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E Seidman

Showing results (321-330 of 533) with videos related to

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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.
Developmental Biology|July 28, 2006
Tbx5-dependent rheostatic control of cardiac gene expression and morphogenesisAlessandro D Mori, Yonghong Zhu, Ilyas Vahora, 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.
American Journal of Human Genetics|May 23, 1998
The Bjornstad syndrome (sensorineural hearing loss and pili torti) disease gene maps to chromosome 2q34-36J F Lubianca Neto, L Lu, R D Eavey, 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. Cardiovascular Genetics|January 25, 2017
The Long Noncoding RNA Landscape of the Ischemic Human Left VentricleLouis A Saddic, Martin I Sigurdsson, Tzuu-Wang Chang, 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.
Biology Open|November 30, 2017
Cardiac-enriched BAF chromatin-remodeling complex subunit Baf60c regulates gene expression programs essential for heart development and functionXin Sun, Swetansu K Hota, Yu-Qing Zhou, et al.
The New England Journal of Medicine|September 8, 2010
Myocardial fibrosis as an early manifestation of hypertrophic cardiomyopathyCarolyn Y Ho, Begoña López, Otavio R Coelho-Filho, et al.
Pageof 54

Showing results (321-330 of 533) with videos related to

Sort By:
Pageof 54
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.
Developmental Biology|July 28, 2006
Tbx5-dependent rheostatic control of cardiac gene expression and morphogenesisAlessandro D Mori, Yonghong Zhu, Ilyas Vahora, 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.
American Journal of Human Genetics|May 23, 1998
The Bjornstad syndrome (sensorineural hearing loss and pili torti) disease gene maps to chromosome 2q34-36J F Lubianca Neto, L Lu, R D Eavey, 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. Cardiovascular Genetics|January 25, 2017
The Long Noncoding RNA Landscape of the Ischemic Human Left VentricleLouis A Saddic, Martin I Sigurdsson, Tzuu-Wang Chang, 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.
Biology Open|November 30, 2017
Cardiac-enriched BAF chromatin-remodeling complex subunit Baf60c regulates gene expression programs essential for heart development and functionXin Sun, Swetansu K Hota, Yu-Qing Zhou, et al.
The New England Journal of Medicine|September 8, 2010
Myocardial fibrosis as an early manifestation of hypertrophic cardiomyopathyCarolyn Y Ho, Begoña López, Otavio R Coelho-Filho, et al.
Pageof 54