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M Ware

Showing results (231-240 of 288) with videos related to

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The Journal of Pediatrics|May 21, 2023
Genetic Testing Guidelines Impact Care in Newborns with Congenital Heart DefectsMatthew D Durbin, Korre Fairman, Lindsey R Helvaty, et al.
Global Change Biology|January 20, 2019
Climate-driven reduction of genetic variation in plant phenology alters soil communities and nutrient poolsIan M Ware, Michael E Van Nuland, Jennifer A Schweitzer, et al.
The Journal of Clinical Investigation|May 17, 2019
Imbalanced mitochondrial function provokes heterotaxy via aberrant ciliogenesisMartin D Burkhalter, Arthi Sridhar, Pedro Sampaio, et al.
Nutrients|December 17, 2024
Study Protocol for a Randomized Controlled Trial Investigating the Effects of the Daily Consumption of Ruminant Milk on Digestive Comfort and Nutrition in Older Women: The YUMMI StudyShien Ping Ong, Jody C Miller, Warren C McNabb, et al.
Heart Rhythm|June 24, 2019
Genetic testing and cascade screening in pediatric long QT syndrome and hypertrophic cardiomyopathyLinda M Knight, Erin Miller, Joshua Kovach, et al.
Journal of Medical Genetics|February 4, 2009
Infantile cardiomyopathy caused by a mutation in the overlapping region of mitochondrial ATPase 6 and 8 genesS M Ware, N El-Hassan, S G Kahler, et al.
Journal of the American Heart Association|September 29, 2022
Learning to Crawl: Determining the Role of Genetic Abnormalities on Postoperative Outcomes in Congenital Heart DiseaseBenjamin J Landis, Benjamin M Helm, Jeremy L Herrmann, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 24, 2004
Serum leptin level is a regulator of bone massF Elefteriou, S Takeda, K Ebihara, et al.
HGG Advances|December 17, 2021
Identification of a common polymorphism in <i>COQ8B</i> acting as a modifier of thoracic aortic aneurysm severityBenjamin J Landis, Dongbing Lai, Dong-Chuan Guo, et al.
Human Molecular Genetics|December 10, 2008
Identification and functional characterization of NODAL rare variants in heterotaxy and isolated cardiovascular malformationsBhagyalaxmi Mohapatra, Brett Casey, Hua Li, et al.
Pageof 29

Showing results (231-240 of 288) with videos related to

Sort By:
Pageof 29
The Journal of Pediatrics|May 21, 2023
Genetic Testing Guidelines Impact Care in Newborns with Congenital Heart DefectsMatthew D Durbin, Korre Fairman, Lindsey R Helvaty, et al.
Global Change Biology|January 20, 2019
Climate-driven reduction of genetic variation in plant phenology alters soil communities and nutrient poolsIan M Ware, Michael E Van Nuland, Jennifer A Schweitzer, et al.
The Journal of Clinical Investigation|May 17, 2019
Imbalanced mitochondrial function provokes heterotaxy via aberrant ciliogenesisMartin D Burkhalter, Arthi Sridhar, Pedro Sampaio, et al.
Nutrients|December 17, 2024
Study Protocol for a Randomized Controlled Trial Investigating the Effects of the Daily Consumption of Ruminant Milk on Digestive Comfort and Nutrition in Older Women: The YUMMI StudyShien Ping Ong, Jody C Miller, Warren C McNabb, et al.
Heart Rhythm|June 24, 2019
Genetic testing and cascade screening in pediatric long QT syndrome and hypertrophic cardiomyopathyLinda M Knight, Erin Miller, Joshua Kovach, et al.
Journal of Medical Genetics|February 4, 2009
Infantile cardiomyopathy caused by a mutation in the overlapping region of mitochondrial ATPase 6 and 8 genesS M Ware, N El-Hassan, S G Kahler, et al.
Journal of the American Heart Association|September 29, 2022
Learning to Crawl: Determining the Role of Genetic Abnormalities on Postoperative Outcomes in Congenital Heart DiseaseBenjamin J Landis, Benjamin M Helm, Jeremy L Herrmann, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 24, 2004
Serum leptin level is a regulator of bone massF Elefteriou, S Takeda, K Ebihara, et al.
HGG Advances|December 17, 2021
Identification of a common polymorphism in <i>COQ8B</i> acting as a modifier of thoracic aortic aneurysm severityBenjamin J Landis, Dongbing Lai, Dong-Chuan Guo, et al.
Human Molecular Genetics|December 10, 2008
Identification and functional characterization of NODAL rare variants in heterotaxy and isolated cardiovascular malformationsBhagyalaxmi Mohapatra, Brett Casey, Hua Li, et al.
Pageof 29