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Longitudinal study of Pex1-G844D NMRI mouse model: A robust pre-clinical model for mild Zellweger spectrum disorder.
Demaret T, Roumain M, Ambroise J, Evraerts J, Ravau J, Bouzin C, Bearzatto B, Gala JL, Stepman H, Marie S, Vincent MF, Muccioli GG, Najimi M, Sokal EM. Demaret T, et al. Among authors: marie s. Biochim Biophys Acta Mol Basis Dis. 2020 Nov 1;1866(11):165900. doi: 10.1016/j.bbadis.2020.165900. Epub 2020 Jul 18. Biochim Biophys Acta Mol Basis Dis. 2020. PMID: 32693164 Free article.
Prenatal diagnosis in adenylosuccinate lyase deficiency.
Marie S, Flipsen JW, Duran M, Poll-The BT, Beemer FA, Bosschaart AN, Vincent MF, Van den Berghe G. Marie S, et al. Prenat Diagn. 2000 Jan;20(1):33-6. doi: 10.1002/(sici)1097-0223(200001)20:1<33::aid-pd751>3.0.co;2-3. Prenat Diagn. 2000. PMID: 10701848
Adenylosuccinate lyase deficiency: study of physiopathologic mechanism(s).
Race V, Marie S, Kienlen-Campard P, Hermans E, Octave JN, Van den Berghe G, Vincent MF. Race V, et al. Among authors: marie s. Nucleosides Nucleotides Nucleic Acids. 2004 Oct;23(8-9):1227-9. doi: 10.1081/NCN-200027491. Nucleosides Nucleotides Nucleic Acids. 2004. PMID: 15571234
A mouse model of L-2-hydroxyglutaric aciduria, a disorder of metabolite repair.
Rzem R, Achouri Y, Marbaix E, Schakman O, Wiame E, Marie S, Gailly P, Vincent MF, Veiga-da-Cunha M, Van Schaftingen E. Rzem R, et al. Among authors: marie s. PLoS One. 2015 Mar 12;10(3):e0119540. doi: 10.1371/journal.pone.0119540. eCollection 2015. PLoS One. 2015. PMID: 25763823 Free PMC article.
477 results