Výsledky vyhledávání - Robert Olaso
- Zobrazuji výsledky 1 - 20 z 35
- Přejít na další stránku
-
1
-
2
-
3
Hypermethylation of the IGF2 differentially methylated region 2 is a specific event in insulinomas leading to loss-of-imprinting and overexpression Autor Emelyne Dejeux, Robert Olaso, B. Dousset, Anne Audebourg, Marta Gut, Benoı̂t Terris, Jörg Tost
Vydáno 2009Artigo -
4
-
5
-
6
Transcriptome Analysis Describing New Immunity and Defense Genes in Peripheral Blood Mononuclear Cells of Rheumatoid Arthritis Patients Autor Vitor H. Teixeira, Robert Olaso, Marie‐Laure Martin‐Magniette, Sandra Lasbleiz, Laurent Jacq, Catarina R. Oliveira, Pascal Hilliquin, Marta Gut, François Cornélis, Élisabeth Petit
Vydáno 2009Artigo -
7
Performance comparison of three DNA extraction kits on human whole-exome data from formalin-fixed paraffin-embedded normal and tumor samples Autor Eric Bonnet, Marie-Laure Moutet, Céline Baulard, Delphine Bacq‐Daian, Florian Sandron, Lilia Mesrob, Bertrand Fin, Marc Delépine, Marie-Ange Palomares, Claire Jubin, Hélène Blanché, Vincent Meyer, Anne Boland, Robert Olaso, Jean‐François Deleuze
Vydáno 2018Artigo -
8
Strong selection during the last millennium for African ancestry in the admixed population of Madagascar Autor Denis Pierron, Margit Heiske, Harilanto Razafindrazaka, Veronica Pereda‐Loth, Jazmin Andrea Cifuentes Sanchez, Omar Alva, Amal Arachiche, Anne Boland, Robert Olaso, Jean‐François Deleuze, François‐Xavier Ricaut, Jean-Aimé Rakotoarisoa, Chantal Radimilahy, Mark Stoneking, Thierry Letellier
Vydáno 2018Artigo -
9
A new titinopathy Autor Rafael de Cid, Rabah Ben Yaou, Carinne Roudaut, Karine Charton, Sylvain Baulande, France Leturcq, Norma B. Romero, Edoardo Malfatti, Maud Beuvin, Anna Vihola, Audrey Criqui, Isabelle Nelson, Juliette Nectoux, Laurène Ben Aim, Christophe Caloustian, Robert Olaso, Bjarne Udd, Gisèle Bonne, B. Eymard, Isabelle Richard
Vydáno 2015Artigo -
10
Mutations in Eml1 lead to ectopic progenitors and neuronal heterotopia in mouse and human Autor Michel Kielar, Françoise Phan Dinh Tuy, Sara Bizzotto, Cécile Lebrand, Camino de Juan Romero, Karine Poirier, Renske Oegema, Grazia M.S. Mancini, Nadia Bahi‐Buisson, Robert Olaso, Anne‐Gaëlle Le Moing, Katia Boutourlinsky, Dominique Boucher, Wassila Carpentier, Patrick Berquin, Jean‐François Deleuze, Richard Belvindrah, Vı́ctor Borrell, Egbert Welker, Jamel Chelly, Alexandre Croquelois, Fiona Francis
Vydáno 2014Artigo -
11
Genome-wide nucleosome specificity and function of chromatin remodellers in ES cells Autor Maud de Dieuleveult, Kuangyu Yen, Isabelle Hmitou, Arnaud Depaux, Fayçal Boussouar, Daria Bou Dargham, Sylvie Jounier, Hélène Humbertclaude, Florence Ribiérre, Céline Baulard, Nina Farrell, Bongsoo Park, Céline Keime, Lucie Carrière, Soizick Berlivet, Marta Gut, Marta Gut, Michel Werner, Jean‐François Deleuze, Robert Olaso, Jean-Christophe Aude, Sophie Chantalat, B. Franklin Pugh, Matthieu Gérard
Vydáno 2016Artigo -
12
