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


Alpha-2 macroglobulin is genetically associated with Alzheimer disease.

Nat. Genet.
Blacker D, Wilcox MA, Laird NM, Rodes L, Horvath SM, Go RC, Perry R, Watson B, Bassett SS, McInnis MG, Albert MS, Hyman BT, Tanzi RE.
| 8 11, 1998

BRCA1 protein is linked to the RNA polymerase II holoenzyme complex via RNA helicase A.

Nat. Genet.
Anderson SF, Schlegel BP, Nakajima T, Wolpin ES, Parvin JD.
| 7 14, 1998

Loss of E2F-1 reduces tumorigenesis and extends the lifespan of Rb1(+/-)mice.

Nat. Genet.
Yamasaki L, Bronson R, Williams BO, Dyson NJ, Harlow E, Jacks T.
| 4 16, 1998

A microsatellite genetic linkage map for zebrafish (Danio rerio).

Nat. Genet.
Knapik EW, Goodman A, Ekker M, Chevrette M, Delgado J, Neuhauss S, Shimoda N, Driever W, Fishman MC, Jacob HJ.
| 4 16, 1998

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

FGFR1 is fused with a novel zinc-finger gene, ZNF198, in the t(8;13) leukaemia/lymphoma syndrome.

Nat. Genet.
Xiao S, Nalabolu SR, Aster JC, Ma J, Abruzzo L, Jaffe ES, Stone R, Weissman SM, Hudson TJ, Fletcher JA.
| 1 13, 1998

The Fanconi anaemia proteins, FAA and FAC, interact to form a nuclear complex.

Nat. Genet.
Kupfer GM, Näf D, Suliman A, Pulsipher M, D'Andrea AD.
| 12 17, 1997

Rapid accumulation of genome rearrangements in liver but not in brain of old mice.

Nat. Genet.
Dollé ME, Giese H, Hopkins CL, Martus HJ, Hausdorff JM, Vijg J.
| 12 17, 1997

Huntingtin is required for neurogenesis and is not impaired by the Huntington's disease CAG expansion.

Nat. Genet.
White JK, Auerbach W, Duyao MP, Vonsattel JP, Gusella JF, Joyner AL, MacDonald ME.
| 12 17, 1997

The EWS-WT1 translocation product induces PDGFA in desmoplastic small round-cell tumour.

Nat. Genet.
Lee SB, Kolquist KA, Nichols K, Englert C, Maheswaran S, Ladanyi M, Gerald WL, Haber DA.
| 11 14, 1997

Perinatal lethality with kidney and pancreas defects in mice with a targetted Pkd1 mutation.

Nat. Genet.
Lu W, Peissel B, Babakhanlou H, Pavlova A, Geng L, Fan X, Larson C, Brent G, Zhou J.
| 11 5, 1997

The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein.

Nat. Genet.
Ozelius LJ, Hewett JW, Page CE, Bressman SB, Kramer PL, Shalish C, de Leon D, Brin MF, Raymond D, Corey DP, Fahn S, Risch NJ, Buckler AJ, Gusella JF, Breakefield XO.
| 9 1, 1997

atm and p53 cooperate in apoptosis and suppression of tumorigenesis, but not in resistance to acute radiation toxicity.

Nat. Genet.
Westphal CH, Rowan S, Schmaltz C, Elson A, Fisher DE, Leder P.
| 8 1, 1997

Academic-industry research relationships in genetics: a field apart.

Nat. Genet.
Blumenthal D, Causino N, Campbell EG.
| 5 1, 1997

Heterozygous ATM mutations do not contribute to early onset of breast cancer.

Nat. Genet.
FitzGerald MG, Bean JM, Hegde SR, Unsal H, MacDonald DJ, Harkin DP, Finkelstein DM, Isselbacher KJ, Haber DA.
| 3 1, 1997

Embryonic lethality and impairment of haematopoiesis in mice heterozygous for an AML1-ETO fusion gene.

Nat. Genet.
Yergeau DA, Hetherington CJ, Wang Q, Zhang P, Sharpe AH, Binder M, Marín-Padilla M, Tenen DG, Speck NA, Zhang DE.
| 3 1, 1997

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

Pancreatic agenesis attributable to a single nucleotide deletion in the human IPF1 gene coding sequence.

Nat. Genet.
Stoffers DA, Zinkin NT, Stanojevic V, Clarke WL, Habener JF.
| 1 1, 1997

UBE3A/E6-AP mutations cause Angelman syndrome.

Nat. Genet.
Kishino T, Lalande M, Wagstaff J.
| 1 1, 1997

Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome.

Nat. Genet.
Basson CT, Bachinsky DR, Lin RC, Levi T, Elkins JA, Soults J, Grayzel D, Kroumpouzou E, Traill TA, Leblanc-Straceski J, Renault B, Kucherlapati R, Seidman JG, Seidman CE.
| 1 1, 1997