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137 results for Hérault,+Yann

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ArticlesPeer ReviewedFull Text
The DNA methyltransferase DNMT3C protects male germ cells from transposon activity
Author / Creator:Barau, Joan ; Teissandier, Aurélie ; Zamudio, Natasha ; Roy, Stéphanie ; Nalesso, Valérie ; Hérault, Yann ; Guillou, Florian ; Bourc'his, Déborah
Publisher:United States: American Association for the Advancement of Science
Journal title:Science (American Association for the Advancement of Science), 2016-11, Vol.354 (6314), p.909-912
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Distinct fibroblast lineages determine dermal architecture in skin development and repair
Author / Creator:Driskell, Ryan R. ; Lichtenberger, Beate M. ; Hoste, Esther ; Kretzschmar, Kai ; Simons, Ben D. ; Charalambous, Marika ; Ferron, Sacri R. ; Herault, Yann ; Pavlovic, Guillaume ; Ferguson-Smith, Anne C. ; Watt, Fiona M.
Publisher:London: Nature Publishing Group UK
Journal title:Nature (London), 2013-12, Vol.504 (7479), p.277-281
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How much do we know about the function of mammalian genes?
Author / Creator:Teboul, Lydia ; Hérault, Yann ; Wells, Sara ; Pavlovic, Guillaume
Publisher:England: BioMed Central Ltd
Journal title:BMC biology, 2023-12, Vol.21 (1), p.301-301, Article 301
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Dyrk1a from Gene Function in Development and Physiology to Dosage Correction across Life Span in Down Syndrome
Author / Creator:Atas-Ozcan, Helin ; Brault, Véronique ; Duchon, Arnaud ; Herault, Yann
Publisher:Switzerland: MDPI AG
Journal title:Genes, 2021-11, Vol.12 (11), p.1833
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Gdaphen, R pipeline to identify the most important qualitative and quantitative predictor variables from phenotypic data
Author / Creator:Muñiz Moreno, Maria del Mar ; Gavériaux-Ruff, Claire ; Herault, Yann
Publisher:England: BioMed Central Ltd
Journal title:BMC bioinformatics, 2023-01, Vol.24 (1), p.28-28, Article 28
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Identification of the translocation breakpoints in the Ts65Dn and Ts1Cje mouse lines: relevance for modeling down syndrome
Author / Creator:Duchon, Arnaud ; Raveau, Matthieu ; Chevalier, Claire ; Nalesso, Valérie ; Sharp, Andrew J ; Herault, Yann
Publisher:New York: Springer-Verlag
Journal title:Mammalian genome, 2011-12, Vol.22 (11-12), p.674-684
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Dissecting the autism-associated 16p11.2 locus identifies multiple drivers in neuroanatomical phenotypes and unveils a male-specific role for the major vault protein
Author / Creator:Kretz, Perrine F. ; Wagner, Christel ; Mikhaleva, Anna ; Montillot, Charlotte ; Hugel, Sylvain ; Morella, Ilaria ; Kannan, Meghna ; Fischer, Marie-Christine ; Milhau, Maxence ; Yalcin, Ipek ; Brambilla, Riccardo ; Selloum, Mohammed ; Herault, Yann ; Reymond, Alexandre ; Collins, Stephan C. ; Yalcin, Binnaz
Publisher:England: BioMed Central Ltd
Journal title:Genome Biology, 2023-11, Vol.24 (1), p.261-22, Article 261
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The COL6A5-p.Glu2272 mutation induces chronic itch in mice
Author / Creator:Rasheed, Ameer Abu Bakr ; Birling, Marie-Christine ; Lauria, Giuseppe ; Gaveriaux-Ruff, Claire ; Herault, Yann
Publisher:New York: Springer US
Journal title:Mammalian genome, 2024-06, Vol.35 (2), p.122-134
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Efficient and rapid generation of large genomic variants in rats and mice using CRISMERE
Author / Creator:Birling, Marie-Christine ; Schaeffer, Laurence ; André, Philippe ; Lindner, Loic ; Maréchal, Damien ; Ayadi, Abdel ; Sorg, Tania ; Pavlovic, Guillaume ; Hérault, Yann
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2017-03, Vol.7 (1), p.43331-43331, Article 43331
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Prenatal treatment with EGCG enriched green tea extract rescues GAD67 related developmental and cognitive defects in Down syndrome mouse models
Author / Creator:Souchet, Benoit ; Duchon, Arnaud ; Gu, Yuchen ; Dairou, Julien ; Chevalier, Claire ; Daubigney, Fabrice ; Nalesso, Valérie ; Créau, Nicole ; Yu, Yuejin ; Janel, Nathalie ; Herault, Yann ; Delabar, Jean Maurice
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2019-03, Vol.9 (1), p.3914-3914, Article 3914
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Dyrk1a gene dosage in glutamatergic neurons has key effects in cognitive deficits observed in mouse models of MRD7 and Down syndrome
Author / Creator:Brault, Véronique ; Nguyen, Thu Lan ; Flores-Gutiérrez, Javier ; Iacono, Giovanni ; Birling, Marie-Christine ; Lalanne, Valérie ; Meziane, Hamid ; Manousopoulou, Antigoni ; Pavlovic, Guillaume ; Lindner, Loïc ; Selloum, Mohammed ; Sorg, Tania ; Yu, Eugene ; Garbis, Spiros D. ; Hérault, Yann
