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Showing results (231-240 of 333) with videos related to

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Cancer Discovery|November 4, 2015
All the World's a Stage: Facilitating Discovery Science and Improved Cancer Care through the Global Alliance for Genomics and HealthMark Lawler, Lillian L Siu, Heidi L Rehm, et al.
American Journal of Human Genetics|March 11, 2025
The expanding global genomics landscape: Converging priorities from national genomics programsCaitlin Howley, Matilda A Haas, Wadha A Al Muftah, et al.
Experimental Gerontology|November 30, 2010
The effect of α-actinin-3 deficiency on muscle agingJane T Seto, Stephen Chan, Nigel Turner, et al.
Cardiovascular Research|January 22, 2016
Lack of MG53 in human heart precludes utility as a biomarker of myocardial injury or endogenous cardioprotective factorFrances A Lemckert, Adam Bournazos, Daniel M Eckert, et al.
Cancers|July 29, 2023
Sensory Processing in Children and Adolescents with Neurofibromatosis Type 1Natalie A Pride, Kristina M Haebich, Karin S Walsh, et al.
European Journal of Human Genetics : EJHG|September 4, 2014
Recessive ACTA1 variant causes congenital muscular dystrophy with rigid spineGina L O'Grady, Heather A Best, Emily C Oates, et al.
Muscle & Nerve|June 16, 2011
Epidermolysis bullosa with late-onset muscular dystrophy and plectin deficiencyEppie M Yiu, Alfred Klausegger, Leigh B Waddell, et al.
Neuromuscular Disorders : NMD|January 25, 2014
Approach to the diagnosis of congenital myopathiesKathryn N North, Ching H Wang, Nigel Clarke, et al.
Human Molecular Genetics|December 19, 2015
Analysis of the ACTN3 heterozygous genotype suggests that α-actinin-3 controls sarcomeric composition and muscle function in a dose-dependent fashionMarshall W Hogarth, Fleur C Garton, Peter J Houweling, et al.
American Journal of Human Genetics|November 26, 2008
Mutations in contactin-1, a neural adhesion and neuromuscular junction protein, cause a familial form of lethal congenital myopathyAlison G Compton, Douglas E Albrecht, Jane T Seto, et al.
Pageof 34

Showing results (231-240 of 333) with videos related to

Sort By:
Pageof 34
Cancer Discovery|November 4, 2015
All the World's a Stage: Facilitating Discovery Science and Improved Cancer Care through the Global Alliance for Genomics and HealthMark Lawler, Lillian L Siu, Heidi L Rehm, et al.
American Journal of Human Genetics|March 11, 2025
The expanding global genomics landscape: Converging priorities from national genomics programsCaitlin Howley, Matilda A Haas, Wadha A Al Muftah, et al.
Experimental Gerontology|November 30, 2010
The effect of α-actinin-3 deficiency on muscle agingJane T Seto, Stephen Chan, Nigel Turner, et al.
Cardiovascular Research|January 22, 2016
Lack of MG53 in human heart precludes utility as a biomarker of myocardial injury or endogenous cardioprotective factorFrances A Lemckert, Adam Bournazos, Daniel M Eckert, et al.
Cancers|July 29, 2023
Sensory Processing in Children and Adolescents with Neurofibromatosis Type 1Natalie A Pride, Kristina M Haebich, Karin S Walsh, et al.
European Journal of Human Genetics : EJHG|September 4, 2014
Recessive ACTA1 variant causes congenital muscular dystrophy with rigid spineGina L O'Grady, Heather A Best, Emily C Oates, et al.
Muscle & Nerve|June 16, 2011
Epidermolysis bullosa with late-onset muscular dystrophy and plectin deficiencyEppie M Yiu, Alfred Klausegger, Leigh B Waddell, et al.
Neuromuscular Disorders : NMD|January 25, 2014
Approach to the diagnosis of congenital myopathiesKathryn N North, Ching H Wang, Nigel Clarke, et al.
Human Molecular Genetics|December 19, 2015
Analysis of the ACTN3 heterozygous genotype suggests that α-actinin-3 controls sarcomeric composition and muscle function in a dose-dependent fashionMarshall W Hogarth, Fleur C Garton, Peter J Houweling, et al.
American Journal of Human Genetics|November 26, 2008
Mutations in contactin-1, a neural adhesion and neuromuscular junction protein, cause a familial form of lethal congenital myopathyAlison G Compton, Douglas E Albrecht, Jane T Seto, et al.
Pageof 34