Recherche - Archive ouverte HAL

63 résultats

	Pour les 63 documents Envoyer sur ORCID RSS ATOM Exporter BibTeX XML-TEI CSV RTF EndNote PDF HTML Export avancé	Page : Page précédente 1 2 3 Page suivante	triés par Pertinence Auteur A→Z Auteur Z→A Titre A→Z Titre Z→A Date de publication croissante Date de publication décroissante Date de dépôt croissante Date de dépôt décroissante

		Coupling of D2R Short but not D2R Long receptor isoform to the Rho/ROCK signaling pathway renders striatal neurons vulnerable to mutant huntingtin Jocelyne Caboche , Galan-Rodriguez Beatriz , Martin Elodie , Emmanuel ; Déglon , Betuing Sandrine , et al. European Journal of Neuroscience, 2017, 45 (1), pp.198-206. ⟨10.1111/ejn.13415⟩ Article dans une revue hal-03365878v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Impaired brain energy metabolism in the BACHD mouse model of Huntington's disease: critical role of astrocyte-neuron interactions Lydie Boussicault , Anne-Sophie Herard , Noel Calingasan , Fanny Petit , Carole Malgorn , et al. Journal of Cerebral Blood Flow and Metabolism, 2014, 34 (9), pp.1500-1510. ⟨10.1038/jcbfm.2014.110⟩ Article dans une revue hal-01545792v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Calpain is a major cell death effector in selective striatal degeneration induced $in\ vivo$ by 3-nitropropionate: implications for Huntington's disease. Nicolas Bizat , Jean-Michel Hermel , Frédéric Boyer , Carine Jacquard , Christophe Créminon , et al. Journal of Neuroscience, 2003, 23 (12), pp.5020-30 Article dans une revue cea-02290630v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Time-Course of Alterations in the Endocannabinoid System after Viral-Mediated Overexpression of α-Synuclein in the Rat Brain Rachel Kelly , Alexis-Pierre Bemelmans , Charlène Joséphine , Emmanuel Brouillet , Declan P Mckernan , et al. Molecules, 2022, 27 (2), pp.507. ⟨10.3390/molecules27020507⟩ Article dans une revue hal-04419946v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Diffusion-weighted magnetic resonance spectroscopy enables cell-specific monitoring of astrocyte reactivity $in\ vivo$ Clémence Ligneul , Marco Palombo , Edwin Hernández-Garzón , Maria-Angeles Carrillo-de Sauvage , Julien Flament , et al. NeuroImage, 2019, 191, pp.457-469. ⟨10.1016/j.neuroimage.2019.02.046⟩ Article dans une revue cea-02155405v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		CA150 expression delays striatal cell death in overexpression and knock-in conditions for mutant huntingtin neurotoxicity Margarita Arango , Sébastien Holbert , Dania Zala , Emmanuel Brouillet , James Pearson , et al. Journal of Neuroscience, 2006, 26 (17), pp.4649 - 4659. ⟨10.1523/JNEUROSCI.5409-05.2006⟩ Article dans une revue hal-02666883v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Mitochondria in Huntington's disease Maria Damiano , Laurie Galvan , Nicole Déglon , Emmanuel Brouillet Biochimica et Biophysica Acta - Molecular Basis of Disease, 2010, 1802 (1), pp.52-61. ⟨10.1016/j.bbadis.2009.07.012⟩ Article dans une revue hal-02459756v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Imaging and spectroscopic approaches to probe brain energy metabolism dysregulation in neurodegenerative diseases Gilles Bonvento , Julien Valette , Julien Flament , Fanny Mochel , Emmanuel Brouillet Journal of Cerebral Blood Flow and Metabolism, 2017, 37 (6), pp.1927-1943. ⟨10.1177/0271678X17697989⟩ Article dans une revue hal-01539753v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		$In\ Vivo$ Calpain/Caspase Cross-talk during 3-Nitropropionic Acid-induced Striatal Degeneration Nicolas Bizat , Jean-Michel Hermel , Sandrine Humbert , Carine Jacquard , Christophe Créminon , et al. Journal of Biological Chemistry, 2003, 278 (44), pp.43245-43253. ⟨10.1074/jbc.M305057200⟩ Article dans une revue cea-02290633v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Energy