• The University of Western Australia (M518), 35 Stirling Highway,

    6009 Perth

    Australia

  • 3242 Citations
  • 27 h-Index
1988 …2019
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Personal profile

Keywords

  • Genetic therapies
  • Molecular medicine
  • Muscular dystrophy

Fingerprint Dive into the research topics where Susan Fletcher is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 17 Similar Profiles
Dystrophin Medicine & Life Sciences
Exons Medicine & Life Sciences
Antisense Oligonucleotides Medicine & Life Sciences
Duchenne Muscular Dystrophy Medicine & Life Sciences
Inbred mdx Mouse Medicine & Life Sciences
Genes Medicine & Life Sciences
Morpholinos Medicine & Life Sciences
Muscular Dystrophies Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Research Output 1988 2019

Altered myogenesis and premature senescence underlie human TRIM32-related myopathy

Servián-Morilla, E., Cabrera-Serrano, M., Rivas-Infante, E., Carvajal, A., Lamont, P. J., Pelayo-Negro, A. L., Ravenscroft, G., Junckerstorff, R., Dyke, J. M., Fletcher, S., Adams, A. M., Mavillard, F., Fernández-García, M. A., Nieto-González, J. L., Laing, N. G. & Paradas, C., 1 Mar 2019, In : Acta Neuropathologica Communications. 7, 1, 1 p.

Research output: Contribution to journalArticle

Open Access
Muscle Development
Muscular Diseases
Muscles
Bardet-Biedl Syndrome
Mutation

Antisense-mediated splice intervention to treat human disease: the odyssey continues

Pitout, I., Flynn, L. L., Wilton, S. D. & Fletcher, S., 22 May 2019, In : F1000Research. 8, 710.

Research output: Contribution to journalReview article

Open Access
Oligonucleotides
Nucleic Acids
Pharmaceutical Preparations
Safety
Degradation

Breakpoint junction features of seven DMD deletion mutations

Keegan, N. P., Wilton, S. D. & Fletcher, S., 1 Dec 2019, In : Human Genome Variation. 6, 1, 39.

Research output: Contribution to journalArticle

Open Access
Duchenne Muscular Dystrophy
Sequence Deletion
Bioinformatics
Muscle
Exons
6 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 othersHool, 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
Cell-Penetrating Peptides
Cytoplasm
Peptide Nucleic Acids
Cell Engineering
Bacterial Genomes
6 Citations (Scopus)

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
Gaucher Disease
Rare Diseases
Registries
Orphan Drug Production
Conservation of Natural Resources

Projects 1997 2016