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Vidu Garg

Showing results (61-70 of 110) with videos related to

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Arteriosclerosis, Thrombosis, and Vascular Biology|October 23, 2012
Inhibition of Notch1 signaling reduces abdominal aortic aneurysm in mice by attenuating macrophage-mediated inflammationChetan P Hans, Sara N Koenig, Nianyuan Huang, et al.
Stem Cell Research|August 20, 2022
Generation of an induced pluripotent stem cell line NCHi003-A from a 11-year-old male with pulmonary atresia with intact ventricular septum (PA-IVS)Javier Contreras, Matthew Alonzo, Shiqiao Ye, et al.
Stem Cell Research|August 20, 2022
Characterization of an iPSC line NCHi006-A from a patient with hypoplastic left heart syndrome (HLHS)Matthew Alonzo, Javier Contreras, Shiqiao Ye, et al.
Gene Expression Patterns : GEP|June 27, 2025
Expression of Netrin-1 in the developing mouse heartAdrianna Matos-Nieves, Sarah C Greskovich, Talita Z Choudhury, et al.
Vascular Pharmacology|July 6, 2022
Loss of Jagged1 in mature endothelial cells causes vascular dysfunction with alterations in smooth muscle phenotypesRanda M Breikaa, Kimberly Denman, Yukie Ueyama, et al.
Circulation. Genomic and Precision Medicine|February 10, 2026
Assessing Genetic Testing in Adult Congenital Heart Disease: Current State and Patient PerspectivesAngela Onorato, Kara Klinkebiel, Rachel Levenseller, et al.
Heart Rhythm|February 2, 2025
Extensive cardiac involvement in laminopathies diagnosed in pediatric-aged patients: A single-center studyEmily A Hayes, Kaitlyn Foreman, Lydia K Wright, et al.
Human Mutation|June 15, 2013
Genetic abnormalities in FOXP1 are associated with congenital heart defectsSheng-Wei Chang, Mona Mislankar, Chaitali Misra, et al.
Circulation. Cardiovascular Genetics|July 16, 2016
Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart DiseaseStephanie LaHaye, Don Corsmeier, Madhumita Basu, et al.
Pediatric Research|June 7, 2008
Cryptic chromosomal abnormalities identified in children with congenital heart diseaseAshleigh A Richards, Lane Jaeckle Santos, Haley A Nichols, et al.
Pageof 11

Showing results (61-70 of 110) with videos related to

Sort By:
Pageof 11
Arteriosclerosis, Thrombosis, and Vascular Biology|October 23, 2012
Inhibition of Notch1 signaling reduces abdominal aortic aneurysm in mice by attenuating macrophage-mediated inflammationChetan P Hans, Sara N Koenig, Nianyuan Huang, et al.
Stem Cell Research|August 20, 2022
Generation of an induced pluripotent stem cell line NCHi003-A from a 11-year-old male with pulmonary atresia with intact ventricular septum (PA-IVS)Javier Contreras, Matthew Alonzo, Shiqiao Ye, et al.
Stem Cell Research|August 20, 2022
Characterization of an iPSC line NCHi006-A from a patient with hypoplastic left heart syndrome (HLHS)Matthew Alonzo, Javier Contreras, Shiqiao Ye, et al.
Gene Expression Patterns : GEP|June 27, 2025
Expression of Netrin-1 in the developing mouse heartAdrianna Matos-Nieves, Sarah C Greskovich, Talita Z Choudhury, et al.
Vascular Pharmacology|July 6, 2022
Loss of Jagged1 in mature endothelial cells causes vascular dysfunction with alterations in smooth muscle phenotypesRanda M Breikaa, Kimberly Denman, Yukie Ueyama, et al.
Circulation. Genomic and Precision Medicine|February 10, 2026
Assessing Genetic Testing in Adult Congenital Heart Disease: Current State and Patient PerspectivesAngela Onorato, Kara Klinkebiel, Rachel Levenseller, et al.
Heart Rhythm|February 2, 2025
Extensive cardiac involvement in laminopathies diagnosed in pediatric-aged patients: A single-center studyEmily A Hayes, Kaitlyn Foreman, Lydia K Wright, et al.
Human Mutation|June 15, 2013
Genetic abnormalities in FOXP1 are associated with congenital heart defectsSheng-Wei Chang, Mona Mislankar, Chaitali Misra, et al.
Circulation. Cardiovascular Genetics|July 16, 2016
Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart DiseaseStephanie LaHaye, Don Corsmeier, Madhumita Basu, et al.
Pediatric Research|June 7, 2008
Cryptic chromosomal abnormalities identified in children with congenital heart diseaseAshleigh A Richards, Lane Jaeckle Santos, Haley A Nichols, et al.
Pageof 11