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Non-coding RNA
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inferredcites →https://doi.org/10.1002/(sici)1097-4644(19990315)72:4<492::aid-jcb5>3.0.co;2-hopenalex-snapshot
Characterization of the promoter for the human antisense fibroblast growth factor-2 gene; Regulation by Ets in Jurkat T cells
inferredcites →https://doi.org/10.1002/bies.10332openalex-snapshot
Challenging the dogma: the hidden layer of non‐protein‐coding RNAs in complex organisms
inferredcites →https://doi.org/10.1002/bies.10394openalex-snapshot
The spliceosome: the most complex macromolecular machine in the cell?
inferredcites →https://doi.org/10.1002/bies.950191010openalex-snapshot
Problems and paradigms: Multifunctional proteins suggest connections between transcriptional and post‐transcriptional processes
inferredcites →https://doi.org/10.1002/ijc.21425openalex-snapshot
The steroid receptor RNA activator protein is expressed in breast tumor tissues
inferredcites →https://doi.org/10.1002/jcp.20528openalex-snapshot
siRNA depletion of 7SK snRNA induces apoptosis but does not affect expression of the HIV‐1 LTR or P‐TEFb‐dependent cellular genes
inferredcites →https://doi.org/10.1007/bf02708978openalex-snapshot
Developmental regulation and complex organization of the promoter of the non-codinghsrω gene ofDrosophila melanogaster
inferredcites →https://doi.org/10.1007/s00412-005-0333-9openalex-snapshot
The many facets of H/ACA ribonucleoproteins
inferredcites →https://doi.org/10.1016/0959-437x(94)90066-3openalex-snapshot
Introns: evolution and function
inferredcites →https://doi.org/10.1016/j.bbrc.2004.07.159openalex-snapshot
Non-coding RNA directed DNA demethylation of Sphk1 CpG island
inferredcites →https://doi.org/10.1016/j.cbpa.2005.09.016openalex-snapshot
Riboswitches and the role of noncoding RNAs in bacterial metabolic control
inferredcites →https://doi.org/10.1016/j.cell.2004.12.031openalex-snapshot
Phylogenetic Shadowing and Computational Identification of Human microRNA Genes
inferredcites →https://doi.org/10.1016/j.cell.2004.12.035openalex-snapshot
Conserved Seed Pairing, Often Flanked by Adenosines, Indicates that Thousands of Human Genes are MicroRNA Targets
inferredcites →https://doi.org/10.1016/j.cell.2005.06.036openalex-snapshot
miRNAs, Cancer, and Stem Cell Division
inferredcites →https://doi.org/10.1016/j.cell.2005.07.028openalex-snapshot
Mutually Exclusive Splicing of the Insect Dscam Pre-mRNA Directed by Competing Intronic RNA Secondary Structures
inferredcites →https://doi.org/10.1016/j.cell.2005.08.033openalex-snapshot
Regulating Gene Expression through RNA Nuclear Retention
inferredcites →https://doi.org/10.1016/j.conb.2005.08.011openalex-snapshot
Role reversal: the regulation of neuronal gene expression by microRNAs
inferredcites →https://doi.org/10.1016/j.cub.2003.12.036openalex-snapshot
A Noncoding RNA Is Required for the Repression of RNApolII-Dependent Transcription in Primordial Germ Cells
inferredcites →https://doi.org/10.1016/j.cub.2004.01.034openalex-snapshot
The Spinocerebellar Ataxia 8 Noncoding RNA Causes Neurodegeneration and Associates with Staufen in Drosophila
inferredcites →https://doi.org/10.1016/j.cub.2004.11.003openalex-snapshot
Guide RNAs with 5′ Caps and Novel Box C/D snoRNA-like Domains for Modification of snRNAs in Metazoa
inferredcites →https://doi.org/10.1016/j.cub.2005.02.027openalex-snapshot
The Noncoding RNA Taurine Upregulated Gene 1 Is Required for Differentiation of the Murine Retina
inferredcites →https://doi.org/10.1016/j.cub.2005.02.060openalex-snapshot
RNAi-Mediated Allelic trans-Interaction at the Imprinted Rtl1/Peg11 Locus
inferredcites →https://doi.org/10.1016/j.devcel.2004.09.004openalex-snapshot
Retrotransposons Regulate Host Genes in Mouse Oocytes and Preimplantation Embryos
inferredcites →https://doi.org/10.1016/j.febslet.2004.03.104openalex-snapshot
The steroid receptor RNA activator is the first functional RNA encoding a protein
inferredcites →https://doi.org/10.1016/j.febslet.2004.03.117openalex-snapshot
Employment opportunities for non-coding RNAs
inferredcites →https://doi.org/10.1016/j.febslet.2005.08.083openalex-snapshot
RNAi‐directed assembly of heterochromatin in fission yeast
inferredcites →https://doi.org/10.1016/j.mib.2004.02.015openalex-snapshot
Controlling mRNA stability and translation with small, noncoding RNAs
inferredcites →https://doi.org/10.1016/j.mib.2005.10.013openalex-snapshot
Small non-coding RNAs in Archaea
inferredcites →https://doi.org/10.1016/j.molcel.2004.06.044openalex-snapshot
Regulation of Nuclear Receptor Activity by a Pseudouridine Synthase through Posttranscriptional Modification of Steroid Receptor RNA Activator
inferredcites →https://doi.org/10.1016/j.molcel.2005.06.011openalex-snapshot
Histone H3 Lysine 9 Methylation and HP1γ Are Associated with Transcription Elongation through Mammalian Chromatin
inferredcites →https://doi.org/10.1016/j.sbi.2004.05.006openalex-snapshot
