Cargando…
HEK‐293 cells expressing the cystic fibrosis transmembrane conductance regulator (CFTR): a model for studying regulation of Cl(−) transport
The Human Embryonic Kidney 293 cell line (HEK‐293) readily lends itself to genetic manipulation and is a common tool for biologists to overexpress proteins of interest and study their function and molecular regulation. Although these cells have some limitations, such as an inability to form resistiv...
Autores principales: | Domingue, Jada C., Ao, Mei, Sarathy, Jayashree, George, Alvin, Alrefai, Waddah A., Nelson, Deborah J., Rao, Mrinalini C. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wiley Periodicals, Inc.
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4270233/ https://www.ncbi.nlm.nih.gov/pubmed/25263207 http://dx.doi.org/10.14814/phy2.12158 |
Ejemplares similares
-
The Mechanistic Links between Insulin and Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Cl(−) Channel
por: Marunaka, Yoshinori
Publicado: (2017) -
Molecular dynamics study of Cl(−) permeation through cystic fibrosis transmembrane conductance regulator (CFTR)
por: Zeng, Zhi Wei, et al.
Publicado: (2023) -
The cystic fibrosis transmembrane conductance regulator (CFTR) and its stability
por: Meng, Xin, et al.
Publicado: (2016) -
Calcitonin receptor-mediated CFTR activation in human intestinal epithelial cells
por: Liu, Hongguang, et al.
Publicado: (2011) -
Relating the Disease Mutation Spectrum to the Evolution of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR)
por: Rishishwar, Lavanya, et al.
Publicado: (2012)