Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Elisabeth Normand"'
Autor:
Remco V. Klaassen, Jasper Stroeder, Françoise Coussen, Anne-Sophie Hafner, Jennifer D. Petersen, Cedric Renancio, Leanne J. M. Schmitz, Elisabeth Normand, Johannes C. Lodder, Diana C. Rotaru, Priyanka Rao-Ruiz, Sabine Spijker, Huibert D. Mansvelder, Daniel Choquet, August B. Smit
Publikováno v:
Nature Communications, Vol 7, Iss 1, Pp 1-12 (2016)
Auxiliary AMPA receptor subunits can affect gating and surface mobility. Here the authors show that Shisa6 traps AMPA receptors at postsynaptic sites via PSD-95, and keeps them in an activated state in the presence of glutamate, preventing full desen
Externí odkaz:
https://doaj.org/article/3618aa11f0194d7bb076e4d881df1108
Autor:
Elsa Diguet, Pierre-Olivier Fernagut, Elisabeth Normand, Laurie Centelles, Christophe Mulle, François Tison
Publikováno v:
Neurobiology of Disease, Vol 15, Iss 3, Pp 667-675 (2004)
Age of onset of Huntington's disease (HD) statistically correlates with the length of expanded CAG repeats in the IT15 gene. However, other factors such as polymorphism in the 3′ untranslated region of the GluR6 kainate receptor gene subunit may co
Externí odkaz:
https://doaj.org/article/89cb3264aaab48938d21ace22b1f1d57
Autor:
Yann Humeau, Emilie Laheranne, Xander Houbaert, Mattia Aime, Pierre Billuart, Jamel Chelly, Elisabeth Normand, Hajer El Oussini, Chun-Lei Zhang, Etienne Herzog, Christelle Martin, Marilyn Lepleux
Publikováno v:
The Journal of neuroscience : the official journal of the Society for Neuroscience
The Journal of neuroscience : the official journal of the Society for Neuroscience, 2017, 37 (46), pp.11114-11126. ⟨10.1523/JNEUROSCI.0351-17.2017⟩
The Journal of neuroscience : the official journal of the Society for Neuroscience, 2017, 37 (46), pp.11114-11126. ⟨10.1523/JNEUROSCI.0351-17.2017⟩
Classical and systems genetics have identified wide networks of genes associated with cognitive and neurodevelopmental diseases. In parallel to deciphering the role of each of these genes in neuronal or synaptic function, evaluating the response of n
Autor:
Elisabeth Normand, Massimo Barresi, Cristina Miguelez, Stéphanie Morin, Andreas Frick, Lionel Froux, Jérôme Baufreton, Stéphanie Fioramonti, Anne Taupignon, Morgane Le Bon-Jego
Publikováno v:
Scientific Reports
Scientific Reports, Nature Publishing Group, 2018, 8 (1), pp.8858. ⟨10.1038/s41598-018-27195-6⟩
Addi. Archivo Digital para la Docencia y la Investigación
instname
Scientific Reports, 2018, 8 (1), pp.8858. ⟨10.1038/s41598-018-27195-6⟩
Scientific Reports, Vol 8, Iss 1, Pp 1-14 (2018)
Scientific Reports, Nature Publishing Group, 2018, 8 (1), pp.8858. ⟨10.1038/s41598-018-27195-6⟩
Addi. Archivo Digital para la Docencia y la Investigación
instname
Scientific Reports, 2018, 8 (1), pp.8858. ⟨10.1038/s41598-018-27195-6⟩
Scientific Reports, Vol 8, Iss 1, Pp 1-14 (2018)
Corticofugal fibers target the subthalamic nucleus (STN), a component nucleus of the basal ganglia, in addition to the striatum, their main input. The cortico-subthalamic, or hyperdirect, pathway, is thought to supplement the cortico-striatal pathway
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30604ebcca2a60ebfca35f24874a0429
https://hal.archives-ouvertes.fr/hal-02275288
https://hal.archives-ouvertes.fr/hal-02275288
Autor:
Jérôme, Baufreton, Tomislav, Milekovic, Qin, Li, Steve, McGuire, Eduardo Martin, Moraud, Grégory, Porras, Shiqi, Sun, Wai Kin D, Ko, Marine, Chazalon, Stéphanie, Morin, Elisabeth, Normand, Géraldine, Farjot, Aude, Milet, Jan, Pype, Elsa, Pioli, Gregoire, Courtine, Baptiste, Bessière, Erwan, Bezard
Publikováno v:
Movement Disorders
