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yippee like 3 (ypel3) is a novel gene required for myelinating and perineurial glia development.
Blanco-Sánchez, Bernardo; Clément, Aurélie; Stednitz, Sara J; Kyle, Jennifer; Peirce, Judy L; McFadden, Marcie; Wegner, Jeremy; Phillips, Jennifer B; Macnamara, Ellen; Huang, Yan; Adams, David R; Toro, Camilo; Gahl, William A; Malicdan, May Christine V; Tifft, Cynthia J; Zink, Erika M; Bloodsworth, Kent J; Stratton, Kelly G; Koeller, David M; Metz, Thomas O; Washbourne, Philip; Westerfield, Monte.
Afiliação
  • Blanco-Sánchez B; Institute of Neuroscience, University of Oregon, Eugene, Oregon, United States of America.
  • Clément A; Institute of Neuroscience, University of Oregon, Eugene, Oregon, United States of America.
  • Stednitz SJ; Institute of Neuroscience, University of Oregon, Eugene, Oregon, United States of America.
  • Kyle J; Pacific Northwest National Laboratory, Richland, Washington, United States of America.
  • Peirce JL; Institute of Neuroscience, University of Oregon, Eugene, Oregon, United States of America.
  • McFadden M; Institute of Neuroscience, University of Oregon, Eugene, Oregon, United States of America.
  • Wegner J; Institute of Neuroscience, University of Oregon, Eugene, Oregon, United States of America.
  • Phillips JB; Institute of Neuroscience, University of Oregon, Eugene, Oregon, United States of America.
  • Macnamara E; National Institutes of Health Undiagnosed Diseases Program, Common Fund, Office of the Director, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Huang Y; Office of the Clinical Director, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Adams DR; National Institutes of Health Undiagnosed Diseases Program, Common Fund, Office of the Director, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Toro C; National Institutes of Health Undiagnosed Diseases Program, Common Fund, Office of the Director, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Gahl WA; Office of the Clinical Director, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Malicdan MCV; National Institutes of Health Undiagnosed Diseases Program, Common Fund, Office of the Director, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Tifft CJ; Office of the Clinical Director, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Zink EM; National Institutes of Health Undiagnosed Diseases Program, Common Fund, Office of the Director, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Bloodsworth KJ; Section of Human Biochemical Genetics, Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Stratton KG; National Institutes of Health Undiagnosed Diseases Program, Common Fund, Office of the Director, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Koeller DM; National Institutes of Health Undiagnosed Diseases Program, Common Fund, Office of the Director, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Metz TO; Office of the Clinical Director, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Washbourne P; Pacific Northwest National Laboratory, Richland, Washington, United States of America.
  • Westerfield M; Pacific Northwest National Laboratory, Richland, Washington, United States of America.
PLoS Genet ; 16(6): e1008841, 2020 06.
Article em En | MEDLINE | ID: mdl-32544203
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Regulação da Expressão Gênica no Desenvolvimento / Doenças Desmielinizantes Hereditárias do Sistema Nervoso Central / Proteínas Supressoras de Tumor / Neurogênese / Bainha de Mielina Tipo de estudo: Prognostic_studies Limite: Animals / Child / Female / Humans Idioma: En Revista: PLoS Genet Assunto da revista: GENETICA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
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Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Regulação da Expressão Gênica no Desenvolvimento / Doenças Desmielinizantes Hereditárias do Sistema Nervoso Central / Proteínas Supressoras de Tumor / Neurogênese / Bainha de Mielina Tipo de estudo: Prognostic_studies Limite: Animals / Child / Female / Humans Idioma: En Revista: PLoS Genet Assunto da revista: GENETICA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos