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J Dowling

Showing results (391-400 of 493) with videos related to

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Gastroenterology|November 20, 2019
Drug Screen Identifies Leflunomide for Treatment of Inflammatory Bowel Disease Caused by TTC7A DeficiencySasha Jardine, Sierra Anderson, Stephen Babcock, et al.
ACS Chemical Biology|August 26, 2022
Shaping Neonatal Immunization by Tuning the Delivery of Synergistic Adjuvants via NanocarriersSoumik Barman, Francesco Borriello, Byron Brook, et al.
Vaccine|November 28, 2018
Increasing FIM2/3 antigen-content improves efficacy of Bordetella pertussis vaccines in mice in vivo without altering vaccine-induced human reactogenicity biomarkers in vitroAnne Marie Queenan, David J Dowling, Wing Ki Cheng, et al.
Developmental Cognitive Neuroscience|February 13, 2022
Measuring retention within the adolescent brain cognitive development (ABCD)<sup>SM</sup> studySarah W Feldstein Ewing, Genevieve F Dash, Wesley K Thompson, et al.
Nature Medicine|June 28, 2024
AAV gene therapy for hereditary spastic paraplegia type 50: a phase 1 trial in a single patientJames J Dowling, Terry Pirovolakis, Keshini Devakandan, et al.
The Journal of Adolescent Health : Official Publication of the Society for Adolescent Medicine|May 16, 2023
Pandemic-Related Changes in the Prevalence of Early Adolescent Alcohol and Drug Use, 2020-2021: Data From a Multisite Cohort StudyWilliam E Pelham, Susan F Tapert, María Luisa Zúñiga, et al.
Neuromuscular Disorders : NMD|December 7, 2023
The myotubular and centronuclear myopathy patient registry: a multifunctional tool for translational researchJoanne Bullivant, Anando Sen, Jess Page, et al.
Neurobiology of Disease|January 26, 2016
Single amino acid deletion in transmembrane segment D4S6 of sodium channel Scn8a (Nav1.6) in a mouse mutant with a chronic movement disorderJulie M Jones, Louise Dionne, James Dell'Orco, et al.
HGG Advances|April 25, 2024
A systematic assessment of the impact of rare canonical splice site variants on splicing using functional and in silico methodsRachel Y Oh, Ali AlMail, David Cheerie, et al.
Human Molecular Genetics|November 10, 2011
Modeling the human MTM1 p.R69C mutation in murine Mtm1 results in exon 4 skipping and a less severe myotubular myopathy phenotypeChristopher R Pierson, Ashley N Dulin-Smith, Ashley N Durban, et al.
Pageof 50

Showing results (391-400 of 493) with videos related to

Sort By:
Pageof 50
Gastroenterology|November 20, 2019
Drug Screen Identifies Leflunomide for Treatment of Inflammatory Bowel Disease Caused by TTC7A DeficiencySasha Jardine, Sierra Anderson, Stephen Babcock, et al.
ACS Chemical Biology|August 26, 2022
Shaping Neonatal Immunization by Tuning the Delivery of Synergistic Adjuvants via NanocarriersSoumik Barman, Francesco Borriello, Byron Brook, et al.
Vaccine|November 28, 2018
Increasing FIM2/3 antigen-content improves efficacy of Bordetella pertussis vaccines in mice in vivo without altering vaccine-induced human reactogenicity biomarkers in vitroAnne Marie Queenan, David J Dowling, Wing Ki Cheng, et al.
Developmental Cognitive Neuroscience|February 13, 2022
Measuring retention within the adolescent brain cognitive development (ABCD)<sup>SM</sup> studySarah W Feldstein Ewing, Genevieve F Dash, Wesley K Thompson, et al.
Nature Medicine|June 28, 2024
AAV gene therapy for hereditary spastic paraplegia type 50: a phase 1 trial in a single patientJames J Dowling, Terry Pirovolakis, Keshini Devakandan, et al.
The Journal of Adolescent Health : Official Publication of the Society for Adolescent Medicine|May 16, 2023
Pandemic-Related Changes in the Prevalence of Early Adolescent Alcohol and Drug Use, 2020-2021: Data From a Multisite Cohort StudyWilliam E Pelham, Susan F Tapert, María Luisa Zúñiga, et al.
Neuromuscular Disorders : NMD|December 7, 2023
The myotubular and centronuclear myopathy patient registry: a multifunctional tool for translational researchJoanne Bullivant, Anando Sen, Jess Page, et al.
Neurobiology of Disease|January 26, 2016
Single amino acid deletion in transmembrane segment D4S6 of sodium channel Scn8a (Nav1.6) in a mouse mutant with a chronic movement disorderJulie M Jones, Louise Dionne, James Dell'Orco, et al.
HGG Advances|April 25, 2024
A systematic assessment of the impact of rare canonical splice site variants on splicing using functional and in silico methodsRachel Y Oh, Ali AlMail, David Cheerie, et al.
Human Molecular Genetics|November 10, 2011
Modeling the human MTM1 p.R69C mutation in murine Mtm1 results in exon 4 skipping and a less severe myotubular myopathy phenotypeChristopher R Pierson, Ashley N Dulin-Smith, Ashley N Durban, et al.
Pageof 50