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Author

  • Susan Fletcher
Abstract/Meeting Abstract

RESCUE OF CFTR FUNCTION IMPAIRED BY MUTATIONS IN EXON 15 IN CHILDREN WITH CYSTIC FIBROSIS

AREST CF & WAERP, Sep 2018, In : Pediatric Pulmonology. 53, p. 224-224 1 p.

Research output: Contribution to journalAbstract/Meeting Abstract

14 Citations (Scopus)

Treatment of Adult mdx Mice with Phosphorodiamidate Morpholino Oligomer Restores Cardiac Mitochondrial Energetics and Prevents the Dystrophic Cardiomyopathy

Viola, H. M., Johnstone, V. P. A., Adams, A. M., Fletcher, S. & Hool, L. C., 3 Feb 2017, In : Biophysical Journal. 112, 3, p. 245A-245A 1 p.

Research output: Contribution to journalAbstract/Meeting Abstract

Article

Antisense oligonucleotide induction of progerin in human myogenic cells

Luo, Y., Mitrpant, C., Adams, A., Johnsen, R., Fletcher, S., Mastaglia, F. & Wilton, S., 2014, In : PLoS One. 9, 6, p. 9pp

Research output: Contribution to journalArticle

Open Access
8 Citations (Scopus)

Antisense suppression of donor splice site mutations in the dystrophin gene transcript

Fletcher, S., Meloni, P., Johnsen, R., Wong, B. L., Muntoni, F. & Wilton, S., 2013, In : Molecular genetics & genomic medicine. 1, 3, p. 162-173

Research output: Contribution to journalArticle

Open Access
9 Citations (Scopus)

A platform for discovery of functional cell-penetrating peptides for efficient multi-cargo intracellular delivery

Hoffmann, K., Milech, N., Juraja, S. M., Cunningham, P. T., Stone, S. R., Francis, R. W., Anastasas, M., Hall, C. M., Heinrich, T., Bogdawa, H. M., Winslow, S., Scobie, M. N., Dewhurst, R. E., Florez, L., Ong, F., Kerfoot, M., Champain, D., Adams, A. M., Fletcher, S., Viola, H. M. & 10 others, Hool, L. C., Connor, T., Longville, B. A. C., Tan, Y. F., Kroeger, K., Morath, V., Weiss, G. A., Skerra, A., Hopkins, R. M. & Watt, P. M., 1 Dec 2018, In : Scientific Reports. 8, 1, 12538.

Research output: Contribution to journalArticle

Open Access
19 Citations (Scopus)

A splice intervention therapy for autosomal recessive juvenile parkinson’s disease arising from parkin mutations

Li, D., Aung-Htut, M. T., Ham, K. A., Fletcher, S. & Wilton, S. D., 1 Oct 2020, In : International Journal of Molecular Sciences. 21, 19, p. 1-15 15 p., 7282.

Research output: Contribution to journalArticle

Open Access

Deletion of dystrophin in-frame exon 5 leads to a severe phenotype: Guidance for exon skipping strategies

Toh, Z. Y. C., Aung-Htut, M. T., Pinniger, G., Adams, A., Krishnaswarmy, S., Wong, B. L., Fletcher, S. & Wilton, S., 8 Jan 2016, In : PLoS One. 11, 1, p. 1-17 e0145620.

Research output: Contribution to journalArticle

Open Access
File
13 Citations (Scopus)
381 Downloads (Pure)

Design of a framework for the deployment of collaborative independent rare disease-centric registries: Gaucher disease registry model

Bellgard, M. I., Napier, K. R., Bittles, A. H., Szer, J., Fletcher, S., Zeps, N., Hunter, A. A. & Goldblatt, J., Feb 2018, In : Blood Cells, Molecules, and Diseases. 68, p. 232-238

Research output: Contribution to journalArticle

Open Access
11 Citations (Scopus)

Gene therapy: Therapeutic applications and relevance to pathology

Both, G., Alexander, I., Fletcher, S., Nicolson, T. J., Rasko, J. E. J., Wilton, S. & Symonds, G., 2011, In : Pathology. 43, 6, p. 642-656

