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Pathogenic TRIO variants associated with neurodevelopmental disorders perturb the molecular regulation of TRIO and axon pathfinding in vivo.
Bonnet, Maxime; Roche, Fiona; Fagotto-Kaufmann, Christine; Gazdagh, Gabriella; Truong, Iona; Comunale, Franck; Barbosa, Sonia; Bonhomme, Marion; Nafati, Nicolas; Hunt, David; Rodriguez, Monserrat Pons; Chaudhry, Ayeshah; Shears, Deborah; Madruga, Marcos; Vansenne, Fleur; Curie, Aurore; Kajava, Andrey V; Baralle, Diana; Fassier, Coralie; Debant, Anne; Schmidt, Susanne.
Afiliação
  • Bonnet M; Centre de Recherche en Biologie Cellulaire de Montpellier (CRBM), University of Montpellier, CNRS, Montpellier, France.
  • Roche F; Institut de la Vision, Sorbonne University, CNRS, INSERM, Paris, France.
  • Fagotto-Kaufmann C; Centre de Recherche en Biologie Cellulaire de Montpellier (CRBM), University of Montpellier, CNRS, Montpellier, France.
  • Gazdagh G; Faculty of Medicine, University of Southampton, Southampton, SO16 5YA, UK.
  • Truong I; Wessex Clinical Genetics Service, University Hospital Southampton National Health Service Foundation Trust, Southampton, SO16 5YA, UK.
  • Comunale F; Centre de Recherche en Biologie Cellulaire de Montpellier (CRBM), University of Montpellier, CNRS, Montpellier, France.
  • Barbosa S; Institut de Génomique Fonctionnelle (IGF), Université de Montpellier, CNRS, INSERM, Montpellier, France.
  • Bonhomme M; Centre de Recherche en Biologie Cellulaire de Montpellier (CRBM), University of Montpellier, CNRS, Montpellier, France.
  • Nafati N; Centre de Recherche en Biologie Cellulaire de Montpellier (CRBM), University of Montpellier, CNRS, Montpellier, France.
  • Hunt D; Centre de Recherche en Biologie Cellulaire de Montpellier (CRBM), University of Montpellier, CNRS, Montpellier, France.
  • Rodriguez MP; Montpellier Ressources Imagerie, BioCampus, University of Montpellier, CNRS, INSERM, 34293, Montpellier, France.
  • Chaudhry A; Wessex Clinical Genetics Service, Princess Anne Hospital, Southampton, SO16 5YA, UK.
  • Shears D; Hospital Universitari Son Espases, 07120, Palma, Illes Balears, Spain.
  • Madruga M; Department of Laboratory Medicine and Genetics, Trillium Health Partners, Mississauga, ON, Canada.
  • Vansenne F; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada.
  • Curie A; Oxford Centre for Genomic Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Kajava AV; Hospital Viamed Santa Ángela De la Cruz, Sevilla, 41014, Spain.
  • Baralle D; Department of Clinical Genetics, University Medical Center, Groningen, 9713 GZ, Groningen, The Netherlands.
  • Fassier C; Reference Center for Intellectual Disability from rare causes, Department of Child Neurology, Woman Mother and Child Hospital, Hospices Civils de Lyon, Lyon Neuroscience Research Centre, CNRS UMR5292, INSERM U1028, Université de Lyon, Bron, France.
  • Debant A; Centre de Recherche en Biologie Cellulaire de Montpellier (CRBM), University of Montpellier, CNRS, Montpellier, France.
  • Schmidt S; Faculty of Medicine, University of Southampton, Southampton, SO16 5YA, UK.
Mol Psychiatry ; 28(4): 1527-1544, 2023 04.
Article em En | MEDLINE | ID: mdl-36717740
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos do Neurodesenvolvimento / Orientação de Axônios Tipo de estudo: Guideline / Prognostic_studies / Risk_factors_studies Limite: Animals / Humans Idioma: En Revista: Mol Psychiatry Assunto da revista: BIOLOGIA MOLECULAR / PSIQUIATRIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: França
Texto completo
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XML
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos do Neurodesenvolvimento / Orientação de Axônios Tipo de estudo: Guideline / Prognostic_studies / Risk_factors_studies Limite: Animals / Humans Idioma: En Revista: Mol Psychiatry Assunto da revista: BIOLOGIA MOLECULAR / PSIQUIATRIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: França