Enhancer ID: | E_02_0316 |
Species: | human |
Position : | chr18:59217032-59219032 |
Biosample name: | |
Experiment class : | High+Lowthroughput |
Enhancer type: | Enhancer |
Disease: | Spinal cord injury (sci) |
Pubmed ID: | 29731818 |
Enhancer experiment: | Basso, Beattie and Bresnahan (BBB) scoring,MTT colorimetric assay,Western blot,Apoptosis assay,Terminal deoxynucleotidyl?transferase?mediated dUTP nick end (TUNEL),ELISA,flow cytometry, |
Enhancer experiment description: | Furthermore, levels of ERS-associated proteins, including caspase-3, activating transcription factor 6, serine/threonine-protein kinase/endoribonuclease inositol-requiring enzyme 1 ?, eukaryotic initiation factor 2 ? and GRP78, were significantly increased following SCI; however, administration of MTX for 7 days significantly reversed this effect (P<0.05, P<0.01 and P<0.001). Therefore, MTX may improve SCI by suppressing ERS-induced apoptosis in vitro and in vivo. |
Target gene : | GRP |
Strong evidence: | qRT-PCR,qPCR,ChIP,3C |
Less strong evidence: | RNA-Seq |
Target gene experiment description: | Furthermore, levels of ERS-associated proteins, including caspase-3, activating transcription factor 6, serine/threonine-protein kinase/endoribonuclease inositol-requiring enzyme 1 ?, eukaryotic initiation factor 2 ? and GRP78, were significantly increased following SCI; however, administration of MTX for 7 days significantly reversed this effect (P<0.05, P<0.01 and P<0.001). Therefore, MTX may improve SCI by suppressing ERS-induced apoptosis in vitro and in vivo. |
TF name : | -- |
TF experiment: | Basso, Beattie and Bresnahan (BBB) scoring,MTT colorimetric assay,Western blot,Apoptosis assay,Terminal deoxynucleotidyl?transferase?mediated dUTP nick end (TUNEL),ELISA,flow cytometry, |
TF experiment description: | Furthermore, levels of ERS-associated proteins, including caspase-3, activating transcription factor 6, serine/threonine-protein kinase/endoribonuclease inositol-requiring enzyme 1 ?, eukaryotic initiation factor 2 ? and GRP78, were significantly increased following SCI; however, administration of MTX for 7 days significantly reversed this effect (P<0.05, P<0.01 and P<0.001). Therefore, MTX may improve SCI by suppressing ERS-induced apoptosis in vitro and in vivo. |
Enhancer function : | Furthermore, levels of ERS-associated proteins, including caspase-3, activating transcription factor 6, serine/threonine-protein kinase/endoribonuclease inositol-requiring enzyme 1 ?, eukaryotic initiation factor 2 ? and GRP78, were significantly increased following SCI; however, administration of MTX for 7 days significantly reversed this effect (P<0.05, P<0.01 and P<0.001). Therefore, MTX may improve SCI by suppressing ERS-induced apoptosis in vitro and in vivo. |
Enhancer function experiment: | Immunohistochemical staining |
Enhancer function experiment description: |
Furthermore, levels of ERS-associated proteins, including caspase-3, activating transcription factor 6, serine/threonine-protein kinase/endoribonuclease inositol-requiring enzyme 1 ?, eukaryotic initiation factor 2 ? and GRP78, were significantly increased following SCI; however, administration of MTX for 7 days significantly reversed this effect (P<0.05, P<0.01 and P<0.001). Therefore, MTX may improve SCI by suppressing ERS-induced apoptosis in vitro and in vivo. |
SNP ID: | -- |
GeneName | Pathway Name | Source | Gene Number |
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