Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 52 Records) |
| Query Trace: Disease and UCP2[original query] |
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| Mitochondrial uncoupling protein gene cluster variation (UCP2-UCP3) and the risk of incident type 2 diabetes mellitus: the Women's Genome Health Study. Atherosclerosis 2011 Jan 214 (1): 107-9. Zee Robert Y L, Ridker Paul M, Chasman Daniel |
| Genetic variants in eleven telomere-associated genes and the risk of incident cardio/cerebrovascular disease: The Women's Genome Health Study. Clinica chimica acta; international journal of clinical chemistry 2011 Jan 412 (1-2): 199-202. Zee Robert Y L, Ridker Paul M, Chasman Daniel |
| The interactive effect of SIRT1 promoter region polymorphism on type 2 diabetes susceptibility in the North Indian population. PloS one 2012 7 (11): e48621. Rai Ekta, Sharma Swarkar, Kaul Surabhi, Jain Kamal, Matharoo Kawaljit, Bhanwer Amarjit S, Bamezai Rameshwar N |
| Association of genetic variants of ghrelin, leptin and UCP2 with malnutrition inflammation syndrome and survival in end-stage renal disease patients. Genes & nutrition 2013 Nov 8 (6): 611-21. Sharma Richa, Agrawal Suraksha, Saxena Anita, Pandey Manmohan, Sharma R |
| Uncoupling protein 2 -866G/A and uncoupling protein 3 -55C/T polymorphisms in young South African Indian coronary artery disease patients. Gene 2013 Jul 524 (2): 79-83. Phulukdaree Alisa, Moodley Devapregasan, Khan Sajidah, Chuturgoon Anil |
| Association between UCP2 A55V polymorphism and risk of cardiovascular events in patients with multi-vessel coronary arterial disease. BMC medical genetics 2013 14 (1): 40. Gioli-Pereira Luciana, Santos Paulo Cjl, Sugaya Luisa S, Ferreira Noely E, Krieger José Eduardo, Pereira Alexandre C, Hueb Whady |
| Associations between UCP1 -3826A/G, UCP2 -866G/A, Ala55Val and Ins/Del, and UCP3 -55C/T polymorphisms and susceptibility to type 2 diabetes mellitus: case-control study and meta-analysis. PloS one 2013 8 (1): 1. de Souza BM, Brondani LA, Bouças AP, Sortica DA, Kramer CK, Canani LH, Leitão CB, Crispim D |
| Polymorphisms of the UCP2 Gene Are Associated with Glomerular Filtration Rate in Type 2 Diabetic Patients and with Decreased UCP2 Gene Expression in Human Kidney. PloS one 2015 10 (7): e0132938. Souza Bianca Marmontel de, Michels Marcus, Sortica Denise Alves, Bouças Ana Paula, Rheinheimer Jakeline, Buffon Marjoriê Piuco, Bauer Andrea Carla, Canani Luís Henrique, Crispim Dai |
| Combined genetic effects of EGLN1 and VWF modulate thrombotic outcome in hypoxia revealed by Ayurgenomics approach. Journal of translational medicine 2015 13 184. Aggarwal Shilpi, Gheware Atish, Agrawal Anurag, Ghosh Saurabh, Prasher Bhavana, Mukerji Mitali, |
| Major components of metabolic syndrome and nutritional intakes in different genotype of UCP2 -866G/A gene polymorphisms in patients with NAFLD. Journal of translational medicine 2016 14 (1): 177. Abbasalizad Farhangi Mahdieh, Mohseni Fatemeh, Farajnia Safar, Jafarabadi Mohammad-Asgha |
| The Genetic Variability of UCP4 Affects the Individual Susceptibility to Late-Onset Alzheimer's Disease and Modifies the Disease's Risk in APOE-?4 Carriers. Journal of Alzheimer's disease : JAD 2016 Feb . Montesanto Alberto, Crocco Paolina, Anfossi Maria, Smirne Nicoletta, Puccio Gianfranco, Colao Rosanna, Maletta Raffaele, Passarino Giuseppe, Bruni Amalia C, Rose Giuseppi |
