Cargando…

Erratum to “Optical Recording of Action Potentials in Human Induced Pluripotent Stem Cell-Derived Cardiac Single Cells and Monolayers Generated from Long QT Syndrome Type 1 Patients”

Detalles Bibliográficos
Autores principales:	Takaki, Tadashi, Inagaki, Azusa, Chonabayashi, Kazuhisa, Inoue, Keiji, Miki, Kenji, Ohno, Seiko, Makiyama, Takeru, Horie, Minoru, Yoshida, Yoshinori
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Hindawi 2020
Materias:	Erratum
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7204173/ https://www.ncbi.nlm.nih.gov/pubmed/32399053 http://dx.doi.org/10.1155/2020/8765895

Ejemplares similares

Optical Recording of Action Potentials in Human Induced Pluripotent Stem Cell-Derived Cardiac Single Cells and Monolayers Generated from Long QT Syndrome Type 1 Patients
por: Takaki, Tadashi, et al.
Publicado: (2019)

Propranolol Attenuates Late Sodium Current in a Long QT Syndrome Type 3-Human Induced Pluripotent Stem Cell Model
por: Hirose, Sayako, et al.
Publicado: (2020)

Cardiac conduction defects and Brugada syndrome: A family with overlap syndrome carrying a nonsense SCN5A mutation()
por: Aoki, Hisaaki, et al.
Publicado: (2017)

Phenotype-Based High-Throughput Classification of Long QT Syndrome Subtypes Using Human Induced Pluripotent Stem Cells
por: Yoshinaga, Daisuke, et al.
Publicado: (2019)

Non-missense variants of KCNH2 show better outcomes in type 2 long QT syndrome
por: Aizawa, Takanori, et al.
Publicado: (2023)

Computerized misinterpretation of QT interval in 12‐lead electrocardiogram and its clinical consequences: A case of recurrent syncope
por: Hasegawa, Kanae, et al.
Publicado: (2023)

Pueraria mirifica, an estrogenic tropical herb, unveiled the severity of Type 1 LQTS caused by KCNQ1‐T587M
por: Kashiwa, Asami, et al.
Publicado: (2021)

Three cases of catecholaminergic polymorphic ventricular tachycardia with prolonged QT intervals including two cases of compound mutations
por: Saito, Aki, et al.
Publicado: (2018)

Patient-Specific Human Induced Pluripotent Stem Cell Model Assessed with Electrical Pacing Validates S107 as a Potential Therapeutic Agent for Catecholaminergic Polymorphic Ventricular Tachycardia
por: Sasaki, Kenichi, et al.
Publicado: (2016)

Genetic variants of alcohol‐metabolizing enzymes in Brugada syndrome: Insights into syncope after drinking alcohol
por: Wu, Qi, et al.
Publicado: (2019)

Targeted deep sequencing analyses of long QT syndrome in a Japanese population
por: Nagata, Yuki, et al.
Publicado: (2022)

Successful Management of a Young Athlete with Type 2 Long QT Syndrome by Genotype-specific Risk Stratification and Bridging Therapy with a Wearable Cardioverter Defibrillator
por: Kojima, Katsumi, et al.
Publicado: (2022)

Azacitidine is a potential therapeutic drug for pyridoxine-refractory female X-linked sideroblastic anemia
por: Morimoto, Yuki, et al.
Publicado: (2022)

Increased Ca(V)1.2 late current by a CACNA1C p.R412M variant causes an atypical Timothy syndrome without syndactyly
por: Ozawa, Junichi, et al.
Publicado: (2022)

Modeling Hippocampal Neurogenesis Using Human Pluripotent Stem Cells
por: Yu, Diana Xuan, et al.
Publicado: (2014)

Multiple sclerosis: getting personal with induced pluripotent stem cells
por: Di Ruscio, A, et al.
Publicado: (2016)

Two-step protocol for regeneration of immunocompetent T cells from mouse pluripotent stem cells
Publicado: (2022)

Exercise worsening of electromechanical disturbances: A predictor of arrhythmia in long QT syndrome
por: Charisopoulou, Dafni, et al.
Publicado: (2019)

Cell-Cycle Control of Developmentally Regulated Transcription Factors Accounts for Heterogeneity in Human Pluripotent Cells
por: Singh, Amar M., et al.
Publicado: (2014)

Erratum: “Genome-wide Association Study of Susceptibility to Particulate Matter-Associated QT Prolongation”
por: Gondalia, Rahul, et al.
Publicado: (2017)

Erratum to: Induced Pluripotent Stem Cell Lines Derived from Equine Fibroblasts
por: Nagy, Kristina, et al.
Publicado: (2011)

Gender Differences in the Inheritance Mode of RYR2 Mutations in Catecholaminergic Polymorphic Ventricular Tachycardia Patients
por: Ohno, Seiko, et al.
Publicado: (2015)

Correction: Gender Differences in the Inheritance Mode of RYR2 Mutations in Catecholaminergic Polymorphic Ventricular Tachycardia Patients
por: Ohno, Seiko, et al.
Publicado: (2021)

Erratum to “A Model for Spheroid versus Monolayer Response of SK-N-SH Neuroblastoma Cells to Treatment with 15-Deoxy-PGJ(2)”
por: Wallace, Dorothy I., et al.
Publicado: (2017)

Molecular pathogenesis of long QT syndrome type 1
por: Wu, Jie, et al.
Publicado: (2016)

Enhanced engraftment, proliferation, and therapeutic potential in heart using optimized human iPSC-derived cardiomyocytes
por: Funakoshi, Shunsuke, et al.
Publicado: (2016)

ERRATUM: Establishment of a primed pluripotent epiblast stem cell in FGF4-based conditions
por: Joo, Jin Young, et al.
Publicado: (2015)

Erratum: Laminin E8 fragments support efficient adhesion and expansion of dissociated human pluripotent stem cells
por: Miyazaki, Takamichi, et al.
Publicado: (2013)

Efficient Differentiation of Human Pluripotent Stem Cells to Endothelial Progenitors via Small-Molecule Activation of WNT Signaling
por: Lian, Xiaojun, et al.
Publicado: (2015)

Cell Adhesion Molecule 1 Contributes to Cell Survival in Crowded Epithelial Monolayers
por: Hagiyama, Man, et al.
Publicado: (2020)

A hERG mutation E1039X produced a synergistic lesion on I(Ks) together with KCNQ1-R174C mutation in a LQTS family with three compound mutations
por: Wu, Jie, et al.
Publicado: (2018)

Unique genetic background and outcome of non‐Caucasian Japanese probands with arrhythmogenic right ventricular dysplasia/cardiomyopathy
por: Wada, Yuko, et al.
Publicado: (2017)

Bradycardia Is a Specific Phenotype of Catecholaminergic Polymorphic Ventricular Tachycardia Induced by RYR2 Mutations
por: Miyata, Kazuaki, et al.
Publicado: (2018)

Erratum: YAP determines the cell fate of injured mouse hepatocytes in vivo
por: Miyamura, Norio, et al.
Publicado: (2017)

A case of long QT syndrome type 2 that developed torsades de pointes two days after the initiation of oral β-blocker therapy
por: Yoneda, Fumiya, et al.
Publicado: (2022)

Erratum to: Closed-form analytical expressions for the potential fields generated by triangular monolayers with linearly distributed source strength
por: van Oosterom, Adriaan
Publicado: (2015)

Erratum to: Novel trigenic CACNA1C/DES/MYPN mutations in a family of hypertrophic cardiomyopathy with early repolarization and short QT syndrome
por: Chen, Yanhong, et al.
Publicado: (2017)

Naïve Induced Pluripotent Stem Cells Generated From β-Thalassemia Fibroblasts Allow Efficient Gene Correction With CRISPR/Cas9
por: Yang, Yuanyuan, et al.
Publicado: (2016)

Erratum: Induced pluripotent stem cell-derived neuronal cells from a sporadic Alzheimer's disease donor as a model for investigating AD-associated gene regulatory networks
por: Hossini, Amir M, et al.
Publicado: (2015)

Base Editing of Human Pluripotent Stem Cells for Modeling Long QT Syndrome
por: Wu, Fujian, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_0q9g7lgfh8n4gln0iinv28a29t