Human Genome Epidemiology Literature Finder
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Records 1 - 29 (of 29 Records) |
| Query Trace: Coronary Artery Disease and INS[original query] |
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| Apolipoprotein B gene polymorphisms: prevalence and impact on serum lipid concentrations in hypercholesterolemic individuals from Brazil. Clinica chimica acta; international journal of clinical chemistry 2000 Dec 302 (1-2): 189-203. Cavalli S A, Hirata M H, Salazar L A, Diament J, Forti N, Giannini S D, Nakandakare E R, Bertolami M C, Hirata R |
| Interaction between SREBP-1a and APOB polymorphisms influences total and low-density lipoprotein cholesterol levels in patients with coronary artery disease. Clinical genetics 2003 May 63 (5): 380-5. Rios D L S, Vargas A F, Torres M R, Zago A J, Callegari-Jacques S M, Hutz M |
| A common haplotype at the CD36 locus is associated with high free fatty acid levels and increased cardiovascular risk in Caucasians. Human molecular genetics 2004 Oct 13 (19): 2197-205. Ma Xiaowei, Bacci Simonetta, Mlynarski Wojciech, Gottardo Lucia, Soccio Teresa, Menzaghi Claudia, Iori Elisabetta, Lager Robert A, Shroff Adhir R, Gervino Ernest V, Nesto Richard W, Johnstone Michael T, Abumrad Nada A, Avogaro Angelo, Trischitta Vincenzo, Doria Alessand |
| Five polymorphisms in gene candidates for cardiovascular disease in Afro-Brazilian individuals. Journal of clinical laboratory analysis 2004 18 (6): 309-16. Sakuma Tatsuya, Hirata Rosario D C, Hirata Mario |
| The effects of three factor VII polymorphisms on factor VII coagulant levels in healthy Singaporean Chinese, Malay and Indian newborns. Annals of human genetics 2006 Nov 70 (Pt 6): 951-7. Quek S C, Low P S, Saha N, Heng C |
| Risk of coronary artery disease as influenced by variants of the human endothelin and endothelin-converting enzyme genes. Pharmacogenetics and genomics 2007 Jan 17 (1): 77-83. Bühler Katrin, Ufer Mike, Müller-Marbach Alexis, Brinkmann Ulrich, Laule Michael, Stangl Verena, Roots Ivar, Stangl Karl, Cascorbi Ingo |
| Association of the insertion/deletion gene polymorphism of the apolipoprotein B signal peptide with myocardial infarction in Tunisian patients. Clinical chemistry and laboratory medicine : CCLM / FESCC 2008 46 (8): 1097-101. Kallel Amani, Ben Ali Samir, Sediri Yosra, Chabrak Sonia, Elasmi Monia, Sanhaji Haïfa, Souheil Omar, Haj-Taieb Sameh, Feki Moncef, Mechmeche Rachid, Jemaa Riadh, Kaabachi Nazi |
| 5' ins/del and 3' VNTR polymorphisms in the apolipoprotein B gene in relation to lipids and coronary artery disease. Clinical chemistry and laboratory medicine : CCLM / FESCC 2008 46 (3): 329-34. Rebhi Lamia, Omezzine Asma, Kchok Kaouther, Belkahla Radhia, Ben Hadjmbarek Ibtihel, Rejeb Jihen, Ben Rejeb Nabila, Nabli Naoufel, Bibi Amina, Massoud Taieb, Abdelaziz Ahmed, Boughzala Essia, Bouslama A |
| Combined effect of hemostatic gene polymorphisms and the risk of myocardial infarction in patients with advanced coronary atherosclerosis. PloS one 2008 3 (2): e1523. Martinelli Nicola, Trabetti Elisabetta, Pinotti Mirko, Olivieri Oliviero, Sandri Marco, Friso Simonetta, Pizzolo Francesca, Bozzini Claudia, Caruso Pier Paolo, Cavallari Ugo, Cheng Suzanne, Pignatti Pier Franco, Bernardi Francesco, Corrocher Roberto, Girelli Domeni |
