2020 The Authors Dermal fibroblasts were donated by a 43 year old male patient with clinically diagnosed familial amyotrophic lateral sclerosis (ALS), carrying the SOD1E101G mutation. The induced pluripotent stem cell (iPSC) line UOWi007-A was generated using repeated mRNA transfections for pluripotency transcription factors Oct4, Klf4, Sox2, c-Myc, Lin28 and Nanog. The iPSCs carried the SOD1E101G genotype and had a normal karyotype, expressed expected pluripotency markers and were capable of in vitro differentiation into endodermal, mesodermal and ectodermal lineages. This iPSC line may be useful for investigating familial ALS resulting from a SOD1 E101G mutation
AbstractInduced pluripotent stem cells (iPSCs) were generated from skin fibroblasts isolated from a ...
The induced pluripotent stem cell (iPSC) lines UOWi002-A and UOWi003-A were reprogrammed from dermal...
AbstractHuman lymphoblast cells from a male patient diagnosed with Alzheimer's disease (AD) expressi...
Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease affecting upper and l...
Amyotrophic lateral sclerosis (ALS) is an incurable neurodegenerative condition with phenotypic and ...
Amyotrophic lateral sclerosis (ALS) is a complex neurodegenerative disease with cellular and molecul...
Abstract Amyotrophic lateral sclerosis (ALS) is a complex neurodegenerative disease with cellular an...
Amyotrophic lateral sclerosis is a progressive disease characterized by the loss of upper and lower ...
SummaryAmyotrophic lateral sclerosis (ALS) is a late-onset motor neuron disorder. Although its neuro...
Amyotrophic lateral sclerosis is a progressive disease characterized by the loss of upper and lower ...
Fibroblasts isolated from an Amyotrophic Lateral Sclerosis (ALS)-patient carrying a mutation in Matr...
Human neurodegenerative disorders are among the most difficult to study. In particular, the inabilit...
The induced pluripotent stem cell (iPSC) lines UOWi002-A and UOWi003-A were reprogrammed from dermal...
AbstractMutations in presenilin 1 (PSEN1) lead to the most aggressive form of familial Alzheimer's d...
Amyotrophic Lateral Sclerosis (ALS) is a fatal disease affecting both upper and lower motoneurons. T...
AbstractInduced pluripotent stem cells (iPSCs) were generated from skin fibroblasts isolated from a ...
The induced pluripotent stem cell (iPSC) lines UOWi002-A and UOWi003-A were reprogrammed from dermal...
AbstractHuman lymphoblast cells from a male patient diagnosed with Alzheimer's disease (AD) expressi...
Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease affecting upper and l...
Amyotrophic lateral sclerosis (ALS) is an incurable neurodegenerative condition with phenotypic and ...
Amyotrophic lateral sclerosis (ALS) is a complex neurodegenerative disease with cellular and molecul...
Abstract Amyotrophic lateral sclerosis (ALS) is a complex neurodegenerative disease with cellular an...
Amyotrophic lateral sclerosis is a progressive disease characterized by the loss of upper and lower ...
SummaryAmyotrophic lateral sclerosis (ALS) is a late-onset motor neuron disorder. Although its neuro...
Amyotrophic lateral sclerosis is a progressive disease characterized by the loss of upper and lower ...
Fibroblasts isolated from an Amyotrophic Lateral Sclerosis (ALS)-patient carrying a mutation in Matr...
Human neurodegenerative disorders are among the most difficult to study. In particular, the inabilit...
The induced pluripotent stem cell (iPSC) lines UOWi002-A and UOWi003-A were reprogrammed from dermal...
AbstractMutations in presenilin 1 (PSEN1) lead to the most aggressive form of familial Alzheimer's d...
Amyotrophic Lateral Sclerosis (ALS) is a fatal disease affecting both upper and lower motoneurons. T...
AbstractInduced pluripotent stem cells (iPSCs) were generated from skin fibroblasts isolated from a ...
The induced pluripotent stem cell (iPSC) lines UOWi002-A and UOWi003-A were reprogrammed from dermal...
AbstractHuman lymphoblast cells from a male patient diagnosed with Alzheimer's disease (AD) expressi...