An adhesion test system based on Schneider cells to determine genotype–phenotype correlations for mutated P0 proteins-Reference-Cited by-同舟云学术

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An adhesion test system based on Schneider cells to determine genotype–phenotype correlations for mutated P0 proteins

Published:1998-10 Issue:4 Volume:14 Page:117-119
ISSN:1050-3862
Container-title:Genetic Analysis: Biomolecular Engineering
language:en
Short-container-title:Genetic Analysis: Biomolecular Engineering

Author:

Bülent Ekici Arif,Fuchs Christina,Nelis Eva,Hillenbrand Rainer,Schachner Melitta,Van Broeckhoven Christine,Rautenstrauss Bernd

Publisher

Elsevier BV

Subject

Genetics,Applied Microbiology and Biotechnology

Reference22 articles.

1. Identification of a de novo insertional mutation in P0 in a patient with a Déjérine–Sottas syndrome (DSS) phenotype;Rautenstrauss;Hum Mol Genet,1994

2. Charcot-Marie-Tooth disease and related peripheral neuropathies;De Jonghe;J Peripher Nerv Syst,1997

3. Protein zero (P0)-deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathies;Martini;Nat Genet,1995

4. Molecular biology of the major myelin genes;Lemke;Trends Neurosci,1986

5. Molecular bases of myelin formation as revealed by investigations on mice deficient in glial cell surface molecules;Martini;GLIA,1997

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3. Myelin protein zero/P0 phosphorylation and function require an adaptor protein linking it to RACK1 and PKCα;Journal of Cell Biology;2007-05-14

4. Clinical and genetic description of a family with Charcot-Marie-Tooth disease type 1B from a transmembraneMPZ mutation;Muscle & Nerve;2004

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