Cargando…

Association between MIF gene promoter rs755622 and susceptibility to coronary artery disease and inflammatory cytokines in the Chinese Han population

Macrophage migration inhibitory factor (MIF) is an essential mediator of atherosclerotic plaque progression and instability leading to intracoronary thrombosis, therefore contributing to coronary artery disease (CAD). In this study, we investigated the relationship between MIF gene polymorphism and...

Descripción completa

Detalles Bibliográficos
Autores principales:	Luo, Jun-Yi, Fang, Bin-Bin, Du, Guo-Li, Liu, Fen, Li, Yan-Hong, Tian, Ting, Li, Xiao-Mei, Gao, Xiao-Ming, Yang, Yi-Ning
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Nature Publishing Group UK 2021
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8044220/ https://www.ncbi.nlm.nih.gov/pubmed/33850223 http://dx.doi.org/10.1038/s41598-021-87580-6

Ejemplares similares

MIF gene rs755622 polymorphism positively associated with acute coronary syndrome in Chinese Han population: case–control study
por: Du, Guo-Li, et al.
Publicado: (2020)

MIF Gene Polymorphism rs755622 Is Associated With Coronary Artery Disease and Severity of Coronary Lesions in a Chinese Kazakh Population: A Case–Control Study
por: Luo, Jun-Yi, et al.
Publicado: (2016)

Association Between MIF-AS rs755622 and Nephrolithiasis Risk in a Chinese Population
por: Ma, Gaoxiang, et al.
Publicado: (2016)

MIF -173G/C (rs755622) polymorphism modulates coronary artery disease risk: evidence from a systematic meta-analysis
por: Li, De-Yang, et al.
Publicado: (2020)

The MIF promoter SNP rs755622 is associated with immune activation in glioblastoma
por: Alban, Tyler J., et al.
Publicado: (2023)

MIF rs755622 and IL6 rs1800795 Are Implied in Genetic Susceptibility to End-Stage Renal Disease (ESRD)
por: Guarneri, Marco, et al.
Publicado: (2022)

MIF Variant rs755622 Is Associated with Severe Crohn’s Disease and Better Response to Anti-TNF Adalimumab Therapy
por: Jezernik, Gregor, et al.
Publicado: (2023)

NFKB1 gene rs28362491 ins/del variation is associated with higher susceptibility to myocardial infarction in a Chinese Han population
por: Luo, Jun-Yi, et al.
Publicado: (2020)

Genetic profile of MIF single nucleotide polymorphism (rs755622 G>C) in hepatocellular carcinoma among Egyptian patients
por: Osman, Heba Ahmed, et al.
Publicado: (2023)

The Macrophage Migration Inhibitory Factor (MIF) Promoter Polymorphisms (rs3063368, rs755622) Predict Acute Kidney Injury and Death after Cardiac Surgery
por: Averdunk, Luisa, et al.
Publicado: (2020)

Association between CCN1 gene polymorphism and acute coronary syndrome in Chinese Han and Uygur populations
por: Li, Yan-Hong, et al.
Publicado: (2021)

MIF -173 G > C (rs755622) Gene Polymorphism Modulates Tuberculosis Risk: Evidence from a Meta-analysis and Trial Sequential Analysis
por: Areeshi, Mohammed Y., et al.
Publicado: (2017)

HDAC9 Variant Rs2107595 Modifies Susceptibility to Coronary Artery Disease and the Severity of Coronary Atherosclerosis in a Chinese Han Population
por: Wang, Xue-bin, et al.
Publicado: (2016)

NFKB1 gene rs28362491 polymorphism is associated with the susceptibility of acute coronary syndrome
por: Jin, Si-Yu, et al.
Publicado: (2019)

Macrophage migration inhibitory factor gene rs755622 G/C polymorphism and coronary artery disease: A meta-analysis of 8,488 participants
por: Li, Yan-yan, et al.
Publicado: (2022)

ACAT-1 gene polymorphism is associated with increased susceptibility to coronary artery disease in Chinese Han population: a case-control study
por: Wang, Yong-Tao, et al.
Publicado: (2017)

A coronary artery disease-associated SNP rs6903956 contributed to asymptomatic hyperuricemia susceptibility in Han Chinese
por: Meng, Jianfen, et al.
Publicado: (2015)

