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Showing results (251-260 of 333) with videos related to

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Human Molecular Genetics|October 29, 2013
NF1 is a critical regulator of muscle development and metabolismKate Sullivan, Jad El-Hoss, Kate G R Quinlan, et al.
Neuromuscular Disorders : NMD|March 4, 2014
Diagnostic approach to the congenital muscular dystrophiesCarsten G Bönnemann, Ching H Wang, Susana Quijano-Roy, et al.
Neuromuscular Disorders : NMD|September 28, 2007
Limb-girdle muscular dystrophy: diagnostic evaluation, frequency and clues to pathogenesisHarriet P Lo, Sandra T Cooper, Frances J Evesson, et al.
Stem Cell Research|June 22, 2021
Generating an iPSC line (with isogenic control) from the PBMCs of an ACTA1 (p.Gly148Asp) nemaline myopathy patientPeter J Houweling, Chantal A Coles, Chrystal F Tiong, et al.
American Journal of Human Genetics|January 5, 2019
Integrating Genomics into Healthcare: A Global ResponsibilityZornitza Stark, Lena Dolman, Teri A Manolio, et al.
Neuromuscular Disorders : NMD|February 8, 2011
Mosaic caveolin-3 expression in acquired rippling muscle disease without evidence of myasthenia gravis or acetylcholine receptor autoantibodiesHarriet P Lo, Enrico Bertini, Massimiliano Mirabella, et al.
American Journal of Human Genetics|February 18, 2021
Loss of α-actinin-3 during human evolution provides superior cold resilience and muscle heat generationVictoria L Wyckelsma, Tomas Venckunas, Peter J Houweling, et al.
The Journal of Clinical Investigation|October 5, 2013
ACTN3 genotype influences muscle performance through the regulation of calcineurin signalingJane T Seto, Kate G R Quinlan, Monkol Lek, et al.
The Journal of Thoracic and Cardiovascular Surgery|April 22, 2009
Myocardial membrane injury in pediatric cardiac surgery: An animal modelJonathan R Egan, Tanya L Butler, Andrew D Cole, et al.
Developmental Medicine and Child Neurology|March 18, 2020
Social skills and autism spectrum disorder symptoms in children with neurofibromatosis type 1: evidence for clinical trial outcomesJonathan M Payne, Karin S Walsh, Natalie A Pride, et al.
Pageof 34

Showing results (251-260 of 333) with videos related to

Sort By:
Pageof 34
Human Molecular Genetics|October 29, 2013
NF1 is a critical regulator of muscle development and metabolismKate Sullivan, Jad El-Hoss, Kate G R Quinlan, et al.
Neuromuscular Disorders : NMD|March 4, 2014
Diagnostic approach to the congenital muscular dystrophiesCarsten G Bönnemann, Ching H Wang, Susana Quijano-Roy, et al.
Neuromuscular Disorders : NMD|September 28, 2007
Limb-girdle muscular dystrophy: diagnostic evaluation, frequency and clues to pathogenesisHarriet P Lo, Sandra T Cooper, Frances J Evesson, et al.
Stem Cell Research|June 22, 2021
Generating an iPSC line (with isogenic control) from the PBMCs of an ACTA1 (p.Gly148Asp) nemaline myopathy patientPeter J Houweling, Chantal A Coles, Chrystal F Tiong, et al.
American Journal of Human Genetics|January 5, 2019
Integrating Genomics into Healthcare: A Global ResponsibilityZornitza Stark, Lena Dolman, Teri A Manolio, et al.
Neuromuscular Disorders : NMD|February 8, 2011
Mosaic caveolin-3 expression in acquired rippling muscle disease without evidence of myasthenia gravis or acetylcholine receptor autoantibodiesHarriet P Lo, Enrico Bertini, Massimiliano Mirabella, et al.
American Journal of Human Genetics|February 18, 2021
Loss of α-actinin-3 during human evolution provides superior cold resilience and muscle heat generationVictoria L Wyckelsma, Tomas Venckunas, Peter J Houweling, et al.
The Journal of Clinical Investigation|October 5, 2013
ACTN3 genotype influences muscle performance through the regulation of calcineurin signalingJane T Seto, Kate G R Quinlan, Monkol Lek, et al.
The Journal of Thoracic and Cardiovascular Surgery|April 22, 2009
Myocardial membrane injury in pediatric cardiac surgery: An animal modelJonathan R Egan, Tanya L Butler, Andrew D Cole, et al.
Developmental Medicine and Child Neurology|March 18, 2020
Social skills and autism spectrum disorder symptoms in children with neurofibromatosis type 1: evidence for clinical trial outcomesJonathan M Payne, Karin S Walsh, Natalie A Pride, et al.
Pageof 34