PMP2 Gene - GeneCards | MYP2 Protein | MYP2 Antibody
2024年10月2日 · PMP2 (Peripheral Myelin Protein 2) is a Protein Coding gene. Diseases associated with PMP2 include Charcot-Marie-Tooth Disease, Demyelinating, Type 1G and …
PMP2 - Wikipedia
Myelin P2 protein is a protein that in humans is encoded by the PMP2 gene. [5][6][7] Myelin protein P2 is a constituent of peripheral nervous system (PNS) myelin, also present in small …
PMP2 peripheral myelin protein 2 [ (human)] - National Center …
High PMP2 expression is associated with melanoma cell invasion. These findings demonstrate that altered biophysical properties and functional dynamics of P2 may cause myelin defects in …
PMP2 peripheral myelin protein 2 [ Homo sapiens (human) ]
2024年11月27日 · Title: The myelin protein PMP2 is regulated by SOX10 and drives melanoma cell invasion. These findings demonstrate that altered biophysical properties and functional …
Entry - *170715 - PERIPHERAL MYELIN PROTEIN 2; PMP2 - OMIM
2019年1月14日 · The PMP2 gene encodes a peripheral myelin protein important for lipid dynamics and myelin membrane stability. It is predominantly expressed in Schwann cells …
A Mutation in PMP2 Causes Dominant Demyelinating Charcot …
2016年2月1日 · First of all, PMP2 encodes a myelin protein that is an important component of the peripheral nervous system. In addition, the PMP2 mutation cosegregated within extended …
PMP2 protein expression summary - The Human Protein Atlas
Detection or not of the gene in blood, based on spectral count estimations from a publicly available mass spectrometry-based plasma proteomics data set obtained from the PeptideAtlas.
PMP2 regulates myelin thickening and ATP production during ...
Surprisingly, Pmp2, encoding for a myelin fatty acid binding protein, is the only gene whose expression increases in Schwann cells following overexpression of axonal NRG1t3. Here, we …
Peripheral myelin protein 2 – a novel cluster of mutations causing ...
2019年8月14日 · Recently, the gene encoding peripheral myelin protein 2 (PMP2) was identified as a novel cause for CMT neuropathy with three mutations that structurally cluster together …
Human myelin protein P2: from crystallography to time-lapse
Mutations in the PMP2 gene, encoding P2, are associated with Charcot-Marie-Tooth disease (CMT). Recent studies have revealed three novel PMP2 mutations in CMT patients.