Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: Recurrence and C3[original query] |
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The dyslipidemia-associated SNP on the APOA1/C3/A5 gene cluster predicts post-surgery poor outcome in Taiwanese breast cancer patients: a 10-year follow-up study. BMC cancer 2013 13 330. Hsu Mei-Chi, Lee Kuo-Ting, Hsiao Wei-Chiang, Wu Chih-Hsing, Sun Hung-Yu, Lin I-Ling, Young Kung-Ch |
Complement genes strongly predict recurrence and graft outcome in adult renal transplant recipients with atypical hemolytic and uremic syndrome. American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons 2013 Mar 13 (3): 663-75. Le Quintrec M, Zuber J, Moulin B, Kamar N, Jablonski M, Lionet A, Chatelet V, Mousson C, Mourad G, Bridoux F, Cassuto E, Loirat C, Rondeau E, Delahousse M, Frémeaux-Bacchi |
Genetic factors associated with response to as-needed aflibercept therapy for typical neovascular age-related macular degeneration and polypoidal choroidal vasculopathy. Scientific reports 2020 Apr 10 (1): 7188. Yoneyama Seigo, Sakurada Yoichi, Kikushima Wataru, Sugiyama Atsushi, Matsubara Mio, Fukuda Yoshiko, Tanabe Naohiko, Parikh Ravi, Mabuchi Fumihiko, Kashiwagi Kenji, Iijima Hiroyu |
The implication of genetic variation in the complement C3 allotypes on the first-year allograft outcome after live donor liver transplantation. Transplant immunology 2020 Apr 101294. Awad Samah Mohamed, Taha Mohammed, Omar Mahmoud, Khalil Ashr |
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 |
Clinicopathologic Implications of Complement Genetic Variants in Kidney Transplantation. Frontiers in medicine 2021 12 8 775280. Ren Zhen, Perkins Stephen J, Love-Gregory Latisha, Atkinson John P, Java Anu |
Genetic and molecular features of seizure-freedom following surgical resections for focal epilepsy: A pilot study. Frontiers in neurology 2022 10 13 942643. Louis Shreya, Busch Robyn M, Lal Dennis, Hockings Jennifer, Hogue Olivia, Morita-Sherman Marcia, Vegh Deborah, Najm Imad, Ghosh Chaitali, Bazeley Peter, Eng Charis, Jehi Lara, Rotroff Daniel |
Association between HLA alleles and sub-phenotype of childhood steroid-sensitive nephrotic syndrome. World journal of pediatrics : WJP 2022 1 18 (2): 109-119. Lee Hao, Wang Li, Ni Fen-Fen, Yang Xue-Ying, Feng Shi-Pin, Gao Xiao-Jie, Chi Huan, Luo Ye-Tao, Chen Xue-Lan, Yang Bao-Hui, Wan Jun-Li, Jiao Jia, Wu Dao-Qi, Zhang Gao-Fu, Wang Mo, Yang Hai-Ping, Chan Han, Li Q |
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 |
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 |
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- Page last updated:Mar 25, 2024
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