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Natural variants of human SARM1 cause both intrinsic and dominant loss-of-function influencing axon...

Natural variants of human SARM1 cause both intrinsic and dominant loss-of-function influencing axon...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_7f17fb24f1fc49849a24f8c3c7c31436

Natural variants of human SARM1 cause both intrinsic and dominant loss-of-function influencing axon survival

About this item

Full title

Natural variants of human SARM1 cause both intrinsic and dominant loss-of-function influencing axon survival

Publisher

London: Nature Publishing Group UK

Journal title

Scientific reports, 2022-08, Vol.12 (1), p.13846-14, Article 13846

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

SARM1 is a central executioner of programmed axon death, and this role requires intrinsic NAD(P)ase or related enzyme activity. A complete absence of SARM1 robustly blocks axon degeneration in mice, but even a partial depletion confers meaningful protection. Since axon loss contributes substantially to the onset and progression of multiple neurodeg...

Alternative Titles

Full title

Natural variants of human SARM1 cause both intrinsic and dominant loss-of-function influencing axon survival

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_7f17fb24f1fc49849a24f8c3c7c31436

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_7f17fb24f1fc49849a24f8c3c7c31436

Other Identifiers

ISSN

2045-2322

E-ISSN

2045-2322

DOI

10.1038/s41598-022-18052-8

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