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206 results for “protein”

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  1. Applications of Cas9 as an RNA-programmed RNA-binding protein.

    BioEssays : news and reviews in molecular, cellular and developmental biology · 2015 · 37(7): 732-9

    The Streptococcus pyogenes CRISPR-Cas system has gained widespread application as a genome editing and gene regulation tool as simultaneous cellular delivery of the Cas9 protein and guide RNAs enables recognition of specific DNA sequences. The recent discovery that Cas9 can …

    PMID 25880497 DOI ↗

  2. RNA-binding proteins in neurodegeneration: Seq and you shall receive.

    Trends in neurosciences · 2015 · 38(4): 226-36

    As critical players in gene regulation, RNA binding proteins (RBPs) are taking center stage in our understanding of cellular function and disease. In our era of bench-top sequencers and unprecedented computational power, biological questions can be addressed in a systematic, …

    PMID 25765321 DOI ↗

  3. Regulation of asymmetric division and CD8+ T lymphocyte fate specification by protein kinase Cζ and protein kinase Cλ/ι.

    Journal of immunology (Baltimore, Md. : 1950) · 2015 · 194(5): 2249-59

    During an immune response against a microbial pathogen, activated naive T lymphocytes give rise to effector cells that provide acute host defense and memory cells that provide long-lived immunity. It has been shown that T lymphocytes can undergo asymmetric division, …

    PMID 25617472 DOI ↗

  4. ALS-causative mutations in FUS/TLS confer gain and loss of function by altered association with SMN and U1-snRNP.

    Nature communications · 2015 · 6: 6171

    The RNA-binding protein FUS/TLS, mutation in which is causative of the fatal motor neuron disease amyotrophic lateral sclerosis (ALS), is demonstrated to directly bind to the U1-snRNP and SMN complexes. ALS-causative mutations in FUS/TLS are shown to abnormally enhance their …

    PMID 25625564 DOI ↗

  5. A novel splice-site mutation in ALS2 establishes the diagnosis of juvenile amyotrophic lateral sclerosis in a family with early onset anarthria and generalized dystonias.

    PloS one · 2014 · 9(12): e113258

    The diagnosis of childhood neurological disorders remains challenging given the overlapping clinical presentation across subgroups and heterogeneous presentation within subgroups. To determine the underlying genetic cause of a severe neurological disorder in a large consanguineous Pakistani family presenting with severe …

    PMID 25474699 DOI ↗

  6. The Period protein homolog LIN-42 negatively regulates microRNA biogenesis in C. elegans.

    Developmental biology · 2014 · 390(2): 126-35

    MicroRNAs (miRNAs) are small RNAs that post-transcriptionally regulate gene expression in many multicellular organisms. They are encoded in the genome and transcribed into primary (pri-) miRNAs before two processing steps that ultimately produce the mature miRNA. In order to generate …

    PMID 24699545 DOI ↗

  7. The dsRBP and inactive editor ADR-1 utilizes dsRNA binding to regulate A-to-I RNA editing across the C. elegans transcriptome.

    Cell reports · 2014 · 6(4): 599-607

    Inadequate adenosine-to-inosine editing of noncoding regions occurs in disease but is often uncorrelated with ADAR levels, underscoring the need to study deaminase-independent control of editing. C. elegans have two ADAR proteins, ADR-2 and the theoretically catalytically inactive ADR-1. Using high-throughput …

    PMID 24508457 DOI ↗

  8. Functional genomic analysis of the let-7 regulatory network in Caenorhabditis elegans.

    PLoS genetics · 2013 · 9(3): e1003353

    The let-7 microRNA (miRNA) regulates cellular differentiation across many animal species. Loss of let-7 activity causes abnormal development in Caenorhabditis elegans and unchecked cellular proliferation in human cells, which contributes to tumorigenesis. These defects are due to improper expression of …

    PMID 23516374 DOI ↗

  9. Rbfox proteins regulate alternative mRNA splicing through evolutionarily conserved RNA bridges.

    Nature structural & molecular biology · 2013 · 20(12): 1434-42

    Alternative splicing (AS) enables programmed diversity of gene expression across tissues and development. We show here that binding in distal intronic regions (>500 nucleotides (nt) from any exon) by Rbfox splicing factors important in development is extensive and is an …