RNA structure and function in C/D and H/ACA s(no)RNPs
inferredcites →https://doi.org/10.1016/j.sbi.2005.01.006openalex-snapshot
Zinc finger proteins: getting a grip on RNA
inferredcites →https://doi.org/10.1016/j.sbi.2005.01.013openalex-snapshot
The signal recognition particle and its interactions during protein targeting
inferredcites →https://doi.org/10.1016/j.sbi.2005.05.003openalex-snapshot
Riboswitches as versatile gene control elements
inferredcites →https://doi.org/10.1016/j.str.2005.08.005openalex-snapshot
Structure and Function of Argonaute Proteins
inferredcites →https://doi.org/10.1016/j.thbio.2005.02.002openalex-snapshot
Inherent size constraints on prokaryote gene networks due to ?accelerating? growth
inferredcites →https://doi.org/10.1016/j.tibs.2005.09.007openalex-snapshot
Regulating mammalian transcription with RNA
inferredcites →https://doi.org/10.1016/j.tig.2003.11.008openalex-snapshot
Riboswitches: the oldest mechanism for the regulation of gene expression?
inferredcites →https://doi.org/10.1016/j.tig.2005.03.007openalex-snapshot
Non-coding RNAs: hope or hype?
inferredcites →https://doi.org/10.1016/j.tig.2005.04.008openalex-snapshot
Mammalian microRNAs derived from genomic repeats
inferredcites →https://doi.org/10.1016/j.tig.2005.05.007openalex-snapshot
RNA-directed transcriptional gene silencing in mammals
inferredcites →https://doi.org/10.1016/j.tig.2005.06.008openalex-snapshot
A census of mammalian imprinting
inferredcites →https://doi.org/10.1016/j.tig.2005.10.003openalex-snapshot
Rapid evolution of noncoding RNAs: lack of conservation does not mean lack of function
inferredcites →https://doi.org/10.1016/j.ydbio.2005.07.030openalex-snapshot
Dynamic developmental regulation of the large non-coding RNA associated with the mouse 7C imprinted chromosomal region
inferredcites →https://doi.org/10.1016/j.ydbio.2005.11.047openalex-snapshot
Overgrowth caused by misexpression of a microRNA with dispensable wild-type function
inferredcites →https://doi.org/10.1016/j.ygeno.2004.07.012openalex-snapshot
Evidence for turnover of functional noncoding DNA in mammalian genome evolution
inferredcites →https://doi.org/10.1016/j.ygeno.2005.01.007openalex-snapshot
Sense and antisense Foxl2 transcripts in mouse
inferredcites →https://doi.org/10.1016/s0014-5793(03)01335-8openalex-snapshot
Thiamine‐regulated gene expression of Aspergillus oryzae thiA requires splicing of the intron containing a riboswitch‐like domain in the 5′‐UTR
inferredcites →https://doi.org/10.1016/s0022-2836(61)80072-7openalex-snapshot
Genetic regulatory mechanisms in the synthesis of proteins
inferredcites →https://doi.org/10.1016/s0092-8674(04)00127-8openalex-snapshot
Unbiased Mapping of Transcription Factor Binding Sites along Human Chromosomes 21 and 22 Points to Widespread Regulation of Noncoding RNAs
inferredcites →https://doi.org/10.1016/s0092-8674(04)00248-xopenalex-snapshot
A Small Modulatory dsRNA Specifies the Fate of Adult Neural Stem Cells
inferredcites →https://doi.org/10.1016/s0168-9525(03)00082-9openalex-snapshot
The callipyge locus: evidence for the trans interaction of reciprocally imprinted genes
inferredcites →https://doi.org/10.1016/s0168-9525(03)00203-8openalex-snapshot
Scaling laws in the functional content of genomes
inferredcites →https://doi.org/10.1016/s0300-9084(02)01402-5openalex-snapshot
The expanding snoRNA world
inferredcites →https://doi.org/10.1016/s0960-9822(01)00401-8openalex-snapshot
Computational identification of noncoding RNAs in E. coli by comparative genomics
inferredcites →https://doi.org/10.1016/s0968-0004(03)00169-5openalex-snapshot
RNA, the first macromolecular catalyst: the ribosome is a ribozyme
inferredcites →https://doi.org/10.1017/s1355838299981190openalex-snapshot
The stability and fate of a spliced intron from vertebrate cells
inferredcites →https://doi.org/10.1038/35030169openalex-snapshot
Chromodomains are protein–RNA interaction modules
inferredcites →https://doi.org/10.1038/35096585openalex-snapshot
The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita
inferredcites →https://doi.org/10.1038/35104575openalex-snapshot
The 7SK small nuclear RNA inhibits the CDK9/cyclin T1 kinase to control transcription
inferredcites →https://doi.org/10.1038/86850openalex-snapshot
Retrotransposons as epigenetic mediators of phenotypic variation in mammals
inferredcites →https://doi.org/10.1038/nature01858openalex-snapshot
Comparative analyses of multi-species sequences from targeted genomic regions
inferredcites →https://doi.org/10.1038/nature02064openalex-snapshot
A regulatory mutation in IGF2 causes a major QTL effect on muscle growth in the pig
inferredcites →https://doi.org/10.1038/nature02255openalex-snapshot
A microRNA controlling left/right neuronal asymmetry in Caenorhabditis elegans
inferredcites →https://doi.org/10.1038/nature02538openalex-snapshot
Intergenic transcription is required to repress the Saccharomyces cerevisiae SER3 gene
inferredcites →https://doi.org/10.1038/nature03001openalex-snapshot
