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.

Bone morphogenetic protein signaling by hemojuvelin regulates hepcidin expression.

Nat. Genet.
Babitt JL, Huang FW, Wrighting DM, Xia Y, Sidis Y, Samad TA, Campagna JA, Chung RT, Schneyer AL, Woolf CJ, Andrews NC, Lin HY.
| 04 09, 2006
122.

Mitochondrial DNA deletions are abundant and cause functional impairment in aged human substantia nigra neurons.

Nat. Genet.
Kraytsberg Y, Kudryavtseva E, McKee AC, Geula C, Kowall NW, Khrapko K.
| 04 09, 2006
123.

Long-range polony haplotyping of individual human chromosome molecules.

Nat. Genet.
Zhang K, Zhu J, Shendure J, Porreca GJ, Aach JD, Mitra RD, Church GM.
| 02 19, 2006
124.

Common deletion polymorphisms in the human genome.

Nat. Genet.
McCarroll SA, Hadnott TN, Perry GH, Sabeti PC, Zody MC, Barrett JC, Dallaire S, Gabriel SB, Lee C, Daly MJ, Altshuler DM.
| 2 10, 2006
125.

Polygenic control of Caenorhabditis elegans fat storage.

Nat. Genet.
Mak HY, Nelson LS, Basson M, Johnson CD, Ruvkun G.
| 02 05, 2006
126.

Nalp1b controls mouse macrophage susceptibility to anthrax lethal toxin.

Nat. Genet.
Boyden ED, Dietrich WF.
| 01 22, 2006
127.

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
128.

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
129.

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
130.

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
131.

Genetic variation in laboratory mice.

Nat. Genet.
Wade CM, Daly MJ.
| 10 29, 2005
132.

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
133.

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
134.

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
135.

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
136.

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
137.

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
138.

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
140.

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