Li Yang

ORCID: 0000-0001-8833-7473
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About
Contact & Profiles
Research Areas
  • RNA modifications and cancer
  • RNA Research and Splicing
  • Circular RNAs in diseases
  • Cancer-related molecular mechanisms research
  • MicroRNA in disease regulation
  • CRISPR and Genetic Engineering
  • Immune cells in cancer
  • Cancer, Hypoxia, and Metabolism
  • RNA and protein synthesis mechanisms
  • RNA regulation and disease
  • Cancer-related gene regulation
  • Virus-based gene therapy research
  • Epigenetics and DNA Methylation
  • Analytical chemistry methods development
  • Analytical Chemistry and Chromatography
  • Advanced biosensing and bioanalysis techniques
  • TGF-β signaling in diseases
  • Chemokine receptors and signaling
  • RNA Interference and Gene Delivery
  • Plant Gene Expression Analysis
  • Phagocytosis and Immune Regulation
  • Plant Molecular Biology Research
  • Adipose Tissue and Metabolism
  • Insect Resistance and Genetics
  • Ubiquitin and proteasome pathways

Children's Hospital of Fudan University
2023-2025

Sichuan Animal Science Academy
2019-2025

Chinese Academy of Sciences
2015-2025

Fudan University
2016-2025

Zhejiang Cancer Hospital
2024-2025

Pudong Medical Center
2025

Southern Medical University
2023-2024

Third Affiliated Hospital of Zhengzhou University
2022-2024

Chongqing University
2014-2024

Shanxi Medical University
2015-2024

Sushmita Roy Jason Ernst Peter V. Kharchenko Pouya Kheradpour Nicolas Nègre and 95 more Matthew L. Eaton Jane M. Landolin Christopher A. Bristow Lijia Ma Michael F. Lin Stefan Washietl Bradley I. Arshinoff Ferhat Ay Patrick Meyer Nicolas Robine Nicole L. Washington Luisa Di Stefano Eugène Berezikov Christopher D. Brown Rogerio Candeias Joseph W. Carlson Adrian R. Carr Irwin Jungreis Daniel Marbach Rachel Sealfon Michael Tolstorukov Sebastian Will Artyom A. Alekseyenko Carlo G. Artieri Benjamin W. Booth Angela N. Brooks Qi Dai Carrie Davis Michael O. Duff Xin Feng Andrey A. Gorchakov Tingting Gu Jorja G. Henikoff Philipp Kapranov Renhua Li Heather K. MacAlpine John H. Malone Aki Minoda Jared T. Nordman Katsutomo Okamura Marc D. Perry Sara Powell Nicole C. Riddle A. Sakai Anastasia Samsonova Jeremy E. Sandler Yuri B. Schwartz Noa Sher Rebecca Spokony David Sturgill Marijke van Baren Kenneth H. Wan Li Yang Charles Yu Elise A. Feingold Peter J. Good Mark S. Guyer Rebecca F. Lowdon Kami Ahmad Justen Andrews Bonnie Berger Steven E. Brenner Michael R. Brent Lucy Cherbas Sarah C. R. Elgin T Gingeras Robert L. Grossman Roger A. Hoskins Thomas C. Kaufman W. James Kent Mitzi I. Kuroda Terry L. Orr‐Weaver Norbert Perrimon Vincenzo Pirrotta James W. Posakony Bing Ren Steven Russell Peter Cherbas Brenton R. Graveley Suzanna Lewis Gos Micklem Brian Oliver Peter J. Park S Celniker Steven Henikoff Gary H. Karpen Eric C. Lai David M. MacAlpine Lincoln Stein Kevin P. White Manolis Kellis David Acevedo Richard P. Auburn Galt P Barber Hugo J. Bellen

From Genome to Regulatory Networks For biologists, having a genome in hand is only the beginning—much more investigation still needed characterize how used help produce functional organism (see Perspective by Blaxter ). In this vein, Gerstein et al. (p. 1775 ) summarize for Caenorhabditis elegans genome, and The modENCODE Consortium 1787 Drosophila melanogaster full transcriptome analyses over developmental stages, genome-wide identification of transcription factor binding sites,...

