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Altered distribution of ATG9A and accumulation of axonal aggregates in neurons from a mouse model of AP-4 deficiency syndrome.
De Pace, Raffaella; Skirzewski, Miguel; Damme, Markus; Mattera, Rafael; Mercurio, Jeffrey; Foster, Arianne M; Cuitino, Loreto; Jarnik, Michal; Hoffmann, Victoria; Morris, H Douglas; Han, Tae-Un; Mancini, Grazia M S; Buonanno, Andrés; Bonifacino, Juan S.
  • De Pace R; Cell Biology and Neurobiology Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Skirzewski M; Section of Molecular Neurobiology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Damme M; Institute of Biochemistry, Christian-Albrechts University of Kiel, Kiel, Germany.
  • Mattera R; Cell Biology and Neurobiology Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Mercurio J; Cell Biology and Neurobiology Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Foster AM; Cell Biology and Neurobiology Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Cuitino L; Cell Biology and Neurobiology Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Jarnik M; Cell Biology and Neurobiology Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Hoffmann V; Division of Veterinary Resources, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Morris HD; NIH Mouse Imaging Facility/NIH Magnetic Resonance Facility, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Han TU; Laboratory of Communication Disorders, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Mancini GMS; Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Buonanno A; Section of Molecular Neurobiology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Bonifacino JS; Cell Biology and Neurobiology Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, United States of America.
PLoS Genet ; 14(4): e1007363, 2018 04.
Article en En | MEDLINE | ID: mdl-29698489
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Paraplejía Espástica Hereditaria / Proteínas de Transporte Vesicular / Complejo 4 de Proteína Adaptadora / Proteínas Relacionadas con la Autofagia / Proteínas de la Membrana Tipo de estudio: Prognostic_studies Límite: Animals / Female / Humans / Male Idioma: En Año: 2018 Tipo del documento: Article
Texto completo
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Paraplejía Espástica Hereditaria / Proteínas de Transporte Vesicular / Complejo 4 de Proteína Adaptadora / Proteínas Relacionadas con la Autofagia / Proteínas de la Membrana Tipo de estudio: Prognostic_studies Límite: Animals / Female / Humans / Male Idioma: En Año: 2018 Tipo del documento: Article