Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: CYBRD1[original query] |
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Analysis of genes implicated in iron regulation in individuals presenting with primary iron overload. Human genetics 2004 Oct 115 (5): 409-17. Zaahl Monique G, Merryweather-Clarke Alison T, Kotze Maritha J, van der Merwe Schalk, Warnich Louise, Robson Kathryn J |
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 |
Duodenal cytochrome b (Cybrd1) ferric reductase functional studies in cells. Metallomics : integrated biometal science 2017 9 9 (10): 1389-1393. Schlottmann F, Vera-Aviles M, Latunde-Dada G |
A single-nucleotide polymorphism in transferrin is associated with soluble transferrin receptor in Chinese adolescents. Asia Pacific journal of clinical nutrition 2017 26 (6): 1170-1178. Piao Wei, Wang Li, Zhang Ting, Wang Zhen, Shangguan Shaofang, Sun Jing, Huo Junshe |
SLC40A1 and CP single nucleotide polymorphisms in porphyria cutanea tarda patients of mixed ancestry. Annals of human genetics 2018 May . Succi Isabella Brasil, Pôrto Luís Cristóvão, Silva Dayse, Nascimento Adriana, Neto Ronald Costa, Fonseca João Carl |
Genome-wide association study identifies TNFSF15 associated with childhood asthma.
Allergy 2021 May . Kim Kyung Won, Kim Dong Yun, Yoon Dankyu, Kim Ka-Kyung, Jang Haerin, Schoettler Nathan, Kim Eun Gyul, Kim Mi Na, Hong Jung Yeon, Lee Jeom-Kyu, Kim Sangwoo, Ober Carole, Gee Heon Yung, Sohn Myung Hy |
Anemia in female adolescents at Karanganyar regency: A cross-sectional study associated with polymorphism of duodenal cytochrome B gene and daily consumptions of fruits and vegetables. Nutrition and health 2023 9 2601060231201891. Liyana Ilmiyati, Dono Indarto, Brian Wasi |
Polymorphisms Related to Iron Homeostasis Associate with Liver Disease in Chronic Hepatitis C. Viruses 2023 8 15 (8): . Anna Wróblewska, Anna Woziwodzka, Magda Rybicka, Krzysztof P Bielawski, Katarzyna Sikors |
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- Page last updated:Apr 22, 2024
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