Human Genome Epidemiology Literature Finder
Records 1 - 14 (of 14 Records) |
Query Trace: Inflammation and C2[original query] |
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Analysis of polymorphisms affecting immune complex handling in systemic lupus erythematosus. Rheumatology (Oxford, England) 2003 Mar 42 (3): 446-52. Sullivan K E, Jawad A F, Piliero L M, Kim N, Luan X, Goldman D, Petri |
The sodium-dependent glucose cotransporter SLC5A11 as an autoimmune modifier gene in SLE. Tissue antigens 2008 Feb 71 (2): 114-26. Tsai L-J, Hsiao S-H, Tsai L-M, Lin C-Y, Tsai J-J, Liou D-M, Lan J |
Genetic variation in complement component 2 of the classical complement pathway is associated with increased mortality and infection: a study of 627 patients with trauma. The Journal of trauma 2009 May 66 (5): 1265-70; discussion 1270-2. Morris John A, Francois Cedric, Olson Paul K, Cotton Bryan A, Summar Marshall, Jenkins Judith M, Norris Patrick R, Moore Jason H, Williams Anna E, McNew Brent S, Canter Jeffrey |
Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits.
BMC medical genetics 2011 12 (1): 123. Middelberg Rita P S, Ferreira Manuel A R, Henders Anjali K, Heath Andrew C, Madden Pamela A F, Montgomery Grant W, Martin Nicholas G, Whitfield John |
Conjunctival scarring in trachoma is associated with the HLA-C ligand of KIR and is exacerbated by heterozygosity at KIR2DL2/KIR2DL3. PLoS neglected tropical diseases 2014 Mar 8 (3): e2744. Roberts Chrissy H, Molina Sandra, Makalo Pateh, Joof Hassan, Harding-Esch Emma M, Burr Sarah E, Mabey David C W, Bailey Robin L, Burton Matthew J, Holland Martin |
HLA-G*14bp Insertion and the KIR2DS1-HLAC2 Complex Impact on Behavioral Impairment in Children with Autism Spectrum Disorders. Neuroscience 2017 Jun . Guerini Franca R, Bolognesi Elisabetta, Chiappedi Matteo, Ghezzo Alessandro, Manca Salvatorica, Zanette Michela, Sotgiu Stefano, Martina Mensi Maria, Zanzottera Milena, Agliardi Cristina, Costa Andrea S, Balottin Umberto, Clerici Mar |
Functional polymorphism rs1024611 in the MCP1 gene is associated with the risk of varicose veins of lower extremities. Journal of vascular surgery. Venous and lymphatic disorders 2017 Jul 5 (4): 561-566. Shadrina Alexandra S, Smetanina Mariya A, Sevost'ianova Kseniya S, Seliverstov Evgenii I, Ilyukhin Evgeny A, Voronina Elena N, Zolotukhin Igor A, Filipenko Maxim |
Association of Natural Killer Cell Ligand Polymorphism HLA-C Asn80Lys With the Development of Anti-SSA/Ro-Associated Congenital Heart Block. Arthritis & rheumatology (Hoboken, N.J.) 2017 11 69 (11): 2170-2174. Ainsworth Hannah C, Marion Miranda C, Bertero Tiziana, Brucato Antonio, Cimaz Rolando, Costedoat-Chalumeau Nathalie, Fredi Micaela, Gaffney Patrick, Kelly Jennifer, Levesque Kateri, Maltret Alice, Morel Nathalie, Ramoni Veronique, Ruffatti Amelia, Langefeld Carl D, Buyon Jill P, Clancy Robert |
MS4A2-rs573790 Is Associated With Aspirin-Exacerbated Respiratory Disease: Replicative Study Using a Candidate Gene Strategy. Frontiers in genetics 2018 9 363. Pavón-Romero Gandhi F, Pérez-Rubio Gloria, Ramírez-Jiménez Fernando, Ambrocio-Ortiz Enrique, Bañuelos-Ortiz Elisé, Alvarado-Franco Norma, Xochipa-Ruiz Karen E, Hernández-Juárez Elizabeth, Flores-García Beatriz A, Camarena Ángel E, Terán Luis M, Falfán-Valencia Ramc |
The combination of maternal KIR-B and fetal HLA-C2 is associated with decidua basalis acute atherosis in pregnancies with preeclampsia. Journal of reproductive immunology 2018 7 129 23-29. Johnsen Guro M, Størvold Gro L, Drabbels Jos J M, Haasnoot Geert W, Eikmans Michael, Spruyt-Gerritse Marijke J, Alnæs-Katjavivi Patji, Scherjon Sicco A, Redman Christopher W G, Claas Frans H J, Staff Anne Cathri |
Cough hypersensitivity in patients with obstructive sleep apnea hypopnea syndrome. Sleep & breathing = Schlaf & Atmung 2018 2 23 (1): 33-39. Shi Cuiqin, Liang Siwei, Xu Xianghuai, Chen Qiang, Wang Lan, Yu Li, Lv Hanjing, Qiu Zhongm |
Protective and causative killer Ig-like receptor (KIR) and metalloproteinase genetic patterns associated with Herpes simplex virus 1 (HSV-1) encephalitis occurrence. Journal of neuroimmunology 2020 Apr 344 577241. Tuttolomondo Antonino, Di Raimondo Domenico, Vasto Sonya, Casuccio Alessandra, Colomba Claudia, Norrito Rosario Luca, Di Bona Danilo, Arnao Valentina, Siciliano Luisa, Cascio Antonio, Pinto Antonio, |
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 |
Polymorphism of genes encoding drug-metabolizing and inflammation-related enzymes for susceptibility to cholangiocarcinoma in Thailand. World journal of gastrointestinal pathophysiology 2023 4 14 (2): 21-33. You Gyokukou, Zeng Lu, Tanaka Hideaki, Ohta Emi, Fujii Takahiro, Ohshima Kazuhiko, Tanaka Masakazu, Hamajima Nobuyuki, Viwatthanasittiphong Chutiwan, Muangphot Mantana, Chenvidhya Dhiraphol, Jedpiyawongse Adisorn, Sripa Banchob, Miwa Masanao, Honjo Satos |
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- Page last updated:Apr 16, 2024
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