Human Genome Epidemiology Literature Finder
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Records 1 - 16 (of 16 Records) |
| Query Trace: Disease and PSMA6[original query] |
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| 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 |
| Association between inflammatory gene polymorphisms and coronary artery disease in an Indian population. Journal of thrombosis and thrombolysis 2009 Jan 27 (1): 88-94. Banerjee Indranil, Pandey Umeshwar, Hasan Omer M, Parihar Rashmi, Tripathi Vijaya, Ganesh Subramani |
| 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 |
| Replication studies for the association of PSMA6 polymorphism with coronary artery disease in East Asian populations. Journal of human genetics 2009 Apr 54 (4): 248-51. Hinohara Kunihiko, Nakajima Toshiaki, Sasaoka Taishi, Sawabe Motoji, Lee Bok-Soo, Ban Jimin, Park Jeong-Euy, Izumi Toru, Kimura Akino |
| 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 |
| 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 |
| Genetic variations in the PSMA3, PSMA6 and PSMC6 genes are associated with type 1 diabetes in Latvians and with expression level of number of UPS-related and T1DM-susceptible genes in HapMap individuals. Molecular genetics and genomics : MGG 2015 Dec . Sjakste Tatjana, Paramonova Natalia, Osina Kristine, Dokane Kristine, Sokolovska Jelizaveta, Sjakste Nikola |
| 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 |
| ASSOSIATION ANALYSYS OF 11 POLYMORPHISMS OF SNPS WITH ENDOTHELIUM DEPENDENT VASODILATATION IN CHILDREN WITH DIABETES MELLITUS TYPE 1. Fiziolohichnyi zhurnal (Kiev, Ukraine : 1994) 0 62 (1): 43-52. Pranik N B, Goncharov S V, Gurianova V L, Maidannik V G, Khaitovych M V, Moibenko A A, Dosenko V |
| Immunochip Meta-Analysis of Inflammatory Bowel Disease Identifies Three Novel Loci and Four Novel Associations in Previously Reported Loci. Journal of Crohn's & colitis 2018 Mar . Hong Myunghee, Ye Byong Duk, Yang Suk-Kyun, Jung Seulgi, Lee Ho-Su, Kim Byoung Mok, Lee Soo Bin, Hong Jeonghoon, Baek Jiwon, Park Sang Hyoung, Han Buhm, Li Yi, Liu Wenting, Haritunians Talin, Taylor Kent D, Rotter Jerome I, Bang So-Young, Kim Tae-Hwan, McGovern Dermot P B, Liu Jianjun, Song Kyuyou |
| The Impact of the NOD2/CARD15 Variant (3020insC) and PSMA6 Polymorphism (-8C>G) on the Development and Outcome of Multiple Myeloma. BioMed research international 2020 6 2020 7629456. Zmorzy?ski S, Popek-Marciniec S, Styk W, Wojcierowska-Litwin M, Korsze?-Pilecka I, Szudy-Szczyrek A, Chocholska S, Hus M, Filip A |
| Polymorphism of Proteasomal Genes Can Be a Risk Factor for Systemic Autoimmune Diseases in Children. Journal of pediatric genetics 2021 5 10 (2): 98-104. Bakutenko Ivan Y, Hileuskaya Irena D, Nikitchenko Natalia V, Sechko Elena V, Tchitchko Alexej M, Batyan Galina M, Sukalo Alexander V, Ryabokon Nadezhda |
| Genetic variations in the PSMA6 and PSMC6 proteasome genes are associated with multiple sclerosis and response to interferon-? therapy in Latvians. Experimental and therapeutic medicine 2021 May 21 (5): 478. Paramonova Natalia, Kalnina Jolanta, Dokane Kristine, Dislere Kristine, Trapina Ilva, Sjakste Tatjana, Sjakste Nikola |
| 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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