HuGE Literature Finder
Records 1-17
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Association of Single-Nucleotide Polymorphism in the Hepcidin Promoter Gene with Susceptibility to Extrapulmonary Tuberculosis.
Genetic testing and molecular biomarkers 2017 May . Liang Li, Liu Huijuan, Yue Jun, Liu Li-Rong, Han Min, Luo Liu-Lin, Zhao Yan-Lin, Xiao Hepi |
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Interferon lambda polymorphisms associate with body iron indices and hepatic expression of interferon-responsive long non-coding RNA in chronic hepatitis C.
Clinical and experimental medicine 2017 May 17 (2): 225-232. Wróblewska Anna, Bernat Agnieszka, Woziwodzka Anna, Markiewicz Joanna, Romanowski Tomasz, Bielawski Krzysztof P, Smiatacz Tomasz, Sikorska Katarzy |
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Rare HFE Variants are the Most Frequent Cause of Hemochromatosis in non C282Y Homozygous Patients with Hemochromatosis.
American journal of hematology 2016 Aug . Hamdi-Rozé Houda, Beaumont-Epinette Marie-Pascale, Ben Ali Zeineb, Le Lan Caroline, Loustaud Ratti Véronique, Causse Xavier, Loreal Olivier, Deugnier Yves, Brissot Pierre, Jouanolle Anne-Marie, Bardou-Jacquet Edoua |
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The global prevalence of HFE and non-HFE hemochromatosis estimated from analysis of next-generation sequencing data.
Genetics in medicine : official journal of the American College of Medical Genetics 2015 Dec . Wallace Daniel F, Subramaniam V Nath |
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The role of genetic factors in patients with hepatocellular carcinoma and iron overload - a prospective series of 234 patients.
Liver international : official journal of the International Association for the Study of the Liver 2015 Oct . Funakoshi Natalie, Chaze Iphigénie, Alary Anne-Sophie, Tachon Gaëlle, Cunat Séverine, Giansily-Blaizot Muriel, Bismuth Michael, Larrey Dominique, Pageaux Georges-Philippe, Schved Jean-François, Donnadieu-Rigole Hélène, Blanc Pierre, Aguilar-Martinez Patric |
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The hepcidin gene promoter nc.-1010C > T; -582A > G haplotype modulates serum ferritin in individuals carrying the common H63D mutation in HFE gene.
Annals of hematology 2014 Dec 93 (12): 2063-6. Silva Bruno, Pita Lina, Gomes Susana, Gonçalves João, Faustino Pau |
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Influence of iron regulating genes mutations on iron status in Egyptian patients with sickle cell disease.
Annals of clinical and laboratory science 2014 44 (3): 304-9. Abdel Rahman Hala A, Abou-Elew Heba H, El-Shorbagy Reem M, Fawzy Rania, Youssry Ilh |
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Cardiac iron overload in transfusion-dependent patients with myelodysplastic syndromes.
British journal of haematology 2011 Jun . Roy NB, Myerson S, Schuh AH, Bignell P, Patel R, Wainscoat JS, McGowan S, Marchi E, Atoyebi W, Littlewood T, Chacko J, Vyas P, Killick SB |
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Hemojuvelin and hepcidin genes sequencing in Brazilian patients with primary iron overload.
Genetic testing and molecular biomarkers 2010 Dec 14 (6): 803-6. de Lima Santos Paulo Caleb Júnior, Pereira Alexandre C, Cançado Rodolfo D, Schettert Isolmar T, Hirata Rosario D C, Hirata Mario H, Figueiredo Maria Stella, Chiattone Carlos S, Krieger Jose E, Guerra-Shinohara Elvira |
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Genetic study of the hepcidin gene (HAMP) promoter and functional analysis of the c.-582A > G variant.
BMC genetics 2010 11 110. Parajes Silvia, González-Quintela Arturo, Campos Joaquín, Quinteiro Celsa, Domínguez Fernando, Loidi Lourd |
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Non-classical hereditary hemochromatosis in Portugal: novel mutations identified in iron metabolism-related genes.
Annals of hematology 2009 Mar 88 (3): 229-34. Mendes Ana Isabel, Ferro Ana, Martins Rute, Picanço Isabel, Gomes Susana, Cerqueira Rute, Correia Manuel, Nunes António Robalo, Esteves Jorge, Fleming Rita, Faustino Pau |
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Down-regulation of hepcidin in porphyria cutanea tarda.
Blood 2008 Dec 112 (12): 4723-8. Ajioka Richard S, Phillips John D, Weiss Robert B, Dunn Diane M, Smit Maria W, Proll Sean C, Katze Michael G, Kushner James |
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H63D homozygotes with hyperferritinaemia: Is this genotype, the primary cause of iron overload?
European journal of haematology 2007 Jan 78 (1): 66-71. de Diego Carles, Opazo Sonsoles, Murga Maria J, Martínez-Castro Ped |
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HFE C282Y homozygotes aged 25-29 years at HEIRS Study initial screening.
Genetic testing 2007 11 (3): 269-75. Barton James C, Acton Ronald T, Leiendecker-Foster Catherine, Lovato Laura, Adams Paul C, McLaren Gordon D, Eckfeldt John H, McLaren Christine E, Reboussin David M, Gordeuk Victor R, Speechley Mark R, Reiss Jacob A, Press Richard D, Dawkins Fitzroy W, |
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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 |
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The recently identified type 2A juvenile haemochromatosis gene (HJV), a second candidate modifier of the C282Y homozygous phenotype.
Human molecular genetics 2004 Sep 13 (17): 1913-8. Le Gac Gérald, Scotet Virginie, Ka Chandran, Gourlaouen Isabelle, Bryckaert Laurence, Jacolot Sandrine, Mura Catherine, Férec Clau |
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HAMP as a modifier gene that increases the phenotypic expression of the HFE pC282Y homozygous genotype.
Blood 2004 Apr 103 (7): 2835-40. Jacolot Sandrine, Le Gac Gerald, Scotet Virginie, Quere Isabelle, Mura Catherine, Ferec Clau |
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- Page last updated:Jan 15, 2021
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