Literature DB >> 1672471

Subtle cerebellar phenotype in mice homozygous for a targeted deletion of the En-2 homeobox.

A L Joyner1, K Herrup, B A Auerbach, C A Davis, J Rossant.   

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.

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Year:  1991        PMID: 1672471     DOI: 10.1126/science.1672471

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  91 in total

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10.  Fatal infantile encephalopathy with olivopontocerebellar hypoplasia and micrencephaly. Report of three siblings.

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