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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Zhou, Rongjia, Bonneaud, Nathalie, Yuan, Chao-Xing, de Santa Barbara, Pascal, Boizet, Brigitte, Tibor, Schomber, Scherer, Gerd, Roeder, Robert G., Poulat, Francis, Berta, Philippe
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Oxford University Press 2002
Pynciau:
Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC135763/
https://ncbi.nlm.nih.gov/pubmed/12136106
Tagiau: Ychwanegu Tag
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