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Genome Medicine
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January 31, 2019
Quantitative approaches to variant classification increase the yield and precision of genetic testing in Mendelian diseases: the case of hypertrophic cardiomyopathy
Roddy Walsh, Francesco Mazzarotto, Nicola Whiffin, et al.
Circulation
|
July 10, 2019
Widespread Translational Control of Fibrosis in the Human Heart by RNA-Binding Proteins
Sonia Chothani, Sebastian Schäfer, Eleonora Adami, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 27, 2021
Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies
Francesco Mazzarotto, Megan H Hawley, Matteo Beltrami, et al.
Nature Communications
|
August 11, 2019
WWP2 regulates pathological cardiac fibrosis by modulating SMAD2 signaling
Huimei Chen, Aida Moreno-Moral, Francesco Pesce, et al.
Nature Communications
|
September 11, 2019
Author Correction: WWP2 regulates pathological cardiac fibrosis by modulating SMAD2 signaling
Huimei Chen, Aida Moreno-Moral, Francesco Pesce, et al.
The Journal of Clinical Investigation
|
March 30, 2023
Modulating fast skeletal muscle contraction protects skeletal muscle in animal models of Duchenne muscular dystrophy
Alan J Russell, Mike DuVall, Ben Barthel, et al.
Physical Review Letters
|
February 28, 2015
Grain-size-independent plastic flow at ultrahigh pressures and strain rates
H-S Park, R E Rudd, R M Cavallo, et al.
Circulation
|
January 28, 2020
Reevaluating the Genetic Contribution of Monogenic Dilated Cardiomyopathy
Francesco Mazzarotto, Upasana Tayal, Rachel J Buchan, et al.
The New England Journal of Medicine
|
February 17, 2012
Truncations of titin causing dilated cardiomyopathy
Daniel S Herman, Lien Lam, Matthew R G Taylor, et al.
Circulation Research
|
July 30, 2011
Telethonin deficiency is associated with maladaptation to biomechanical stress in the mammalian heart
Ralph Knöll, Wolfgang A Linke, Peijian Zou, et al.
Page
of 68
Search research articles
Search
Showing results (641-650 of 672) with videos related to
Sort By:
Page
of 68
Genome Medicine
|
January 31, 2019
Quantitative approaches to variant classification increase the yield and precision of genetic testing in Mendelian diseases: the case of hypertrophic cardiomyopathy
Roddy Walsh, Francesco Mazzarotto, Nicola Whiffin, et al.
Circulation
|
July 10, 2019
Widespread Translational Control of Fibrosis in the Human Heart by RNA-Binding Proteins
Sonia Chothani, Sebastian Schäfer, Eleonora Adami, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 27, 2021
Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies
Francesco Mazzarotto, Megan H Hawley, Matteo Beltrami, et al.
Nature Communications
|
August 11, 2019
WWP2 regulates pathological cardiac fibrosis by modulating SMAD2 signaling
Huimei Chen, Aida Moreno-Moral, Francesco Pesce, et al.
Nature Communications
|
September 11, 2019
Author Correction: WWP2 regulates pathological cardiac fibrosis by modulating SMAD2 signaling
Huimei Chen, Aida Moreno-Moral, Francesco Pesce, et al.
The Journal of Clinical Investigation
|
March 30, 2023
Modulating fast skeletal muscle contraction protects skeletal muscle in animal models of Duchenne muscular dystrophy
Alan J Russell, Mike DuVall, Ben Barthel, et al.
Physical Review Letters
|
February 28, 2015
Grain-size-independent plastic flow at ultrahigh pressures and strain rates
H-S Park, R E Rudd, R M Cavallo, et al.
Circulation
|
January 28, 2020
Reevaluating the Genetic Contribution of Monogenic Dilated Cardiomyopathy
Francesco Mazzarotto, Upasana Tayal, Rachel J Buchan, et al.
The New England Journal of Medicine
|
February 17, 2012
Truncations of titin causing dilated cardiomyopathy
Daniel S Herman, Lien Lam, Matthew R G Taylor, et al.
Circulation Research
|
July 30, 2011
Telethonin deficiency is associated with maladaptation to biomechanical stress in the mammalian heart
Ralph Knöll, Wolfgang A Linke, Peijian Zou, et al.
Page
of 68