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Clinical Genetics
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October 1, 2019
Targeted panel sequencing in pediatric primary cardiomyopathy supports a critical role of TNNI3
Jirko 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 myocytes
Konstantina Stathopoulou, Josef Schnittger, Janice Raabe, et al.
Nature Communications
|
December 3, 2014
Mybpc3 gene therapy for neonatal cardiomyopathy enables long-term disease prevention in mice
Giulia 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 Vivo
Christian 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 activity
Felix 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 defects
Fabian Witthoff, Niels Pietsch, Philipp Henning, et al.
Circulation Research
|
July 21, 2023
EGFR/IGF1R Signaling Modulates Relaxation in Hypertrophic Cardiomyopathy
Sila 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 cardiomyocytes
Atsushi 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 toxicity
Marie-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 communication
Diederik W D Kuster, Vasco Sequeira, Aref Najafi, et al.
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of 15
Search research articles
Search
Showing results (101-110 of 145) with videos related to
Sort By:
Page
of 15
Clinical Genetics
|
October 1, 2019
Targeted panel sequencing in pediatric primary cardiomyopathy supports a critical role of TNNI3
Jirko 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 myocytes
Konstantina Stathopoulou, Josef Schnittger, Janice Raabe, et al.
Nature Communications
|
December 3, 2014
Mybpc3 gene therapy for neonatal cardiomyopathy enables long-term disease prevention in mice
Giulia 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 Vivo
Christian 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 activity
Felix 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 defects
Fabian Witthoff, Niels Pietsch, Philipp Henning, et al.
Circulation Research
|
July 21, 2023
EGFR/IGF1R Signaling Modulates Relaxation in Hypertrophic Cardiomyopathy
Sila 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 cardiomyocytes
Atsushi 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 toxicity
Marie-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 communication
Diederik W D Kuster, Vasco Sequeira, Aref Najafi, et al.
Page
of 15