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.

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
162.

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
163.

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
164.

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
165.

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
166.

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
167.

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
168.

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
169.

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
170.

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
171.

A common polymorphism acts as an intragenic modifier of mutant p53 behaviour.

Nat. Genet.
Marin MC, Jost CA, Brooks LA, Irwin MS, O'Nions J, Tidy JA, James N, McGregor JM, Harwood CA, Yulug IG, Vousden KH, Allday MJ, Gusterson B, Ikawa S, Hinds PW, Crook T, Kaelin WG.
| 5 10, 2000
172.

Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation.

Nat. Genet.
Satokata I, Ma L, Ohshima H, Bei M, Woo I, Nishizawa K, Maeda T, Takano Y, Uchiyama M, Heaney S, Peters H, Tang Z, Maxson R, Maas R.
| 3 31, 2000
173.

Familial dyserythropoietic anaemia and thrombocytopenia due to an inherited mutation in GATA1.

Nat. Genet.
Nichols KE, Crispino JD, Poncz M, White JG, Orkin SH, Maris JM, Weiss MJ.
| 3 4, 2000
174.

Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis.

Nat. Genet.
Kaplan JM, Kim SH, North KN, Rennke H, Correia LA, Tong HQ, Mathis BJ, Rodríguez-Pérez JC, Allen PG, Beggs AH, Pollak MR.
| 3 4, 2000
175.

Gene-target recognition among members of the myc superfamily and implications for oncogenesis.

Nat. Genet.
O'Hagan RC, Schreiber-Agus N, Chen K, David G, Engelman JA, Schwab R, Alland L, Thomson C, Ronning DR, Sacchettini JC, Meltzer P, DePinho RA.
| 2 2, 2000
176.

Reversibility of acute B-cell leukaemia induced by BCR-ABL1.

Nat. Genet.
Huettner CS, Zhang P, Van Etten RA, Tenen DG.
| 12 30, 1999
177.

Retinopathy and attenuated circadian entrainment in Crx-deficient mice.

Nat. Genet.
Furukawa T, Morrow EM, Li T, Davis FC, Cepko CL.
| 12 2, 1999
178.

Mutations in NEUROD1 are associated with the development of type 2 diabetes mellitus.

Nat. Genet.
Malecki MT, Jhala US, Antonellis A, Fields L, Doria A, Orban T, Saad M, Warram JH, Montminy M, Krolewski AS.
| 11 5, 1999
179.

Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia.

Nat. Genet.
Song WJ, Sullivan MG, Legare RD, Hutchings S, Tan X, Kufrin D, Ratajczak J, Resende IC, Haworth C, Hock R, Loh M, Felix C, Roy DC, Busque L, Kurnit D, Willman C, Gewirtz AM, Speck NA, Bushweller JH, Li FP, Gardiner K, Poncz M, Maris JM, Gilliland DG.
| 10 3, 1999
180.

Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia.

Nat. Genet.
Xu PX, Adams J, Peters H, Brown MC, Heaney S, Maas R.
| 9 2, 1999