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The transcriptome of circulating cells indicates potential biomarkers and therapeutic targets in the course of hypertension-related myocardial infarction 被引量:1
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作者 Zilun wei Yining Yang +7 位作者 Qiaoling Li Yong Yin zhonghai wei Wenfeng Zhang Dan Mu Jie Ni Xuan Sun Biao Xu 《Genes & Diseases》 SCIE 2021年第4期555-568,共14页
Hypertension(HT)is the most common public-health challenge andshows a high inci-dence around the world.Cardiovascular diseases are the leadingcause of mortality and morbidity among the elderly(age>65 years)in the U... Hypertension(HT)is the most common public-health challenge andshows a high inci-dence around the world.Cardiovascular diseases are the leadingcause of mortality and morbidity among the elderly(age>65 years)in the UnitedStates.Now,there is widespread acceptanceof the causal link between HT and acute myocardial infarction(MI).This is the first data-mining study to identify co-expressed differentially expressed genes(Co-DEGs)between HT and MI(rela-tive to nommal control)and to uncover potential biomarkers and therapeutic targets of HT-related MI.In thismanuscript,HT-specfcDEGs andMl-specific DEGs and dffretially expressed microRNAs(DE-miRNAs)were identifhed in Gene Expression Omnibus(GEO)datasets GSE24752,GSE60993,GSE62646,and GSE24548 after data consolidation and batch correction.Subse-quently,enichmentin Gene Ontology(GO)terms and Kyoto Encyclopedia of Genes and Genomes(KEGG)pathways as well as protein-protein interaction networks were identified,and single-gene gene set enrichment analysis was performed to determine the affected biological cate-gories and networks.Cross-matching of the results on cCo-DE-miRNAs and predicted miRNAs tar-geting the Co-DEGs wasconducted and discussed as well.We found thatMYC and HIST1H2BO may be associatedwith HT,whereas FCGR 1A,FYN,KLRD1,KLRB1,and FOLR3 may be implicated in MI.Moreover,Co-DEGs FOLR3 and NFE2 with predicted miRNAs and DE-miRNAs,especially miR-7 and miR-548,may be significantly associated and show huge potential as a new set of novel bio-markers and important molecular targets in the course of HT-related MI. 展开更多
关键词 Biological function BLOOD HYPERTENSION MICROARRAY Myocardial infarction PATHWAY
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