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Brown, SJ
ORCID: https://orcid.org/0000-0001-9671-7054, Kline, RA, Synowsky, SA, Shirran, SL, Holt, I, Sillence, KA, Claus, P, Wirth, B, Wishart, TM and Fuller, HR
ORCID: https://orcid.org/0000-0001-8868-896X
(2022)
The proteome signatures of fibroblasts from patients with severe, intermediate and mild spinal muscular atrophy show limited overlap.
Cells, 11 (17).
Llavero Hurtado, M, Fuller, HR
ORCID: https://orcid.org/0000-0001-8868-896X, Wong, AMS, Eaton, SL, Gillingwater, TH, Pennetta, G, Cooper, JD and Wishart, TM
(2017)
Proteomic mapping of differentially vulnerable pre-synaptic populations identifies regulators of neuronal stability in vivo.
Scientific Reports (12412).
Fuller, HR
ORCID: https://orcid.org/0000-0001-8868-896X, Graham, LC, Llavero Hurtado, M and Wishart, TM
(2016)
Understanding the molecular consequences of inherited muscular dystrophies: advancements through proteomic experimentation.
Expert Review of Proteomics, 13 (7).
pp. 659-671.
Fuller, HR
ORCID: https://orcid.org/0000-0001-8868-896X, Gillingwater, TH and Wishart, TM
(2016)
Commonality amid diversity: multi-study proteomic identification of conserved disease mechanisms in spinal muscular atrophy.
Neuromuscular Disorders, 26 (9).
pp. 560-569.
Fuller, HR
ORCID: https://orcid.org/0000-0001-8868-896X, Hurtado, ML, Wishart, TM and Gates, MA
(2014)
The rat striatum responds to nigro-striatal degeneration via the increased expression of proteins associated with growth and regeneration of neuronal circuitry.
Proteome Science, 12.
pp. 1-20.
Wishart, TM, Mutsaers, CA, Riessland, M, Reimer, MM, Hunter, G, Hannam, ML, Eaton, SL, Fuller, HR
ORCID: https://orcid.org/0000-0001-8868-896X, Roche, SL, Somers, E, Morse, R, Young, PJ, Lamont, DJ, Hammerschmidt, M, Joshi, A, Hohenstein, P, Morris, GE, Parson, SH, Skehel, PA, Becker, T, Robinson, IM, Becker, CG, Wirth, B and Gillingwater, TH
(2014)
Dysregulation of ubiquitin homeostasis and β-catenin signaling promote spinal muscular atrophy.
Journal of Clinical Investigation, 124 (4).
1821 -1834.

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