Essential functions of the Williams-Beuren syndrome-associated TFII-I genes in embryonic development

GTF2I and GTF2IRD1 encoding the multifunctional transcription factors TFII-I and BEN are clustered at the 7q11.23 region hemizygously deleted in Williams-Beuren syndrome (WBS), a complex multisystemic neurodevelopmental disorder. Although the biochemical properties of TFII-I family transcription fac...

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Detaylı Bibliyografya
Asıl Yazarlar: Enkhmandakh, Badam, Makeyev, Aleksandr V., Erdenechimeg, Lkhamsuren, Ruddle, Frank H., Chimge, Nyam-Osor, Tussie-Luna, Maria Isabel, Roy, Ananda L., Bayarsaihan, Dashzeveg
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: National Academy of Sciences 2009
Konular:
Biological Sciences
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2629217/
https://ncbi.nlm.nih.gov/pubmed/19109438
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0811531106
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