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


Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein.

Nat. Genet.
Watts GD, Wymer J, Kovach MJ, Mehta SG, Mumm S, Darvish D, Pestronk A, Whyte MP, Kimonis VE.
| 03 21, 2004

Gene expression-based high-throughput screening(GE-HTS) and application to leukemia differentiation.

Nat. Genet.
Stegmaier K, Ross KN, Colavito SA, O'Malley S, Stockwell BR, Golub TR.
| 02 08, 2004

The hyh mutation uncovers roles for alpha Snap in apical protein localization and control of neural cell fate.

Nat. Genet.
Chae TH, Kim S, Marz KE, Hanson PI, Walsh CA.
| 02 01, 2004

Elastic fiber homeostasis requires lysyl oxidase-like 1 protein.

Nat. Genet.
Liu X, Zhao Y, Gao J, Pawlyk B, Starcher B, Spencer JA, Yanagisawa H, Zuo J, Li T.
| 01 25, 2004

Mutations in ARFGEF2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortex.

Nat. Genet.
Sheen VL, Ganesh VS, Topcu M, Sebire G, Bodell A, Hill RS, Grant PE, Shugart YY, Imitola J, Khoury SJ, Guerrini R, Walsh CA.
| 11 30, 2003

Cryptic boundaries in roof plate and choroid plexus identified by intersectional gene activation.

Nat. Genet.
Awatramani R, Soriano P, Rodriguez C, Mai JJ, Dymecki SM.
| 08 17, 2003

C. elegans ORFeome version 1.1: experimental verification of the genome annotation and resource for proteome-scale protein expression.

Nat. Genet.
Reboul J, Vaglio P, Rual JF, Lamesch P, Martinez M, Armstrong CM, Li S, Jacotot L, Bertin N, Janky R, Moore T, Hudson JR, Hartley JL, Brasch MA, Vandenhaute J, Boulton S, Endress GA, Jenna S, Chevet E, Papasotiropoulos V, Tolias PP, Ptacek J, Snyder M, Huang R, Chance MR, Lee H, Doucette-Stamm L, Hill DE, Vidal M.
| 4 8, 2003

Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells.

Nat. Genet.
Nauli SM, Alenghat FJ, Luo Y, Williams E, Vassilev P, Li X, Elia AE, Lu W, Brown EM, Quinn SJ, Ingber DE, Zhou J.
| 01 06, 2003

A systematic RNAi screen identifies a critical role for mitochondria in C. elegans longevity.

Nat. Genet.
Lee SS, Lee RY, Fraser AG, Kamath RS, Ahringer J, Ruvkun G.
| 11 25, 2002

beta-cell-specific deletion of the Igf1 receptor leads to hyperinsulinemia and glucose intolerance but does not alter beta-cell mass.

Nat. Genet.
Kulkarni RN, Holzenberger M, Shih DQ, Ozcan U, Stoffel M, Magnuson MA, Kahn CR.
| 04 01, 2002

Efficient generation and mapping of recessive developmental mutations using ENU mutagenesis.

Nat. Genet.
Herron BJ, Lu W, Rao C, Liu S, Peters H, Bronson RT, Justice MJ, McDonald JD, Beier DR.
| 01 02, 2002

Identification of foreign gene sequences by transcript filtering against the human genome.

Nat. Genet.
Weber G, Shendure J, Tanenbaum DM, Church GM, Meyerson M.
| 01 14, 2002

Cardiomyopathy in zebrafish due to mutation in an alternatively spliced exon of titin.

Nat. Genet.
Xu X, Meiler SE, Zhong TP, Mohideen M, Crossley DA, Burggren WW, Fishman MC.
| 01 14, 2002

MLL translocations specify a distinct gene expression profile that distinguishes a unique leukemia.

Nat. Genet.
Armstrong SA, Staunton JE, Silverman LB, Pieters R, den Boer ML, Minden MD, Sallan SE, Lander ES, Golub TR, Korsmeyer SJ.
| 12 03, 2001

Correlation between transcriptome and interactome mapping data from Saccharomyces cerevisiae.

Nat. Genet.
Ge H, Liu Z, Church GM, Vidal M.
| 11 6, 2001

Homozygous mutations in ARIX(PHOX2A) result in congenital fibrosis of the extraocular muscles type 2.

Nat. Genet.
Nakano M, Yamada K, Fain J, Sener EC, Selleck CJ, Awad AH, Zwaan J, Mullaney PB, Bosley TM, Engle EC.
| 10 16, 2001

Identifying regulatory networks by combinatorial analysis of promoter elements.

Nat. Genet.
Pilpel Y, Sudarsanam P, Church GM.
| 9 8, 2001