Human Genome Epidemiology Literature Finder
Records 1 - 16 (of 16 Records) |
Query Trace: Glomerulonephritis and C3[original query] |
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Mannose-binding lectin-low genotypes are associated with milder systemic and immunological disease expression in primary Sjögren's syndrome. Rheumatology (Oxford, England) 2009 Jan 48 (1): 65-9. Ramos-Casals M, Brito-Zerón P, Soria N, Nardi N, Vargas A, Muñoz S, Bové A, Suárez B, Lozano |
Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies. Kidney international 2012 Mar . Servais A, Noël LH, Roumenina LT, Le Quintrec M, Ngo S, Dragon-Durey MA, Macher MA, Zuber J, Karras A, Provot F, Moulin B, Grünfeld JP, Niaudet P, Lesavre P, Frémeaux-Bacchi V |
Complement factor H gene associations with end-stage kidney disease in African Americans. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2014 Jul 29 (7): 1409-14. Bonomo Jason A, Palmer Nicholette D, Hicks Pamela J, Lea Janice P, Okusa Mark D, Langefeld Carl D, Bowden Donald W, Freedman Barry |
C3 glomerulonephritis and autoimmune disease: more than a fortuitous association? Journal of nephrology 2015 Jul . Alexander Mariam P, Fervenza Fernando C, De Vriese An S, Smith Richard J H, Nasr Samih H, Cornell Lynn D, Herrera Hernandez Loren P, Zhang Yuzhou, Sethi Sanje |
Complement gene variants determine the risk of immunoglobulin-associated MPGN and C3 glomerulopathy and predict long-term renal outcome. Molecular immunology 2016 Feb 71 131-142. Iatropoulos Paraskevas, Noris Marina, Mele Caterina, Piras Rossella, Valoti Elisabetta, Bresin Elena, Curreri Manuela, Mondo Elena, Zito Anna, Gamba Sara, Bettoni Serena, Murer Luisa, Fremeaux-Bacchi Veronique, Vivarelli Marina, Emma Francesco, Daina Erica, Remuzzi Giusep |
Outcome of membranoproliferative glomerulonephritis and C3-glomerulopathy in children and adolescents. Pediatric nephrology (Berlin, Germany) 2018 9 33 (12): 2289-2298. Holle Johannes, Berenberg-Goßler Lena, Wu Kaiyin, Beringer Ortraud, Kropp Florian, Müller Dominik, Thumfart Jul |
Genetic polymorphism in C3 is associated with progression in chronic kidney disease (CKD) patients with IgA nephropathy but not in other causes of CKD. PloS one 2020 15 (1): e0228101. Ibrahim Sara T, Chinnadurai Rajkumar, Ali Ibrahim, Payne Debbie, Rice Gillian I, Newman William G, Algohary Eman, Adam Ahmed G, Kalra Philip |
The contribution of the LOC105371267 and MRPS30-DT genetic polymorphisms to IgA nephropathy in the Chinese Han population. American journal of translational research 2021 11 13 (10): 11718-11727. Chen Xiaoyan, Li Haiyue, Liu Yuanwei, Liu Jianfeng, Sun Yao, Wu Jiamin, Xiong Zichao, Cao W |
Role of fluid-phase complement system regulation in the development of hepatitis C virus-associated glomerulonephritis. PloS one 2022 17 (10): e0276017. Ibrahim Sara T, Abdelhamid Marwa R, Lewis Neveen, Baddour Nahed, Adam Ahmed |
Genetic investigation of Nordic patients with complement-mediated kidney diseases. Frontiers in immunology 2023 9 14 1254759. Viktor Rydberg, Sigridur Sunna Aradottir, Ann-Charlotte Kristoffersson, Naila Svitacheva, Diana Karpm |
Mesangial C3 Deposition, Complement-Associated Variant, and Disease Progression in IgA Nephropathy. Clinical journal of the American Society of Nephrology : CJASN 2023 8 . Yuqi Kang, Boyang Xu, Sufang Shi, Xujie Zhou, Pei Chen, Lijun Liu, Yebei Li, Yueqi Leng, Jicheng Lv, Li Zhu, Hong Zha |
Rare Variants in Complement Gene in C3 Glomerulopathy and Immunoglobulin-Mediated Membranoproliferative Glomerulonephritis. Clinical journal of the American Society of Nephrology : CJASN 2023 8 . Marie Sophie Meuleman, Paula Vieira Martins, Carine El Sissy, Vincent Audard, Véronique Baudouin, Dominique Bertrand, Frank Bridoux, Férielle Louillet, Claire Dossier, Vincent Esnault, Noémie Jourde-Chiche, Alexandre Karras, Marie-Pascale Morin, François Provot, Philippe Remy, David Ribes, Caroline Rousset-Rouviere, Aude Servais, Eric Thervet, Leila Tricot, Mohamad Zaidan, Alain Wynckel, Julien Zuber, Moglie Le Quintrec, Véronique Frémeaux-Bacchi, Sophie Chauv |
Complement alternative pathway determines disease susceptibility and severity in antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis. Kidney international 2023 11 . Laura Lucientes-Continente, Gema Fernández-Juárez, Bárbara Márquez-Tirado, Laura Jiménez-Villegas, Mercedes Acevedo, Teresa Cavero, Luís Sánchez Cámara, Juliana Draibe, Paula Anton-Pampols, Fernando Caravaca-Fontán, Manuel Praga, Javier Villacorta, Elena Goicoechea de Jor |
Low C3 in a 4-month-old baby: is it a problem? Pediatric nephrology (Berlin, Germany) 2023 11 . Gül?ah Kaya Aksoy, Mustafa Gökhan Ertosun, Mustafa Koyun, Elif Çomak, Sema Akm |
Evaluation of the significance of complement-related genes mutations in atypical postinfectious glomerulonephritis: a pilot study. International urology and nephrology 2023 10 . Feng Xu, Changming Zhang, Mingchao Zhang, Xiaodong Zhu, Shuiqin Cheng, Zhen Cheng, Caihong Zeng, Song Jia |
Anti-factor B antibodies in atypical hemolytic uremic syndrome. Pediatric nephrology (Berlin, Germany) 2024 1 . Priyanka Khandelwal, Shreesha Nambiar, Rahul Saini, Savita Saini, Poonam Coshic, Aditi Sinha, Pankaj Hari, Jayanth Kumar Palanichamy, Arvind Bag |
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- Page last updated:Apr 22, 2024
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