(Q73635193)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10751670%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

review article

1 reference

title

Connexin channels in Schwann cells and the development of the X-linked form of Charcot-Marie-Tooth disease (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10751670%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

0 references

C Ressot

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10751670%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

R Bruzzone

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10751670%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

publication date

1 April 2000

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10751670%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

volume

32

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10751670%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10751670%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

page(s)

192-202

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10751670%20AND%20SRC:MED&resulttype=core&format=json

Connections with connexins: the molecular basis of direct intercellular signaling

5 November 2019

cites work

1 reference

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7 January 2021

Gap junctions: getting the message through

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Genetic diseases and gene knockouts reveal diverse connexin functions.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Altered connexin expression after peripheral nerve injury

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Connexin32 in the Peripheral Nervous System: Functional Analysis of Mutations Associated with X-linked Charcot-Marie-Tooth Syndrome and Implications for the Pathophysiology of the Disease

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

From the syndrome of Charcot, Marie and Tooth to disorders of peripheral myelin proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Biology and Genetics of Hereditary Motor and Sensory Neuropathies

1 reference

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7 January 2021

The clinical features of hereditary motor and sensory neuropathy types I and II

1 reference

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7 January 2021

Unwrapping the genes of myelin

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Krox-20 controls myelination in the peripheral nervous system

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

X-linked dominant Charcot-Marie-Tooth disease: suggestion of linkage with a cloned DNA sequence from the proximal Xq.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

X-linked neuropathy: gene localization with DNA probes

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Hereditary motor and sensory neuropathy, X-linked: a half century follow-up

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

X-linked dominant hereditary motor and sensory neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Mapping of the gene for X-linked dominant Charcot-Marie-Tooth neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Intermediate nerve conduction velocities define X-linked Charcot-Marie-Tooth neuropathy families

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

X-linked Charcot-Marie-Tooth disease with connexin 32 mutations: clinical and electrophysiologic study.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Genotype/phenotype correlation in affected individuals of a family with a deletion of the entire coding sequence of the connexin 32 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Mutations of the noncoding region of the connexin32 gene in X-linked dominant Charcot-Marie-Tooth neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Use of alternate promoters for tissue-specific expression of the gene coding for connexin32

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Molecular cloning of cDNA for rat liver gap junction protein

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Cloning and characterization of human and rat liver cDNAs coding for a gap junction protein

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Identification of a rat liver cDNA and mRNA coding for the 28 kDa gap junction protein

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Tight junction contact events and temporary gap junctions in the sciatic nerve fibres of the chicken during Wallerian degeneration and subsequent regeneration

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Distribution of PASII/PMP22 and connexin 32 proteins in the peripheral nervous system

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

From neuro-glue ('Nervenkitt') to glia: a prologue

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

The bicellular and reflexive membrane junctions of renomedullary interstitial cells: functional implications of reflexive gap junctions

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Autocellular coupling by gap junctions in cultured astrocytes: a new view on cellular autoregulation during process formation.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Functional gap junctions in the schwann cell myelin sheath

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Dye coupling between spinal cord oligodendrocytes: differences in coupling efficiency between gray and white matter

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Slowing of central conduction in X-linked Charcot-Marie-Tooth neuropathy shown by brain stem auditory evoked responses

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Central visual, acoustic, and motor pathway involvement in a Charcot-Marie-Tooth family with an Asn205Ser mutation in the connexin 32 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Sensorineural deafness in X-linked Charcot-Marie-Tooth disease with connexin 32 mutation (R142Q)

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Connexin32-null mice develop demyelinating peripheral neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Connexin 32 gap junctions enhance stimulation of glucose output by glucagon and noradrenaline in mouse liver.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Enhanced secretion of amylase from exocrine pancreas of connexin32-deficient mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Coexpression of connexin45 and -32 in oligodendrocytes of rat brain

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Nerve injury and inflammatory cytokines modulate gap junctions in the peripheral nervous system

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Differential expression of three gap junction proteins in developing and mature brain tissues

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Connexin43 and connexin45 form gap junctions with different molecular permeabilities in osteoblastic cells.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Transfected connexin45 alters gap junction permeability in cells expressing endogenous connexin43.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Functional analysis of selective interactions among rodent connexins

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Selectivity of connexin-specific gap junctions does not correlate with channel conductance.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Size and selectivity of gap junction channels formed from different connexins

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Isoform composition of connexin channels determines selectivity among second messengers and uncharged molecules

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Disruption of alpha3 connexin gene leads to proteolysis and cataractogenesis in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Targeted ablation of connexin50 in mice results in microphthalmia and zonular pulverulent cataracts.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Altered trafficking of mutant connexin32

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Mutations of connexin32 in Charcot-Marie-Tooth disease type X interfere with cell-to-cell communication but not cell proliferation and myelin-specific gene expression.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

A cellular mechanism governing the severity of Pelizaeus-Merzbacher disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Overloaded endoplasmic reticulum-Golgi compartments, a possible pathomechanism of peripheral neuropathies caused by mutations of the peripheral myelin protein PMP22.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Impaired intracellular trafficking is a common disease mechanism of PMP22 point mutations in peripheral neuropathies

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Changes in permeability caused by connexin 32 mutations underlie X-linked Charcot-Marie-Tooth disease

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Connexin32 mutations associated with X-linked Charcot-Marie-Tooth disease show two distinct behaviors: loss of function and altered gating properties.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Specific permeability and selective formation of gap junction channels in connexin-transfected HeLa cells

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Cell-free synthesis and assembly of connexins into functional gap junction membrane channels

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Dominant inhibition of intercellular communication by two chimeric connexins.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Heart malformations in transgenic mice exhibiting dominant negative inhibition of gap junctional communication in neural crest cells.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Heterotypic gap junction channels (connexin26 ? connexin32) violate the paradigm of unitary conductance

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Analysis of compound heterozygous mice reveals that the Trembler mutation can behave as a gain-of-function allele

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Transcriptional controls underlying Schwann cell differentiation and myelination

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

The second messenger, cyclic AMP, is not sufficient for myelin gene induction in the peripheral nervous system

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Connexin43: a protein from rat heart homologous to a gap junction protein from liver

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Abnormalities in the axonal cytoskeleton induced by a connexin32 mutation in nerve xenografts.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

Gap junctions formed by connexins 26 and 32 alone and in combination are differently affected by applied voltage

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900081-8

7 January 2021

10.1016/S0165-0173(99)00081-8

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10751670%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

1 reference