Wei Chen

ORCID: 0000-0003-3263-1627
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About
Contact & Profiles
Research Areas
  • RNA Research and Splicing
  • RNA modifications and cancer
  • RNA and protein synthesis mechanisms
  • Epigenetics and DNA Methylation
  • Cancer-related molecular mechanisms research
  • Genetics and Neurodevelopmental Disorders
  • MicroRNA in disease regulation
  • Cancer-related gene regulation
  • Genomics and Chromatin Dynamics
  • CRISPR and Genetic Engineering
  • Genomics and Phylogenetic Studies
  • Genomic variations and chromosomal abnormalities
  • Cancer Cells and Metastasis
  • Single-cell and spatial transcriptomics
  • Genomics and Rare Diseases
  • Chromosomal and Genetic Variations
  • Congenital heart defects research
  • Cancer Genomics and Diagnostics
  • Molecular Biology Techniques and Applications
  • RNA regulation and disease
  • Bioinformatics and Genomic Networks
  • Animal Genetics and Reproduction
  • Advanced biosensing and bioanalysis techniques
  • RNA Interference and Gene Delivery
  • DNA Repair Mechanisms

Huazhong University of Science and Technology
2012-2025

Zhengzhou University
2021-2025

Southern University of Science and Technology
2016-2024

Huazhong Agricultural University
2024

University of Birmingham
2024

Guilin Medical University
2017-2024

Sun Yat-sen University
2007-2024

Army Medical University
2011-2024

Guangxi University
2024

National Clinical Research Center for Digestive Diseases
2024

microRNAs (miRNAs) are a large class of small non-coding RNAs which post-transcriptionally regulate the expression fraction all animal genes and important in wide range biological processes. Recent advances high-throughput sequencing allow miRNA detection at unprecedented sensitivity, but computational task accurately identifying miRNAs background sequenced remains challenging. For this purpose, we have designed miRDeep2, substantially improved algorithm identifies canonical non-canonical...

10.1093/nar/gkr688 article EN cc-by-nc Nucleic Acids Research 2011-09-10

As the human life span increases, number of people suffering from cognitive decline is rising dramatically. The mechanisms underlying age-associated memory impairment are, however, not understood. Here we show that disturbances in aging brain mouse are associated with altered hippocampal chromatin plasticity. During learning, aged mice display a specific deregulation histone H4 lysine 12 (H4K12) acetylation and fail to initiate gene expression program consolidation. Restoration physiological...

10.1126/science.1186088 article EN Science 2010-05-06

SummaryData on absolute molecule numbers will empower the modeling, understanding, and comparison of cellular functions biological systems. We quantified transcriptomes proteomes in fission yeast during proliferation quiescence. This rich resource provides first comprehensive reference for all RNA most protein concentrations a eukaryote under two key physiological conditions. The integrated data set supports quantitative biology affords unique insights into cell regulation. Although mRNAs...

10.1016/j.cell.2012.09.019 article EN cc-by Cell 2012-10-01
H.G. Stunnenberg Martin Hirst Sergio Abrignani David J. Adams Melanie de Almeida and 95 more Lucia Altucci Viren Amin Ido Amit Stylianos E. Antonarakis Samuel Aparício Takahiro Arima Laura Arrigoni Rob J.W. Arts Vahid Asnafi Manel Esteller Jae‐Bum Bae Kevin Baßler Stephan Beck Benjamin E. Berkman B Bernstein Mikhail Bilenky Adrian Bird Christoph Bock Bernhard O. Boehm Guillaume Bourque Charles E. Breeze Benedikt Brors David Bujold Oliver S. Burren Marion J.G. Bussemakers Adam S. Butterworth Elı́as Campo Enrique Carrillo de Santa Pau Lisa H. Chadwick Kui Ming Chan Wei Chen Tom H. Cheung Luca Chiapperino Nam‐Kyong Choi Ho‐Ryun Chung Laura Clarke Joseph M. Connors Philippe Cronet John Danesh Manolis Dermitzakis Gerard Drewes Pawel Durek Stephanie O. M. Dyke Tomasz Dyląg Connie J. Eaves Peter Ebert Roland Eils Roland Eils Catherine Ennis Tariq Enver Elise A. Feingold Bärbel Felder Anne C. Ferguson‐Smith Jude Fitzgibbon Paul Flicek Roger Foo Peter Fraser Mattia Frontini Eileen E. M. Furlong Sitanshu Gakkhar Nina Gasparoni Gilles Gasparoni Daniel H. Geschwind Petar Glažar Thomas Graf Frank Grosveld Xin‐Yuan Guan Roderic Guigó Marta Gut Alf Hamann Bok-Ghee Han R. Alan Harris Simon Heath Kristian Helin Jan G. Hengstler Alireza Heravi‐Moussavi Karl Herrup Steven Hill Jason A. Hilton Benjamin C. Hitz Bernhard Horsthemke Ming Hu Joo-Yeon Hwang Nancy Y. Ip Takashi Ito Biola M. Javierre Sasa Jenko Thomas Jenuwein Yann Joly Steven J.M. Jones Yae Kanai Hee Gyung Kang Aly Karsan Alexandra K. Kiemer Song Cheol Kim

