© 2020 Fibroblasts from an amyotrophic lateral sclerosis patient with simultaneous mutations in the MATR3 gene and KIF5A gene were isolated and reprogrammed into induced pluripotent stem cells via a non-integrating Sendai viral vector. The generated iPSC clones demonstrated normal karyotype, expression of pluripotency markers, and the capacity to differentiate into three germ layers. The unique presence of two simultaneous mutations in ALS-associated genes represent a novel tool for the study of ALS disease mechanisms
Amyotrophic lateral sclerosis (ALS) is a late-onset motor neuron disorder. Although its neuropatholo...
Amyotrophic lateral sclerosis (ALS) is an adult-onset neurodegenerative disease affecting primarily ...
Amyotrophic lateral sclerosis (ALS) is a fatal and progressive neurodegenerative disease characteriz...
Fibroblasts isolated from an Amyotrophic Lateral Sclerosis (ALS)-patient carrying a mutation in Matr...
Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease affecting upper and l...
Amyotrophic Lateral Sclerosis (ALS) is a severe and fatal neurodegenerative disease characterized by...
AbstractAmyotrophic Lateral Sclerosis (ALS) is a severe and fatal neurodegenerative disease characte...
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease that selectively affects mo...
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease that primarily affects moto...
Induced pluripotent stem cells (iPSCs), which are generated through reprogramming adult somatic cell...
Amyotrophic lateral sclerosis (ALS) is a severe neurodegenerative disease, mainly affecting the moto...
Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease affecting upper and l...
Abstract Amyotrophic lateral sclerosis (ALS) is a complex neurodegenerative disease with cellular an...
Amyotrophic Lateral Sclerosis (ALS) is a complex multifactorial disorder, characterized by motor neu...
Amyotrophic lateral sclerosis (ALS) is a complex neurodegenerative disease with cellular and molecul...
Amyotrophic lateral sclerosis (ALS) is a late-onset motor neuron disorder. Although its neuropatholo...
Amyotrophic lateral sclerosis (ALS) is an adult-onset neurodegenerative disease affecting primarily ...
Amyotrophic lateral sclerosis (ALS) is a fatal and progressive neurodegenerative disease characteriz...
Fibroblasts isolated from an Amyotrophic Lateral Sclerosis (ALS)-patient carrying a mutation in Matr...
Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease affecting upper and l...
Amyotrophic Lateral Sclerosis (ALS) is a severe and fatal neurodegenerative disease characterized by...
AbstractAmyotrophic Lateral Sclerosis (ALS) is a severe and fatal neurodegenerative disease characte...
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease that selectively affects mo...
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease that primarily affects moto...
Induced pluripotent stem cells (iPSCs), which are generated through reprogramming adult somatic cell...
Amyotrophic lateral sclerosis (ALS) is a severe neurodegenerative disease, mainly affecting the moto...
Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease affecting upper and l...
Abstract Amyotrophic lateral sclerosis (ALS) is a complex neurodegenerative disease with cellular an...
Amyotrophic Lateral Sclerosis (ALS) is a complex multifactorial disorder, characterized by motor neu...
Amyotrophic lateral sclerosis (ALS) is a complex neurodegenerative disease with cellular and molecul...
Amyotrophic lateral sclerosis (ALS) is a late-onset motor neuron disorder. Although its neuropatholo...
Amyotrophic lateral sclerosis (ALS) is an adult-onset neurodegenerative disease affecting primarily ...
Amyotrophic lateral sclerosis (ALS) is a fatal and progressive neurodegenerative disease characteriz...