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Caroline Godfrey

Showing results (11-20 of 24) with videos related to

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Human Molecular Genetics|September 20, 2015
Multi-level omics analysis in a murine model of dystrophin loss and therapeutic restorationThomas C Roberts, Henrik J Johansson, Graham McClorey, et al.
Annals of Neurology|October 18, 2006
Fukutin gene mutations in steroid-responsive limb girdle muscular dystrophyCaroline Godfrey, Diana Escolar, Martin Brockington, et al.
Human Molecular Genetics|May 3, 2015
How much dystrophin is enough: the physiological consequences of different levels of dystrophin in the mdx mouseCaroline Godfrey, Sofia Muses, Graham McClorey, et al.
Archives of Neurology|January 16, 2008
Mild POMGnT1 mutations underlie a novel limb-girdle muscular dystrophy variantEmma M Clement, Caroline Godfrey, Jenny Tan, et al.
Scientific Reports|June 27, 2015
Implications for Cardiac Function Following Rescue of the Dystrophic Diaphragm in a Mouse Model of Duchenne Muscular DystrophyCorinne A Betts, Amer F Saleh, Carolyn A Carr, et al.
Scientific Reports|March 12, 2015
Prevention of exercised induced cardiomyopathy following Pip-PMO treatment in dystrophic mdx miceCorinne A Betts, Amer F Saleh, Carolyn A Carr, et al.
Molecular Therapy. Nucleic Acids|November 26, 2014
Correlating In Vitro Splice Switching Activity With Systemic In Vivo Delivery Using Novel ZEN-modified OligonucleotidesSuzan M Hammond, Graham McClorey, Joel Z Nordin, et al.
The Journal of Thoracic and Cardiovascular Surgery|February 15, 2023
Improving lung cancer diagnosis with cancer, fungal, and imaging biomarkersHannah N Marmor, Michael N Kammer, Stephen A Deppen, et al.
Molecular Therapy. Nucleic Acids|September 17, 2018
Comprehensive RNA-Sequencing Analysis in Serum and Muscle Reveals Novel Small RNA Signatures with Biomarker Potential for DMDAnna M L Coenen-Stass, Helena Sork, Sole Gatto, et al.
Human Molecular Genetics|October 4, 2018
Cmah-dystrophin deficient mdx mice display an accelerated cardiac phenotype that is improved following peptide-PMO exon skipping treatmentCorinne A Betts, Graham McClorey, Richard Healicon, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Human Molecular Genetics|September 20, 2015
Multi-level omics analysis in a murine model of dystrophin loss and therapeutic restorationThomas C Roberts, Henrik J Johansson, Graham McClorey, et al.
Annals of Neurology|October 18, 2006
Fukutin gene mutations in steroid-responsive limb girdle muscular dystrophyCaroline Godfrey, Diana Escolar, Martin Brockington, et al.
Human Molecular Genetics|May 3, 2015
How much dystrophin is enough: the physiological consequences of different levels of dystrophin in the mdx mouseCaroline Godfrey, Sofia Muses, Graham McClorey, et al.
Archives of Neurology|January 16, 2008
Mild POMGnT1 mutations underlie a novel limb-girdle muscular dystrophy variantEmma M Clement, Caroline Godfrey, Jenny Tan, et al.
Scientific Reports|June 27, 2015
Implications for Cardiac Function Following Rescue of the Dystrophic Diaphragm in a Mouse Model of Duchenne Muscular DystrophyCorinne A Betts, Amer F Saleh, Carolyn A Carr, et al.
Scientific Reports|March 12, 2015
Prevention of exercised induced cardiomyopathy following Pip-PMO treatment in dystrophic mdx miceCorinne A Betts, Amer F Saleh, Carolyn A Carr, et al.
Molecular Therapy. Nucleic Acids|November 26, 2014
Correlating In Vitro Splice Switching Activity With Systemic In Vivo Delivery Using Novel ZEN-modified OligonucleotidesSuzan M Hammond, Graham McClorey, Joel Z Nordin, et al.
The Journal of Thoracic and Cardiovascular Surgery|February 15, 2023
Improving lung cancer diagnosis with cancer, fungal, and imaging biomarkersHannah N Marmor, Michael N Kammer, Stephen A Deppen, et al.
Molecular Therapy. Nucleic Acids|September 17, 2018
Comprehensive RNA-Sequencing Analysis in Serum and Muscle Reveals Novel Small RNA Signatures with Biomarker Potential for DMDAnna M L Coenen-Stass, Helena Sork, Sole Gatto, et al.
Human Molecular Genetics|October 4, 2018
Cmah-dystrophin deficient mdx mice display an accelerated cardiac phenotype that is improved following peptide-PMO exon skipping treatmentCorinne A Betts, Graham McClorey, Richard Healicon, et al.
Pageof 3