Finishing the euchromatic sequence of the human genome
inferredcites →https://doi.org/10.1038/nature03016openalex-snapshot
Neutral evolution of ‘non-coding’ complementary DNAs
inferredcites →https://doi.org/10.1038/nature03552openalex-snapshot
A microRNA polycistron as a potential human oncogene
inferredcites →https://doi.org/10.1038/nature03677openalex-snapshot
c-Myc-regulated microRNAs modulate E2F1 expression
inferredcites →https://doi.org/10.1038/nature03702openalex-snapshot
MicroRNA expression profiles classify human cancers
inferredcites →https://doi.org/10.1038/nature03816openalex-snapshot
Stem cell division is regulated by the microRNA pathway
inferredcites →https://doi.org/10.1038/nature03959openalex-snapshot
Genome sequencing in microfabricated high-density picolitre reactors
inferredcites →https://doi.org/10.1038/nature04107openalex-snapshot
Adaptive evolution of non-coding DNA in Drosophila
inferredcites →https://doi.org/10.1038/nature04338openalex-snapshot
Genome sequence, comparative analysis and haplotype structure of the domestic dog
inferredcites →https://doi.org/10.1038/nbt1144openalex-snapshot
Mapping of conserved RNA secondary structures predicts thousands of functional noncoding RNAs in the human genome
inferredcites →https://doi.org/10.1038/ncb1373openalex-snapshot
The microRNA miR-181 targets the homeobox protein Hox-A11 during mammalian myoblast differentiation
inferredcites →https://doi.org/10.1038/nchembio725openalex-snapshot
Inhibiting gene expression at transcription start sites in chromosomal DNA with antigene RNAs
inferredcites →https://doi.org/10.1038/ng1171openalex-snapshot
Imprinted microRNA genes transcribed antisense to a reciprocally imprinted retrotransposon-like gene
inferredcites →https://doi.org/10.1038/ng1421openalex-snapshot
MicroRNA-responsive 'sensor' transgenes uncover Hox-like and other developmentally regulated patterns of vertebrate microRNA expression
inferredcites →https://doi.org/10.1038/ng1590openalex-snapshot
Identification of hundreds of conserved and nonconserved human microRNAs
inferredcites →https://doi.org/10.1038/ng1602openalex-snapshot
Comprehensive analysis of heterochromatin- and RNAi-mediated epigenetic control of the fission yeast genome
inferredcites →https://doi.org/10.1038/ng1611openalex-snapshot
Short double-stranded RNA induces transcriptional gene silencing in human cancer cells in the absence of DNA methylation
inferredcites →https://doi.org/10.1038/nrg1125openalex-snapshot
The power of the 3′ UTR: translational control and development
inferredcites →https://doi.org/10.1038/nrm1488openalex-snapshot
Molecular mechanisms of translational control
inferredcites →https://doi.org/10.1038/nsb862openalex-snapshot
U1 snRNA associates with TFIIH and regulates transcriptional initiation
inferredcites →https://doi.org/10.1038/nsmb0705-569openalex-snapshot
MicroRNAs directing siRNA biogenesis
inferredcites →https://doi.org/10.1038/nsmb1041openalex-snapshot
Modulation of microRNA processing and expression through RNA editing by ADAR deaminases
inferredcites →https://doi.org/10.1038/nsmb812openalex-snapshot
B2 RNA binds directly to RNA polymerase II to repress transcript synthesis
inferredcites →https://doi.org/10.1038/nsmb813openalex-snapshot
The SINE-encoded mouse B2 RNA represses mRNA transcription in response to heat shock
inferredcites →https://doi.org/10.1038/sj.ejhg.5201459openalex-snapshot
Genomics: The amazing complexity of the human transcriptome
inferredcites →https://doi.org/10.1038/sj.emboj.7600275openalex-snapshot
Binding of the 7SK snRNA turns the HEXIM1 protein into a P‐TEFb (CDK9/cyclin T) inhibitor
inferredcites →https://doi.org/10.1038/sj.emboj.7600385openalex-snapshot
MicroRNA genes are transcribed by RNA polymerase II
inferredcites →https://doi.org/10.1042/bst0330447openalex-snapshot
Towards understanding the catalytic core structure of the spliceosome
inferredcites →https://doi.org/10.1056/nejmoa050995openalex-snapshot
A MicroRNA Signature Associated with Prognosis and Progression in Chronic Lymphocytic Leukemia
inferredcites →https://doi.org/10.1073/pnas.0403423101openalex-snapshot
Identification of tandem duplicate regulatory small RNAs in Pseudomonas aeruginosa involved in iron homeostasis
inferredcites →https://doi.org/10.1073/pnas.0409169102openalex-snapshot
Fast and reliable prediction of noncoding RNAs
inferredcites →https://doi.org/10.1073/pnas.192571399openalex-snapshot
Distinct RNA motifs are important for coactivation of steroid hormone receptors by steroid receptor RNA activator (SRA)
inferredcites →https://doi.org/10.1073/pnas.222671299openalex-snapshot
Characterization of the intergenic RNA profile at abdominal-A and Abdominal-B in the Drosophila bithorax complex
inferredcites →https://doi.org/10.1073/pnas.250426397openalex-snapshot
Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization
inferredcites →https://doi.org/10.1073/pnas.90.24.11563openalex-snapshot
BC200 RNA: a neural RNA polymerase III product encoded by a monomeric Alu element.
