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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Publicado en:	Nucleic Acids Res
Autores principales:	Zhou, Rongjia, Bonneaud, Nathalie, Yuan, Chao-Xing, de Santa Barbara, Pascal, Boizet, Brigitte, Tibor, Schomber, Scherer, Gerd, Roeder, Robert G., Poulat, Francis, Berta, Philippe
Formato:	Artigo
Lenguaje:	Inglês
Publicado:	Oxford University Press 2002
Materias:	Article
Acceso en línea:	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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