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.

Generation of hair cells by stepwise differentiation of embryonic stem cells.

Proc. Natl. Acad. Sci. U.S.A.
Li H, Roblin G, Liu H, Heller S.
| Nov 11, 2003
42.

Pluripotent stem cells from the adult mouse inner ear.

Nat. Med.
Li H, Liu H, Heller S.
| 08 31, 2003
43.

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 1, 2003
44.

Chlamydia pneumoniae as an emerging risk factor in cardiovascular disease.

JAMA.
Kalayoglu MV, Libby P, Byrne GI.
| Dec 4, 2002
45.

Revised estimates of human cochlear tuning from otoacoustic and behavioral measurements.

Proc. Natl. Acad. Sci. U.S.A.
Shera CA, Guinan JJ, Oxenham AJ.
| Mar 5, 2002
47.

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
50.

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
51.

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
52.

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
53.

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
55.

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
56.

Images in clinical medicine. Herpes simplex virus corneal dendrite.

N. Engl. J. Med.
Ciulla TA, Johnson K.
| Dec 28, 1995
57.

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
59.

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
60.

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