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Model matchmaking via the Solve-RD Rare Disease Models & Mechanisms Network (RDMM-Europe).
Ellwanger, Kornelia; Brill, Julie A; de Boer, Elke; Efthymiou, Stephanie; Elgersma, Ype; Icmat, Marynelle; Lecoquierre, François; Lobato, Amanda G; Morleo, Manuela; Ori, Michela; Schaffer, Ashleigh E; Vitobello, Antonio; Wells, Sara; Yalcin, Binnaz; Zhai, R Grace; Sturm, Marc; Zurek, Birte; Graessner, Holm; Bermejo-Sánchez, Eva; Evangelista, Teresinha; Hoogerbrugge, Nicoline; Nigro, Vincenzo; Schüle, Rebecca; Verloes, Alain; Brunner, Han; Campeau, Philippe M; Lasko, Paul; Riess, Olaf.
Afiliación
  • Ellwanger K; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany. kornelia.ellwanger@med.uni-tuebingen.de.
  • Brill JA; The Hospital for Sick Children, Toronto, Ontario, Canada.
  • de Boer E; Department of Molecular Genetics, University of Toronto, Ontario, Canada.
  • Efthymiou S; Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Elgersma Y; Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Icmat M; Department of Neuromuscular Disorders, Queen Square Institute of Neurology, University College London, London, UK.
  • Lecoquierre F; Department of Clinical Genetics, Erasmus Medical Centre, Rotterdam, the Netherlands.
  • Lobato AG; The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Morleo M; Department of Molecular Genetics, University of Toronto, Ontario, Canada.
  • Ori M; Normandie Univ, UNIROUEN, Inserm U1245, CHU Rouen, Department of Genetics, FHU G4 Génomique, Rouen, France.
  • Schaffer AE; Department of Molecular and Cellular Pharmacology, University of Miami Miller School of Medicine, Miami, FL, USA.
  • Vitobello A; Graduate Program in Human Genetics and Genomics, University of Miami Miller School of Medicine, Miami, FL, USA.
  • Wells S; Department of Neurology, University of Chicago, Chicago, IL, USA.
  • Yalcin B; Telethon Institute of Genetics and Medicine (TIGEM), Pozzuoli (Na), Italy.
  • Zhai RG; Department of Precision Medicine, University of Campania Luigi Vanvitelli, Napoli, Italy.
  • Sturm M; Department of Biology, University of Pisa, Pisa, Italy.
  • Zurek B; Department of Genetics and Genome Sciences, Case Western Reserve University, Cleveland, OH, USA.
  • Graessner H; INSERM-Université de Bourgogne UMR1231 GAD «Génétique Des Anomalies du Développement¼, FHU-TRANSLAD, UFR Des Sciences de Santé, Dijon, France.
  • Bermejo-Sánchez E; Dijon University Hospital- UF innovation en diagnostic génomique, Dijon, France.
  • Evangelista T; The Mary Lyon Centre at MRC Harwell, Harwell Science Campus, Oxon, UK.
  • Hoogerbrugge N; Inserm Unit 1231, University of Bourgogne Franche-Comté, Dijon, France.
  • Nigro V; Department of Molecular and Cellular Pharmacology, University of Miami Miller School of Medicine, Miami, FL, USA.
  • Schüle R; Department of Neurology, University of Chicago, Chicago, IL, USA.
  • Verloes A; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
  • Brunner H; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
  • Campeau PM; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
  • Lasko P; Institute of Rare Diseases Research (IIER), Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
  • Riess O; Sorbonne Université, Inserm, Institut de Myologie, Centre de Recherche en Myologie, Paris, France.
Lab Anim (NY) ; 53(7): 161-165, 2024 Jul.
Article en En | MEDLINE | ID: mdl-38914824
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Enfermedades Raras / Modelos Animales de Enfermedad País/Región como asunto: Europa Idioma: En Revista: Lab Anim (NY) Año: 2024 Tipo del documento: Article
Texto completo
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Enfermedades Raras / Modelos Animales de Enfermedad País/Región como asunto: Europa Idioma: En Revista: Lab Anim (NY) Año: 2024 Tipo del documento: Article