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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Autors principals: Zhou, Rongjia, Bonneaud, Nathalie, Yuan, Chao-Xing, de Santa Barbara, Pascal, Boizet, Brigitte, Tibor, Schomber, Scherer, Gerd, Roeder, Robert G., Poulat, Francis, Berta, Philippe
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 2002
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Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC135763/
https://ncbi.nlm.nih.gov/pubmed/12136106
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