Human Genome Epidemiology Literature Finder
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Records 1 - 7 (of 7 Records) |
| Query Trace: Inflammation and UCP2[original query] |
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| Association of common variants of UCP2 gene with low-grade inflammation in Swedish children and adolescents; the European Youth Heart Study. Pediatric research 2009 Jun . Labayen I, Ortega FB, Sjöström M, Nilsson TK, Olsson LA, Ruiz JR |
| 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 |
| 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 |
| The Role of Genetic Profile in Functional Performance Adaptations to Exercise Training or Physical Activity: A Systematic Review of the Literature. Journal of aging and physical activity 2019 1 27 (4): 594-616. Wilson Guy C, Mavros Yorgi, Tajouri Lotti, Singh Maria Fiataro |
| 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 |
- Page last reviewed:Feb 1, 2024
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