Aglycemia triggers alternative electron transport to sustain mesenchymal stem cell survival under anoxia.
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| Title: | Aglycemia triggers alternative electron transport to sustain mesenchymal stem cell survival under anoxia. |
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| Authors: | Refeyton A; Etablissement Français du Sang, Nouvelle Aquitaine, France; Rare disease genetics and metabolism, Inserm U1211, University of Bordeux, France; Children's Hospital of Philadelphia, Philadelphia, USA., Amoedo ND; Etablissement Français du Sang, Nouvelle Aquitaine, France; Rare disease genetics and metabolism, Inserm U1211, University of Bordeux, France., Labat V; Etablissement Français du Sang, Nouvelle Aquitaine, France; Rare disease genetics and metabolism, Inserm U1211, University of Bordeux, France., Vignane T; Leibniz Institute for Analytical Sciences, ISAS e.V., Dortmund, Germany; Institute of Molecular Systems Medicine, Goethe University of Frankfurt, Faculty of Medicine, Frankfurt, Germany., Buré C; Service Analyses Métaboliques-TBMCore University of Bordeaux, UAR CNRS 3427, US05 INSERM, France., Pinson B; Service Analyses Métaboliques-TBMCore University of Bordeaux, UAR CNRS 3427, US05 INSERM, France; Institute of Cellular Biochemistry and Genetics, UMR 5095 CNRS, University of Bordeaux, France., Ley-Ngardigal S; Rare disease genetics and metabolism, Inserm U1211, University of Bordeux, France., Debeissat C; Etablissement Français du Sang, Nouvelle Aquitaine, France; Rare disease genetics and metabolism, Inserm U1211, University of Bordeux, France., Bursac B; Institute of Cellular Biochemistry and Genetics, UMR 5095 CNRS, University of Bordeaux, France; Department of Biochemistry, Institute for Biological Research, University of Belgrade, Serbia., Claverol S; University of Bordeaux, Bordeaux Proteome, Bordeaux, France., Khelifi R; Etablissement Français du Sang, Nouvelle Aquitaine, France; Rare disease genetics and metabolism, Inserm U1211, University of Bordeux, France., Rodriguez L; Etablissement Français du Sang, Nouvelle Aquitaine, France; Rare disease genetics and metabolism, Inserm U1211, University of Bordeux, France., de la Grange PB; Etablissement Français du Sang, Nouvelle Aquitaine, France; Rare disease genetics and metabolism, Inserm U1211, University of Bordeux, France., Rossignol R; Rare disease genetics and metabolism, Inserm U1211, University of Bordeux, France., Filipovic MR; Leibniz Institute for Analytical Sciences, ISAS e.V., Dortmund, Germany; Institute of Cellular Biochemistry and Genetics, UMR 5095 CNRS, University of Bordeaux, France; School of Molecular Biosciences, University of Glasgow, Scotland, UK. Electronic address: Milos.Filipovic@glasgow.ac.uk., Ivanovic Z; Etablissement Français du Sang, Nouvelle Aquitaine, France; Rare disease genetics and metabolism, Inserm U1211, University of Bordeux, France. Electronic address: Zoran.ivanovic@efs.sante.fr., Vlaski-Lafarge M; Etablissement Français du Sang, Nouvelle Aquitaine, France; Rare disease genetics and metabolism, Inserm U1211, University of Bordeux, France. Electronic address: Marija.vlaski@efs.sante.fr. |
| Source: | Redox biology [Redox Biol] 2026 Jul 14; Vol. 96, pp. 104304. Date of Electronic Publication: 2026 Jul 14. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Elsevier, B.V Country of Publication: Netherlands NLM ID: 101605639 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2213-2317 (Electronic) Linking ISSN: 22132317 NLM ISO Abbreviation: Redox Biol Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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