Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
4 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
CFAP54 is required for proper ciliary motility and assembly of the central pair apparatus in mice.
Mol Biol Cell. 2015 Sep 15;26(18):3140-9. doi: 10.1091/mbc.E15-02-0121. Epub 2015 Jul 29.
Mol Biol Cell. 2015.
PMID: 26224312
Free PMC article.
Genetic interaction between central pair apparatus genes CFAP221, CFAP54, and SPEF2 in mouse models of primary ciliary dyskinesia.
McKenzie CW, Lee L.
McKenzie CW, et al.
Sci Rep. 2020 Jul 23;10(1):12337. doi: 10.1038/s41598-020-69359-3.
Sci Rep. 2020.
PMID: 32704025
Free PMC article.
Item in Clipboard
Strain-specific differences in brain gene expression in a hydrocephalic mouse model with motile cilia dysfunction.
McKenzie CW, Preston CC, Finn R, Eyster KM, Faustino RS, Lee L.
McKenzie CW, et al.
Sci Rep. 2018 Sep 6;8(1):13370. doi: 10.1038/s41598-018-31743-5.
Sci Rep. 2018.
PMID: 30190587
Free PMC article.
Item in Clipboard
Enhanced response to pulmonary Streptococcus pneumoniae infection is associated with primary ciliary dyskinesia in mice lacking Pcdp1 and Spef2.
McKenzie CW, Klonoski JM, Maier T, Trujillo G, Vitiello PF, Huber VC, Lee L.
McKenzie CW, et al.
Cilia. 2013 Dec 20;2(1):18. doi: 10.1186/2046-2530-2-18.
Cilia. 2013.
PMID: 24360193
Free PMC article.
Item in Clipboard
Cite
Cite