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A genetic model for a central (septum transversum) congenital diaphragmatic hernia in mice lacking Slit3
Congenital diaphragmatic hernia (CDH) is a significant cause of pediatric mortality in humans with a heterogeneous and poorly understood etiology. Here we show that mice lacking Slit3 developed a central (septum transversum) CDH. Slit3 encodes a member of the Slit family of guidance molecules and is...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The National Academy of Sciences
2003
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC154325/ https://ncbi.nlm.nih.gov/pubmed/12702769 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0730709100 |
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