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Stem Cell Research
|
August 26, 2023
Generation of a homozygous CRYAB p.Arg120Gly mutant (UKEi001-A-1) from a human iPSC line
Niels Pietsch, Jiancheng Cheng, Antonietta Fazio, et al.
Biomolecules
|
July 25, 2019
Association of Asymmetric Dimethylarginine and Diastolic Dysfunction in Patients with Hypertrophic Cardiomyopathy
Kathrin Cordts, Doreen Seelig, Natalie Lund, et al.
Journal of Molecular and Cellular Cardiology
|
June 15, 2007
Decreased phosphorylation levels of cardiac myosin-binding protein-C in human and experimental heart failure
Ali El-Armouche, Lutz Pohlmann, Saskia Schlossarek, et al.
International Journal of Cardiology. Heart & Vasculature
|
August 9, 2017
I-1-deficiency negatively impacts survival in a cardiomyopathy mouse model
Felix W Friedrich, Hannieh Sotoud, Birgit Geertz, et al.
Journal of Cardiac Failure
|
March 29, 2016
Serum Matrix Metalloproteinases as Quantitative Biomarkers for Myocardial Fibrosis and Sudden Cardiac Death Risk Stratification in Patients With Hypertrophic Cardiomyopathy
Julia Münch, Maxim Avanesov, Peter Bannas, et al.
Journal of Molecular and Cellular Cardiology
|
March 11, 2004
Human homozygous R403W mutant cardiac myosin presents disproportionate enhancement of mechanical and enzymatic properties
Dagmar I Keller, Catherine Coirault, Thomas Rau, et al.
The Journal of Biological Chemistry
|
February 17, 2005
A minimal structural analogue of cyclic ADP-ribose: synthesis and calcium release activity in mammalian cells
Andreas H Guse, Xianfeng Gu, Liangren Zhang, et al.
Stem Cells and Development
|
October 15, 2010
Distinction between two populations of islet-1-positive cells in hearts of different murine strains
Patricia Khattar, Felix W Friedrich, Gisèle Bonne, et al.
Fundamental & Clinical Pharmacology
|
April 23, 2013
AT1 blockade abolishes left ventricular hypertrophy in heterozygous cMyBP-C null mice: role of FHL1
Nicolas Vignier, Philippe Le Corvoisier, Charlotte Blard, et al.
Human Mutation
|
March 30, 2019
Biallelic mutation in MYH7 and MYBPC3 leads to severe cardiomyopathy with left ventricular noncompaction phenotype
Konstantinos Kolokotronis, Jirko Kühnisch, Eva Klopocki, et al.
Page
of 15
Search research articles
Search
Showing results (41-50 of 145) with videos related to
Sort By:
Page
of 15
Stem Cell Research
|
August 26, 2023
Generation of a homozygous CRYAB p.Arg120Gly mutant (UKEi001-A-1) from a human iPSC line
Niels Pietsch, Jiancheng Cheng, Antonietta Fazio, et al.
Biomolecules
|
July 25, 2019
Association of Asymmetric Dimethylarginine and Diastolic Dysfunction in Patients with Hypertrophic Cardiomyopathy
Kathrin Cordts, Doreen Seelig, Natalie Lund, et al.
Journal of Molecular and Cellular Cardiology
|
June 15, 2007
Decreased phosphorylation levels of cardiac myosin-binding protein-C in human and experimental heart failure
Ali El-Armouche, Lutz Pohlmann, Saskia Schlossarek, et al.
International Journal of Cardiology. Heart & Vasculature
|
August 9, 2017
I-1-deficiency negatively impacts survival in a cardiomyopathy mouse model
Felix W Friedrich, Hannieh Sotoud, Birgit Geertz, et al.
Journal of Cardiac Failure
|
March 29, 2016
Serum Matrix Metalloproteinases as Quantitative Biomarkers for Myocardial Fibrosis and Sudden Cardiac Death Risk Stratification in Patients With Hypertrophic Cardiomyopathy
Julia Münch, Maxim Avanesov, Peter Bannas, et al.
Journal of Molecular and Cellular Cardiology
|
March 11, 2004
Human homozygous R403W mutant cardiac myosin presents disproportionate enhancement of mechanical and enzymatic properties
Dagmar I Keller, Catherine Coirault, Thomas Rau, et al.
The Journal of Biological Chemistry
|
February 17, 2005
A minimal structural analogue of cyclic ADP-ribose: synthesis and calcium release activity in mammalian cells
Andreas H Guse, Xianfeng Gu, Liangren Zhang, et al.
Stem Cells and Development
|
October 15, 2010
Distinction between two populations of islet-1-positive cells in hearts of different murine strains
Patricia Khattar, Felix W Friedrich, Gisèle Bonne, et al.
Fundamental & Clinical Pharmacology
|
April 23, 2013
AT1 blockade abolishes left ventricular hypertrophy in heterozygous cMyBP-C null mice: role of FHL1
Nicolas Vignier, Philippe Le Corvoisier, Charlotte Blard, et al.
Human Mutation
|
March 30, 2019
Biallelic mutation in MYH7 and MYBPC3 leads to severe cardiomyopathy with left ventricular noncompaction phenotype
Konstantinos Kolokotronis, Jirko Kühnisch, Eva Klopocki, et al.
Page
of 15