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

221.

A human MSX1 homeodomain missense mutation causes selective tooth agenesis.

Nat. Genet.
Vastardis H, Karimbux N, Guthua SW, Seidman JG, Seidman CE.
| 8 1, 1996
223.

Renal disease susceptibility and hypertension are under independent genetic control in the fawn-hooded rat.

Nat. Genet.
Brown DM, Provoost AP, Daly MJ, Lander ES, Jacob HJ.
| 1 1, 1996
224.

A mutation in the gene encoding the alpha 2 chain of the fibril-associated collagen IX, COL9A2, causes multiple epiphyseal dysplasia (EDM2).

Nat. Genet.
Muragaki Y, Mariman EC, van Beersum SE, Perälä M, van Mourik JB, Warman ML, Olsen BR, Hamel BC.
| 1 1, 1996
225.

Autosomal recessive retinitis pigmentosa caused by mutations in the alpha subunit of rod cGMP phosphodiesterase.

Nat. Genet.
Huang SH, Pittler SJ, Huang X, Oliveira L, Berson EL, Dryja TP.
| 12 1, 1995
226.

A mouse model of human familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism.

Nat. Genet.
Ho C, Conner DA, Pollak MR, Ladd DJ, Kifor O, Warren HB, Brown EM, Seidman JG, Seidman CE.
| 12 1, 1995
227.

Gene therapy of metastatic cancer by in vivo retroviral gene targeting.

Nat. Genet.
Hurford RK, Dranoff G, Mulligan RC, Tepper RI.
| 8 1, 1995
228.

Detection of mutations by cleavage of DNA heteroduplexes with bacteriophage resolvases.

Nat. Genet.
Mashal RD, Koontz J, Sklar J.
| 2 1, 1995
229.

A genetic linkage map of the laboratory rat, Rattus norvegicus.

Nat. Genet.
Jacob HJ, Brown DM, Bunker RK, Daly MJ, Dzau VJ, Goodman A, Koike G, Kren V, Kurtz T, Lernmark A.
| 1 1, 1995
230.

Autosomal dominant hypocalcaemia caused by a Ca(2+)-sensing receptor gene mutation.

Nat. Genet.
Pollak MR, Brown EM, Estep HL, McLaine PN, Kifor O, Park J, Hebert SC, Seidman CE, Seidman JG.
| 11 1, 1994
231.

A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1.

Nat. Genet.
Kass S, MacRae C, Graber HL, Sparks EA, McNamara D, Boudoulas H, Basson CT, Baker PB, Cody RJ, Fishman MC.
| 8 1, 1994
232.

PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anophthalmia and central nervous system defects.

Nat. Genet.
Glaser T, Jepeal L, Edwards JG, Young SR, Favor J, Maas RL.
| 8 1, 1994
235.

A complex bilateral polysyndactyly disease locus maps to chromosome 7q36.

Nat. Genet.
Tsukurov O, Boehmer A, Flynn J, Nicolai JP, Hamel BC, Traill S, Zaleske D, Mankin HJ, Yeon H, Ho C.
| 3 1, 1994
236.

Isolation of genes from complex sources of mammalian genomic DNA using exon amplification.

Nat. Genet.
Church DM, Stotler CJ, Rutter JL, Murrell JR, Trofatter JA, Buckler AJ.
| 1 1, 1994
238.

Inactivation of WT1 in nephrogenic rests, genetic precursors to Wilms' tumour.

Nat. Genet.
Park S, Bernard A, Bove KE, Sens DA, Hazen-Martin DJ, Garvin AJ, Haber DA.
| 12 1, 1993
239.

The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene.

Nat. Genet.
Tanzi RE, Petrukhin K, Chernov I, Pellequer JL, Wasco W, Ross B, Romano DM, Parano E, Pavone L, Brzustowicz LM.
| 12 1, 1993
240.

Homozygosity mapping of the gene for alkaptonuria to chromosome 3q2.

Nat. Genet.
Pollak MR, Chou YH, Cerda JJ, Steinmann B, La Du BN, Seidman JG, Seidman CE.
| 10 1, 1993