1 - 25 of 33 results for uniprot:P60900 in Computationally mapped citations
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| 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) |
| 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) |
| 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) |
| 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) |
| 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) |
| 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) |
| 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) |
| 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) |
| 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 -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) |
| 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) |
| 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) |
| 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) |
| 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) |
| 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) |
| Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip. BRIGHT Consortium Am. J. Hum. Genet. 85:628-642(2009) GeneRIF 5687 · Mapped (10,092) |
| 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) |
| 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) |
| 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) |
| 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) |
| 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) |

