Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Stephanie M Ware

Showing results (111-120 of 147) with videos related to

Pageof 15
Sort By:
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.
Scientific Reports|September 14, 2016
The analysis of heterotaxy patients reveals new loss-of-function variants of GRK5Davor Lessel, Tariq Muhammad, Teresa Casar Tena, et al.
Circulation|December 21, 2018
Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart AssociationMary Ella Pierpont, Martina Brueckner, Wendy K Chung, et al.
Research Square|April 2, 2024
Rapid Genome Sequencing Shows Diagnostic Utility In Infants With Congenital Heart DefectsMatthew D Durbin, Lindsey R Helvaty, Alyx Posorske, et al.
Pediatrics|October 7, 2004
Clinical spectrum, morbidity, and mortality in 113 pediatric patients with mitochondrial diseaseFernando Scaglia, Jeffrey A Towbin, William J Craigen, et al.
Circulation. Genomic and Precision Medicine|April 10, 2026
Rapid Genome Sequencing Shows Diagnostic Utility in Infants With Congenital Heart DefectsMatthew D Durbin, Lindsey R Helvaty, Alyx Posorske, et al.
The American Journal of Cardiology|February 23, 2015
Dystrophin genotype-cardiac phenotype correlations in Duchenne and Becker muscular dystrophies using cardiac magnetic resonance imagingAnimesh Tandon, John L Jefferies, Chet R Villa, et al.
Circulation|November 16, 2022
Cardiac Troponin I-Interacting Kinase Affects Cardiomyocyte S-Phase Activity but Not Cardiomyocyte ProliferationSean P Reuter, Mark H Soonpaa, Dorothy Field, et al.
Pediatric Cardiology|May 7, 2024
Genetic Testing Resources and Practice Patterns Among Pediatric Cardiomyopathy ProgramsJustin Godown, Emily H Kim, Melanie D Everitt, et al.
Pageof 15

Showing results (111-120 of 147) with videos related to

Sort By:
Pageof 15
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.
Scientific Reports|September 14, 2016
The analysis of heterotaxy patients reveals new loss-of-function variants of GRK5Davor Lessel, Tariq Muhammad, Teresa Casar Tena, et al.
Circulation|December 21, 2018
Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart AssociationMary Ella Pierpont, Martina Brueckner, Wendy K Chung, et al.
Research Square|April 2, 2024
Rapid Genome Sequencing Shows Diagnostic Utility In Infants With Congenital Heart DefectsMatthew D Durbin, Lindsey R Helvaty, Alyx Posorske, et al.
Pediatrics|October 7, 2004
Clinical spectrum, morbidity, and mortality in 113 pediatric patients with mitochondrial diseaseFernando Scaglia, Jeffrey A Towbin, William J Craigen, et al.
Circulation. Genomic and Precision Medicine|April 10, 2026
Rapid Genome Sequencing Shows Diagnostic Utility in Infants With Congenital Heart DefectsMatthew D Durbin, Lindsey R Helvaty, Alyx Posorske, et al.
The American Journal of Cardiology|February 23, 2015
Dystrophin genotype-cardiac phenotype correlations in Duchenne and Becker muscular dystrophies using cardiac magnetic resonance imagingAnimesh Tandon, John L Jefferies, Chet R Villa, et al.
Circulation|November 16, 2022
Cardiac Troponin I-Interacting Kinase Affects Cardiomyocyte S-Phase Activity but Not Cardiomyocyte ProliferationSean P Reuter, Mark H Soonpaa, Dorothy Field, et al.
Pediatric Cardiology|May 7, 2024
Genetic Testing Resources and Practice Patterns Among Pediatric Cardiomyopathy ProgramsJustin Godown, Emily H Kim, Melanie D Everitt, et al.
Pageof 15