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Lucie Carrier

Showing results (101-110 of 145) with videos related to

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Clinical Genetics|October 1, 2019
Targeted panel sequencing in pediatric primary cardiomyopathy supports a critical role of TNNI3Jirko Kühnisch, Christopher Herbst, Nadya Al-Wakeel-Marquard, et al.
The FEBS Journal|February 17, 2022
CMYA5 is a novel interaction partner of FHL2 in cardiac myocytesKonstantina Stathopoulou, Josef Schnittger, Janice Raabe, et al.
Nature Communications|December 3, 2014
Mybpc3 gene therapy for neonatal cardiomyopathy enables long-term disease prevention in miceGiulia Mearini, Doreen Stimpel, Birgit Geertz, et al.
JACC. Basic to Translational Science|May 17, 2021
FYCO1 Regulates Cardiomyocyte Autophagy and Prevents Heart Failure Due to Pressure Overload In VivoChristian Kuhn, Maja Menke, Frauke Senger, et al.
European Journal of Heart Failure|November 16, 2012
A novel genetic variant in the transcription factor Islet-1 exerts gain of function on myocyte enhancer factor 2C promoter activityFelix W Friedrich, Gilles Dilanian, Patricia Khattar, et al.
Stem Cell Research|February 21, 2026
Generation of human induced pluripotent stem cell lines carrying a heterozygous and homozygous PRKD1 c.1774G > A genetic variant causing syndromic congenital defectsFabian Witthoff, Niels Pietsch, Philipp Henning, et al.
Circulation Research|July 21, 2023
EGFR/IGF1R Signaling Modulates Relaxation in Hypertrophic CardiomyopathySila Algül, Maike Schuldt, Emmy Manders, et al.
Journal of the American Heart Association|November 13, 2014
Endothelin-1 induces myofibrillar disarray and contractile vector variability in hypertrophic cardiomyopathy-induced pluripotent stem cell-derived cardiomyocytesAtsushi Tanaka, Shinsuke Yuasa, Giulia Mearini, et al.
Human Molecular Genetics|April 12, 2013
Heterozygous LmnadelK32 mice develop dilated cardiomyopathy through a combined pathomechanism of haploinsufficiency and peptide toxicityMarie-Elodie Cattin, Anne T Bertrand, Saskia Schlossarek, et al.
Circulation Research|January 2, 2013
GSK3β phosphorylates newly identified site in the proline-alanine-rich region of cardiac myosin-binding protein C and alters cross-bridge cycling kinetics in human: short communicationDiederik W D Kuster, Vasco Sequeira, Aref Najafi, et al.
Pageof 15

Showing results (101-110 of 145) with videos related to

Sort By:
Pageof 15
Clinical Genetics|October 1, 2019
Targeted panel sequencing in pediatric primary cardiomyopathy supports a critical role of TNNI3Jirko Kühnisch, Christopher Herbst, Nadya Al-Wakeel-Marquard, et al.
The FEBS Journal|February 17, 2022
CMYA5 is a novel interaction partner of FHL2 in cardiac myocytesKonstantina Stathopoulou, Josef Schnittger, Janice Raabe, et al.
Nature Communications|December 3, 2014
Mybpc3 gene therapy for neonatal cardiomyopathy enables long-term disease prevention in miceGiulia Mearini, Doreen Stimpel, Birgit Geertz, et al.
JACC. Basic to Translational Science|May 17, 2021
FYCO1 Regulates Cardiomyocyte Autophagy and Prevents Heart Failure Due to Pressure Overload In VivoChristian Kuhn, Maja Menke, Frauke Senger, et al.
European Journal of Heart Failure|November 16, 2012
A novel genetic variant in the transcription factor Islet-1 exerts gain of function on myocyte enhancer factor 2C promoter activityFelix W Friedrich, Gilles Dilanian, Patricia Khattar, et al.
Stem Cell Research|February 21, 2026
Generation of human induced pluripotent stem cell lines carrying a heterozygous and homozygous PRKD1 c.1774G > A genetic variant causing syndromic congenital defectsFabian Witthoff, Niels Pietsch, Philipp Henning, et al.
Circulation Research|July 21, 2023
EGFR/IGF1R Signaling Modulates Relaxation in Hypertrophic CardiomyopathySila Algül, Maike Schuldt, Emmy Manders, et al.
Journal of the American Heart Association|November 13, 2014
Endothelin-1 induces myofibrillar disarray and contractile vector variability in hypertrophic cardiomyopathy-induced pluripotent stem cell-derived cardiomyocytesAtsushi Tanaka, Shinsuke Yuasa, Giulia Mearini, et al.
Human Molecular Genetics|April 12, 2013
Heterozygous LmnadelK32 mice develop dilated cardiomyopathy through a combined pathomechanism of haploinsufficiency and peptide toxicityMarie-Elodie Cattin, Anne T Bertrand, Saskia Schlossarek, et al.
Circulation Research|January 2, 2013
GSK3β phosphorylates newly identified site in the proline-alanine-rich region of cardiac myosin-binding protein C and alters cross-bridge cycling kinetics in human: short communicationDiederik W D Kuster, Vasco Sequeira, Aref Najafi, et al.
Pageof 15