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Human Dermal Fibroblasts Derived from Oculodentodigital Dysplasia Patients Suggest that Patients may have Wound Healing Defects
Oculodentodigital dysplasia (ODDD) is primarily an autosomal dominant human disease caused by any one of over 60 mutations in the GJA1 gene encoding the gap junction protein Cx43. In the present study, wound healing was investigated in a G60S ODDD mutant mouse model and by using dermal fibroblasts i...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3180923/ https://ncbi.nlm.nih.gov/pubmed/21305658 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/humu.21472 |
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