Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 63 Records) |
| Query Trace: Disease and C5[original query] |
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| Lack of association of variants previously associated with anti-TNF medication response in rheumatoid arthritis patients: results from a homogeneous Greek population. PloS one 2013 8 (9): e74375. Zervou Maria I, Myrthianou Efsevia, Flouri Irene, Plant Darren, Chlouverakis Gregory, Castro-Giner Francesc, Rapsomaniki Panayiota, Barton Anne, Boumpas Dimitrios T, Sidiropoulos Prodromos, Goulielmos George |
| Investigation of juvenile idiopathic arthritis susceptibility loci: results from a Greek population. Human immunology 2013 Sep 74 (9): 1194-8. Dimopoulou D G, Zervou M I, Trachana M, Myrthianou E, Pratsidou-Gertsi P, Kardassis D, Garyfallos A, Goulielmos G |
| A genetic role for macrophage migration inhibitory factor (MIF) in adult-onset Still's disease. Arthritis research & therapy 2013 15 (3): R65. Wang Fang-Fang, Huang Xin-Fang, Shen Nan, Leng Lin, Bucala Richard, Chen Shun-Le, Lu Liang-Ji |
| Independent replication analysis of genetic loci with previous evidence of association with juvenile idiopathic arthritis. Pediatric rheumatology online journal 2013 11 (1): 12. Ellis Justine A, Chavez Raul A, Pezic Angela, Ponsonby Anne-Louise, Akikusa Jonathan D, Allen Roger C, Munro Jane |
| Susceptibility to childhood-onset rheumatoid arthritis: investigation of a weighted genetic risk score that integrates cumulative effects of variants at five genetic loci. Arthritis and rheumatism 2013 Jun 65 (6): 1663-7. Prahalad Sampath, Conneely Karen N, Jiang Yunxuan, Sudman Marc, Wallace Carol A, Brown Milton R, Ponder Lori A, Rohani-Pichavant Mina, Zwick Michael E, Cutler David J, Angeles-Han Sheila T, Vogler Larry B, Kennedy Christine, Rouster-Stevens Kelly, Wise Carol A, Punaro Marilynn, Reed Ann M, Mellins Elizabeth D, Bohnsack John F, Glass David N, Thompson Susan |
| Association between polymorphism in TRAF1/C5 gene and risk of rheumatoid arthritis: a meta-analysis. Molecular biology reports 2014 Jan 41 (1): 317-24. Zhang Xingang, Li Wei, Zhang Xinpeng, Zhang Xiaoli, Jiang Li, Guo Yun, Wang Xiaof |
| Common genetic variants of the human steroid 21-hydroxylase gene (CYP21A2) are related to differences in circulating hormone levels. PloS one 2014 9 (9): e107244. Doleschall Márton, Szabó Julianna Anna, Pázmándi Júlia, Szilágyi Ágnes, Koncz Klára, Farkas Henriette, Tóth Miklós, Igaz Péter, Gláz Edit, Prohászka Zoltán, Korbonits Márta, Rácz Károly, Füst George, Patócs Atti |
| A complement C5 gene mutation, c.754G>A:p.A252T, is common in the Western Cape, South Africa and found to be homozygous in seven percent of Black African meningococcal disease cases. Molecular immunology 2015 Mar 64 (1): 170-6. Owen E Patricia, Würzner Reinhard, Leisegang Felicity, Rizkallah Pierre, Whitelaw Andrew, Simpson John, Thomas Andrew D, Harris Claire L, Giles Joanna L, Hellerud Bernt C, Mollnes Tom E, Morgan B Paul, Potter Paul C, Orren A |
| Copy number variations and gene polymorphisms of complement components in ocular Behcet's disease and Vogt-Koyanagi-Harada syndrome. Scientific reports 2015 5 12989. Xu Dengfeng, Hou Shengping, Zhang Jun, Jiang Yanni, Kijlstra Aize, Yang Peize |
