Researcher Profile

Miss Abbie Adams

Abbie Adams
Abbie Adams
  1. 2016
  2. 1

    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

  3. 2014
  4. 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

  5. 2012
  6. 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

  7. 2011
  8. 2010
  9. Dystrophin isoform induction in vivo by antisense-mediated alternative splicing

    Fletcher, S., Adams, A., Johnsen, R., Greer, K., Moutlon, H. M. & Wilton, S. 2010 In : Molecular Therapy. 18, 6, p. 1218-1223

    Research output: Contribution to journalArticle

  10. 2009
  11. Rational design of antisense oligomers to induce dystrophin exon skipping

    Mitrpant, C., Adams, A., Meloni, P., Muntoni, F., Fletcher, S. & Wilton, S. 2009 In : Molecular Therapy. 17, 8, p. 1418-1426

    Research output: Contribution to journalArticle

  12. 2008
  13. Antisense oligomer design: Targeting and assay systems

    Wilton, S., Mitrpant, C., Meloni, P., Adams, A. & Fletcher, S. 2008 NEUROMUSCULAR DISORDERS. Vol. 18, p. 756-756

    Research output: Chapter in Book/Conference paperConference paper

  14. 2007
  15. Antisense oligonucleotide induced exon skipping and the dystrophin gene transcript: cocktails and chemistries

    Adams, A., Meloni, P., Iversen, P. L., Coleman, C., Fletcher, S. & Wilton, S. 2007 In : BMC Molecular Biology. 8, p. 1-8

    Research output: Contribution to journalArticle

  16. Antisense oligonucleotide-induced exon skipping across the human dystrophin gene transcript

    Wilton, S., Adams, A., Meloni, P., Mcclorey, G., Coleman, C. & Fletcher, S. 2007 In : Molecular Therapy. 15, 7, p. 1288-1296

    Research output: Contribution to journalArticle

  17. Comparative analysis of antisense oligonucleotide sequences for targeted skipping of exon 51 during dystrophin pre-mRNA splicing in human muscle

    Arechavala-Gomeza, V., Graham, I. R., Popplewell, L. J., Adams, A., Aartsma-Rus, A., Kinali, M., Morgan, J. E., Van Deutekom, J. C., Wilton, S., Dickson, G. & Muntoni, F. 2007 In : Human Gene Therapy. 18, 9, p. 798-810

    Research output: Contribution to journalArticle

  18. Morpholino oligomer-mediated exon skipping averts the onset of dystrophic pathology in the mdx mouse

    Fletcher, S., Wright, K., Adams, A., Meloni, P., Johnsen, R., Steinhaus, J. P., Moulton, H. M., Iversen, P. L. & Wilton, S. 2007 In : Molecular Therapy. 15, 9, p. 1587-1592

    Research output: Contribution to journalArticle

  19. The influence of antisense oligonucleotide length on dystrophin exon skipping

    Harding, P., Fall, A., Honeyman, K., Fletcher, S. & Wilton, S. 2007 In : Molecular Therapy. 15, 1, p. 157-166

    Research output: Contribution to journalArticle

  20. 2006
  21. Induced dystrophin exon skipping in human muscle explants

    Mcclorey, G., Fall, A., Moulton, H. M., Iversen, P. L., Rasko, J. E., Ryan, M., Fletcher, S. & Wilton, S. 2006 In : Neuromuscular Disorders. 16, 9-10, p. 583-590

    Research output: Contribution to journalArticle

  22. 2004
  23. 2003
  24. A possible role for the axon guidance molecule ephrin-A2 in activity-dependent refinement of regenerating central nerve connections

    King, C., Fall, A., Quach, T., Bartlett, C., Rodger, J., Dunlop, S. & Beazley, L. 2003 22nd Symposium of Western Australian Neuroscience. Fall, A., Madja, B. & Byrnes, M. (eds.). Nedlands, WA ed. Australia: Symposium of Western Australian Neuroscience, Vol. 1, p. 30

    Research output: Chapter in Book/Conference paperConference paper

  25. A possible role for the axon guidance molecule eprhin-A2 in activity-dependent refinement of regenerating central nerve connections

    Quach, T., Fall, A., King, C., Bartlett, C., Rodger, J., Dunlop, S. & Beazley, L. 2003 Fourteenth Annual Combined Biological Sciences Meeting. Newberry, J. A., Quail, E. A. & Watson, M. (eds.). Scarborough, WA ed. Australia: BioMed Chem, Vol. 1, p. 38

    Research output: Chapter in Book/Conference paperConference paper

  26. The Axon Repulsive Molecule Ephrin-A2 Is Up-Regulated After Insertion Of A Peripheral Nerve Into The Rate Superior Colliculus

    Symonds, A., Sauce, Y., Rodger, J., King, C., Bartlett, C., Fall, A., Dunlop, S., Lund, R. & Beazley, L. 2003 Fourteenth Annual Combined Biological Science Meeting. Newberry, J. A., Quail, E. A. & Watson, M. (eds.). Scarborough, WA ed. Australia: BioMed Chem, Vol. 1, p. 43

    Research output: Chapter in Book/Conference paperConference paper

  27. Up-regulation of the axon guidance molecule ephrin-A2 after insertion of a peripheral nerve into the rat superior colliculus

    Symonds, A., Sauve, Y., Rodger, J., King, C., Bartlett, C., Fall, A., Dunlop, S., Lund, R. & Beazley, L. 2003 22nd Symposium of Western Australian Neuroscience. Nedlands, WA ed. Australia: Symposium of Western Australian Neuroscience, Vol. 1, p. 27

    Research output: Chapter in Book/Conference paperConference paper

ID: 85657

Most frequent journals
  • Molecular Therapy

    ISSNs: 1525-0016

    Nature Publishing Group

    Scopus rating (2015): SJR 3.374 SNIP 1.339

    Journal

  • Neuromuscular Disorders

    ISSNs: 0960-8966

    Elsevier Limited

    Scopus rating (2015): SJR 1.447 SNIP 1.159

    Journal

  • PLoS One

    ISSNs: 1932-6203

    PUBLIC LIBRARY SCIENCE

    Scopus rating (2015): SJR 1.395 SNIP 1.044

    Journal

  • Journal of Gene Medicine

    ISSNs: 1099-498X

    John Wiley and Sons Ltd

    Scopus rating (2015): SJR 1.025 SNIP 0.742

    Journal

  • BMC Medical Genetics

    ISSNs: 1471-2350

    BioMed Central

    Scopus rating (2015): SJR 1.062 SNIP 0.798

    Journal

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Most frequent publishers