    PMID 24213538 DOI ↗

  10. Reactivation of fetal splicing programs in diabetic hearts is mediated by protein kinase C signaling.

    The Journal of biological chemistry · 2013 · 288(49): 35372-86

    Diabetic cardiomyopathy is one of the complications of diabetes that eventually leads to heart failure and death. Aberrant activation of PKC signaling contributes to diabetic cardiomyopathy by mechanisms that are poorly understood. Previous reports indicate that PKC is implicated in …

    PMID 24151077 DOI ↗

  11. Differential L1 regulation in pluripotent stem cells of humans and apes.

    Nature · 2013 · 503(7477): 525-529

    Identifying cellular and molecular differences between human and non-human primates (NHPs) is essential to the basic understanding of the evolution and diversity of our own species. Until now, preserved tissues have been the main source for most comparative studies between …

    PMID 24153179 DOI ↗

  12. Coordinate Nodal and BMP inhibition directs Baf60c-dependent cardiomyocyte commitment.

    Genes & development · 2013 · 27(21): 2332-44

    A critical but molecularly uncharacterized step in heart formation and regeneration is the process that commits progenitor cells to differentiate into cardiomyocytes. Here, we show that the endoderm-derived dual Nodal/bone morphogenetic protein (BMP) antagonist Cerberus-1 (Cer1) in embryonic stem cell …

    PMID 24186978 DOI ↗

  13. Genome-wide analysis reveals SR protein cooperation and competition in regulated splicing.

    Molecular cell · 2013 · 50(2): 223-35

    SR proteins are well-characterized RNA binding proteins that promote exon inclusion by binding to exonic splicing enhancers (ESEs). However, it has been unclear whether regulatory rules deduced on model genes apply generally to activities of SR proteins in the cell. …

    PMID 23562324 DOI ↗

  14. ALS-linked TDP-43 mutations produce aberrant RNA splicing and adult-onset motor neuron disease without aggregation or loss of nuclear TDP-43.

    Proceedings of the National Academy of Sciences of the United States of America · 2013 · 110(8): E736-45

    Transactivating response region DNA binding protein (TDP-43) is the major protein component of ubiquitinated inclusions found in amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration (FTLD) with ubiquitinated inclusions. Two ALS-causing mutants (TDP-43(Q331K) and TDP-43(M337V)), but not wild-type human TDP-43, …

    PMID 23382207 DOI ↗

  15. Genome-wide approaches to dissect the roles of RNA binding proteins in translational control: implications for neurological diseases.

    Frontiers in neuroscience · 2012 · 6: 144

    Translational control of messenger RNAs (mRNAs) is a key aspect of neurobiology, defects of which can lead to neurological diseases. In response to stimuli, local translation of mRNAs is activated at synapses to facilitate long-lasting forms of synaptic plasticity, the …

    PMID 23060744 DOI ↗

  16. Divergent roles of ALS-linked proteins FUS/TLS and TDP-43 intersect in processing long pre-mRNAs.

    Nature neuroscience · 2012 · 15(11): 1488-97

    FUS/TLS (fused in sarcoma/translocated in liposarcoma) and TDP-43 are integrally involved in amyotrophic lateral sclerosis (ALS) and frontotemporal dementia. We found that FUS/TLS binds to RNAs from >5,500 genes in mouse and human brain, primarily through a GUGGU-binding motif. We …

    PMID 23023293 DOI ↗

  17. LIN28 binds messenger RNAs at GGAGA motifs and regulates splicing factor abundance.

    Molecular cell · 2012 · 48(2): 195-206

    LIN28 is a conserved RNA-binding protein implicated in pluripotency, reprogramming, and oncogenesis. It was previously shown to act primarily by blocking let-7 microRNA (miRNA) biogenesis, but here we elucidate distinct roles of LIN28 regulation via its direct messenger RNA (mRNA) …

    PMID 22959275 DOI ↗

  18. Misregulated RNA processing in amyotrophic lateral sclerosis.

    Brain research · 2012 · 1462: 3-15

    Amyotrophic lateral sclerosis (ALS) research is undergoing an era of unprecedented discoveries with the identification of new genes as major genetic causes of this disease. These discoveries reinforce the genetic, clinical and pathological overlap between ALS and frontotemporal lobar degeneration …

