SOX9 interacts with a component of the human thyroid hormone receptor-associated protein complex

SOX9 transcription factor is involved in chondrocyte differentiation and male sex determination. Heterozygous defects in the human SOX9 gene cause campomelic dysplasia. The mechanisms behind SOX9 function are not understood despite the description of different target genes. This study therefore sets...

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Bibliografische gegevens

Gepubliceerd in:	Nucleic Acids Res
Hoofdauteurs:	Zhou, Rongjia, Bonneaud, Nathalie, Yuan, Chao-Xing, de Santa Barbara, Pascal, Boizet, Brigitte, Tibor, Schomber, Scherer, Gerd, Roeder, Robert G., Poulat, Francis, Berta, Philippe
Formaat:	Artigo
Taal:	Inglês
Gepubliceerd in:	Oxford University Press 2002
Onderwerpen:	Article
Online toegang:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC135763/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/12136106/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/gkf443
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