inferredcites →https://doi.org/10.1074/jbc.m005104200openalex-snapshot
Localization and Stability of Introns Spliced from thePem Homeobox Gene
inferredcites →https://doi.org/10.1074/jbc.m103544200openalex-snapshot
A Novel Brain-specific Box C/D Small Nucleolar RNA Processed from Tandemly Repeated Introns of a Noncoding RNA Gene in Rats
inferredcites →https://doi.org/10.1074/jbc.m404930200openalex-snapshot
An RNA-binding Domain in the Thyroid Hormone Receptor Enhances Transcriptional Activation
inferredcites →https://doi.org/10.1074/jbc.m409070200openalex-snapshot
Components of the DNA Methylation System of Chromatin Control Are RNA-binding Proteins
inferredcites →https://doi.org/10.1074/jbc.m500912200openalex-snapshot
Compensatory Contributions of HEXIM1 and HEXIM2 in Maintaining the Balance of Active and Inactive Positive Transcription Elongation Factor b Complexes for Control of Transcription
inferredcites →https://doi.org/10.1074/jbc.m502712200openalex-snapshot
Analysis of the Large Inactive P-TEFb Complex Indicates That It Contains One 7SK Molecule, a Dimer of HEXIM1 or HEXIM2, and Two P-TEFb Molecules Containing Cdk9 Phosphorylated at Threonine 186
inferredcites →https://doi.org/10.1074/jbc.m505791200openalex-snapshot
Analysis of U1 Small Nuclear RNA Interaction with Cyclin H
inferredcites →https://doi.org/10.1083/jcb.200310138openalex-snapshot
Human telomerase RNA and box H/ACA scaRNAs share a common Cajal body–specific localization signal
inferredcites →https://doi.org/10.1089/154545704322988067openalex-snapshot
Modification of Alternative Splicing by Antisense Therapeutics
inferredcites →https://doi.org/10.1091/mbc.e04-12-1078openalex-snapshot
Structural and Functional Characterization of Noncoding Repetitive RNAs Transcribed in Stressed Human Cells
inferredcites →https://doi.org/10.1093/dnares/8.1.11openalex-snapshot
Complete Genome Sequence of Enterohemorrhagic Eschelichia coli O157:H7 and Genomic Comparison with a Laboratory Strain K-12
inferredcites →https://doi.org/10.1093/embo-reports/kve230openalex-snapshot
Non‐coding RNAs: the architects of eukaryotic complexity
inferredcites →https://doi.org/10.1093/embo-reports/kvf194openalex-snapshot
Coordinated methyl and RNA binding is required for heterochromatin localization of mammalian HP1α
inferredcites →https://doi.org/10.1093/emboj/20.11.2943openalex-snapshot
RNomics: an experimental approach that identifies 201 candidates for novel, small, non‐messenger RNAs in mouse
inferredcites →https://doi.org/10.1093/emboj/cdg187openalex-snapshot
Modification of Sm small nuclear RNAs occurs in the nucleoplasmic Cajal body following import from the cytoplasm
inferredcites →https://doi.org/10.1093/emboj/cdg337openalex-snapshot
Structure, function and evolution of the signal recognition particle
inferredcites →https://doi.org/10.1093/genetics/163.1.453openalex-snapshot
Mosaicism of Solid Gold Supports the Causality of a Noncoding A-to-G Transition in the Determinism of the Callipyge Phenotype
inferredcites →https://doi.org/10.1093/hmg/11.13.1527openalex-snapshot
Identification of tandemly-repeated C/D snoRNA genes at the imprinted human 14q32 domain reminiscent of those at the Prader-Willi/Angelman syndrome region
inferredcites →https://doi.org/10.1093/hmg/ddg196openalex-snapshot
Morpholino antisense oligonucleotide induced dystrophin exon 23 skipping in mdx mouse muscle
inferredcites →https://doi.org/10.1093/hmg/ddi084openalex-snapshot
Natural antisense transcripts associated with genes involved in eye development
inferredcites →https://doi.org/10.1093/hmg/ddi257openalex-snapshot
Analysis of intronic conserved elements indicates that functional complexity might represent a major source of negative selection on non-coding sequences
