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Jonathan G Seidman

Showing results (61-70 of 170) with videos related to

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Microsystems & Nanoengineering|September 27, 2021
Probing the subcellular nanostructure of engineered human cardiomyocytes in 3D tissueJosh Javor, Jourdan K Ewoldt, Paige E Cloonan, et al.
Genetics in Medicine Open|December 13, 2024
Genetic diagnosis of facioscapulohumeral muscular dystrophy type 1 using rare-variant linkage analysis and long-read genome sequencingKun Li, Daniel Quiat, Fei She, et al.
Physiological Genomics|February 3, 2011
Age-related autocrine diabetogenic effects of transgenic resistin in spontaneously hypertensive rats: gene expression profile analysisMichal Pravenec, Václav Zídek, Vladimír Landa, et al.
Frontiers in Genetics|January 13, 2018
A Novel Role for <i>CSRP1</i> in a Lebanese Family with Congenital Cardiac DefectsAmina Kamar, Akl C Fahed, Kamel Shibbani, et al.
Scientific Reports|December 28, 2022
Mechanism based therapies enable personalised treatment of hypertrophic cardiomyopathyFrancesca Margara, Yiangos Psaras, Zhinuo Jenny Wang, et al.
Circulation. Genomic and Precision Medicine|May 13, 2020
Congenital Heart Defects Due to <i>TAF1</i> Missense VariantsSarah U Morton, Radhika Agarwal, Jill A Madden, et al.
JCI Insight|May 31, 2016
Molecular profiling of dilated cardiomyopathy that progresses to heart failureMichael A Burke, Stephen Chang, Hiroko Wakimoto, et al.
The Journal of Thoracic and Cardiovascular Surgery|August 29, 2024
Predictive modeling of endocardial fibroelastosis recurrence in patients with congenital heart diseaseDaniel Diaz-Gil, Natalia Silva-Gomez, Sarah U Morton, et al.
Human Mutation|June 19, 2013
HOXA2 haploinsufficiency in dominant bilateral microtia and hearing lossKerry K Brown, Lucas M Viana, Cecilia C Helwig, et al.
The Journal of Clinical Investigation|May 3, 2005
A novel COL1A1 mutation in infantile cortical hyperostosis (Caffey disease) expands the spectrum of collagen-related disordersRobert C Gensure, Outi Mäkitie, Catherine Barclay, et al.
Pageof 17

Showing results (61-70 of 170) with videos related to

Sort By:
Pageof 17
Microsystems & Nanoengineering|September 27, 2021
Probing the subcellular nanostructure of engineered human cardiomyocytes in 3D tissueJosh Javor, Jourdan K Ewoldt, Paige E Cloonan, et al.
Genetics in Medicine Open|December 13, 2024
Genetic diagnosis of facioscapulohumeral muscular dystrophy type 1 using rare-variant linkage analysis and long-read genome sequencingKun Li, Daniel Quiat, Fei She, et al.
Physiological Genomics|February 3, 2011
Age-related autocrine diabetogenic effects of transgenic resistin in spontaneously hypertensive rats: gene expression profile analysisMichal Pravenec, Václav Zídek, Vladimír Landa, et al.
Frontiers in Genetics|January 13, 2018
A Novel Role for <i>CSRP1</i> in a Lebanese Family with Congenital Cardiac DefectsAmina Kamar, Akl C Fahed, Kamel Shibbani, et al.
Scientific Reports|December 28, 2022
Mechanism based therapies enable personalised treatment of hypertrophic cardiomyopathyFrancesca Margara, Yiangos Psaras, Zhinuo Jenny Wang, et al.
Circulation. Genomic and Precision Medicine|May 13, 2020
Congenital Heart Defects Due to <i>TAF1</i> Missense VariantsSarah U Morton, Radhika Agarwal, Jill A Madden, et al.
JCI Insight|May 31, 2016
Molecular profiling of dilated cardiomyopathy that progresses to heart failureMichael A Burke, Stephen Chang, Hiroko Wakimoto, et al.
The Journal of Thoracic and Cardiovascular Surgery|August 29, 2024
Predictive modeling of endocardial fibroelastosis recurrence in patients with congenital heart diseaseDaniel Diaz-Gil, Natalia Silva-Gomez, Sarah U Morton, et al.
Human Mutation|June 19, 2013
HOXA2 haploinsufficiency in dominant bilateral microtia and hearing lossKerry K Brown, Lucas M Viana, Cecilia C Helwig, et al.
The Journal of Clinical Investigation|May 3, 2005
A novel COL1A1 mutation in infantile cortical hyperostosis (Caffey disease) expands the spectrum of collagen-related disordersRobert C Gensure, Outi Mäkitie, Catherine Barclay, et al.
Pageof 17