Research output: Contribution to journalArticle

12 Citations (Scopus)
Open Access
28 Citations (Scopus)

Improved Antisense Oligonucleotide Design to Suppress Aberrant SMN2 Gene Transcript Processing: Towards a Treatment for Spinal Muscular Atrophy

Mitrpant, C., Porensky, P. N., Zhou, H., Price, L., Muntoni, F., Fletcher, S., Wilton, S. & Burghes, A. H. M., 2013, In : PLoS One. 8, 4, p. 10pp

Research output: Contribution to journalArticle

Open Access
54 Citations (Scopus)
5 Citations (Scopus)

Mismatched single stranded antisense oligonucleotides can induce efficient dystrophin splice switching

Fragall, C., Adams, A., Johnsen, R., Kole, R., Fletcher, S. & Wilton, S., 2011, In : BMC Medical Genetics. 12, p. 141

Research output: Contribution to journalArticle

Open Access
6 Citations (Scopus)
28 Citations (Scopus)

Multiple exon skipping strategies to by-pass dystrophin mutations

Adkin, C., Meloni, P., Fletcher, S., Adams, A., Muntoni, F., Wong, B. & Wilton, S., 2012, In : Neuromuscular Disorders. 22, 4, p. 297-305

Research output: Contribution to journalArticle

Open Access
12 Citations (Scopus)

Novel mutations found in individuals with adult-onset pompe disease

Aung-Htut, M. T., Ham, K. A., Tchan, M. C., Fletcher, S. & Wilton, S. D., 1 Feb 2020, In : Genes. 11, 2, 135.

Research output: Contribution to journalArticle

Open Access
2 Citations (Scopus)

Phenotype–genotype correlations in a pseudodominant Stargardt disease pedigree due to a novel ABCA4 deletion–insertion variant causing a splicing defect

Huang, D., Thompson, J. A., Charng, J., Chelva, E., McLenachan, S., Chen, S. C., Zhang, D., McLaren, T. L., Lamey, T. M., Constable, I. J., De Roach, J. N., Aung-Htut, M. T., Adams, A., Fletcher, S., Wilton, S. D. & Chen, F. K., 1 Jul 2020, In : Molecular Genetics and Genomic Medicine. 8, 7, e1259.

Research output: Contribution to journalArticle

Open Access
1 Citation (Scopus)

Pseudoexon activation increases phenotype severity in a Becker muscular dystrophy patient

Greer, K., Mizzi, K., Rice, E., Kuster, L., Barrero, R. A., Bellgard, M. I., Lynch, B. J., Foley, A. R., O Rathallaigh, E., Wilton, S. & Fletcher, S., 2015, In : Molecular Genetics and Genomics. 3, 4, p. 320-326

Research output: Contribution to journalArticle

Open Access
13 Citations (Scopus)

Rare Disease Research Roadmap: Navigating the bioinformatics and translational challenges for improved patient health outcomes

Bellgard, M. I., Sleeman, M. W., Guerrero, F. D., Fletcher, S., Baynam, G., Goldblatt, J., Rubinstein, Y. R., Bell, C., Groft, S. C., Barrero, R., Bittles, A. H., Wilton, S., Mason, C. E. & Weeramanthri, T. S., 2014, In : Health Policy And Technology. 3, 4, p. 325-335

Research output: Contribution to journalArticle

7 Citations (Scopus)
Open Access
281 Citations (Scopus)

Revertant Fibers in the mdx Murine Model of Duchenne Muscular Dystrophy: An Age and Muscle-Related Reappraisal

Pigozzo, S., Da Re, L., Romualdi, C., Mazzara, P. G., Galletta, E., Fletcher, S., Wilton, S. & Vitiello, L., 2013, In : PLoS One. 8, 8, p. 6pp

Research output: Contribution to journalArticle

Open Access
13 Citations (Scopus)
14 Citations (Scopus)

