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

41.

A retinitis pigmentosa GTPase regulator (RPGR)-deficient mouse model for X-linked retinitis pigmentosa (RP3).

Proc. Natl. Acad. Sci. U.S.A.
Hong DH, Pawlyk BS, Shang J, Sandberg MA, Berson EL, Li T.
| Mar 28, 2000
44.

Effect of vitamin A supplementation on rhodopsin mutants threonine-17 --> methionine and proline-347 --> serine in transgenic mice and in cell cultures.

Proc. Natl. Acad. Sci. U.S.A.
Li T, Sandberg MA, Pawlyk BS, Rosner B, Hayes KC, Dryja TP, Berson EL.
| Sep 29, 1998
45.

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
46.

Recessive mutations in the gene encoding the tubby-like protein TULP1 in patients with retinitis pigmentosa.

Nat. Genet.
Hagstrom SA, North MA, Nishina PL, Berson EL, Dryja TP.
| 2 14, 1998
47.

Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness.

Nat. Genet.
Yamamoto S, Sippel KC, Berson EL, Dryja TP.
| 2 1, 1997
49.

A prospective study of cigarette smoking and age-related macular degeneration in women.

JAMA.
Seddon JM, Willett WC, Speizer FE, Hankinson SE.
| Oct 9, 1996
50.

Images in clinical medicine. Herpes simplex virus corneal dendrite.

N. Engl. J. Med.
Ciulla TA, Johnson K.
| Dec 28, 1995
51.

Mutations in the gene encoding the alpha subunit of the rod cGMP-gated channel in autosomal recessive retinitis pigmentosa.

Proc. Natl. Acad. Sci. U.S.A.
Dryja TP, Finn JT, Peng YW, McGee TL, Berson EL, Yau KW.
| Oct 24, 1995
53.

Constitutive activation of phototransduction by K296E opsin is not a cause of photoreceptor degeneration.

Proc. Natl. Acad. Sci. U.S.A.
Li T, Franson WK, Gordon JW, Berson EL, Dryja TP.
| Apr 11, 1995
54.

Mutation spectrum of the gene encoding the beta subunit of rod phosphodiesterase among patients with autosomal recessive retinitis pigmentosa.

Proc. Natl. Acad. Sci. U.S.A.
McLaughlin ME, Ehrhart TL, Berson EL, Dryja TP.
| Apr 11, 1995
55.

Dietary carotenoids, vitamins A, C, and E, and advanced age-related macular degeneration. Eye Disease Case-Control Study Group.

JAMA.
Seddon JM, Ajani UA, Sperduto RD, Hiller R, Blair N, Burton TC, Farber MD, Gragoudas ES, Haller J, Miller DT.
| Nov 9, 1994
56.

Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci.

Science.
Kajiwara K, Berson EL, Dryja TP.
| Jun 10, 1994
59.

A null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa.

Nat. Genet.
Rosenfeld PJ, Cowley GS, McGee TL, Sandberg MA, Berson EL, Dryja TP.
| 6 1, 1992
60.

Prevalence and spectrum of germline mutations of the p53 gene among patients with sarcoma.

N. Engl. J. Med.
Toguchida J, Yamaguchi T, Dayton SH, Beauchamp RL, Herrera GE, Ishizaki K, Yamamuro T, Meyers PA, Little JB, Sasaki MS.
| May 14, 1992