    PMID 22444279 DOI ↗

  19. Integrative genome-wide analysis reveals cooperative regulation of alternative splicing by hnRNP proteins.

    Cell reports · 2012 · 1(2): 167-78

    Understanding how RNA binding proteins control the splicing code is fundamental to human biology and disease. Here, we present a comprehensive study to elucidate how heterogeneous nuclear ribonucleoparticle (hnRNP) proteins, among the most abundant RNA binding proteins, coordinate to regulate …

    PMID 22574288 DOI ↗

  20. Comprehensive identification of miRNA target sites in live animals.

    Methods in molecular biology (Clifton, N.J.) · 2011 · 732: 169-85

    MicroRNAs (miRNAs) are small RNA molecules that posttranscriptionally regulate the expression of protein-coding genes. The mature miRNAs are loaded into Argonaute-containing protein complexes (miRISC, miRNA Induced S ilencing Complex), and guide these complexes to the 3' UTR of targeted mRNA …

    PMID 21431713 DOI ↗

  21. Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43.

    Nature neuroscience · 2011 · 14(4): 459-68

    We used cross-linking and immunoprecipitation coupled with high-throughput sequencing to identify binding sites in 6,304 genes as the brain RNA targets for TDP-43, an RNA binding protein that, when mutated, causes amyotrophic lateral sclerosis. Massively parallel sequencing and splicing-sensitive junction …

    PMID 21358643 DOI ↗

  22. LIN-28 co-transcriptionally binds primary let-7 to regulate miRNA maturation in Caenorhabditis elegans.

    Nature structural & molecular biology · 2011 · 18(3): 302-8

    The highly conserved let-7 microRNA (miRNA) regulates developmental pathways across animal phyla. Mis-expression of let-7 causes lethality in C. elegans and has been associated with several human diseases. We show that timing of let-7 expression in developing worms is under …

    PMID 21297634 DOI ↗

  23. Comprehensive discovery of endogenous Argonaute binding sites in Caenorhabditis elegans.

    Nature structural & molecular biology · 2010 · 17(2): 173-9

    MicroRNAs (miRNAs) regulate gene expression by guiding Argonaute proteins to specific target mRNA sequences. Identification of bona fide miRNA target sites in animals is challenging because of uncertainties regarding the base-pairing requirements between miRNA and target as well as the …

    PMID 20062054 DOI ↗

  24. An RNA code for the FOX2 splicing regulator revealed by mapping RNA-protein interactions in stem cells.

    Nature structural & molecular biology · 2009 · 16(2): 130-7

    The elucidation of a code for regulated splicing has been a long-standing goal in understanding the control of post-transcriptional gene expression events that are crucial for cell survival, differentiation and development. We decoded functional RNA elements in vivo by constructing …

    PMID 19136955 DOI ↗

  25. Divergent transcription from active promoters.

    Science (New York, N.Y.) · 2008 · 322(5909): 1849-51

    Transcription initiation by RNA polymerase II (RNAPII) is thought to occur unidirectionally from most genes. Here, we present evidence of widespread divergent transcription at protein-encoding gene promoters. Transcription start site-associated RNAs (TSSa-RNAs) nonrandomly flank active promoters, with peaks of antisense …

    PMID 19056940 DOI ↗

Datasets 25+

GSE302600 GSE · GEO

Zfp697/ZNF697 is an RNA-binding protein that modulates TGF-β1 2 signaling and hepatic inflammation in liver disease

Mus musculus · GPL30172

GSE254209 GSE · GEO

Inhibition of RNA splicing triggers CHMP7 nuclear entry impacting TDP-43 function and leading to onset of ALS (eCLIP).

Homo sapiens · GPL24676

GSE254208 GSE · GEO

Inhibition of RNA splicing triggers CHMP7 nuclear entry impacting TDP-43 function and leading to onset of ALS (RNA-Seq).