defects in Huntington's disease: Why “in vivo” evidence matters Géraldine Liot , Julien Valette , Jérémy Pépin , Julien Flament , Emmanuel Brouillet Biochemical and Biophysical Research Communications, 2017, 483 (4), pp.1084-1095. ⟨10.1016/j.bbrc.2016.09.065⟩ Article dans une revue hal-04476989v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Possible involvement of self-defense mechanisms in the preferential vulnerability of the striatum in Huntington's disease Laetitia Francelle , Laurie Galvan , Emmanuel Brouillet Frontiers in Cellular Neuroscience, 2014, ⟨10.3389/fncel.2014.00295⟩ Article dans une revue hal-02459873v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Striatal long noncoding RNA Abhd11os is neuroprotective against an N-terminal fragment of mutant huntingtin in vivo. Laetitia Francelle , Laurie Galvan , Marie-Claude Gaillard , Fanny Petit , Benoît Bernay , et al. Neurobiology of Aging, 2015, pp.1601.e7-16. ⟨10.1016/j.neurobiolaging.2014.11.014⟩ Article dans une revue hal-01465910v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		SET translocation is associated with increase in caspase cleaved amyloid precursor protein in CA1 of Alzheimer and Down syndrome patients. Patricia Facchinetti , Emilie Dorard , Vincent Contremoulins , Marie-Claude Gaillard , Nicole Déglon , et al. Neurobiol Aging, 2014, 35 (5), pp.958-68. ⟨10.1016/j.neurobiolaging.2013.08.039⟩ Article dans une revue hal-00946234v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		The C-Terminal Domain of LRRK2 with the G2019S Substitution Increases Mutant A53T α-Synuclein Toxicity in Dopaminergic Neurons In Vivo Noémie Cresto , Camille Gardier , Marie-Claude Gaillard , Francesco Gubinelli , Pauline Roost , et al. International Journal of Molecular Sciences, 2021, 22 (13), pp.6760. ⟨10.3390/ijms22136760⟩ Article dans une revue hal-03452142v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		What is gained or ‘lost in translation’ in Huntington’s disease Emmanuel Brouillet , Karine Merienne Brain - A Journal of Neurology , 2019, 142 (10), pp.2900-2902. ⟨10.1093/brain/awz274⟩ Article dans une revue hal-03058364v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Corticostriatopallidal Neuroprotection by Adenovirus-Mediated Ciliary Neurotrophic Factor Gene Transfer in a Rat Model of Progressive Striatal Degeneration Vincent Mittoux , Stephane Ouary , Christelle Monville , Fabrice Lisovoski , Thomas Poyot , et al. Journal of Neuroscience, 2002, 22 (11), pp.4478-86 Article dans une revue cea-02290628v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Perseverative behavior underlying attentional set-shifting deficits in rats chronically treated with the neurotoxin 3-nitropropionic acid. Nicole El Massioui , Stéphane Ouary , Fabrice Chéruel , Philippe Hantraye , Emmanuel Brouillet Experimental Neurology, 2001, 172 (1), pp.172-81. ⟨10.1006/exnr.2001.7766⟩ Article dans une revue istex hal-01467542v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		A role of mitochondrial complex II defects in genetic models of Huntington's disease expressing N-terminal fragments of mutant huntingtin Maria Damiano , Elsa Diguet , Carole Malgorn , Marilena d'Aurelio , Laurie Galvan , et al. Human Molecular Genetics, 2013, 22 (19), pp.3869-3882. ⟨10.1093/hmg/ddt242⟩ Article dans une revue hal-02459752v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		The Mitochondrial Toxin 3-Nitropropionic Acid Induces Striatal Neurodegeneration via a c-Jun N-Terminal Kinase/c-Jun Module Marta Garcia , Peter Vanhoutte , Christiane Pagès , Marie-Jo Besson , Emmanuel Brouillet , et al. Journal of Neuroscience, 2002, 22 (6), pp.2174-2184. ⟨10.1523/JNEUROSCI.22-06-02174.2002⟩ Article dans une revue hal-02372666v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Ectosomes: a new mechanism for non-exosomal secretion of tau protein. Simon Dujardin , Séverine Bégard , Raphaëlle Caillierez , Cédrick Lachaud , Lucie Delattre , et al. PLoS ONE, 2013, 9 (6), pp.e100760. ⟨10.1371/journal.pone.0100760⟩ Article dans une revue hal-01181185v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Discovering new bioactive neuropeptides in the striatum secretome using in vivo microdialysis and versatile proteomics. Benoît Bernay , Marie-Claude Gaillard , Vilém Guryca , Anouk Emadali , Lauriane Kuhn , et al. Molecular and Cellular Proteomics, 2009, 8 (5), pp.946-58. ⟨10.1074/mcp.M800501-MCP200⟩ Article dans une revue inserm-00410894v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Contribution of Neuroepigenetics to Huntington’s Disease Laetitia Francelle , Caroline Lotz , Tiago Outeiro , Emmanuel Brouillet , Karine Merienne Frontiers in Human Neuroscience, 2017, 11, ⟨10.3389/fnhum.2017.00017⟩ Article dans une revue hal-03060269v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Contribution of Neuroepigenetics to Huntington’s Disease Laetitia Francelle , Caroline Lotz , Tiago Outeiro , Emmanuel Brouillet , Karine Merienne Frontiers in Human Neuroscience, 2017, 11, ⟨10.3389/fnhum.2017.00017⟩ Article dans une revue cea-01751739v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Activation of Astrocytes by CNTF Induces Metabolic Plasticity and Increases Resistance to Metabolic Insults Carole Escartin , Karin Pierre , Angélique Colin , Emmanuel Brouillet , Thierry Delzescaux , et al. Journal of Neuroscience, 2007, 27 (27), pp.7094-7104. ⟨10.1523/JNEUROSCI.0174-07.2007⟩ Article dans une revue cea-02290623v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		The Neuroprotective Agent CNTF Decreases Neuronal Metabolites in the Rat Striatum: An $in\ Vivo$ Multimodal Magnetic Resonance Imaging Study Maria-Angeles Carrillo-de Sauvage , Julien Flament , Yann Bramoullé , Lucile Ben Haim , Martine Guillermier , et al. Journal of Cerebral Blood Flow and Metabolism, 2015, 35 (6), pp.917-921. ⟨10.1038/jcbfm.2015.48⟩ Article dans une revue cea-02168367v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		The striatal kinase DCLK3 produces neuroprotection against mutant huntingtin Laurie Galvan , Laetitia Francelle , Marie-Claude Gaillard , Lucie de Longprez , Maria-Angeles Carrillo-de Sauvage , et al. Brain - A Journal of Neurology , 2018, 141 (5), pp.1434-1454. ⟨10.1093/brain/awy057⟩ Article dans une revue hal-02074093v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		THY-Tau22 mouse model accumulates more tauopathy at late stage of the disease in response to microglia deactivation through TREM2 deficiency Audrey Vautheny , Charlotte Duwat , Gwennaëlle Aurégan , Charlène Joséphine , Anne-Sophie Hérard , et al. Neurobiology of Disease, 2021, 155, pp.105398. ⟨10.1016/j.nbd.2021.105398⟩ Article dans une revue inserm-03366724v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Mitochondria in Huntington's disease Maria Damiano , Laurie Galvan , Nicole Déglon , Emmanuel Brouillet Biochimica et Biophysica Acta - Molecular Basis of Disease, 2009, 1802 (1), pp.52. ⟨10.1016/j.bbadis.2009.07.012⟩ Article dans une revue hal-00543005v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Extreme conservation of the poly-glutamine tract in huntingtin is related to neurodevelopmental functions: the “better” may become the “enemy of the good” in the course of evolution Emmanuel Brouillet Cell Death and Differentiation, 2022, 29 (2), pp.266-268. ⟨10.1038/s41418-021-00927-4⟩ Article dans une revue hal-04312713v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Energy defects in Huntington's disease: Why “in vivo” evidence matters Géraldine Liot , Julien Valette , Jérémy Pépin , Julien Flament , Emmanuel Brouillet Biochemical and Biophysical Research Communications, 2017, 483, pp.1084 - 1095. ⟨10.1016/j.bbrc.2016.09.065⟩ Article dans une revue cea-01752431v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More