inferredcites →https://doi.org/10.1093/hmg/ddi271openalex-snapshot
Camels and zebrafish, viruses and cancer: a microRNA update
inferredcites →https://doi.org/10.1093/jhered/esj022openalex-snapshot
Primate MicroRNAs miR-220 and miR-492 Lie within Processed Pseudogenes
inferredcites →https://doi.org/10.1093/nar/gkg849openalex-snapshot
Identification of 13 novel human modification guide RNAs
inferredcites →https://doi.org/10.1093/nar/gkg867openalex-snapshot
RNomics in Escherichia coli detects new sRNA species and indicates parallel transcriptional output in bacteria
inferredcites →https://doi.org/10.1093/nar/gkh818openalex-snapshot
Over 20% of human transcripts might form sense-antisense pairs
inferredcites →https://doi.org/10.1093/nar/gki041openalex-snapshot
NONCODE: an integrated knowledge database of non-coding RNAs
inferredcites →https://doi.org/10.1093/nar/gki256openalex-snapshot
Detection of 5'- and 3'-UTR-derived small RNAs and cis-encoded antisense RNAs in Escherichia coli
inferredcites →https://doi.org/10.1093/nar/gki809openalex-snapshot
Human vault-associated non-coding RNAs bind to mitoxantrone, a chemotherapeutic compound
inferredcites →https://doi.org/10.1093/nar/gki810openalex-snapshot
Distribution of SR protein exonic splicing enhancer motifs in human protein-coding genes
inferredcites →https://doi.org/10.1093/nar/gki863openalex-snapshot
Real-time expression profiling of microRNA precursors in human cancer cell lines
inferredcites →https://doi.org/10.1093/nar/gkj112openalex-snapshot
miRBase: microRNA sequences, targets and gene nomenclature
inferredcites →https://doi.org/10.1093/nar/gkj144openalex-snapshot
The UCSC Genome Browser Database: update 2006
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a003951openalex-snapshot
The Evolution of Controlled Multitasked Gene Networks: The Role of Introns and Other Noncoding RNAs in the Development of Complex Organisms
inferredcites →https://doi.org/10.1101/gad.1.3.307openalex-snapshot
Novel transcripts from the Ultrabithorax domain of the bithorax complex.
inferredcites →https://doi.org/10.1101/gad.11.19.2494openalex-snapshot
Intergenic transcription and transinduction of the human β-globin locus
inferredcites →https://doi.org/10.1101/gad.1165404openalex-snapshot
The C. elegans microRNA let-7 binds to imperfect let-7 complementary sites from the lin-41 3′UTR
inferredcites →https://doi.org/10.1101/gad.326205openalex-snapshot
Intergenic transcription through a Polycomb group response element counteracts silencing
inferredcites →https://doi.org/10.1101/gr.1011603openalex-snapshot
Identification of Putative Noncoding RNAs Among the RIKEN Mouse Full-Length cDNA Collection
inferredcites →https://doi.org/10.1101/gr.1208803openalex-snapshot
Intronic Sequences Flanking Alternatively Spliced Exons Are Conserved Between Human and Mouse
inferredcites →https://doi.org/10.1101/gr.152902openalex-snapshot
Comparative Sequence Analysis of the X-Inactivation Center Region in Mouse, Human, and Bovine
inferredcites →https://doi.org/10.1101/gr.172701openalex-snapshot
Human–Ovine Comparative Sequencing of a 250-kb Imprinted Domain Encompassing the Callipyge (clpg) Locus and Identification of Six Imprinted Transcripts: DLK1, DAT, GTL2, PEG11, antiPEG11, and MEG8
inferredcites →https://doi.org/10.1101/gr.2722704openalex-snapshot
Identification of Mammalian microRNA Host Genes and Transcription Units
inferredcites →https://doi.org/10.1101/gr.3155905openalex-snapshot
Disclosing hidden transcripts: Mouse natural sense–antisense transcripts tend to be poly(A) negative and nuclear localized
inferredcites →https://doi.org/10.1101/gr.3308405openalex-snapshot
Naturally occurring antisense: Transcriptional leakage or real overlap?
