Induced pluripotent stem cells (iPSCs) were generated from peripheral blood mononuclear cells (PBMCs) isolated from the whole blood of a 43-year-old male with hypertrophic cardiomyopathy (HCM) who carries the pathogenic variant p.Val698Ala in beta-myosin heavy chain (MYH7). Patient-derived PBMCs were reprogrammed using non-integrative episomal vectors containing reprogramming factors OCT4, SOX2, LIN28, KLF4 and L-MYC. iPSCs were shown to express pluripotent markers, have trilineage differentiation potential, carry the pathogenic MYH7 variant p.Val698Ala, have a normal karyotype and no longer carry the episomal reprogramming vector. This line is useful for studying the link between variants in MYH7 and the pathogenesis of HCM
Modeling a disease “in a dish,” a new research tool to study human heart disease mechanisms, is beco...
AbstractWe generated an induced pluripotent stem cell (iPSC) line from a Bernard–Soulier Syndrome (B...
Arrhythmogenic Cardiomyopathy (ACM) is a genetically based cardiomyopathy associated with ventricula...
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...
Hypertrophic cardiomyopathy is an inherited cardiomyopathy with a prevalence of up to 1 in 200, whic...
Aims Familial hypertrophic cardiomyopathy (HCM) is one the most common heart disorders, with gene mu...
Cardiac laminopathy caused by mutations in the LMNA gene are common and highly penetrant with a poor...
Mutations in the gene that encodes the nuclear envelope proteins lamin A/C (LMNA) are considered to ...
MYBPC3 is the most frequently affected gene in hypertrophic cardiomyopathy (HCM), which is an autoso...
Summary: A novel myosin heavy chain 7 mutation (E848G) identified in a familial cardiomyopathy was s...
Dilated cardiomyopathy (DCM) is a heart muscle disease that causes heart failure and is the leading ...
Peripheral blood mononuclear cells (PBMCs) were derived from a 67-year-old Chinese male. We used non...
Left Ventricular Noncompaction Cardiomyopathy (LVNC) is characterized by abnormal number and promine...
We generated human induced pluripotent stem cells (hiPSCs) from dermal fibroblasts of a woman carrie...
Modeling a disease “in a dish,” a new research tool to study human heart disease mechanisms, is beco...
AbstractWe generated an induced pluripotent stem cell (iPSC) line from a Bernard–Soulier Syndrome (B...
Arrhythmogenic Cardiomyopathy (ACM) is a genetically based cardiomyopathy associated with ventricula...
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...
Hypertrophic cardiomyopathy is an inherited cardiomyopathy with a prevalence of up to 1 in 200, whic...
Aims Familial hypertrophic cardiomyopathy (HCM) is one the most common heart disorders, with gene mu...
Cardiac laminopathy caused by mutations in the LMNA gene are common and highly penetrant with a poor...
Mutations in the gene that encodes the nuclear envelope proteins lamin A/C (LMNA) are considered to ...
MYBPC3 is the most frequently affected gene in hypertrophic cardiomyopathy (HCM), which is an autoso...
Summary: A novel myosin heavy chain 7 mutation (E848G) identified in a familial cardiomyopathy was s...
Dilated cardiomyopathy (DCM) is a heart muscle disease that causes heart failure and is the leading ...
Peripheral blood mononuclear cells (PBMCs) were derived from a 67-year-old Chinese male. We used non...
Left Ventricular Noncompaction Cardiomyopathy (LVNC) is characterized by abnormal number and promine...
We generated human induced pluripotent stem cells (hiPSCs) from dermal fibroblasts of a woman carrie...
Modeling a disease “in a dish,” a new research tool to study human heart disease mechanisms, is beco...
AbstractWe generated an induced pluripotent stem cell (iPSC) line from a Bernard–Soulier Syndrome (B...
Arrhythmogenic Cardiomyopathy (ACM) is a genetically based cardiomyopathy associated with ventricula...