Cargando…
Regulatory dynamics of 11p13 suggest a role for EHF in modifying CF lung disease severity
Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene cause cystic fibrosis (CF), but are not good predictors of lung phenotype. Genome-wide association studies (GWAS) previously identified additional genomic sites associated with CF lung disease severity. One of these, at...
Autores principales: | Stolzenburg, Lindsay R., Yang, Rui, Kerschner, Jenny L., Fossum, Sara, Xu, Matthew, Hoffmann, Andrew, Lamar, Kay-Marie, Ghosh, Sujana, Wachtel, Sarah, Leir, Shih-Hsing, Harris, Ann |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5587731/ https://www.ncbi.nlm.nih.gov/pubmed/28549169 http://dx.doi.org/10.1093/nar/gkx482 |
Ejemplares similares
-
Looping of upstream cis-regulatory elements is required for CFTR expression in human airway epithelial cells
por: NandyMazumdar, Monali, et al.
Publicado: (2020) -
Differential contribution of cis-regulatory elements to higher order chromatin structure and expression of the CFTR locus
por: Yang, Rui, et al.
Publicado: (2016) -
Nucleosome mapping across the CFTR locus identifies novel regulatory factors
por: Yigit, Erbay, et al.
Publicado: (2013) -
Ets homologous factor regulates pathways controlling response to injury in airway epithelial cells
por: Fossum, Sara L., et al.
Publicado: (2014) -
Coordinate regulation of ELF5 and EHF at the chr11p13 CF modifier region
por: Swahn, Hannah, et al.
Publicado: (2019)