(Q28587855)

31 January 2017

title

Specific disruption of a schwann cell dystrophin-related protein complex in a demyelinating neuropathy (English)

1 reference

Dystrophin related protein 2

31 January 2017

main subject

1 reference

GOA release 2020-03-11

Dystroglycan 1

1 reference

GOA release 2020-03-11

Periaxin

1 reference

GOA release 2020-03-11

Schwann cell

0 references

author name string

D. L. Sherman

1

1 reference

31 January 2017

C. Fabrizi

2

1 reference

31 January 2017

C. S. Gillespie

3

1 reference

31 January 2017

P. J. Brophy

4

1 reference

31 January 2017

language of work or name

English

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publication date

1 June 2001

1 reference

31 January 2017

1 reference

31 January 2017

volume

30

1 reference

31 January 2017

issue

3

1 reference

31 January 2017

page(s)

677–687

1 reference

The three human syntrophin genes are expressed in diverse tissues, have distinct chromosomal locations, and each bind to dystrophin and its relatives

31 January 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

The structural and functional diversity of dystrophin

1 reference

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7 January 2021

Periaxin mutations cause recessive Dejerine-Sottas neuropathy

1 reference

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7 January 2021

Schwann cell function depends upon axonal signals and basal lamina components

1 reference

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7 January 2021

Evidence that contact with connective tissue matrix is required for normal interaction between Schwann cells and nerve fibers

1 reference

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7 January 2021

Linkage between axonal ensheathment and basal lamina production by Schwann cells

1 reference

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7 January 2021

Schwann cell myelination: induction by exogenous basement membrane-like extracellular matrix

1 reference

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7 January 2021

Requirement for the PDZ domain protein, INAD, for localization of the TRP store-operated channel to a signaling complex

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

A G+1-->A transversion at the 5' splice site of intron 69 of the dystrophin gene causing the absence of peripheral nerve Dp116 and severe clinical involvement in a DMD patient.

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

PDZ motifs in PTP-BL and RIL bind to internal protein segments in the LIM domain protein RIL.

1 reference

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7 January 2021

Expression of the dystrophin-related protein 2 (Drp2) transcript in the mouse.

1 reference

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7 January 2021

Crystal structures of a complexed and peptide-free membrane protein-binding domain: molecular basis of peptide recognition by PDZ

1 reference

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7 January 2021

Laminin A, B1, and B2 chain gene expression in transected and regenerating nerves: regulation by axonal signals

1 reference

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7 January 2021

Origins of cell polarity

1 reference

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7 January 2021

Non-muscle alpha-dystroglycan is involved in epithelial development

1 reference

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7 January 2021

Two PDZ domain proteins encoded by the murine periaxin gene are the result of alternative intron retention and are differentially targeted in Schwann cells

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

Axonal regulation of Schwann cell integrin expression suggests a role for alpha 6 beta 4 in myelination.

1 reference

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7 January 2021

Differentiation of axon-related Schwann cells in vitro: II. Control of myelin formation by basal lamina.

1 reference

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7 January 2021

Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle

1 reference

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7 January 2021

PDZ domains in synapse assembly and signalling

1 reference

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7 January 2021

Periaxin, a novel protein of myelinating Schwann cells with a possible role in axonal ensheathment

1 reference

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7 January 2021

Peripheral demyelination and neuropathic pain behavior in periaxin-deficient mice

1 reference

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7 January 2021

Reduced levels of dystrophin associated proteins in the brains of mice deficient for Dp71.

1 reference

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7 January 2021

A mutation in periaxin is responsible for CMT4F, an autosomal recessive form of Charcot-Marie-Tooth disease

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

Unexpected modes of PDZ domain scaffolding revealed by structure of nNOS-syntrophin complex

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

A sarcoglycan-dystroglycan complex anchors Dp116 and utrophin in the peripheral nervous system

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

Identification and characterization of the dystrophin anchoring site on beta-dystroglycan

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

A PDZ-containing scaffold related to the dystrophin complex at the basolateral membrane of epithelial cells

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

Interaction of ion channels and receptors with PDZ domain proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

TRP and the PDZ protein, INAD, form the core complex required for retention of the signalplex in Drosophila photoreceptor cells

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

An autosomal transcript in skeletal muscle with homology to dystrophin

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

A role of dystroglycan in schwannoma cell adhesion to laminin

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

Peripheral nerve involvement in merosin-deficient congenital muscular dystrophy and dy mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

Differential expression of dystrophin, utrophin and dystrophin-associated proteins in peripheral nerve

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

An epitope structure for the C-terminal domain of dystrophin and utrophin

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

Mechanical function of dystrophin in muscle cells

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

Dystrophin protects the sarcolemma from stresses developed during muscle contraction

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

Characterization of DRP2, a novel human dystrophin homologue

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

Association of dystrophin-related protein 2 (DRP2) with postsynaptic densities in rat brain

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

Characterization of the transmembrane molecular architecture of the dystroglycan complex in schwann cells

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

A tripartite nuclear localization signal in the PDZ-domain protein L-periaxin

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

Dystrophin is not a specific component of the cardiac costamere

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

Muscular dystrophies and the dystrophin-glycoprotein complex

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

Molecular organization at the glycoprotein-complex-binding site of dystrophin. Three dystrophin-associated proteins bind directly to the carboxy-terminal portion of dystrophin

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

Contribution of the different modules in the utrophin carboxy-terminal region to the formation and regulation of the DAP complex

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

A multivalent PDZ-domain protein assembles signalling complexes in a G-protein-coupled cascade

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

Influence of laminin-2 on Schwann cell-axon interactions

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

Hereditary peripheral neuropathies: clinical forms, genetics, and molecular mechanisms

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

The membrane-cytoskeleton interface: the role of dystrophin and utrophin

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

Murine muscular dystrophy caused by a mutation in the laminin alpha 2 (Lama2) gene

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

Coordination of an array of signaling proteins through homo- and heteromeric interactions between PDZ domains and target proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

Characterization of dp6troglycan-laminin interaction in peripheral nerve.

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

Dystroglycan is a dual receptor for agrin and laminin-2 in Schwann cell membrane

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

Dystroglycan is a binding protein of laminin and merosin in peripheral nerve

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

Synaptic clustering of Fascilin II and Shaker: essential targeting sequences and role of Dlg.

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900327-0

7 January 2021

10.1016/S0896-6273(01)00327-0

Identifiers

DOI

0 references

1 reference