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Dominant-acting CSF1R variants cause microglial depletion and altered astrocytic phenotype in zebrafish and adult-onset leukodystrophy.
Berdowski, Woutje M; van der Linde, Herma C; Breur, Marjolein; Oosterhof, Nynke; Beerepoot, Shanice; Sanderson, Leslie; Wijnands, Lieve I; de Jong, Patrick; Tsai-Meu-Chong, Elisa; de Valk, Walter; de Witte, Moniek; van IJcken, Wilfred F J; Demmers, Jeroen; van der Knaap, Marjo S; Bugiani, Marianna; Wolf, Nicole I; van Ham, Tjakko J.
Afiliación
  • Berdowski WM; Department of Clinical Genetics, Erasmus MC, University Medical Center Rotterdam, PO Box 2040, 3000 CA, Rotterdam, The Netherlands.
  • van der Linde HC; Department of Clinical Genetics, Erasmus MC, University Medical Center Rotterdam, PO Box 2040, 3000 CA, Rotterdam, The Netherlands.
  • Breur M; Department of Child Neurology, Amsterdam Leukodystrophy Center, Emma Children's Hospital, Amsterdam University Medical Centers, Vrije Universiteit, De Boelelaan 1117, 1081 HV, Amsterdam, The Netherlands.
  • Oosterhof N; Amsterdam Neuroscience, Amsterdam University Medical Centers, Vrije Universiteit, De Boelelaan 1117, 1081 HV, Amsterdam, The Netherlands.
  • Beerepoot S; Department of Pathology, Neuroscience Campus Amsterdam, VU University Medical Center, Amsterdam, The Netherlands.
  • Sanderson L; European Research Institute for the Biology of Ageing (ERIBA), University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
  • Wijnands LI; Department of Child Neurology, Amsterdam Leukodystrophy Center, Emma Children's Hospital, Amsterdam University Medical Centers, Vrije Universiteit, De Boelelaan 1117, 1081 HV, Amsterdam, The Netherlands.
  • de Jong P; Amsterdam Neuroscience, Amsterdam University Medical Centers, Vrije Universiteit, De Boelelaan 1117, 1081 HV, Amsterdam, The Netherlands.
  • Tsai-Meu-Chong E; Department of Clinical Genetics, Erasmus MC, University Medical Center Rotterdam, PO Box 2040, 3000 CA, Rotterdam, The Netherlands.
  • de Valk W; Department of Clinical Genetics, Erasmus MC, University Medical Center Rotterdam, PO Box 2040, 3000 CA, Rotterdam, The Netherlands.
  • de Witte M; Department of Clinical Genetics, Erasmus MC, University Medical Center Rotterdam, PO Box 2040, 3000 CA, Rotterdam, The Netherlands.
  • van IJcken WFJ; Department of Clinical Genetics, Erasmus MC, University Medical Center Rotterdam, PO Box 2040, 3000 CA, Rotterdam, The Netherlands.
  • Demmers J; Department of Clinical Genetics, Erasmus MC, University Medical Center Rotterdam, PO Box 2040, 3000 CA, Rotterdam, The Netherlands.
  • van der Knaap MS; Hematology Department, University Medical Center, Utrecht, The Netherlands.
  • Bugiani M; Center for Biomics, Erasmus MC University Medical Center, Rotterdam, The Netherlands.
  • Wolf NI; Proteomics Center, Erasmus University Medical Center, Wytemaweg 80, 3015 CN, Rotterdam, The Netherlands.
  • van Ham TJ; Department of Child Neurology, Amsterdam Leukodystrophy Center, Emma Children's Hospital, Amsterdam University Medical Centers, Vrije Universiteit, De Boelelaan 1117, 1081 HV, Amsterdam, The Netherlands.
Acta Neuropathol ; 144(2): 211-239, 2022 08.
Article en En | MEDLINE | ID: mdl-35713703
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades Desmielinizantes / Enfermedades por Almacenamiento Lisosomal / Proteínas Tirosina Quinasas Receptoras / Enfermedades Neurodegenerativas / Proteínas de Pez Cebra / Leucoencefalopatías Tipo de estudio: Prognostic_studies Límite: Adult / Animals / Humans Idioma: En Revista: Acta Neuropathol Año: 2022 Tipo del documento: Article País de afiliación: Países Bajos Pais de publicación: Alemania
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades Desmielinizantes / Enfermedades por Almacenamiento Lisosomal / Proteínas Tirosina Quinasas Receptoras / Enfermedades Neurodegenerativas / Proteínas de Pez Cebra / Leucoencefalopatías Tipo de estudio: Prognostic_studies Límite: Adult / Animals / Humans Idioma: En Revista: Acta Neuropathol Año: 2022 Tipo del documento: Article País de afiliación: Países Bajos Pais de publicación: Alemania