Human Genome Epidemiology Literature Finder
Records 1 - 19 (of 19 Records) |
Query Trace: CXCL16[original query] |
---|
Severity of coronary artery stenosis is associated with a polymorphism in the CXCL16/SR-PSOX gene. Journal of internal medicine 2005 May 257 (5): 415-22. Lundberg G A, Kellin A, Samnegård A, Lundman P, Tornvall P, Dimmeler S, Zeiher A M, Hamsten A, Hansson G K, Eriksson |
Genotype-phenotype analysis of the CXCL16 p.Ala181Val polymorphism in inflammatory bowel disease. Clinical immunology (Orlando, Fla.) 2008 Apr 127 (1): 49-55. Seiderer Julia, Dambacher Julia, Leistner Dorothea, Tillack Cornelia, Glas Jürgen, Niess Jan-Hendrik, Pfennig Simone, Jürgens Matthias, Müller-Myhsok Bertram, Göke Burkhard, Ochsenkühn Thomas, Lohse Peter, Reinecker Hans-Christian, Brand Steph |
An intron polymorphism in the CXCL16 gene is associated with increased risk of coronary artery disease in Chinese Han population: a large angiography-based study. Atherosclerosis 2010 May 210 (1): 160-5. Huang Mingfang, Han Yaling, Zhang Xiaolin, Pei Fang, Deng Jie, Kang Jian, Yan Chengh |
Chemokine CXC Ligand 16 serum concentration but not A181V genotype is associated with atherosclerotic stroke. Clinica chimica acta; international journal of clinical chemistry 2010 Oct 411 (19-20): 1447-51. Wang Ke-di, Liu Zhi-zhong, Wang Rui-min, Wang Ya-jie, Zhang Guo-jun, Su Jian-rong, Kang Xi-xio |
The CXCL16 A181V mutation selectively inhibits monocyte adhesion to CXCR6 but is not associated with human coronary heart disease. Arteriosclerosis, thrombosis, and vascular biology 2011 Apr 31 (4): 914-20. Petit Sarah J, Wise Emma L, Chambers John C, Sehmi Jobanpreet, Chayen Naomi E, Kooner Jaspal S, Pease James |
Pathway analysis of a genome-wide association study in schizophrenia. Gene 2013 Aug 525 (1): 107-15. Lee Young Ho, Kim Jae-Hoon, Song Gwan G |
The gender-specific association of CXCL16 A181V gene polymorphism with susceptibility to multiple sclerosis, and its effects on PBMC mRNA and plasma soluble CXCL16 levels: preliminary findings. Journal of neurology 2014 Aug 261 (8): 1544-51. Stojkovi? Ljiljana, Stankovi? Aleksandra, Djuri? Tamara, Din?i? Evica, Alavanti? Dragan, Zivkovi? Ma |
PPARG, AGTR1, CXCL16 and LGALS2 polymorphisms are correlated with the risk for coronary heart disease. International journal of clinical and experimental pathology 2015 8 (3): 3138-43. Tian Jianwei, Hu Shunying, Wang Feng, Yang Xuedong, Li Yuqian, Huang Congch |
IL-9 induces IL-8 production via STIM1 activation and ERK phosphorylation in epidermal keratinocytes: A plausible mechanism of IL-9R in atopic dermatitis. Journal of dermatological science 2015 Jun 78 (3): 206-14. Hong Chien-Hui, Chang Kee-Lung, Wang Hung-Jen, Yu Hsin-Su, Lee Chih-Hu |
Association of NOD1, CXCL16, STAT6 and TLR4 gene polymorphisms with Malaysian patients with Crohn's disease. PeerJ 2016 4 e1843. Chua Kek Heng, Ng Jin Guan, Ng Ching Ching, Hilmi Ida, Goh Khean Lee, Kee Boon P |
The Impact of tagSNPs in CXCL16 Gene on the Risk of Myocardial Infarction in a Chinese Han Population. Disease markers 2017 2017 9463272. Xu Shun, Cheng Jie, Cai Meng-Yun, Liang Li-Li, Cen Jin-Ming, Yang Xi-Li, Chen Can, Liu Xinguang, Xiong Xing-Do |
