Search Results - "Freckleton, Sarah"

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  1. 1

    Theme 3 In vitro experimental models.

    Authors: Yang, Shu Wu, Sharlynn Fifita, Jennifer et al.

    Source: Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 2019 Supplement, Vol. 20, p135-159. 25p.

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  2. 2

    Accumulation of dysfunctional SOD1 protein in Parkinson's disease is not associated with mutations in the SOD1 gene.

    Authors: Trist, Benjamin G. Fifita, Jennifer A. Freckleton, Sarah E. et al.

    Source: Acta Neuropathologica. Jan2018, Vol. 135 Issue 1, p155-156. 2p.

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  3. 3

    Pathogenic mutation in the ALS/FTD gene, CCNF, causes elevated Lys48-linked ubiquitylation and defective autophagy.

    Authors: Lee, Albert Rayner, Stephanie L. Gwee, Serene S. L. et al.

    Source: Cellular & Molecular Life Sciences. Jan2018, Vol. 75 Issue 2, p335-354. 20p. 3 Color Photographs, 1 Diagram, 4 Graphs.

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  4. 4

    Genetic and immunopathological analysis of CHCHD10 in Australian amyotrophic lateral sclerosis and frontotemporal dementia and transgenic TDP-43 mice.

    Authors: McCann EP Fifita JA Grima N et al.

    Source: Journal of neurology, neurosurgery, and psychiatry [J Neurol Neurosurg Psychiatry] 2020 Feb; Vol. 91 (2), pp. 162-171. Date of Electronic Publication: 2019 Nov 05.

    Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

    Journal Info: Publisher: BMJ Publishing Group Country of Publication: England NLM ID: 2985191R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1468-330X (Electronic) Linking ISSN: 00223050 NLM ISO Abbreviation: J Neurol Neurosurg Psychiatry Subsets: MEDLINE

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