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

181.

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
182.

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
183.

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

Nat. Genet.
Huettner CS, Zhang P, Van Etten RA, Tenen DG.
| 12 30, 1999
184.

Retinopathy and attenuated circadian entrainment in Crx-deficient mice.

Nat. Genet.
Furukawa T, Morrow EM, Li T, Davis FC, Cepko CL.
| 12 2, 1999
185.

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
186.

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
187.

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
188.

Irs-2 coordinates Igf-1 receptor-mediated beta-cell development and peripheral insulin signalling.

Nat. Genet.
Withers DJ, Burks DJ, Towery HH, Altamuro SL, Flint CL, White MF.
| 9 2, 1999
189.

The gene mutated in thiamine-responsive anaemia with diabetes and deafness (TRMA) encodes a functional thiamine transporter.

Nat. Genet.
Fleming JC, Tartaglini E, Steinkamp MP, Schorderet DF, Cohen N, Neufeld EJ.
| 7 3, 1999
190.

Systematic determination of genetic network architecture.

Nat. Genet.
Tavazoie S, Hughes JD, Campbell MJ, Cho RJ, Church GM.
| 7 3, 1999
191.

Mutations in the gene encoding 11-cis retinol dehydrogenase cause delayed dark adaptation and fundus albipunctatus.

Nat. Genet.
Yamamoto H, Simon A, Eriksson U, Harris E, Berson EL, Dryja TP.
| 6 16, 1999
192.

Pharmacogenetic association between ALOX5 promoter genotype and the response to anti-asthma treatment.

Nat. Genet.
Drazen JM, Yandava CN, Dubé L, Szczerback N, Hippensteel R, Pillari A, Israel E, Schork N, Silverman ES, Katz DA, Drajesk J.
| 6 16, 1999
193.

Tsix, a gene antisense to Xist at the X-inactivation centre.

Nat. Genet.
Lee JT, Davidow LS, Warshawsky D.
| 4 7, 1999
194.

Transferrin receptor is necessary for development of erythrocytes and the nervous system.

Nat. Genet.
Levy JE, Jin O, Fujiwara Y, Kuo F, Andrews NC.
| 4 7, 1999
195.

Receptors for polytropic and xenotropic mouse leukaemia viruses encoded by a single gene at Rmc1.

Nat. Genet.
Yang YL, Guo L, Xu S, Holland CA, Kitamura T, Hunter K, Cunningham JM.
| 2 13, 1999
196.

Prolongation of ovarian lifespan into advanced chronological age by Bax-deficiency.

Nat. Genet.
Perez GI, Robles R, Knudson CM, Flaws JA, Korsmeyer SJ, Tilly JL.
| 2 13, 1999
197.

Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction.

Nat. Genet.
Robertson NG, Lu L, Heller S, Merchant SN, Eavey RD, McKenna M, Nadol JB, Miyamoto RT, Linthicum FH, Lubianca Neto JF, Hudspeth AJ, Seidman CE, Morton CC, Seidman JG.
| 11 7, 1998
198.

Positional cloning of the zebrafish sauternes gene: a model for congenital sideroblastic anaemia.

Nat. Genet.
Brownlie A, Donovan A, Pratt SJ, Paw BH, Oates AC, Brugnara C, Witkowska HE, Sassa S, Zon LI.
| 11 7, 1998
199.

Identification of a candidate modifying gene for spinal muscular atrophy by comparative genomics.

Nat. Genet.
Scharf JM, Endrizzi MG, Wetter A, Huang S, Thompson TG, Zerres K, Dietrich WF, Wirth B, Kunkel LM.
| 9 10, 1998
200.

PAK3 mutation in nonsyndromic X-linked mental retardation.

Nat. Genet.
Allen KM, Gleeson JG, Bagrodia S, Partington MW, MacMillan JC, Cerione RA, Mulley JC, Walsh CA.
| 9 10, 1998