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New TFII-I family target genes involved in embryonic development
Two members of the TFII-I family transcription factor genes, GTF2I and GTF2IRD1, are the prime candidates responsible for the craniofacial and cognitive abnormalities of Williams syndrome patients. We have previously generated mouse lines with targeted disruption of Gtf2ird1 and Gtf2i. Microarray an...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3092703/ https://ncbi.nlm.nih.gov/pubmed/19527686 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bbrc.2009.06.045 |
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