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TNNT2
FLNC Pathogenic Variants in Patients with Cardiomyopathies
Genetic Variation Screening of TNNT2 Gene in a Cohort of Patients with Hypertrophic and Dilated Cardiomyopathy
Genetic Mutations and Mechanisms in Dilated Cardiomyopathy
Tnnt2
Inhibition of Β-Catenin Signaling Respecifies Anterior-Like Endothelium Into Beating Human Cardiomyocytes Nathan J
Novel Pathogenic Variants in Filamin C Identified in Pediatric Restrictive Cardiomyopathy
Disrupted Mechanobiology Links the Molecular and Cellular Phenotypes
Illuminating the Divergent Role of Filamin C Mutations in Human Cardiomyopathy
Transcriptomic Uniqueness and Commonality of the Ion Channels and Transporters in the Four Heart Chambers Sanda Iacobas1, Bogdan Amuzescu2 & Dumitru A
Genetic Cardiomyopathies: the Lesson Learned from Hipscs
Variant Interpretation for Dilated Cardiomyopathy
Human Induced Pluripotent Stem Cell–Derived Podocytes Mature Into Vascularized Glomeruli Upon Experimental Transplantation
Mutation Location of HCM-Causing Troponin T Mutations Defines The
In Vitro Generation of Functional Murine Heart Organoids Via FGF4
The Function of Wnt/Beta-Catenin Signaling in Ewing Sarcoma and Its Contribution to Pathogenesis
TNNT2 Mutations in the Tropomyosin Binding Region of TNT1 Disrupt Its Role in Contractile Inhibition and Stimulate Cardiac Dysfunction
TNNT2 Gene Troponin T2, Cardiac Type
Transcriptional Profiling Reveals Extraordinary Diversity Among
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ALPK2 Promotes Cardiogenesis in Zebrafish and Human Pluripotent
Muscle-Specific Mis-Splicing and Heart Disease Exemplified by RBM20
Telomere Shortening Is a Hallmark of Genetic Cardiomyopathies
Clinical and Genetic Issues in Dilated Cardiomyopathy: a Review for Genetics Professionals Ray E
A Yeast-Based Model for Hereditary Motor and Sensory Neuropathies: a Simple System for Complex, Heterogeneous Diseases
Crucial Genes Associated with Diabetic Nephropathy Explored by Microarray Analysis Zhikui Wang, Zhaoxia Wang*, Zhongqi Zhou and Yueqin Ren
Tet Proteins Influence the Balance Between Neuroectodermal and Mesodermal Fate Choice by Inhibiting Wnt Signaling
N-Cadherin Prevents the Premature Differentiation of Anterior Heart Field Progenitors in the Pharyngeal Mesodermal Microenvironment
Brain Pathology in Myotonic Dystrophy: When Tauopathy Meets Spliceopathy and Rnaopathy
Mono- and Bi-Allelic Protein Truncating Variants in Alpha-Actinin 2 Cause Cardiomyopathy Through Distinct Mechanisms
Differentiation of Human Cardiac Atrial Appendage Stem Cells Into Adult
Hereditary Dilated Cardiomyopathy: Recent Advances in Genetic
Α-Cardiac Actin Is a Novel Disease Gene in Familial Hypertrophic Cardiomyopathy
Regulation of Pluripotency and Differentiation by Chromatin Remodeling Factors
Mutation P.A337P Is Associated with Left-Ventricular Non-Compaction Cardiomyopathy
Titin in Muscular Dystrophy and Cardiomyopathy Urinary Titin As a Novel Marker
Variant R94C in TNNT2‐Encoded Troponin T Predisposes to Pediatric
Yield of Rare Variants Detected by Targeted Next-Generation Sequencing in a Cohort of Romanian Index Patients with Hypertrophic Cardiomyopathy