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Isogenic cell models of cystic fibrosis-causing variants in natively expressing pulmonary epithelial cells.

Resource Type

CF Research News

Authors

Valley HC, Bukis KM, Bell A, Cheng Y, Wong E, Jordan NJ, Allaire NE, Sivachenko A, Liang F, Bihler H, Thomas PJ, Mahiou J, Mense

References

J Cyst Fibros. 2018 Dec 15. pii: S1569-1993(18)30940-8. doi: 10.1016/j.jcf.2018.12.001. 

Document

PDF icon CF Research News Article [1]

Link

Scientific Abstract [2]

Keywords

CFTR [3]
CRISPR/Cas9 [4]
Model system [5]
Nonsense mutation [6]
Premature termination codon [7]

Date

Saturday, December 15, 2018

Featured resource article

Yes

Resource - Guideline Type

Other Guidelines [8]
Source URL:https://www.ecfs.eu/resource-article/cf-research-news/isogenic-cell-models-cystic-fibrosis-causing-variants-natively

Links
[1] https://www.ecfs.eu/sites/default/files/cf-research-article-files/JCF-D-18-00255R2_Mense_FINAL_070319_0.pdf [2] https://www.ncbi.nlm.nih.gov/pubmed/?term=ISOGENIC%20CELL%20MODELS%20OF%20CYSTIC%20FIBROSIS-CAUSING%20VARIANTS%20IN%20NATIVELY%20EXPRESSING%20PULMONARY%20EPITHELIAL%20CELLS [3] https://www.ecfs.eu/research-article-keywords/cftr [4] https://www.ecfs.eu/research-article-keywords/crisprcas9 [5] https://www.ecfs.eu/research-article-keywords/model-system [6] https://www.ecfs.eu/research-article-keywords/nonsense-mutation [7] https://www.ecfs.eu/research-article-keywords/premature-termination-codon [8] https://www.ecfs.eu/resource-guideline-type/other-guidelines