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Arran Babbs

Showing results (11-20 of 18) with videos related to

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Molecular Therapy. Methods & Clinical Development|November 13, 2018
Micro-utrophin Improves Cardiac and Skeletal Muscle Function of Severely Affected D2/<i>mdx</i> MiceTahnee L Kennedy, Simon Guiraud, Ben Edwards, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 7, 2007
A dominant mutation in Snap25 causes impaired vesicle trafficking, sensorimotor gating, and ataxia in the blind-drunk mouseAlexander F Jeans, Peter L Oliver, Reuben Johnson, et al.
Human Molecular Genetics|November 11, 2010
Diaphragm rescue alone prevents heart dysfunction in dystrophic miceAlastair Crisp, Haifang Yin, Aurelie Goyenvalle, et al.
Human Molecular Genetics|May 3, 2015
Second-generation compound for the modulation of utrophin in the therapy of DMDSimon Guiraud, Sarah E Squire, Benjamin Edwards, et al.
Nature Medicine|February 3, 2015
Functional correction in mouse models of muscular dystrophy using exon-skipping tricyclo-DNA oligomersAurélie Goyenvalle, Graziella Griffith, Arran Babbs, et al.
Journal of Medicinal Chemistry|June 20, 2020
2-Arylbenzo[<i>d</i>]oxazole Phosphinate Esters as Second-Generation Modulators of Utrophin for the Treatment of Duchenne Muscular DystrophyArran Babbs, Adam Berg, Maria Chatzopoulou, et al.
The Journal of Infection|August 22, 2025
Evaluation of Hepatitis B core-related antigen (HBcrAg) as a biomarker in cohorts from the United Kingdom and South AfricaLouise O Downs, Marion Delphin, Marije van Schalkwyk, et al.
Tetrahedron|July 28, 2020
Synthesis of SMT022357 enantiomers and <i>in vivo</i> evaluation in a Duchenne muscular dystrophy mouse modelArran Babbs, Adam Berg, Maria Chatzopoulou, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Molecular Therapy. Methods & Clinical Development|November 13, 2018
Micro-utrophin Improves Cardiac and Skeletal Muscle Function of Severely Affected D2/<i>mdx</i> MiceTahnee L Kennedy, Simon Guiraud, Ben Edwards, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 7, 2007
A dominant mutation in Snap25 causes impaired vesicle trafficking, sensorimotor gating, and ataxia in the blind-drunk mouseAlexander F Jeans, Peter L Oliver, Reuben Johnson, et al.
Human Molecular Genetics|November 11, 2010
Diaphragm rescue alone prevents heart dysfunction in dystrophic miceAlastair Crisp, Haifang Yin, Aurelie Goyenvalle, et al.
Human Molecular Genetics|May 3, 2015
Second-generation compound for the modulation of utrophin in the therapy of DMDSimon Guiraud, Sarah E Squire, Benjamin Edwards, et al.
Nature Medicine|February 3, 2015
Functional correction in mouse models of muscular dystrophy using exon-skipping tricyclo-DNA oligomersAurélie Goyenvalle, Graziella Griffith, Arran Babbs, et al.
Journal of Medicinal Chemistry|June 20, 2020
2-Arylbenzo[<i>d</i>]oxazole Phosphinate Esters as Second-Generation Modulators of Utrophin for the Treatment of Duchenne Muscular DystrophyArran Babbs, Adam Berg, Maria Chatzopoulou, et al.
The Journal of Infection|August 22, 2025
Evaluation of Hepatitis B core-related antigen (HBcrAg) as a biomarker in cohorts from the United Kingdom and South AfricaLouise O Downs, Marion Delphin, Marije van Schalkwyk, et al.
Tetrahedron|July 28, 2020
Synthesis of SMT022357 enantiomers and <i>in vivo</i> evaluation in a Duchenne muscular dystrophy mouse modelArran Babbs, Adam Berg, Maria Chatzopoulou, et al.
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