HuGE Literature Finder
Records
1
-
4
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 |
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 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 |
- Page last reviewed:Oct 1, 2021
- Page last updated:Jun 22, 2022
- Content source: