2019
DOI: 10.3892/etm.2019.8009
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Exploration of vascular adhesion protein-1 expression in patients with conjunctivitis associated systemic lupus erythematosus using 2D-DIGE

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Cited by 9 publications
(6 citation statements)
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“…[ 57 ] Overactive immune system following COVID-19 vaccination and increased specific auto-antibodies and certain factors in the serum might have led to this injury. [ 58 ]…”
Section: Discussionmentioning
confidence: 99%
“…[ 57 ] Overactive immune system following COVID-19 vaccination and increased specific auto-antibodies and certain factors in the serum might have led to this injury. [ 58 ]…”
Section: Discussionmentioning
confidence: 99%
“…IGHG3, which is also involved in acute rejection [27], may contribute to platelet activation during ischemic stroke, and it is expected to be a potential target for the treatment of the early phase of stroke [28]. Studies from other groups have found that IGHM is abnormally expressed in patients with conjunctivitis-related systemic lupus erythematosus and cholangiocarcinoma [29,30]. In our study, several of the proteins involved in immune regulation were significantly reduced in plasma, indicating considerable immunosuppression in patients with SAP and suggesting that these proteins may be potential biomarkers for SAP.…”
Section: Discussionmentioning
confidence: 99%
“…19,20 2D-DIGE allows covalent labeling of proteins in various samples (e.g., a control and a test group) with different fluorescent dyes, followed by mixing and simultaneous separation by two-dimensional gel electrophoresis (2D-GE) in a single gel. 21,22 Common dyes used are cyan fluorescent dyes, binding to the epsilon amino-group of lysine residues and infrared (IR) maleimide dyes, binding to free thiolgroups of cysteines. 23,24 For detection, the distinct fluorescence of the dyes is recorded, which intensity depends on the amount of the protein-attached dye.…”
Section: Introductionmentioning
confidence: 99%
“…For the investigation of proteome variations, the technique of fluorescent two‐dimensional difference gel electrophoresis (2D‐DIGE) presented for the first time by Ünlü et al has been established 19,20 . 2D‐DIGE allows covalent labeling of proteins in various samples (e.g., a control and a test group) with different fluorescent dyes, followed by mixing and simultaneous separation by two‐dimensional gel electrophoresis (2D‐GE) in a single gel 21,22 . Common dyes used are cyan fluorescent dyes, binding to the epsilon amino‐group of lysine residues and infrared (IR) maleimide dyes, binding to free thiol‐groups of cysteines 23,24 .…”
Section: Introductionmentioning
confidence: 99%