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Enhanced axonal regeneration of ALS patient iPSC-derived motor neurons harboring SOD1A4V mutation

Enhanced axonal regeneration of ALS patient iPSC-derived motor neurons harboring SOD1A4V mutation

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_618425bc3da44c26b14ec76b7174e164

Enhanced axonal regeneration of ALS patient iPSC-derived motor neurons harboring SOD1A4V mutation

About this item

Full title

Enhanced axonal regeneration of ALS patient iPSC-derived motor neurons harboring SOD1A4V mutation

Publisher

London: Nature Publishing Group UK

Journal title

Scientific reports, 2023-04, Vol.13 (1), p.5597-5597, Article 5597

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease, characterized by degeneration of upper and lower motor neurons that leads to muscle weakness, paralysis, and death, but the effects of disease-causing mutations on axonal outgrowth of neurons derived from human induced pluripotent stem cells (iPSC)-derived motor neurons...

Alternative Titles

Full title

Enhanced axonal regeneration of ALS patient iPSC-derived motor neurons harboring SOD1A4V mutation

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_618425bc3da44c26b14ec76b7174e164

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_618425bc3da44c26b14ec76b7174e164

Other Identifiers

ISSN

2045-2322

E-ISSN

2045-2322

DOI

10.1038/s41598-023-31720-7

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