HuGE Literature Finder
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Targeted genotyping of COVID-19 patients reveals a signature of complement C3 and factor B coding SNPs associated with severe infection. Immunobiology 2023 2 228 (2): 152351. Tsiftsoglou Stefanos A, Gavriilaki Eleni, Touloumenidou Tasoula, Koravou Evaggelia-Evdoxia, Koutra Maria, Papayanni Penelope Georgia, Karali Vassiliki, Papalexandri Apostolia, Varelas Christos, Chatzopoulou Fani, Chatzidimitriou Maria, Chatzidimitriou Dimitrios, Veleni Anastasia, Rapti Evdoxia, Kioumis Ioannis, Kaimakamis Evaggelos, Bitzani Milly, Boumpas Dimitrios T, Tsantes Argyris, Sotiropoulos Damianos, Papadopoulou Anastasia, Sakellari Ioanna, Kokoris Styliani, Anagnostopoulos Achill |
CD46 Genetic Variability and HIV-1 Infection Susceptibility. Cells 2021 11 10 (11): . Serrano-Rísquez Carmen, Omar Mohamed, Gómez-Vidal María Amparo, Real Luis Miguel, Pineda Juan Antonio, Rivero Antonio, Rivero-Juárez Antonio, Forthal Donald, Márquez Francisco J, Lo Caputo Sergio, Clerici Mario, Biasin Mara, Caruz Anton |
Genetic Polymorphisms in the Host and COVID-19 Infection. Advances in experimental medicine and biology 2021 5 1318 109-118. Delanghe Joris R, De Buyzere Marc L, Speeckaert Marijn |
Hepatitis B Virus Infection Among Leprosy Patients: A Case for Polymorphisms Compromising Activation of the Lectin Pathway and Complement Receptors. Frontiers in immunology 2021 3 11 574457. Boldt Angelica Beate Winter, Oliveira-Toré Camila de Freitas, Kretzschmar Gabriela Canalli, Weinschutz Mendes Hellen, Stinghen Sérvio Túlio, Andrade Fabiana Antunes, Bumiller-Bini Valéria, Gonçalves Letícia Boslooper, Braga Anna Carolina de Moraes, Stahlke Ewalda von Rosen Seeling, Velavan Thirumalaisamy P, Thiel Steffen, de Messias-Reason Iara José Tabor |
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 |
Abnormal DNA methylation patterns in patients with infection?caused leukocytopenia based on methylation microarrays. Molecular medicine reports 2020 4 21 (6): 2335-2348. Wu Chao, Muhataer Xirennayi, Wang Wenyi, Deng Mingqin, Jin Rong, Lian Zhichuang, Luo Dan, Li Yafang, Yang Xiaoho |
Interactive Impacts from Hepatitis C Virus Infection and Mixed Cryoglobulinemia on Complement Levels. Digestive diseases and sciences 2020 8 66 (7): 2407-2416. Chang Ming-Ling, Hu Jing-Hong, Chen Wei-Ting, Lin Ming-Shyan, Kuo Chia-Jung, Chen Shiang-Chi, Chien Rong-N |
Newborn Screening for Methylmalonic Acidemia in a Chinese Population: Molecular Genetic Confirmation and Genotype Phenotype Correlations. Frontiers in genetics 2019 2 9 726. Zhou Wei, Li Huizhong, Wang Chuanxia, Wang Xiuli, Gu Maoshe |
MBL2 gene polymorphism rs1800450 and rheumatic fever with and without rheumatic heart disease: an Egyptian pilot study. Pediatric rheumatology online journal 2018 Apr 16 (1): 24. Gomaa Maher Hassan, Ali Shawkey Sadik, Fattouh Aya Mohamed, Hamza Hala Salah, Badr Mohamed Moham |
A novel quantitative hemolytic assay coupled with restriction fragment length polymorphisms analysis enabled early diagnosis of atypical hemolytic uremic syndrome and identified unique predisposing mutations in Japan. PloS one 2015 10 (5): e0124655. Yoshida Yoko, Miyata Toshiyuki, Matsumoto Masanori, Shirotani-Ikejima Hiroko, Uchida Yumiko, Ohyama Yoshifumi, Kokubo Tetsuro, Fujimura Yoshihi |
Complement alternative pathway genetic variation and Dengue infection in the Thai population. Clinical and experimental immunology 2013 Nov 174 (2): 326-34. Kraivong R, Vasanawathana S, Limpitikul W, Malasit P, Tangthawornchaikul N, Botto M, Screaton G R, Mongkolsapaya J, Pickering M |
Common polymorphisms in the complement system and susceptiblity to bacterial meningitis. The Journal of infection 2013 Mar 66 (3): 255-62. Adriani Kirsten S, Brouwer Matthijs C, Geldhoff Madelijn, Baas Frank, Zwinderman Aeilko H, Paul Morgan B, Harris Claire L, van der Ende Arie, van de Beek Dieder |
Complement and mannose-binding lectin 2 polymorphism in meningococcal disease. Clinical laboratory 2012 58 (11-12): 11-12. Lima Filho A, Carmo R, Cavalcanti M, Vasconcelos L, Moura P, Silva A, Sarinho E |
IL10 family member genes IL19 and IL20 are associated with recurrent wheeze after respiratory syncytial virus bronchiolitis. Pediatric research 2011 Nov 70 (5): 518-23. Ermers Marieke J J, Janssen Riny, Onland-Moret N Charlotte, Hodemaekers Hennie M, Rovers Maroeska M, Houben Michiel L, Kimpen Jan L L, Bont Louis |
Cystic fibrosis modifier genes related to Pseudomonas aeruginosa infection. Genes and immunity 2011 Jul 12 (5): 370-7. Park J E, Yung R, Stefanowicz D, Shumansky K, Akhabir L, Durie P R, Corey M, Zielenski J, Dorfman R, Daley D, Sandford A |
Association of mannose binding lectin (MBL) gene polymorphism and serum MBL concentration with characteristics and progression of systemic lupus erythematosus. Annals of the rheumatic diseases 2005 Feb 64 (2): 311-4. Takahashi R, Tsutsumi A, Ohtani K, Muraki Y, Goto D, Matsumoto I, Wakamiya N, Sumida |
[Study on the polymorphisme of human leucocyte antigen-DRB1, -DQA1 and -DQB1 alleles in patients with hepatitis B]. Zhonghua liu xing bing xue za zhi = Zhonghua liuxingbingxue zazhi 2004 Apr 25 (4): 337-40. Jiang Ye-gui, Wang Yu-mi |
Prevalence and clinical significance of circulating cryoglobulins in HIV-positive patients with and without co-infection with hepatitis C virus. Journal of medical virology 2003 1 69 (3): 339-43. Fabris Paolo, Tositti Giulia, Giordani Maria Teresa, Romanò Luisa, Betterle Corrado, Pignattari Elena, Tagliaferri Cinzia, Muratori Paolo, Manfrin Vinicio, de Lalla Faus |
[Mannose-binding protein gene polymorphism influences the patterns of glomerular immune deposition in IgA nephropathy]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2001 Apr 18 (2): 83-7. Gong R, Liu Z, Chen Z, Liu D, Li L |
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- Page last updated:Mar 22, 2023
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