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Compact RNA editors with small Cas13 proteins from soil microbes
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创建时间：
2024-03-28
相关数据集
Evolution of a Reverse Transcriptase to Map N1-Methyladenosine in Human mRNA. Evolution of a Reverse Transcriptase to Map N1-Methyladenosine in Human mRNA
Chemical modifications on mRNA are increasingly recognized as a critical regulatory layer of the flow of genetic information, but quantitative tools to monitor RNA modifications in a whole-transcripto
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Identification of differentially expressed genes from limited amounts of RNA
The identification of cellular RNA expression profiles by differential display (DD) involves the visualization of RT–PCR products from the RNA. Traditionally, DD protocols require 200–500 ng RNA for e
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ExtFig3E_RACE_BCAP31_R1_LG274.tif
HEK293T ishXrn1 cells were treated with doxycycline for 3-4 days to induce knock down of Xrn1, then transfected with the luciferase reporters containing 99 bp insertions from the BCAP1, INSIG1, SLC7A5
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Phospho-small RNA-seq reveals circulating, extracellular mRNA/lncRNAs as potential biomarkers in human plasma: PNK evaluation on synthetic, equimolar pool [SYNTHETICPNK]. Phospho-small RNA-seq reveals circulating, extracellular mRNA/lncRNAs as potential biomarkers in human plasma: PNK evaluation on synthetic, equimolar pool [SYNTHETICPNK]
Extracellular RNAs (exRNAs) in blood and other biofluids have attracted great interest as potential biomarkers in liquid biopsy applications, as well as for their potential biological functions. Where
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Programmable C to U editing of RNA with CRISPR-Cas13. Homo sapiens
Programmable C to U editing of RNA with CRISPR-Cas13 data
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