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


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

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

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

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

Images in clinical medicine. Herpes simplex virus corneal dendrite.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Perforin-mediated myocardial damage in acute myocarditis.

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