The genetic landscape of cardiomyopathy and its role in heart failure.
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The Role of Leucine-Rich Repeat Containing Protein 10 (LRRC10) in Dilated CardiomyopathyMicroRNAs Based Therapy of Hypertrophic Cardiomyopathy: The Road Traveled So FarThe Role of Genetic Testing in the Identification of Young Athletes with Inherited Primitive Cardiac Disorders at Risk of Exercise Sudden DeathRecent Advances in the Molecular Genetics of Familial Hypertrophic Cardiomyopathy in South Asian DescendantsGenetic Dissection of Cardiac Remodeling in an Isoproterenol-Induced Heart Failure Mouse Model.A CRISPR Path to Engineering New Genetic Mouse Models for Cardiovascular ResearchSex dimorphisms of crossbridge cycling kinetics in transgenic hypertrophic cardiomyopathy miceHigh-Throughput Diagnostic Assay for a Highly Prevalent Cardiomyopathy-Associated MYBPC3 Variant.Systems Genetics Approach Identifies Gene Pathways and Adamts2 as Drivers of Isoproterenol-Induced Cardiac Hypertrophy and Cardiomyopathy in MiceWhole gene sequencing identifies deep-intronic variants with potential functional impact in patients with hypertrophic cardiomyopathy.A multidimensional sight on cardiac failure: uncovered from structural to molecular level.Analysis of SCN5A Gene Variants in East Slovak Patients with Cardiomyopathy.Bioinformatics method identifies potential biomarkers of dilated cardiomyopathy in a human induced pluripotent stem cell-derived cardiomyocyte model.Knock-in mice harboring a Ca(2+) desensitizing mutation in cardiac troponin C develop early onset dilated cardiomyopathy.Cardiomyocyte-Specific Telomere Shortening is a Distinct Signature of Heart Failure in Humans.Experimental Modeling Supports a Role for MyBP-HL as a Novel Myofilament Component in Arrhythmia and Dilated Cardiomyopathy.Dystrophic Cardiomyopathy: Complex Pathobiological Processes to Generate Clinical Phenotype.Genetic determinants of heart failure: facts and numbers.LRRC10 (Leucine-Rich Repeat Containing Protein 10) and REEP5 (Receptor Accessory Protein 5) as Novel Regulators of Cardiac Excitation-Contraction Coupling Structure and Function.Dilated Cardiomyopathy: Genetic Determinants and Mechanisms.ALPK3-deficient cardiomyocytes generated from patient-derived induced pluripotent stem cells and mutant human embryonic stem cells display abnormal calcium handling and establish that ALPK3 deficiency underlies familial cardiomyopathy.A Genome-Wide Association Study of Idiopathic Dilated Cardiomyopathy in African Americans.Myocardial Induction of Type 3 Deiodinase in Dilated Cardiomyopathy.[Cardiac pathologies and aging: lessons from a tiny heart].Whole exome sequencing identified 1 base pair novel deletion in BCL2-associated athanogene 3 (BAG3) gene associated with severe dilated cardiomyopathy (DCM) requiring heart transplant in multiple family members.Data on whole length myosin binding protein C stabilizes myosin S2 as measured by gravitational force spectroscopy.Lycium barbarum polysaccharides restore adverse structural remodelling and cardiac contractile dysfunction induced by overexpression of microRNA-1
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P2860
The genetic landscape of cardiomyopathy and its role in heart failure.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
The genetic landscape of cardiomyopathy and its role in heart failure.
@en
type
label
The genetic landscape of cardiomyopathy and its role in heart failure.
@en
prefLabel
The genetic landscape of cardiomyopathy and its role in heart failure.
@en
P2860
P1433
P1476
The genetic landscape of cardiomyopathy and its role in heart failure
@en
P2093
Elizabeth M McNally
Megan J Puckelwartz
P2860
P304
P356
10.1016/J.CMET.2015.01.013
P577
2015-02-01T00:00:00Z