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PXMP2 gene

Known as: PMP22, PXMP2, peroxisomal membrane protein 2 
National Institutes of Health

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PMP22 gene

Papers overview

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2019
2019
RUNX represses Pmp22 to drive neurofibromagenesis
RUNX 1 and RUNX3 drive Nf1 neurofibromagenesis by mediating the promoter usage and inducing levels of protein expression of PMP22… 
2016
2016
Alternative Splicing in the Human PMP22 Gene: Implications in CMT1A Neuropathy
CMT1A patients commonly share PMP22 genetic overloading but they show phenotypic heterogeneity and variability in PMP22 mRNA and… 
2016
2016
SP110 and PMP22 polymorphisms are associated with tuberculosis risk in a Chinese-Tibetan population
Susceptibility to tuberculosis (TB) is partially dependent on host genetic variability. SP110 and PMP22 are candidate genes… 
2015
2015
P192. Small hairpin RNA against PMP22 is effective in vitro but fails to improve the phenotype of a CMT1A rat model in vivo
2014
2014
Peroxisomal membrane channel Pxmp2 in the mammary fat pad is essential for stromal lipid homeostasis and for development of mammary gland epithelium in mice.
2011
2011
Neuropathy in a human without the PMP22 gene.
BACKGROUND Haploinsufficiency of PMP22 causes hereditary neuropathy with liability to pressure palsies. However, the biological… 
2008
2008
Solute traffic across the mammalian peroxisomal membrane—the role of Pxmp2
Peroxisomes are small oxidative organelles found in all eukaryotes. They contain a matrix which is surrounded by a single… 
2003
2003
The Pxmp2 and PoleI genes are linked by a bidirectional promoter in an evolutionary conserved fashion.
1999
1999
Regulation and expression of the murine Pmp22 gene
Mutations in the gene encoding the peripheral myelin protein PMP22 account for several hereditary neuropathies in human and mouse… 
1998
1998
Purification of PASII/PMP22– an extremely hydrophobic glycoprotein of PNS myelin membrane
PASII/PMP22 protein (mol. wt 2 2 kDa, pI 8.8) is an abundant and extremely hydrophobic glycoprotein of PNS myelin which is… 
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