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Modeling the Mutational and Phenotypic Landscapes of Pelizaeus-Merzbacher Disease with Human iPSC-Derived Oligodendrocytes.
Nevin, Zachary S; Factor, Daniel C; Karl, Robert T; Douvaras, Panagiotis; Laukka, Jeremy; Windrem, Martha S; Goldman, Steven A; Fossati, Valentina; Hobson, Grace M; Tesar, Paul J.
Afiliación
  • Nevin ZS; Department of Genetics and Genome Sciences, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA.
  • Factor DC; Department of Genetics and Genome Sciences, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA.
  • Karl RT; Department of Genetics and Genome Sciences, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA.
  • Douvaras P; New York Stem Cell Foundation Research Institute, New York, NY 10032, USA.
  • Laukka J; Departments of Neurology and Neuroscience, College of Medicine and Life Science, University of Toledo, Toledo, OH 43614, USA.
  • Windrem MS; Center for Translational Neuromedicine, University of Rochester Medical Center, Rochester, NY 14642, USA.
  • Goldman SA; Center for Translational Neuromedicine, University of Rochester Medical Center, Rochester, NY 14642, USA; Center for Neuroscience, Faculty of Medicine and Health Sciences, University of Copenhagen, 2200 Copenhagen, Denmark.
  • Fossati V; New York Stem Cell Foundation Research Institute, New York, NY 10032, USA.
  • Hobson GM; Nemours Biomedical Research, Alfred I. duPont Hospital for Children, Wilmington, DE 19803, USA; Department of Biological Sciences, University of Delaware, Newark, DE 19716, USA; Department of Pediatrics, Jefferson Medical College, Thomas Jefferson University, Philadelphia, PA 19107, USA.
  • Tesar PJ; Department of Genetics and Genome Sciences, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA. Electronic address: paul.tesar@case.edu.
Am J Hum Genet ; 100(4): 617-634, 2017 Apr 06.
Article en En | MEDLINE | ID: mdl-28366443

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Oligodendroglía / Enfermedad de Pelizaeus-Merzbacher Límite: Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Am J Hum Genet Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Oligodendroglía / Enfermedad de Pelizaeus-Merzbacher Límite: Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Am J Hum Genet Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos
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