White Blood Cell Count procedure
|
0.100 |
GeneticVariation
|
phenotype |
GWASDB |
Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT).
|
21738479 |
2011 |
Sepsis
|
0.040 |
GeneticVariation
|
disease |
BEFREE |
We hypothesized that CXCL2 polymorphisms may confer susceptibility to sepsis and performed an association study using 178 severe sepsis patients and 357 population-based controls.
|
16421598 |
2006 |
Sepsis
|
0.040 |
GeneticVariation
|
disease |
LHGDN |
A CXCL2 tandem repeat promoter polymorphism is associated with susceptibility to severe sepsis in the Spanish population.
|
16421598 |
2006 |
Septicemia
|
0.030 |
GeneticVariation
|
disease |
BEFREE |
We hypothesized that CXCL2 polymorphisms may confer susceptibility to sepsis and performed an association study using 178 severe sepsis patients and 357 population-based controls.
|
16421598 |
2006 |
Virus Diseases
|
0.020 |
GeneticVariation
|
group |
BEFREE |
In addition, T-LGL clones were characterized by an overexpression of chemokines and chemokine receptors that are typically associated with viral infections (CXCL2, Hepatitis A virus cellular receptor 1, IL-18, CCR2).
|
18086899 |
2008 |
Ischemic stroke
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
This is a pilot study analysing association of chemokine gene polymorphisms (CXCL1, rs3117604; CXCL2, rs3806792; CCL2, rs2857656 and rs3760396; CCL5, rs2107538) in Korean patients with ischemic stroke (IS) (n = 120) and age-matched controls (n = 267).
|
23198952 |
2013 |
Severe Sepsis
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
Although replicate studies and functional assays are needed, these results suggest that CXCL2 gene variants may contribute to the development of severe sepsis.
|
16421598 |
2006 |
Severe Sepsis
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
We hypothesized that a tandem repeat polymorphism (AC)n in the CXCL2 gene, previously associated with susceptibility to severe sepsis, contributes to morbidity and mortality in severe sepsis.
|
17944017 |
2007 |
Alopecia
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Polymorphisms in the promoter regions of the CXCL1 and CXCL2 genes contribute to increased risk of alopecia areata in the Korean population.
|
26345899 |
2015 |
Alopecia Areata
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Polymorphisms in the promoter regions of the CXCL1 and CXCL2 genes contribute to increased risk of alopecia areata in the Korean population.
|
26345899 |
2015 |
Reperfusion Injury
|
0.500 |
Biomarker
|
disease |
RGD |
The ratio of ELR+ to ELR- CXC chemokines affects the lung and liver injury following hepatic ischemia/ reperfusion in the rat.
|
10655268 |
2000 |
Reperfusion Injury
|
0.500 |
Biomarker
|
disease |
RGD |
Lung and liver injury following hepatic ischemia/reperfusion in the rat is increased by exogenous lipopolysaccharide which also increases hepatic TNF production in vivo and in vitro.
|
11580116 |
2001 |
Reperfusion Injury
|
0.500 |
Biomarker
|
disease |
CTD_human |
Peroxisome proliferator-activated receptor-gamma (PPAR-gamma) activation suppresses ischemic induction of Egr-1 and its inflammatory gene targets.
|
12468449 |
2002 |
Reperfusion Injury
|
0.500 |
Biomarker
|
disease |
RGD |
A novel ELR-CXC chemokine antagonist reduces intestinal ischemia reperfusion-induced mortality, and local and remote organ injury.
|
19691980 |
2010 |
Acute Lung Injury
|
0.500 |
Biomarker
|
disease |
CTD_human |
Protective effect of quercetin on acute lung injury in rats with sepsis and its influence on ICAM-1 and MIP-2 expression.
|
27525872 |
2016 |
Acute Lung Injury
|
0.500 |
Biomarker
|
disease |
RGD |
Delay of LPS-induced acute lung injury resolution by soluble immune complexes is neutrophil dependent.
|
19106808 |
2009 |
Degenerative polyarthritis
|
0.330 |
Biomarker
|
disease |
CTD_human |
While these differences may represent differential behaviour of synovial fibroblasts in in vitro culture, these observations suggest that TFPI2, GRObeta (CXCL2), MnSOD and GCP-2 (CXCL6) may represent new targets for treatments specifically tailored to osteoarthritis.
|
15292528 |
2004 |
Degenerative polyarthritis
|
0.330 |
Biomarker
|
disease |
BEFREE |
While these differences may represent differential behaviour of synovial fibroblasts in in vitro culture, these observations suggest that TFPI2, GRObeta (CXCL2), MnSOD and GCP-2 (CXCL6) may represent new targets for treatments specifically tailored to osteoarthritis.
|
15292528 |
2004 |
Rheumatoid Arthritis
|
0.320 |
Biomarker
|
disease |
CTD_human |
Detection of differentially expressed genes in synovial fibroblasts by restriction fragment differential display.
|
15292528 |
2004 |
Rheumatoid Arthritis
|
0.320 |
Biomarker
|
disease |
BEFREE |
Plasminogen (PLG) and related DEGs such as chemokine (C-X-C motif) ligand 2 (CXCL2), laminin, alpha 3 (LAMA3), complement component 7 (C7), and coagulation factor X (F10) were identified in 4 submodules.Our results indicate that DLG1, GUCY1A2, GRIN2A, KCNA1, PLG, CXCL2, LAMA3, C7, and F10 may play key roles in the progression of RA and may serve as putative therapeutic targets for treating RA.
|
28767591 |
2017 |
Esophageal Neoplasms
|
0.310 |
Biomarker
|
group |
CTD_human |
The analyses pointed out the potential importance of CXCL2, and monitoring CXCL2 with quantitative videomicroscopy indicated that its biologic activity was silenced in OE21 esophageal cancer cells.
|
21509778 |
2011 |
Chronic Obstructive Airway Disease
|
0.310 |
Biomarker
|
disease |
BEFREE |
Within this context, we now show increased expression of the C-X-C chemokines (CXCL1 and CXCL2) and their receptor CXCR2, and the intercellular cellular adhesion molecule-1 (ICAM-1), in the lung tissues of patients with COPD.
|
26747783 |
2016 |
Chronic Obstructive Airway Disease
|
0.310 |
Biomarker
|
disease |
CTD_human |
Aberrantly activated EGFR contributes to enhanced IL-8 expression in COPD airways epithelial cells via regulation of nuclear FoxO3A.
|
23099361 |
2013 |
Malignant neoplasm of esophagus
|
0.310 |
Biomarker
|
disease |
CTD_human |
The analyses pointed out the potential importance of CXCL2, and monitoring CXCL2 with quantitative videomicroscopy indicated that its biologic activity was silenced in OE21 esophageal cancer cells.
|
21509778 |
2011 |
Mammary Neoplasms
|
0.310 |
Biomarker
|
group |
LHGDN |
Curcumin downregulates the inflammatory cytokines CXCL1 and -2 in breast cancer cells via NFkappaB.
|
17999991 |
2008 |