Search research articles
Contact Us
Filters
Showing results (251-260 of 333) with videos related to
Page
of 34
Sort By:
Human Molecular Genetics
|
October 29, 2013
NF1 is a critical regulator of muscle development and metabolism
Kate Sullivan, Jad El-Hoss, Kate G R Quinlan, et al.
Neuromuscular Disorders : NMD
|
March 4, 2014
Diagnostic approach to the congenital muscular dystrophies
Carsten 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 pathogenesis
Harriet 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 patient
Peter J Houweling, Chantal A Coles, Chrystal F Tiong, et al.
American Journal of Human Genetics
|
January 5, 2019
Integrating Genomics into Healthcare: A Global Responsibility
Zornitza 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 autoantibodies
Harriet 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 generation
Victoria 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 signaling
Jane 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 model
Jonathan 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 outcomes
Jonathan M Payne, Karin S Walsh, Natalie A Pride, et al.
Page
of 34
Search research articles
Search
Showing results (251-260 of 333) with videos related to
Sort By:
Page
of 34
Human Molecular Genetics
|
October 29, 2013
NF1 is a critical regulator of muscle development and metabolism
Kate Sullivan, Jad El-Hoss, Kate G R Quinlan, et al.
Neuromuscular Disorders : NMD
|
March 4, 2014
Diagnostic approach to the congenital muscular dystrophies
Carsten 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 pathogenesis
Harriet 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 patient
Peter J Houweling, Chantal A Coles, Chrystal F Tiong, et al.
American Journal of Human Genetics
|
January 5, 2019
Integrating Genomics into Healthcare: A Global Responsibility
Zornitza 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 autoantibodies
Harriet 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 generation
Victoria 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 signaling
Jane 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 model
Jonathan 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 outcomes
Jonathan M Payne, Karin S Walsh, Natalie A Pride, et al.
Page
of 34