(Q48210622)

9 February 2018

title

Connatal Pelizaeus-Merzbacher disease associated with the jimpy(msd) mice mutation (English)

1 reference

9 February 2018

Pelizaeus-Merzbacher disease

main subject

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Komaki H

1

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9 February 2018

Sasaki M

2

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9 February 2018

Yamamoto T

3

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9 February 2018

Iai M

4

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9 February 2018

Takashima S

5

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9 February 2018

publication date

1 April 1999

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9 February 2018

published in

Pediatric Neurology

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9 February 2018

volume

20

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9 February 2018

issue

4

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9 February 2018

page(s)

309-311

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9 February 2018

The proteolipid protein gene

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2898%2900160-X

7 January 2021

Neuropathology and genetics of Pelizaeus-Merzbacher disease

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2898%2900160-X

7 January 2021

Mutation of the proteolipid protein gene PLP in a human X chromosome-linked myelin disorder

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2898%2900160-X

7 January 2021

Pelizaeus-Merzbacher disease: a point mutation in exon 6 of the proteolipid protein (PLP) gene

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2898%2900160-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2898%2900160-X

7 January 2021

Conservative amino acid substitution in the myelin proteolipid protein of jimpymsd mice

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2898%2900160-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2898%2900160-X

7 January 2021

Oligodendroglial cell death in jimpy mice: an explanation for the myelin deficit

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2898%2900160-X

7 January 2021

Monoclonal antibody O10 defines a conformationally sensitive cell-surface epitope of proteolipid protein (PLP): evidence that PLP misfolding underlies dysmyelination in mutant mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2898%2900160-X

7 January 2021

Assembly of CNS myelin in the absence of proteolipid protein

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2898%2900160-X

7 January 2021

Girl with signs of Pelizaeus-Merzbacher disease heterozygous for a mutation in exon 2 of the proteolipid protein gene

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2898%2900160-X

7 January 2021

10.1016/S0887-8994(98)00160-X

Identifiers

DOI

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9 February 2018

1 reference

9 February 2018