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

JAMA.
Seddon JM, Willett WC, Speizer FE, Hankinson SE.
| Oct 9, 1996
42.

Images in clinical medicine. Herpes simplex virus corneal dendrite.

N. Engl. J. Med.
Ciulla TA, Johnson K.
| Dec 28, 1995
43.

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
45.

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
46.

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
47.

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
48.

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

Science.
Kajiwara K, Berson EL, Dryja TP.
| Jun 10, 1994
51.

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
52.

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
53.

Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa.

Nature.
Kajiwara K, Hahn LB, Mukai S, Travis GH, Berson EL, Dryja TP.
| Dec 12, 1991
54.

Mutation spectrum of the rhodopsin gene among patients with autosomal dominant retinitis pigmentosa.

Proc. Natl. Acad. Sci. U.S.A.
Dryja TP, Hahn LB, Cowley GS, McGee TL, Berson EL.
| Oct 15, 1991
55.

Oncogenic germ-line mutations in Sp1 and ATF sites in the human retinoblastoma gene.

Nature.
Sakai T, Ohtani N, McGee TL, Robbins PD, Dryja TP.
| Sep 5, 1991
56.

Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa.

N. Engl. J. Med.
Dryja TP, McGee TL, Hahn LB, Cowley GS, Olsson JE, Reichel E, Sandberg MA, Berson EL.
| Nov 8, 1990
57.

Perforin-mediated myocardial damage in acute myocarditis.

Lancet.
Young LH, Joag SV, Zheng LM, Lee CP, Lee YS, Young JD.
| Oct 27, 1990
58.

A point mutation of the rhodopsin gene in one form of retinitis pigmentosa.

Nature.
Dryja TP, McGee TL, Reichel E, Hahn LB, Cowley GS, Yandell DW, Sandberg MA, Berson EL.
| Jan 25, 1990
60.

Short, direct repeats at the breakpoints of deletions of the retinoblastoma gene.

Proc. Natl. Acad. Sci. U.S.A.
Canning S, Dryja TP.
| 7 1, 1989