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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Main Authors: van Bueren, Kelly Lammerts, Papangeli, Irinna, Rochais, Francesca, Pearce, Kerra, Roberts, Catherine, Calmont, Amelie, Szumska, Dorota, Kelly, Robert G., Bhattacharya, Shoumo, Scambler, Peter J.
Formato: Artigo
Idioma:Inglês
Publicado em: Elsevier 2010
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Article
Acesso em linha: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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