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Ectodysplasin regulates the lymphotoxin-β pathway for hair differentiation
Mutations in the EDA gene cause anhidrotic/hypohidrotic ectodermal dysplasia, a disorder characterized by defective formation of hair, sweat glands, and teeth in humans and in a mouse model, “Tabby” (Ta). The gene encodes ectodysplasin, a TNF ligand family member that activates the NF-κB-signaling p...
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| Autors principals: | , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
National Academy of Sciences
2006
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1482580/ https://ncbi.nlm.nih.gov/pubmed/16738056 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0509678103 |
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