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Generation of the human induced pluripotent stem cell (hiPSC) line PSMi007-A from a Long QT Syndrome type 1 patient carrier of two common variants in the NOS1AP gene.
Mura, Manuela; Pisano, Federica; Stefanello, Manuela; Ginevrino, Monia; Boni, Marina; Calabrò, Federica; Crotti, Lia; Valente, Enza Maria; Schwartz, Peter J; Brink, Paul A; Gnecchi, Massimiliano.
Affiliation
  • Mura M; Coronary Care Unit and Laboratory of Experimental Cardiology for Cell and Molecular Therapy, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Pisano F; Coronary Care Unit and Laboratory of Experimental Cardiology for Cell and Molecular Therapy, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.; Department of Molecular Medicine, Unit of Cardiology, Università degli studi di Pavia, Pavia, Italy.
  • Stefanello M; Coronary Care Unit and Laboratory of Experimental Cardiology for Cell and Molecular Therapy, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Ginevrino M; Department of Molecular Medicine, Unit of Genetics, Università degli studi di Pavia, Pavia, Italy.; Neurogenetics Unit, Fondazione IRCCS Santa Lucia, Rome, Italy.
  • Boni M; Laboratory of Oncohaematological Cytogenetic and Molecular Diagnostics, Division of Haematology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Calabrò F; Coronary Care Unit and Laboratory of Experimental Cardiology for Cell and Molecular Therapy, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Crotti L; Istituto Auxologico Italiano, IRCCS, Center for Cardiac Arrhythmias of Genetic Origin and Laboratory of Cardiovascular Genetics, Milan, Italy.; Istituto Auxologico Italiano, IRCCS, Department of Cardiovascular, Neural and Metabolic Sciences, San Luca Hospital, Milan, Italy.; Department of Medicine a
  • Valente EM; Department of Molecular Medicine, Unit of Genetics, Università degli studi di Pavia, Pavia, Italy.; Neurogenetics Unit, Fondazione IRCCS Santa Lucia, Rome, Italy.
  • Schwartz PJ; Istituto Auxologico Italiano, IRCCS, Center for Cardiac Arrhythmias of Genetic Origin and Laboratory of Cardiovascular Genetics, Milan, Italy.
  • Brink PA; Department of Internal Medicine, University of Stellenbosch, Tygerberg, South Africa.
  • Gnecchi M; Coronary Care Unit and Laboratory of Experimental Cardiology for Cell and Molecular Therapy, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.; Department of Molecular Medicine, Unit of Cardiology, Università degli studi di Pavia, Pavia, Italy.; Department of Medicine, University of Cape Town,
Stem Cell Res ; 36: 101416, 2019 04.
Article de En | MEDLINE | ID: mdl-30878014

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Lignée cellulaire / Syndrome de Romano-Ward / Protéines adaptatrices de la transduction du signal / Canal potassique KCNQ1 / Cellules souches pluripotentes induites Limites: Female / Humans / Middle aged Langue: En Journal: Stem Cell Res Année: 2019 Type de document: Article Pays d'affiliation: Italie Pays de publication: Royaume-Uni

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Lignée cellulaire / Syndrome de Romano-Ward / Protéines adaptatrices de la transduction du signal / Canal potassique KCNQ1 / Cellules souches pluripotentes induites Limites: Female / Humans / Middle aged Langue: En Journal: Stem Cell Res Année: 2019 Type de document: Article Pays d'affiliation: Italie Pays de publication: Royaume-Uni