Peripheral neuropathies caused by mutations in the myelin protein zero
about
Charcot-Marie-Tooth disease and intracellular trafficClinical features and molecular modelling of novel MPZ mutations in demyelinating and axonal neuropathiesMyelination and regional domain differentiation of the axon.Identification and in silico analysis of 14 novel GJB1, MPZ and PMP22 gene mutations.ENU mutagenesis screen to establish motor phenotypes in wild-type mice and modifiers of a pre-existing motor phenotype in tau mutant mice.Progesterone synthesis in the nervous system: implications for myelination and myelin repair.Gain of glycosylation: a new pathomechanism of myelin protein zero mutations.L-MPZ, a novel isoform of myelin P0, is produced by stop codon readthrough.Intermediate Charcot-Marie-Tooth disease due to a novel Trp101Stop myelin protein zero mutation associated with debilitating neuropathic pain.Rapid progression of late onset axonal Charcot-Marie-Tooth disease associated with a novel MPZ mutation in the extracellular domain.Myelin sheaths are formed with proteins that originated in vertebrate lineages.Erbin regulates NRG1 signaling and myelination.GlcNAc6ST-1 regulates sulfation of N-glycans and myelination in the peripheral nervous systemRecent advances in the genetics of hereditary axonal sensory-motor neuropathies type 2.Demyelinating prenatal and infantile developmental neuropathies.Murine therapeutic models for Charcot-Marie-Tooth (CMT) disease.Animal models and therapeutic prospects for Charcot-Marie-Tooth disease.Endoplasmic Reticulum Protein Quality Control Failure in Myelin Disorders.Genomic variants at 20p11 associated with body fat mass in the European population.Peripheral myelin protein 22 alters membrane architecture.Proteolipid protein modulates preservation of peripheral axons and premature death when myelin protein zero is lacking.Neural mobilization promotes nerve regeneration by nerve growth factor and myelin protein zero increased after sciatic nerve injury.Novel MPZ mutations and congenital hypomyelinating neuropathyDysmyelinating and demyelinating Charcot-Marie-Tooth disease associated with two myelin protein zero gene mutations.Phylogenetically Conserved Sequences Around Myelin P0 Stop Codon are Essential for Translational Readthrough to Produce L-MPZ.DHTKD1 deficiency causes Charcot-Marie-Tooth disease in mice.Two novel MPZ mutations in Chinese CMT patients.
P2860
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P2860
Peripheral neuropathies caused by mutations in the myelin protein zero
description
2006 nî lūn-bûn
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2006 թուականի Մարտին հրատարակուած գիտական յօդուած
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2006 թվականի մարտին հրատարակված գիտական հոդված
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2006年の論文
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2006年学术文章
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2006年学术文章
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2006年学术文章
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2006年学术文章
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2006年學術文章
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name
Peripheral neuropathies caused by mutations in the myelin protein zero
@ast
Peripheral neuropathies caused by mutations in the myelin protein zero
@en
Peripheral neuropathies caused by mutations in the myelin protein zero
@nl
type
label
Peripheral neuropathies caused by mutations in the myelin protein zero
@ast
Peripheral neuropathies caused by mutations in the myelin protein zero
@en
Peripheral neuropathies caused by mutations in the myelin protein zero
@nl
prefLabel
Peripheral neuropathies caused by mutations in the myelin protein zero
@ast
Peripheral neuropathies caused by mutations in the myelin protein zero
@en
Peripheral neuropathies caused by mutations in the myelin protein zero
@nl
P1476
Peripheral neuropathies caused by mutations in the myelin protein zero
@en
P2093
Michael E Shy
P356
10.1016/J.JNS.2005.11.015
P407
P577
2006-03-15T00:00:00Z