Lack in treatment options for virus-induced inflammatory cardiomyopathy: Can iPS-derived cardiomyocytes close the gap?

Circulation Research

Volumn 115, Issue 6, 2014, Pages 540-541

  Van Linthout, Sophie ^a   Tschöpe, Carsten ^a   Schultheiss, Heinz Peter ^a  

^a CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

Author keywords

cardiac; drug evaluation; myocytes; preclinical

Indexed keywords

ANTIVIRUS AGENT; COXSACKIE VIRUS AND ADENOVIRUS RECEPTOR; KRUPPEL LIKE FACTOR 4; MYC PROTEIN; OCTAMER TRANSCRIPTION FACTOR 4; TRANSCRIPTION FACTOR NANOG; TRANSCRIPTION FACTOR SOX2;

ANTIVIRAL THERAPY; BRUGADA SYNDROME; CARDIAC PATIENT; CARDIOMYOPATHY; CATECHOLAMINERGIC POLYMORPHIC VENTRICULAR TACHYCARDIA; CELL REGENERATION; CONGESTIVE CARDIOMYOPATHY; CYTOPATHOGENIC EFFECT; DRUG EFFICACY; EDITORIAL; HEART MUSCLE BIOPSY; HEART MUSCLE CELL; HUMAN; HUMAN PARVOVIRUS B19; LEOPARD SYNDROME; LONG QT SYNDROME; PHENOTYPE; PLURIPOTENT STEM CELL; PRIORITY JOURNAL; PROTEIN EXPRESSION; VIRUS INDUCED INFLAMMATORY CARDIOMYOPATHY; VIRUS MYOCARDITIS; VIRUS REPLICATION;

DRUG EVALUATION, PRECLINICAL; MYOCYTES, CARDIAC;

ANTIVIRAL AGENTS; ENTEROVIRUS B, HUMAN; ENTEROVIRUS INFECTIONS; HUMANS; MODELS, CARDIOVASCULAR; MYOCARDITIS; MYOCYTES, CARDIAC; PLURIPOTENT STEM CELLS;

EID: 84906997974     PISSN: 00097330     EISSN: 15244571     Source Type: Journal    
DOI: 10.1161/CIRCRESAHA.114.304951     Document Type: Editorial

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