10.1126/science.1198374 article EN Science 2010-12-23

Circular RNAs (circRNAs) derived from back-spliced exons have been widely identified as being co-expressed with their linear counterparts. A single gene locus can produce multiple circRNAs through alternative back-splice site selection and/or splice selection; however, a detailed map of back-splicing/splicing in is lacking. Here, the upgraded CIRCexplorer2 pipeline, we systematically annotated different types back-splicing and splicing events various cell lines. Compared cognate RNAs,...

10.1101/gr.202895.115 article EN cc-by-nc Genome Research 2016-06-30

The human 8q24 gene desert contains multiple enhancers that form tissue-specific long-range chromatin loops with the MYC oncogene, but how looping at locus is regulated remains poorly understood. Here we demonstrate a long noncoding RNA (lncRNA), CCAT1-L, transcribed specifically in colorectal cancers from 515 kb upstream of MYC. This lncRNA plays role transcriptional regulation and promotes looping. Importantly, CCAT1-L located within strong super-enhancer spatially close to Knockdown...

10.1038/cr.2014.35 article EN cc-by-nc-nd Cell Research 2014-03-25

Steady-state circular RNAs (circRNAs) have been mapped to thousands of genomic loci in mammals. We studied circRNA processing using metabolic tagging nascent with 4-thiouridine (4sU). Strikingly, the efficiency from pre-mRNA is extremely low endogenously. Additional studies revealed that back-splicing outcomes correlate fast RNA Polymerase II elongation rate and are tightly controlled by cis-elements vivo. Additionally, prolonged 4sU labeling cells shows circRNAs largely processed...

10.1016/j.celrep.2016.03.058 article EN cc-by-nc-nd Cell Reports 2016-04-01

Abstract Background RNAs can be physically classified into poly(A)+ or poly(A)- transcripts according to the presence absence of a poly(A) tail at their 3' ends. Current deep sequencing approaches largely depend on enrichment with tail, and therefore offer little insight nature expression that lack tails. Results We have used explore repertoire both from HeLa cells H9 human embryonic stem (hESCs). Using stringent criteria, we found while majority are poly(A)+, significant portion either...

10.1186/gb-2011-12-2-r16 article EN cc-by Genome biology 2011-02-16

Uniform processing and detailed annotation of human, worm fly RNA-sequencing data reveal ancient, conserved features the transcriptome, shared co-expression modules (many enriched in developmental genes), matched expression patterns across development similar extent non-canonical, non-coding transcription; furthermore, are used to create a single, universal model predict gene-expression levels for all three organisms from chromatin at promoter. In this paper modENCODE consortium reports on...

10.1038/nature13424 article EN cc-by-nc-sa Nature 2014-08-26

Drosophila melanogaster cell lines are important resources for biologists. Here, we catalog the expression of exons, genes, and unannotated transcriptional signals 25 lines. Unannotated transcription is substantial (typically 19% euchromatic signal). Conservatively, identify 1405 novel transcribed regions; 684 these appear to be new exons neighboring, often distant, genes. Sixty-four percent genes expressed detectably in at least one line, but only 21% detected all Each line expresses, on...

10.1101/gr.112961.110 article EN Genome Research 2010-12-22

Abstract Circular RNAs (circRNAs) from back-splicing of exon(s) have been recently identified to be broadly expressed in eukaryotes, tissue- and species-specific manners. Although functions most circRNAs remain elusive, some are shown functional gene expression regulation potentially relate diseases. Due their stability, can also used as biomarkers for diagnosis. Profiling by integrating among different samples thus provides molecular basis further study potential application clinic. Here,...

10.1016/j.gpb.2018.08.001 article EN cc-by Genomics Proteomics & Bioinformatics 2018-08-01
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