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PEA15 loss of function and defective cerebral development in the domestic cat.
Graff, Emily C; Cochran, J Nicholas; Kaelin, Christopher B; Day, Kenneth; Gray-Edwards, Heather L; Watanabe, Rie; Koehler, Jey W; Falgoust, Rebecca A; Prokop, Jeremy W; Myers, Richard M; Cox, Nancy R; Barsh, Gregory S; Martin, Douglas R.
Afiliación
  • Graff EC; Department of Pathobiology, College of Veterinary Medicine, Auburn University, Auburn, United States of America.
  • Cochran JN; Scott-Ritchey Research Center, College of Veterinary Medicine, Auburn University, Auburn, Alabama, United States of America.
  • Kaelin CB; Center for Neuroscience Initiative, Auburn University, Auburn, AL, United States of America Alabama, United States of America.
  • Day K; HudsonAlpha Institute for Biotechnology, Huntsville, AL, United States of America.
  • Gray-Edwards HL; HudsonAlpha Institute for Biotechnology, Huntsville, AL, United States of America.
  • Watanabe R; HudsonAlpha Institute for Biotechnology, Huntsville, AL, United States of America.
  • Koehler JW; Scott-Ritchey Research Center, College of Veterinary Medicine, Auburn University, Auburn, Alabama, United States of America.
  • Falgoust RA; Department of Anatomy Physiology and Pharmacology, College of Veterinary Medicine, Auburn University, Auburn, Alabama, United States of America.
  • Prokop JW; Department of Pathobiology, College of Veterinary Medicine, Auburn University, Auburn, United States of America.
  • Myers RM; Department of Pathobiology, College of Veterinary Medicine, Auburn University, Auburn, United States of America.
  • Cox NR; Center for Neuroscience Initiative, Auburn University, Auburn, AL, United States of America Alabama, United States of America.
  • Barsh GS; Scott-Ritchey Research Center, College of Veterinary Medicine, Auburn University, Auburn, Alabama, United States of America.
  • Martin DR; HudsonAlpha Institute for Biotechnology, Huntsville, AL, United States of America.
PLoS Genet ; 16(12): e1008671, 2020 12.
Article en En | MEDLINE | ID: mdl-33290415
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fosfoproteínas / Encefalopatías / Enfermedades de los Gatos / Corteza Cerebral / Proteínas Reguladoras de la Apoptosis / Mutación con Pérdida de Función Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: PLoS Genet Asunto de la revista: GENETICA Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fosfoproteínas / Encefalopatías / Enfermedades de los Gatos / Corteza Cerebral / Proteínas Reguladoras de la Apoptosis / Mutación con Pérdida de Función Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: PLoS Genet Asunto de la revista: GENETICA Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos