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Showing results (221-230 of 333) with videos related to

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International Journal of Obesity (2005)|March 16, 2017
Exploring the relationship between α-actinin-3 deficiency and obesity in mice and humansP J Houweling, Y D Berman, N Turner, et al.
Neurology|September 11, 2002
Gliomas presenting after age 10 in individuals with neurofibromatosis type 1 (NF1)D H Gutmann, S A Rasmussen, P Wolkenstein, et al.
Cell Motility and the Cytoskeleton|October 31, 2007
Tropomyosin 4 defines novel filaments in skeletal muscle associated with muscle remodelling/regeneration in normal and diseased muscleNicole Vlahovich, Galina Schevzov, Visalini Nair-Shaliker, et al.
Neurology|January 17, 2007
Outcome of noninvasive ventilation in children with neuromuscular diseaseH K Young, A Lowe, D A Fitzgerald, et al.
Molecular Psychiatry|December 5, 2024
Brain volumes in genetic syndromes associated with mTOR dysregulation: a systematic review and meta-analysisJonathan M Payne, Kristina M Haebich, Rebecca Mitchell, et al.
Stem Cell Research|January 26, 2024
Generation of a human ACTA1-tdTomato reporter iPSC line using CRISPR/Cas9 editingPeter J Houweling, Vanessa Crossman, Chrystal F Tiong, et al.
Annals of Neurology|August 21, 2007
Intranuclear rod myopathy: molecular pathogenesis and mechanisms of weaknessAna Domazetovska, Biljana Ilkovski, Vikash Kumar, et al.
Neurology|October 10, 2001
Congenital muscular dystrophy with primary partial laminin alpha2 chain deficiency: molecular studyY He, K J Jones, N Vignier, et al.
Human Molecular Genetics|February 7, 2001
A mutation in alpha-tropomyosin(slow) affects muscle strength, maturation and hypertrophy in a mouse model for nemaline myopathyM A Corbett, C S Robinson, G F Dunglison, et al.
The Journal of Biological Chemistry|August 24, 2010
Collagen VI microfibril formation is abolished by an {alpha}2(VI) von Willebrand factor type A domain mutation in a patient with Ullrich congenital muscular dystrophyLeona D Tooley, Laura K Zamurs, Nicola Beecher, et al.
Pageof 34

Showing results (221-230 of 333) with videos related to

Sort By:
Pageof 34
International Journal of Obesity (2005)|March 16, 2017
Exploring the relationship between α-actinin-3 deficiency and obesity in mice and humansP J Houweling, Y D Berman, N Turner, et al.
Neurology|September 11, 2002
Gliomas presenting after age 10 in individuals with neurofibromatosis type 1 (NF1)D H Gutmann, S A Rasmussen, P Wolkenstein, et al.
Cell Motility and the Cytoskeleton|October 31, 2007
Tropomyosin 4 defines novel filaments in skeletal muscle associated with muscle remodelling/regeneration in normal and diseased muscleNicole Vlahovich, Galina Schevzov, Visalini Nair-Shaliker, et al.
Neurology|January 17, 2007
Outcome of noninvasive ventilation in children with neuromuscular diseaseH K Young, A Lowe, D A Fitzgerald, et al.
Molecular Psychiatry|December 5, 2024
Brain volumes in genetic syndromes associated with mTOR dysregulation: a systematic review and meta-analysisJonathan M Payne, Kristina M Haebich, Rebecca Mitchell, et al.
Stem Cell Research|January 26, 2024
Generation of a human ACTA1-tdTomato reporter iPSC line using CRISPR/Cas9 editingPeter J Houweling, Vanessa Crossman, Chrystal F Tiong, et al.
Annals of Neurology|August 21, 2007
Intranuclear rod myopathy: molecular pathogenesis and mechanisms of weaknessAna Domazetovska, Biljana Ilkovski, Vikash Kumar, et al.
Neurology|October 10, 2001
Congenital muscular dystrophy with primary partial laminin alpha2 chain deficiency: molecular studyY He, K J Jones, N Vignier, et al.
Human Molecular Genetics|February 7, 2001
A mutation in alpha-tropomyosin(slow) affects muscle strength, maturation and hypertrophy in a mouse model for nemaline myopathyM A Corbett, C S Robinson, G F Dunglison, et al.
The Journal of Biological Chemistry|August 24, 2010
Collagen VI microfibril formation is abolished by an {alpha}2(VI) von Willebrand factor type A domain mutation in a patient with Ullrich congenital muscular dystrophyLeona D Tooley, Laura K Zamurs, Nicola Beecher, et al.
Pageof 34