Parkinson's disease motor symptoms are treated with levodopa, but long‐term treatment leads to disabling dyskinesia. Altered synaptic transmission and maladaptive plasticity of corticostriatal glutamatergic projections play a critical role in the p
Autor:
Nadège Loaëc, Tania Sorg, Jamel Chelly, Elisabeth Normand, Yann Humeau, Aline Dubos, Guillaume Pavlovic, Aurore Curie, Giovanni Iacono, Gaëlle Friocourt, Yann Herault, Hamid Meziane, Mohammed Selloum, Fabrice Riet, Henk Stunnenberg, Marie-Christine Birling, Christelle Martin
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, 2018, 27 (12), pp.2138-2153. ⟨10.1093/hmg/ddy122⟩
Human Molecular Genetics, 27, 12, pp. 2138-2153
Human Molecular Genetics, 27, 2138-2153
Human Molecular Genetics, 2018, 27 (12), pp.2138-2153. ⟨10.1093/hmg/ddy122⟩
Human Molecular Genetics, 27, 12, pp. 2138-2153
Human Molecular Genetics, 27, 2138-2153
The aristaless-related homeobox (ARX) transcription factor is involved in the development of GABAergic and cholinergic neurons in the forebrain. ARX mutations have been associated with a wide spectrum of neurodevelopmental disorders in humans, among
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28517c1b180db0f702bc5eb2d2fe4487
https://hal.science/hal-03664342
https://hal.science/hal-03664342
Autor:
Alexandre Favereaux, Pierre-Olivier Fernagut, Federico N. Soria, Marta Martinez-Vicente, Erwan Bezard, François Georges, Christophe Lo Bianco, Miquel Vila, Christelle Glangetas, Sandra Dovero, Benjamin Dehay, María José López-González, Michel Engeln, Elisabeth Normand
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2017, 26 (14), pp.2603-2615. ⟨10.1093/hmg/ddx120⟩
Human Molecular Genetics, 2017, 26 (14), pp.2603-2615. ⟨10.1093/hmg/ddx120⟩
Human Molecular Genetics, Oxford University Press (OUP), 2017, 26 (14), pp.2603-2615. ⟨10.1093/hmg/ddx120⟩
Human Molecular Genetics, 2017, 26 (14), pp.2603-2615. ⟨10.1093/hmg/ddx120⟩
International audience; Mutations in the GBA1 gene encoding the lysosomal enzyme glucocerebrosidase (GBA1) are important risk factors for Parkinson's disease (PD). In vitro, altered GBA1 activity promotes alpha-synuclein accumulation whereas elevated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd2c4f2523288de15966a00174248330
https://www.hal.inserm.fr/inserm-02439478
https://www.hal.inserm.fr/inserm-02439478
Publikováno v:
Hippocampus. 24:1059-1069
Autism is a complex neurodevelopmental disorder with high heritability. grik2 (which encodes the GluK2 subunit of kainate receptors) has been identified as a susceptibility gene in Autism Spectrum Disorders (ASD), but its role in the core and associa
Publikováno v:
Journal of Biological Chemistry. 285:40060-40071
The trafficking of ionotropic glutamate receptors to and from synaptic sites is regulated by proteins that interact with their cytoplasmic C-terminal domain. Profilin IIa (PfnIIa), an actin-binding protein expressed in the brain and recruited to syna
Autor:
Marilyn Lepleux, Elisabeth Normand, Chun-Lei Zhang, Frédéric Gambino, Melissa Deshors, Yann Humeau, Xander Houbaert, Etienne Herzog
Publikováno v:
Brain Structure and Function
Brain Structure and Function, Springer Verlag, 2015, 220 (6), pp.3673-3682. ⟨10.1007/s00429-014-0882-x⟩
Brain Structure and Function, Springer Verlag, 2015, 220 (6), pp.3673-3682. ⟨10.1007/s00429-014-0882-x⟩
The process of learning mainly depends on the ability to store new information, while the ability to retrieve this information and express appropriate behaviors are also crucial for the adaptation of individuals to environmental cues. Thereby, all th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::413383ee4a911dc8fa3034f39a1dcb09
https://hal.archives-ouvertes.fr/hal-02392401
https://hal.archives-ouvertes.fr/hal-02392401