Tuberculosis
|
0.020 |
GeneticVariation
|
disease |
LHGDN |
Moreover, the VDR gene variants might regulate cytotoxic T-cell response via 1, 25(OH)(2) D(3) mediated suppression of granzyme A expression in tuberculosis.
|
19014932 |
2009 |
Malignant neoplasm of stomach
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
The expression of CTLA4, CD3, and granzyme A (GZMA) were validated on 30 cases of Chinese GC.
|
30422018 |
2019 |
Stomach Carcinoma
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
The expression of CTLA4, CD3, and granzyme A (GZMA) were validated on 30 cases of Chinese GC.
|
30422018 |
2019 |
Liver Cirrhosis, Experimental
|
0.300 |
Biomarker
|
disease |
CTD_human |
Systems level analysis and identification of pathways and networks associated with liver fibrosis.
|
25380136 |
2014 |
Malignant Neoplasms
|
0.040 |
Biomarker
|
group |
BEFREE |
In contrast to exposure to mf, exposure to cancer cell lines increased the phagocytic ability of monocytes and reduced their ability to induce T cell proliferation and to expand Granzyme A+ CD8+ T cells.
|
29668679 |
2018 |
Malignant Neoplasms
|
0.040 |
Biomarker
|
group |
BEFREE |
Integrated methylation and expression data (along with publicly available, ENCODE-generated histone ChIP Seq and DNAse hypersensitivity data) predict that epigenetic regulation is a primary factor driving transcriptional activation of a number of genes crucial to immunity in cancer, including T cell receptor genes (e.g., CD3D, CD3E), CTLA4, and GZMA.
|
30885360 |
2019 |
Primary malignant neoplasm
|
0.040 |
Biomarker
|
group |
BEFREE |
Integrated methylation and expression data (along with publicly available, ENCODE-generated histone ChIP Seq and DNAse hypersensitivity data) predict that epigenetic regulation is a primary factor driving transcriptional activation of a number of genes crucial to immunity in cancer, including T cell receptor genes (e.g., CD3D, CD3E), CTLA4, and GZMA.
|
30885360 |
2019 |
Primary malignant neoplasm
|
0.040 |
Biomarker
|
group |
BEFREE |
In contrast to exposure to mf, exposure to cancer cell lines increased the phagocytic ability of monocytes and reduced their ability to induce T cell proliferation and to expand Granzyme A+ CD8+ T cells.
|
29668679 |
2018 |
Rheumatoid Arthritis
|
0.030 |
Biomarker
|
disease |
BEFREE |
The purpose of this study was to evaluate the contribution of GzmA to the pathogenesis of RA in vivo and to examine the possibility that GzmA acting via tumor necrosis factor (TNF) stimulates osteoclastogenesis.
|
27598995 |
2017 |
Multiple Sclerosis
|
0.030 |
Biomarker
|
disease |
BEFREE |
Astrocyte cluster 8 (MMP7, SERPINA3, GZMA and CLIC1) and microglial cluster 2 (DSG2 and TNFRSF25) were reproducibly elevated in MS and had a significant and reproducible correlation with MS severity suggesting their pathogenic role.
|
30553167 |
2019 |
Multiple Sclerosis
|
0.030 |
Biomarker
|
disease |
BEFREE |
This study identified many DNA methylations and genes as important risk factors for MS and provided novel evidence on the association between circulating MICB and Granzyme A and MS. We also showed that the interaction among DDR1, MICB and GZMA and interaction among METTL21B, METTL1 and TSFM may participate in the pathogenesis of MS.
|
31321514 |
2019 |
Arthritis
|
0.020 |
Biomarker
|
disease |
BEFREE |
Chikungunya virus requires host granzyme A to drive joint inflammation.
|
28356507 |
2017 |
Arthritis
|
0.020 |
Biomarker
|
disease |
BEFREE |
Granzyme A Contributes to Inflammatory Arthritis in Mice Through Stimulation of Osteoclastogenesis.
|
27598995 |
2017 |
Chikungunya Fever
|
0.020 |
Biomarker
|
disease |
BEFREE |
RNA-Seq analysis of chikungunya virus infection and identification of granzyme A as a major promoter of arthritic inflammation.
|
28207896 |
2017 |
Chikungunya Fever
|
0.020 |
Biomarker
|
disease |
BEFREE |
Chikungunya virus requires host granzyme A to drive joint inflammation.
|
28356507 |
2017 |
Acute HIV infection
|
0.020 |
Biomarker
|
disease |
BEFREE |
This article describes a defect in the coexpression of perforin in granzyme A-positive CD8(+) T cells in lymphoid tissue from patients with acute HIV infection and a reduction in the perforin-dependent nuclear translocation of granzyme A.
|
12001057 |
2002 |
Acute HIV infection
|
0.020 |
Biomarker
|
disease |
BEFREE |
Moreover, these data suggest that expansion of granzyme A(+) HIV-specific cytolytic CD4 T cell responses early during acute HIV infection contributes substantially to the control of viral replication.
|
22378925 |
2012 |
Arthritis, Psoriatic
|
0.010 |
Biomarker
|
disease |
BEFREE |
TCRβ sequencing showed these cells are polyclonal in PsA (median clonality = 0.08), whilst RNA-seq and deep-immunophenotyping revealed that PsA synovial Tc17 cells have hallmarks of Th17 (RORC/IL23R/CCR6/CD161) and Tc1 cells (granzyme A/B).
|
31677365 |
2020 |
Ulcerative Colitis
|
0.010 |
Biomarker
|
disease |
BEFREE |
Levels of GZMA and ITGAE mRNAs in colon tissues can identify patients with UC who are most likely to benefit from etrolizumab; expression levels decrease with etrolizumab administration in biomarker(high) patients.
|
26522261 |
2016 |
Eclampsia
|
0.010 |
Biomarker
|
disease |
BEFREE |
GZMA) are predicted to play significant roles in the progress of EOPET, which will be confirmed by experiments in future.
|
28759171 |
2017 |
Ectromelia
|
0.010 |
Biomarker
|
disease |
BEFREE |
In this paper, we show that mice lacking both granzyme A (gzmA) and granzyme B (gzmB), which are, beside perforin, key constituents of cytolytic vesicles, are as incapable as are perforin-deficient mice of controlling primary infections by the natural mouse pathogen ectromelia, a poxvirus.
|
10570179 |
1999 |
Graft-vs-Host Disease
|
0.010 |
Biomarker
|
disease |
BEFREE |
We herewith identify GZMA as critical effector molecule of human Treg function for gastrointestinal immune response in an experimental GvHD model.
|
25928296 |
2015 |
Herpes Simplex Infections
|
0.010 |
Biomarker
|
group |
BEFREE |
Granzyme A, a noncytolytic component of CD8(+) cell granules, restricts the spread of herpes simplex virus in the peripheral nervous systems of experimentally infected mice.
|
10623769 |
2000 |
Inflammation
|
0.010 |
Biomarker
|
phenotype |
LHGDN |
Thus, the granule secretory pathway plays an unexpected role in inflammation, with GzmA acting as an endogenous modulator.
|
18951048 |
2008 |
Acute lymphocytic leukemia
|
0.010 |
Biomarker
|
disease |
BEFREE |
GC-induced GZMA expression could thus be a useful early biomarker for "personalized" ALL therapy.
|
17310274 |
2007 |