Homo sapiens · Illumina

GSE328331 GSE · GEO

Modulation of the DNA/RNA Binding Protein ARID5A Regulates Microglial Activation and Response [RIP-Seq]

Homo sapiens · Illumina

GSE290625 GSE · GEO

Modulation of the DNA/RNA Binding Protein ARID5A Regulates Microglial Activation and Response [eclip]

Homo sapiens · Illumina

GSE290765 GSE · GEO

Modulation of the DNA/RNA Binding Protein ARID5A Regulates Microglial Activation and Response [cutnrun]

Homo sapiens · Illumina

GSE290755 GSE · GEO

Modulation of the DNA/RNA Binding Protein ARID5A Regulates Microglial Activation and Response [rna-seq]

Homo sapiens · Illumina

GSE227455 GSE · GEO

RBP Footprint Grand Challenge: An evaluation of novel computational approaches to RNA-binding protein target prediction from structural data

Homo sapiens · GPL20301

GSE145805 GSE · GEO

RNA secondary structome of different cell lines

Homo sapiens, Mus musculus · GPL20795, GPL21273

GSE302649 GSE · GEO

Mapping CCR4-NOT recruitment elements at high resolution reveals transcriptome-wide determinants of mRNA decay [miRNA-Seq]

GPL18573

GSE302648 GSE · GEO

Mapping CCR4-NOT recruitment elements at high resolution reveals transcriptome-wide determinants of mRNA decay [RIP-Seq]

GPL18573

GSE290248 GSE · GEO

Large-scale tethered screen of RNA-binding proteins reveals novel regulators of poly(A) site selection [PAS-seq]

Homo sapiens · Illumina

GSE290282 GSE · GEO

Large-scale tethered screen of RNA-binding proteins reveals novel regulators of poly(A) site selection [RNA-Seq]

Homo sapiens · Illumina

GSE290281 GSE · GEO

Large-scale tethered screen of RNA-binding proteins reveals novel regulators of poly(A) site selection [eCLIP]

Homo sapiens · Illumina

GSE244832 GSE · GEO

Multi-Modal Comparison of human Hepatic Stellate Cells identifies novel therapeutic targets for Metabolic Dysfunction-Associated Steatotic Liver Disease

Homo sapiens · GPL24676, GPL37309

GSE151788 GSE · GEO

Ythdf m6A readers compensate each other in a context dependent manner [eCLIP]

GPL17021

GSE148536 GSE · GEO

Ythdf m6A readers compensate each other in a context dependent manner [Ribo-seq]

GPL21626

GSE148038 GSE · GEO

Ythdf m6A readers compensate each other in a context dependent manner [3'UTR RNA-seq]

GPL13112

GSE147849 GSE · GEO

Ythdf m6A readers compensate each other in a context dependent manner [RNA-seq]

GPL21626

GSE315443 GSE · GEO

MBNL2 dysfunction in outer radial glial cells is associated with disrupted corticogenesis in congenital myotonic dystrophy [scRNA-Seq]

GPL24676

GSE315407 GSE · GEO

Comprehensive RNA-binding protein analyses using enhanced CLIP (ENCORE)

GPL20301, GPL24676, GPL34284

GSE315406 GSE · GEO

Comprehensive RNA-binding protein analyses using enhanced CLIP (ENCORE) [dataset2]

GPL20301, GPL24676, GPL34284

GSE315347 GSE · GEO

Comprehensive RNA-binding protein analyses using enhanced CLIP (ENCORE) [dataset1]

GPL20301, GPL24676

GSE315026 GSE · GEO

MBNL2 dysfunction in outer radial glial cells is associated with disrupted corticogenesis in congenital myotonic dystrophy [eCLIP]

GPL24676

GSE314059 GSE · GEO

Single-cell and isoform-specific translational profiling of the mouse brain with long-read sequencing [scRNA-Seq, longread]

GPL34585

Showing first 25 dataset results.

Analyses 25+

GSE244832 scRNA-seq Data Processing

GSE244832 · 9 steps · scRNA-seq · geo_data_processing

RNA-binding protein LARP6 coordinates hepatic stellate cell activation and liver fibrosis. (2026)

GSE290248 Data Processing

GSE290248 · 1 step · geo_data_processing

Large-scale tethered screen of RNA-binding proteins reveals novel regulators of poly(A) site selection. (2026)

GSE290281 eCLIP Data Processing

GSE290281 · 1 step · eCLIP · geo_data_processing

Large-scale tethered screen of RNA-binding proteins reveals novel regulators of poly(A) site selection. (2026)

GSE290282 RNA-seq Data Processing

GSE290282 · 3 steps · RNA-seq · geo_data_processing

Large-scale tethered screen of RNA-binding proteins reveals novel regulators of poly(A) site selection. (2026)

GSE299099 Processing Pipeline

GSE299099 · 3 steps · RNA-Seq · code_examples

Structural and mechanistic analysis of covalent ligands targeting the RNA-binding protein NONO. (2026)

