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E Seidman

Showing results (121-130 of 611) with videos related to

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The American Journal of Physiology|September 1, 1988
Ouabain induces secretion of proatrial natriuretic factor by rat atrial cardiocytesK D Bloch, N Zamir, D Lichtstein, et al.
Human Molecular Genetics|January 1, 1996
Hereditary inclusion body myopathy maps to chromosome 9p1-q1S Mitrani-Rosenbaum, Z Argov, A Blumenfeld, et al.
Alimentary Pharmacology & Therapeutics|September 26, 2007
Evidence of allelic heterogeneity for associations between the NOD2/CARD15 gene and ulcerative colitis among North IndiansG Juyal, D Amre, V Midha, et al.
Nature Genetics|August 1, 1996
A human MSX1 homeodomain missense mutation causes selective tooth agenesisH Vastardis, N Karimbux, S W Guthua, et al.
American Journal of Human Genetics|July 1, 1997
Characterization of endoglin and identification of novel mutations in hereditary hemorrhagic telangiectasiaC L Shovlin, J M Hughes, J Scott, et al.
Circulation|November 11, 2024
Gene Therapy in Cardiovascular Disease: Recent Advances and Future Directions in Science: A Science Advisory From the American Heart AssociationYuri Kim, Andrew P Landstrom, Svati H Shah, et al.
Genes & Development|September 1, 1987
Localized expression of the atrial natriuretic factor gene during cardiac embryogenesisR Zeller, K D Bloch, B S Williams, et al.
The Journal of Clinical Investigation|March 13, 1999
Altered cardiac excitation-contraction coupling in mutant mice with familial hypertrophic cardiomyopathyW D Gao, N G Pérez, C E Seidman, et al.
Human Molecular Genetics|December 1, 1994
A dinucleotide repeat polymorphism in the MYBPH geneH Watkins, C A MacRae, D A Fischman, et al.
Mayo Clinic Proceedings|July 1, 1997
A new autosomal dominant disorder of pyogenic sterile arthritis, pyoderma gangrenosum, and acne: PAPA syndromeN M Lindor, T M Arsenault, H Solomon, et al.
Pageof 62

Showing results (121-130 of 611) with videos related to

Sort By:
Pageof 62
The American Journal of Physiology|September 1, 1988
Ouabain induces secretion of proatrial natriuretic factor by rat atrial cardiocytesK D Bloch, N Zamir, D Lichtstein, et al.
Human Molecular Genetics|January 1, 1996
Hereditary inclusion body myopathy maps to chromosome 9p1-q1S Mitrani-Rosenbaum, Z Argov, A Blumenfeld, et al.
Alimentary Pharmacology & Therapeutics|September 26, 2007
Evidence of allelic heterogeneity for associations between the NOD2/CARD15 gene and ulcerative colitis among North IndiansG Juyal, D Amre, V Midha, et al.
Nature Genetics|August 1, 1996
A human MSX1 homeodomain missense mutation causes selective tooth agenesisH Vastardis, N Karimbux, S W Guthua, et al.
American Journal of Human Genetics|July 1, 1997
Characterization of endoglin and identification of novel mutations in hereditary hemorrhagic telangiectasiaC L Shovlin, J M Hughes, J Scott, et al.
Circulation|November 11, 2024
Gene Therapy in Cardiovascular Disease: Recent Advances and Future Directions in Science: A Science Advisory From the American Heart AssociationYuri Kim, Andrew P Landstrom, Svati H Shah, et al.
Genes & Development|September 1, 1987
Localized expression of the atrial natriuretic factor gene during cardiac embryogenesisR Zeller, K D Bloch, B S Williams, et al.
The Journal of Clinical Investigation|March 13, 1999
Altered cardiac excitation-contraction coupling in mutant mice with familial hypertrophic cardiomyopathyW D Gao, N G Pérez, C E Seidman, et al.
Human Molecular Genetics|December 1, 1994
A dinucleotide repeat polymorphism in the MYBPH geneH Watkins, C A MacRae, D A Fischman, et al.
Mayo Clinic Proceedings|July 1, 1997
A new autosomal dominant disorder of pyogenic sterile arthritis, pyoderma gangrenosum, and acne: PAPA syndromeN M Lindor, T M Arsenault, H Solomon, et al.
Pageof 62