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Generation and characterization of Six2 conditional mice
Heterozygous deletion of SIX2, which encodes a member of sine oculis homeobox family transcription factors, has recently been associated with the frontonasal dysplasia syndrome FND4. Previous studies showed that Six2 is expressed in multiple tissues during craniofacial development in mice, including...
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| Publicado no: | Genesis |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7363584/ https://ncbi.nlm.nih.gov/pubmed/32277572 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/dvg.23365 |
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