Single Exon Skipping Can Address a Multi-Exon Duplication in the Dystrophin Gene

Greer, K., Johnsen, R., Nevo, Y., Fellig, Y., Fletcher, S. & Wilton, S. D., 25 Jun 2020, In : International Journal of Molecular Sciences. 21, 12

Research output: Contribution to journalArticle

Open Access

Splice modulating antisense oligonucleotides restore some acid-alpha-glucosidase activity in cells derived from patients with late-onset Pompe disease

Aung-Htut, M. T., Ham, K. A., Tchan, M., Johnsen, R., Schnell, F. J., Fletcher, S. & Wilton, S. D., 1 Dec 2020, In : Scientific Reports. 10, 1, 6702.

Research output: Contribution to journalArticle

Open Access
1 Citation (Scopus)

Structural Variants May Be a Source of Missing Heritability in sALS

Theunissen, F., Flynn, L. L., Anderton, R. S., Mastaglia, F., Pytte, J., Jiang, L., Hodgetts, S., Burns, D. K., Saunders, A., Fletcher, S., Wilton, S. D. & Akkari, P. A., 31 Jan 2020, In : Frontiers in Neuroscience. 14, 47.

Research output: Contribution to journalArticle

Open Access
1 Citation (Scopus)

Targeted exon skipping to address "leaky" mutations in the dystrophin gene

Fletcher, S., Adkin, C., Meloni, P., Wong, B., Muntoni, F., Kole, R., Fragall, C., Greer, K., Johnsen, R. & Wilton, S., 2012, In : Molecular Therapy-Nucleic Acids. 1, p. e48

Research output: Contribution to journalArticle

Open Access
15 Citations (Scopus)

Targeted Exon Skipping to Correct Exon Duplications in the Dystrophin Gene

Greer, K. L., Lochmueller, H., Flanigan, K., Fletcher, S. & Wilton, S. D., 18 Mar 2014, In : Molecular Therapy-Nucleic Acids. 3, p. 1-7 7 p., 155.

Research output: Contribution to journalArticle

Open Access
18 Citations (Scopus)
Chapter

Optimizing splice-switching oligomer sequences using 2'-o-methyl phosphorothioate chemistry

Adkin, C., Fletcher, S. & Wilton, S., 2012, Exon Skipping: Methods and Protocols. Aartsma-Rus, A. (ed.). United States: Humana Press, Vol. 867. p. 169-188 (Methods in Molecular Biology).

Research output: Chapter in Book/Conference paperChapter

3 Citations (Scopus)

Skipping of Duplicated Dystrophin Exons: In Vitro Induction and Assessment

Greer, K., Fletcher, S. & Wilton, S. D., 1 Jan 2018, Methods in Molecular Biology. Yokota, T. & Maruyama, R. (eds.). USA: Humana Press, p. 219-228 10 p. (Methods in Molecular Biology; vol. 1828).

Research output: Chapter in Book/Conference paperChapter

1 Citation (Scopus)
Editorial

Comprehending the Health informatics Spectrum: Grappling with System Entropy and Advancing Quality Clinical Research

Bellgard, M. I., Chartres, N., Watts, G. F., Wilton, S., Fletcher, S., Hunter, A. & Snelling, T., 14 Sep 2017, In : Frontiers in Public Health. 5, 5 p., 224.

Research output: Contribution to journalEditorial

Open Access
Review article

Precision Medicine through Antisense Oligonucleotide-Mediated Exon Skipping

Li, D., Mastaglia, F. L., Fletcher, S. & Wilton, S. D., 1 Nov 2018, In : Trends in Pharmacological Sciences. 39, 11, p. 982-994 13 p.

Research output: Contribution to journalReview article

13 Citations (Scopus)
Open Access
Open Access

Translational development of splice-modifying antisense oligomers

Fletcher, S., Bellgard, M., Price, L., Akkari, A. & Wilton, S., 2 Jan 2017, In : Expert Opinion on Biological Therapy. 17, 1, p. 15-30 16 p.

Research output: Contribution to journalReview article

14 Citations (Scopus)