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Innate frequency-discrimination hyperacuity in Williams-Beuren syndrome mice.
Davenport, Christopher M; Teubner, Brett J W; Han, Seung Baek; Patton, Mary H; Eom, Tae-Yeon; Garic, Dusan; Lansdell, Benjamin J; Shirinifard, Abbas; Chang, Ti-Cheng; Klein, Jonathon; Pruett-Miller, Shondra M; Blundon, Jay A; Zakharenko, Stanislav S.
Afiliación
  • Davenport CM; Department of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
  • Teubner BJW; Department of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
  • Han SB; Department of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
  • Patton MH; Department of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
  • Eom TY; Department of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
  • Garic D; Department of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
  • Lansdell BJ; Department of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
  • Shirinifard A; Department of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
  • Chang TC; Center for Applied Bioinformatics, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
  • Klein J; Department of Cell and Molecular Biology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
  • Pruett-Miller SM; Department of Cell and Molecular Biology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
  • Blundon JA; Department of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
  • Zakharenko SS; Department of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA. Electronic address: stanislav.zakharenko@stjude.org.
Cell ; 185(21): 3877-3895.e21, 2022 10 13.
Article en En | MEDLINE | ID: mdl-36152627
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Corteza Auditiva / Síndrome de Williams Tipo de estudio: Prognostic_studies Idioma: En Revista: Cell Año: 2022 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Corteza Auditiva / Síndrome de Williams Tipo de estudio: Prognostic_studies Idioma: En Revista: Cell Año: 2022 Tipo del documento: Article