Cargando…
Peripheral myelin protein 22 alters membrane architecture
Peripheral myelin protein 22 (PMP22) is highly expressed in myelinating Schwann cells of the peripheral nervous system. PMP22 genetic alterations cause the most common forms of Charcot-Marie-Tooth disease (CMTD), which is characterized by severe dysmyelination in the peripheral nerves. However, the...
Autores principales: | Mittendorf, Kathleen F., Marinko, Justin T., Hampton, Cheri M., Ke, Zunlong, Hadziselimovic, Arina, Schlebach, Jonathan P., Law, Cheryl L., Li, Jun, Wright, Elizabeth R., Sanders, Charles R., Ohi, Melanie D. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5498104/ https://www.ncbi.nlm.nih.gov/pubmed/28695207 http://dx.doi.org/10.1126/sciadv.1700220 |
Ejemplares similares
-
Peripheral myelin protein 22 preferentially partitions into ordered phase membrane domains
por: Marinko, Justin T., et al.
Publicado: (2020) -
How T118M peripheral myelin protein 22 predisposes humans to Charcot–Marie–Tooth disease
por: Stefanski, Katherine M., et al.
Publicado: (2022) -
Glycosylation limits forward trafficking of the tetraspan membrane protein PMP22
por: Marinko, Justin T., et al.
Publicado: (2021) -
Modest Effects of Lipid Modifications on the Structure
of Caveolin-3
por: Kim, Ji-Hun, et al.
Publicado: (2014) -
Conformational
Stability and Pathogenic Misfolding
of the Integral Membrane Protein PMP22
por: Schlebach, Jonathan P., et al.
Publicado: (2015)