Publisher:United States: Public Library of Science
Journal title:PLoS genetics, 2021-09, Vol.17 (9), p.e1009777-e1009777
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Fluorescent nanodiamond tracking reveals intraneuronal transport abnormalities induced by brain-disease-related genetic risk factors
Author / Creator:Haziza, Simon ; Mohan, Nitin ; Loe-Mie, Yann ; Lepagnol-Bestel, Aude-Marie ; Massou, Sophie ; Adam, Marie-Pierre ; Le, Xuan Loc ; Viard, Julia ; Plancon, Christine ; Daudin, Rachel ; Koebel, Pascale ; Dorard, Emilie ; Rose, Christiane ; Hsieh, Feng-Jen ; Wu, Chih-Che ; Potier, Brigitte ; Herault, Yann ; Sala, Carlo ; Corvin, Aiden ; Allinquant, Bernadette ; Chang, Huan-Cheng ; Treussart, François ; Simonneau, Michel
Publisher:London: Nature Publishing Group UK
Journal title:Nature nanotechnology, 2017-04, Vol.12 (4), p.322-328
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Day-to-day spontaneous social behaviours is quantitatively and qualitatively affected in a 16p11.2 deletion mouse model
Author / Creator:Rusu, Anna ; Chevalier, Claire ; de Chaumont, Fabrice ; Nalesso, Valérie ; Brault, Véronique ; Hérault, Yann ; Ey, Elodie
Publisher:Switzerland: Frontiers Research Foundation
Journal title:Frontiers in behavioral neuroscience, 2023-12, Vol.17, p.1294558-1294558
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Targeting the RHOA pathway improves learning and memory in adult Kctd13 and 16p11.2 deletion mouse models
Author / Creator:Martin Lorenzo, Sandra ; Nalesso, Valérie ; Chevalier, Claire ; Birling, Marie-Christine ; Herault, Yann
Publisher:England: BioMed Central Ltd
Journal title:Molecular autism, 2021-01, Vol.12 (1), p.1-1, Article 1
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The Rogdi knockout mouse is a model for Kohlschütter–Tönz syndrome
Author / Creator:Jimenez-Armijo, Alexandra ; Morkmued, Supawich ; Ahumada, José Tomás ; Kharouf, Naji ; de Feraudy, Yvan ; Gogl, Gergo ; Riet, Fabrice ; Niederreither, Karen ; Laporte, Jocelyn ; Birling, Marie Christine ; Selloum, Mohammed ; Herault, Yann ; Hernandez, Magali ; Bloch-Zupan, Agnès
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2024-01, Vol.14 (1), p.445-445, Article 445
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BAHD1 haploinsufficiency results in anxiety-like phenotypes in male mice
Author / Creator:Pourpre, Renaud ; Naudon, Laurent ; Meziane, Hamid ; Lakisic, Goran ; Jouneau, Luc ; Varet, Hugo ; Legendre, Rachel ; Wendling, Olivia ; Selloum, Mohammed ; Proux, Caroline ; Coppée, Jean-Yves ; Herault, Yann ; Bierne, Hélène
Publisher:United States: Public Library of Science
Journal title:PloS one, 2020-05, Vol.15 (5), p.e0232789-e0232789
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Correction of cognitive deficits in mouse models of Down syndrome by a pharmacological inhibitor of DYRK1A
Author / Creator:Nguyen, Thu Lan ; Duchon, Arnaud ; Manousopoulou, Antigoni ; Loaëc, Nadège ; Villiers, Benoît ; Pani, Guillaume ; Karatas, Meltem ; Mechling, Anna E. ; Harsan, Laura-Adela ; Limanton, Emmanuelle ; Bazureau, Jean-Pierre ; Carreaux, François ; Garbis, Spiros D. ; Meijer, Laurent ; Herault, Yann
Publisher:England: The Company of Biologists Ltd
Journal title:Disease models & mechanisms, 2018-09, Vol.11 (9)
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Identifying foetal forebrain interneurons as a target for monogenic autism risk factors and the polygenic 16p11.2 microdeletion
Author / Creator:Yang, Yifei ; Booker, Sam A. ; Clegg, James M. ; Quintana-Urzainqui, Idoia ; Sumera, Anna ; Kozic, Zrinko ; Dando, Owen ; Martin Lorenzo, Sandra ; Herault, Yann ; Kind, Peter C. ; Price, David J. ; Pratt, Thomas
Publisher:England: BioMed Central Ltd
Journal title:BMC neuroscience, 2023-01, Vol.24 (1), p.5-5, Article 5
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BIN1 recovers tauopathy-induced long-term memory deficits in mice and interacts with Tau through Thr348 phosphorylation
Author / Creator:Sartori, Maxime ; Mendes, Tiago ; Desai, Shruti ; Lasorsa, Alessia ; Herledan, Adrien ; Malmanche, Nicolas ; Mäkinen, Petra ; Marttinen, Mikael ; Malki, Idir ; Chapuis, Julien ; Flaig, Amandine ; Vreulx, Anaïs-Camille ; Ciancia, Marion ; Amouyel, Philippe ; Leroux, Florence ; Déprez, Benoit ; Cantrelle, François-Xavier ; Maréchal, Damien ; Pradier, Laurent ; Hiltunen, Mikko ; Landrieu, Isabelle ; Kilinc, Devrim ; Herault, Yann ; Laporte, Jocelyn ; Lambert, Jean-Charles
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Acta neuropathologica, 2019-10, Vol.138 (4), p.631-652
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ArticlesPeer ReviewedFull Text
Introduction to Mammalian Genome Special Issue: Genome Editing
Author / Creator:Teboul, Lydia ; Hérault, Yann ; Smith, Cynthia ; Whitelaw, Bruce
Publisher:New York: Springer US
Journal title:Mammalian genome, 2017-08, Vol.28 (7-8), p.235-236
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Showing 1 to 20 of 137 results

