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Peripheral Myelin Protein 22

Known as: GAS-3, Growth Arrest-Specific Protein 3, PMP-22 
Peripheral myelin protein 22 (160 aa, ~18 kDa) is encoded by the human PMP22 gene. This protein is involved in the determination of the structure and… 
National Institutes of Health

Related topics

Related topics

7 relations
Charcot-Marie-Tooth Disease, Type Ia (disorder)Homo sapiensMyelin SheathNeurogenesis

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
399 Down-Regulation of Peripheral Myelin Protein 22 (PMP22) Contributes to Impairment of Intestinal Barrier Integrity in Sepsis: Role of TNF-α and IFN-γ
2014
2014
Protective Effect of a cAMP Analogue on Behavioral Deficits and Neuropathological Changes in Cuprizone Model of Demyelination
Multiple sclerosis (MS) is an inflammatory demyelinating disease that leads to neuronal cell loss. Cyclic AMP and its analogs are… 
2012
2012
Myelinating and demyelinating phenotype of Trembler‐J mouse (a model of Charcot–Marie–Tooth human disease) analyzed by atomic force microscopy and confocal microscopy
The accumulation of misfolded proteins is associated with various neurodegenerative conditions. Mutations in PMP‐22 are… 
2009
2009
Notch independent signalling mediates Schwann cell-like differentiation of Adipose Derived Stem Cells
2009
2009
研究PERP (p53 apoptosis effect related to PMP-22) 基因對人類肺癌細胞株生長的影響
PERP (p53 apoptosis effect related to PMP-22) is a membrane protein with a tetra-span transmembrane domain. PERP is located at… 
2001
2001
Early Electrophysiological Changes In Transgenic Rat Model Of Charcot‐Marie‐Tooth
Recently, a reliable transgenic rat model of human Charcot-Marie-Tooth type 1 A has been developed. So far, neurophysiological… 
1999
1999
The role of PMP-22 as an autoantigen in GBS and CIDP
1995
1995
[A case of hereditary motor and sensory neuropathy type I with a new type of peripheral myelin protein (PMP)-22 mutation].
A 16-year-old school boy suffered from an insidious foot deformity. Slight degrees of symmetrical muscular weakness of the distal… 
1992
1992
Isolation and sequence determination of cDNA encoding PMP-22 (PAS-II/SR13/Gas-3) of human peripheral myelin.
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