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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...

Deskribapen osoa

Gorde:
Argitaratua izan da:Nucleic Acids Res
Egile Nagusiak: Zhou, Rongjia, Bonneaud, Nathalie, Yuan, Chao-Xing, de Santa Barbara, Pascal, Boizet, Brigitte, Tibor, Schomber, Scherer, Gerd, Roeder, Robert G., Poulat, Francis, Berta, Philippe
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Oxford University Press 2002
Gaiak:
Article
Sarrera elektronikoa: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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