inferredcites →https://doi.org/10.1101/gr.3455305openalex-snapshot
Examples of the complex architecture of the human transcriptome revealed by RACE and high-density tiling arrays
inferredcites →https://doi.org/10.1101/gr.3545105openalex-snapshot
Ultraconserved elements in insect genomes: A highly conserved intronic sequence implicated in the control of homothorax mRNA splicing
inferredcites →https://doi.org/10.1101/gr.3715005openalex-snapshot
Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes
inferredcites →https://doi.org/10.1101/gr.4041005openalex-snapshot
An atlas of human gene expression from massively parallel signature sequencing (MPSS)
inferredcites →https://doi.org/10.1101/gr.4139206openalex-snapshot
Organization of the Caenorhabditis elegans small non-coding transcriptome: Genomic features, biogenesis, and expression
inferredcites →https://doi.org/10.1101/gr.4200206openalex-snapshot
Experimental validation of the regulated expression of large numbers of non-coding RNAs from the mouse genome
inferredcites →https://doi.org/10.1101/gr.4624306openalex-snapshot
Transposon-free regions in mammalian genomes
inferredcites →https://doi.org/10.1101/gr.955503openalex-snapshot
A Comprehensive Transcript Map of the Mouse Gnas Imprinted Complex
inferredcites →https://doi.org/10.1126/science.1087047openalex-snapshot
Evolutionary Discrimination of Mammalian Conserved Non-Genic Sequences (CNGs)
inferredcites →https://doi.org/10.1126/science.1097434openalex-snapshot
MicroRNA-Directed Cleavage of HOXB8 mRNA
inferredcites →https://doi.org/10.1126/science.1098119openalex-snapshot
Ultraconserved Elements in the Human Genome
inferredcites →https://doi.org/10.1126/science.1101372openalex-snapshot
Small Interfering RNA-Induced Transcriptional Gene Silencing in Human Cells
inferredcites →https://doi.org/10.1126/science.1103388openalex-snapshot
Global Identification of Human Transcribed Sequences with Genome Tiling Arrays
inferredcites →https://doi.org/10.1126/science.1108625openalex-snapshot
Transcriptional Maps of 10 Human Chromosomes at 5-Nucleotide Resolution
inferredcites →https://doi.org/10.1126/science.1109020openalex-snapshot
MicroRNAs Regulate Brain Morphogenesis in Zebrafish
inferredcites →https://doi.org/10.1126/science.1111443openalex-snapshot
From Birth to Death: The Complex Lives of Eukaryotic mRNAs
inferredcites →https://doi.org/10.1126/science.1111444openalex-snapshot
Ribo-gnome: The Big World of Small RNAs
inferredcites →https://doi.org/10.1126/science.1111771openalex-snapshot
RNA Structure: Reading the Ribosome
inferredcites →https://doi.org/10.1126/science.1112009openalex-snapshot
Antisense Transcription in the Mammalian Transcriptome
inferredcites →https://doi.org/10.1126/science.1112014openalex-snapshot
The Transcriptional Landscape of the Mammalian Genome
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Human Box H/ACA Pseudouridylation Guide RNA Machinery
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microPrimer: the biogenesis and function of microRNA
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What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Downregulation of lnRNA‐NEF is involved in the postoperative cancer distant recurrence in prostate carcinoma patients
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lncRNA mortal obligate RNA transcript was downregulated in ovarian carcinoma and inhibits cancer cell proliferation by downregulating miRNA‐21
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The various regulatory functions of long noncoding RNAs in apoptosis, cell cycle, and cellular senescence
inferred← citeshttps://doi.org/10.1002/jcla.24106openalex-snapshot
Long noncoding RNA TUG1 upregulates VEGFA to enhance malignant behaviors in stomach adenocarcinoma by sponging miR‐29c‐3p
inferred← citeshttps://doi.org/10.1002/jcp.26911openalex-snapshot
Implications of the noncoding RNAs in rheumatoid arthritis pathogenesis
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Clinicopathological and prognostic value of lncRNA PANDAR expression in solid tumors: Evidence from a systematic review and meta‐analysis
inferred← citeshttps://doi.org/10.1002/jcp.27612openalex-snapshot
New insights into the roles and regulation of SphK2 as a therapeutic target in cancer chemoresistance
inferred← citeshttps://doi.org/10.1002/jcp.27727openalex-snapshot
Knockdown of NEAT1 repressed the malignant progression of glioma through sponging miR‐107 and inhibiting CDK14
inferred← citeshttps://doi.org/10.1002/jcp.27772openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/jcp.28153openalex-snapshot
Deregulation of long noncoding RNA (TUG1) contributes to excessive podocytes apoptosis by activating endoplasmic reticulum stress in the development of diabetic nephropathy
inferred← citeshttps://doi.org/10.1002/jcp.28449openalex-snapshot
Circular RNA expression profile in human fibroblast premature senescence after repeated ultraviolet B irradiations revealed by microarray
inferred← citeshttps://doi.org/10.1002/jcp.28486openalex-snapshot