| Genetic variants in hypertensive patients with coronary artery disease and coexisting atheromatous renal artery stenosis. Medical science monitor : international medical journal of experimental and clinical research 2008 Dec 14 (12): CR611-6. Szperl Malgorzata, Dzielinska Zofia, Roszczynko Marta, Malek Lukasz A, Makowiecka-Ciesla Magdalena, Demkow Marcin, Kadziela Jacek, Prejbisz Aleksander, Florczak Elzbieta, Zielinski Tomasz, Januszewicz Andrzej, Ruzyllo Wito |
| Lack of association between endothelin-1 gene variants and myocardial infarction. Journal of atherosclerosis and thrombosis 2009 Aug 16 (4): 388-95. Palacín María, Rodriguez-Pascual Fernando, Reguero Julián R, Rodríguez Isabel, Avanzas Pablo, Lozano Iñigo, Morís Cesar, Alvarez Victoria, Cannata-Andía Jorge B, Lamas Santiago, García-Castro Monica, Coto Eliec |
| Evaluation of the contribution of renin angiotensin system polymorphisms to the risk of coronary artery disease among Tunisians. Genetic testing and molecular biomarkers 2010 Oct 14 (5): 661-6. Abboud Nesrine, Ghazouani Lakhder, Kaabi Belhassen, Ben-Hadj-Khalifa Sonia, Addad Fawzi, Marwen Mahjoub, Almawi Wassim Y, Mahjoub Touha |
| Apolipoprotein C-I genotype and serum levels of triglycerides, C-reactive protein and coronary heart disease. Metabolism: clinical and experimental 2010 Dec 59 (12): 1736-41. Olsson Bob, Gigante Bruna, Mehlig Kirsten, Bergsten Alicia, Leander Karin, de Faire Ulf, Lissner Lauren, Thelle Dag S, Carlsson Lena M |
| Combined renin-angiotensin system gene polymorphisms and outcomes in coronary artery disease - a preliminary report. Kardiologia polska 2011 69 (7): 688-95. Dzieli?ska Zofia, Ma?ek Lukasz A, Roszczynko Marta, Szperl Ma?gorzata, Demkow Marcin, K?dziela Jacek, Prejbisz Aleksander, Zieli?ski Tomasz, Januszewicz Andrzej, Ru?y??o Wito |
| Association between two polymorphisms in the HLA-G gene and angiographic coronary artery disease. Molecular medicine reports 2012 May 5 (5): 1141-5. Boiocchi Chiara, Bozzini Sara, Zorzetto Michele, Pelissero Gabriele, Cuccia Mariaclara, Falcone Colom |
| Role of inflammatory gene polymorphisms in left ventricular dysfunction (LVD) susceptibility in coronary artery disease (CAD) patients. Cytokine 2013 Mar 61 (3): 856-61. Mishra Avshesh, Srivastava Anshika, Mittal T, Garg N, Mittal |
| Genetic predisposition to left ventricular dysfunction: a multigenic and multi-analytical approach. Gene 2014 Aug 546 (2): 309-17. Mishra Avshesh, Srivastava Anshika, Mittal Tulika, Garg Naveen, Mittal Balr |
| -94 ATTG insertion/deletion polymorphism of the NFKB1 gene is associated with coronary artery disease in Han and Uygur women in China. Genetic testing and molecular biomarkers 2014 Jun 18 (6): 430-8. Yang Yi-Ning, Zhang Jin-Yu, Ma Yi-Tong, Xie Xiang, Li Xiao-Mei, Liu Fen, Chen Bang-Dang, Dong Xing-Hui, Zheng Ying-Ying, Pan Shuo, Zhai Hui, Li Dong-Ze, Chen Qing-J |
