TTN mutations are the common genetic cause for various types of cardiomyopathies (e.g., dilated cardiomyopathy, hypertrophic cardiomyopathy, restrictive cardiomyopathy, and arrhythmogenic right ventricular cardiomyopathy) and skeletal myopathies. Here, we generated three TTN knock-out human induced pluripotent stem cell (iPSC) lines using CRISPR/Cas9 system. These cell lines, which exhibit normal karyotype, typical morphology and pluripotency, could provide useful platform for investigating the role of TTN in associated disorders.ope
Induced pluripotent stem cells (iPSCs) originate from the reprogramming of adult somatic cells using...
Hypertrophic cardiomyopathy (HCM) is a prevalent genetic cardiovascular disease affecting 1:500 indi...
GNB5 loss-of-function pathogenic variants cause IDDCA, a rare autosomal recessive human genetic dise...
Dilated cardiomyopathy (DCM) is a heart muscle disease that causes heart failure and is the leading ...
E192K missense mutation of TPM1 has been found in different types of cardiomyopathies (e.g., hypertr...
Rationale: Targeted genetic engineering using programmable nucleases such as transcription activator...
Arrhythmogenic Cardiomyopathy (ACM) is a rare genetic cardiac disease predominantly associated with ...
We derived an integration-free induced pluripotent stem cell (iPSC) line from the peripheral blood m...
Dilated cardiomyopathy (DCM) is one of the leading causes of heart transplantation. The clinical fea...
Cardiac laminopathy caused by mutations in the LMNA gene are common and highly penetrant with a poor...
MYBPC3 is the most frequently affected gene in hypertrophic cardiomyopathy (HCM), which is an autoso...
Patient-derived induced pluripotent stem cells (iPSC) are a valuable approach to model cardiovascula...
Left Ventricular Noncompaction Cardiomyopathy (LVNC) is characterized by excessive trabeculation of ...
As the most common cause of heart failure, dilated cardiomyopathy (DCM) is characterized by dilated ...
Induced pluripotent stem cells (iPSCs) originate from the reprogramming of adult somatic cells using...
Induced pluripotent stem cells (iPSCs) originate from the reprogramming of adult somatic cells using...
Hypertrophic cardiomyopathy (HCM) is a prevalent genetic cardiovascular disease affecting 1:500 indi...
GNB5 loss-of-function pathogenic variants cause IDDCA, a rare autosomal recessive human genetic dise...
Dilated cardiomyopathy (DCM) is a heart muscle disease that causes heart failure and is the leading ...
E192K missense mutation of TPM1 has been found in different types of cardiomyopathies (e.g., hypertr...
Rationale: Targeted genetic engineering using programmable nucleases such as transcription activator...
Arrhythmogenic Cardiomyopathy (ACM) is a rare genetic cardiac disease predominantly associated with ...
We derived an integration-free induced pluripotent stem cell (iPSC) line from the peripheral blood m...
Dilated cardiomyopathy (DCM) is one of the leading causes of heart transplantation. The clinical fea...
Cardiac laminopathy caused by mutations in the LMNA gene are common and highly penetrant with a poor...
MYBPC3 is the most frequently affected gene in hypertrophic cardiomyopathy (HCM), which is an autoso...
Patient-derived induced pluripotent stem cells (iPSC) are a valuable approach to model cardiovascula...
Left Ventricular Noncompaction Cardiomyopathy (LVNC) is characterized by excessive trabeculation of ...
As the most common cause of heart failure, dilated cardiomyopathy (DCM) is characterized by dilated ...
Induced pluripotent stem cells (iPSCs) originate from the reprogramming of adult somatic cells using...
Induced pluripotent stem cells (iPSCs) originate from the reprogramming of adult somatic cells using...
Hypertrophic cardiomyopathy (HCM) is a prevalent genetic cardiovascular disease affecting 1:500 indi...
GNB5 loss-of-function pathogenic variants cause IDDCA, a rare autosomal recessive human genetic dise...