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Steve D Wilton

Showing results (31-40 of 109) with videos related to

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FEBS Letters|December 21, 2018
YAPping about and not forgetting TAZBernard A Callus, Megan L Finch-Edmondson, Sue Fletcher, et al.
Journal of Cellular and Molecular Medicine|January 22, 2011
Evaluation of exon-skipping strategies for Duchenne muscular dystrophy utilizing dystrophin-deficient zebrafishJoachim Berger, Silke Berger, Arie S Jacoby, et al.
The Clinical Biochemist. Reviews|September 14, 2011
Molecular diagnosis of duchenne muscular dystrophy: past, present and future in relation to implementing therapiesNigel G Laing, Mark R Davis, Klair Bayley, et al.
Molecular Therapy. Nucleic Acids|June 3, 2018
Antisense Oligonucleotide-Mediated Terminal Intron Retention of the SMN2 TranscriptLoren L Flynn, Chalermchai Mitrpant, Ianthe L Pitout, et al.
Frontiers in Molecular Neuroscience|August 8, 2024
Down syndrome and DYRK1A overexpression: relationships and future therapeutic directionsAidan J Murphy, Steve D Wilton, May T Aung-Htut, et al.
Current Opinion in Lipidology|October 15, 2021
Splice correction therapies for familial hypercholesterolemic patients with low-density lipoprotein receptor mutationsCraig S McIntosh, Gerald F Watts, Steve D Wilton, et al.
Molecular Therapy. Nucleic Acids|November 24, 2020
Morpholino Oligomer-Induced Dystrophin Isoforms to Map the Functional Domains in the Dystrophin ProteinDunhui Li, Abbie M Adams, Russell D Johnsen, et al.
Plos One|October 19, 2017
Functional improvement of dystrophic muscle by repression of utrophin: let-7c interactionManoj K Mishra, Emanuele Loro, Kasturi Sengupta, et al.
International Journal of Molecular Sciences|July 8, 2020
Single Exon Skipping Can Address a Multi-Exon Duplication in the Dystrophin GeneKane Greer, Russell Johnsen, Yoram Nevo, et al.
Neuromuscular Disorders : NMD|September 7, 2010
Personalized exon skipping strategies to address clustered non-deletion dystrophin mutationsSarah Forrest, Penny L Meloni, Francesco Muntoni, et al.
Pageof 11

Showing results (31-40 of 109) with videos related to

Sort By:
Pageof 11
FEBS Letters|December 21, 2018
YAPping about and not forgetting TAZBernard A Callus, Megan L Finch-Edmondson, Sue Fletcher, et al.
Journal of Cellular and Molecular Medicine|January 22, 2011
Evaluation of exon-skipping strategies for Duchenne muscular dystrophy utilizing dystrophin-deficient zebrafishJoachim Berger, Silke Berger, Arie S Jacoby, et al.
The Clinical Biochemist. Reviews|September 14, 2011
Molecular diagnosis of duchenne muscular dystrophy: past, present and future in relation to implementing therapiesNigel G Laing, Mark R Davis, Klair Bayley, et al.
Molecular Therapy. Nucleic Acids|June 3, 2018
Antisense Oligonucleotide-Mediated Terminal Intron Retention of the SMN2 TranscriptLoren L Flynn, Chalermchai Mitrpant, Ianthe L Pitout, et al.
Frontiers in Molecular Neuroscience|August 8, 2024
Down syndrome and DYRK1A overexpression: relationships and future therapeutic directionsAidan J Murphy, Steve D Wilton, May T Aung-Htut, et al.
Current Opinion in Lipidology|October 15, 2021
Splice correction therapies for familial hypercholesterolemic patients with low-density lipoprotein receptor mutationsCraig S McIntosh, Gerald F Watts, Steve D Wilton, et al.
Molecular Therapy. Nucleic Acids|November 24, 2020
Morpholino Oligomer-Induced Dystrophin Isoforms to Map the Functional Domains in the Dystrophin ProteinDunhui Li, Abbie M Adams, Russell D Johnsen, et al.
Plos One|October 19, 2017
Functional improvement of dystrophic muscle by repression of utrophin: let-7c interactionManoj K Mishra, Emanuele Loro, Kasturi Sengupta, et al.
International Journal of Molecular Sciences|July 8, 2020
Single Exon Skipping Can Address a Multi-Exon Duplication in the Dystrophin GeneKane Greer, Russell Johnsen, Yoram Nevo, et al.
Neuromuscular Disorders : NMD|September 7, 2010
Personalized exon skipping strategies to address clustered non-deletion dystrophin mutationsSarah Forrest, Penny L Meloni, Francesco Muntoni, et al.
Pageof 11