A carregar...
Absence of Chx10 Causes Neural Progenitors to Persist in the Adult Retina
PURPOSE: Mutation of the Chx10 homeobox gene in mice and humans causes congenital blindness and microphthalmia (small eyes). This study used Chx10(−/−) (ocular retardation) mice to investigate how lack of Chx10 affects progenitor/stem cell behavior in the retina and ciliary epithelium (CE). METHODS:...
Na minha lista:
| Main Authors: | , , , , , , |
|---|---|
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2006
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2423807/ https://ncbi.nlm.nih.gov/pubmed/16384989 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.05-0428 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|
A carregar...