Induced pluripotent stem cells (iPSCs) were generated from peripheral blood mononuclear cells (PBMCs) obtained from a 62-year-old female with familial hypertrophic cardiomyopathy (HCM). PBMCs were reprogrammed to a pluripotent state following transfection with non-integrative episomal vectors carrying reprogramming factors OCT4, SOX2, LIN28, KLF4 and L-MYC. iPSCs were shown to express pluripotency markers, possess trilineage differentiation potential, carry rare variants identified in DNA isolated directly from the patient's whole blood, have a normal karyotype and no longer carry episomal vectors for reprogramming. This line is a useful resource for identifying unknown genetic causes of HCM
One of the recent breakthroughs in stem cell research has been the reprogramming of human somatic ce...
AbstractIn this work we describe for the first time the generation and characterization of human ind...
In the last few decades, many pathogenic or likely pathogenic genetic mutations in over hundred diff...
Induced pluripotent stem cells (iPSCs) were generated from peripheral blood mononuclear cells (PBMCs...
Hypertrophic cardiomyopathy (HCM) is an inherited cardiomyopathy characterized by left ventricular h...
Aims Familial hypertrophic cardiomyopathy (HCM) is one the most common heart disorders, with gene mu...
Hypertrophic cardiomyopathy is an inherited cardiomyopathy with a prevalence of up to 1 in 200, whic...
Dilated cardiomyopathy (DCM) is one of the most common cardiac defects that contribute to heart fai...
Peripheral blood mononuclear cells (PBMCs) were derived from a 67-year-old Chinese male. We used non...
Cardiac laminopathy caused by mutations in the LMNA gene are common and highly penetrant with a poor...
Modeling a disease “in a dish,” a new research tool to study human heart disease mechanisms, is beco...
We generated human induced pluripotent stem cells (hiPSCs) from dermal fibroblasts of a woman carrie...
Peripheral blood was collected from a 39-year-old unaffected female carrier of an X-linked recessive...
Abstract: We describe the generation and characterization of 5 human induced pluripotent stem cell (...
We generated human induced pluripotent stem cells (hiPSCs) from dermal fibroblasts of a woman carrie...
One of the recent breakthroughs in stem cell research has been the reprogramming of human somatic ce...
AbstractIn this work we describe for the first time the generation and characterization of human ind...
In the last few decades, many pathogenic or likely pathogenic genetic mutations in over hundred diff...
Induced pluripotent stem cells (iPSCs) were generated from peripheral blood mononuclear cells (PBMCs...
Hypertrophic cardiomyopathy (HCM) is an inherited cardiomyopathy characterized by left ventricular h...
Aims Familial hypertrophic cardiomyopathy (HCM) is one the most common heart disorders, with gene mu...
Hypertrophic cardiomyopathy is an inherited cardiomyopathy with a prevalence of up to 1 in 200, whic...
Dilated cardiomyopathy (DCM) is one of the most common cardiac defects that contribute to heart fai...
Peripheral blood mononuclear cells (PBMCs) were derived from a 67-year-old Chinese male. We used non...
Cardiac laminopathy caused by mutations in the LMNA gene are common and highly penetrant with a poor...
Modeling a disease “in a dish,” a new research tool to study human heart disease mechanisms, is beco...
We generated human induced pluripotent stem cells (hiPSCs) from dermal fibroblasts of a woman carrie...
Peripheral blood was collected from a 39-year-old unaffected female carrier of an X-linked recessive...
Abstract: We describe the generation and characterization of 5 human induced pluripotent stem cell (...
We generated human induced pluripotent stem cells (hiPSCs) from dermal fibroblasts of a woman carrie...
One of the recent breakthroughs in stem cell research has been the reprogramming of human somatic ce...
AbstractIn this work we describe for the first time the generation and characterization of human ind...
In the last few decades, many pathogenic or likely pathogenic genetic mutations in over hundred diff...