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

161.

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
162.

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
163.

Correlation between transcriptome and interactome mapping data from Saccharomyces cerevisiae.

Nat. Genet.
Ge H, Liu Z, Church GM, Vidal M.
| 11 6, 2001
164.

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
165.

Identifying regulatory networks by combinatorial analysis of promoter elements.

Nat. Genet.
Pilpel Y, Sudarsanam P, Church GM.
| 9 8, 2001
166.

Aromatic hydrocarbon receptor-driven Bax gene expression is required for premature ovarian failure caused by biohazardous environmental chemicals.

Nat. Genet.
Matikainen T, Perez GI, Jurisicova A, Pru JK, Schlezinger JJ, Ryu HY, Laine J, Sakai T, Korsmeyer SJ, Casper RF, Sherr DH, Tilly JL.
| 7 17, 2001
167.

Association analysis of NOTCH4 loci in schizophrenia using family and population-based controls.

Nat. Genet.
Sklar P, Schwab SG, Williams NM, Daly M, Schaffner S, Maier W, Albus M, Trixler M, Eichhammer P, Lerer B, Hallmayer J, Norton N, Williams H, Zammit S, Cardno AG, Jones S, McCarthy G, Milanova V, Kirov G, O'Donovan MC, Lander ES, Owen MJ, Wildenauer DB.
| 6 6, 2001
168.

Telomere dysfunction and evolution of intestinal carcinoma in mice and humans.

Nat. Genet.
Rudolph KL, Millard M, Bosenberg MW, DePinho RA.
| 5 31, 2001
169.

Mutations in the gene encoding c-Abl-binding protein SH3BP2 cause cherubism.

Nat. Genet.
Ueki Y, Tiziani V, Santanna C, Fukai N, Maulik C, Garfinkle J, Ninomiya C, doAmaral C, Peters H, Habal M, Rhee-Morris L, Doss JB, Kreiborg S, Olsen BR, Reichenberger E.
| 5 31, 2001
170.

Mouse models of cell death.

Nat. Genet.
Ranger AM, Malynn BA, Korsmeyer SJ.
| 5 31, 2001
171.

Open-reading-frame sequence tags (OSTs) support the existence of at least 17,300 genes in C. elegans.

Nat. Genet.
Reboul J, Vaglio P, Tzellas N, Thierry-Mieg N, Moore T, Jackson C, Shin-i T, Kohara Y, Thierry-Mieg D, Thierry-Mieg J, Lee H, Hitti J, Doucette-Stamm L, Hartley JL, Temple GF, Brasch MA, Vandenhaute J, Lamesch PE, Hill DE, Vidal M.
| 3 10, 2001
172.

Dominant-negative mutations of CEBPA, encoding CCAAT/enhancer binding protein-alpha (C/EBPalpha), in acute myeloid leukemia.

Nat. Genet.
Pabst T, Mueller BU, Zhang P, Radomska HS, Narravula S, Schnittger S, Behre G, Hiddemann W, Tenen DG.
| 3 10, 2001
173.

SPTLC1 is mutated in hereditary sensory neuropathy, type 1.

Nat. Genet.
Bejaoui K, Wu C, Scheffler MD, Haan G, Ashby P, Wu L, de Jong P, Brown RH.
| 3 10, 2001
174.

Multigenic control of Listeria monocytogenes susceptibility in mice.

Nat. Genet.
Boyartchuk VL, Broman KW, Mosher RE, D'Orazio SE, Starnbach MN, Dietrich WF.
| 3 10, 2001
175.

Localized Igf-1 transgene expression sustains hypertrophy and regeneration in senescent skeletal muscle.

Nat. Genet.
Musarò A, McCullagh K, Paul A, Houghton L, Dobrowolny G, Molinaro M, Barton ER, Sweeney HL, Rosenthal N.
| 2 15, 2001
176.

MAML1, a human homologue of Drosophila mastermind, is a transcriptional co-activator for NOTCH receptors.

Nat. Genet.
Wu L, Aster JC, Blacklow SC, Lake R, Artavanis-Tsakonas S, Griffin JD.
| 12 2, 2000
177.

Hypoglycaemia, liver necrosis and perinatal death in mice lacking all isoforms of phosphoinositide 3-kinase p85 alpha.

Nat. Genet.
Fruman DA, Mauvais-Jarvis F, Pollard DA, Yballe CM, Brazil D, Bronson RT, Kahn CR, Cantley LC.
| 11 4, 2000
178.

A computational analysis of whole-genome expression data reveals chromosomal domains of gene expression.

Nat. Genet.
Cohen BA, Mitra RD, Hughes JD, Church GM.
| 10 4, 2000
179.

Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations.

Nat. Genet.
Hong SE, Shugart YY, Huang DT, Shahwan SA, Grant PE, Hourihane JO, Martin ND, Walsh CA.
| 9 6, 2000
180.

Telomere dysfunction impairs DNA repair and enhances sensitivity to ionizing radiation.

Nat. Genet.
Wong KK, Chang S, Weiler SR, Ganesan S, Chaudhuri J, Zhu C, Artandi SE, Rudolph KL, Gottlieb GJ, Chin L, Alt FW, DePinho RA.
| 9 6, 2000