Impaired neural development in a zebrafish model for Lowe syndrome

Lowe syndrome, which is characterized by defects in the central nervous system, eyes and kidneys, is caused by mutation of the phosphoinositide 5-phosphatase OCRL1. The mechanisms by which loss of OCRL1 leads to the phenotypic manifestations of Lowe syndrome are currently unclear, in part, owing to...

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Detalles Bibliográficos
Autores principales: Ramirez, Irene Barinaga-Rementeria, Pietka, Grzegorz, Jones, David R., Divecha, Nullin, Alia, A., Baraban, Scott C., Hurlstone, Adam F. L., Lowe, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2012
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3313792/
https://www.ncbi.nlm.nih.gov/pubmed/22210625
http://dx.doi.org/10.1093/hmg/ddr608

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3313792/
https://www.ncbi.nlm.nih.gov/pubmed/22210625
http://dx.doi.org/10.1093/hmg/ddr608

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