Zobrazeno 1 - 5
of 5
pro vyhledávání: '"PMP22, peripheral myelin protein 22"'
Autor:
Umber Alam, Derek Kennedy
Publikováno v:
Biochimica et Biophysica Acta. Molecular Cell Research
Ras-GTPase-activating protein (SH3 domain)-binding proteins (G3BPs, also known as Rasputin) are a family of RNA binding proteins that regulate gene expression in response to environmental stresses by controlling mRNA stability and translation. G3BPs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75fb9fdcf6daf1cd6b8230b6d96cc695
https://doi.org/10.1016/j.bbamcr.2018.09.001
https://doi.org/10.1016/j.bbamcr.2018.09.001
Autor:
Darren R. Heintzman, Jonathan P. Schlebach, Madison T. Wright, Katherine R. Clowes, Justin T. Marinko, Lars Plate, Charles R. Sanders
Publikováno v:
The Journal of Biological Chemistry
Peripheral myelin protein 22 (PMP22) folds and trafficks inefficiently, with only 20% of newly expressed protein trafficking to the cell surface. This behavior is exacerbated in many of the mutants associated with Charcot–Marie–Tooth disease, mot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04f7aa822492ff0debb73ba9d1a8ad87
https://pubmed.ncbi.nlm.nih.gov/33933451
https://pubmed.ncbi.nlm.nih.gov/33933451
Autor:
Irina Madorsky, Lee Sooyeon, Jordan T. Schmidt, Jessica Nicks, Lucia Notterpek, Vinita G. Chittoor, Sunitha Rangaraju, Diana C. Narvaez
Publikováno v:
ASN Neuro, Vol 5 (2013)
ASN NEURO
ASN NEURO
Charcot–Marie–Tooth disease type 1A (CMT1A) is a hereditary demyelinating neuropathy linked with duplication of the peripheral myelin protein 22 (PMP22) gene. Transgenic C22 mice, a model of CMT1A, display many features of the human disease, incl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1cd3f919617a01bb16f04c551c1b30f9
https://doaj.org/article/48ad42821b82448abca2e113d6cd0950
https://doaj.org/article/48ad42821b82448abca2e113d6cd0950
Publikováno v:
ASN NEURO
ASN Neuro, Vol 4 (2012)
ASN Neuro, Vol 4 (2012)
Modulating molecular chaperones is emerging as an attractive approach to treat neurodegenerative diseases associated with protein aggregation, DPN (diabetic peripheral neuropathy) and possibly, demyelinating neuropathies. KU-32 [ N-(7-((2 R,3 R,4 S,5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37626863c920cce013581455d45367d9
http://europepmc.org/articles/PMC3517131
http://europepmc.org/articles/PMC3517131
Autor:
Vinita G. Chittoor, Sooyeon Lee, Lucia Notterpek, Sunitha Rangaraju, Susie J. Zoltewicz, Steven M. Freeland, David A. Zacharias
Publikováno v:
ASN NEURO
ASN Neuro, Vol 4 (2012)
ASN Neuro, Vol 4 (2012)
PMP22 (peripheral myelin protein 22), also known as GAS 3 (growth-arrest-specific protein 3), is a disease-linked tetraspan glycoprotein of peripheral nerve myelin and constituent of intercellular junctions in epithelia. To date, our knowledge of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10142c56e22448518a50a8093eff27f4
https://doi.org/10.1042/an20120045
https://doi.org/10.1042/an20120045