Paper Chase is a research database designed to offer abstracts of research articles published in journals that have a highly rated impact factor as determined by ISI Impact Factor and PageRank. Abstracts are organized by date, with the most recently published papers listed first. 

Paper Chase


AIPL1, the protein that is defective in Leber congenital amaurosis, is essential for the biosynthesis of retinal rod cGMP phosphodiesterase.

Proc. Natl. Acad. Sci. U.S.A.
Liu X, Bulgakov OV, Wen XH, Woodruff ML, Pawlyk B, Yang J, Fain GL, Sandberg MA, Makino CL, Li T.
| Sep 21, 2004

The retinitis pigmentosa GTPase regulator (RPGR)- interacting protein: subserving RPGR function and participating in disk morphogenesis.

Proc. Natl. Acad. Sci. U.S.A.
Zhao Y, Hong DH, Pawlyk B, Yue G, Adamian M, Grynberg M, Godzik A, Li T.
| Apr 01, 2003

Functional domains of the cone-rod homeobox (CRX) transcription factor.

J. Biol. Chem.
Chau KY, Chen S, Zack DJ, Ono SJ.
| Nov 24, 2000

Retinopathy and attenuated circadian entrainment in Crx-deficient mice.

Nat. Genet.
Furukawa T, Morrow EM, Li T, Davis FC, Cepko CL.
| 12 2, 1999

Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis.

Proc. Natl. Acad. Sci. U.S.A.
Morimura H, Fishman GA, Grover SA, Fulton AB, Berson EL, Dryja TP.
| Mar 17, 1998
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