Genomic insights into population history and biological adaptation in Oceania Autor Jérémy Choin, Javier Mendoza‐Revilla, Lara R. Arauna, Sebastián Cuadros-Espinoza, Olivier Cassar, Maximilian Larena, Albert Min‐Shan Ko, Christine Harmant, R. Laurent, Paul Verdu, Guillaume Laval, Anne Boland, Robert Olaso, Jean‐François Deleuze, Frédérique Valentin, Ying‐Chin Ko, Mattias Jakobsson, Antoine Gessain, Laurent Excoffier, Mark Stoneking, Étienne Patin, Lluı́s Quintana-Murci
Vydáno 2021Artigo -
13
Histone variant H2A.J accumulates in senescent cells and promotes inflammatory gene expression Autor Kévin Contrepois, Clément Coudereau, Bérénice A. Benayoun, Nadine Schuler, Pierre‐François Roux, Oliver Bischof, Régis Courbeyrette, Cyril Carvalho, Jean‐Yves Thuret, Zhihai Ma, Céline Derbois, Marie‐Claire Nevers, Hervé Volland, Christophe E. Redon, William M. Bonner, Jean‐François Deleuze, Clotilde Wiel, David Bernard, M Snyder, Claudia E. Rübe, Robert Olaso, François Fenaille, Carl Mann
Vydáno 2017Artigo -
14
POLR1B and neural crest cell anomalies in Treacher Collins syndrome type 4 Autor Elodie Sanchez, Béryl Laplace-Builhé, Frédéric Tran Mau‐Them, Eric Richard, Alice Goldenberg, Tomi L. Toler, Thomas Guignard, Vincent Gâtinois, Marie Vincent, Catherine Blanchet, Anne Boland, Marie Thérèse Bihoreau, Jean‐François Deleuze, Robert Olaso, Walton Nephi, Hermann‐Josef Lüdecke, Joanne Verheij, Florence Moreau-Lenoir, Françoise Denoyelle, Jean‐Baptiste Rivière, Jean Laplanche, Marcia Willing, Guillaume Captier, Florence Apparailly, Dagmar Wieczorek, Corinne Collet, Farida Djouad, David Geneviève
Vydáno 2019Artigo -
15
Modulation of astrocyte reactivity improves functional deficits in mouse models of Alzheimer’s disease Autor Kelly Ceyzériat, Lucile Ben Haim, Audrey Denizot, Dylan Pommier, Marco Matos, Océane Guillemaud, Marie-Ange Palomares, Laurene Abjean, Fanny Petit, Pauline Gipchtein, Marie‐Claude Gaillard, Martine Guillermier, Suéva Bernier, Mylène Gaudin, Gwenaëlle Aurégan, Charlène Joséphine, Nathalie Déchamps, Julien Veran, Valentin Langlais, Karine Cambon, Alexis‐Pierre Bemelmans, Jan Baijer, Gilles Bonvento, Marc Dhénain, Jean‐François Deleuze, Stéphane H. R. Oliet, Emmanuel Brouillet, Philippe Hantraye, María-Angeles Carrillo-de Sauvage, Robert Olaso, Aude Panatier, Carole Escartin
Vydáno 2018Artigo -
16
Reactive astrocytes promote proteostasis in Huntington’s disease through the JAK2-STAT3 pathway Autor Laurene Abjean, Lucile Ben Haim, Miriam Riquelme-Pérez, Pauline Gipchtein, Céline Derbois, Marie-Ange Palomares, Fanny Petit, Anne‐Sophie Hérard, Marie‐Claude Gaillard, Martine Guillermier, Mylène Gaudin-Guérif, Gwennaëlle Aurégan, Nisrine Sagar, Cameron Héry, Noëlle Dufour, Noémie Robil, Mehdi Kabani, Ronald Melki, Pierre de la Grange, Alexis‐Pierre Bemelmans, Gilles Bonvento, Jean‐François Deleuze, Philippe Hantraye, Julien Flament, Eric Bonnet, Solène Brohard, Robert Olaso, Emmanuel Brouillet, María-Angeles Carrillo-de Sauvage, Carole Escartin
Vydáno 2022Artigo -
17
