Altered MAM function shifts mitochondrial metabolism in SOD1-mutant models of ALS
Altered MAM function shifts mitochondrial metabolism in SOD1-mutant models of ALS
About this item
Full title
Author / Creator
Publisher
Cold Spring Harbor: Cold Spring Harbor Laboratory Press
Journal title
Language
English
Formats
Publication information
Publisher
Cold Spring Harbor: Cold Spring Harbor Laboratory Press
Subjects
More information
Scope and Contents
Contents
Mitochondrial defects are a common hallmark of familial and sporadic forms of amyotrophic lateral sclerosis (ALS). However, the origin of these defects, including reduced pyruvate metabolism and reduced oxygen consumption, is poorly understood. These metabolic functions are regulated in specialized endoplasmic reticulum (ER) domains in close contac...
Alternative Titles
Full title
Altered MAM function shifts mitochondrial metabolism in SOD1-mutant models of ALS
Authors, Artists and Contributors
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_proquest_journals_2716765089
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2716765089
Other Identifiers
E-ISSN
2692-8205
DOI
10.1101/2022.09.22.508778
How to access this item
https://www.proquest.com/docview/2716765089?pq-origsite=primo&accountid=13902