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Jennifer A Sullivan

Showing results (21-30 of 45) with videos related to

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Cardiovascular Research|July 19, 2002
Adenovirus-mediated expression of p35 prevents hypoxia/reoxygenation injury by reducing reactive oxygen species and caspase activityTaro Date, Adam J Belanger, Seibu Mochizuki, et al.
Journal of Hepatology|July 20, 2007
Resection of hepatocellular adenoma in patients with glycogen storage disease type IaSrinevas K Reddy, Priya S Kishnani, Jennifer A Sullivan, et al.
Clinical Genetics|October 19, 2023
The best of both worlds: Blending cutting-edge research with clinical processes for a productive exome clinicJennifer A Sullivan, Rebecca C Spillmann, Kelly Schoch, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 21, 2024
Substrate specificity controlled by the exit site of human P4-ATPases, revealed by de novo point mutations in neurological disordersDavid C Calianese, Tomoyasu Noji, Jennifer A Sullivan, et al.
Journal of Child and Adolescent Psychopharmacology|January 5, 2007
Safety and efficacy of rivastigmine in adolescents with Down syndrome: a preliminary 20-week, open-label studyJames H Heller, Gail A Spiridigliozzi, Blythe G Crissman, et al.
Gene Therapy|May 23, 2018
Rationally designed AAV2 and AAVrh8R capsids provide improved transduction in the retina and brainJennifer A Sullivan, Lisa M Stanek, Michael J Lukason, et al.
Human Gene Therapy|March 13, 2014
Translational fidelity of intrathecal delivery of self-complementary AAV9-survival motor neuron 1 for spinal muscular atrophyMarco A Passini, Jie Bu, Amy M Richards, et al.
Molecular Genetics & Genomic Medicine|July 31, 2020
Missed diagnoses: Clinically relevant lessons learned through medical mysteries solved by the Undiagnosed Diseases NetworkHeidi Cope, Rebecca Spillmann, Jill A Rosenfeld, et al.
American Journal of Medical Genetics. Part A|May 18, 2021
De novo variants in TCF7L2 are associated with a syndromic neurodevelopmental disorderCaroline Dias, Rolph Pfundt, Tjitske Kleefstra, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 16, 2017
Looking beyond the exome: a phenotype-first approach to molecular diagnostic resolution in rare and undiagnosed diseasesLoren D M Pena, Yong-Hui Jiang, Kelly Schoch, et al.
Pageof 5

Showing results (21-30 of 45) with videos related to

Sort By:
Pageof 5
Cardiovascular Research|July 19, 2002
Adenovirus-mediated expression of p35 prevents hypoxia/reoxygenation injury by reducing reactive oxygen species and caspase activityTaro Date, Adam J Belanger, Seibu Mochizuki, et al.
Journal of Hepatology|July 20, 2007
Resection of hepatocellular adenoma in patients with glycogen storage disease type IaSrinevas K Reddy, Priya S Kishnani, Jennifer A Sullivan, et al.
Clinical Genetics|October 19, 2023
The best of both worlds: Blending cutting-edge research with clinical processes for a productive exome clinicJennifer A Sullivan, Rebecca C Spillmann, Kelly Schoch, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 21, 2024
Substrate specificity controlled by the exit site of human P4-ATPases, revealed by de novo point mutations in neurological disordersDavid C Calianese, Tomoyasu Noji, Jennifer A Sullivan, et al.
Journal of Child and Adolescent Psychopharmacology|January 5, 2007
Safety and efficacy of rivastigmine in adolescents with Down syndrome: a preliminary 20-week, open-label studyJames H Heller, Gail A Spiridigliozzi, Blythe G Crissman, et al.
Gene Therapy|May 23, 2018
Rationally designed AAV2 and AAVrh8R capsids provide improved transduction in the retina and brainJennifer A Sullivan, Lisa M Stanek, Michael J Lukason, et al.
Human Gene Therapy|March 13, 2014
Translational fidelity of intrathecal delivery of self-complementary AAV9-survival motor neuron 1 for spinal muscular atrophyMarco A Passini, Jie Bu, Amy M Richards, et al.
Molecular Genetics & Genomic Medicine|July 31, 2020
Missed diagnoses: Clinically relevant lessons learned through medical mysteries solved by the Undiagnosed Diseases NetworkHeidi Cope, Rebecca Spillmann, Jill A Rosenfeld, et al.
American Journal of Medical Genetics. Part A|May 18, 2021
De novo variants in TCF7L2 are associated with a syndromic neurodevelopmental disorderCaroline Dias, Rolph Pfundt, Tjitske Kleefstra, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 16, 2017
Looking beyond the exome: a phenotype-first approach to molecular diagnostic resolution in rare and undiagnosed diseasesLoren D M Pena, Yong-Hui Jiang, Kelly Schoch, et al.
Pageof 5