review article | Q7318358 |
scholarly article | Q13442814 |
P356 | DOI | 10.1016/S0378-1119(01)00695-3 |
P698 | PubMed publication ID | 11602343 |
P2093 | author name string | A L Greenleaf | |
M A Garcia-Blanco | |||
A C Goldstrohm | |||
P2860 | cites work | Initial sequencing and analysis of the human genome | Q21045365 |
Oncoprotein TLS interacts with serine-arginine proteins involved in RNA splicing | Q22003961 | ||
Evidence that P-TEFb alleviates the negative effect of DSIF on RNA polymerase II-dependent transcription in vitro | Q22008559 | ||
A novel transcriptional coactivator, p52, functionally interacts with the essential splicing factor ASF/SF2 | Q22008652 | ||
Mediator of Transcriptional Regulation | Q22065418 | ||
The Sequence of the Human Genome | Q22065842 | ||
Functional association of U2 snRNP with the ATP-independent spliceosomal complex E | Q22254390 | ||
The apoptosis-promoting factor TIA-1 is a regulator of alternative pre-mRNA splicing | Q24290594 | ||
Mass spectrometry and EST-database searching allows characterization of the multi-protein spliceosome complex | Q24311408 | ||
The transcriptional repressor ZFM1 interacts with and modulates the ability of EWS to activate transcription | Q24313686 | ||
A nuclear cap-binding complex binds Balbiani ring pre-mRNA cotranscriptionally and accompanies the ribonucleoprotein particle during nuclear export | Q24322859 | ||
EWS, but not EWS-FLI-1, is associated with both TFIID and RNA polymerase II: interactions between two members of the TET family, EWS and hTAFII68, and subunits of TFIID and RNA polymerase II complexes. | Q24522406 | ||
CUS2, a yeast homolog of human Tat-SF1, rescues function of misfolded U2 through an unusual RNA recognition motif | Q24522636 | ||
SAF-B protein couples transcription and pre-mRNA splicing to SAR/MAR elements | Q24548190 | ||
TLS-ERG leukemia fusion protein inhibits RNA splicing mediated by serine-arginine proteins | Q24554236 | ||
Transcriptional cofactor CA150 regulates RNA polymerase II elongation in a TATA-box-dependent manner | Q24554483 | ||
hnRNP H is a component of a splicing enhancer complex that activates a c-src alternative exon in neuronal cells | Q24554786 | ||
The HIV-1 Tat cellular coactivator Tat-SF1 is a general transcription elongation factor | Q24596637 | ||
The spliceosome assembly pathway in mammalian extracts | Q24601223 | ||
Three functional classes of transcriptional activation domain | Q24649917 | ||
WW domain-mediated interactions reveal a spliceosome-associated protein that binds a third class of proline-rich motif: the proline glycine and methionine-rich motif | Q24657609 | ||
Protein-interaction modules that organize nuclear function: FF domains of CA150 bind the phosphoCTD of RNA polymerase II | Q24672654 | ||
The splicing factor BBP interacts specifically with the pre-mRNA branchpoint sequence UACUAAC. | Q27934071 | ||
Modulation of RNA polymerase II elongation efficiency by C-terminal heptapeptide repeat domain kinase I. | Q27934205 | ||
Cross-intron bridging interactions in the yeast commitment complex are conserved in mammals | Q27936705 | ||
Transcriptional activation domains stimulate initiation and elongation at different times and via different residues | Q41810274 | ||
Coupled in vitro synthesis and splicing of RNA polymerase II transcripts | Q42040067 | ||
Capping of eucaryotic mRNAs | Q44537736 | ||
Both subunits of U2AF recognize the 3' splice site in Caenorhabditis elegans | Q47069458 | ||
mRNA-type introns in U6 small nuclear RNA genes: implications for the catalysis in pre-mRNA splicing | Q48222905 | ||
Mutually exclusive splicing of alpha-tropomyosin exons enforced by an unusual lariat branch point location: implications for constitutive splicing | Q48302007 | ||
Transcriptional elongation by RNA polymerase II is stimulated by transactivators. | Q49101405 | ||
The splicing factor, Prp40, binds the phosphorylated carboxyl-terminal domain of RNA polymerase II. | Q51075771 | ||
RNP particles at splice junction sequences on Drosophila chorion transcripts. | