about
MicroRNA-driven developmental remodeling in the brain distinguishes humans from other primatesDe novo assembly and validation of planaria transcriptome by massive parallel sequencing and shotgun proteomicsComparative analysis of transposable element vector systems in human cellsCGHPRO -- a comprehensive data analysis tool for array CGH.Global quantification of mammalian gene expression controlComparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophreniaDiscovering microRNAs from deep sequencing data using miRDeepA human snoRNA with microRNA-like functionsQuantitative analysis of fission yeast transcriptomes and proteomes in proliferating and quiescent cellsExtension of cortical synaptic development distinguishes humans from chimpanzees and macaquesEstimating accuracy of RNA-Seq and microarrays with proteomicsSequence features associated with microRNA strand selection in humans and fliesDeciphering the porcine intestinal microRNA transcriptome.Comprehensive survey of human brain microRNA by deep sequencing.Intergenic and repeat transcription in human, chimpanzee and macaque brains measured by RNA-Seq.MicroRNA expression and regulation in human, chimpanzee, and macaque brains.MicroRNA, mRNA, and protein expression link development and aging in human and macaque brainGenomic analysis of miRNAs in an extreme mammalian hibernator, the Arctic ground squirrel.Altered histone acetylation is associated with age-dependent memory impairment in mice.Integrated epigenome profiling of repressive histone modifications, DNA methylation and gene expression in normal and malignant urothelial cells.ST3GAL3 mutations impair the development of higher cognitive functions.Breakpoint analysis of balanced chromosome rearrangements by next-generation paired-end sequencing.A novel X-linked recessive mental retardation syndrome comprising macrocephaly and ciliary dysfunction is allelic to oral-facial-digital type I syndrome.Next generation sequencing in a family with autosomal recessive Kahrizi syndrome (OMIM 612713) reveals a homozygous frameshift mutation in SRD5A3Two distinct auto-regulatory loops operate at the PU.1 locus in B cells and myeloid cells.Hybridisation-based resequencing of 17 X-linked intellectual disability genes in 135 patients reveals novel mutations in ATRX, SLC6A8 and PQBP1.Comparative genomic integration profiling of Sleeping Beauty transposons mobilized with high efficacy from integrase-defective lentiviral vectors in primary human cells.Widespread expression of piRNA-like molecules in somatic tissues.miRDeep2 accurately identifies known and hundreds of novel microRNA genes in seven animal clades.Gene expression of pluripotency determinants is conserved between mammalian and planarian stem cells.Retargeting transposon insertions by the adeno-associated virus Rep protein.Retargeting sleeping beauty transposon insertions by engineered zinc finger DNA-binding domains.Widespread splicing changes in human brain development and aging.Mapping translocation breakpoints by next-generation sequencingA unilateral negative feedback loop between miR-200 microRNAs and Sox2/E2F3 controls neural progenitor cell-cycle exit and differentiation.Pervasive isoform-specific translational regulation via alternative transcription start sites in mammals.Large-scale sorting of C. elegans embryos reveals the dynamics of small RNA expression.Global analysis of regulatory divergence in the evolution of mouse alternative polyadenylation.Tumor necrosis factor receptor superfamily member 19 (TNFRSF19) regulates differentiation fate of human mesenchymal (stromal) stem cells through canonical Wnt signaling and C/EBP.Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci.
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description
hulumtues
@sq
researcher
@en
հետազոտող
@hy
name
Wei Chen
@ast
Wei Chen
@en
Wei Chen
@es
Wei Chen
@fr
Wei Chen
@nl
Wei Chen
@sl
type
label
Wei Chen
@ast
Wei Chen
@en
Wei Chen
@es
Wei Chen
@fr
Wei Chen
@nl
Wei Chen
@sl
prefLabel
Wei Chen
@ast
Wei Chen
@en
Wei Chen
@es
Wei Chen
@fr
Wei Chen
@nl
Wei Chen
@sl
P106
P21
P2456
c/WeiChen29
P31
P496
0000-0003-3263-1627