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Ketty Schwartz

Showing results (1-10 of 21) with videos related to

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The Journal of Clinical Investigation|September 4, 2003
Cardiac troponin T and familial hypertrophic cardiomyopathy: an energetic affairKetty Schwartz, Jean-Jacques Mercadier
European Journal of Human Genetics : EJHG|April 26, 2002
Emery-Dreifuss muscular dystrophyAnne Helbling-Leclerc, Gisèle Bonne, Ketty Schwartz
Swiss Medical Weekly|November 13, 2002
Genetics of familial cardiomyopathies and arrhythmiasDagmar I Keller, Lucie Carrier, Ketty Schwartz
Cardiovascular Research|November 14, 2003
Biomolecular interactions between human recombinant beta-MyHC and cMyBP-Cs implicated in familial hypertrophic cardiomyopathyJeanne Flavigny, Philippe Robert, Jean-Claude Camelin, et al.
Journal of Molecular and Cellular Cardiology|June 24, 2003
Identification of the genotypes causing hypertrophic cardiomyopathy in northern SwedenStellan Mörner, Pascale Richard, Elsadig Kazzam, et al.
Experimental Cell Research|December 4, 2003
Nuclear envelope alterations in fibroblasts from LGMD1B patients carrying nonsense Y259X heterozygous or homozygous mutation in lamin A/C geneAntoine Muchir, Baziel G van Engelen, Martin Lammens, et al.
Stem Cells and Development|October 15, 2010
Distinction between two populations of islet-1-positive cells in hearts of different murine strainsPatricia Khattar, Felix W Friedrich, Gisèle Bonne, et al.
European Journal of Human Genetics : EJHG|August 27, 2003
Polymorphisms of genes of the cardiac calcineurin pathway and cardiac hypertrophyOdette Poirier, Viviane Nicaud, Theresa McDonagh, et al.
Radiology|July 26, 2003
Electrotransfer at MR imaging: tool for optimization of gene transfer protocols--feasibility study in miceMarion Paturneau-Jouas, Elodie Parzy, Giovanni Vidal, et al.
European Journal of Heart Failure|December 17, 2003
Apical left ventricular aneurysm without atrio-ventricular block due to a lamin A/C gene mutationJean-François Forissier, Gisèle Bonne, Christiane Bouchier, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
The Journal of Clinical Investigation|September 4, 2003
Cardiac troponin T and familial hypertrophic cardiomyopathy: an energetic affairKetty Schwartz, Jean-Jacques Mercadier
European Journal of Human Genetics : EJHG|April 26, 2002
Emery-Dreifuss muscular dystrophyAnne Helbling-Leclerc, Gisèle Bonne, Ketty Schwartz
Swiss Medical Weekly|November 13, 2002
Genetics of familial cardiomyopathies and arrhythmiasDagmar I Keller, Lucie Carrier, Ketty Schwartz
Cardiovascular Research|November 14, 2003
Biomolecular interactions between human recombinant beta-MyHC and cMyBP-Cs implicated in familial hypertrophic cardiomyopathyJeanne Flavigny, Philippe Robert, Jean-Claude Camelin, et al.
Journal of Molecular and Cellular Cardiology|June 24, 2003
Identification of the genotypes causing hypertrophic cardiomyopathy in northern SwedenStellan Mörner, Pascale Richard, Elsadig Kazzam, et al.
Experimental Cell Research|December 4, 2003
Nuclear envelope alterations in fibroblasts from LGMD1B patients carrying nonsense Y259X heterozygous or homozygous mutation in lamin A/C geneAntoine Muchir, Baziel G van Engelen, Martin Lammens, et al.
Stem Cells and Development|October 15, 2010
Distinction between two populations of islet-1-positive cells in hearts of different murine strainsPatricia Khattar, Felix W Friedrich, Gisèle Bonne, et al.
European Journal of Human Genetics : EJHG|August 27, 2003
Polymorphisms of genes of the cardiac calcineurin pathway and cardiac hypertrophyOdette Poirier, Viviane Nicaud, Theresa McDonagh, et al.
Radiology|July 26, 2003
Electrotransfer at MR imaging: tool for optimization of gene transfer protocols--feasibility study in miceMarion Paturneau-Jouas, Elodie Parzy, Giovanni Vidal, et al.
European Journal of Heart Failure|December 17, 2003
Apical left ventricular aneurysm without atrio-ventricular block due to a lamin A/C gene mutationJean-François Forissier, Gisèle Bonne, Christiane Bouchier, et al.
Pageof 3