Human Genome Epidemiology Literature Finder
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Records 1 - 22 (of 22 Records) |
| Query Trace: Disease and TFR2[original query] |
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| Can defects in transferrin receptor 2 and hereditary hemochromatosis genes account for iron overload in HbH disease? Blood cells, molecules & diseases 0 30 (1): 107-11. Chan Vivian, Wong Man Sim, Ooi Clara, Chen F E, Chim C S, Liang R H S, Todd D, Chan T |
| Comprehensive hereditary hemochromatosis genotyping. Tissue antigens 2002 Dec 60 (6): 481-8. Jones D C, Young N T, Pigott C, Fuggle S V, Barnardo M C N M, Marshall S E, Bunce |
| Investigation of genetic variants of genes of the hemochromatosis pathway and their role in breast cancer. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2005 May 14 (5): 1102-7. Abraham Benny K, Justenhoven Christina, Pesch Beate, Harth Volker, Weirich Gregor, Baisch Christian, Rabstein Sylvia, Ko Yon-Dschun, Brüning Thomas, Fischer Hans-Peter, Haas Susanne, Brod Sandra, Oberkanins Christian, Hamann Ute, Brauch Hiltrud, |
| 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 |
| Common variants in the BMP2, BMP4, and HJV genes of the hepcidin regulation pathway modulate HFE hemochromatosis penetrance. American journal of human genetics 2007 Oct 81 (4): 799-807. Milet Jacqueline, Dehais Valerie, Bourgain Catherine, Jouanolle Anne Marie, Mosser Annick, Perrin Michele, Morcet Jeff, Brissot Pierre, David Veronique, Deugnier Yves, Mosser Je |
| The A Allele of the -576G>A polymorphism of the transferrin gene is associated with the increased risk of age-related macular degeneration in smokers. The Tohoku journal of experimental medicine 2011 223 (4): 253-61. Wysokinski Daniel, Szaflik Jerzy, Sklodowska Anna, Kolodziejska Urszula, Dorecka Mariola, Romaniuk Dorota, Wozniak Katarzyna, Blasiak Janusz, Szaflik Jacek Paw |
| TFR2-related hereditary hemochromatosis as a frequent cause of primary iron overload in patients from Central-Southern Italy. Blood cells, molecules & diseases 2013 Sep . Radio FC, Majore S, Binni F, Valiante M, Ricerca BM, De Bernardo C, Morrone A, Grammatico P |
| Association between genetic variations in TFR2 gene and coronary heart disease in Chinese: a case-control study. Journal of cardiovascular medicine (Hagerstown, Md.) 2013 Jun . Shi Y, Lian Y, Zhou L, Huang L, Zhang X, Guo H, Wu T, Cheng L, He M |
| Genetic and biochemical markers in patients with Alzheimer's disease support a concerted systemic iron homeostasis dysregulation. Neurobiology of aging 2014 Apr 35 (4): 777-85. Crespo Ângela C, Silva Bruno, Marques Liliana, Marcelino Erica, Maruta Carolina, Costa Sónia, Timóteo Angela, Vilares Arminda, Couto Frederico Simões, Faustino Paula, Correia Ana Paula, Verdelho Ana, Porto Graça, Guerreiro Manuela, Herrero Ana, Costa Cristina, de Mendonça Alexandre, Costa Luciana, Martins Madale |
| Pooled analysis of iron-related genes in Parkinson's disease: association with transferrin. Neurobiology of disease 2014 Feb 62 172-8. Rhodes Shannon L, Buchanan Daniel D, Ahmed Ismaïl, Taylor Kent D, Loriot Marie-Anne, Sinsheimer Janet S, Bronstein Jeff M, Elbaz Alexis, Mellick George D, Rotter Jerome I, Ritz Bea |
| Evaluation of genome-wide loci of iron metabolism in hereditary hemochromatosis identifies PCSK7 as a host risk factor of liver cirrhosis. Human molecular genetics 2014 Jul 23 (14): 3883-90. Stickel Felix, Buch Stephan, Zoller Heinz, Hultcrantz Rolf, Gallati Sabina, Österreicher Christoph, Finkenstedt Armin, Stadlmayr Andreas, Aigner Elmar, Sahinbegovic Enijad, Sarrazin Christoph, Schafmayer Clemens, Braun Felix, Erhart Wiebke, Nothnagel Michael, Lerch Markus M, Mayerle Julia, Völzke Henry, Schaller André, Kratzer Wolfgang, Boehm Bernhard O, Sipos Bence, D'Amato Mauro, Torkvist Leif, Stal Per, Arlt Alexander, Franke Andre, Becker Thomas, Krawczak Michael, Zwerina Jochen, Berg Thomas, Hinrichsen Holger, Krones Elisabeth, Dejaco Christian, Strasser Michael, Datz Christian, Hampe Joch |
Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis.
