Using a Sendai Virus based vector delivering Yamanaka Factors, we generated induced Pluripotent Stem Cells (iPSCs) from peripheral blood mononuclear cells of a patient affected by Ataxia Telangiectasia (AT), caused by a novel homozygous deletion in ATM, spanning exons 5–7. Three clones were fully characterized for pluripotency and capability to differentiate. These clones preserved the causative mutation of parental cells and genomic stability over time (>100 passages). Furthermore, in AT derived iPSCs we confirmed the impaired DNA damage response after ionizing radiation. All these data underline potential usefulness of our clones as in vitro AT disease model
Ataxia Telangiectasia (AT) and Aicardi Goutières syndrome (AGS) are inherited disorders of immunity ...
The β-amyloid precursor protein (APP) is a crucial pathogenic gene linked to Alzheimer's disease (AD...
Induced pluripotent stem cells (iPSCs) were generated from dermal fibroblasts from a 60-year-old cer...
Peripheral blood was obtained from a 12-year old male carrying bialleleic inactivating mutations at ...
AbstractPeripheral blood was obtained from a 12-year old male carrying bialleleic inactivating mutat...
Pluripotent stem cells can differentiate into every cell type of the human body. Reprogramming of so...
Ataxia-telangiectasia (A-T) is a complex disease arising from mutations in the ATM gene (Ataxia-Tela...
Ataxia Telangiectasia is a rare autosomal recessive disorder caused by a mutated ATM gene. The most ...
Biallelic mutations in ATM result in the neurodegenerative syndrome Ataxia-Telangiectasia, while ATM...
Ataxia-telangiectasia (A-T) is a rare hereditary, early onset neurodegenerative disorder caused by i...
AbstractBiallelic mutations in ATM result in the neurodegenerative syndrome Ataxia-Telangiectasia, w...
Ataxia telangiectasia (AT) and Aicardi–Goutières syndrome (AGS) are inherited disorders of immunity ...
textabstractSpinocerebellar ataxia type 1 (SCA1) is a hereditary neurodegenerative disease caused by...
Hereditary deficiencies in DNA damage signaling are invariably associated with cancer predisposition...
IPSC line RCPCMi004-8 was generated from skin fibroblasts collected from a male patient with spinoce...
Ataxia Telangiectasia (AT) and Aicardi Goutières syndrome (AGS) are inherited disorders of immunity ...
The β-amyloid precursor protein (APP) is a crucial pathogenic gene linked to Alzheimer's disease (AD...
Induced pluripotent stem cells (iPSCs) were generated from dermal fibroblasts from a 60-year-old cer...
Peripheral blood was obtained from a 12-year old male carrying bialleleic inactivating mutations at ...
AbstractPeripheral blood was obtained from a 12-year old male carrying bialleleic inactivating mutat...
Pluripotent stem cells can differentiate into every cell type of the human body. Reprogramming of so...
Ataxia-telangiectasia (A-T) is a complex disease arising from mutations in the ATM gene (Ataxia-Tela...
Ataxia Telangiectasia is a rare autosomal recessive disorder caused by a mutated ATM gene. The most ...
Biallelic mutations in ATM result in the neurodegenerative syndrome Ataxia-Telangiectasia, while ATM...
Ataxia-telangiectasia (A-T) is a rare hereditary, early onset neurodegenerative disorder caused by i...
AbstractBiallelic mutations in ATM result in the neurodegenerative syndrome Ataxia-Telangiectasia, w...
Ataxia telangiectasia (AT) and Aicardi–Goutières syndrome (AGS) are inherited disorders of immunity ...
textabstractSpinocerebellar ataxia type 1 (SCA1) is a hereditary neurodegenerative disease caused by...
Hereditary deficiencies in DNA damage signaling are invariably associated with cancer predisposition...
IPSC line RCPCMi004-8 was generated from skin fibroblasts collected from a male patient with spinoce...
Ataxia Telangiectasia (AT) and Aicardi Goutières syndrome (AGS) are inherited disorders of immunity ...
The β-amyloid precursor protein (APP) is a crucial pathogenic gene linked to Alzheimer's disease (AD...
Induced pluripotent stem cells (iPSCs) were generated from dermal fibroblasts from a 60-year-old cer...