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J Dowling

Showing results (431-440 of 493) with videos related to

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Neurology|March 24, 2019
X-linked myotubular myopathy: A prospective international natural history studyMélanie Annoussamy, Charlotte Lilien, Teresa Gidaro, et al.
Iscience|November 21, 2024
The BNT162b2 mRNA vaccine demonstrates reduced age-associated T<sub>H</sub>1 support <i>in vitro</i> and <i>in vivo</i>Byron Brook, Abhinav Kumar Checkervarty, Soumik Barman, et al.
JCI Insight|March 30, 2017
TLR7/8 adjuvant overcomes newborn hyporesponsiveness to pneumococcal conjugate vaccine at birthDavid J Dowling, Simon D van Haren, Annette Scheid, et al.
Research Square|January 4, 2023
The mRNA vaccine BNT162b2 demonstrates impaired T<sub>H</sub>1 immunogenicity in human elders <i>in vitro</i> and aged mice <i>in vivo</i>Byron Brook, Benoit Fatou, Abhinav Kumar Checkervarty, et al.
Stroke|May 17, 2019
Response to Late-Window Endovascular Revascularization Is Associated With Collateral Status in Basilar Artery OcclusionFana Alemseged, Erik Van der Hoeven, Francesca Di Giuliano, et al.
The Journal of Adolescent Health : Official Publication of the Society for Adolescent Medicine|August 28, 2021
Early Adolescent Substance Use Before and During the COVID-19 Pandemic: A Longitudinal Survey in the ABCD Study CohortWilliam E Pelham, Susan F Tapert, Marybel Robledo Gonzalez, et al.
Neurology|January 17, 2020
Randomized controlled trial of <i>N</i>-acetylcysteine therapy for <i>RYR1</i>-related myopathiesJoshua J Todd, Tokunbor A Lawal, Jessica W Witherspoon, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 15, 2025
Screening rare genetic diagnoses for amenability to bespoke antisense oligonucleotide therapy development: A retrospective cohort studyDavid Cheerie, Marlen C Lauffer, Logan Newton, et al.
Neurology. Genetics|May 2, 2019
Clinical, genetic, and pathologic characterization of <i>FKRP</i> Mexican founder mutation c.1387A>GAngela J Lee, Karra A Jones, Russell J Butterfield, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 1, 2023
Monoallelic loss-of-function BMP2 variants result in BMP2-related skeletal dysplasia spectrumJessica R C Priestley, Ashish R Deshwar, Harsha Murthy, et al.
Pageof 50

Showing results (431-440 of 493) with videos related to

Sort By:
Pageof 50
Neurology|March 24, 2019
X-linked myotubular myopathy: A prospective international natural history studyMélanie Annoussamy, Charlotte Lilien, Teresa Gidaro, et al.
Iscience|November 21, 2024
The BNT162b2 mRNA vaccine demonstrates reduced age-associated T<sub>H</sub>1 support <i>in vitro</i> and <i>in vivo</i>Byron Brook, Abhinav Kumar Checkervarty, Soumik Barman, et al.
JCI Insight|March 30, 2017
TLR7/8 adjuvant overcomes newborn hyporesponsiveness to pneumococcal conjugate vaccine at birthDavid J Dowling, Simon D van Haren, Annette Scheid, et al.
Research Square|January 4, 2023
The mRNA vaccine BNT162b2 demonstrates impaired T<sub>H</sub>1 immunogenicity in human elders <i>in vitro</i> and aged mice <i>in vivo</i>Byron Brook, Benoit Fatou, Abhinav Kumar Checkervarty, et al.
Stroke|May 17, 2019
Response to Late-Window Endovascular Revascularization Is Associated With Collateral Status in Basilar Artery OcclusionFana Alemseged, Erik Van der Hoeven, Francesca Di Giuliano, et al.
The Journal of Adolescent Health : Official Publication of the Society for Adolescent Medicine|August 28, 2021
Early Adolescent Substance Use Before and During the COVID-19 Pandemic: A Longitudinal Survey in the ABCD Study CohortWilliam E Pelham, Susan F Tapert, Marybel Robledo Gonzalez, et al.
Neurology|January 17, 2020
Randomized controlled trial of <i>N</i>-acetylcysteine therapy for <i>RYR1</i>-related myopathiesJoshua J Todd, Tokunbor A Lawal, Jessica W Witherspoon, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 15, 2025
Screening rare genetic diagnoses for amenability to bespoke antisense oligonucleotide therapy development: A retrospective cohort studyDavid Cheerie, Marlen C Lauffer, Logan Newton, et al.
Neurology. Genetics|May 2, 2019
Clinical, genetic, and pathologic characterization of <i>FKRP</i> Mexican founder mutation c.1387A>GAngela J Lee, Karra A Jones, Russell J Butterfield, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 1, 2023
Monoallelic loss-of-function BMP2 variants result in BMP2-related skeletal dysplasia spectrumJessica R C Priestley, Ashish R Deshwar, Harsha Murthy, et al.
Pageof 50