Skip Header

1 - 25 of 33 results for uniprot:P60900 in Computationally mapped citations

Page of 2 | Next »

to top of page·  

Results Customize

Validation of the association between the gene encoding proteasome subunit alpha type 6 and myocardial infarction in a Japanese population.

Takashima N., Shioji K., Kokubo Y., Okayama A., Goto Y., Nonogi H., Iwai N.

Circ. J. 71:495-498(2007) GAD 152892 GeneRIF 5687 · Mapped (4)
Not Associated with CARDIOVASCULAR: myocardial infarct; GAD 152892 The reported genotype in PSMA6 appears not to contribute appreciably to myocardial infarction but may contribute slightly to atherosclerosis in the present study population; Observational study of gene-disease association. (HuGE Navigator) GeneRIF 5687

The functional variant rs1048990 in PSMA6 is associated with susceptibility to myocardial infarction in a Chinese population.

Liu X., Wang X., Shen Y., Wu L., Ruan X., Lindpaintner K., Yusuf S., Engert J.C., Anand S., Tan X. et al.

Atherosclerosis 206:199-203(2009) GAD 595775 GeneRIF 5687 · Mapped (4)
Associated with CARDIOVASCULAR: Myocardial Infarction; GAD 595775 Observational study of gene-disease association. (HuGE Navigator); Our results indicate that the PSMA6 variant rs1048990 is a risk factor of myocardial infarction in the Chinese population. GeneRIF 5687

Haplotypes encompassing the KIAA0391 and PSMA6 gene cluster confer a genetic link for myocardial infarction and coronary artery disease.

Alsmadi O., Muiya P., Khalak H., Al-Saud H., Meyer B.F., Al-Mohanna F., Alshahid M., Dzimiri N.

Ann. Hum. Genet. 73:475-483(2009) GAD 161102 GeneRIF 5687 · Mapped (5)
Associated with CARDIOVASCULAR: Cardiovascular; GAD 161102 Observational study of gene-disease association. (HuGE Navigator); Haplotypes in KIAA0391 and PSMA6 genes is a genetic link for myocardial infarction and coronary artery disease. GeneRIF 5687

A functional SNP in PSMA6 confers risk of myocardial infarction in the Japanese population.

Ozaki K., Sato H., Iida A., Mizuno H., Nakamura T., Miyamoto Y., Takahashi A., Tsunoda T., Ikegawa S., Kamatani N. et al.

Nat. Genet. 38:921-925(2006) GeneRIF 5687 · Mapped (4)
common SNP (minor allele frequency of 0.35) in the proteasome subunit alpha type 6 gene (PSMA6) conferring risk of myocardial infarction in the Japanese population GeneRIF 5687

Association of microsatellite polymorphisms of the human 14q13.2 region with type 2 diabetes mellitus in Latvian and Finnish populations.

Sjakste T., Kalis M., Poudziunas I., Pirags V., Lazdins M., Groop L., Sjakste N.

Ann. Hum. Genet. 71:772-776(2007) GeneRIF 5687 GAD 152893 · Mapped (4)
Associated with METABOLIC: diabetes, type 2; GAD 152893 Observational study of gene-disease association. (HuGE Navigator) GeneRIF 5687

SNPs of PSMA6 gene--investigation of possible association with myocardial infarction and type 2 diabetes mellitus.

Sjakste T., Poudziunas I., Ninio E., Perret C., Pirags V., Nicaud V., Lazdins M., Evanss A., Morrison C., Cambien F. et al.

Genetika 43:553-559(2007) GeneRIF 5687 · Mapped (4)
2 SNPs at positions -110 & -8 from translation start in the promoter region & 5'UTR of PSMA6 were analyzed; genotype -8CG was more frequent in type 2 diabetes patients & haplotype C-110/G-8 compared to C-110/C-8 was associated with higher risk of NIDDM GeneRIF 5687

Association between inflammatory gene polymorphisms and coronary artery disease in an Indian population.

Banerjee I., Pandey U., Hasan O.M., Parihar R., Tripathi V., Ganesh S.