Host Genetic Variant in CXCL16 May Be Associated With Hepatitis B Virus-Related Acute Liver Failure. Cellular and molecular gastroenterology and hepatology 2019 7 (2): 477-479.e4. Ajmera Veeral, Huang Hailiang, Dao Doan, Feld Jordan J, Lau Daryl T, Patel Keyur, Rule Jody A, Daly Mark, Lee William M, Chung Raymond |
Plasma chemokine CXC motif-ligand 16 as a predictor of renal prognosis in immunoglobulin A nephropathy. Annals of translational medicine 2020 5 8 (6): 381. Luo Ran, Yang Yi, Cheng Yi-Chun, Chang Dan, Liu Ting-Ting, Li Yue-Qiang, Dai Wei, Zuo Mei-Ying, Xu Yu-Lin, Zhang Chun-Xiu, Ge Shu-Wang, Xu Ga |
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Nature metabolism 2020 10 2 (10): 1135-1148. Folkersen Lasse, Gustafsson Stefan, Wang Qin, Hansen Daniel Hvidberg, Hedman Åsa K, Schork Andrew, Page Karen, Zhernakova Daria V, Wu Yang, Peters James, Eriksson Niclas, Bergen Sarah E, Boutin Thibaud S, Bretherick Andrew D, Enroth Stefan, Kalnapenkis Anette, Gådin Jesper R, Suur Bianca E, Chen Yan, Matic Ljubica, Gale Jeremy D, Lee Julie, Zhang Weidong, Quazi Amira, Ala-Korpela Mika, Choi Seung Hoan, Claringbould Annique, Danesh John, Davey Smith George, de Masi Federico, Elmståhl Sölve, Engström Gunnar, Fauman Eric, Fernandez Celine, Franke Lude, Franks Paul W, Giedraitis Vilmantas, Haley Chris, Hamsten Anders, Ingason Andres, Johansson Åsa, Joshi Peter K, Lind Lars, Lindgren Cecilia M, Lubitz Steven, Palmer Tom, Macdonald-Dunlop Erin, Magnusson Martin, Melander Olle, Michaelsson Karl, Morris Andrew P, Mägi Reedik, Nagle Michael W, Nilsson Peter M, Nilsson Jan, Orho-Melander Marju, Polasek Ozren, Prins Bram, Pålsson Erik, Qi Ting, Sjögren Marketa, Sundström Johan, Surendran Praveen, Võsa Urmo, Werge Thomas, Wernersson Rasmus, Westra Harm-Jan, Yang Jian, Zhernakova Alexandra, Ärnlöv Johan, Fu Jingyuan, Smith J Gustav, Esko Tõnu, Hayward Caroline, Gyllensten Ulf, Landen Mikael, Siegbahn Agneta, Wilson James F, Wallentin Lars, Butterworth Adam S, Holmes Michael V, Ingelsson Erik, Mälarstig Ande |
A Functional Variant of CXCL16 Is Associated With Predisposition to Sepsis and MODS in Trauma Patients: Genetic Association Studies. Frontiers in genetics 2021 12 720313. Sun Jianhui, Zhang Huacai, Liu Di, Cui Li, Wang Qiang, Gan Lebin, Wen Dalin, Wang Jun, Du Juan, Huang Hong, Zhang Anqiang, Deng Jin, Jiang Jianxin, Zeng Li |
Elevated plasma levels of CXCL16 in severe COVID-19 patients. Cytokine 2022 2 152 155810. Smieszek Sandra P, Polymeropoulos Vasilios M, Polymeropoulos Christos M, Przychodzen Bartlomiej P, Birznieks Gunther, Polymeropoulos Mihael |
GENETIC VARIANTS AND SERUM PROFILES OF CYTOKINES IN COVID-19 SEVERITY. Shock (Augusta, Ga.) 2022 11 59 (1): 58-65. Alefishat Eman, Mousa Mira, Albreiki Mohammed, Jelinek Herbert F, Al Halwachi Zainab, Khalili Mariam, Waasia Fathimathuz, Uddin Maimunah, Al Kaabi Nawal, Mahboub Bassam, Albataineh Mohammad T, Tay Guan K, Alsafar Habiba S, |
Metformin attenuates symptoms of osteoarthritis: role of genetic diversity of Bcl2 and CXCL16 in OA. Arthritis research & therapy 2023 3 25 (1): 35. Alimoradi Nahid, Tahami Mohammad, Firouzabadi Negar, Haem Elham, Ramezani Am |
Convergent transcriptomic and genomic evidence supporting a dysregulation of CXCL16 and CCL5 in Alzheimer's disease. Alzheimer's research & therapy 2023 1 15 (1): 17. Li Xiao, Zhang Deng-Feng, Bi Rui, Tan Li-Wen, Chen Xiaogang, Xu Min, Yao Yong-Ga |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: