Disease mechanisms in ALS: misfolded SOD1 transferred through exosome-dependent and exosome-independent pathways

Full text for this resource is not available from the Research Repository.

Silverman, Judith M, Fernando, Sarah M, Grad, Leslie I, Hill, Andrew F ORCID: 0000-0001-5581-2354, Turner, Bradley J, Yerbury, Justin J and Cashman, Neil R (2016) Disease mechanisms in ALS: misfolded SOD1 transferred through exosome-dependent and exosome-independent pathways. Cellular and Molecular Neurobiology, 36 (3). pp. 377-381. ISSN 0272-4340

Dimensions Badge

Altmetric Badge

Item type Article
URI https://vuir.vu.edu.au/id/eprint/45720
DOI 10.1007/s10571-015-0294-3
Official URL https://link.springer.com/article/10.1007/s10571-0...
Subjects Current > FOR (2020) Classification > 3205 Medical biochemistry and metabolomics
Current > FOR (2020) Classification > 3209 Neurosciences
Current > Division/Research > Chancellery
Keywords disease mechanism, ALS, misfolded protein, amyotrophic lateral sclerosis
Citations in Scopus 67 - View on Scopus
Download/View statistics View download statistics for this item

Search Google Scholar

Repository staff login