| Functional analysis of a complement polymorphism (rs17611) associated with rheumatoid arthritis. Journal of immunology (Baltimore, Md. : 1950) 2015 Apr 194 (7): 3029-34. Giles Joanna L, Choy Ernest, van den Berg Carmen, Morgan B Paul, Harris Claire |
| Epistasis analysis links immune cascades and cerebral amyloidosis. Journal of neuroinflammation 2015 12 (1): 227. Benedet Andréa L, Labbe Aurélie, Lemay Philippe, Zimmer Eduardo R, Pascoal Tharick A, Leuzy Antoine, Mathotaarachchi Sulantha, Mohades Sara, Shin Monica, Dionne-Laporte Alexandre, Beaudry Thomas, Picard Cynthia, Gauthier Serge, Poirier Judes, Rouleau Guy, Rosa-Neto Pedro, |
| Genetic Predictors of Poor Prognosis in Portuguese Patients with Juvenile Idiopathic Arthritis: Data from Reuma.pt. Journal of immunology research 2015 2015 706515. Mourão Ana Filipa, Santos Maria José, Mendonça Sílvia, Oliveira-Ramos Filipa, Salgado Manuel, Estanqueiro Paula, Melo-Gomes José, Martins Fernando, Lopes Ana, Bettencourt Bruno Filipe, Bruges-Armas Jácome, Costa José, Furtado Carolina, Figueira Ricardo, Brito Iva, Branco Jaime, Fonseca João Eurico, Canhão Hele |
| Butyrylcholinesterase: K variant, plasma activity, molecular forms and rivastigmine treatment in Alzheimer's disease in a Southern Brazilian population. Neurochemistry international 2015 Feb 81 57-62. Bono G F, Simão-Silva D P, Batistela M S, Josviak N D, Dias P F R, Nascimento G A, Souza R L R, Piovezan M R, Souza R K M, Furtado-Alle |
| Systemic complement activation and complement gene analysis in enterohaemorrhagic Escherichia coli-associated paediatric haemolytic uraemic syndrome. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2016 May . Ahlenstiel-Grunow Thurid, Hachmeister Svenja, Bange Franz Christoph, Wehling Cyrill, Kirschfink Michael, Bergmann Carsten, Pape La |
| Genetic Investigation of Complement Pathway Genes in Type 2 Diabetic Retinopathy: An Inflammatory Perspective. Mediators of inflammation 2016 2016 1313027. Yang Ming Ming, Wang Jun, Ren Hong, Sun Yun Duan, Fan Jiao Jie, Teng Yan, Li Yan |
| Single-Nucleotide Polymorphism rs17611 of Complement Component 5 Shows Association with Ischemic Stroke in Northeast Chinese Population. Genetic testing and molecular biomarkers 2016 Oct . Guo Liang, Zheng Liqiang, Guo Xiaofan, Chang Ye, Zhou Xinghu, Sun Yingxi |
| GLCE rs3865014 (Val597Ile) polymorphism is associated with breast cancer susceptibility and triple-negative breast cancer in Siberian population. Gene 2017 Jul . Belyavskaya Valentina A, Prudnikova Tatiana Y, Domanitskaya Natalya V, Litviakov Nikolay V, Maksimov Vladimir N, Cherdyntseva Nadezhda V, Grigorieva Elvira |
| Association of TRAF1/C5 Locus Polymorphisms with Epilepsy and Clinical Traits in Mexican Patients with Neurocysticercosis. Infection and immunity 2019 10 87 (12): . Villegas Marcela, Sciutto Edda, Rosetti Marcos, Fleury Agnes, Fragoso Glad |
| Relationship between Aflibercept Efficacy and Genetic Variants of Genes Associated with Neovascular Age-Related Macular Degeneration: The BIOIMAGE Trial. Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde 2020 May . Burés Jelstrup Anniken, Pomares Esther, Navarro Rafael, |
| Cough hypersensitivity in patients with metabolic syndrome: a clinical finding and its possible mechanisms. BMC pulmonary medicine 2021 9 21 (1): 284. Cheng Jiafen, Xie Zhuangli, Wang Shengyuan, Wen Siwan, Niu Shanshan, Shi Cuiqin, Yu Li, Xu Xianghu |
