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Steve D Wilton

Showing results (61-70 of 109) with videos related to

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Vision (Basel, Switzerland)|November 20, 2019
Inherited Retinal Disease Therapies Targeting Precursor Messenger Ribonucleic AcidDi Huang, Sue Fletcher, Steve D Wilton, et al.
Neuromuscular Disorders : NMD|December 21, 2011
Multiple exon skipping strategies to by-pass dystrophin mutationsCarl F Adkin, Penelope L Meloni, Susan Fletcher, et al.
Pathology|September 8, 2011
Gene therapy: therapeutic applications and relevance to pathologyGerald Both, Ian Alexander, Sue Fletcher, et al.
Molecular and Cellular Pediatrics|February 8, 2018
The potential of antisense oligonucleotide therapies for inherited childhood lung diseasesKelly M Martinovich, Nicole C Shaw, Anthony Kicic, et al.
Frontiers in Genetics|January 21, 2020
Consequences of Making the Inactive Active Through Changes in Antisense Oligonucleotide ChemistriesKhine Zaw, Kane Greer, May Thandar Aung-Htut, et al.
Scientific Reports|April 23, 2020
Splice modulating antisense oligonucleotides restore some acid-alpha-glucosidase activity in cells derived from patients with late-onset Pompe diseaseMay Thandar Aung-Htut, Kristin A Ham, Michel Tchan, et al.
International Journal of Clinical and Experimental Pathology|September 17, 2013
Investigation of splicing changes and post-translational processing of LMNA in sporadic inclusion body myositisYue-Bei Luo, Chalermchai Mitrpant, Russell Johnsen, et al.
International Journal of Clinical and Experimental Pathology|December 3, 2013
Investigation of age-related changes in LMNA splicing and expression of progerin in human skeletal musclesYue-Bei Luo, Chalermchai Mitrpant, Russell D Johnsen, et al.
Plos One|June 4, 2014
Antisense oligonucleotide induction of progerin in human myogenic cellsYue-Bei Luo, Chalermchai Mitrpant, Abbie M Adams, et al.
Nature Medicine|January 31, 2006
Systemic delivery of morpholino oligonucleotide restores dystrophin expression bodywide and improves dystrophic pathologyJulia Alter, Fang Lou, Adam Rabinowitz, et al.
Pageof 11

Showing results (61-70 of 109) with videos related to

Sort By:
Pageof 11
Vision (Basel, Switzerland)|November 20, 2019
Inherited Retinal Disease Therapies Targeting Precursor Messenger Ribonucleic AcidDi Huang, Sue Fletcher, Steve D Wilton, et al.
Neuromuscular Disorders : NMD|December 21, 2011
Multiple exon skipping strategies to by-pass dystrophin mutationsCarl F Adkin, Penelope L Meloni, Susan Fletcher, et al.
Pathology|September 8, 2011
Gene therapy: therapeutic applications and relevance to pathologyGerald Both, Ian Alexander, Sue Fletcher, et al.
Molecular and Cellular Pediatrics|February 8, 2018
The potential of antisense oligonucleotide therapies for inherited childhood lung diseasesKelly M Martinovich, Nicole C Shaw, Anthony Kicic, et al.
Frontiers in Genetics|January 21, 2020
Consequences of Making the Inactive Active Through Changes in Antisense Oligonucleotide ChemistriesKhine Zaw, Kane Greer, May Thandar Aung-Htut, et al.
Scientific Reports|April 23, 2020
Splice modulating antisense oligonucleotides restore some acid-alpha-glucosidase activity in cells derived from patients with late-onset Pompe diseaseMay Thandar Aung-Htut, Kristin A Ham, Michel Tchan, et al.
International Journal of Clinical and Experimental Pathology|September 17, 2013
Investigation of splicing changes and post-translational processing of LMNA in sporadic inclusion body myositisYue-Bei Luo, Chalermchai Mitrpant, Russell Johnsen, et al.
International Journal of Clinical and Experimental Pathology|December 3, 2013
Investigation of age-related changes in LMNA splicing and expression of progerin in human skeletal musclesYue-Bei Luo, Chalermchai Mitrpant, Russell D Johnsen, et al.
Plos One|June 4, 2014
Antisense oligonucleotide induction of progerin in human myogenic cellsYue-Bei Luo, Chalermchai Mitrpant, Abbie M Adams, et al.
Nature Medicine|January 31, 2006
Systemic delivery of morpholino oligonucleotide restores dystrophin expression bodywide and improves dystrophic pathologyJulia Alter, Fang Lou, Adam Rabinowitz, et al.
Pageof 11