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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Hlavní autoři: Zhou, Rongjia, Bonneaud, Nathalie, Yuan, Chao-Xing, de Santa Barbara, Pascal, Boizet, Brigitte, Tibor, Schomber, Scherer, Gerd, Roeder, Robert G., Poulat, Francis, Berta, Philippe
Médium: Artigo
Jazyk:Inglês
Vydáno: Oxford University Press 2002
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Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC135763/
https://ncbi.nlm.nih.gov/pubmed/12136106
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