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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Enkhmandakh, Badam, Makeyev, Aleksandr V., Erdenechimeg, Lkhamsuren, Ruddle, Frank H., Chimge, Nyam-Osor, Tussie-Luna, Maria Isabel, Roy, Ananda L., Bayarsaihan, Dashzeveg
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: National Academy of Sciences 2009
Aiheet:
Biological Sciences
Linkit: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
Tagit: Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!

Samankaltaisia teoksia