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Altered MAM function shifts mitochondrial metabolism in SOD1-mutant models of ALS

Altered MAM function shifts mitochondrial metabolism in SOD1-mutant models of ALS

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2716765089

Altered MAM function shifts mitochondrial metabolism in SOD1-mutant models of ALS

About this item

Full title

Altered MAM function shifts mitochondrial metabolism in SOD1-mutant models of ALS

Publisher

Cold Spring Harbor: Cold Spring Harbor Laboratory Press

Journal title

bioRxiv, 2022-09

Language

English

Formats

Publication information

Publisher

Cold Spring Harbor: Cold Spring Harbor Laboratory Press

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

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