| Genetic variation and coronary atherosclerosis in patients with systemic lupus erythematosus. Lupus 2014 Aug 23 (9): 876-80. Chung C P, Solus J F, Oeser A, Li C, Raggi P, Smith J R, Stein C |
| Genetic Variation in NFKB1 and NFKBIA and Susceptibility to Coronary Artery Disease in a Chinese Uygur Population. PloS one 2015 10 (6): e0129144. Lai Hong-Mei, Li Xiao-Mei, Yang Yi-Ning, Ma Yi-Tong, Xu Rui, Pan Shuo, Zhai Hui, Liu Fen, Chen Bang-Dang, Zhao Qi |
| Association between genetic polymorphism in NFKB1 and NFKBIA and coronary artery disease in a Chinese Han population. International journal of clinical and experimental medicine 2015 8 (11): 21487-96. Lai Hongmei, Chen Qingjie, Li Xiaomei, Ma Yitong, Xu Rui, Zhai Hui, Liu Fen, Chen Bangdang, Yang Yini |
| Polymorphic variants of Caspase genes (8 & 3) in the risk prediction of Coronary Artery Disease. Gene 2017 Jun . Gundapaneni Kishore Kumar, Shyamala Nivas, Galimudi Rajesh Kumar, Kupsal Keerthi, Gantala Srilatha Reddy, Padala Chiranjeevi, Gunda Padma, Tupurani Mohini Aiyengar, Puranam Kaushik, Sahu Sanjib Kumar, Hanumanth Surekha Ra |
| Mutant DD genotype of NFKB1 gene is associated with the susceptibility and severity of coronary artery disease. Journal of molecular and cellular cardiology 2017 Jan 103 56-64. Luo Jun-Yi, Li Xiao-Mei, Zhou Yun, Zhao Qiang, Chen Bang-Dang, Liu Fen, Chen Xiao-Cui, Zheng Hong, Ma Yi-Tong, Gao Xiao-Ming, Yang Yi-Ni |
| The association between NFKB1 -94ATTG ins/del and NFKB1A 826C/T genetic variations and coronary artery disease risk. Molecular biology research communications 2018 Mar 7 (1): 17-24. Seidi Abbas, Mirzaahmadi Sina, Mahmoodi Khalil, Soleiman-Soltanpour Mohamm |
| Association of MMP-1 (rs1799750)-1607 2G/2G and MMP-3 (rs3025058)-1612 6A/6A Genotypes With Coronary Artery Disease Risk Among Iranian Turks. Journal of cardiovascular pharmacology 2019 Jul . Ghaffarzadeh Ayda, Bagheri Morteza, Khadem-Vatani Kamal, Abdi Rad I |
| The Syntaxin-1A gene single nucleotide polymorphism rs4717806 associates with the risk of ischemic heart disease. Medicine 2019 Jun 98 (24): e15846. Guerini Franca R, Ripamonti Enrico, Costa Andrea S, Zanzottera Milena, Agliardi Cristina, Bolognesi Elisabetta, Clerici Mario, Racca Vittor |
| Evaluation of Cases with Myotonia Congenita for Cardiovascular Risk. Medeniyet medical journal 2020 8 34 (4): 374-379. Damar Ibrahim Halil, Eroz Rec |
| Modulation of STIM1 by a risk insertion/deletion polymorphism underlying genetics susceptibility to sudden cardiac death originated from coronary artery disease. Forensic science international 2021 9 328 111010. Zhang Qing, He Yan, Xu Hongfei, Li Lijuan, Guo Yadong, Zhang Jianhua, Cheng Lei, Yu Huan, Dai Yunda, Yang Qi, Yang Zhenzhen, Li Chengtao, Zhang Suhua, Zhu Shaohua, Luo Bin, Gao Yuzh |
| NFKB1 Gene Mutant Was Associated with Prognosis of Coronary Artery Disease and Exacerbated Endothelial Mitochondrial Fission and Dysfunction. Oxidative medicine and cellular longevity 2022 11 2022 9494926. Luo Jun-Yi, Liu Fen, Fang Bin-Bin, Tian Ting, Li Yan-Hong, Zhang Tong, Li Xiao-Mei, Yang Yi-Ni |
- Page last reviewed:Feb 1, 2024
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