Add to ORKGAllele-specific RNA interference rescues the long-QT syndrome phenotype in human-induced pluripotency stem cell cardiomyocytes. European Heart Journal. ISSN 0195-668X Access from the University of Nottingham repository
Calmodulin (CaM) is a small protein, encoded by three genes (CALM1-3), exerting multiple Ca2+-depend...
Abstract Human induced pluripotent stem cells (hiPSC) have enabled a major step forwar...
Cardiovascular genetic diseases are a major cause of morbidity and the leading cause of sudden cardi...
Aims Long-QT syndromes (LQTS) are mostly autosomal-dominant congenital disorders associated with a 1...
Aims Long-QT syndromes (LQTS) are mostly autosomal-dominant congenital disorders associated with a 1...
Aims Long-QT syndromes (LQTS) are mostly autosomal-dominant congenital disorders associated with a 1...
Aims Long-QT syndromes (LQTS) are mostly autosomal-dominant congenital disorders associated with a 1...
Aims Long-QT syndromes (LQTS) are mostly autosomal-dominant congenital disorders associated with a 1...
Aims Long-QT syndromes (LQTS) are mostly autosomal-dominant congenital disorders associated with a 1...
Human induced pluripotent stem cells (hiPSCs) have been widely used in cardiac disease modelling, dr...
Long QT syndrome (LQTS) is a potentially severe arrhythmogenic disorder, associated with a prolonged...
Long QT syndrome (LQTS) is a potentially severe arrhythmogenic disorder, associated with a prolonged...
Calmodulin (CaM) is a small protein, encoded by three genes (CALM1-3), exerting multiple Ca2+-depend...
Long-QT syndrome type 1 (LQT1) is caused by mutations in KCNQ1. Patients heterozygous for such a mut...
Human induced pluripotent stem cells (hiPSC) have enabled a major step forward in pathophysiologic s...
Calmodulin (CaM) is a small protein, encoded by three genes (CALM1-3), exerting multiple Ca2+-depend...
Abstract Human induced pluripotent stem cells (hiPSC) have enabled a major step forwar...
Cardiovascular genetic diseases are a major cause of morbidity and the leading cause of sudden cardi...
Aims Long-QT syndromes (LQTS) are mostly autosomal-dominant congenital disorders associated with a 1...
Aims Long-QT syndromes (LQTS) are mostly autosomal-dominant congenital disorders associated with a 1...
Aims Long-QT syndromes (LQTS) are mostly autosomal-dominant congenital disorders associated with a 1...
Aims Long-QT syndromes (LQTS) are mostly autosomal-dominant congenital disorders associated with a 1...
Aims Long-QT syndromes (LQTS) are mostly autosomal-dominant congenital disorders associated with a 1...
Aims Long-QT syndromes (LQTS) are mostly autosomal-dominant congenital disorders associated with a 1...
Human induced pluripotent stem cells (hiPSCs) have been widely used in cardiac disease modelling, dr...
Long QT syndrome (LQTS) is a potentially severe arrhythmogenic disorder, associated with a prolonged...
Long QT syndrome (LQTS) is a potentially severe arrhythmogenic disorder, associated with a prolonged...
Calmodulin (CaM) is a small protein, encoded by three genes (CALM1-3), exerting multiple Ca2+-depend...
Long-QT syndrome type 1 (LQT1) is caused by mutations in KCNQ1. Patients heterozygous for such a mut...
Human induced pluripotent stem cells (hiPSC) have enabled a major step forward in pathophysiologic s...
Calmodulin (CaM) is a small protein, encoded by three genes (CALM1-3), exerting multiple Ca2+-depend...
Abstract Human induced pluripotent stem cells (hiPSC) have enabled a major step forwar...
Cardiovascular genetic diseases are a major cause of morbidity and the leading cause of sudden cardi...