Filtrer vos résultats

Coupling of D2R Short but not D2R Long receptor isoform to the Rho/ROCK signaling pathway renders striatal neurons vulnerable to mutant huntingtin

Impaired brain energy metabolism in the BACHD mouse model of Huntington's disease: critical role of astrocyte-neuron interactions

Calpain is a major cell death effector in selective striatal degeneration induced $in\ vivo$ by 3-nitropropionate: implications for Huntington's disease.

Time-Course of Alterations in the Endocannabinoid System after Viral-Mediated Overexpression of α-Synuclein in the Rat Brain

Diffusion-weighted magnetic resonance spectroscopy enables cell-specific monitoring of astrocyte reactivity $in\ vivo$

CA150 expression delays striatal cell death in overexpression and knock-in conditions for mutant huntingtin neurotoxicity

Mitochondria in Huntington's disease

Imaging and spectroscopic approaches to probe brain energy metabolism dysregulation in neurodegenerative diseases

$In\ Vivo$ Calpain/Caspase Cross-talk during 3-Nitropropionic Acid-induced Striatal Degeneration

Energy defects in Huntington's disease: Why “in vivo” evidence matters

Possible involvement of self-defense mechanisms in the preferential vulnerability of the striatum in Huntington's disease

Striatal long noncoding RNA Abhd11os is neuroprotective against an N-terminal fragment of mutant huntingtin in vivo.

SET translocation is associated with increase in caspase cleaved amyloid precursor protein in CA1 of Alzheimer and Down syndrome patients.

The C-Terminal Domain of LRRK2 with the G2019S Substitution Increases Mutant A53T α-Synuclein Toxicity in Dopaminergic Neurons In Vivo

What is gained or ‘lost in translation’ in Huntington’s disease

Corticostriatopallidal Neuroprotection by Adenovirus-Mediated Ciliary Neurotrophic Factor Gene Transfer in a Rat Model of Progressive Striatal Degeneration

Perseverative behavior underlying attentional set-shifting deficits in rats chronically treated with the neurotoxin 3-nitropropionic acid.

A role of mitochondrial complex II defects in genetic models of Huntington's disease expressing N-terminal fragments of mutant huntingtin

The Mitochondrial Toxin 3-Nitropropionic Acid Induces Striatal Neurodegeneration via a c-Jun N-Terminal Kinase/c-Jun Module

Ectosomes: a new mechanism for non-exosomal secretion of tau protein.

Discovering new bioactive neuropeptides in the striatum secretome using in vivo microdialysis and versatile proteomics.

Contribution of Neuroepigenetics to Huntington’s Disease

Contribution of Neuroepigenetics to Huntington’s Disease

Activation of Astrocytes by CNTF Induces Metabolic Plasticity and Increases Resistance to Metabolic Insults

The Neuroprotective Agent CNTF Decreases Neuronal Metabolites in the Rat Striatum: An $in\ Vivo$ Multimodal Magnetic Resonance Imaging Study

The striatal kinase DCLK3 produces neuroprotection against mutant huntingtin

THY-Tau22 mouse model accumulates more tauopathy at late stage of the disease in response to microglia deactivation through TREM2 deficiency

Mitochondria in Huntington's disease

Extreme conservation of the poly-glutamine tract in huntingtin is related to neurodevelopmental functions: the “better” may become the “enemy of the good” in the course of evolution

Energy defects in Huntington's disease: Why “in vivo” evidence matters