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Frontiers in Cell and Developmental Biology|June 7, 2021
Loss of Pde6a Induces Rod Outer Segment Shrinkage and Visual Alterations in <i>pde6a</i> Mutant Zebrafish, a Relevant Model of Retinal DystrophyLucie Crouzier, Camille Diez, Elodie M Richard, et al.
Toxicology Mechanisms and Methods|March 22, 2022
Developmental exposure to the A6-pesticide causes changes in tyrosine hydroxylase gene expression, neurochemistry, and locomotors behavior in larval zebrafishAhmed Nasri, Pierre-André Lafon, Amine Mezni, et al.
Molecular Therapy. Methods & Clinical Development|November 2, 2022
NCS1 overexpression restored mitochondrial activity and behavioral alterations in a zebrafish model of Wolfram syndromeLucie Crouzier, Elodie M Richard, Camille Diez, et al.
Redox Biology|November 28, 2022
Sigma-1 receptor agonist PRE-084 confers protection against TAR DNA-binding protein-43 toxicity through NRF2 signallingChristelle Lasbleiz, Amandine Peyrel, Pauline Tarot, et al.
The Science of the Total Environment|January 26, 2021
Ethinylestradiol (EE2) residues from birth control pills impair nervous system development and swimming behavior of zebrafish larvaeAhmed Nasri, Ali Mezni, Pierre-André Lafon, et al.
Plos One|December 2, 2014
Zebrafish prion protein PrP2 controls collective migration process during lateral line sensory system developmentSylvaine Huc-Brandt, Nelson Hieu, Thibaut Imberdis, et al.
Neurobiology of Disease|August 10, 2018
Regenerating islet-derived 1α (REG-1α) protein increases tau phosphorylation in cell and animal models of tauopathiesMireille Moussaed, Sylvaine Huc-Brandt, Nicolas Cubedo, et al.
Human Molecular Genetics|March 24, 2022
Morphological, behavioral and cellular analyses revealed different phenotypes in Wolfram syndrome wfs1a and wfs1b zebrafish mutant linesLucie Crouzier, Elodie M Richard, Camille Diez, et al.
Translational Neurodegeneration|December 14, 2025
Positive modulation of sigma-1 receptor: a new weapon to mitigate disease progression in amyotrophic lateral sclerosisJulien Le Friec, Hugo Mourier, Simon Couly, et al.
European Journal of Human Genetics : EJHG|May 12, 2023
Identification and in vivo functional investigation of a HOMER2 nonstop variant causing hearing lossChristel Vaché, Nicolas Cubedo, Luke Mansard, et al.
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