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Showing results (271-280 of 333) with videos related to

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Human Molecular Genetics|August 27, 2015
Muscle weakness in TPM3-myopathy is due to reduced Ca2+-sensitivity and impaired acto-myosin cross-bridge cycling in slow fibresMichaela Yuen, Sandra T Cooper, Steve B Marston, et al.
American Journal of Human Genetics|May 3, 2001
Nemaline myopathy caused by mutations in the muscle alpha-skeletal-actin geneB Ilkovski, S T Cooper, K Nowak, et al.
Medicine and Sport Science|June 12, 2016
The Future of Genomic Research in Athletic Performance and Adaptation to TrainingGuan Wang, Masashi Tanaka, Nir Eynon, et al.
Brain : a Journal of Neurology|November 10, 2011
Hypertrophy and dietary tyrosine ameliorate the phenotypes of a mouse model of severe nemaline myopathyMai-Anh T Nguyen, Josephine E Joya, Anthony J Kee, et al.
Physiological Genomics|December 31, 2015
Athlome Project Consortium: a concerted effort to discover genomic and other "omic" markers of athletic performanceYannis P Pitsiladis, Masashi Tanaka, Nir Eynon, et al.
Neuropsychology|February 13, 2025
Agreement, reliability, feasibility, and acceptability of home-based telehealth versus face-to-face pediatric neuropsychological testing: A within-person crossover studyKristina M Haebich, Hayley Darke, Francesca Lami, et al.
Nature Reviews. Genetics|October 7, 2024
A call to action to scale up research and clinical genomic data sharingZornitza Stark, David Glazer, Oliver Hofmann, et al.
Annals of Neurology|October 1, 2008
Collagen VI glycine mutations: perturbed assembly and a spectrum of clinical severityRishika A Pace, Rachel A Peat, Naomi L Baker, et al.
Human Mutation|June 29, 2010
Recessive mutations in RYR1 are a common cause of congenital fiber type disproportionNigel F Clarke, Leigh B Waddell, Sandra T Cooper, et al.
Molecular Autism|January 5, 2022
Delineating the autistic phenotype in children with neurofibromatosis type 1Anita K Chisholm, Kristina M Haebich, Natalie A Pride, et al.
Pageof 34

Showing results (271-280 of 333) with videos related to

Sort By:
Pageof 34
Human Molecular Genetics|August 27, 2015
Muscle weakness in TPM3-myopathy is due to reduced Ca2+-sensitivity and impaired acto-myosin cross-bridge cycling in slow fibresMichaela Yuen, Sandra T Cooper, Steve B Marston, et al.
American Journal of Human Genetics|May 3, 2001
Nemaline myopathy caused by mutations in the muscle alpha-skeletal-actin geneB Ilkovski, S T Cooper, K Nowak, et al.
Medicine and Sport Science|June 12, 2016
The Future of Genomic Research in Athletic Performance and Adaptation to TrainingGuan Wang, Masashi Tanaka, Nir Eynon, et al.
Brain : a Journal of Neurology|November 10, 2011
Hypertrophy and dietary tyrosine ameliorate the phenotypes of a mouse model of severe nemaline myopathyMai-Anh T Nguyen, Josephine E Joya, Anthony J Kee, et al.
Physiological Genomics|December 31, 2015
Athlome Project Consortium: a concerted effort to discover genomic and other "omic" markers of athletic performanceYannis P Pitsiladis, Masashi Tanaka, Nir Eynon, et al.
Neuropsychology|February 13, 2025
Agreement, reliability, feasibility, and acceptability of home-based telehealth versus face-to-face pediatric neuropsychological testing: A within-person crossover studyKristina M Haebich, Hayley Darke, Francesca Lami, et al.
Nature Reviews. Genetics|October 7, 2024
A call to action to scale up research and clinical genomic data sharingZornitza Stark, David Glazer, Oliver Hofmann, et al.
Annals of Neurology|October 1, 2008
Collagen VI glycine mutations: perturbed assembly and a spectrum of clinical severityRishika A Pace, Rachel A Peat, Naomi L Baker, et al.
Human Mutation|June 29, 2010
Recessive mutations in RYR1 are a common cause of congenital fiber type disproportionNigel F Clarke, Leigh B Waddell, Sandra T Cooper, et al.
Molecular Autism|January 5, 2022
Delineating the autistic phenotype in children with neurofibromatosis type 1Anita K Chisholm, Kristina M Haebich, Natalie A Pride, et al.
Pageof 34