10.1016/j.cell.2016.11.007 article EN publisher-specific-oa Cell 2016-11-01

Copy number variations (CNVs) account for a substantial proportion of human genomic variation, and have been shown to cause neurodevelopmental disorders.We sought determine the relevance CNVs aetiology schizophrenia (SZ).Whole-genome, high-resolution, tiling path BAC array comparative hybridization (array CGH) was employed test DNA from 93 individuals with DSM-IV SZ.Common copy changes that are unlikely be directly pathogenic in SZ were filtered out by comparison reference dataset 372...

10.1093/hmg/ddm323 article EN Human Molecular Genetics 2007-10-03

We have developed a transcriptome-wide approach to identify genes affected by promoter CpG island DNA hypermethylation and transcriptional silencing in colorectal cancer. By screening cell lines validating tumor-specific panel of primary human cancer samples, we estimate that nearly 5% or more all known may be methylated an individual tumor. When directly compared gene mutations, find larger numbers hypermethylated tumors, higher frequency within harboring either genetic epigenetic changes....

10.1371/journal.pgen.0030157 article EN cc-by PLoS Genetics 2007-09-18

Do young and old protein molecules have the same probability to be degraded? We addressed this question using metabolic pulse-chase labeling quantitative mass spectrometry obtain degradation profiles for thousands of proteins. find that >10% proteins are degraded non-exponentially. Specifically, less stable in first few hours their life stabilize with age. Degradation conserved similar two cell types. Many non-exponentially (NED) subunits complexes produced super-stoichiometric amounts...

10.1016/j.cell.2016.09.015 article EN publisher-specific-oa Cell 2016-10-01

Changes in gene expression levels determine differentiation of tissues involved development and are associated with functional decline aging. Although is tightly regulated, the transition between aging, as well regulation post-developmental changes, not understood. Here, we measured messenger RNA (mRNA), microRNA (miRNA), protein prefrontal cortex humans rhesus macaques over species' life spans. We find that few changes unique to Instead, vast majority miRNA occur aging represent reversals...

10.1101/gr.106849.110 article EN Genome Research 2010-07-20

Abstract Background Microarrays revolutionized biological research by enabling gene expression comparisons on a transcriptome-wide scale. Microarrays, however, do not estimate absolute level accurately. At present, high throughput sequencing is emerging as an alternative methodology for transcriptome studies. Although free of many limitations imposed microarray design, its potential to transcript levels unknown. Results In this study, we evaluate relative accuracy microarrays and (RNA-Seq)...

10.1186/1471-2164-10-161 article EN cc-by BMC Genomics 2009-04-16

Cellular metabolism was recently shown to regulate endothelial cell phenotype profoundly. Whether the atheroprotective biomechanical stimulus elicited by laminar shear stress modulates is not known.Here, we show that flow exposure reduced glucose uptake and mitochondrial content in endothelium. Shear stress-mediated reduction of reversed silencing flow-sensitive transcription factor Krüppel-like 2 (KLF2). Endothelial-specific deletion KLF2 mice induced cells perfused hearts. overexpression...

10.1161/atvbaha.114.304277 article EN Arteriosclerosis Thrombosis and Vascular Biology 2014-10-31

Over the course of ontogenesis, human brain and cognitive abilities develop in parallel, resulting a phenotype strikingly distinct from that other primates. Here, we used microarrays RNA-sequencing to examine human-specific gene expression changes taking place during postnatal development prefrontal cortex cerebellum humans, chimpanzees, rhesus macaques. We show most prominent change affects genes associated with synaptic functions represents an extreme shift timing cortex, but not...

10.1101/gr.127324.111 article EN Genome Research 2012-02-02

While splicing differences between tissues, sexes and species are well documented, little is known about the extent nature of changes that take place during human or mammalian development aging. Here, using high‐throughput transcriptome sequencing, we have characterized whole lifespan in two brain regions: prefrontal cortex cerebellum. Identified were confirmed independent rhesus macaque RNA‐seq data sets, exon arrays PCR, detected at protein level mass spectrometry. Splicing across abundant...

10.1038/msb.2012.67 article EN cc-by-nc-sa Molecular Systems Biology 2013-01-01

Abstract Current treatments for clear cell renal cancer (ccRCC) are insufficient because two-thirds of patients with metastases progress within two years. Here we report the identification and characterization a stem (CSC) population in ccRCC. CSCs quantitatively correlated tumor aggressiveness metastasis. Transcriptional profiling single sequencing reveal that these exhibit an activation WNT NOTCH signaling. A significant obstacle to development rational has been discrepancy between model...

10.1038/s41467-020-14700-7 article EN cc-by Nature Communications 2020-02-17
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