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A new mouse model of ARX dup24 recapitulates the patients' behavioral and fine motor alterations.
Dubos, Aline; Meziane, Hamid; Iacono, Giovanni; Curie, Aurore; Riet, Fabrice; Martin, Christelle; Loaëc, Nadège; Birling, Marie-Christine; Selloum, Mohammed; Normand, Elisabeth; Pavlovic, Guillaume; Sorg, Tania; Stunnenberg, Henk G; Chelly, Jamel; Humeau, Yann; Friocourt, Gaëlle; Hérault, Yann.
Afiliação
  • Dubos A; Institut de Génétique et de Biologie Moléculaire et Cellulaire, Université de Strasbourg, 67404 Illkirch, France.
  • Meziane H; Centre National de la Recherche Scientifique, UMR7104, 67404 Illkirch, France.
  • Iacono G; Institut National de la Santé et de la Recherche Médicale, U1258, 67404 Illkirch, France.
  • Curie A; CELPHEDIA, PHENOMIN, Institut Clinique de la Souris, 67404 Illkirch, France.
  • Riet F; CELPHEDIA, PHENOMIN, Institut Clinique de la Souris, 67404 Illkirch, France.
  • Martin C; Department of Molecular Biology, Radboud Institute for Molecular Life Sciences, Radboud University, 6500 HB Nijmegen, The Netherlands.
  • Loaëc N; Centre de Référence Déficiences Intellectuelles de Causes Rares, Hôpital Femmes Mères Enfants, Hospices Civils de Lyon, Institut des Sciences Cognitives, CNRS UMR5304, Université Claude Bernard Lyon1, 69675 Bron, France.
  • Birling MC; CELPHEDIA, PHENOMIN, Institut Clinique de la Souris, 67404 Illkirch, France.
  • Selloum M; Team Synapse in Cognition, Institut Interdisciplinaire de NeuroScience, Centre National de la Recherche Scientifique CNRS UMR5297, Université de Bordeaux, 33077 Bordeaux, France.
  • Normand E; Inserm UMR 1078, Université de Bretagne Occidentale, Faculté de Médecine et des Sciences de la Santé, Etablissement Français du Sang (EFS) Bretagne, CHRU Brest, Hôpital Morvan, Laboratoire de Génétique Moléculaire, 29200 Brest, France.
  • Pavlovic G; CELPHEDIA, PHENOMIN, Institut Clinique de la Souris, 67404 Illkirch, France.
  • Sorg T; CELPHEDIA, PHENOMIN, Institut Clinique de la Souris, 67404 Illkirch, France.
  • Stunnenberg HG; Team Synapse in Cognition, Institut Interdisciplinaire de NeuroScience, Centre National de la Recherche Scientifique CNRS UMR5297, Université de Bordeaux, 33077 Bordeaux, France.
  • Chelly J; Pole In Vivo, Institut Interdisciplinaire de NeuroScience, Centre National de la Recherche Scientifique CNRS UMR5297, Université de Bordeaux, 33077 Bordeaux, France.
  • Humeau Y; CELPHEDIA, PHENOMIN, Institut Clinique de la Souris, 67404 Illkirch, France.
  • Friocourt G; CELPHEDIA, PHENOMIN, Institut Clinique de la Souris, 67404 Illkirch, France.
  • Hérault Y; Department of Molecular Biology, Radboud Institute for Molecular Life Sciences, Radboud University, 6500 HB Nijmegen, The Netherlands.
Hum Mol Genet ; 27(12): 2138-2153, 2018 06 15.
Article em En | MEDLINE | ID: mdl-29659809
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Proteínas de Homeodomínio / Epilepsia / Transtornos do Neurodesenvolvimento Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Animals / Child / Child, preschool / Humans / Infant / Male Idioma: En Ano de publicação: 2018 Tipo de documento: Article
Texto completo
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Proteínas de Homeodomínio / Epilepsia / Transtornos do Neurodesenvolvimento Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Animals / Child / Child, preschool / Humans / Infant / Male Idioma: En Ano de publicação: 2018 Tipo de documento: Article