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The NHS Delivery Plan for Access to Primary Care | PASociety
The therapeutic potential of genetic approaches has been demonstrated in certain in vitro studies, such as a nanoparticle-delivered siRNA to suppress oncogene CFL1 639 and a CRISPR/Cas9 system-delivered LncRNA PANDAR (promoter of CDKN1A antisense DNA damage activated RNA) to interact with p53 and competitively regulate CDKN1A transcription in GC cell lines
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KEGG: Kyoto encyclopedia of genes and genomes
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