We report the generation of human induced pluripotent stem cells (hiPSCs) from dermal fibroblasts of a female patient carrier of the two compound heterozygous mutations c.568 C>T p.R190W (maternal allele), and c.1781 G>A p.R594Q (paternal allele) on the KCNQ1 gene, causing Jervell and Lange-Nielsen Syndrome (JLNS). To obtain hiPSCs, we used the classical approach of the four retroviruses each encoding for a reprogramming factor OCT4, SOX2, KLF4, cMYC. The obtained hiPSC clones display pluripotent stem cell characteristics, and differentiate into spontaneously beating cardiomyocytes (hiPSC-CMs)
The human iPS cell line, hiPS-SPG76 (FJMUi001-A), derived from skin fibroblasts from a 42-year-old m...
Arrhythmogenic Cardiomyopathy (ACM) is a rare inherited heart muscle disease characterised by progre...
Left Ventricular Noncompaction Cardiomyopathy (LVNC) is characterized by abnormal number and promine...
We report the generation of human induced pluripotent stem cells (hiPSCs) from dermal fibroblasts of...
We generated human induced pluripotent stem cells (hiPSCs) from dermal fibroblasts of a woman carrie...
We generated human induced pluripotent stem cells (hiPSCs) from dermal fibroblasts of a male carrier...
We generated human induced pluripotent stem cells (hiPSCs) from dermal fibroblasts of a 51 years old...
We generated human induced pluripotent stem cells (hiPSCs) from dermal fibroblasts of a 40 years old...
We generated human induced pluripotent stem cells (hiPSCs) from a symptomatic Long QT Syndrome (LQTS...
Four human iPSC cell lines (one Jervell and Lange-Nielsen Syndrome, one Long QT Syndrome-type 1 and ...
In this study we describe the generation and characterization of an human induced pluripotent stem c...
Induced pluripotent stem cells (iPSCs) were generated from peripheral blood mononuclear cells (PBMCs...
AbstractIn this work we describe for the first time the generation and characterization of human ind...
Hypomyelinating Leukodystrophy 22 (HLD22) is caused by a stoploss mutation in CLDN11. To study the m...
Induced pluripotent stem cells (iPSCs) were generated from peripheral blood mononuclear cells (PBMCs...
The human iPS cell line, hiPS-SPG76 (FJMUi001-A), derived from skin fibroblasts from a 42-year-old m...
Arrhythmogenic Cardiomyopathy (ACM) is a rare inherited heart muscle disease characterised by progre...
Left Ventricular Noncompaction Cardiomyopathy (LVNC) is characterized by abnormal number and promine...
We report the generation of human induced pluripotent stem cells (hiPSCs) from dermal fibroblasts of...
We generated human induced pluripotent stem cells (hiPSCs) from dermal fibroblasts of a woman carrie...
We generated human induced pluripotent stem cells (hiPSCs) from dermal fibroblasts of a male carrier...
We generated human induced pluripotent stem cells (hiPSCs) from dermal fibroblasts of a 51 years old...
We generated human induced pluripotent stem cells (hiPSCs) from dermal fibroblasts of a 40 years old...
We generated human induced pluripotent stem cells (hiPSCs) from a symptomatic Long QT Syndrome (LQTS...
Four human iPSC cell lines (one Jervell and Lange-Nielsen Syndrome, one Long QT Syndrome-type 1 and ...
In this study we describe the generation and characterization of an human induced pluripotent stem c...
Induced pluripotent stem cells (iPSCs) were generated from peripheral blood mononuclear cells (PBMCs...
AbstractIn this work we describe for the first time the generation and characterization of human ind...
Hypomyelinating Leukodystrophy 22 (HLD22) is caused by a stoploss mutation in CLDN11. To study the m...
Induced pluripotent stem cells (iPSCs) were generated from peripheral blood mononuclear cells (PBMCs...
The human iPS cell line, hiPS-SPG76 (FJMUi001-A), derived from skin fibroblasts from a 42-year-old m...
Arrhythmogenic Cardiomyopathy (ACM) is a rare inherited heart muscle disease characterised by progre...
Left Ventricular Noncompaction Cardiomyopathy (LVNC) is characterized by abnormal number and promine...