AbstractInduced pluripotent stem cells (iPSCs) were generated from skin fibroblasts isolated from a 58-year old male with a L150P mutation in the presenilin 1 (PSEN-1) gene, which is responsible for the majority of familial cases of Alzheimer's disease (AD). The iPSCs were established by co-electroporation with episomal plasmids containing hOCT4, hSOX2, hL-MYC, hKLF4, hNANOG, hLIN28, and short hairpin RNA against TP53. The iPSCs contained the specific heterozygous mutation c.449C>T, had normal karyotype, expressed the expected pluripotency genes and displayed in vitro differentiation potential to the three germ layers. The iPSCs may be useful for studying familial AD pathology in vitro
A double mutation (KM670/671NL) in amyloid precursor protein gene (APP) is causative for familial Al...
AbstractPeripheral blood mononuclear cells (PBMCs) were collected from a clinically characterised 75...
Skin fibroblasts were obtained from a 48-year-old presymptomatic woman carrying a A79V mutation in t...
AbstractSkin fibroblasts were obtained from a 46-year-old symptomatic man carrying a M146I mutation ...
AbstractMutations in presenilin 1 (PSEN1) lead to the most aggressive form of familial Alzheimer's d...
AbstractPeripheral blood mononuclear cells (PBMCs) were collected from a clinically characterised, e...
AbstractInduced pluripotent stem cells (iPSCs) were generated from skin fibroblasts isolated from a ...
AbstractPeripheral blood mononuclear cells (PBMCs) were collected from a clinically characterised 57...
AbstractMutations in the presenilin 1 (PSEN1) gene lead to the most aggressive form of familial Alzh...
AbstractSkin fibroblasts were obtained from a 57-year-old woman diagnosed with frontotemporal dement...
AbstractSkin fibroblasts were obtained from a 28-year-old pre-symptomatic woman carrying a R406W mut...
The induced pluripotent stem cell (iPSC) lines UOWi002-A and UOWi003-A were reprogrammed from dermal...
AbstractSkin fibroblasts were obtained from a 59-year-old woman diagnosed with frontotemporal dement...
AbstractPeripheral blood mononuclear cells (PBMCs) were collected from a clinically characterised 84...
A double mutation (KM670/671NL) in amyloid precursor protein gene (APP) is causative for familial Al...
A double mutation (KM670/671NL) in amyloid precursor protein gene (APP) is causative for familial Al...
AbstractPeripheral blood mononuclear cells (PBMCs) were collected from a clinically characterised 75...
Skin fibroblasts were obtained from a 48-year-old presymptomatic woman carrying a A79V mutation in t...
AbstractSkin fibroblasts were obtained from a 46-year-old symptomatic man carrying a M146I mutation ...
AbstractMutations in presenilin 1 (PSEN1) lead to the most aggressive form of familial Alzheimer's d...
AbstractPeripheral blood mononuclear cells (PBMCs) were collected from a clinically characterised, e...
AbstractInduced pluripotent stem cells (iPSCs) were generated from skin fibroblasts isolated from a ...
AbstractPeripheral blood mononuclear cells (PBMCs) were collected from a clinically characterised 57...
AbstractMutations in the presenilin 1 (PSEN1) gene lead to the most aggressive form of familial Alzh...
AbstractSkin fibroblasts were obtained from a 57-year-old woman diagnosed with frontotemporal dement...
AbstractSkin fibroblasts were obtained from a 28-year-old pre-symptomatic woman carrying a R406W mut...
The induced pluripotent stem cell (iPSC) lines UOWi002-A and UOWi003-A were reprogrammed from dermal...
AbstractSkin fibroblasts were obtained from a 59-year-old woman diagnosed with frontotemporal dement...
AbstractPeripheral blood mononuclear cells (PBMCs) were collected from a clinically characterised 84...
A double mutation (KM670/671NL) in amyloid precursor protein gene (APP) is causative for familial Al...
A double mutation (KM670/671NL) in amyloid precursor protein gene (APP) is causative for familial Al...
AbstractPeripheral blood mononuclear cells (PBMCs) were collected from a clinically characterised 75...
Skin fibroblasts were obtained from a 48-year-old presymptomatic woman carrying a A79V mutation in t...