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Joshua M Gorham

Showing results (31-40 of 54) with videos related to

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Biorxiv : the Preprint Server for Biology|May 3, 2023
<i>Tbx5</i> maintains atrial identity by regulating an atrial enhancer networkMason E Sweat, Yangpo Cao, Xiaoran Zhang, et al.
The Journal of Clinical Investigation|February 11, 2014
5'RNA-Seq identifies Fhl1 as a genetic modifier in cardiomyopathyDanos C Christodoulou, Hiroko Wakimoto, Kenji Onoue, et al.
Molecular Systems Biology|June 24, 2010
Dissecting spatio-temporal protein networks driving human heart development and related disordersKasper Lage, Kjeld Møllgård, Steven Greenway, et al.
American Journal of Human Genetics|April 9, 2022
Neither cardiac mitochondrial DNA variation nor copy number contribute to congenital heart disease riskJon A L Willcox, Joshua T Geiger, Sarah U Morton, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 18, 2022
An ancient founder mutation located between <i>ROBO1</i> and <i>ROBO2</i> is responsible for increased microtia risk in Amerindigenous populationsDaniel Quiat, Seong Won Kim, Qi Zhang, et al.
Human Molecular Genetics|August 27, 2013
Loss of FHL1 induces an age-dependent skeletal muscle myopathy associated with myofibrillar and intermyofibrillar disorganization in miceAndrea A Domenighetti, Pao-Hsien Chu, Tongbin Wu, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 21, 2012
Genetic and environmental risk factors in congenital heart disease functionally converge in protein networks driving heart developmentKasper Lage, Steven C Greenway, Jill A Rosenfeld, et al.
The Journal of Clinical Investigation|June 3, 2024
Increased endothelial sclerostin caused by elevated DSCAM mediates multiple trisomy 21 phenotypesDavid M McKean, Qi Zhang, Priyanka Narayan, et al.
Science (New York, N.Y.)|September 4, 2025
Reversible compromise of physiological resilience by accumulation of heteroplasmic mtDNA mutationsHuihui Huang, Yi Wang, Zsuzsanna K Zsengeller, et al.
Circulation. Genomic and Precision Medicine|February 16, 2026
<i>ROBO2</i> Variants Associated With Atrial Septal Defect Define a Novel Regulatory ElementSeong Won Kim, Michael Parfenov, Laura Rodriguez-Murillo, et al.
Pageof 6

Showing results (31-40 of 54) with videos related to

Sort By:
Pageof 6
Biorxiv : the Preprint Server for Biology|May 3, 2023
<i>Tbx5</i> maintains atrial identity by regulating an atrial enhancer networkMason E Sweat, Yangpo Cao, Xiaoran Zhang, et al.
The Journal of Clinical Investigation|February 11, 2014
5'RNA-Seq identifies Fhl1 as a genetic modifier in cardiomyopathyDanos C Christodoulou, Hiroko Wakimoto, Kenji Onoue, et al.
Molecular Systems Biology|June 24, 2010
Dissecting spatio-temporal protein networks driving human heart development and related disordersKasper Lage, Kjeld Møllgård, Steven Greenway, et al.
American Journal of Human Genetics|April 9, 2022
Neither cardiac mitochondrial DNA variation nor copy number contribute to congenital heart disease riskJon A L Willcox, Joshua T Geiger, Sarah U Morton, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 18, 2022
An ancient founder mutation located between <i>ROBO1</i> and <i>ROBO2</i> is responsible for increased microtia risk in Amerindigenous populationsDaniel Quiat, Seong Won Kim, Qi Zhang, et al.
Human Molecular Genetics|August 27, 2013
Loss of FHL1 induces an age-dependent skeletal muscle myopathy associated with myofibrillar and intermyofibrillar disorganization in miceAndrea A Domenighetti, Pao-Hsien Chu, Tongbin Wu, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 21, 2012
Genetic and environmental risk factors in congenital heart disease functionally converge in protein networks driving heart developmentKasper Lage, Steven C Greenway, Jill A Rosenfeld, et al.
The Journal of Clinical Investigation|June 3, 2024
Increased endothelial sclerostin caused by elevated DSCAM mediates multiple trisomy 21 phenotypesDavid M McKean, Qi Zhang, Priyanka Narayan, et al.
Science (New York, N.Y.)|September 4, 2025
Reversible compromise of physiological resilience by accumulation of heteroplasmic mtDNA mutationsHuihui Huang, Yi Wang, Zsuzsanna K Zsengeller, et al.
Circulation. Genomic and Precision Medicine|February 16, 2026
<i>ROBO2</i> Variants Associated With Atrial Septal Defect Define a Novel Regulatory ElementSeong Won Kim, Michael Parfenov, Laura Rodriguez-Murillo, et al.
Pageof 6