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Cancer Discovery
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November 4, 2015
All the World's a Stage: Facilitating Discovery Science and Improved Cancer Care through the Global Alliance for Genomics and Health
Mark 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 programs
Caitlin Howley, Matilda A Haas, Wadha A Al Muftah, et al.
Experimental Gerontology
|
November 30, 2010
The effect of α-actinin-3 deficiency on muscle aging
Jane 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 factor
Frances A Lemckert, Adam Bournazos, Daniel M Eckert, et al.
Cancers
|
July 29, 2023
Sensory Processing in Children and Adolescents with Neurofibromatosis Type 1
Natalie 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 spine
Gina 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 deficiency
Eppie M Yiu, Alfred Klausegger, Leigh B Waddell, et al.
Neuromuscular Disorders : NMD
|
January 25, 2014
Approach to the diagnosis of congenital myopathies
Kathryn 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 fashion
Marshall 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 myopathy
Alison G Compton, Douglas E Albrecht, Jane T Seto, et al.
Page
of 34
Search research articles
Search
Showing results (231-240 of 333) with videos related to
Sort By:
Page
of 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 Health
Mark 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 programs
Caitlin Howley, Matilda A Haas, Wadha A Al Muftah, et al.
Experimental Gerontology
|
November 30, 2010
The effect of α-actinin-3 deficiency on muscle aging
Jane 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 factor
Frances A Lemckert, Adam Bournazos, Daniel M Eckert, et al.
Cancers
|
July 29, 2023
Sensory Processing in Children and Adolescents with Neurofibromatosis Type 1
Natalie 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 spine
Gina 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 deficiency
Eppie M Yiu, Alfred Klausegger, Leigh B Waddell, et al.
Neuromuscular Disorders : NMD
|
January 25, 2014
Approach to the diagnosis of congenital myopathies
Kathryn 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 fashion
Marshall 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 myopathy
Alison G Compton, Douglas E Albrecht, Jane T Seto, et al.
Page
of 34