J. Thromb. Thrombolysis 27:88-94(2009) GeneRIF 5687 · Mapped (24)
Observational study of gene-disease association. (HuGE Navigator) GeneRIF 5687

Inflammatory system gene polymorphism and the risk of stroke: a case-control study in an Indian population.

Banerjee I., Gupta V., Ahmed T., Faizaan M., Agarwal P., Ganesh S.

Brain Res. Bull. 75:158-165(2008) GeneRIF 5687 · Mapped (22)
Observational study of gene-disease association. (HuGE Navigator) GeneRIF 5687

The exon 1-8C/G SNP in the PSMA6 gene contributes only a small amount to the burden of myocardial infarction in 6946 cases and 2720 controls from a United Kingdom population.

Bennett D.A., Xu P., Clarke R., Zondervan K., Parish S., Palmer A., Cardon L., Peto R., Lathrop M., Collins R.

Eur. J. Hum. Genet. 16:480-486(2008) GeneRIF 5687 · Mapped (4)
The GG genotype for rs1048990 was less frequent in the UK population than in the Japanese population and was associated with an odds ratio for mi of 1.09 per G allele in a co-dominant genetic model and 1.32 in a recessive genetic model; Observational study and meta-analysis of gene-disease association. (HuGE Navigator) GeneRIF 5687

The -8 UTR C/G polymorphism of PSMA6 gene is associated with susceptibility to myocardial infarction in type 2 diabetic patients.

Barbieri M., Marfella R., Rizzo M.R., Boccardi V., Siniscalchi M., Schiattarella C., Siciliano S., Lemme P., Paolisso G.

Atherosclerosis 201:117-123(2008) GeneRIF 5687 · Mapped (4)
Observational study of gene-disease association. (HuGE Navigator); PSMA6 rs_1048990 polymorphism may contribute to MI susceptibility in type 2 diabetes. GeneRIF 5687

Association of a polymorphism of the apolipoprotein E gene with chronic kidney disease in Japanese individuals with metabolic syndrome.

Yoshida T., Kato K., Fujimaki T., Yokoi K., Oguri M., Watanabe S., Metoki N., Yoshida H., Satoh K., Aoyagi Y. et al.

Genomics 93:221-226(2009) GeneRIF 5687 · Mapped (324)
Observational study of gene-disease association. (HuGE Navigator) GeneRIF 5687

Genetic variation in the lymphotoxin-alpha pathway and the risk of ischemic stroke in European populations.

Freilinger T., Bevan S., Ripke S., Gschwendtner A., Lichtner P., Muller-Myhsok B., Wichmann H.E., Markus H.S., Meitinger T., Dichgans M.

Stroke 40:970-972(2009) GeneRIF 5687 · Mapped (23)
Observational study of gene-disease association. (HuGE Navigator) GeneRIF 5687

Replication studies for the association of PSMA6 polymorphism with coronary artery disease in East Asian populations.

Hinohara K., Nakajima T., Sasaoka T., Sawabe M., Lee B.S., Ban J., Park J.E., Izumi T., Kimura A.

J. Hum. Genet. 54:248-251(2009) GeneRIF 5687 · Mapped (4)
Observational study and meta-analysis of gene-disease association. (HuGE Navigator); A total of 1330 cases and 2554 controls from Japanese and Korean populations for PSMA6 genotypes were investigated and no evidence of the association was obtained in both Japanese and Korean populations. GeneRIF 5687

Integrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease risk.

Drenos F., Talmud P.J., Casas J.P., Smeeth L., Palmen J., Humphries S.E., Hingorani A.D.

Hum. Mol. Genet. 18:2305-2316(2009) GeneRIF 5687 · Mapped (329)
Observational study of gene-disease association. (HuGE Navigator) GeneRIF 5687

Allele polymorphism of genes coding proteasome subunits is associated with an enhanced risk for arterial hypertension in adolescents.

Honcharov S.V., Dosenko V.I.e., Khaitovych M.V., Moibenko O.O.

