2016
DOI: 10.1093/bioinformatics/btw089
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Computationally expanding infinium HumanMethylation450 BeadChip array data to reveal distinct DNA methylation patterns of rheumatoid arthritis

Abstract: Supplementary data are available at Bioinformatics online.

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Cited by 26 publications
(31 citation statements)
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“…Methylation levels of cg23700278, cg27427581, cg04334751, cg26764200 are found increased significantly after MTX treatment (Nair et al, 2019). In addition, DNA methylation of LBH, CASP8, OLIG3, IRF5, HLA-G, ELMO1, TRHDE, SLCO1C1, PLD4, AIRE and HLA-DQA1 are demonstrated involved in pathogenesis of RA and then are recommended as promising therapeutic markers (Fan et al, 2016). AZU1, LTBR, RTEL1 are hypomethylated and related to the trigger of autoimmune signaling cascade indicating the potential roles as epigenetic susceptibility markers (Wang et al, 2018).…”
Section: Dna Methylation Mediated Disease Risk Disease Activity and mentioning
confidence: 97%
“…Methylation levels of cg23700278, cg27427581, cg04334751, cg26764200 are found increased significantly after MTX treatment (Nair et al, 2019). In addition, DNA methylation of LBH, CASP8, OLIG3, IRF5, HLA-G, ELMO1, TRHDE, SLCO1C1, PLD4, AIRE and HLA-DQA1 are demonstrated involved in pathogenesis of RA and then are recommended as promising therapeutic markers (Fan et al, 2016). AZU1, LTBR, RTEL1 are hypomethylated and related to the trigger of autoimmune signaling cascade indicating the potential roles as epigenetic susceptibility markers (Wang et al, 2018).…”
Section: Dna Methylation Mediated Disease Risk Disease Activity and mentioning
confidence: 97%
“…Tyrosinase acts as an enzyme meant to control melanogenesis. With the widespread presence of melanoma, it is seen that there is an overexpression of tyrosinase [33][34][35][36][37][38][39][40] . This has led to the growth of dopamine which in turn produces dopamine quinone and dopaquinone 5 .…”
Section: Inhibitors For Melanomamentioning
confidence: 99%
“…The process of antipsychotic delivery is not researched in depth. However, nanoparticle-based administration to the treatment of psychotic problems tends to enhance the life of the affected individual and prove biocompatibility [33][34][35][36][37][38] For the brain tumor, it is a severe case though nanoparticles are available in abundance in the market. The problem is the absence of a substance that can control brain tumor-like glioblastoma at an earlier stage.…”
Section: Impact Of Nanoparticles On Brain Problemsmentioning
confidence: 99%