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Seidman

Showing results (801-810 of 3,143) with videos related to

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Clinical and Investigative Medicine. Medecine Clinique Et Experimentale|December 1, 1996
Lactose handling by women with lactose malabsorption is improved during pregnancyA Szilagyi, R Salomon, M Martin, et al.
American Journal of Community Psychology|August 1, 1996
The impact of the transition to high school on the self-system and perceived social context of poor urban youthE Seidman, J L Aber, L Allen, et al.
Nature Cardiovascular Research|August 26, 2025
Endocardial primary cilia and blood flow regulate EndoMT during endocardial cushion developmentKathryn Berg, Joshua Gorham, Faith Lundt, et al.
Biochemistry|July 24, 1979
Interaction between wheat germ RNA polymerase II and adenovirus 2 DNA. Evidence for two types of stable binary complexesS Seidman, S J Surzycki, W DeLorbe, et al.
The Journal of Clinical Investigation|March 6, 2003
IL-12 is required for differentiation of pathogenic CD8+ T cell effectors that cause myocarditisNir Grabie, Michael W Delfs, Jason R Westrich, et al.
Molecular and Cellular Biochemistry|November 5, 2004
Reduced cross-bridge dependent stiffness of skinned myocardium from mice lacking cardiac myosin binding protein-CBradley M Palmer, Bradley K McConnell, Guo Hua Li, et al.
The Journal of Clinical Investigation|December 6, 2000
An abnormal Ca(2+) response in mutant sarcomere protein-mediated familial hypertrophic cardiomyopathyD Fatkin, B K McConnell, J O Mudd, et al.
Journal of Molecular and Cellular Cardiology|September 1, 1986
Atrial natriuretic factor: assessment of its structure in atria and regulation of its biosynthesis with volume depletionJ B Zisfein, G R Matsueda, J T Fallon, et al.
Heart Rhythm|July 13, 2010
Optimizing catecholaminergic polymorphic ventricular tachycardia therapy in calsequestrin-mutant miceGuy Katz, Assad Khoury, Efrat Kurtzwald, et al.
Cell|December 31, 1993
Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidismM R Pollak, E M Brown, Y H Chou, et al.
Pageof 315

Showing results (801-810 of 3,143) with videos related to

Sort By:
Pageof 315
Clinical and Investigative Medicine. Medecine Clinique Et Experimentale|December 1, 1996
Lactose handling by women with lactose malabsorption is improved during pregnancyA Szilagyi, R Salomon, M Martin, et al.
American Journal of Community Psychology|August 1, 1996
The impact of the transition to high school on the self-system and perceived social context of poor urban youthE Seidman, J L Aber, L Allen, et al.
Nature Cardiovascular Research|August 26, 2025
Endocardial primary cilia and blood flow regulate EndoMT during endocardial cushion developmentKathryn Berg, Joshua Gorham, Faith Lundt, et al.
Biochemistry|July 24, 1979
Interaction between wheat germ RNA polymerase II and adenovirus 2 DNA. Evidence for two types of stable binary complexesS Seidman, S J Surzycki, W DeLorbe, et al.
The Journal of Clinical Investigation|March 6, 2003
IL-12 is required for differentiation of pathogenic CD8+ T cell effectors that cause myocarditisNir Grabie, Michael W Delfs, Jason R Westrich, et al.
Molecular and Cellular Biochemistry|November 5, 2004
Reduced cross-bridge dependent stiffness of skinned myocardium from mice lacking cardiac myosin binding protein-CBradley M Palmer, Bradley K McConnell, Guo Hua Li, et al.
The Journal of Clinical Investigation|December 6, 2000
An abnormal Ca(2+) response in mutant sarcomere protein-mediated familial hypertrophic cardiomyopathyD Fatkin, B K McConnell, J O Mudd, et al.
Journal of Molecular and Cellular Cardiology|September 1, 1986
Atrial natriuretic factor: assessment of its structure in atria and regulation of its biosynthesis with volume depletionJ B Zisfein, G R Matsueda, J T Fallon, et al.
Heart Rhythm|July 13, 2010
Optimizing catecholaminergic polymorphic ventricular tachycardia therapy in calsequestrin-mutant miceGuy Katz, Assad Khoury, Efrat Kurtzwald, et al.
Cell|December 31, 1993
Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidismM R Pollak, E M Brown, Y H Chou, et al.
Pageof 315