Silencing of a novel lncRNA LOC105369748 suppresses the progression of hepatocellular carcinoma by sponging miR‐5095 from MBD2
inferred← citeshttps://doi.org/10.1002/jcp.29538openalex-snapshot
The chromosome 19 microRNA cluster, regulated by promoter hypomethylation, is associated with tumour burden and poor prognosis in patients with hepatocellular carcinoma
inferred← citeshttps://doi.org/10.1002/jcp.30104openalex-snapshot
Epigenetic regulation of angiogenesis in lung cancer
inferred← citeshttps://doi.org/10.1002/jcp.30271openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/jlb.3ma0320-327rrropenalex-snapshot
The regulated profile of noncoding RNAs associated with inflammation by tanshinone IIA on atherosclerosis
inferred← citeshttps://doi.org/10.1002/jms.4465openalex-snapshot
High‐resolution ion mobility spectrometry‐mass spectrometry of isomeric/isobaric ribonucleotide variants
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inferred← citeshttps://doi.org/10.1002/lci2.20openalex-snapshot
Role of epigenetic alterations in aflatoxin‐induced hepatocellular carcinoma
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Analyzing RNA posttranscriptional modifications to decipher the epitranscriptomic code
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Epigenetic inactivation of microRNA gene hsa‐mir‐9‐1 in human breast cancer
inferred← citeshttps://doi.org/10.1002/pros.23953openalex-snapshot
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Controlled Delivery of Target-Specific MicroRNA Analogs as a Key to RNAi Therapeutics in Cancer
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Epigenetic Dysregulation in Alcohol-Associated Behaviors: Preclinical and Clinical Evidence
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inferred← citeshttps://doi.org/10.1007/978-0-387-92808-1_14openalex-snapshot
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RNA Structure and Its Function
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microRNA in Cutaneous Wound Healing
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The Non-coding Landscape of the Genome of Arabidopsis thaliana
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MicroRNAs in Cell Death and Cancer
inferred← citeshttps://doi.org/10.1007/978-1-4614-6182-1_8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-1-4614-6280-4_7openalex-snapshot
Microsatellite Repeats: Canaries in the Coalmine
inferred← citeshttps://doi.org/10.1007/978-1-4614-8624-4_11openalex-snapshot
Transcription Through Chromatin
inferred← citeshttps://doi.org/10.1007/978-1-4939-2547-6_13openalex-snapshot
cDNA Library Generation for the Analysis of Small RNAs by High-Throughput Sequencing
inferred← citeshttps://doi.org/10.1007/978-1-4939-2547-6_19openalex-snapshot
Efficient and Selective Knockdown of Small Non-Coding RNAs
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PARIS: Psoralen Analysis of RNA Interactions and Structures with High Throughput and Resolution
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Comparative Genome Annotation
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MicroRNA Networks in Breast Cancer Cells
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Gene Regulatory Networks: A Primer in Biological Processes and Statistical Modelling
inferred← citeshttps://doi.org/10.1007/978-1-4939-8982-9_11openalex-snapshot
Controllability Methods for Identifying Associations Between Critical Control ncRNAs and Human Diseases
inferred← citeshttps://doi.org/10.1007/978-1-4939-8982-9_14openalex-snapshot
Quantitative Characteristic of ncRNA Regulation in Gene Regulatory Networks
inferred← citeshttps://doi.org/10.1007/978-1-59745-033-1_10openalex-snapshot
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Role of DNA Methylation and Epigenetics in Stem Cells
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Gene and Promoter Structures of the Dopamine Receptors
inferred← citeshttps://doi.org/10.1007/978-1-60761-175-2_17openalex-snapshot
miRNAs: From Biogenesis to Networks
inferred← citeshttps://doi.org/10.1007/978-1-60761-259-9_4openalex-snapshot
Beyond PSA: Promising New Markers for Prostate Cancer
inferred← citeshttps://doi.org/10.1007/978-1-61779-018-8_15openalex-snapshot
Functional Analysis of Noncoding RNAs in Trypanosomes: RNA Walk, a Novel Approach to Study RNA–RNA Interactions Between Small RNA and Its Target
inferred← citeshttps://doi.org/10.1007/978-1-61779-027-0_14openalex-snapshot
Bioinformatics for RNomics
inferred← citeshttps://doi.org/10.1007/978-1-61779-854-2_15openalex-snapshot
High-Resolution Quantitative Methylation Analysis of MicroRNA Genes Using Pyrosequencing™
inferred← citeshttps://doi.org/10.1007/978-1-62703-011-3_14openalex-snapshot
Generation of cDNA Libraries from RNP-Derived Regulatory Noncoding RNAs
inferred← citeshttps://doi.org/10.1007/978-1-62703-709-9_15openalex-snapshot
De Novo Discovery of Structured ncRNA Motifs in Genomic Sequences
inferred← citeshttps://doi.org/10.1007/978-1-62703-709-9_6openalex-snapshot
An Introduction to RNA Databases
inferred← citeshttps://doi.org/10.1007/978-3-030-17938-0_31openalex-snapshot