Nature communications 2014 5 4926. Benyamin Beben, Esko Tonu, Ried Janina S, Radhakrishnan Aparna, Vermeulen Sita H, Traglia Michela, Gögele Martin, Anderson Denise, Broer Linda, Podmore Clara, Luan Jian'an, Kutalik Zoltan, Sanna Serena, van der Meer Peter, Tanaka Toshiko, Wang Fudi, Westra Harm-Jan, Franke Lude, Mihailov Evelin, Milani Lili, Hälldin Jonas, Häldin Jonas, Winkelmann Juliane, Meitinger Thomas, Thiery Joachim, Peters Annette, Waldenberger Melanie, Rendon Augusto, Jolley Jennifer, Sambrook Jennifer, Kiemeney Lambertus A, Sweep Fred C, Sala Cinzia F, Schwienbacher Christine, Pichler Irene, Hui Jennie, Demirkan Ayse, Isaacs Aaron, Amin Najaf, Steri Maristella, Waeber Gérard, Verweij Niek, Powell Joseph E, Nyholt Dale R, Heath Andrew C, Madden Pamela A F, Visscher Peter M, Wright Margaret J, Montgomery Grant W, Martin Nicholas G, Hernandez Dena, Bandinelli Stefania, van der Harst Pim, Uda Manuela, Vollenweider Peter, Scott Robert A, Langenberg Claudia, Wareham Nicholas J, , van Duijn Cornelia, Beilby John, Pramstaller Peter P, Hicks Andrew A, Ouwehand Willem H, Oexle Konrad, Gieger Christian, Metspalu Andres, Camaschella Clara, Toniolo Daniela, Swinkels Dorine W, Whitfield John |
| Hereditary hemochromatosis type 1 phenotype modifiers in Italian patients. The controversial role of variants in HAMP, BMP2, FTL and SLC40A1 genes. Blood cells, molecules & diseases 2015 Jun 55 (1): 71-5. Radio Francesca Clementina, Majore Silvia, Aurizi Caterina, Sorge Fiammetta, Biolcati Gianfranco, Bernabini Sara, Giotti Irene, Torricelli Francesca, Giannarelli Diana, De Bernardo Carmelilia, Grammatico Pao |
| 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 |
| HJV and HFE Play Distinct Roles in Regulating Hepcidin. Antioxidants & redox signaling 2015 May 22 (15): 1325-36. Wu Qian, Wang Hao, An Peng, Tao Yunlong, Deng Jiali, Zhang Zhuzhen, Shen Yuanyuan, Chen Caiyong, Min Junxia, Wang Fu |
| 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 |
| Association of SNPs in transferrin and transferrin receptor genes with blood iron levels in human. Legal medicine (Tokyo, Japan) 2018 Oct 36 17-20. Fujihara Junko, Yasuda Toshihiro, Kimura-Kataoka Kaori, Takeshita Har |
| Role of TfR2-Y250X and TfR1- rs3817672 Single Nucleotide Polymorphism on Pathophysiology of Iron Deficiency Anemia. The Journal of the Association of Physicians of India 2019 Nov 67 (11): 36-39. Pandey Sweta, Pandey Sanjay Kumar, Shah Vine |
| Hepcidin (rs10421768), Transferrin (rs3811647, rs1049296) and Transferrin Receptor 2 (rs7385804) Gene Polymorphism Might Be Associated with the Origin of Multiple Sclerosis. International journal of environmental research and public health 2022 06 19 (11): . Stachowska Laura, Koziarska Dorota, Karakiewicz Beata, Kotwas Artur, Knyszy?ska Anna, Folwarski Marcin, Dec Karolina, Stachowska Ewa, Hawry?kowicz Viktoria, Kulaszy?ska Monika, So?ek-Pastuszka Joanna, Skonieczna-?ydecka Karoli |
| Genetic variants in promoter region of TFR2 is associated with the risk of non-alcoholic fatty liver disease in a Chinese Han population: a case-control study. Gastroenterology report 2022 11 10 goac060. Pan Xinting, Peng Hewei, Zhang Junchao, Wu Yunli, Hu Zhijian, Peng Xian |
| 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 |
| Transcriptome-wide association study and Mendelian randomization in pancreatic cancer identifies susceptibility genes and causal relationships with type 2 diabetes and venous thromboembolism. EBioMedicine 2024 7 106 105233. Marcus C B Tan, Chelsea A Isom, Yangzi Liu, David-Alexandre Trégouët, , Lang Wu, Dan Zhou, Eric R Gamaz |
- Page last reviewed:Feb 1, 2024
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