Modelling renal defects in Bardet-Biedl syndrome patients using human iPS cells.
Bardet-Biedl syndrome
CRISPR
ciliopathy
iPSC (induced pluripotent stem cell)
kidney
Journal
Frontiers in cell and developmental biology
ISSN: 2296-634X
Titre abrégé: Front Cell Dev Biol
Pays: Switzerland
ID NLM: 101630250
Informations de publication
Date de publication:
2023
2023
Historique:
received:
11
02
2023
accepted:
19
05
2023
medline:
19
6
2023
pubmed:
19
6
2023
entrez:
19
6
2023
Statut:
epublish
Résumé
Bardet-Biedl syndrome (BBS) is a ciliopathy with pleiotropic effects on multiple tissues, including the kidney. Here we have compared renal differentiation of iPS cells from healthy and BBS donors. High content image analysis of WT1-expressing kidney progenitors showed that cell proliferation, differentiation and cell shape were similar in healthy,
Identifiants
pubmed: 37333983
doi: 10.3389/fcell.2023.1163825
pii: 1163825
pmc: PMC10272764
doi:
Types de publication
Journal Article
Langues
eng
Pagination
1163825Informations de copyright
Copyright © 2023 Williams, Hurling, Munir, Harley, Machado, Cujba, Alvarez-Fallas, Danovi, Lieberam, Sancho, Beales and Watt.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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