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E Seidman

Showing results (281-290 of 533) with videos related to

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Genomics|July 1, 1995
Cloning, expression, and chromosomal location of SHH and IHH: two human homologues of the Drosophila segment polarity gene hedgehogV Marigo, D J Roberts, S M Lee, et al.
The New England Journal of Medicine|November 16, 1989
Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1J A Jarcho, W McKenna, J A Pare, et al.
The Annals of Thoracic Surgery|July 21, 2018
Molecular Genetics of Lidocaine-Containing Cardioplegia in the Human Heart During Cardiac SurgeryMahyar Heydarpour, Julius Ejiofor, Michael Gilfeather, et al.
BMC Medical Genomics|July 27, 2025
Enrichment of tandem repeat element variants near CHD genes identified by short- and long-read genome sequencingAbhilash Suresh, Sarah U Morton, Daniel Quiat, et al.
Nature Genetics|July 1, 1992
The gene responsible for familial hypocalciuric hypercalcemia maps to chromosome 3q in four unrelated familiesY H Chou, E M Brown, T Levi, et al.
Circulation Research|May 25, 2004
Effect of cardiac myosin binding protein-C on mechanoenergetics in mouse myocardiumBradley M Palmer, Teruo Noguchi, Yuan Wang, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 20, 2006
Cardiac myosin missense mutations cause dilated cardiomyopathy in mouse models and depress molecular motor functionJoachim P Schmitt, Edward P Debold, Ferhaan Ahmad, et al.
JACC. Basic to Translational Science|September 1, 2018
The Role of the L-Type Ca<sup>2+</sup> Channel in Altered Metabolic Activity in a Murine Model of Hypertrophic CardiomyopathyHelena M Viola, Victoria P A Johnstone, Henrietta Cserne Szappanos, et al.
Annals of Neurology|April 29, 2014
UBQLN2 mutation causing heterogeneous X-linked dominant neurodegenerationAkl C Fahed, Barbara McDonough, Cynthia M Gouvion, et al.
Molecular and Cellular Biology|September 19, 1998
Haploinsufficiency of MSX1: a mechanism for selective tooth agenesisG Hu, H Vastardis, A J Bendall, et al.
Pageof 54

Showing results (281-290 of 533) with videos related to

Sort By:
Pageof 54
Genomics|July 1, 1995
Cloning, expression, and chromosomal location of SHH and IHH: two human homologues of the Drosophila segment polarity gene hedgehogV Marigo, D J Roberts, S M Lee, et al.
The New England Journal of Medicine|November 16, 1989
Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1J A Jarcho, W McKenna, J A Pare, et al.
The Annals of Thoracic Surgery|July 21, 2018
Molecular Genetics of Lidocaine-Containing Cardioplegia in the Human Heart During Cardiac SurgeryMahyar Heydarpour, Julius Ejiofor, Michael Gilfeather, et al.
BMC Medical Genomics|July 27, 2025
Enrichment of tandem repeat element variants near CHD genes identified by short- and long-read genome sequencingAbhilash Suresh, Sarah U Morton, Daniel Quiat, et al.
Nature Genetics|July 1, 1992
The gene responsible for familial hypocalciuric hypercalcemia maps to chromosome 3q in four unrelated familiesY H Chou, E M Brown, T Levi, et al.
Circulation Research|May 25, 2004
Effect of cardiac myosin binding protein-C on mechanoenergetics in mouse myocardiumBradley M Palmer, Teruo Noguchi, Yuan Wang, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 20, 2006
Cardiac myosin missense mutations cause dilated cardiomyopathy in mouse models and depress molecular motor functionJoachim P Schmitt, Edward P Debold, Ferhaan Ahmad, et al.
JACC. Basic to Translational Science|September 1, 2018
The Role of the L-Type Ca<sup>2+</sup> Channel in Altered Metabolic Activity in a Murine Model of Hypertrophic CardiomyopathyHelena M Viola, Victoria P A Johnstone, Henrietta Cserne Szappanos, et al.
Annals of Neurology|April 29, 2014
UBQLN2 mutation causing heterogeneous X-linked dominant neurodegenerationAkl C Fahed, Barbara McDonough, Cynthia M Gouvion, et al.
Molecular and Cellular Biology|September 19, 1998
Haploinsufficiency of MSX1: a mechanism for selective tooth agenesisG Hu, H Vastardis, A J Bendall, et al.
Pageof 54