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D Overton

Showing results (41-50 of 242) with videos related to

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Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|April 16, 1998
Demonstration of dose-dependent global and regional cocaine-induced reductions in brain blood flow using a novel approach to quantitative single photon emission computerized tomographyB Johnson, L Lamki, B Fang, et al.
Psychopharmacology|May 26, 1998
Isradipine prevents global and regional cocaine-induced changes in brain blood flow: a preliminary studyB Johnson, B Barron, B Fang, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 20, 2013
Molecular chaperone Hsp110 rescues a vesicle transport defect produced by an ALS-associated mutant SOD1 protein in squid axoplasmYuyu Song, Maria Nagy, Weiming Ni, et al.
Cell Reports|January 18, 2016
Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in DevelopmentNick D L Owens, Ira L Blitz, Maura A Lane, et al.
Scientific Reports|August 12, 2025
Use of an anatomical atlas in real-time EIT reconstructions of ventilation and pulsatile perfusion in preterm infantsChristopher J Rocheleau, Trevor D Overton, Nilton Barbosa da Rosa, et al.
The Journal of Clinical Endocrinology and Metabolism|August 13, 2024
Deficiency of Peptidylglycine-alpha-amidating Monooxygenase, a Cause of Sarcopenic Diabetes MellitusAlice Giontella, Mikael Åkerlund, Kevin Bronton, et al.
Human Molecular Genetics|January 12, 2018
Large-scale exome datasets reveal a new class of adaptor-related protein complex 2 sigma subunit (AP2σ) mutations, located at the interface with the AP2 alpha subunit, that impair calcium-sensing receptor signallingCaroline M Gorvin, Raghu Metpally, Victoria J Stokes, et al.
Bioinformatics (Oxford, England)|September 19, 2015
CLAMMS: a scalable algorithm for calling common and rare copy number variants from exome sequencing dataJonathan S Packer, Evan K Maxwell, Colm O'Dushlaine, et al.
Journal of Personalized Medicine|December 24, 2021
Association of Thyroid Function with Blood Pressure and Cardiovascular Disease: A Mendelian RandomizationAlice Giontella, Luca A Lotta, John D Overton, et al.
Journal of Human Genetics|March 24, 2019
A novel TUFM homozygous variant in a child with mitochondrial cardiomyopathy expands the phenotype of combined oxidative phosphorylation deficiency 4Tova Hershkovitz, Alina Kurolap, Claudia Gonzaga-Jauregui, et al.
Pageof 25

Showing results (41-50 of 242) with videos related to

Sort By:
Pageof 25
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|April 16, 1998
Demonstration of dose-dependent global and regional cocaine-induced reductions in brain blood flow using a novel approach to quantitative single photon emission computerized tomographyB Johnson, L Lamki, B Fang, et al.
Psychopharmacology|May 26, 1998
Isradipine prevents global and regional cocaine-induced changes in brain blood flow: a preliminary studyB Johnson, B Barron, B Fang, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 20, 2013
Molecular chaperone Hsp110 rescues a vesicle transport defect produced by an ALS-associated mutant SOD1 protein in squid axoplasmYuyu Song, Maria Nagy, Weiming Ni, et al.
Cell Reports|January 18, 2016
Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in DevelopmentNick D L Owens, Ira L Blitz, Maura A Lane, et al.
Scientific Reports|August 12, 2025
Use of an anatomical atlas in real-time EIT reconstructions of ventilation and pulsatile perfusion in preterm infantsChristopher J Rocheleau, Trevor D Overton, Nilton Barbosa da Rosa, et al.
The Journal of Clinical Endocrinology and Metabolism|August 13, 2024
Deficiency of Peptidylglycine-alpha-amidating Monooxygenase, a Cause of Sarcopenic Diabetes MellitusAlice Giontella, Mikael Åkerlund, Kevin Bronton, et al.
Human Molecular Genetics|January 12, 2018
Large-scale exome datasets reveal a new class of adaptor-related protein complex 2 sigma subunit (AP2σ) mutations, located at the interface with the AP2 alpha subunit, that impair calcium-sensing receptor signallingCaroline M Gorvin, Raghu Metpally, Victoria J Stokes, et al.
Bioinformatics (Oxford, England)|September 19, 2015
CLAMMS: a scalable algorithm for calling common and rare copy number variants from exome sequencing dataJonathan S Packer, Evan K Maxwell, Colm O'Dushlaine, et al.
Journal of Personalized Medicine|December 24, 2021
Association of Thyroid Function with Blood Pressure and Cardiovascular Disease: A Mendelian RandomizationAlice Giontella, Luca A Lotta, John D Overton, et al.
Journal of Human Genetics|March 24, 2019
A novel TUFM homozygous variant in a child with mitochondrial cardiomyopathy expands the phenotype of combined oxidative phosphorylation deficiency 4Tova Hershkovitz, Alina Kurolap, Claudia Gonzaga-Jauregui, et al.
Pageof 25