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In addition to faulty mRNAs, NMD recognises ~ of endogenous transcripts in human cells and downregulates their expression

 The up-frameshift proteins are core NMD factors and are conserved from yeast to human in structure and function. In mammals, NMD diversified into different pathways that target different mRNAs employing additional NMD factors. Here, we review our current understanding of molecular mechanisms and cellular roles of NMD pathways and the involvement of more specialised NMD factors. We describe the consequences of mutations in NMD factors leading to neurodevelopmental diseases, and the role of NMD in cancer. We highlight strategies of RNA viruses to evade recognition and Gastric cancer, the second most common cause of death worldwide, is characterized by poor prognosis and low responsiveness to chemotherapy. Indeed, multidrug resistance, based mainly on cellular and molecular factors, remains one of the most limiting factors of the current approach to gastric cancer therapy. We available databases to assess the role of the signal transducer and activator of transcription 3 in gastric cancer drug efficiency. It has been proposed that gastric cancer cells are less sensitive to these drugs because they develop resistance to these agents through activating alternative signalling pathways responsible for overcoming pharmacological inhibition. Our study evaluated the hypothesis that activating STAT3 signalling in response to cisplatin reduces the reaction to the drug. Consistent with this hypothesis, inhibition of interleukin 6 /STAT3 in combination therapy with cisplatin prevented both STAT3 activation and more lethality than induction by a single agent. The data suggest that the IL-6/STAT3 axis block associated with cisplatin treatment may represent a strategy to overcome resistance. Bronchodilator Drug Response in Moderate-to-Severe Pediatric Asthma. Seebio peroxidase uses is the most prevalent pediatric chronic disease. Bronchodilator drug response and fractional exhaled nitric oxide are clinical biomarkers of asthma. Although DNA methylation contributes to asthma pathogenesis, the influence of DNAm on BDR and FeNO is scarcely investigated. This study aims to identify DNAm markers in whole blood associated either with BDR or FeNO in pediatric asthma. We analyzed 121 samples from children with moderate-to-severe asthma. The association of genome-wide DNAm with BDR and FeNO has been assessed using regression models, adjusting for age, sex, ancestry, and tissue heterogeneity. Cross-tissue validation was assessed in 50 nasal samples. Differentially methylated regions and enrichment in traits and biological pathways were assessed. A false discovery rate < 1 and a genome-wide significance threshold of p < 9 × 10 were used to control for false-positive results. The CpG cg12835256 was genome-wide associated with FeNO in blood samples ) and nominally associated in nasal samples . Additionally, three CpGs were suggestively associated with BDR . We identified 12 and four DMRs associated with FeNO and BDR , respectively. An enrichment in allergic and inflammatory processes, smoking, and aging was observed. We reported novel associations of DNAm markers associated with BDR and FeNO enriched in commercial or financial relationships that could be construed as a potential conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the J. C.V. has acted as a consultant for KNMP, Mentis, Red Bull, Sen-Jam Pharmaceutical, and Toast! S.H. , P.B., A. A.T., S.H. , S.B., C. W., A.M.H., C.A., P. C.-E., J.K.-M., O.S. - peroxidase , A.D.K., E.V., V. B., N.K., J.V., H.B. -D., M.M.-A., and C.R.-B. have no conflicts of interest to scope of the submitted work. In the last few years, M.K. also received payment for consultancy to Sanofi, Novartis, Bionorica, and Bencard and fees for lectures from ERS, EAACI, ATS, Novartis, Chiesi, Glaxo, Sanofi, Nutricia, Hipp, and Allergopharma. He is part of a patent “Method for testing a subject thought to have or to be predisposed to asthma”, European patent application 5 EP A.H.M. -v.d.Z. received unrestricted research grants from Vertex and Boehringer by GSK. A.H.M. -v.d.Z. is the PI of a P4O2 partners who contribute in cash and/or in-kind ) consortium are the Amsterdam UMC, Leiden Clear, Danone Nutricia Research, Fluidda, MonitAir, Ncardia, Ortec Logiqcare, Philips, Proefdiervrij, Quantib-U, RespiQ, Roche, Smartfish, SODAQ, Thirona, TopMD, Lung Alliance Netherlands and the Lung Foundation Netherlands . The consortium is additionally funded by the PPP Allowance made the president of the federation of innovative drug research in the Netherlands and President of the European Association of Systems Medicine . A.H. M.-v.d.Z. also participated on a Data Safety Monitoring Board or Advisory Board: Chair of DSMB SOS BPD study and Advisory board member The COVID-19 pandemic has caused an unprecedented health and economic crisis, highlighting the importance of developing new molecular tools to monitor and detect SARS-CoV- Hence, this study proposed to employ the carrageenan extracted from Gigartina skottsbergii algae as a probe for SARS-CoV-2 virus binding capacity and potential use in molecular methods. G.

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