Human sex reversal is caused by duplication or deletion of core enhancers upstream of SOX9
SRY and its target SOX9 are known key determinants in testis development. Here the authors by studying duplications and deletions upstream of SOX9 from patient samples with disorders of sex development (DSD) reveal enhancers for SOX9 critical for human sex development and DSD.
Guardado en:
Autores principales: | Brittany Croft, Thomas Ohnesorg, Jacqueline Hewitt, Josephine Bowles, Alexander Quinn, Jacqueline Tan, Vincent Corbin, Emanuele Pelosi, Jocelyn van den Bergen, Rajini Sreenivasan, Ingrid Knarston, Gorjana Robevska, Dung Chi Vu, John Hutson, Vincent Harley, Katie Ayers, Peter Koopman, Andrew Sinclair |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2018
|
Materias: | |
Acceso en línea: | https://doaj.org/article/e81c5e53ca074ef49a72aa8ab16f5fd8 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Author Correction: Human sex reversal is caused by duplication or deletion of core enhancers upstream of SOX9
por: Brittany Croft, et al.
Publicado: (2019) -
Failure of SOX9 regulation in 46XY disorders of sex development with SRY, SOX9 and SF1 mutations.
por: Kevin C Knower, et al.
Publicado: (2011) -
SOX17 regulates uterine epithelial–stromal cross-talk acting via a distal enhancer upstream of Ihh
por: Xiaoqiu Wang, et al.
Publicado: (2018) -
SOX9 duplication linked to intersex in deer.
por: Regina Kropatsch, et al.
Publicado: (2013) -
Formation of the embryonic organizer is restricted by the competitive influences of Fgf signaling and the SoxB1 transcription factors.
por: Cheng-Liang Kuo, et al.
Publicado: (2013)