Hes1 expression is reduced in Tbx1 null cells and is required for the development of structures affected in 22q11 deletion syndrome

22q11 deletion syndrome (22q11DS) is characterised by aberrant development of the pharyngeal apparatus and the heart with haploinsufficiency of the transcription factor TBX1 being considered the major underlying cause of the disease. Tbx1 mutations in mouse phenocopy the disorder. In order to identi...

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Detaylı Bibliyografya
Asıl Yazarlar: van Bueren, Kelly Lammerts, Papangeli, Irinna, Rochais, Francesca, Pearce, Kerra, Roberts, Catherine, Calmont, Amelie, Szumska, Dorota, Kelly, Robert G., Bhattacharya, Shoumo, Scambler, Peter J.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Elsevier 2010
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Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2877781/
https://ncbi.nlm.nih.gov/pubmed/20122914
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ydbio.2010.01.020
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