[HTML][HTML] Transcriptomes of Dravet syndrome iPSC derived GABAergic cells reveal dysregulated pathways for chromatin remodeling and neurodevelopment
Dravet syndrome (DS) is an early onset refractory epilepsy typically caused by de novo
heterozygous variants in SCN1A encoding the α-subunit of the neuronal sodium channel Na …
heterozygous variants in SCN1A encoding the α-subunit of the neuronal sodium channel Na …
Non integrative strategy decreases chromosome instability and improves endogenous pluripotency genes reactivation in porcine induced pluripotent-like stem cells
A Congras, H Barasc, K Canale-Tabet… - Scientific Reports, 2016 - nature.com
The pig is an emerging animal model, complementary to rodents for basic research and for
biomedical and agronomical purposes. However despite the progress made on mouse and …
biomedical and agronomical purposes. However despite the progress made on mouse and …
Current reprogramming systems in regenerative medicine: from somatic cells to induced pluripotent stem cells
C Hu, L Li - Regenerative medicine, 2016 - Taylor & Francis
Induced pluripotent stem cells (iPSCs) paved the way for research fields including cell
therapy, drug screening, disease modeling and the mechanism of embryonic development …
therapy, drug screening, disease modeling and the mechanism of embryonic development …
[HTML][HTML] Mowat-Wilson syndrome: Generation of two human iPS cell lines (UUIGPi004A and UUIGPi005A) from siblings with a truncating ZEB2 gene variant
Mowat-Wilson syndrome (MWS) is a complex developmental syndrome caused by
heterozygous mutations in the Zinc finger E-box-binding homeobox 2 gene (ZEB2). We …
heterozygous mutations in the Zinc finger E-box-binding homeobox 2 gene (ZEB2). We …