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Cellular and Molecular Life Sciences : CMLS|August 12, 2016
Liver X receptors: from cholesterol regulation to neuroprotection-a new barrier against neurodegeneration in amyotrophic lateral sclerosis?Kevin Mouzat, Cédric Raoul, Anne Polge, et al.
International Journal of Molecular Sciences|August 11, 2019
Regulation of Brain Cholesterol: What Role Do Liver X Receptors Play in Neurodegenerative Diseases?Kevin Mouzat, Aleksandra Chudinova, Anne Polge, et al.
Clinical Genetics|April 23, 2023
Discovering the ANK2-related autism phenotypeClaire Guissart, Anne Polge, Nelly Durand, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|November 29, 2016
Slowly progressive motor neuron disease with multi-system involvement related to p.E121G SOD1 mutationGuillaume Taieb, Anne Polge, Raul Juntas-Morales, et al.
Clinical Biochemistry|June 19, 2007
Earlier detection of myocardial infarction by an improved cardiac TnI assayEstelle Le Moal, Isabelle Giuliani, Jean-Pierre Bertinchant, et al.
Scientific Reports|November 27, 2020
Premature termination codons in SOD1 causing Amyotrophic Lateral Sclerosis are predicted to escape the nonsense-mediated mRNA decayClaire Guissart, Kevin Mouzat, Jovana Kantar, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 18, 2005
Prognostic value of cardiac troponin T in patients with both acute and chronic stable congestive heart failure: comparison with atrial natriuretic peptide, brain natriuretic peptide and plasma norepinephrineJean-Pierre Bertinchant, Nicolas Combes, Anne Polge, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|October 20, 2021
Compound heterozygous P67S/D91A SOD1 mutations in an ALS family with apparently sporadic caseElisa De La Cruz, Claire Guissart, Florence Esselin, et al.
BMC Medical Genetics|October 28, 2011
A common polymorphism in NR1H2 (LXRbeta) is associated with preeclampsiaKevin Mouzat, Eric Mercier, Anne Polge, et al.
Therapeutic Drug Monitoring|December 17, 2009
High-resolution melting analysis of sequence variations in the cytidine deaminase gene (CDA) in patients with cancer treated with gemcitabineCaroline Raynal, Joseph Ciccolini, Cédric Mercier, et al.
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