Proteolipid protein gene: Pelizaeus-Merzbacher disease in humans and neurodegeneration in mice (Q28141588)

Pelizaeus-Merzbacher disease

Europe PubMed Central

title

Proteolipid protein gene: Pelizaeus-Merzbacher disease in humans and neurodegeneration in mice (English)

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main subject

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K Woodward

1

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S Malcolm

series ordinal

2

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language of work or name

English

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publication date

April 1999

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published in

Trends in Genetics

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volume

15

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issue

4

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page(s)

125-8

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cites work

X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locus

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901716-3

7 January 2021

Proteolipid protein gene dosage effect in Pelizaeus-Merzbacher disease

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7 January 2021

Pelizaeus-Merzbacher disease: identification of Xq22 proteolipid-protein duplications and characterization of breakpoints by interphase FISH.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901716-3

7 January 2021

Duplication of the proteolipid protein gene is the major cause of Pelizaeus-Merzbacher disease

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901716-3

7 January 2021

Glial cell degeneration and hypomyelination caused by overexpression of myelin proteolipid protein gene

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901716-3

7 January 2021

Premature arrest of myelin formation in transgenic mice with increased proteolipid protein gene dosage

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901716-3

7 January 2021

Overexpression of DM20 messenger RNA in two brothers with Pelizaeus-Merzbacher disease

1 reference

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7 January 2021

Cell death of oligodendrocytes or demyelination induced by overexpression of proteolipid protein depending on expressed gene dosage

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901716-3

7 January 2021

Over-expression of the DM-20 myelin proteolipid causes central nervous system demyelination in transgenic mice

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901716-3

7 January 2021

Late-onset neurodegeneration in mice with increased dosage of the proteolipid protein gene

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901716-3

7 January 2021

Disrupted proteolipid protein trafficking results in oligodendrocyte apoptosis in an animal model of Pelizaeus-Merzbacher disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901716-3

7 January 2021

Distinct phenotypes associated with increasing dosage of the PLP gene: implications for CMT1A due to PMP22 gene duplication

1 reference

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7 January 2021

Genetics of Pelizaeus-Merzbacher disease

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7 January 2021

Many naturally occurring mutations of myelin proteolipid protein impair its intracellular transport.

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Phenotypic severity of murine Plp mutants reflects in vivo and in vitro variations in transport of PLP isoproteins

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7 January 2021

The rumpshaker mutation in spastic paraplegia

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Jimpy(msd) mouse mutation and connatal Pelizaeus-Merzbacher disease

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7 January 2021

A combination of PLP and DM20 transgenes promotes partial myelination in the jimpy mouse

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7 January 2021

A (G-to-A) mutation in the initiation codon of the proteolipid protein gene causing a relatively mild form of Pelizaeus-Merzbacher disease in a Dutch family

1 reference

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7 January 2021

Proteolipid protein is necessary in peripheral as well as central myelin.

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Assembly of CNS myelin in the absence of proteolipid protein

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7 January 2021

Axonal swellings and degeneration in mice lacking the major proteolipid of myelin

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7 January 2021

Paralytic tremor (pt) rabbit: a sex-linked mutation affecting proteolipid protein-gene expression

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7 January 2021

Oligodendrocyte survival and function in the long-lived strain of the myelin deficient rat

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7 January 2021

10.1016/S0168-9525(99)01716-3

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

10203813

1 reference

Consolidated OpenCitations Corpus – April 2017