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FEBS Letters
|
December 21, 2018
YAPping about and not forgetting TAZ
Bernard 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 zebrafish
Joachim 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 therapies
Nigel 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 Transcript
Loren 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 directions
Aidan 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 mutations
Craig 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 Protein
Dunhui 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 interaction
Manoj 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 Gene
Kane Greer, Russell Johnsen, Yoram Nevo, et al.
Neuromuscular Disorders : NMD
|
September 7, 2010
Personalized exon skipping strategies to address clustered non-deletion dystrophin mutations
Sarah Forrest, Penny L Meloni, Francesco Muntoni, et al.
Page
of 11
Search research articles
Search
Showing results (31-40 of 109) with videos related to
Sort By:
Page
of 11
FEBS Letters
|
December 21, 2018
YAPping about and not forgetting TAZ
Bernard 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 zebrafish
Joachim 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 therapies
Nigel 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 Transcript
Loren 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 directions
Aidan 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 mutations
Craig 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 Protein
Dunhui 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 interaction
Manoj 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 Gene
Kane Greer, Russell Johnsen, Yoram Nevo, et al.
Neuromuscular Disorders : NMD
|
September 7, 2010
Personalized exon skipping strategies to address clustered non-deletion dystrophin mutations
Sarah Forrest, Penny L Meloni, Francesco Muntoni, et al.
Page
of 11