Publications: Pitout, Ianthe
Journal Article
Pytte, J., Anderton, R.S., Flynn, L.L., Theunissen, F., Jiang, L., Pitout, I., James, I., Mastaglia, F.L., Saunders, A.M., Bedlack, R., Siddique, T., Siddique, N. and Akkari, P.A. (2020) Association of a structural variant within the SQSTM1 gene with amyotrophic lateral sclerosis. Neurology Genetics, 6 (2). Art. e406.
Mejzini, R., Flynn, L.L., Pitout, I.L., Fletcher, S., Wilton, S.D. and Akkari, P.A. (2019) ALS genetics, mechanisms, and therapeutics: Where are we now? Frontiers in Neuroscience, 13 .
Pitout, I., Flynn, L.L., Wilton, S.D. and Fletcher, S. (2019) Antisense-mediated splice intervention to treat human disease: the odyssey continues. F1000Research, 8 .
Aung-Htut, M.T., McIntosh, C.S., Ham, K.A.
ORCID: 0000-0002-7036-5334, Pitout, I.L., Flynn, L.L., Greer, K., Fletcher, S. and Wilton, S.D.
(2019)
Systematic approach to developing splice modulating antisense oligonucleotides.
International Journal of Molecular Sciences, 20
(20).
Article 5030.
Flynn, L.L., Mitrpant, C., Pitout, I.L., Fletcher, S. and Wilton, S.D. (2018) Antisense oligonucleotide mediated terminal intron retention of the SMN2 transcript. Molecular Therapy - Nucleic Acids, 11 . pp. 91-102.
Pitout, I., Fletcher, S., Etherington, S.ORCID: 0000-0002-6589-8793 and Wilton, S.
(2015)
A spanner in the works of human transformer 2 β1 autoregulation may reduce the severity of spinal muscular atrophy.
The Journal of Gene Medicine, 17
(8 - 9).
pp. 173-217.
Conference Item
Pitout, I., Fletcher, S., Etherington, S.ORCID: 0000-0002-6589-8793 and Wilton, S.
(2015)
A spanner in the works of human Transformer-2-β1 autoregulation may reduce the severity of spinal muscular atrophy.
In: 9th Australasian Gene and Cell Therapy Society meeting, 29 April - 1 May, Parkville, Victoria, Australia.
Thesis
Pitout, Ianthe (2018) Modulation of modifiers of Pre-mRNA splicing: A therapeutic strategy for Amenable Inherited Diseases. PhD thesis, Murdoch University.