Multisystem involvement, defective lysosomes and impaired autophagy in a novel rat model of nephropathic cystinosis

Recessive mutations in the CTNS gene encoding the lysosomal transporter cystinosin cause cystinosis, a lysosomal storage disease leading to kidney failure and multisystem manifestations. A Ctns knockout mouse model recapitulates features of cystinosis, but the delayed onset of kidney manifestations,...

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Detalles Bibliográficos
Autores principales: Krohn, Patrick, Rega, Laura Rita, Harvent, Marianne, Festa, Beatrice Paola, Taranta, Anna, Luciani, Alessandro, Dewulf, Joseph, Cremonesi, Alessio, Camassei, Francesca Diomedi, Hanson, James V M, Gerth-Kahlert, Christina, Emma, Francesco, Berquez, Marine, Devuyst, Olivier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9262394/
https://www.ncbi.nlm.nih.gov/pubmed/35137071
http://dx.doi.org/10.1093/hmg/ddac033

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9262394/
https://www.ncbi.nlm.nih.gov/pubmed/35137071
http://dx.doi.org/10.1093/hmg/ddac033

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