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Tian Chen

Researcher at Laboratory of Molecular Biology

Publications -  5
Citations -  2381

Tian Chen is an academic researcher from Laboratory of Molecular Biology. The author has contributed to research in topics: Gene & RNA. The author has an hindex of 5, co-authored 5 publications receiving 1878 citations.

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Circular Intronic Long Noncoding RNAs

TL;DR: A cis-regulatory role of noncoding intronic transcripts on their parent coding genes is suggested, which largely accumulates to its sites of transcription, associates with elongation Pol II machinery, and acts as a positive regulator of Pol II transcription.
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Human colorectal cancer-specific CCAT1-L lncRNA regulates long-range chromatin interactions at the MYC locus

TL;DR: It is demonstrated that a long noncoding RNA, CCAT1-L, is transcribed specifically in human colorectal cancers from a locus 515 kb upstream of MYC, and this lncRNA plays a role in MYC transcriptional regulation and promotes long-range chromatin looping.
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ADAR1 is required for differentiation and neural induction by regulating microRNA processing in a catalytically independent manner

TL;DR: It is observed that ADAR1 deficiency in human embryonic stem cells (hESCs) significantly affected hESC differentiation and neural induction with widespread changes in mRNA and miRNA expression, including upregulation of self-renewal-related miRNAs, such as miR302s.
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Species-specific alternative splicing leads to unique expression of sno-lncRNAs

TL;DR: Comparative transcriptomes of non-polyadenylated RNAs among human, rhesus and mouse revealed that the expression of sno-lncRNAs is species-specific and that their processing is closely linked to alternative splicing of their parent genes.
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Prediction of constitutive A-to-I editing sites from human transcriptomes in the absence of genomic sequences

TL;DR: A new strategy to accurately predict constitutive RNA editing sites from publicly available human RNA-seq datasets in the absence of relevant genomic sequences is developed and new parameters are established to increase the ability to map mismatches and to minimize sequencing/mapping errors and unreported genome variations.