Defective Cystinosin, Aberrant Autophagy-Endolysosome Pathways, and Storage Disease: Towards Assembling the Puzzle.

Rega, Laura Rita; De Leo, Ester; Nieri, Daniela; Luciani, Alessandro

Rega, Laura Rita; De Leo, Ester; Nieri, Daniela; Luciani, Alessandro.

Afiliación

Rega LR; Renal Diseases Research Unit, Genetic and Rare Diseases Research Area, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy.
De Leo E; Renal Diseases Research Unit, Genetic and Rare Diseases Research Area, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy.
Nieri D; Mechanisms of Inherited Kidney Diseases Group, Institute of Physiology, University of Zurich, 8057 Zurich, Switzerland.
Luciani A; Mechanisms of Inherited Kidney Diseases Group, Institute of Physiology, University of Zurich, 8057 Zurich, Switzerland.

Cells ; 11(3)2022 01 19.

Article en En | MEDLINE | ID: mdl-35159136

Asunto(s)

Cistinosis; Enfermedades Metabólicas; Autofagia; Cistinosis/metabolismo; Ecosistema; Endosomas/metabolismo; Humanos; Lisosomas/metabolismo; Enfermedades Metabólicas/metabolismo

Palabras clave

autophagy; endolysosome; epithelial cell differentiation; homeostasis; kidney proximal tubule; lysosomal storage diseases; mitochondrial distress

Texto completo

Añadir a Mi BVS

Imprimir

XML

PubMed Links

Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cistinosis / Enfermedades Metabólicas Límite: Humans Idioma: En Revista: Cells Año: 2022 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Suiza

Texto completo

Añadir a Mi BVS

Imprimir

XML

PubMed Links

Buscar en Google