| The association of uncoupling protein 2 (UCP2) exon 8 insertion/deletion polymorphism and ECG derived QRS duration: A cross-sectional study in an Australian rural population. International journal of cardiology 2017 Feb 228 507-510. Lee Yvonne Yin Leng, Zhou Yuling, Jelinek Herbert F, Hambly Brett D, McLachlan Craig |
| Association of UCP2 -866G>A Polymorphism With Nonalcoholic Fatty Liver Disease in Patients From North-West of Iran. Laboratory medicine 2016 Oct . Mohseni Fatemeh, Farajnia Safar, Farhangi Mahdieh Abbasalizad, Khoshbaten Manouchehr, Jafarabadi Mohammad-Asgha |
| Uncovering the molecular pathogenesis of congenital hyperinsulinism by panel gene sequencing in 32 Chinese patients. Molecular genetics & genomic medicine 2015 Nov 3 (6): 526-36. Fan Zi-Chuan, Ni Jin-Wen, Yang Lin, Hu Li-Yuan, Ma Si-Min, Mei Mei, Sun Bi-Jun, Wang Hui-Jun, Zhou Wen-H |
| Genetic variants within telomere-associated genes, leukocyte telomere length and the risk of acute coronary syndrome in Czech women. Clinica chimica acta; international journal of clinical chemistry 2016 Jan 454 62-65. Dlouha Dana, Pitha Jan, Mesanyova Jana, Mrazkova Jolana, Fellnerova Adela, Stanek Vladimir, Lanska Vera, Hubacek Jaroslav |
| Obesity phenotype in relation to gene polymorphism among samples of Egyptian children and their mothers. Genes & diseases 2018 Jun 5 (2): 150-157. Hassan Nayera E, El-Masry Sahar A, Zarouk Waheba, El Banna Rokia A, Mosaad Rehab M, Al-Tohamy Muhammad, Salamah Abeer Ramad |
| The UCP2 -866G/A, Ala55Val and UCP3 -55C/T polymorphisms are associated with premature coronary artery disease and cardiovascular risk factors in Mexican population. Genetics and molecular biology 2018 May . Gamboa Ricardo, Huesca-Gómez Claudia, López-Pérez Vanessa, Posadas-Sánchez Rosalinda, Cardoso-Saldaña Guillermo, Medina-Urrutia Aida, Juárez-Rojas Juan Gabriel, Soto María Elena, Posadas-Romero Carlos, Vargas-Alarcón Gilber |
| Genetic determinants of steatosis and fibrosis progression in paediatric non-alcoholic fatty liver disease. Liver international : official journal of the International Association for the Study of the Liver 2019 Mar 39 (3): 540-556. Hudert Christian A, Selinski Silvia, Rudolph Birgit, Bläker Hendrik, Loddenkemper Christoph, Thielhorn Ria, Berndt Nikolaus, Golka Klaus, Cadenas Cristina, Reinders Jörg, Henning Stephan, Bufler Philip, Jansen Peter L M, Holzhütter Hermann-Georg, Meierhofer David, Hengstler Jan G, Wiegand Susan |
| -866G/A and Ins/Del polymorphisms in the UCP2 gene and diabetic kidney disease: case-control study and meta-analysis. Genetics and molecular biology 2019 Sep . Dieter Cristine, Assmann Taís Silveira, Lemos Natália Emerim, Massignam Eloísa Toscan, Souza Bianca Marmontel de, Bauer Andrea Carla, Crispim Dai |
| Genetic Associations with Aging Muscle: A Systematic Review. Cells 2019 12 9 (1): . Pratt Jedd, Boreham Colin, Ennis Sean, Ryan Anthony W, De Vito Giusep |
