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Subtle cerebellar phenotype in mice homozygous for a targeted deletion of the En-2 homeobox.
Joyner, A L; Herrup, K; Auerbach, B A; Davis, C A; Rossant, J.
Afiliación
  • Joyner AL; Samuel Lunenfeld Research Institute, Mount Sinai Hospital, Toronto, Ontario, Canada.
Science ; 251(4998): 1239-43, 1991 Mar 08.
Article en En | MEDLINE | ID: mdl-1672471
ABSTRACT
The two mouse genes, En-1 and En-2, that are homologs of the Drosophila segmentation gene engrailed, show overlapping spatially restricted patterns of expression in the neural tube during embryogenesis, suggestive of a role in regional specification. Mice homozygous for a targeted mutation that deletes the homeobox were viable and showed no obvious defects in embryonic development. This may be due to functional redundancy of En-2 and the related En-1 gene product during embryogenesis. Consistent with this hypothesis, the mutant mice showed abnormal foliation in the adult cerebellum, where En-2, and not En-1, is normally expressed.
Asunto(s)
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Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Cerebelo / Genes Homeobox / Deleción Cromosómica Límite: Animals Idioma: En Revista: Science Año: 1991 Tipo del documento: Article País de afiliación: Canadá
Buscar en Google
Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Cerebelo / Genes Homeobox / Deleción Cromosómica Límite: Animals Idioma: En Revista: Science Año: 1991 Tipo del documento: Article País de afiliación: Canadá