Modeling cartilage pathology in mucopolysaccharidosis VI using iPSCs reveals early dysregulation of chondrogenic and metabolic gene expression.
cartilage
disease modeling
induced pluripotent stem cells
lysosomal storage disease
mucopolysaccharidosis type VI
Journal
Frontiers in bioengineering and biotechnology
ISSN: 2296-4185
Titre abrégé: Front Bioeng Biotechnol
Pays: Switzerland
ID NLM: 101632513
Informations de publication
Date de publication:
2022
2022
Historique:
received:
20
05
2022
accepted:
09
11
2022
entrez:
23
12
2022
pubmed:
24
12
2022
medline:
24
12
2022
Statut:
epublish
Résumé
Mucopolysaccharidosis type VI (MPS VI) is a metabolic disorder caused by disease-associated variants in the Arylsulfatase B (
Identifiants
pubmed: 36561048
doi: 10.3389/fbioe.2022.949063
pii: 949063
pmc: PMC9763729
doi:
Types de publication
Journal Article
Langues
eng
Pagination
949063Informations de copyright
Copyright © 2022 Broeders, van Rooij, Oussoren, van Gestel, Smith, Kimber, Verdijk, Wagenmakers, van den Hout, van der Ploeg, Narcisi and Pijnappel.
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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