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
3 results
Filters applied: . Clear all
Page 1
Leber congenital amaurosis linked to AIPL1: a mouse model reveals destabilization of cGMP phosphodiesterase.
Proc Natl Acad Sci U S A. 2004 Sep 21;101(38):13897-902. doi: 10.1073/pnas.0404197101. Epub 2004 Sep 13.
Proc Natl Acad Sci U S A. 2004.
PMID: 15365178
Free PMC article.
AIPL1, the protein that is defective in Leber congenital amaurosis, is essential for the biosynthesis of retinal rod cGMP phosphodiesterase.
Liu X, Bulgakov OV, Wen XH, Woodruff ML, Pawlyk B, Yang J, Fain GL, Sandberg MA, Makino CL, Li T.
Liu X, et al.
Proc Natl Acad Sci U S A. 2004 Sep 21;101(38):13903-8. doi: 10.1073/pnas.0405160101. Epub 2004 Sep 13.
Proc Natl Acad Sci U S A. 2004.
PMID: 15365173
Free PMC article.
Item in Clipboard
Retinal degeneration in Aipl1-deficient mice: a new genetic model of Leber congenital amaurosis.
Dyer MA, Donovan SL, Zhang J, Gray J, Ortiz A, Tenney R, Kong J, Allikmets R, Sohocki MM.
Dyer MA, et al.
Brain Res Mol Brain Res. 2004 Dec 20;132(2):208-20. doi: 10.1016/j.molbrainres.2004.10.011.
Brain Res Mol Brain Res. 2004.
PMID: 15582159
Item in Clipboard
Cite
Cite