Fiziol Zh 55:3-10(2009) GeneRIF 5687 · Mapped (7)
Obtained data suggest the LMP2 and PSMA6 gene polymorphisms significance as the risk factors of essential hypertension in adolescents; Observational study of gene-disease association. (HuGE Navigator) GeneRIF 5687

Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.

BRIGHT Consortium
Talmud P.J., Drenos F., Shah S., Shah T., Palmen J., Verzilli C., Gaunt T.R., Pallas J., Lovering R., Li K. et al.

Am. J. Hum. Genet. 85:628-642(2009) GeneRIF 5687 · Mapped (10,092)
Observational study of gene-disease association. (HuGE Navigator) GeneRIF 5687

The G-Allele of the PSMA6-8C>G polymorphism is associated with poor outcome in multiple myeloma independently of circulating proteasome serum levels.

Bachmann H.S., Novotny J., Sixt S., Liebisch P., Frey U.H., Duhrsen U., Siffert W., Nuckel H.

Eur. J. Haematol. 85:108-113(2010) GeneRIF 5687 · Mapped (4)
Observational study of gene-disease association. (HuGE Navigator); the G-allele of the PSMA6-8C>G polymorphism is a possible survival prognosticator in multiple myeloma GeneRIF 5687

Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.

Bailey S.D., Xie C., Do R., Montpetit A., Diaz R., Mohan V., Keavney B., Yusuf S., Gerstein H.C., Engert J.C. et al.

Diabetes Care 33:2250-2253(2010) GeneRIF 5687 · Mapped (10,071)
Observational study of gene-disease association gene-environment interaction and pharmacogenomic / toxicogenomic. (HuGE Navigator) GeneRIF 5687

Genome-wide association analysis identifies three psoriasis susceptibility loci.

Stuart P.E., Nair R.P., Ellinghaus E., Ding J., Tejasvi T., Gudjonsson J.E., Li Y., Weidinger S., Eberlein B., Gieger C. et al.

Nat. Genet. 42:1000-1004(2010) GeneRIF 5687 · Mapped (9)
Observational study and genome-wide association study of gene-disease association. (HuGE Navigator) GeneRIF 5687

Polymorphisms of LTA, LGALS2, and PSMA6 genes and coronary atherosclerosis: a pathological study of 1503 consecutive autopsy cases.

Ikeda S., Tanaka N., Arai T., Chida K., Muramatsu M., Sawabe M.

Atherosclerosis 221:458-460(2012) GeneRIF 5687 · Mapped (23)
PSMA6 polymorphisms were not associated with phenotype of coronary atherosclerosis. GeneRIF 5687

Inhibition of eukaryotic DNA replication by geminin binding to Cdt1.

Wohlschlegel J.A., Dwyer B.T., Dhar S.K., Cvetic C., Walter J.C., Dutta A.

Science 290:2309-2312(2000) Reactome REACT_383 · UniProtKB (1) · Mapped (50)

Geminin, an inhibitor of DNA replication, is degraded during mitosis.

McGarry T.J., Kirschner M.W.

Cell 93:1043-1053(1998) Reactome REACT_383 · UniProtKB (4) · Mapped (42)

Human origin recognition complex large subunit is degraded by ubiquitin-mediated proteolysis after initiation of DNA replication.

Mendez J., Zou-Yang X.H., Kim S.Y., Hidaka M., Tansey W.P., Stillman B.

Mol. Cell 9:481-491(2002) Reactome REACT_383 · UniProtKB (1) · Mapped (65)

Chromatin association of human origin recognition complex, cdc6, and minichromosome maintenance proteins during the cell cycle: assembly of prereplication complexes in late mitosis.

Mendez J., Stillman B.

Mol. Cell. Biol. 20:8602-8612(2000) Reactome REACT_383 · Mapped (49)

Anaphase-promoting complex/cyclosome-dependent proteolysis of human cyclin A starts at the beginning of mitosis and is not subject to the spindle assembly checkpoint.

Geley S., Kramer E., Gieffers C., Gannon J., Peters J.M., Hunt T.

J. Cell Biol. 153:137-148(2001) Reactome REACT_6850 · Mapped (62)

to top of page·

Page of 2 | Next »