| [Association of maternal diabetes mellitus and UCP2 gene polymorphisms with congenital heart disease in offspring: a case-control study]. Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics 2020 Oct 22 (10): 1092-1099. Luo Liu, Huang Peng, Wang Ting-Ting, Zhao Li-Juan, Ye Zi-Wei, Zhang Sen-Mao, Chen Le-Tao, Diao Jing-Yi, Li Jin-Qi, Li Yi-Huan, Qin Jia- |
| Association of UCP1, UCP2 and UCP3 gene polymorphisms with cardiovascular disease risk factors in European adolescents: the HELENA study. Pediatric research 2020 Jan . Pascual-Gamarra Jose M, Salazar-Tortosa Diego F, Labayen Idoia, Rupérez Azahara I, Leclercq Catherine, Marcos Ascension, Gómez Sonia, Moreno Luis A, Meirhaeghe Aline, Castillo Manuel J, R Ruiz Jonat |
| Impact of KCNJ11 rs5219, UCP2 rs659366, and MTHFR rs1801133 Polymorphisms on Type 2 Diabetes: A Cross-Sectional Study. The review of diabetic studies : RDS 2021 17 (1): 21-29. Lapik Irina Alexandrovna, Ranjit Rajesh, Galchenko Alexey Vladimirovi |
| Quantile-specific heritability of 8-isoprostane and the modulating effects of smoking, alcohol, cardiovascular disease and diabetes on 8-isoprostane-gene interactions. Free radical biology & medicine 2021 12 178 262-270. Williams Paul |
| [Risk of Multiple Sclerosis: Analysis of Interactions Between Variants of Nuclear and Mitochondrial Genomes]. Molekuliarnaia biologiia 0 55 (6): 956-964. Kozin M S, Kiselev I S, Baulina N M, Pavlova G V, Boyko A N, Kulakova O G, Favorova O |
| Leptin Receptor (rs1137101) and Brain-Derived Neurotrophic Factor (rs925946) Gene Variants Are Associated with Obesity in the Early- but Not in the Late-Onset Population of Hungarian Psoriatic Patients. Life (Basel, Switzerland) 2021 Oct 11 (10): . Szentkereszty-Kovács Zita, Fiatal Szilvia, Janka Eszter Anna, Kovács Dóra, Szegedi Andrea, Remenyik Éva, Tör?csik Dáni |
| The Association of UCP2-866 G/A Genotype with Autoimmune Hypothyroidism in the Southwestern Saudi Arabia Population. International journal of general medicine 2023 3 16 875-879. Habibullah Mahmoud M, Hakamy Ali, Mansor Abdullah S, Atti Ibrahim Mohammed, Alwadani Abbas Ali Jaber, Kaabi Yahia |
| UCP2 polymorphisms, daily step count, and number of teeth associated with all-cause mortality risk in Sado City: A hospital-based cohort study. Heliyon 2024 7 10 (12): e32512. Han Lyu, Noriko Sugita, Shigeki Komatsu, Minako Wakasugi, Akio Yokoseki, Akihiro Yoshihara, Tetsuo Kobayashi, Kenji Sato, Hiroyuki Kawashima, Osamu Onodera, Ichiei Narita, Koichi Tabe |
| Genetic variants in DBC1, SIRT1, UCP2 and ADRB2 as potential biomarkers for severe obesity and metabolic complications. Frontiers in genetics 2024 6 15 1363417. Ana Carolina Proença da Fonseca, Izadora Sthephanie da Silva Assis, Kaio Cezar Rodrigues Salum, Lohanna Palhinha, Gabriella de Medeiros Abreu, Verônica Marques Zembrzuski, Mario Campos Junior, José Firmino Nogueira-Neto, Amanda Cambraia, Mauro Lucio Ferreira Souza Junior, Clarissa Menezes Maya-Monteiro, Pedro Hernán Cabello, Patrícia Torres Bozza, João Regis Ivar Carnei |
| Deletion of the Murine Ortholog of the Human 9p21.3 Locus Leads to Insulin Resistance and Obesity in Hypercholesterolemic Mice. Cells 2024 6 13 (11): . Sanna Kettunen, Tuisku Suoranta, Sadegh Beikverdi, Minja Heikkilä, Anna Slita, Iida Räty, Elias Ylä-Herttuala, Katariina Öörni, Anna-Kaisa Ruotsalainen, Seppo Ylä-Herttua |
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