Genetic Variant rs755622 Regulates Expression of the Multiple Sclerosis Severity Modifier D-Dopachrome Tautomerase in a Sex-Specific Way
por: Han, Zhijie, et al.
Publicado: (2018)

A study of the association of rs12040273 with susceptibility and severity of coronary artery disease in a Chinese Han population
por: Yang, Bo, et al.
Publicado: (2018)

Association of genetic variations in the Wnt signaling pathway genes with myocardial infarction susceptibility in Chinese Han population
por: Tao, Jing, et al.
Publicado: (2016)

Genetic polymorphism of IDOL gene was associated with the susceptibility of coronary artery disease in Han population in Xinjiang, China
por: Adi, Dilare, et al.
Publicado: (2021)

Genetic Variation of Migration Inhibitory Factor Gene rs2070766 Is Associated With Acute Coronary Syndromes in Chinese Population
por: Zhang, Jin-Yu, et al.
Publicado: (2022)

NEXN Is a Novel Susceptibility Gene for Coronary Artery Disease in Han Chinese
por: Wu, Chong, et al.
Publicado: (2013)

Correction to: Genetic polymorphism of IDOL gene was associated with the susceptibility of coronary artery disease in Han population in Xinjiang, China
por: Adi, Dilare, et al.
Publicado: (2021)

TT genotype of rs2941484 in the human HNF4G gene is associated with hyperuricemia in Chinese Han men
por: Chen, Bang-Dang, et al.
Publicado: (2017)

The association of cholesterol absorption gene Numb polymorphism with Coronary Artery Disease among Han Chinese and Uighur Chinese in Xinjiang, China
por: Abudoukelimu, Mayila, et al.
Publicado: (2015)

GLUT4 gene rs5418 polymorphism is associated with increased coronary heart disease risk in a Uygur Chinese population
por: Yu, Fei, et al.
Publicado: (2022)

Rs420137, rs386360 and rs7763726 polymorphisms in fibronectin type III domain containing 1 are associated with susceptibility to coronary heart disease: Analysis in the Han population
por: He, Xiaodan, et al.
Publicado: (2022)

Rs3213758 in the RPGRIP1L Gene Associated with Susceptibility to Segmental Vitiligo in a Chinese Han Population
por: Hu, Man, et al.
Publicado: (2018)

Variant of PAI-2 gene is associated with coronary artery disease and recurrent coronary event risk in Chinese Han population
por: Li, Xia, et al.
Publicado: (2015)

Relationship between CYP17A1 genetic polymorphism and coronary artery disease in a Chinese Han population
por: Dai, Chuan-Fang, et al.
Publicado: (2015)

Lack of Association of the CD247 SNP rs2056626 with Systemic Sclerosis in Han Chinese
por: Wang, Jiucun, et al.
Publicado: (2014)

Association between ABC family variants rs1800977, rs4149313, and rs1128503 and susceptibility to type 2 diabetes in a Chinese Han population
por: Yan, Ruicheng, et al.
Publicado: (2020)

Interleukin-1 Beta Gene Polymorphism rs16944 May Associate with Increased Susceptibility to Extremity Chronic Osteomyelitis in Chinese Han Population
por: Yao, Zi-long, et al.
Publicado: (2019)

Association of the NOTCH4 Gene Polymorphism rs204993 with Schizophrenia in the Chinese Han Population
por: Zhang, Bao, et al.
Publicado: (2015)

AT1R gene rs389566 polymorphism contributes to MACCEs in hypertension patients
por: Luo, Jun-Yi, et al.
Publicado: (2023)

Association Among MIF, IFIH1, and IL6 Gene Polymorphisms and Non-Segmental Vitiligo in a Chinese Han Population
por: Wang, Danfeng, et al.
Publicado: (2022)

Association of rs1137101 polymorphism in LEPR and susceptibility to knee osteoarthritis in a Northwest Chinese Han population
por: Yang, Jianhui, et al.
Publicado: (2016)

Correction to: AT1R gene rs389566 polymorphism contributes to MACCEs in hypertension patients
por: Luo, Jun-Yi, et al.
Publicado: (2023)

Novel KIF6 Polymorphism Increases Susceptibility to Type 2 Diabetes Mellitus and Coronary Heart Disease in Han Chinese Men
por: Wu, Ge, et al.
Publicado: (2014)

Cannot write session to /tmp/vufind_sessions/sess_ug9fg51r4ua8i321mc5jkbraru