Stephen D Wilton

Stephen D Wilton

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Stephen D Wilton

Stephen D Wilton

Publications by authors named "Stephen D Wilton"

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16Publications

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Rational Design of Short Locked Nucleic Acid-Modified 2'-O-Methyl Antisense Oligonucleotides for Efficient Exon-Skipping In Vitro.

Mol Ther Nucleic Acids 2017 Dec 12;9:155-161. Epub 2017 Sep 12.

Centre for Comparative Genomics, Murdoch University, Perth, WA 6150, Australia; Perron Institute for Neurological and Translational Science, Perth, WA 6009, Australia. Electronic address:

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http://dx.doi.org/10.1016/j.omtn.2017.09.002DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5633351PMC
December 2017

Smart functional nucleic acid chimeras: enabling tissue specific RNA targeting therapy.

RNA Biol 2015 ;12(4):412-25

a Nucleic Acid Center; Department of Physics, Chemistry and Pharmacy ; University of Southern Denmark ; Odense , Denmark.

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http://www.tandfonline.com/doi/full/10.1080/15476286.2015.10
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http://dx.doi.org/10.1080/15476286.2015.1017234DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4615226PMC
January 2016

Revertant fibers in the mdx murine model of Duchenne muscular dystrophy: an age- and muscle-related reappraisal.

PLoS One 2013 28;8(8):e72147. Epub 2013 Aug 28.

Centre for Neuromuscular and Neurological Disorders, University of Western Australia Queen Elizabeth II Medical Centre, Nedlands Western Australia, Australia ; Department of Biology, University of Padova, Padova, Italy.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0072147PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3756063PMC
May 2014

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

Mol Genet Genomic Med 2013 Sep 13;1(3):162-73. Epub 2013 Jun 13.

Centre for Comparative Genomics, Murdoch University South St, 6150, Perth, Western Australia, Australia ; Centre for Neuromuscular and Neurological Disorders, University of Western Australia Perth 6009, Western Australia, Australia.

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http://dx.doi.org/10.1002/mgg3.19DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3865583PMC
September 2013

A single administration of morpholino antisense oligomer rescues spinal muscular atrophy in mouse.

Hum Mol Genet 2012 Apr 20;21(7):1625-38. Epub 2011 Dec 20.

Department of Molecular and Cellular Biochemistry, The Ohio State University, Columbus, OH 43210, USA.

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http://dx.doi.org/10.1093/hmg/ddr600DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3298284PMC
April 2012

Long-term administration of antisense oligonucleotides into the paraspinal muscles of mdx mice reduces kyphosis.

J Appl Physiol (1985) 2008 Aug 22;105(2):662-8. Epub 2008 May 22.

Centre for Systems Biology, Faculty of Sciences, University of Southern Queensland, Toowoomba, Queensland 4350, Australia.

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http://dx.doi.org/10.1152/japplphysiol.00068.2008DOI Listing
August 2008

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

Mol Ther 2007 Sep 19;15(9):1587-92. Epub 2007 Jun 19.

Centre for Neuromuscular and Neurological Disorders, University of Western Australia, Nedlands, Perth, Western Australia, Australia.

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http://dx.doi.org/10.1038/sj.mt.6300245DOI Listing
September 2007

Redirecting splicing to address dystrophin mutations: molecular by-pass surgery.

Prog Mol Subcell Biol 2006 ;44:161-97

Experimental Molecular Medicine Group, Centre for Neuromuscular and Neurological Disorders, University of Western Australia.

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January 2007

Induction of revertant fibres in the mdx mouse using antisense oligonucleotides.

Genet Vaccines Ther 2006 May 24;4. Epub 2006 May 24.

Experimental Molecular Medicine Group, Centre for Neuromuscular and Neurological Disorders, University of Western Australia, Nedlands, Perth, 6009, Western Australia.

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http://gvt-journal.biomedcentral.com/articles/10.1186/1479-0
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http://dx.doi.org/10.1186/1479-0556-4-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1481566PMC
May 2006

Terminal antisense oligonucleotide modifications can enhance induced exon skipping.

Neuromuscul Disord 2005 Oct;15(9-10):622-9

Experimental Molecular Medicine Group, Centre for Neuromuscular and Neurological Disorders, University of Western Australia, Nedlands, Perth 6097, Western Australia.

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http://linkinghub.elsevier.com/retrieve/pii/S096089660500190
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http://dx.doi.org/10.1016/j.nmd.2005.06.009DOI Listing
October 2005

Functional amounts of dystrophin produced by skipping the mutated exon in the mdx dystrophic mouse.

Nat Med 2003 Aug 6;9(8):1009-14. Epub 2003 Jul 6.

Muscle Cell Biology, MRC Clinical Science Centre, Hammersmith Hospital, Du Cane Road, London, W12 0NN, UK.

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http://dx.doi.org/10.1038/nm897DOI Listing
August 2003

Morpholino antisense oligonucleotide induced dystrophin exon 23 skipping in mdx mouse muscle.

Hum Mol Genet 2003 Aug;12(15):1801-11

Centre for Neuromuscular and Neurological Disorders, University of Western Australia, 4th Floor, "A" Block, QE II Medical Centre, Verdun Street, Nedlands, Perth, Western Australia 6009, Australia.

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http://dx.doi.org/10.1093/hmg/ddg196DOI Listing
August 2003

Target selection for antisense oligonucleotide induced exon skipping in the dystrophin gene.

J Gene Med 2003 Jun;5(6):518-27

Edith Cowan University, Perth, Western Australia, 6027.

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http://dx.doi.org/10.1002/jgm.361DOI Listing
June 2003

Improved antisense oligonucleotide induced exon skipping in the mdx mouse model of muscular dystrophy.

J Gene Med 2002 Nov-Dec;4(6):644-54

Australian Neuromuscular Research Institute, Centre for Neuromuscular and Neurological Disorders, University of Western Australia, Perth, Western Australia, 6907.

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http://dx.doi.org/10.1002/jgm.295DOI Listing
May 2003