The Amyotrophic Lateral Sclerosis M114T PFN1 Mutation Deregulates Alternative Autophagy Pathways and...
The Amyotrophic Lateral Sclerosis M114T PFN1 Mutation Deregulates Alternative Autophagy Pathways and Mitochondrial Homeostasis
About this item
Full title
Author / Creator
Teyssou, Elisa , Chartier, Laura , Roussel, Delphine , Perera, Nirma D. , Nemazanyy, Ivan , Langui, Dominique , Albert, Mélanie , Larmonier, Thierry , Saker, Safaa , Salachas, François , Pradat, Pierre-François , Meininger, Vincent , Ravassard, Philippe , Côté, Francine , Lobsiger, Christian S. , Boillée, Séverine , Turner, Bradley J. , Seilhean, Danielle and Millecamps, Stéphanie
Publisher
Switzerland: MDPI AG
Journal title
Language
English
Formats
Publication information
Publisher
Switzerland: MDPI AG
Subjects
More information
Scope and Contents
Contents
Mutations in profilin 1 (PFN1) have been identified in rare familial cases of Amyotrophic Lateral Sclerosis (ALS). PFN1 is involved in multiple pathways that could intervene in ALS pathology. However, the specific pathogenic role of PFN1 mutations in ALS is still not fully understood. We hypothesized that PFN1 could play a role in regulating autoph...
Alternative Titles
Full title
The Amyotrophic Lateral Sclerosis M114T PFN1 Mutation Deregulates Alternative Autophagy Pathways and Mitochondrial Homeostasis
Authors, Artists and Contributors
Author / Creator
Chartier, Laura
Roussel, Delphine
Perera, Nirma D.
Nemazanyy, Ivan
Langui, Dominique
Albert, Mélanie
Larmonier, Thierry
Saker, Safaa
Salachas, François
Pradat, Pierre-François
Meininger, Vincent
Ravassard, Philippe
Côté, Francine
Lobsiger, Christian S.
Boillée, Séverine
Turner, Bradley J.
Seilhean, Danielle
Millecamps, Stéphanie
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9143529
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9143529
Other Identifiers
ISSN
1422-0067,1661-6596
E-ISSN
1422-0067
DOI
10.3390/ijms23105694
