Your browser doesn't support javascript.
loading
Impaired mitophagy links mitochondrial disease to epithelial stress in methylmalonyl-CoA mutase deficiency.
Luciani, Alessandro; Schumann, Anke; Berquez, Marine; Chen, Zhiyong; Nieri, Daniela; Failli, Mario; Debaix, Huguette; Festa, Beatrice Paola; Tokonami, Natsuko; Raimondi, Andrea; Cremonesi, Alessio; Carrella, Diego; Forny, Patrick; Kölker, Stefan; Diomedi Camassei, Francesca; Diaz, Francisca; Moraes, Carlos T; Di Bernardo, Diego; Baumgartner, Matthias R; Devuyst, Olivier.
Affiliation
  • Luciani A; Institute of Physiology and NCCR Kidney.CH, University of Zurich, 8057, Zurich, Switzerland. alessandro.luciani@uzh.ch.
  • Schumann A; Institute of Physiology and NCCR Kidney.CH, University of Zurich, 8057, Zurich, Switzerland.
  • Berquez M; Division of Metabolism and Children's Research Center, University Children's Hospital, 8032, Zurich, Switzerland.
  • Chen Z; Institute of Physiology and NCCR Kidney.CH, University of Zurich, 8057, Zurich, Switzerland.
  • Nieri D; Institute of Physiology and NCCR Kidney.CH, University of Zurich, 8057, Zurich, Switzerland.
  • Failli M; Institute of Physiology and NCCR Kidney.CH, University of Zurich, 8057, Zurich, Switzerland.
  • Debaix H; Department of Biomedicine, University of Eastern Finland, 70211, Kuopio, Finland.
  • Festa BP; Institute of Physiology and NCCR Kidney.CH, University of Zurich, 8057, Zurich, Switzerland.
  • Tokonami N; Institute of Physiology and NCCR Kidney.CH, University of Zurich, 8057, Zurich, Switzerland.
  • Raimondi A; Institute of Physiology and NCCR Kidney.CH, University of Zurich, 8057, Zurich, Switzerland.
  • Cremonesi A; San Raffaele Scientific Institute, Experimental Imaging Center, 20132, Milan, Italy.
  • Carrella D; Division of Clinical Chemistry and Biochemistry, University Children's Hospital Zurich, 8032, Zurich, Switzerland.
  • Forny P; Telethon Institute of Genetics and Medicine, Pozzuoli, 80078, Naples, Italy.
  • Kölker S; Division of Metabolism and Children's Research Center, University Children's Hospital, 8032, Zurich, Switzerland.
  • Diomedi Camassei F; Division of Inherited Metabolic Diseases, University Children's Hospital Heidelberg, 69120, Heidelberg, Germany.
  • Diaz F; Department of Laboratories-Pathology Unit, Bambino Gesù Children's Hospital, 00165, Rome, Italy.
  • Moraes CT; Department of Neurology, University of Miami Miller School of Medicine, 33136, Miami, FL, USA.
  • Di Bernardo D; Department of Neurology, University of Miami Miller School of Medicine, 33136, Miami, FL, USA.
  • Baumgartner MR; Telethon Institute of Genetics and Medicine, Pozzuoli, 80078, Naples, Italy.
  • Devuyst O; Division of Metabolism and Children's Research Center, University Children's Hospital, 8032, Zurich, Switzerland.
Nat Commun ; 11(1): 970, 2020 02 20.
Article in En | MEDLINE | ID: mdl-32080200
Subject(s)
Fulltext
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mitochondrial Diseases / Mitophagy / Amino Acid Metabolism, Inborn Errors / Metabolism, Inborn Errors / Methylmalonyl-CoA Mutase Type of study: Prognostic_studies Limits: Animals / Female / Humans / Male Language: En Journal: Nat Commun Year: 2020 Document type: Article
Fulltext
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mitochondrial Diseases / Mitophagy / Amino Acid Metabolism, Inborn Errors / Metabolism, Inborn Errors / Methylmalonyl-CoA Mutase Type of study: Prognostic_studies Limits: Animals / Female / Humans / Male Language: En Journal: Nat Commun Year: 2020 Document type: Article