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

121.

Nalp1b controls mouse macrophage susceptibility to anthrax lethal toxin.

Nat. Genet.
Boyden ED, Dietrich WF.
| 01 22, 2006
122.

Nras loss induces metastatic conversion of Rb1-deficient neuroendocrine thyroid tumor.

Nat. Genet.
Takahashi C, Contreras B, Iwanaga T, Takegami Y, Bakker A, Bronson RT, Noda M, Loda M, Hunt JL, Ewen ME.
| 12 20, 2005
123.

Genetic analysis of cavefish reveals molecular convergence in the evolution of albinism.

Nat. Genet.
Protas ME, Hersey C, Kochanek D, Zhou Y, Wilkens H, Jeffery WR, Zon LI, Borowsky R, Tabin CJ.
| 12 11, 2005
124.

A genome-wide RNA interference screen in Drosophila melanogaster cells for new components of the Hh signaling pathway.

Nat. Genet.
Nybakken K, Vokes SA, Lin TY, McMahon AP, Perrimon N.
| 11 20, 2005
125.

Inherited susceptibility to lung cancer may be associated with the T790M drug resistance mutation in EGFR.

Nat. Genet.
Bell DW, Gore I, Okimoto RA, Godin-Heymann N, Sordella R, Mulloy R, Sharma SV, Brannigan BW, Mohapatra G, Settleman J, Haber DA.
| 10 30, 2005
126.

Genetic variation in laboratory mice.

Nat. Genet.
Wade CM, Daly MJ.
| 10 29, 2005
127.

Efficiency and power in genetic association studies.

Nat. Genet.
de Bakker PI, Yelensky R, Pe'er I, Gabriel SB, Daly MJ, Altshuler D.
| 10 23, 2005
128.

Identification of a ferrireductase required for efficient transferrin-dependent iron uptake in erythroid cells.

Nat. Genet.
Ohgami RS, Campagna DR, Greer EL, Antiochos B, McDonald A, Chen J, Sharp JJ, Fujiwara Y, Barker JE, Fleming MD.
| 10 16, 2005
129.

A whole-genome admixture scan finds a candidate locus for multiple sclerosis susceptibility.

Nat. Genet.
Reich D, Patterson N, De Jager PL, McDonald GJ, Waliszewska A, Tandon A, Lincoln RR, DeLoa C, Fruhan SA, Cabre P, Bera O, Semana G, Kelly MA, Francis DA, Ardlie K, Khan O, Cree BA, Hauser SL, Oksenberg JR, Hafler DA.
| 09 25, 2005
130.

Distinct epigenetic changes in the stromal cells of breast cancers.

Nat. Genet.
Hu M, Yao J, Cai L, Bachman KE, van den Brûle F, Velculescu V, Polyak K.
| 07 10, 2005
131.

TACI is mutant in common variable immunodeficiency and IgA deficiency.

Nat. Genet.
Castigli E, Wilson SA, Garibyan L, Rachid R, Bonilla F, Schneider L, Geha RS.
| 07 10, 2005
132.

TRPC6 is a glomerular slit diaphragm-associated channel required for normal renal function.

Nat. Genet.
Reiser J, Polu KR, Möller CC, Kenlan P, Altintas MM, Wei C, Faul C, Herbert S, Villegas I, Avila-Casado C, McGee M, Sugimoto H, Brown D, Kalluri R, Mundel P, Smith PL, Clapham DE, Pollak MR.
| 05 27, 2005
133.

Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing loss.

Nat. Genet.
Schönberger J, Wang L, Shin JT, Kim SD, Depreux FF, Zhu H, Zon L, Pizard A, Kim JB, Macrae CA, Mungall AJ, Seidman JG, Seidman CE.
| 02 27, 2005
135.

Deletion of the NESP55 differentially methylated region causes loss of maternal GNAS imprints and pseudohypoparathyroidism type Ib.

Nat. Genet.
Bastepe M, Fröhlich LF, Linglart A, Abu-Zahra HS, Tojo K, Ward LM, Jüppner H.
| 12 12, 2004
136.

Modular epistasis in yeast metabolism.

Nat. Genet.
Segrè D, Deluna A, Church GM, Kishony R.
| 12 12, 2004
137.

Rapid analysis of the DNA-binding specificities of transcription factors with DNA microarrays.

Nat. Genet.
Mukherjee S, Berger MF, Jona G, Wang XS, Muzzey D, Snyder M, Young RA, Bulyk ML.
| 11 14, 2004
138.

Targeted gene alteration in Caenorhabditis elegans by gene conversion.

Nat. Genet.
Barrett PL, Fleming JT, Göbel V.
| 10 24, 2004
139.

MicroRNA-responsive 'sensor' transgenes uncover Hox-like and other developmentally regulated patterns of vertebrate microRNA expression.

Nat. Genet.
Mansfield JH, Harfe BD, Nissen R, Obenauer J, Srineel J, Chaudhuri A, Farzan-Kashani R, Zuker M, Pasquinelli AE, Ruvkun G, Sharp PA, Tabin CJ, McManus MT.
| 09 12, 2004
140.

Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome.

Nat. Genet.
Ferland RJ, Eyaid W, Collura RV, Tully LD, Hill RS, Al-Nouri D, Al-Rumayyan A, Topcu M, Gascon G, Bodell A, Shugart YY, Ruvolo M, Walsh CA.
| 08 22, 2004