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...

Descrición completa

Detalles Bibliográficos

Publicado en:	Nucleic Acids Res
Principais autores:	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
Idioma:	Inglês
Publicado:	Oxford University Press 2002
Assuntos:	Article
Acceso en liña:	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
Tags:	Engadir etiqueta Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!