Non-Coding Regions of Chloroplast Genomes Exhibit a Structuredness of Five Types
inferred← citeshttps://doi.org/10.1007/978-3-030-63369-1_8openalex-snapshot
Biomarkers as Putative Therapeutic Targets in Colorectal Cancer
inferred← citeshttps://doi.org/10.1007/978-3-030-87821-4_11openalex-snapshot
Transcriptome Profiling in Autoimmune Diseases
inferred← citeshttps://doi.org/10.1007/978-3-030-90214-8_8openalex-snapshot
Small Noncoding RNA, microRNA in Gene Regulation
inferred← citeshttps://doi.org/10.1007/978-3-030-94475-9_3openalex-snapshot
Laboratory Methods in Epigenetic Epidemiology
inferred← citeshttps://doi.org/10.1007/978-3-031-36390-0_4openalex-snapshot
Unraveling RNA by Mechanical Unzipping
inferred← citeshttps://doi.org/10.1007/978-3-031-36815-8_1openalex-snapshot
Viral RNA as a Branched Polymer
inferred← citeshttps://doi.org/10.1007/978-3-031-59286-7_2openalex-snapshot
Epigenetic Control of Cell Fate Decisions by Enhancer-Derived Long Noncoding RNAs
inferred← citeshttps://doi.org/10.1007/978-3-031-59286-7_21openalex-snapshot
The Role of Epigenetic Communication in the Co-regulation of Holobionts’ Biology: Interspecies Probabilistic Epigenesis
inferred← citeshttps://doi.org/10.1007/978-3-031-62178-9_2openalex-snapshot
Fibonacci’s Blueprint in Lifespan: Integrating Mathematical Predictions with RNA Dynamics and DNA Heritability in Systems Biology
inferred← citeshttps://doi.org/10.1007/978-3-031-70591-5_12openalex-snapshot
From Genes to Worms: A Deep Dive into Helminth Omics
inferred← citeshttps://doi.org/10.1007/978-3-032-06766-1_12openalex-snapshot
Hydra at the Crossroads of Evolution: Insights into Cell-type Diversification, Regeneration, and Epigenetic Regulation
inferred← citeshttps://doi.org/10.1007/978-3-319-11985-4_8openalex-snapshot
Transcriptome Profiling in Autoimmune Diseases
inferred← citeshttps://doi.org/10.1007/978-3-319-12418-6_15openalex-snapshot
Genome-Wide Identification of Non-coding RNAs in Komagatella pastoris str. GS115
inferred← citeshttps://doi.org/10.1007/978-3-319-13689-9_9openalex-snapshot
MicroRNAs with Impact on Adipose Tissue Inflammation in Obesity
inferred← citeshttps://doi.org/10.1007/978-3-319-41324-2_15openalex-snapshot
How Likely Are We? Evolution of Organismal Complexity
inferred← citeshttps://doi.org/10.1007/978-3-319-41761-5_22openalex-snapshot
Noncoding RNAs in Breast Cancer
inferred← citeshttps://doi.org/10.1007/978-3-319-95843-9_5openalex-snapshot
Modeling Nucleic Acids at the Residue–Level Resolution
inferred← citeshttps://doi.org/10.1007/978-3-540-70600-7_9openalex-snapshot
Translational Control by RNA-RNA Interaction: Improved Computation of RNA-RNA Binding Thermodynamics
inferred← citeshttps://doi.org/10.1007/978-3-540-73731-5_14openalex-snapshot
Outlining a Strategy for Screening Non-coding RNAs on a Transcriptome Through Support Vector Machines
inferred← citeshttps://doi.org/10.1007/978-3-642-12168-5_18openalex-snapshot
Noncoding RNAs as Therapeutic Targets
inferred← citeshttps://doi.org/10.1007/978-3-642-15294-8_4openalex-snapshot
Sparsification of RNA Structure Prediction Including Pseudoknots
inferred← citeshttps://doi.org/10.1007/978-3-642-16502-3_1openalex-snapshot
Transcriptional and Posttranscriptional Programming by Long Noncoding RNAs
inferred← citeshttps://doi.org/10.1007/978-3-642-16502-3_9openalex-snapshot
Long Nonprotein-Coding RNAs in Plants
inferred← citeshttps://doi.org/10.1007/978-3-642-17426-1_11openalex-snapshot
Toward an Understanding of the Dynamic Interdependence of Genes and Environment in the Regulation of Phenotype
inferred← citeshttps://doi.org/10.1007/978-3-642-22218-4_10openalex-snapshot
A Data Mining Library for miRNA Annotation and Analysis
inferred← citeshttps://doi.org/10.1007/978-3-642-22517-8_17openalex-snapshot
MicroRNAs in Development, Stem Cell Differentiation, and Regenerative Medicine
inferred← citeshttps://doi.org/10.1007/978-3-642-22517-8_8openalex-snapshot
Long Noncoding RNA Function and Expression in Cancer
inferred← citeshttps://doi.org/10.1007/978-3-642-22517-8_9openalex-snapshot
Expression Profiling of ncRNAs Employing RNP Libraries and Custom LNA/DNA Microarray Analysis
inferred← citeshttps://doi.org/10.1007/978-3-642-25740-7_17openalex-snapshot
RNA Structure Determination by Structural Probing and Mass Spectrometry: MS3D
inferred← citeshttps://doi.org/10.1007/978-3-642-28554-7_5openalex-snapshot
Modeling Nucleic Acids at the Residue-Level Resolution
inferred← citeshttps://doi.org/10.1007/978-3-642-33412-2_65openalex-snapshot
ncRNA-Class Web Tool: Non-coding RNA Feature Extraction and Pre-miRNA Classification Web Tool
inferred← citeshttps://doi.org/10.1007/978-3-642-36853-0_11openalex-snapshot
RNA Nanoparticles for Gene Expression Regulation
inferred← citeshttps://doi.org/10.1007/978-3-642-36853-0_6openalex-snapshot
Gene Expression Analysis Using Conventional and Imaging Methods
inferred← citeshttps://doi.org/10.1007/978-3-642-54842-0_10openalex-snapshot
MS-Based Approaches for Nucleic Acid Structural Determination
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