Behcet Syndrome
|
0.330 |
GeneticVariation
|
disease |
BEFREE |
Single nucleotide polymorphisms of CD11a and CD11c have been suggested as susceptibility loci in Korean patients with Behçet's disease (BD).
|
27309860 |
2017 |
Behcet Syndrome
|
0.330 |
GeneticVariation
|
disease |
BEFREE |
Therefore, the major genotype and haplotype of CD11a/CD18 may play a role in decreasing the susceptibility of BD, whereas the major genotype and haplotype of CD11c/CD18 may play a role in increasing the susceptibility of BD.
|
25155097 |
2014 |
Behcet Syndrome
|
0.330 |
AlteredExpression
|
disease |
BEFREE |
DEX, Col and ILalphaD in vitro differentially affected the stimulus-dependent oxidative burst of BD and caused the down-regulation of CD11a/CD18 surface expression in neutrophils but not monocytes.
|
16428075 |
2006 |
Behcet Syndrome
|
0.330 |
Biomarker
|
disease |
CTD_human |
Neutrophil adhesion to endothelial cells and factors affecting adhesion in patients with Behçet's disease.
|
8712863 |
1996 |
Acute Promyelocytic Leukemia
|
0.320 |
Biomarker
|
disease |
CTD_human |
We demonstrate the clinical usefulness of a panel of beta2 integrins (CD11a, CD11b and CD11c) in accurate prediction of AML-M3, and recommend inclusion of this immunophenotypic analysis to identify patients who require ATRA therapy.
|
16764927 |
2007 |
Acute Promyelocytic Leukemia
|
0.320 |
Biomarker
|
disease |
BEFREE |
In a test group of 58 APL patients, the most predictive immune profile was HLA-DR(low), CD11a(low) (alpha(L) subunit of the leukocyte integrin LFA-1), CD18(low) (beta(2) subunit of LFA-1).
|
15108165 |
2004 |
Acute Promyelocytic Leukemia
|
0.320 |
AlteredExpression
|
disease |
BEFREE |
ATRA was, however, incapable of promoting the up-regulation of CD11a in APL.
|
7815843 |
1994 |
Inflammatory Bowel Diseases
|
0.310 |
Biomarker
|
group |
CTD_human |
Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease.
|
28067908 |
2017 |
Inflammatory Bowel Diseases
|
0.310 |
GeneticVariation
|
group |
BEFREE |
Genetic associations with EN included known IBD susceptibility genes (PTGER4 [P = 8.8 × 10], ITGAL [0.03]) as well as SOCS5 (9.64 × 10), CD207 (3.14 × 10), ITGB3 (7.56 × 10), and rs6828740 (4q26) (P < 5.0 × 10).
|
24487271 |
2014 |
Liver Cirrhosis, Experimental
|
0.300 |
Biomarker
|
disease |
CTD_human |
Systems level analysis and identification of pathways and networks associated with liver fibrosis.
|
25380136 |
2014 |
clinical depression
|
0.300 |
Biomarker
|
disease |
PSYGENET |
Decreased chemotactic response and expression of CD11a found in this experimental model of depression could be important mechanisms to induce impairment immune response in experimental and clinical depression.
|
20516718 |
2010 |
Nephritis
|
0.200 |
Therapeutic
|
disease |
RGD |
We examined the expression of ICAM-1 in renal tissues of Masugi nephritis rats and directly examined the role of ICAM-1 by administration of neutralizing monoclonal antibodies (MAbs) to rat ICAM-1, LFA-1 alpha-subunit (LFA-1 alpha), beta-subunit (LFA-1 beta) and Mac-1 alpha-subunit (Mac-1 alpha).
|
8773354 |
1996 |
Psoriasis
|
0.130 |
Biomarker
|
disease |
BEFREE |
To better understand the relationship between the JCV life cycle and PML pathology, we studied autopsy brain tissue from a 70-year-old psoriasis patient on the integrin alpha-L inhibitor efalizumab following a ~2 month clinical course of PML.
|
27191595 |
2016 |
Psoriasis
|
0.130 |
GeneticVariation
|
disease |
GWASCAT |
Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci.
|
26974007 |
2016 |
Psoriasis
|
0.130 |
Biomarker
|
disease |
BEFREE |
Post-therapeutic relapse of psoriasis after CD11a blockade is associated with T cells and inflammatory myeloid DCs.
|
22348003 |
2012 |
Psoriasis
|
0.130 |
Biomarker
|
disease |
BEFREE |
Targeting of the statin-binding site of LFA-1 could be used to treat diseases such as psoriasis, rheumatoid arthritis, ischemia/reperfusion injury and transplant rejection.
|
11385505 |
2001 |
Ulcerative Colitis
|
0.110 |
GeneticVariation
|
disease |
GWASCAT |
Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci.
|
26974007 |
2016 |
Crohn Disease
|
0.110 |
GeneticVariation
|
disease |
GWASCAT |
Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci.
|
26974007 |
2016 |
Ulcerative Colitis
|
0.110 |
AlteredExpression
|
disease |
LHGDN |
CD11a was more likely to be expressed on CD4(+) cells in both Crohn's disease and ulcerative colitis and compared with controls and less expressed on CD19(+) cells.
|
12139949 |
2002 |
Crohn Disease
|
0.110 |
AlteredExpression
|
disease |
LHGDN |
CD11a was more likely to be expressed on CD4(+) cells in both Crohn's disease and ulcerative colitis and compared with controls and less expressed on CD19(+) cells.
|
12139949 |
2002 |
Red Blood Cell Count measurement
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
|
30595370 |
2019 |
White Blood Cell Count procedure
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
|
30595370 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
C26 cell activation with sICAM-1 enhanced their metastasizing potential in vivo, while tumor LFA-1 blockade reduced tumor burden and LSECs and HSC-derived myofibroblasts recruitment.
|
31511625 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Interestingly, cells from the triplet treated for Hodgkin lymphoma in 1985 contained two subpopulations: one with high expression of CD11a that behaved like control cells and the other with low expression of CD11a that formed large tumors in vivo similar to cells from the undiagnosed triplet.
|
31582539 |
2019 |
Lupus Erythematosus, Systemic
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
The goal of this study was to comprehensively characterize CD4+CD28+ T cells overexpressing CD11a and KIR genes, and examine the relationship between this T cell subset, genetic risk, and disease activity in lupus.
|
29066026 |
2018 |