Molecular genetics of demyelination: new wrinkles on an old membrane (Q41331515)

29 September 2017

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title

Molecular genetics of demyelination: new wrinkles on an old membrane (English)

1 reference

29 September 2017

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Scherer SS

1

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PubMed ID

9010201

29 September 2017

language of work or name

English

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publication date

1 January 1997

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29 September 2017

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29 September 2017

18

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29 September 2017

1

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29 September 2017

13-16

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Disruption of the compacted myelin sheath of axons of the central nervous system in proteolipid protein-deficient mice

29 September 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2980042-8

7 January 2021

Functional breakdown of the lipid bilayer of the myelin membrane in central and peripheral nervous system by disrupted galactocerebroside synthesis

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2980042-8

7 January 2021

Isolation and characterization of a novel oligodendrocyte-specific protein

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2980042-8

7 January 2021

Connections with connexins: the molecular basis of direct intercellular signaling

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2980042-8

7 January 2021

Myelination in the absence of galactocerebroside and sulfatide: normal structure with abnormal function and regional instability.

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2980042-8

7 January 2021

Measurement of Myelin Sheath Resistances: Implications for Axonal Conduction and Pathophysiology

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2980042-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2980042-8

7 January 2021

Assembly of CNS myelin in the absence of proteolipid protein

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2980042-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2980042-8

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%2FS0896-6273%2801%2980042-8

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%2FS0896-6273%2801%2980042-8

7 January 2021

Molecular specializations at nodes and paranodes in peripheral nerve

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2980042-8

7 January 2021

A transgenic rat model of Charcot-Marie-Tooth disease

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2980042-8

7 January 2021

Crystal structure of the extracellular domain from P0, the major structural protein of peripheral nerve myelin

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2980042-8

7 January 2021

Biology and genetics of hereditary motor and sensory neuropathies

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2980042-8

7 January 2021

Epithelial membrane protein-2 and epithelial membrane protein-3: two novel members of the peripheral myelin protein 22 gene family

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2980042-8

7 January 2021

Ultrastructural PMP22 expression in inherited demyelinating neuropathies

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2980042-8

7 January 2021

Dominant-negative effect on adhesion by myelin Po protein truncated in its cytoplasmic domain

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2980042-8

7 January 2021

Parallel evolution and coexpression of the proteolipid proteins and protein zero in vertebrate myelin.

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2980042-8

7 January 2021

10.1016/S0896-6273(01)80042-8

Identifiers

DOI

1 reference

29 September 2017

1 reference

PubMed ID

9010201