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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 14 (of 14 Records)

Query Trace: Myocardial Infarction and PSMA6[original query]
SNPs of PSMA6 gene--investigation of possible association with myocardial infarction and type 2 diabetes mellitus.
Genetika 2007 Apr 43 (4): 553-9.
Sjakste T, Poudziunas I, Ninio E, Perret C, Pirags V, Nicaud V, Lazdins M, Evanss A, Morrison C, Cambien F, Sjakste
Validation of the association between the gene encoding proteasome subunit alpha type 6 and myocardial infarction in a Japanese population.
Circulation journal : official journal of the Japanese Circulation Society 2007 Apr 71 (4): 495-8.
Takashima Naoyuki, Shioji Keisuke, Kokubo Yoshihiro, Okayama Akira, Goto Yoichi, Nonogi Hiroshi, Iwai Naoha
The -8 UTR C/G polymorphism of PSMA6 gene is associated with susceptibility to myocardial infarction in type 2 diabetic patients.
Atherosclerosis 2008 Nov 201 (1): 117-23.
Barbieri Michelangela, Marfella Raffaele, Rizzo Maria Rosaria, Boccardi Virginia, Siniscalchi Mario, Schiattarella Concetta, Siciliano Silvio, Lemme Pietro, Paolisso Giusep
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.
European journal of human genetics : EJHG 2008 Apr 16 (4): 480-6.
Bennett Derrick A, Xu Peng, Clarke Robert, Zondervan Krina, Parish Sarah, Palmer Alison, Cardon Lon, Peto Richard, Lathrop Mark, Collins Rory,
Haplotypes encompassing the KIAA0391 and PSMA6 gene cluster confer a genetic link for myocardial infarction and coronary artery disease.
Annals of human genetics 2009 Sep 73 (Pt 5): 475-83.
Alsmadi Osama, Muiya Paul, Khalak Hanif, Al-Saud Haya, Meyer Brian F, Al-Mohanna Futwan, Alshahid Maie, Dzimiri Ndu
The functional variant rs1048990 in PSMA6 is associated with susceptibility to myocardial infarction in a Chinese population.
Atherosclerosis 2009 Sep 206 (1): 199-203.
Liu Xin, Wang Xingyu, Shen Yue, Wu Lijun, Ruan Xiaoyang, Lindpaintner Klaus, Yusuf Salim, Engert James C, Anand Sonia, Tan Xuerui, Liu Lishe
Genetic variation in the lymphotoxin-alpha pathway and the risk of ischemic stroke in European populations.
Stroke; a journal of cerebral circulation 2009 Mar 40 (3): 970-2.
Freilinger Tobias, Bevan Steve, Ripke Stephan, Gschwendtner Andreas, Lichtner Peter, Müller-Myhsok Bertram, Wichmann H-Erich, Markus Hugh S, Meitinger Thomas, Dichgans Mart
The G-Allele of the PSMA6-8C>G polymorphism is associated with poor outcome in multiple myeloma independently of circulating proteasome serum levels.
European journal of haematology 2010 Aug 85 (2): 108-13.
Bachmann Hagen S, Novotny Jürgen, Sixt Stephan, Liebisch Peter, Frey Ulrich H, Dührsen Ulrich, Siffert Winfried, Nückel Holg
Genetic variants associated with myocardial infarction in the PSMA6 gene and Chr9p21 are also associated with ischaemic stroke.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2013 Feb 20 (2): 300-8.
Heckman M G, Soto-Ortolaza A I, Diehl N N, Rayaprolu S, Brott T G, Wszolek Z K, Meschia J F, Ross O
Polymorphisms of LTA, LGALS2, and PSMA6 genes and coronary atherosclerosis: a pathological study of 1503 consecutive autopsy cases.
Atherosclerosis 2012 Apr 221 (2): 458-60.
Ikeda Shinobu, Tanaka Noriko, Arai Tomio, Chida Kouji, Muramatsu Masaaki, Sawabe Moto
Quantitative assessment of the influence of PSMA6 variant (rs1048990) on coronary artery disease risk.
Molecular biology reports 2012 Oct .
Wang H, Jiang M, Zhu H, Chen Q, Gong P, Lin J, Lu J, Qiu J
Molecular genetics of coronary artery disease.
Journal of human genetics 2015 Jul .
Ozaki Kouichi, Tanaka Toshihi
Association between functional variant of inflammatory system gene (PSMA6) and end-stage kidney disease.
International urology and nephrology 2016 Sep .
Buraczynska Monika, Stec Anna, Filipczak Aleksandra, Ksiazek Andrz
Discovering Genotype Variants in an Infant with VACTERL through Clinical Exome Sequencing: A Support for Personalized Risk Assessment and Disease Prevention.
Pediatric reports 2021 1 13 (1): 45-56.
Pelizzo Gloria, Chiricosta Luigi, Mazzon Emanuela, Zuccotti Gian Vincenzo, Avanzini Maria Antonietta, Croce Stefania, Lima Mario, Bramanti Placido, Calcaterra Valer
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