GSE315347 eCLIP Data Processing

GSE315347 · 4 steps · eCLIP · geo_data_processing

Comprehensive RNA-binding protein analyses and deep learning uncover genetic constraints and disease associations in protein-RNA interfaces. (2026)

GSE315406 eCLIP Data Processing

GSE315406 · 4 steps · eCLIP · geo_data_processing

Comprehensive RNA-binding protein analyses and deep learning uncover genetic constraints and disease associations in protein-RNA interfaces. (2026)

GSE315407 eCLIP Data Processing

GSE315407 · 4 steps · eCLIP · geo_data_processing

Comprehensive RNA-binding protein analyses and deep learning uncover genetic constraints and disease associations in protein-RNA interfaces. (2026)

GSE145805 SHAPE-seq Data Processing

GSE145805 · 7 steps · SHAPE-seq · geo_data_processing

Evaluation of novel computational methods to identify RNA-binding protein footprints from structural data. (2025)

GSE227455 eCLIP Data Processing

GSE227455 · 7 steps · eCLIP · geo_data_processing

Evaluation of novel computational methods to identify RNA-binding protein footprints from structural data. (2025)

GSE262542 Processing Pipeline

GSE262542 · 4 steps · RNA-Seq · code_examples

Evaluation of novel computational methods to identify RNA-binding protein footprints from structural data. (2025)

GSE276985 Processing Pipeline

GSE276985 · 2 steps · RIP-Seq · code_examples

Neuronal aging causes mislocalization of splicing proteins and unchecked cellular stress. (2025)

GSE276986 Processing Pipeline

GSE276986 · 1 step · RNA-Seq · code_examples

Neuronal aging causes mislocalization of splicing proteins and unchecked cellular stress. (2025)

GSE277082 Processing Pipeline

GSE277082 · 2 steps · RNA-Seq · code_examples

Neuronal aging causes mislocalization of splicing proteins and unchecked cellular stress. (2025)

GSE106493 Processing Pipeline

GSE106493 · 4 steps · RIP-Seq · code_examples

Transcriptome regulation by PARP13 in basal and antiviral states in human cells. (2024)

GSE114820 Processing Pipeline

GSE114820 · 4 steps · RNA-Seq · code_examples

Zfp697 is an RNA-binding protein that regulates skeletal muscle inflammation and remodeling. (2024)

GSE143437 Processing Pipeline

GSE143437 · 7 steps · RNA-Seq · code_examples

Zfp697 is an RNA-binding protein that regulates skeletal muscle inflammation and remodeling. (2024)

GSE145480 Processing Pipeline

GSE145480 · 11 steps · RNA-Seq · code_examples

Zfp697 is an RNA-binding protein that regulates skeletal muscle inflammation and remodeling. (2024)

GSE147127 Processing Pipeline

GSE147127 · 5 steps · RNA-Seq · code_examples

Zfp697 is an RNA-binding protein that regulates skeletal muscle inflammation and remodeling. (2024)

GSE193134 Processing Pipeline

GSE193134 · 18 steps · RIP-Seq · code_examples

LARP4 is an RNA-binding protein that binds nuclear-encoded mitochondrial mRNAs to promote mitochondrial function. (2024)

GSE210263 Processing Pipeline

GSE210263 · 10 steps · RNA-Seq · code_examples

Zfp697 is an RNA-binding protein that regulates skeletal muscle inflammation and remodeling. (2024)

GSE230097 Processing Pipeline

GSE230097 · 6 steps · RNA-Seq · code_examples

ePRINT: exonuclease assisted mapping of protein-RNA interactions. (2024)

GSE230717 Processing Pipeline

GSE230717 · 9 steps · RIP-Seq · code_examples

Large-scale map of RNA-binding protein interactomes across the mRNA life cycle. (2024)

GSE232513 Processing Pipeline

GSE232513 · 3 steps · RNA-Seq · code_examples

High-sensitivity in situ capture of endogenous RNA-protein interactions in fixed cells and primary tissues. (2024)

GSE232514 Processing Pipeline

GSE232514 · 5 steps · RNA-Seq · code_examples

High-sensitivity in situ capture of endogenous RNA-protein interactions in fixed cells and primary tissues. (2024)

Showing first 25 analysis results.