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Isabelle Draper

Showing results (11-20 of 26) with videos related to

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Human Molecular Genetics|May 13, 2017
Consequences of MEGF10 deficiency on myoblast function and Notch1 interactionsMadhurima Saha, Satomi Mitsuhashi, Michael D Jones, et al.
The Journal of Clinical Investigation|May 19, 2026
Deficiency of muscular dystrophy-related gene JAG2 causes NOTCH signaling dysfunction in muscle stem cellsMinoru Tanaka, Nam Chul Kim, Isabelle Draper, et al.
Plos Genetics|March 9, 2018
RNA helicase, DDX27 regulates skeletal muscle growth and regeneration by modulation of translational processesAlexis H Bennett, Marie-Francoise O'Donohue, Stacey R Gundry, et al.
Gene Expression Patterns : GEP|May 6, 2023
hnRNPL expression dynamics in the embryo and placentaVineetha Mathew, Ariel Mei, Hamida Giwa, et al.
Muscle & Nerve|March 2, 2021
hnRNP L is essential for myogenic differentiation and modulates myotonic dystrophy pathologiesMatthew S Alexander, Rylie M Hightower, Andrea L Reid, et al.
Human Molecular Genetics|July 4, 2019
Selective serotonin reuptake inhibitors ameliorate MEGF10 myopathyMadhurima Saha, Skylar A Rizzo, Manashwi Ramanathan, et al.
Molecular Genetics & Genomic Medicine|January 29, 2019
Identification of a pathogenic mutation in ATP2A1 via in silico analysis of exome data for cryptic aberrant splice sitesChristine C Bruels, Chengcheng Li, Tonatiuh Mendoza, et al.
Circulation. Cardiovascular Genetics|December 21, 2012
Formin homology 2 domain containing 3 variants associated with hypertrophic cardiomyopathyEric C Wooten, Virginia B Hebl, Matthew J Wolf, et al.
Muscle & Nerve|July 29, 2024
Dominant stop-loss HNRNPA1 variants in juvenile-onset myopathyJohnnie Turner, Christine C Bruels, Audrey L Daugherty, et al.
Physiological Genomics|October 23, 2018
Impact of PYROXD1 deficiency on cellular respiration and correlations with genetic analyses of limb-girdle muscular dystrophy in Saudi Arabia and SudanMadhurima Saha, Hemakumar M Reddy, Mustafa A Salih, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Human Molecular Genetics|May 13, 2017
Consequences of MEGF10 deficiency on myoblast function and Notch1 interactionsMadhurima Saha, Satomi Mitsuhashi, Michael D Jones, et al.
The Journal of Clinical Investigation|May 19, 2026
Deficiency of muscular dystrophy-related gene JAG2 causes NOTCH signaling dysfunction in muscle stem cellsMinoru Tanaka, Nam Chul Kim, Isabelle Draper, et al.
Plos Genetics|March 9, 2018
RNA helicase, DDX27 regulates skeletal muscle growth and regeneration by modulation of translational processesAlexis H Bennett, Marie-Francoise O'Donohue, Stacey R Gundry, et al.
Gene Expression Patterns : GEP|May 6, 2023
hnRNPL expression dynamics in the embryo and placentaVineetha Mathew, Ariel Mei, Hamida Giwa, et al.
Muscle & Nerve|March 2, 2021
hnRNP L is essential for myogenic differentiation and modulates myotonic dystrophy pathologiesMatthew S Alexander, Rylie M Hightower, Andrea L Reid, et al.
Human Molecular Genetics|July 4, 2019
Selective serotonin reuptake inhibitors ameliorate MEGF10 myopathyMadhurima Saha, Skylar A Rizzo, Manashwi Ramanathan, et al.
Molecular Genetics & Genomic Medicine|January 29, 2019
Identification of a pathogenic mutation in ATP2A1 via in silico analysis of exome data for cryptic aberrant splice sitesChristine C Bruels, Chengcheng Li, Tonatiuh Mendoza, et al.
Circulation. Cardiovascular Genetics|December 21, 2012
Formin homology 2 domain containing 3 variants associated with hypertrophic cardiomyopathyEric C Wooten, Virginia B Hebl, Matthew J Wolf, et al.
Muscle & Nerve|July 29, 2024
Dominant stop-loss HNRNPA1 variants in juvenile-onset myopathyJohnnie Turner, Christine C Bruels, Audrey L Daugherty, et al.
Physiological Genomics|October 23, 2018
Impact of PYROXD1 deficiency on cellular respiration and correlations with genetic analyses of limb-girdle muscular dystrophy in Saudi Arabia and SudanMadhurima Saha, Hemakumar M Reddy, Mustafa A Salih, et al.
Pageof 3