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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 08 Dec 2016.

Myelin protein zero

MPP, MPZ, P-0, CMT1
This gene encodes a major structural protein of peripheral myelin. Mutations in this gene result in the autosomal dominant form of Charcot-Marie-Tooth disease type 1 and other polyneuropathies. [provided by RefSeq, Apr 2010] (from NCBI)
Papers using MPP antibodies
Mouse embryo fibroblasts lacking the tumor suppressor menin show altered expression of extracellular matrix protein genes.
Supplier
Laudet Vincent, In PLoS ONE, 2006
... ICI 182780 and the ERα specific antagonist 4,4′,4″-(4-Propyl-[1H] pyrazole-1,3,5-triyl) trisphenol (MPP), were purchased from Tocris (Ellisville, MO) ...
Proof without prejudice: use of the Kolmogorov-Smirnov test for the analysis of histograms from flow systems and other sources
Supplier
Schmidt Ulrike, In PLoS ONE, 1976
... separate experiments, cells were pre-treated with i) 10 mM NAC for 2 h; ii) 100 nM MPP ERα antagonist (Tocris Cookson, Ellisville, MO) for ...
Papers on MPP
Developmental regulation of insulin receptor gene in sciatic nerves and role of insulin on glycoprotein P0 in the Schwann cells.
GeneRIF
Muttagi et al., India. In Peptides, 2012
steady-state levels of insulin receptor mRNA increase during development and after postnatal day 10, when the peak of myelin structural gene (P0) expression occurs, increasing further in parallel with the growth of the myelin sheath
MpzR98C arrests Schwann cell development in a mouse model of early-onset Charcot-Marie-Tooth disease type 1B.
GeneRIF
Shy et al., Detroit, United States. In Brain, 2012
results provide a potential link between the accumulation of MpzR98C in the endoplasmic reticulum and a developmental delay in myelination.
Phenotypic presentation of the Ser63Del MPZ mutation.
GeneRIF
Shy et al., Detroit, United States. In J Peripher Nerv Syst, 2012
Patients with CMT1B caused by Ser63del MPZ have a classical CMT1 phenotype that is much less severe than that of patients with Arg98Cys MPZ
A novel MPZ gene mutation in exon 2 causing late-onset demyelinating Charcot-Marie-Tooth disease.
GeneRIF
Hadjivassiliou et al., Sheffield, United Kingdom. In J Clin Neuromuscul Dis, 2012
Thiss study demonistrated that two affected member of the same family with the same genotype had an 8-base pair deletion, c.160_167delTCCCGGGT in MPZ exon 2.
Defective autoimmune regulator-dependent central tolerance to myelin protein zero is linked to autoimmune peripheral neuropathy.
GeneRIF
Anderson et al., Chapel Hill, United States. In J Immunol, 2012
Mutant autoimmune regulator protein-mediated central tolerance to Mpz initiates an autoimmune T helper type (Th)1 cell effector response toward peripheral nerves.
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