Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Morgane Louessard"'
Autor:
Mathilde Louçã, Donya El Akrouti, Aude Lemesle, Morgane Louessard, Noëlle Dufour, Chloé Baroin, Aurore de la Fouchardière, Laurent Cotter, Hélène Jean-Jacques, Virginie Redeker, Anselme L. Perrier
Publikováno v:
Neurobiology of Disease, Vol 202, Iss , Pp 106703- (2024)
Externí odkaz:
https://doaj.org/article/9b7b2a86457a4b27aeb7d79b1e947592
Autor:
Mathilde Louçã, Donya El Akrouti, Aude Lemesle, Morgane Louessard, Noëlle Dufour, Chloé Baroin, Aurore de la Fouchardière, Laurent Cotter, Hélène Jean-Jacques, Virginie Redeker, Anselme L. Perrier
Publikováno v:
Neurobiology of Disease, Vol 200, Iss , Pp 106630- (2024)
Despite growing descriptions of wild-type Huntingtin (wt-HTT) roles in both adult brain function and, more recently, development, several clinical trials are exploring HTT-lowering approaches that target both wt-HTT and the mutant isoform (mut-HTT) r
Externí odkaz:
https://doaj.org/article/014f66c687ef4b789460f73ea00cc84e
Autor:
Marija Fjodorova, Morgane Louessard, Zongze Li, Daniel C. De La Fuente, Emma Dyke, Simon P. Brooks, Anselme L. Perrier, Meng Li
Publikováno v:
Stem Cell Reports, Vol 13, Iss 3, Pp 448-457 (2019)
Summary: The mechanisms underlying the selective degeneration of medium spiny neurons (MSNs) in Huntington disease (HD) remain largely unknown. CTIP2, a transcription factor expressed by all MSNs, is implicated in HD pathogenesis because of its inter
Externí odkaz:
https://doaj.org/article/951ad28726b04624b556ebadd2e08d26
Autor:
Maria-Victoria Hinckelmann, Frédéric Saudou, Morgane Louessard, Rémi Carpentier, Sophie Lenoir, Patricia Lino, Aurélie Genoux, Sandrine Humbert, Laura Auboyer, Anselm Perrier, Chiara Scaramuzzino, Amandine Virlogeux
Publikováno v:
I: Experimental therapeutics – preclinical.
Background Huntington Disease (HD) involves a complex cascade of pathogenic events, but central to its disruption of the cortico-striatal circuitry is impaired trafficking of Brain-Derived Neurotrophic Factor (BDNF). Aim We hypothesized that improvin
Autor:
Cyrille Orset, Carine Ali, Valérie Carraro, Jérôme Parcq, Benoit D. Roussel, Isabelle Bardou, Audrey M Thiebaut, Anne Terrisse, Denis Vivien, Jérôme Leprince, Eloise Lemarchand, Morgane Louessard, Alain Bruhat, Pierre Fafournoux
Publikováno v:
Cell Death and Differentiation
Cell Death and Differentiation, 2017, 24 (9), pp.1518-1529. ⟨10.1038/cdd.2017.35⟩
Cell Death and Differentiation, Nature Publishing Group, 2017, 24 (9), pp.1518-1529. ⟨10.1038/cdd.2017.35⟩
Cell Death and Differentiation, 2017, 24 (9), pp.1518-1529. ⟨10.1038/cdd.2017.35⟩
Cell Death and Differentiation, Nature Publishing Group, 2017, 24 (9), pp.1518-1529. ⟨10.1038/cdd.2017.35⟩
This project was supported by the Region Basse-Normandie and the AXA postdoctoral fellowship program, the INSERM, and the university of Caen. We thank Mr Gilbert Pigree and Mr Maxime Lemarchand for their help with the production of radioactive tPA (I
Autor:
Emma Dyke, Zongze Li, Marija Fjodorova, Simon Philip Brooks, Morgane Louessard, Anselme L. Perrier, Meng Li, Daniel C. De La Fuente
Publikováno v:
Stem Cell Reports, Vol 13, Iss 3, Pp 448-457 (2019)
Stem Cell Reports
Stem Cell Reports
Summary The mechanisms underlying the selective degeneration of medium spiny neurons (MSNs) in Huntington disease (HD) remain largely unknown. CTIP2, a transcription factor expressed by all MSNs, is implicated in HD pathogenesis because of its intera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6fcd36be9ff2feb5ab560d79435a2f2
https://orca.cardiff.ac.uk/id/eprint/124505/3/1-s2.0-S221367111930267X-main.pdf
https://orca.cardiff.ac.uk/id/eprint/124505/3/1-s2.0-S221367111930267X-main.pdf
Autor:
Åsa Petersén, Johana Tournois, Marie Michael, Gilles Bonvento, Margot Jarrige, Anselme L. Perrier, Barbara Baldo, Morgane Louessard, Deniz Kirik, Gurvan Mahé, Julie Bigarreau
Publikováno v:
Models for HD.
Several studies have outlined a non-cell-autonomous contribution in Huntington Disease (HD). Mutant-HTT (mut-HTT) expressed solely in astrocytes is sufficient for recapitulating the neurological and peripheral symptoms of HD in mice. Our objective is
Autor:
Margot Jarrige, Julie Bigarreau, Gabriel Vachey, Morgane Louessard, Nicole Déglon, Anselme L. Perrier, Michel Cailleret
Publikováno v:
Pathogenic mechanisms.
In Huntington disease (HD), the most affected cells are the GABA-releasing medium spiny neurons (MSN) of the striatum, the subcortical brain structure that controls body movement. DARPP32 (dopamine- and 3’,5’-cyclic adenosine monophosphate-regula
Autor:
Yannick Hommet, Morgane Louessard, Nolwenn Pasquet, Denis Vivien, Isabelle Bardou, Sara Douceau, Mickael Naveau, Flavie Lesept, Laurent Lebouvier
Publikováno v:
Cerebral cortex (New York, N.Y. : 1991). 29(6)
Modifications of neuronal migration during development, including processes that control cortical lamination are associated with functional deficits at adult stage. Here, we report for the first time that the lack of the serine protease tissue-type P
Autor:
Eric Maubert, Alexandre Lacroix, Morgane Louessard, Bertrand Lambolez, Grégoire Mondielli, Denis Vivien, Bruno Cauli, Magalie Martineau, Jean-Pierre Mothet, Flavie Lesept, Axel Montagne
Publikováno v:
Molecular Neurobiology
Molecular Neurobiology, Humana Press, 2016, 53 (7), pp.5000-5012. ⟨10.1007/s12035-015-9432-7⟩
Molecular Neurobiology, 2016, 53 (7), pp.5000-5012. ⟨10.1007/s12035-015-9432-7⟩
Molecular Neurobiology, Humana Press, 2016, 53 (7), pp.5000-5012. ⟨10.1007/s12035-015-9432-7⟩
Molecular Neurobiology, 2016, 53 (7), pp.5000-5012. ⟨10.1007/s12035-015-9432-7⟩
International audience; Although the extracellular serine protease tissue plasminogen activator (tPA) is involved in pathophysiological processes such as learning and memory, anxiety, epilepsy, stroke, and Alzheimer's disease, information about its r