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Human Molecular Genetics
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September 20, 2015
Multi-level omics analysis in a murine model of dystrophin loss and therapeutic restoration
Thomas C Roberts, Henrik J Johansson, Graham McClorey, et al.
Annals of Neurology
|
October 18, 2006
Fukutin gene mutations in steroid-responsive limb girdle muscular dystrophy
Caroline 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 mouse
Caroline Godfrey, Sofia Muses, Graham McClorey, et al.
Archives of Neurology
|
January 16, 2008
Mild POMGnT1 mutations underlie a novel limb-girdle muscular dystrophy variant
Emma 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 Dystrophy
Corinne 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 mice
Corinne 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 Oligonucleotides
Suzan 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 biomarkers
Hannah 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 DMD
Anna 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 treatment
Corinne A Betts, Graham McClorey, Richard Healicon, et al.
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of 3
Search research articles
Search
Showing results (11-20 of 24) with videos related to
Sort By:
Page
of 3
Human Molecular Genetics
|
September 20, 2015
Multi-level omics analysis in a murine model of dystrophin loss and therapeutic restoration
Thomas C Roberts, Henrik J Johansson, Graham McClorey, et al.
Annals of Neurology
|
October 18, 2006
Fukutin gene mutations in steroid-responsive limb girdle muscular dystrophy
Caroline 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 mouse
Caroline Godfrey, Sofia Muses, Graham McClorey, et al.
Archives of Neurology
|
January 16, 2008
Mild POMGnT1 mutations underlie a novel limb-girdle muscular dystrophy variant
Emma 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 Dystrophy
Corinne 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 mice
Corinne 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 Oligonucleotides
Suzan 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 biomarkers
Hannah 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 DMD
Anna 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 treatment
Corinne A Betts, Graham McClorey, Richard Healicon, et al.
Page
of 3