Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Hemochromatosis and CYBRD1[original query] |
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A novel association between a SNP in CYBRD1 and serum ferritin levels in a cohort study of HFE hereditary haemochromatosis. British journal of haematology 2009 Oct 147 (1): 140-9. Constantine Clare C, Anderson Greg J, Vulpe Chris D, McLaren Christine E, Bahlo Melanie, Yeap Heng Lin, Gertig Dorota M, Osborne Nicholas J, Bertalli Nadine A, Beckman Kenneth B, Chen Victoria, Matak Pavel, McKie Andrew T, Delatycki Martin B, Olynyk John K, English Dallas R, Southey Melissa C, Giles Graham G, Hopper John L, Allen Katrina J, Gurrin Lyle |
CYBRD1 as a modifier gene that modulates iron phenotype in HFE p.C282Y homozygous patients. Haematologica 2012 Dec 97 (12): 1818-25. Pelucchi Sara, Mariani Raffaella, Calza Stefano, Fracanzani Anna Ludovica, Modignani Giulia Litta, Bertola Francesca, Busti Fabiana, Trombini Paola, Fraquelli Mirella, Forni Gian Luca, Girelli Domenico, Fargion Silvia, Specchia Claudia, Piperno Alber |
Analysis of polymorphism and hepatic expression of duodenal cytochrome b in chronic hepatitis C. Journal of gastroenterology and hepatology 2017 Feb 32 (2): 482-486. Rudnicka Alina, Woziwodzka Anna, Wróblewska Anna, Rybicka Magda, Bielawski Krzysztof P, Sikorska Katarzyna, Bernat Agniesz |
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