 reference

12 December 2020

Molecular cloning of mouse connexins26 and -32: similar genomic organization but distinct promoter sequences of two gap junction genes

1 reference

12 December 2020

Connections with connexins: the molecular basis of direct intercellular signaling

1 reference

12 December 2020

Impaired differentiation of Schwann cells in transgenic mice with increased PMP22 gene dosage

1 reference

12 December 2020

Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice

1 reference

12 December 2020

Connexin 32 mutations from X-linked Charcot-Marie-Tooth disease patients: functional defects and dominant negative effects

1 reference

12 December 2020

Mouse P0 gene disruption leads to hypomyelination, abnormal expression of recognition molecules, and degeneration of myelin and axons.

1 reference

12 December 2020

Connexin32 is a myelin-related protein in the PNS and CNS

1 reference

12 December 2020

Node-paranode regions as local degradative centres in alpha-motor axons

1 reference

12 December 2020

A transgenic rat model of Charcot-Marie-Tooth disease

1 reference

12 December 2020

Mutations of the Connexin43 gap-junction gene in patients with heart malformations and defects of laterality

1 reference

12 December 2020

X-linked dominant Charcot-Marie-Tooth disease and other potential gap-junction diseases of the nervous system

1 reference

12 December 2020

Linkage and mutation analysis of Charcot-Marie-Tooth neuropathy type 2 families with chromosomes 1p35-p36 and Xq13

1 reference

12 December 2020

Defective propagation of signals generated by sympathetic nerve stimulation in the liver of connexin32-deficient mice

1 reference

12 December 2020

Functional abnormalities in P0-deficient mice resemble human hereditary neuropathies linked to P0 gene mutations

1 reference

12 December 2020

A leucine-to-proline mutation in the putative first transmembrane domain of the 22-kDa peripheral myelin protein in the trembler-J mouse

1 reference

12 December 2020

Protein zero (P0)-deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathies

1 reference

12 December 2020

Null mutations of connexin32 in patients with X-linked Charcot-Marie-Tooth disease.

1 reference

12 December 2020

Crucial role for the myelin-associated glycoprotein in the maintenance of axon-myelin integrity

1 reference

12 December 2020

Connexins, gap junctions and cell-cell signalling in the nervous system

1 reference

12 December 2020

The gap junction communication channel

1 reference

12 December 2020

Trembler mouse carries a point mutation in a myelin gene

1 reference

12 December 2020

10.1523/JNEUROSCI.17-12-04545.1997

Identifiers

DOI

1 reference

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3 November 2019

1 reference

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3 November 2019

PubMed publication ID

9169515

1 reference