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.

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
222.

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

Nat. Genet.
Blumenthal D, Causino N, Campbell EG.
| 5 1, 1997
223.

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
224.

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
225.

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
226.

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
227.

UBE3A/E6-AP mutations cause Angelman syndrome.

Nat. Genet.
Kishino T, Lalande M, Wagstaff J.
| 1 1, 1997
228.

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
229.

A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics Group.

Nat. Genet.
Haines JL, Ter-Minassian M, Bazyk A, Gusella JF, Kim DJ, Terwedow H, Pericak-Vance MA, Rimmler JB, Haynes CS, Roses AD, Lee A, Shaner B, Menold M, Seboun E, Fitoussi RP, Gartioux C, Reyes C, Ribierre F, Gyapay G, Weissenbach J, Hauser SL, Goodkin DE, Lincoln R, Usuku K, Oksenberg JR.
| 8 1, 1996
230.

Chromosomal mapping of quantitative trait loci contributing to stroke in a rat model of complex human disease.

Nat. Genet.
Rubattu S, Volpe M, Kreutz R, Ganten U, Ganten D, Lindpaintner K.
| 8 1, 1996
231.

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
233.

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
234.

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
235.

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
236.

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
237.

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

Nat. Genet.
Hurford RK, Dranoff G, Mulligan RC, Tepper RI.
| 8 1, 1995
238.

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

Nat. Genet.
Mashal RD, Koontz J, Sklar J.
| 2 1, 1995
239.

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
240.

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