Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

N North

Showing results (281-290 of 333) with videos related to

Pageof 34
Sort By:
Nature Genetics|September 11, 2007
Loss of ACTN3 gene function alters mouse muscle metabolism and shows evidence of positive selection in humansDaniel G MacArthur, Jane T Seto, Joanna M Raftery, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 19, 2007
Distinctive patterns of microRNA expression in primary muscular disordersIris Eisenberg, Alal Eran, Ichizo Nishino, et al.
American Journal of Human Genetics|May 1, 2018
The Effect of ACTN3 Gene Doping on Skeletal Muscle PerformanceFleur C Garton, Peter J Houweling, Damjan Vukcevic, et al.
Journal of Neuro-Oncology|June 5, 2025
Psychosocial functioning and determinants of the health-related quality of life in children with neurofibromatosis type 1 and cognitive impairmentsBelinda Barton, Pamela L Wolters, Karin S Walsh, et al.
Journal of Neuropathology and Experimental Neurology|March 18, 2011
Dysferlin, annexin A1, and mitsugumin 53 are upregulated in muscular dystrophy and localize to longitudinal tubules of the T-system with stretchLeigh B Waddell, Frances A Lemckert, Xi F Zheng, et al.
Nature Communications|June 12, 2020
Eosinophil function in adipose tissue is regulated by Krüppel-like factor 3 (KLF3)Alexander J Knights, Emily J Vohralik, Peter J Houweling, et al.
BMJ Open|September 28, 2019
Understanding autism spectrum disorder and social functioning in children with neurofibromatosis type 1: protocol for a cross-sectional multimodal studyKristina M Haebich, Natalie A Pride, Karin S Walsh, et al.
Neurology|September 4, 2016
Variants in SLC18A3, vesicular acetylcholine transporter, cause congenital myasthenic syndromeGina L O'Grady, Corien Verschuuren, Michaela Yuen, et al.
Brain : a Journal of Neurology|February 15, 2015
Expanding the phenotype of GMPPB mutationsMacarena Cabrera-Serrano, Roula Ghaoui, Gianina Ravenscroft, et al.
Journal of Autism and Developmental Disorders|April 21, 2022
Sex- and age-related differences in autistic behaviours in children with neurofibromatosis type 1Anita K Chisholm, Francesca Lami, Kristina M Haebich, et al.
Pageof 34

Showing results (281-290 of 333) with videos related to

Sort By:
Pageof 34
Nature Genetics|September 11, 2007
Loss of ACTN3 gene function alters mouse muscle metabolism and shows evidence of positive selection in humansDaniel G MacArthur, Jane T Seto, Joanna M Raftery, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 19, 2007
Distinctive patterns of microRNA expression in primary muscular disordersIris Eisenberg, Alal Eran, Ichizo Nishino, et al.
American Journal of Human Genetics|May 1, 2018
The Effect of ACTN3 Gene Doping on Skeletal Muscle PerformanceFleur C Garton, Peter J Houweling, Damjan Vukcevic, et al.
Journal of Neuro-Oncology|June 5, 2025
Psychosocial functioning and determinants of the health-related quality of life in children with neurofibromatosis type 1 and cognitive impairmentsBelinda Barton, Pamela L Wolters, Karin S Walsh, et al.
Journal of Neuropathology and Experimental Neurology|March 18, 2011
Dysferlin, annexin A1, and mitsugumin 53 are upregulated in muscular dystrophy and localize to longitudinal tubules of the T-system with stretchLeigh B Waddell, Frances A Lemckert, Xi F Zheng, et al.
Nature Communications|June 12, 2020
Eosinophil function in adipose tissue is regulated by Krüppel-like factor 3 (KLF3)Alexander J Knights, Emily J Vohralik, Peter J Houweling, et al.
BMJ Open|September 28, 2019
Understanding autism spectrum disorder and social functioning in children with neurofibromatosis type 1: protocol for a cross-sectional multimodal studyKristina M Haebich, Natalie A Pride, Karin S Walsh, et al.
Neurology|September 4, 2016
Variants in SLC18A3, vesicular acetylcholine transporter, cause congenital myasthenic syndromeGina L O'Grady, Corien Verschuuren, Michaela Yuen, et al.
Brain : a Journal of Neurology|February 15, 2015
Expanding the phenotype of GMPPB mutationsMacarena Cabrera-Serrano, Roula Ghaoui, Gianina Ravenscroft, et al.
Journal of Autism and Developmental Disorders|April 21, 2022
Sex- and age-related differences in autistic behaviours in children with neurofibromatosis type 1Anita K Chisholm, Francesca Lami, Kristina M Haebich, et al.
Pageof 34