Transgenic expression of human connexin32 in myelinating Schwann cells prevents demyelination in connexin32-null mice (Q81386114)

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8 January 2020

title

Transgenic expression of human connexin32 in myelinating Schwann cells prevents demyelination in connexin32-null mice (English)

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8 January 2020

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Steven S Scherer

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8 January 2020

author name string

Yi-Tian Xu

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8 January 2020

Albee Messing

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8 January 2020

Klaus Willecke

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Kenneth H Fischbeck

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Linda Jo Bone Jeng

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8 January 2020

publication date

1 February 2005

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8 January 2020

published in

Journal of Neuroscience

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volume

25

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issue

6

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page(s)

1550-1559

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Studies in transgenic mice indicate a loss of connexin32 function in X-linked Charcot-Marie-Tooth disease

8 January 2020

cites work

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12 December 2020

Long-term changes in connexin32 gap junction protein and mRNA expression following cocaine self-administration in rats

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X-linked dominant Charcot-Marie-Tooth neuropathy: clinical, electrophysiological, and morphological phenotype in four families with different connexin32 mutations(1).

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P(0) glycoprotein overexpression causes congenital hypomyelination of peripheral nerves

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

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Differential expression of connexin26 and connexin32 in the pre-Bötzinger complex of neonatal and adult rat.

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Nogo-A expressed in Schwann cells impairs axonal regeneration after peripheral nerve injury

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Preserved myelin integrity and reduced axonopathy in connexin32-deficient mice lacking the recombination activating gene-1.

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Tamoxifen-inducible glia-specific Cre mice for somatic mutagenesis in oligodendrocytes and Schwann cells

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Disease mechanisms in inherited neuropathies

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P0 promoter directs expression of reporter and toxin genes to Schwann cells of transgenic mice.

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Connexin32-containing gap junctions in Schwann cells at the internodal zone of partial myelin compaction and in Schmidt-Lanterman incisures

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Subsurface cisterns in alpha-motoneurons of the rat and cat: immunohistochemical detection with antibodies against connexin32.

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Protein zero of peripheral nerve myelin: biosynthesis, membrane insertion, and evidence for homotypic interaction.

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The myelin-associated glycoproteins: membrane disposition, evidence of a novel disulfide linkage between immunoglobulin-like domains, and posttranslational palmitylation.

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FVB/N: an inbred mouse strain preferable for transgenic analyses

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Heterologous introns can enhance expression of transgenes in mice

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Antibody-mediated demyelination in experimental allergic encephalomyelitis is independent of complement membrane attack complex formation

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X-linked dominant hereditary motor and sensory neuropathy

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Differential ultrastructural localization of myelin basic protein, myelin/oligodendroglial glycoprotein, and 2',3'-cyclic nucleotide 3'-phosphodiesterase in the CNS of adult rats

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Isolation and analysis of the gene encoding peripheral myelin protein zero

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Monoclonal antibodies distinguish several differentially phosphorylated states of the two largest rat neurofilament subunits (NF-H and NF-M) and demonstrate their existence in the normal nervous system of adult rats

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Introns increase transcriptional efficiency in transgenic mice

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

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Motoneurons of the rat sciatic nerve

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Factors affecting the efficiency of introducing foreign DNA into mice by microinjecting eggs

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Monoclonal antibodies recognize individual neurofilament triplet proteins

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

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

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Novel E-cadherin-mediated adhesion in peripheral nerve: Schwann cell architecture is stabilized by autotypic adherens junctions

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12 December 2020

Membrane insertion of gap junction connexins: polytopic channel forming membrane proteins

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Connexin 32 mRNA levels in the rat supraoptic nucleus: up-regulation prior to parturition and during lactation

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12 December 2020

The human connexin32 gene is transcribed from two tissue-specific promoters

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12 December 2020

Altered connexin expression after peripheral nerve injury

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12 December 2020

A second alternative transcript of the gap junction gene connexin32 is expressed in murine Schwann cells and modulated in injured sciatic nerve

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12 December 2020

Connexin32 in oligodendrocytes and association with myelinated fibers in mouse and rat brain

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12 December 2020

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

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12 December 2020

Charcot-Marie-Tooth disease type 1A with 17p11.2 duplication. Clinical and electrophysiological phenotype study and factors influencing disease severity in 119 cases

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12 December 2020

Charcot-Marie-Tooth disease with intermediate motor nerve conduction velocities: characterization of 14 Cx32 mutations in 35 families.

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12 December 2020

Charcot-Marie-Tooth disease: histopathological features of the peripheral myelin protein (PMP22) duplication (CMT1A) and connexin32 mutations (CMTX1)

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12 December 2020

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

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12 December 2020

Connexin32-null mice develop demyelinating peripheral neuropathy

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12 December 2020

Functional gap junctions in the schwann cell myelin sheath

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12 December 2020

10.1523/JNEUROSCI.3082-04.2005

Identifiers

DOI

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8 January 2020

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8 January 2020

PubMed publication ID

15703409

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