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Benjamin Edwards

Showing results (21-30 of 33) with videos related to

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Human Molecular Genetics|April 17, 2019
The potential of utrophin and dystrophin combination therapies for Duchenne muscular dystrophySimon Guiraud, Benjamin Edwards, Arran Babbs, et al.
The Journal of Biological Chemistry|August 10, 2014
A novel mouse model of a patient mucolipidosis II mutation recapitulates disease pathologyLeigh Paton, Emmanuelle Bitoun, Janet Kenyon, et al.
Human Molecular Genetics|October 11, 2018
Embryonic myosin is a regeneration marker to monitor utrophin-based therapies for DMDSimon Guiraud, Benjamin Edwards, Sarah E Squire, et al.
American Journal of Critical Care : an Official Publication, American Association of Critical-Care Nurses|April 30, 2025
Longitudinal Evaluation of Implementation of AACN's Healthy Work Environment Framework in an Intensive Care UnitPhilip Parker, Heather Pena, Jason Stokes, et al.
Plos Genetics|October 27, 2011
Oxr1 is essential for protection against oxidative stress-induced neurodegenerationPeter L Oliver, Mattéa J Finelli, Benjamin Edwards, et al.
Cerebral Cortex (New York, N.Y. : 1991)|September 12, 2014
Disruption of Visc-2, a Brain-Expressed Conserved Long Noncoding RNA, Does Not Elicit an Overt Anatomical or Behavioral PhenotypePeter L Oliver, Rebecca A Chodroff, Amrit Gosal, 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.
Journal of Seismology|May 15, 2018
Characterisation of ground motion recording stations in the Groningen gas fieldRik Noorlandt, Pauline P Kruiver, Marco P E de Kleine, et al.
BMJ Open|September 16, 2022
The Australian Temperament Project Generation 3 study: a population-based multigenerational prospective cohort study of socioemotional health and developmentCraig A Olsson, Primrose Letcher, Christopher J Greenwood, et al.
Skeletal Muscle|July 28, 2022
Dysregulation of Tweak and Fn14 in skeletal muscle of spinal muscular atrophy miceKatharina E Meijboom, Emma R Sutton, Eve McCallion, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
Human Molecular Genetics|April 17, 2019
The potential of utrophin and dystrophin combination therapies for Duchenne muscular dystrophySimon Guiraud, Benjamin Edwards, Arran Babbs, et al.
The Journal of Biological Chemistry|August 10, 2014
A novel mouse model of a patient mucolipidosis II mutation recapitulates disease pathologyLeigh Paton, Emmanuelle Bitoun, Janet Kenyon, et al.
Human Molecular Genetics|October 11, 2018
Embryonic myosin is a regeneration marker to monitor utrophin-based therapies for DMDSimon Guiraud, Benjamin Edwards, Sarah E Squire, et al.
American Journal of Critical Care : an Official Publication, American Association of Critical-Care Nurses|April 30, 2025
Longitudinal Evaluation of Implementation of AACN's Healthy Work Environment Framework in an Intensive Care UnitPhilip Parker, Heather Pena, Jason Stokes, et al.
Plos Genetics|October 27, 2011
Oxr1 is essential for protection against oxidative stress-induced neurodegenerationPeter L Oliver, Mattéa J Finelli, Benjamin Edwards, et al.
Cerebral Cortex (New York, N.Y. : 1991)|September 12, 2014
Disruption of Visc-2, a Brain-Expressed Conserved Long Noncoding RNA, Does Not Elicit an Overt Anatomical or Behavioral PhenotypePeter L Oliver, Rebecca A Chodroff, Amrit Gosal, 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.
Journal of Seismology|May 15, 2018
Characterisation of ground motion recording stations in the Groningen gas fieldRik Noorlandt, Pauline P Kruiver, Marco P E de Kleine, et al.
BMJ Open|September 16, 2022
The Australian Temperament Project Generation 3 study: a population-based multigenerational prospective cohort study of socioemotional health and developmentCraig A Olsson, Primrose Letcher, Christopher J Greenwood, et al.
Skeletal Muscle|July 28, 2022
Dysregulation of Tweak and Fn14 in skeletal muscle of spinal muscular atrophy miceKatharina E Meijboom, Emma R Sutton, Eve McCallion, et al.
Pageof 4