Induction of cryptic pre-mRNA splice-switching by antisense oligonucleotides
Ham, Kristin A., Keegan, Niall P., McIntosh, Craig S., Aung-Htut, May T., Zaw, Khine, Greer, Kane, Fletcher, Sue, Wilton, Steve D.
Published in Scientific reports (23.07.2021)
Published in Scientific reports (23.07.2021)
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Structural Variants May Be a Source of Missing Heritability in sALS
Theunissen, Frances, Flynn, Loren L, Anderton, Ryan S, Mastaglia, Frank, Pytte, Julia, Jiang, Leanne, Hodgetts, Stuart, Burns, Daniel K, Saunders, Ann, Fletcher, Sue, Wilton, Steve D, Akkari, Patrick Anthony
Published in Frontiers in neuroscience (31.01.2020)
Published in Frontiers in neuroscience (31.01.2020)
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Longitudinal assessment of social cognition in infants born preterm using eye‐tracking and parent–child play
Dean, Bethan, O'Carroll, Sinéad, Ginnell, Lorna, Ledsham, Victoria, Telford, Emma, Sparrow, Sarah, Boardman, James P., Fletcher‐Watson, Sue
Published in Infant and child development (01.11.2021)
Published in Infant and child development (01.11.2021)
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In Vitro Validation of Phosphorodiamidate Morpholino Oligomers
Aung-Htut, May T, McIntosh, Craig S, West, Kristin A, Fletcher, Sue, Wilton, Steve D
Published in Molecules (Basel, Switzerland) (12.08.2019)
Published in Molecules (Basel, Switzerland) (12.08.2019)
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Prevention of Dystrophic Pathology in Severely Affected Dystrophin/Utrophin-deficient Mice by Morpholino-oligomer-mediated Exon-skipping
Goyenvalle, Aurélie, Babbs, Arran, Powell, Dave, Kole, Ryszard, Fletcher, Sue, Wilton, Steve D, Davies, Kay E
Published in Molecular therapy (01.01.2010)
Published in Molecular therapy (01.01.2010)
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Antisense Oligonucleotide Induction of the hnRNPA1b Isoform Affects Pre-mRNA Splicing of SMN2 in SMA Type I Fibroblasts
Toosaranont, Jarichad, Ruschadaariyachat, Sukanya, Mujchariyakul, Warasinee, Arora, Jantarika Kumar, Charoensawan, Varodom, Suktitipat, Bhoom, Palmer, Thomas N, Fletcher, Sue, Wilton, Steve D, Mitrpant, Chalermchai
Published in International journal of molecular sciences (01.04.2022)
Published in International journal of molecular sciences (01.04.2022)
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Novel STMN2 Variant Linked to Amyotrophic Lateral Sclerosis Risk and Clinical Phenotype
Theunissen, Frances, Anderton, Ryan S, Mastaglia, Frank L, Flynn, Loren L, Winter, Samantha J, James, Ian, Bedlack, Richard, Hodgetts, Stuart, Fletcher, Sue, Wilton, Steve D, Laing, Nigel G, MacShane, Mandi, Needham, Merrilee, Saunders, Ann, Mackay-Sim, Alan, Melamed, Ze'ev, Ravits, John, Cleveland, Don W, Akkari, P Anthony
Published in Frontiers in aging neuroscience (26.03.2021)
Published in Frontiers in aging neuroscience (26.03.2021)
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Systematic Approach to Developing Splice Modulating Antisense Oligonucleotides
Aung-Htut, May T, McIntosh, Craig S, Ham, Kristin A, Pitout, Ianthe L, Flynn, Loren L, Greer, Kane, Fletcher, Sue, Wilton, Steve D
Published in International journal of molecular sciences (11.10.2019)
Published in International journal of molecular sciences (11.10.2019)
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Design of a framework for the deployment of collaborative independent rare disease-centric registries: Gaucher disease registry model
Bellgard, Matthew I., Napier, Kathryn R., Bittles, Alan H., Szer, Jeffrey, Fletcher, Sue, Zeps, Nikolajs, Hunter, Adam A., Goldblatt, Jack
Published in Blood cells, molecules, & diseases (01.02.2018)
Published in Blood cells, molecules, & diseases (01.02.2018)
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Antisense oligonucleotide induction of progerin in human myogenic cells
Luo, Yue-Bei, Mitrpant, Chalermchai, Adams, Abbie M, Johnsen, Russell D, Fletcher, Sue, Mastaglia, Frank L, Wilton, Steve D
Published in PloS one (03.06.2014)
Published in PloS one (03.06.2014)
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Single Stranded Fully Modified-Phosphorothioate Oligonucleotides can Induce Structured Nuclear Inclusions, Alter Nuclear Protein Localization and Disturb the Transcriptome In Vitro
Flynn, Loren L, Li, Ruohan, Pitout, Ianthe L, Aung-Htut, May T, Larcher, Leon M, Cooper, Jack A L, Greer, Kane L, Hubbard, Alysia, Griffiths, Lisa, Bond, Charles S, Wilton, Steve D, Fox, Archa H, Fletcher, Sue
Published in Frontiers in genetics (06.04.2022)
Published in Frontiers in genetics (06.04.2022)
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Deletion of Dystrophin In-Frame Exon 5 Leads to a Severe Phenotype: Guidance for Exon Skipping Strategies
Toh, Zhi Yon Charles, Thandar Aung-Htut, May, Pinniger, Gavin, Adams, Abbie M, Krishnaswarmy, Sudarsan, Wong, Brenda L, Fletcher, Sue, Wilton, Steve D
Published in PloS one (08.01.2016)
Published in PloS one (08.01.2016)
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Functional amounts of dystrophin produced by skipping the mutated exon in the mdx dystrophic mouse
Lu, Qi Long, Partridge, Terence A, Mann, Christopher J, Lou, Fang, Bou-Gharios, George, Morris, Glenn E, Xue, Shao-an, Fletcher, Sue, Wilton, Stephen D
Published in Nature medicine (01.08.2003)
Published in Nature medicine (01.08.2003)
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