Patient-specific induced pluripotent stem cells as a model for familial dilated cardiomyopathy. - Wikidata - wikimedia - TriplyDB

Patient-specific induced pluripotent stem cells as a model for familial dilated cardiomyopathy.

Patient-specific induced pluripotent stem cells as a model for familial dilated cardiomyopathy.

http://www.wikidata.org/entity/Q30539904

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Distilling complexity to advance cardiac tissue engineering Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes Afford New Opportunities in Inherited Cardiovascular Disease Modeling Young at Heart: Pioneering Approaches to Model Nonischaemic Cardiomyopathy with Induced Pluripotent Stem Cells hiPSC-derived iMSCs: NextGen MSCs as an advanced therapeutically active cell resource for regenerative medicine G-protein Coupled Receptor Signaling in Pluripotent Stem Cell-derived Cardiovascular Cells: Implications for Disease Modeling Induced Pluripotency and Gene Editing in Disease Modelling: Perspectives and Challenges Nanopatterned Human iPSC-Based Model of a Dystrophin-Null Cardiomyopathic Phenotype Parkinson's disease proteins: Novel mitochondrial targets for cardioprotection Induced pluripotent stem cells for cardiovascular disease: from product-focused disease modeling to process-focused disease discovery Cardiovascular Disease Modeling Using Patient-Specific Induced Pluripotent Stem Cells Reprogramming and transdifferentiation for cardiovascular development and regenerative medicine: where do we stand?Induced pluripotent stem cell-derived cardiomyocytes for cardiovascular disease modeling and drug screening Human-induced pluripotent stem cell models of inherited cardiomyopathies Modelling human disease with pluripotent stem cells Mitoconfusion: noncanonical functioning of dynamism factors in static mitochondria of the heart Calcium signalling of human pluripotent stem cell-derived cardiomyocytes Endothelial cells derived from nuclear reprogramming Clinical Potentials of Cardiomyocytes Derived from Patient-Specific Induced Pluripotent Stem Cells Maturation status of sarcomere structure and function in human iPSC-derived cardiac myocytes Generation of Functional Cardiomyocytes from Efficiently Generated Human iPSCs and a Novel Method of Measuring Contractility Atomic force mechanobiology of pluripotent stem cell-derived cardiomyocytes Generation of highly purified human cardiomyocytes from peripheral blood mononuclear cell-derived induced pluripotent stem cells Mutation-Specific Phenotypes in hiPSC-Derived Cardiomyocytes Carrying Either Myosin-Binding Protein C Or α-Tropomyosin Mutation for Hypertrophic Cardiomyopathy.Pitx2c is reactivated in the failing myocardium and stimulates myf5 expression in cultured cardiomyocytes Identification and purification of human induced pluripotent stem cell-derived atrial-like cardiomyocytes based on sarcolipin expression Generation and characterization of functional cardiomyocytes derived from human T cell-derived induced pluripotent stem cells Genetics and disease of ventricular muscle.Patient Specific Induced Pluripotent Stem Cell-Derived Cardiomyocytes for Drug Development and Screening In Catecholaminergic Polymorphic Ventricular Tachycardia Key Challenges and Opportunities Associated with the Use of In Vitro Models to Detect Human DILI: Integrated Risk Assessment and Mitigation Plans Translation of Human-Induced Pluripotent Stem Cells: From Clinical Trial in a Dish to Precision Medicine Inherited heart disease - what can we expect from the second decade of human iPS cell research?Human induced pluripotent stem cell-derived cardiomyocytes: insights into molecular, cellular, and functional phenotypes Induced pluripotent stem cell potential in medicine, specifically focused on reproductive medicine hiPSC Modeling of Inherited Cardiomyopathies Study familial hypertrophic cardiomyopathy using patient-specific induced pluripotent stem cells Modelling sarcomeric cardiomyopathies in the dish: from human heart samples to iPSC cardiomyocytes Abnormal calcium handling properties underlie familial hypertrophic cardiomyopathy pathology in patient-specific induced pluripotent stem cells Correction of human phospholamban R14del mutation associated with cardiomyopathy using targeted nucleases and combination therapy.CaMKII inhibition rectifies arrhythmic phenotype in a patient-specific model of catecholaminergic polymorphic ventricular tachycardia.Screening drug-induced arrhythmia [corrected] using human induced pluripotent stem cell-derived cardiomyocytes and low-impedance microelectrode arrays.

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P2860

Patient-specific induced pluripotent stem cells as a model for familial dilated cardiomyopathy.

http://www.wikidata.org/entity/Q30539904

description

2012 nî lūn-bûn

@nan

2012 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2012 թվականի ապրիլին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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name

Patient-specific induced pluri ...... milial dilated cardiomyopathy.

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Patient-specific induced pluri ...... milial dilated cardiomyopathy.

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type

label

Patient-specific induced pluri ...... milial dilated cardiomyopathy.

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Patient-specific induced pluri ...... milial dilated cardiomyopathy.

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prefLabel

Patient-specific induced pluri ...... milial dilated cardiomyopathy.

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Patient-specific induced pluri ...... milial dilated cardiomyopathy.

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SCITRANSLMED.3003552

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Science Translational Medicine

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Patient-specific induced pluri ...... amilial dilated cardiomyopathy

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Aleksandra Pavlovic

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Andrew Lee

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Enrique G Navarrete

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Euan A Ashley

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Jianwei Liu

http://www.w3.org/2001/XMLSchema#string

Li Wang

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Masayuki Yazawa

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Michael P Snyder

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Michael T Longaker

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Ricardo E Dolmetsch

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P2860

Restoration of contractile function in isolated cardiomyocytes from failing human hearts by gene transfer of SERCA2a.

Nexilin mutations destabilize cardiac Z-disks and lead to dilated cardiomyopathy

The cardiac mechanical stretch sensor machinery involves a Z disc complex that is defective in a subset of human dilated cardiomyopathy

Induced pluripotent stem cell lines derived from human somatic cells

Induction of pluripotent stem cells from adult human fibroblasts by defined factors

Cardiac troponin T mutation R141W found in dilated cardiomyopathy stabilizes the troponin T-tropomyosin interaction and causes a Ca2+ desensitization

Cardiac excitation-contraction coupling

Hic-5 is required for fetal gene expression and cytoskeletal organization of neonatal cardiac myocytes

Mutations in Troponin that cause HCM, DCM AND RCM: what can we learn about thin filament function?

Clinical and functional characterization of TNNT2 mutations identified in patients with dilated cardiomyopathy

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130ra47

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4

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Manish J. Butte

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Veronica Sanchez-Freire

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2012-04-01T00:00:00Z

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224770278

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22517884

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