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Ultrasensitive digital immunoassays for SOD1 conformation in amyotrophic lateral sclerosis.
Morichon, Lisa; Hirtz, Christophe; Tiers, Laurent; Mezghrani, Alexandre; Raoul, Cédric; Esselin, Florence; La Cruz, Elisa De; Julien, Jean-Pierre; Camu, William; Lehmann, Sylvain.
Afiliação
  • Morichon L; LBPC-PPC, University of Montpellier, CHU Montpellier, INM INSERM, Montpellier, 34295, France.
  • Hirtz C; LBPC-PPC, University of Montpellier, CHU Montpellier, INM INSERM, Montpellier, 34295, France.
  • Tiers L; LBPC-PPC, University of Montpellier, CHU Montpellier, INM INSERM, Montpellier, 34295, France.
  • Mezghrani A; INM, University of Montpellier, INSERM, Montpellier, 34295, France.
  • Raoul C; INM, University of Montpellier, INSERM, Montpellier, 34295, France.
  • Esselin F; Department of Neurology, University of Montpellier, CHU Montpellier, INM, INSERM, Montpellier, 34295, France.
  • La Cruz E; Department of Neurology, University of Montpellier, CHU Montpellier, INM, INSERM, Montpellier, 34295, France.
  • Julien JP; Department of Psychiatry and Neuroscience, CERVO Brain Research Centre, University Laval, Quebec City, 23027, Canada.
  • Camu W; Department of Neurology, University of Montpellier, CHU Montpellier, INM, INSERM, Montpellier, 34295, France.
  • Lehmann S; LBPC-PPC, University of Montpellier, CHU Montpellier, INM INSERM, Montpellier, 34295, France.
Bioanalysis ; 15(15): 927-936, 2023 Aug.
Article em En | MEDLINE | ID: mdl-37650499
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease associated with protein misfolding, including Cu/Zn SOD1. In this study, we set up a method for detecting normal and pathological misfolded SOD1 in human serum and cerebrospinal fluid. SOD1 was increased in ALS and misfolded SOD1 had low and variable expression in both control and ALS. These assays holds promise for improving our understanding of ALS and its diagnosis.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esclerose Lateral Amiotrófica Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esclerose Lateral Amiotrófica Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article