Literature DB >> 2483101

Unwrapping the genes of myelin.

G Lemke1.   

Abstract

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Year:  1988        PMID： 2483101     DOI： 10.1016/0896-6273(88)90103-1

Source DB:  PubMed          Journal:  Neuron        ISSN： 0896-6273            Impact factor:   17.173


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  41 in total

1.  Protein zero gene expression is regulated by the glial transcription factor Sox10.

Authors:  R I Peirano; D E Goerich; D Riethmacher; M Wegner
Journal:  Mol Cell Biol       Date:  2000-05       Impact factor: 4.272

2.  Tst-1, a member of the POU domain gene family, binds the promoter of the gene encoding the cell surface adhesion molecule P0.

Authors:  X He; R Gerrero; D M Simmons; R E Park; C J Lin; L W Swanson; M G Rosenfeld
Journal:  Mol Cell Biol       Date:  1991-03       Impact factor: 4.272

3.  Neuregulin 1 type III improves peripheral nerve myelination in a mouse model of congenital hypomyelinating neuropathy.

Authors:  Sophie Belin; Francesca Ornaghi; Ghjuvan'Ghjacumu Shackleford; Jie Wang; Cristina Scapin; Camila Lopez-Anido; Nicholas Silvestri; Neil Robertson; Courtney Williamson; Akihiro Ishii; Carla Taveggia; John Svaren; Rashmi Bansal; Markus H Schwab; Klaus Nave; Pietro Fratta; Maurizio D'Antonio; Yannick Poitelon; M Laura Feltri; Lawrence Wrabetz
Journal:  Hum Mol Genet       Date:  2019-04-15       Impact factor: 6.150

4.  Differential expression of sodium channels in acutely isolated myelinating and non-myelinating Schwann cells of rabbits.

Authors:  S Y Chiu
Journal:  J Physiol       Date:  1993-10       Impact factor: 5.182

Review 5.  An introduction to the molecular basis of inherited myelin diseases.

Authors:  J M Matthieu
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

Review 6.  Embryonic Schwann cell development: the biology of Schwann cell precursors and early Schwann cells.

Authors:  K R Jessen; R Mirsky
Journal:  J Anat       Date:  1997-11       Impact factor: 2.610

7.  Charcot-Marie-Tooth disease: a novel Tyr145Ser mutation in the myelin protein zero (MPZ, P0) gene causes different phenotypes in homozygous and heterozygous carriers within one family.

Authors:  Alejandro Leal; Corinna Berghoff; Martin Berghoff; Gerardo Del Valle; Carlos Contreras; Olga Montoya; Erick Hernández; Ramiro Barrantes; Ursula Schlötzer-Schrehardt; Bernhard Neundörfer; André Reis; Bernd Rautenstrauss; Dieter Heuss
Journal:  Neurogenetics       Date:  2003-07-05       Impact factor: 2.660

8.  Two novel missense mutations in the myelin protein zero gene causes Charcot-Marie-Tooth type 2 and Déjérine-Sottas syndrome.

Authors:  Geir J Braathen; Jette C Sand; Michael B Russell
Journal:  BMC Res Notes       Date:  2010-04-12

Review 9.  Molecular anatomy and genetics of myelin proteins in the peripheral nervous system.

Authors:  G J Snipes; U Suter
Journal:  J Anat       Date:  1995-06       Impact factor: 2.610

10.  Identification of an embryonic isoform of myelin basic protein that is expressed widely in the mouse embryo.

Authors:  P M Mathisen; S Pease; J Garvey; L Hood; C Readhead
Journal:  Proc Natl Acad Sci U S A       Date:  1993-11-01       Impact factor: 11.205
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