| A genetic variant in the TRAF1/C5 gene lead susceptibility to active pulmonary tuberculosis by decreased TNF-? levels. Microbial pathogenesis 2021 Aug 159 105117. Souza de Lima Dhêmerson, Fadoul de Brito Carolina, Cavalcante Barbosa Aguyda Rayany, Brasil de Andrade Figueira Mariana, Maciel Bonet Julio César, Walzer Joseph, Ramasawmy Rajendranath, Ogusku Mauricio Morishi, Sadahiro Aya, Boechat Antonio Lu |
| The Influence of an Elastase-Sensitive Complement C5 Variant on Lupus Nephritis and Its Flare. Kidney international reports 2021 Aug 6 (8): 2105-2113. Toy Chris R, Song Huijuan, Nagaraja Haikady N, Scott Julia, Greco Jessica, Zhang Xiaolan, Yu Chack-Yung, Tumlin James A, Rovin Brad H, Hebert Lee A, Birmingham Daniel |
| C5 Variant rs10985126 is Associated with Mortality in Patients with Symptomatic Coronary Artery Disease. Pharmacogenomics and personalized medicine 2021 14 893-903. Henes Jessica Kristin, Groga-Bada Patrick, Schaeffeler Elke, Winter Stefan, Hack Luis, Zdanyte Monika, Mueller Karin, Droppa Michal, Stimpfle Fabian, Gawaz Meinrad, Langer Harald, Schwab Matthias, Geisler Tobias, Rath Domin |
| CFH I62V as a Putative Genetic Marker for Posner-Schlossman Syndrome. Frontiers in immunology 2021 3 12 608723. Yang Ming Ming, Sun Hong Yan, Meng Ting, Qiu Shan Hu, Zeng Qi Qiao, Ng Tsz Kin, Jiang Li, Deng Ting Ming, Zeng Ai Neng, Wang Jun, Luo Xiao Li |
| Genetic analysis of four consanguineous multiplex families with inflammatory bowel disease. Gastroenterology report 2021 12 9 (6): 521-532. Ben-Yosef Noam, Frampton Matthew, Schiff Elena R, Daher Saleh, Abu Baker Fadi, Safadi Rifaat, Israeli Eran, Segal Anthony W, Levine Adam |
| Cytokine TGF? Gene Polymorphism in Asthma: TGF-Related SNP Analysis Enhances the Prediction of Disease Diagnosis (A Case-Control Study With Multivariable Data-Mining Model Development). Frontiers in immunology 2022 13 746360. Panek Micha?, Stawiski Konrad, Kaszkowiak Marcin, Kuna Pio |
| C5 and SRGAP3 Polymorphisms Are Linked to Paediatric Allergic Asthma in the Italian Population. Genes 2022 Jan 13 (2): . Messelodi Daria, Giuliani Cristina, Cipriani Francesca, Armuzzi Silvia, di Palmo Emanuela, Garagnani Paolo, Bertelli Luca, Astolfi Annalisa, Luiselli Donata, Ricci Giampaolo, Pession Andr |
| Rare variants in genes coding for components of the terminal pathway of the complement system in preeclampsia. Research square 2024 4 . A Lokki, Michael Triebwasser, Emma Daly, Finnpec Cohort, Mrtja Kurki, Markus Perola, Kirsi Auro, Jane Salmon, Anuja Java, Mark Daly, John Atkinson, Hannele Laivuori, Seppo Me |
| Understanding rare genetic variants within the terminal pathway of complement system in preeclampsia. Genes and immunity 2024 12 . A Inkeri Lokki, Michael Triebwasser, Emma Daly, , Mitja I Kurki, Markus Perola, Kirsi Auro, Jane E Salmon, Java Anuja, Mark Daly, John P Atkinson, Hannele Laivuori, Seppo Me |
| Using genetics to explore complement C5 as a druggable protein in periodontitis. Frontiers in immunology 2024 10 15 1407431. Zoheir Alayash, Sebastian-Edgar Baumeister, Birte Holtfreter, Thomas Kocher, Hansjörg Baurecht, Benjamin Ehmke, Stefan Lars Reckelkamm, Michael Nol |
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