Hasil Pencarian - Patrick Vourc’h
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Contribution of the dihydropyrimidinase-like proteins family in synaptic physiology and in neurodevelopmental disorders oleh Florence Desprez, Dévina C. Ung, Patrick Vourc’h, Patrick Vourc’h, Patrick Vourc’h, Médéric Jeanne, Médéric Jeanne, Frédéric Laumonnier, Frédéric Laumonnier
Diterbitkan 2023-04-01
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The Relevancy of Data Regarding the Metabolism of Iron to Our Understanding of Deregulated Mechanisms in ALS; Hypotheses and Pitfalls oleh Camille Petillon, Rudolf Hergesheimer, Hervé Puy, Philippe Corcia, Philippe Corcia, Patrick Vourc’h, Patrick Vourc’h, Christian Andres, Christian Andres, Zoubida Karim, Hélène Blasco, Hélène Blasco
Diterbitkan 2019-01-01
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Deep sequencing is an appropriate tool for the selection of unique Hepatitis C virus (HCV) variants after single genomic amplification. oleh Thibault Guinoiseau, Alain Moreau, Guillaume Hohnadel, Nicole Ngo-Giang-Huong, Celine Brulard, Patrick Vourc'h, Alain Goudeau, Catherine Gaudy-Graffin
Diterbitkan 2017-01-01
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Identification of rare copy number variations reveals PJA2, APCS, SYNPO, and TAC1 as novel candidate genes in Autism Spectrum Disorders oleh Tania Bitar, Walid Hleihel, Sylviane Marouillat, Sandrine Vonwill, Marie‐Laure Vuillaume, Michel Soufia, Patrick Vourc'h, Frederic Laumonnier, Christian R. Andres
Diterbitkan 2019-08-01
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The Roles of NEDD4 Subfamily of HECT E3 Ubiquitin Ligases in Neurodevelopment and Neurodegeneration oleh Shanez Haouari, Patrick Vourc’h, Médéric Jeanne, Sylviane Marouillat, Charlotte Veyrat-Durebex, Débora Lanznaster, Frédéric Laumonnier, Philippe Corcia, Hélène Blasco, Christian R. Andres
Diterbitkan 2022-03-01
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Aβ1-42 and Tau as Potential Biomarkers for Diagnosis and Prognosis of Amyotrophic Lateral Sclerosis oleh Débora Lanznaster, Rudolf C. Hergesheimer, Salah Eddine Bakkouche, Stephane Beltran, Patrick Vourc’h, Christian R. Andres, Diane Dufour-Rainfray, Philippe Corcia, Hélène Blasco
Diterbitkan 2020-04-01
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Implication of Central Nervous System Barrier Impairment in Amyotrophic Lateral Sclerosis: Gender-Related Difference in Patients oleh Hugo Alarcan, Patrick Vourc’h, Lise Berton, Isabelle Benz-De Bretagne, Eric Piver, Christian R. Andres, Philippe Corcia, Charlotte Veyrat-Durebex, Hélène Blasco
Diterbitkan 2023-07-01
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TDP-43-Mediated Toxicity in HEK293T Cells: A Fast and Reproducible Protocol To Be Employed in the Search of New Therapeutic Options against Amyotrophic Lateral Sclerosis oleh Débora Lanznaster, Jérôme Bourgeais, Clement Bruno, Rudolf C. Hergesheimer, Rose-Anne Thepault, Patrick Vourc’h, Philippe Corcia, Christian R. Andres, Olivier Herault, Hélène Blasco
Diterbitkan 2019-12-01
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Dysregulations of Expression of Genes of the Ubiquitin/SUMO Pathways in an In Vitro Model of Amyotrophic Lateral Sclerosis Combining Oxidative Stress and SOD1 Gene Mutation oleh Audrey Dangoumau, Sylviane Marouillat, Roxane Coelho, François Wurmser, Céline Brulard, Shanez Haouari, Frédéric Laumonnier, Philippe Corcia, Christian R. Andres, Hélène Blasco, Patrick Vourc’h
Diterbitkan 2021-02-01
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Post-Translational Variants of Major Proteins in Amyotrophic Lateral Sclerosis Provide New Insights into the Pathophysiology of the Disease oleh Léa Bedja-Iacona, Elodie Richard, Sylviane Marouillat, Céline Brulard, Tarek Alouane, Stéphane Beltran, Christian R. Andres, Hélène Blasco, Philippe Corcia, Charlotte Veyrat-Durebex, Patrick Vourc’h
Diterbitkan 2024-08-01
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Inflammatory mediators, lipoproteins and apolipoproteins in early diagnosis of amyotrophic lateral sclerosis oleh Hugo Alarcan, Mélanie Berthet, Laura Suire, Corentin Colas, Loïc Gonzalez, Christophe Paget, Isabelle Benz-de Bretagne, Eric Piver, Patrick Vourc'h, Christian Andres, Philippe Corcia, Hélène Blasco
Diterbitkan 2022-10-01
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Some CSF Kynurenine Pathway Intermediates Associated with Disease Evolution in Amyotrophic Lateral Sclerosis oleh Hugo Alarcan, Romane Chaumond, Patrick Emond, Isabelle Benz-De Bretagne, Antoine Lefèvre, Salah-eddine Bakkouche, Charlotte Veyrat-Durebex, Patrick Vourc’h, Christian Andres, Philippe Corcia, Hélène Blasco
Diterbitkan 2021-05-01
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Study of Ubiquitin Pathway Genes in a French Population with Amyotrophic Lateral Sclerosis: Focus on <i>HECW1</i> Encoding the E3 Ligase NEDL1 oleh Shanez Haouari, Christian Robert Andres, Debora Lanznaster, Sylviane Marouillat, Céline Brulard, Audrey Dangoumau, Devina Ung, Charlotte Veyrat-Durebex, Frédéric Laumonnier, Hélène Blasco, Philippe Couratier, Philippe Corcia, Patrick Vourc’h
Diterbitkan 2023-01-01
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Correction: H-NMR-Based Metabolomic Profiling of CSF in Early Amyotrophic Lateral Sclerosis. oleh Hélène Blasco, Philippe Corcia, Caroline Moreau, Ségolène Veau, Clémentine Fournier, Patrick Vourc'h, Patrick Emond, Paul Gordon, Pierre-François Pradat, Julien Praline, David Devos, Lydie Nadal-Desbarats, Christian R. Andres
Diterbitkan 2010-01-01
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1H-NMR-based metabolomic profiling of CSF in early amyotrophic lateral sclerosis. oleh Hélène Blasco, Philippe Corcia, Caroline Moreau, Ségolène Veau, Clémentine Fournier, Patrick Vourc'h, Patrick Emond, Paul Gordon, Pierre-François Pradat, Julien Praline, David Devos, Lydie Nadal-Desbarats, Christian R Andres
Diterbitkan 2010-01-01
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Metabolic Profile and Pathological Alterations in the Muscle of Patients with Early-Stage Amyotrophic Lateral Sclerosis oleh Débora Lanznaster, Clément Bruno, Jérôme Bourgeais, Patrick Emond, Ilyess Zemmoura, Antoine Lefèvre, Pascal Reynier, Sébastien Eymieux, Emmanuelle Blanchard, Patrick Vourc'h, Christian R. Andres, Salah Eddine Bakkouche, Olivier Herault, Luc Favard, Philippe Corcia, Hélène Blasco
Diterbitkan 2022-06-01
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Search for RASA1 Variants in Capillary Malformations of the Legs in 113 Children: Results from the French National Paediatric Cohort CONAPE oleh Annabel Maruani, Marine Durieux-Verde, Juliette Mazereeuw-Hautier, Olivia Boccara, Ludovic Martin, Christine Chiaverini, Catherine Eschard, Nathalie Bénéton, Pierre Vabres, Xavier Balguerie, Patrice Plantin, Didier Bessis, Sébastien Barbarot, Ali Dadban, Catherine Droitcourt, Aline Berthelot, Gérard Lorette, Sophie Leducq, Mahtab Samimi, Christian Andres, Agnès Caille, Patrick Vourc'h, Groupe de Recherche de la Société Française de Dermatologie
Diterbitkan 2017-11-01
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