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Investigation of mitochondrial phenotypes in motor neurons derived by direct conversion of fibroblas...

Investigation of mitochondrial phenotypes in motor neurons derived by direct conversion of fibroblas...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_3167783905

Investigation of mitochondrial phenotypes in motor neurons derived by direct conversion of fibroblasts from familial ALS subjects

About this item

Full title

Investigation of mitochondrial phenotypes in motor neurons derived by direct conversion of fibroblasts from familial ALS subjects

Publisher

United States: Cold Spring Harbor Laboratory Press

Journal title

bioRxiv, 2025-02

Language

English

Formats

Publication information

Publisher

United States: Cold Spring Harbor Laboratory Press

More information

Scope and Contents

Contents

Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease of motor neurons, leading to fatal muscle paralysis. Familial forms of ALS (fALS) account for approximately 10% of cases and are associated with mutations in numerous genes. Alterations of mitochondrial functions have been proposed to contribute to disease pathogenesis....

Alternative Titles

Full title

Investigation of mitochondrial phenotypes in motor neurons derived by direct conversion of fibroblasts from familial ALS subjects

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_journals_3167783905

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_3167783905

Other Identifiers

ISSN

2692-8205

E-ISSN

2692-8205

DOI

10.1101/2025.02.13.637962