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Showing results (1091-1100 of 1,117) with videos related to

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Frontiers in Genetics|November 7, 2024
Identification of novel 3D-genome altering and complex structural variants underlying retinitis pigmentosa type 17 through a multistep and high-throughput approachSuzanne E de Bruijn, Daan M Panneman, Nicole Weisschuh, et al.
Journal of Clinical Sleep Medicine : JCSM : Official Publication of the American Academy of Sleep Medicine|October 31, 2023
Permanent standard time is the optimal choice for health and safety: an American Academy of Sleep Medicine position statementMuhammad Adeel Rishi, Jocelyn Y Cheng, Abigail R Strang, et al.
Physical Review Letters|January 13, 2019
Piezoelectrically Tuned Multimode Cavity Search for Axion Dark MatterC Boutan, M Jones, B H LaRoque, et al.
Annals of Epidemiology|November 4, 2018
Trends in human immunodeficiency virus diagnoses among men who have sex with men in North America, Western Europe, and Australia, 2000-2014Johanna Chapin-Bardales, Axel J Schmidt, Rebecca J Guy, et al.
American Journal of Human Genetics|June 13, 2009
Mutations in a BTB-Kelch protein, KLHL7, cause autosomal-dominant retinitis pigmentosaJames S Friedman, Joseph W Ray, Naushin Waseem, et al.
The American Journal of Gastroenterology|May 2, 2025
HLA DQA1*05 and Risk of Antitumor Necrosis Factor Treatment Failure and Anti-Drug Antibody Development in Children With Crohn's DiseaseJeremy Adler, Joseph A Galanko, Rana Ammoury, et al.
The American Journal of Gastroenterology|October 18, 2024
HLA DQA1*05 and risk of anti-TNF treatment failure and anti-drug antibody development in children with Crohn's Disease: HLA DQA1*05 and Pediatric Crohn's DiseaseJeremy Adler, Joseph A Galanko, Rana Ammoury, et al.
Human Molecular Genetics|January 11, 2011
A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3Robert C Kaplan, Ann-Kristin Petersen, Ming-Huei Chen, et al.
Physical Review Letters|March 29, 2020
Extended Search for the Invisible Axion with the Axion Dark Matter ExperimentT Braine, R Cervantes, N Crisosto, et al.
Human Genetics|October 25, 2013
Next generation sequencing-based molecular diagnosis of retinitis pigmentosa: identification of a novel genotype-phenotype correlation and clinical refinementsFeng Wang, Hui Wang, Han-Fang Tuan, et al.
Pageof 112

Showing results (1091-1100 of 1,117) with videos related to

Sort By:
Pageof 112
Frontiers in Genetics|November 7, 2024
Identification of novel 3D-genome altering and complex structural variants underlying retinitis pigmentosa type 17 through a multistep and high-throughput approachSuzanne E de Bruijn, Daan M Panneman, Nicole Weisschuh, et al.
Journal of Clinical Sleep Medicine : JCSM : Official Publication of the American Academy of Sleep Medicine|October 31, 2023
Permanent standard time is the optimal choice for health and safety: an American Academy of Sleep Medicine position statementMuhammad Adeel Rishi, Jocelyn Y Cheng, Abigail R Strang, et al.
Physical Review Letters|January 13, 2019
Piezoelectrically Tuned Multimode Cavity Search for Axion Dark MatterC Boutan, M Jones, B H LaRoque, et al.
Annals of Epidemiology|November 4, 2018
Trends in human immunodeficiency virus diagnoses among men who have sex with men in North America, Western Europe, and Australia, 2000-2014Johanna Chapin-Bardales, Axel J Schmidt, Rebecca J Guy, et al.
American Journal of Human Genetics|June 13, 2009
Mutations in a BTB-Kelch protein, KLHL7, cause autosomal-dominant retinitis pigmentosaJames S Friedman, Joseph W Ray, Naushin Waseem, et al.
The American Journal of Gastroenterology|May 2, 2025
HLA DQA1*05 and Risk of Antitumor Necrosis Factor Treatment Failure and Anti-Drug Antibody Development in Children With Crohn's DiseaseJeremy Adler, Joseph A Galanko, Rana Ammoury, et al.
The American Journal of Gastroenterology|October 18, 2024
HLA DQA1*05 and risk of anti-TNF treatment failure and anti-drug antibody development in children with Crohn's Disease: HLA DQA1*05 and Pediatric Crohn's DiseaseJeremy Adler, Joseph A Galanko, Rana Ammoury, et al.
Human Molecular Genetics|January 11, 2011
A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3Robert C Kaplan, Ann-Kristin Petersen, Ming-Huei Chen, et al.
Physical Review Letters|March 29, 2020
Extended Search for the Invisible Axion with the Axion Dark Matter ExperimentT Braine, R Cervantes, N Crisosto, et al.
Human Genetics|October 25, 2013
Next generation sequencing-based molecular diagnosis of retinitis pigmentosa: identification of a novel genotype-phenotype correlation and clinical refinementsFeng Wang, Hui Wang, Han-Fang Tuan, et al.
Pageof 112