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The DNA methyltransferase DNMT3C protects male germ cells from transposon activity

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Distinct fibroblast lineages determine dermal architecture in skin development and repair

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How much do we know about the function of mammalian genes?

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Dyrk1a from Gene Function in Development and Physiology to Dosage Correction across Life Span in Down Syndrome

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Gdaphen, R pipeline to identify the most important qualitative and quantitative predictor variables from phenotypic data

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Identification of the translocation breakpoints in the Ts65Dn and Ts1Cje mouse lines: relevance for modeling down syndrome

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Dissecting the autism-associated 16p11.2 locus identifies multiple drivers in neuroanatomical phenotypes and unveils a male-specific role for the major vault protein

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The COL6A5-p.Glu2272 mutation induces chronic itch in mice

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Efficient and rapid generation of large genomic variants in rats and mice using CRISMERE

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Prenatal treatment with EGCG enriched green tea extract rescues GAD67 related developmental and cognitive defects in Down syndrome mouse models

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Dyrk1a gene dosage in glutamatergic neurons has key effects in cognitive deficits observed in mouse models of MRD7 and Down syndrome

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Fluorescent nanodiamond tracking reveals intraneuronal transport abnormalities induced by brain-disease-related genetic risk factors

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Day-to-day spontaneous social behaviours is quantitatively and qualitatively affected in a 16p11.2 deletion mouse model

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Targeting the RHOA pathway improves learning and memory in adult Kctd13 and 16p11.2 deletion mouse models

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The Rogdi knockout mouse is a model for Kohlschütter–Tönz syndrome

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BAHD1 haploinsufficiency results in anxiety-like phenotypes in male mice

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Correction of cognitive deficits in mouse models of Down syndrome by a pharmacological inhibitor of DYRK1A

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Identifying foetal forebrain interneurons as a target for monogenic autism risk factors and the polygenic 16p11.2 microdeletion

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BIN1 recovers tauopathy-induced long-term memory deficits in mice and interacts with Tau through Thr348 phosphorylation

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Introduction to Mammalian Genome Special Issue: Genome Editing

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