Literature DB >> 7686967

Infantile neuropathy with unstable myelin: study of the P0 protein.

S Peudenier1, J F Deleuze, D Pham-Dinh, C Lacroix, J Boulloche, P Landrieu.   

Abstract

An unusual form of hereditary motor and sensory neuropathy characterized by a prominent disruption of the myelin lamellae is reported. In addition to detailed morphological analysis, we investigated the protein P0, which is the major protein of peripheral myelin involved in adhesion. No major gene rearrangement and no differences in P0 protein expression were observed in the present case.

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Year:  1993        PMID： 7686967     DOI： 10.1007/bf00838164

Source DB:  PubMed          Journal:  J Neurol        ISSN： 0340-5354            Impact factor:   4.849


  13 in total

1.  Role of myelin P0 protein as a homophilic adhesion molecule.

Authors:  M T Filbin; F S Walsh; B D Trapp; J A Pizzey; G I Tennekoon
Journal:  Nature       Date:  1990-04-26       Impact factor: 49.962

2.  Isolation and sequence determination of cDNA encoding the major structural protein of human peripheral myelin.

Authors:  K Hayasaka; K Nanao; M Tahara; W Sato; G Takada; M Miura; K Uyemura
Journal:  Biochem Biophys Res Commun       Date:  1991-10-31       Impact factor: 3.575

3.  Isolation and sequence of a cDNA encoding the major structural protein of peripheral myelin.

Authors:  G Lemke; R Axel
Journal:  Cell       Date:  1985-03       Impact factor: 41.582

4.  Congenital hypo- and hypermyelination neuropathy. Two cases.

Authors:  J M Vallat; R Gil; M J Leboutet; J Hugon; D Moulies
Journal:  Acta Neuropathol       Date:  1987       Impact factor: 17.088

5.  Pelizaeus-Merzbacher disease: a valine to phenylalanine point mutation in a putative extracellular loop of myelin proteolipid.

Authors:  D Pham-Dinh; J L Popot; O Boespflug-Tanguy; P Landrieu; J F Deleuze; J Boué; P Jollès; A Dautigny
Journal:  Proc Natl Acad Sci U S A       Date:  1991-09-01       Impact factor: 11.205

6.  Congenital demyelinating motor and sensory neuropathy with focally folded myelin sheaths.

Authors:  A A Gabreëls-Festen; E M Joosten; F J Gabreëls; D F Stegeman; A J Vos; H F Busch
Journal:  Brain       Date:  1990-12       Impact factor: 13.501

7.  The PO glycoprotein of peripheral nerve myelin.

Authors:  A Ishaque; M W Roomi; I Szymanska; S Kowalski; E H Eylar
Journal:  Can J Biochem       Date:  1980-10

8.  The hypertrophic forms of hereditary motor and sensory neuropathy. A study of hypertrophic Charcot-Marie-Tooth disease (HMSN type I) and Dejerine-Sottas disease (HMSN type III) in childhood.

Authors:  R A Ouvrier; J G McLeod; T E Conchin
Journal:  Brain       Date:  1987-02       Impact factor: 13.501

9.  Autosomal recessive motor and sensory neuropathy with excessive myelin outfolding.

Authors:  A Ohnishi; Y Murai; M Ikeda; T Fujita; H Furuya; Y Kuroiwa
Journal:  Muscle Nerve       Date:  1989-07       Impact factor: 3.217

10.  Isolation and analysis of the gene encoding peripheral myelin protein zero.

Authors:  G Lemke; E Lamar; J Patterson
Journal:  Neuron       Date:  1988-03       Impact factor: 17.173
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  1 in total

Review 1.  Dejerine-Sottas syndrome grown to maturity: overview of genetic and morphological heterogeneity and follow-up of 25 patients.

Authors:  Anneke Gabreëls-Festen
Journal:  J Anat       Date:  2002-04       Impact factor: 2.610
  1 in total

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