Search Results - "Garrigue, Jérôme"

Glutamatergic neuron-targeted loss of LGI1 epilepsy gene results in seizures by BOILLOT, Morgane, HUNEAU, Clément, MARTIN, Benoit, LEGUERN, Eric, ANDERSON, Matthew P, BAULAC, Stéphanie, MARSAN, Elise, LEHONGRE, Katia, NAVARRO, Vincent, ISHIDA, Saeko, DUFRESNOIS, Béatrice, OZKAYNAK, Ekim, GARRIGUE, Jérôme, MILES, Richard

“…Leucin-rich, glioma inactivated 1 (LGI1) is a secreted protein linked to human seizures of both genetic and autoimmune aetiology. Mutations in the LGI1 gene…”
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Parkin deficiency delays motor decline and disease manifestation in a mouse model of synucleinopathy by Fournier, Margot, Vitte, Jérémie, Garrigue, Jérôme, Langui, Dominique, Dullin, Jean-Philippe, Saurini, Françoise, Hanoun, Naïma, Perez-Diaz, Fernando, Cornilleau, Fabien, Joubert, Chantal, Ardila-Osorio, Héctor, Traver, Sabine, Duchateau, René, Goujet-Zalc, Cécile, Paleologou, Katerina, Lashuel, Hilal A, Haass, Christian, Duyckaerts, Charles, Cohen-Salmon, Charles, Kahle, Philipp J, Hamon, Michel, Brice, Alexis, Corti, Olga

“…In synucleinopathies, including Parkinson's disease, partially ubiquitylated alpha-synuclein species phosphorylated on serine 129 (P(S129)-alpha-synuclein)…”
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Parkin depletion delays motor decline dose-dependently without overtly affecting neuropathology in [alpha]-synuclein transgenic mice by Fournier, Margot, Roux, Amandine, Garrigue, Jñrôme, Muriel, Marie-Paule, Blanche, Paul, Lashuel, Hilal A, Anderson, John P, Barbour, Robin, Huang, Jiping, du Montcel, Sophie Tezenas, Brice, Alexis, Co

“…Background Mutations of the gene encoding the major component of Lewy bodies (LB), [alpha]-synuclein ([alpha]-syn), cause autosomal dominant forms of…”
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Parkin depletion delays motor decline dose-dependently without overtly affecting neuropathology in α-synuclein transgenic mice by Fournier, Margot, Roux, Amandine, Garrigue, Jérôme, Muriel, Marie-Paule, Blanche, Paul, Lashuel, Hilal A, Anderson, John P, Barbour, Robin, Huang, Jiping, du Montcel, Sophie Tezenas, Brice, Alexis, Corti, Olga

“…Mutations of the gene encoding the major component of Lewy bodies (LB), α-synuclein (α-syn), cause autosomal dominant forms of Parkinson's disease (PD),…”
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