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Ocular Coloboma and Dorsoventral Neuroretinal Patterning Defects in Lrp6 Mutant Eyes

Coloboma, an ocular birth defect seen in humans and other species, is caused by incomplete closure of the optic fissure. Here, we demonstrate that genetic deletion of Lrp6, a bottleneck coreceptor in the canonical Wnt signaling pathway, results in ocular coloboma and neuroretinal patterning defects...

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Detalhes bibliográficos
Main Authors: Zhou, Cheng-Ji, Molotkov, Andrei, Song, Lanying, Li, Yunhong, Pleasure, David E., Pleasure, Samuel J., Wang, Ya-Zhou
Formato: Artigo
Idioma:Inglês
Publicado em: 2008
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2727282/
https://ncbi.nlm.nih.gov/pubmed/18985738
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/dvdy.21770
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