Association between ABO haplotypes and the risk of venous thrombosis: impact on disease risk estimation Autor Louisa Goumidi, Florian Thibord, Kerri L. Wiggins, Ruifang Li‐Gao, Mickael R. Brown, Astrid van Hylckama Vlieg, Juan Carlos Souto, José Manuel Soria, Manal Ibrahim‐Kosta, Noémie Saut, Delphine Daian, Robert Olaso, Philippe Amouyel, Stéphanie Debette, Anne Boland, Pascal Bailly, Alanna C. Morrison, Denis O. Mook-Kanamori, Jean‐François Deleuze, Andrew D. Johnson, Paul S. de Vries, Maria Sabater‐Lleal, Jacques Chiaroni, Nicholas L. Smith, Frits R. Rosendaal, Daniel I. Chasman, David‐Alexandre Trégouët, Pierre‐Emmanuel Morange
Vydáno 2020Artigo -
18
Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons Autor Gaël Nicolas, David Wallon, Camille Charbonnier, Olivier Quenez, Stéphane Rousseau, Anne‐Claire Richard, Anne Rovelet‐Lecrux, Sophie Coutant, Kilan Le Guennec, Delphine Bacq, Jean-Guillaume Garnier, Robert Olaso, Anne Boland, Vincent Meyer, Jean‐François Deleuze, Hans Markus Münter, Guillaume Bourque, Daniel Auld, Alexandre Montpetit, Mark Lathrop, Lucie Guyant‐Maréchal, Olivier Martinaud, Jérémie Pariente, Adeline Rollin‐Sillaire, Florence Pasquier, Isabelle Le Ber, Marie Sarazin, Bernard Croisile, Claire Boutoleau‐Bretonnière, Catherine Thomas-Antérion, Claire Paquet, Mathilde Sauvée, Olivier Moreaud, Audrey Gabelle, François Sellal, Mathieu Ceccaldi, Ludivine Chamard, Fréderic Blanc, Thierry Frébourg, Dominique Campion, Didier Hannequin
Vydáno 2015Artigo -
19
Mutations in the HECT domain of NEDD4L lead to AKT–mTOR pathway deregulation and cause periventricular nodular heterotopia Autor Loïc Broix, Hélène Jagline, Ekaterina L. Ivanova, Stéphane Schmucker, Nathalie Drouot, Jill Clayton‐Smith, Alistair T. Pagnamenta, Kay Metcalfe, Bertrand Isidor, Ulrike Walther Louvier, Annapurna Poduri, Jenny C. Taylor, Peggy Tilly, Karine Poirier, Yoann Saillour, Nicolas Lebrun, Tristan Stemmelen, Gabrielle Rudolf, Giuseppe Muraca, Benjamin Saintpierre, Adrienne Elmorjani, Martin Moïse, Nathalie Bednarek Weirauch, Renzo Guerrini, Anne Boland, Robert Olaso, Cécile Masson, Ratna Tripathy, David A. Keays, Chérif Beldjord, Laurent Nguyen, Juliette D. Godin, Usha Kini, Patrick Nischké, Jean‐François Deleuze, Nadia Bahi‐Buisson, Izabela Sumara, María-Victoria Hinckelmann, Jamel Chelly
Vydáno 2016Artigo -
20
Mutations and variants of ONECUT1 in diabetes Autor Anne Philippi, Sandra Heller, Ivan G. Costa, Valérie Senée, Markus Breunig, Zhijian Li, Gino Kwon, Ronan Russell, Anett Illing, Qiong Lin, Meike Hohwieler, Anne Degavre, Pierre Zalloua, Stefan Liebau, Michael Schuster, Johannes Krumm, Xi Zhang, Ryan J. Geusz, Jacqueline R. Benthuysen, Allen Wang, Joshua Chiou, Kyle J. Gaulton, Heike Neubauer, Eric J. Simon, Thomas Klein, Martin Wagner, Gopika G. Nair, Céline Besse, Claire Dandine‐Roulland, Robert Olaso, Jean‐François Deleuze, Bernhard Küster, Matthias Hebrok, Thomas Seufferlein, Maike Sander, Bernhard O. Boehm, Franz Oswald, Marc Nicolino, Cécile Julier, Alexander Kleger
Vydáno 2021Artigo
Vyhledávací nástroje:
Související témata
Biology
Genetics
Gene
Medicine
Internal medicine
Disease
Cell biology
Gene expression
Alzheimer's disease
Bioinformatics
Computational biology
Exome sequencing
Mutation
Endocrinology
Allele
Cancer
Cancer research
DNA methylation
Evolutionary biology
Immune system
Immunology
Neuroscience
Phenotype
Receptor
Computer science
DNA
Exome
Genome-wide association study
Genotype
Histone