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Exendin-4 ameliorates motor neuron degeneration in cellular and animal models of amyotrophic lateral...

Exendin-4 ameliorates motor neuron degeneration in cellular and animal models of amyotrophic lateral...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1323851125

Exendin-4 ameliorates motor neuron degeneration in cellular and animal models of amyotrophic lateral sclerosis

About this item

Full title

Exendin-4 ameliorates motor neuron degeneration in cellular and animal models of amyotrophic lateral sclerosis

Publisher

United States: Public Library of Science

Journal title

PloS one, 2012-02, Vol.7 (2), p.e32008

Language

English

Formats

Publication information

Publisher

United States: Public Library of Science

More information

Scope and Contents

Contents

Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease characterized by a progressive loss of lower motor neurons in the spinal cord. The incretin hormone, glucagon-like peptide-1 (GLP-1), facilitates insulin signaling, and the long acting GLP-1 receptor agonist exendin-4 (Ex-4) is currently used as an anti-diabetic drug. GL...

Alternative Titles

Full title

Exendin-4 ameliorates motor neuron degeneration in cellular and animal models of amyotrophic lateral sclerosis

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_plos_journals_1323851125

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1323851125

Other Identifiers

ISSN

1932-6203

E-ISSN

1932-6203

DOI

10.1371/journal.pone.0032008

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