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


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

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

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

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

Expression of transducin in retinal rod photoreceptor outer segments.

Roof DJ, Heth CA.
| Aug 12, 1988

Adult supraglottitis. A prospective analysis.

Shapiro J, Eavey RD, Baker AS.
| 1 22, 1988

Prediction of the risk of hereditary retinoblastoma, using DNA polymorphisms within the retinoblastoma gene.

N. Engl. J. Med.
Wiggs J, Nordenskjöld M, Yandell D, Rapaport J, Grondin V, Janson M, Werelius B, Petersen R, Craft A, Riedel K.
| Jan 21, 1988