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He, Chuan
One or more keywords matched the following items that are connected to He, Chuan
Item TypeName
Concept RNA-Binding Proteins
Academic Article Blockade of miR-150 maturation by MLL-fusion/MYC/LIN-28 is required for MLL-associated leukemia.
Academic Article FTO-mediated formation of N6-hydroxymethyladenosine and N6-formyladenosine in mammalian RNA.
Academic Article N6-methyladenosine-dependent regulation of messenger RNA stability.
Academic Article High-resolution N(6) -methyladenosine (m(6) A) map using photo-crosslinking-assisted m(6) A sequencing.
Academic Article Reading RNA methylation codes through methyl-specific binding proteins.
Academic Article N(6)-methyladenosine Modulates Messenger RNA Translation Efficiency.
Academic Article YTHDF3 facilitates translation and decay of N6-methyladenosine-modified RNA.
Academic Article m6A-dependent maternal mRNA clearance facilitates zebrafish maternal-to-zygotic transition.
Academic Article m6A facilitates hippocampus-dependent learning and memory through YTHDF1.
Academic Article YTHDC1 mediates nuclear export of N6-methyladenosine methylated mRNAs.
Academic Article Circadian Clock Regulation of Hepatic Lipid Metabolism by Modulation of m6A mRNA Methylation.
Academic Article The RNA-binding protein FMRP facilitates the nuclear export of N6-methyladenosine-containing mRNAs.
Academic Article YTHDF2 promotes mitotic entry and is regulated by cell cycle mediators.
Academic Article Control of Early B Cell Development by the RNA N6-Methyladenosine Methylation.
Academic Article N6-Adenosine Methylation of Socs1 mRNA Is Required to Sustain the Negative Feedback Control of Macrophage Activation.
Academic Article METTL14 facilitates global genome repair and suppresses skin tumorigenesis.
Academic Article The mechanism underlying redundant functions of the YTHDF proteins.
Academic Article YTHDF2 inhibition potentiates radiotherapy antitumor efficacy.
Academic Article FMRP phosphorylation modulates neuronal translation through YTHDF1.
Academic Article Profiling of RNA-binding protein binding sites by in situ reverse transcription-based sequencing.
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  • RNA Binding Proteins