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Showing results (181-190 of 333) with videos related to

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Cell Motility and the Cytoskeleton|May 18, 2004
C2C12 co-culture on a fibroblast substratum enables sustained survival of contractile, highly differentiated myotubes with peripheral nuclei and adult fast myosin expressionS T Cooper, A L Maxwell, E Kizana, et al.
Human Mutation|October 4, 2018
Is evolutionary loss our gain? The role of ACTN3 p.Arg577Ter (R577X) genotype in athletic performance, ageing, and diseasePeter J Houweling, Ioannis D Papadimitriou, Jane T Seto, et al.
Neuropsychology|June 29, 2023
Understanding nonliteral language abilities in children with neurofibromatosis type 1Kristina M Haebich, Natalie A Pride, Alana Collins, et al.
Implementation Research and Practice|May 13, 2024
Pilot evaluation of the Fiscal Mapping Process for sustainable financing of evidence-based youth mental health treatments: A comparative case study analysisAlex R Dopp, Maddison N North, Marylou Gilbert, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 20, 2022
A randomized controlled trial of remote microphone listening devices to treat auditory deficits in children with neurofibromatosis type 1Gary Rance, Alice Maier, Julien Zanin, et al.
Neuromuscular Disorders : NMD|February 17, 2007
Dystrophinopathy carrier determination and detection of protein deficiencies in muscular dystrophy using lentiviral MyoD-forced myogenesisSandra T Cooper, Eddy Kizana, Jonathon D Yates, et al.
Journal of Child Neurology|December 15, 2007
Dietary L-tyrosine supplementation in nemaline myopathyMonique M Ryan, Catherine Sy, Sian Rudge, et al.
Journal of Molecular and Cellular Cardiology|May 12, 2004
Expression of aquaporin 1 in human cardiac and skeletal muscleCarol G Au, Sandra T Cooper, Harriet P Lo, et al.
Neuromuscular Disorders : NMD|June 26, 2016
TOR1AIP1 as a cause of cardiac failure and recessive limb-girdle muscular dystrophyRoula Ghaoui, Tatiana Benavides, Monkol Lek, et al.
Human Molecular Genetics|December 2, 2005
Aberrant dysferlin trafficking in cells lacking caveolin or expressing dystrophy mutants of caveolin-3Delia J Hernández-Deviez, Sally Martin, Steven H Laval, et al.
Pageof 34

Showing results (181-190 of 333) with videos related to

Sort By:
Pageof 34
Cell Motility and the Cytoskeleton|May 18, 2004
C2C12 co-culture on a fibroblast substratum enables sustained survival of contractile, highly differentiated myotubes with peripheral nuclei and adult fast myosin expressionS T Cooper, A L Maxwell, E Kizana, et al.
Human Mutation|October 4, 2018
Is evolutionary loss our gain? The role of ACTN3 p.Arg577Ter (R577X) genotype in athletic performance, ageing, and diseasePeter J Houweling, Ioannis D Papadimitriou, Jane T Seto, et al.
Neuropsychology|June 29, 2023
Understanding nonliteral language abilities in children with neurofibromatosis type 1Kristina M Haebich, Natalie A Pride, Alana Collins, et al.
Implementation Research and Practice|May 13, 2024
Pilot evaluation of the Fiscal Mapping Process for sustainable financing of evidence-based youth mental health treatments: A comparative case study analysisAlex R Dopp, Maddison N North, Marylou Gilbert, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 20, 2022
A randomized controlled trial of remote microphone listening devices to treat auditory deficits in children with neurofibromatosis type 1Gary Rance, Alice Maier, Julien Zanin, et al.
Neuromuscular Disorders : NMD|February 17, 2007
Dystrophinopathy carrier determination and detection of protein deficiencies in muscular dystrophy using lentiviral MyoD-forced myogenesisSandra T Cooper, Eddy Kizana, Jonathon D Yates, et al.
Journal of Child Neurology|December 15, 2007
Dietary L-tyrosine supplementation in nemaline myopathyMonique M Ryan, Catherine Sy, Sian Rudge, et al.
Journal of Molecular and Cellular Cardiology|May 12, 2004
Expression of aquaporin 1 in human cardiac and skeletal muscleCarol G Au, Sandra T Cooper, Harriet P Lo, et al.
Neuromuscular Disorders : NMD|June 26, 2016
TOR1AIP1 as a cause of cardiac failure and recessive limb-girdle muscular dystrophyRoula Ghaoui, Tatiana Benavides, Monkol Lek, et al.
Human Molecular Genetics|December 2, 2005
Aberrant dysferlin trafficking in cells lacking caveolin or expressing dystrophy mutants of caveolin-3Delia J Hernández-Deviez, Sally Martin, Steven H Laval, et al.
Pageof 34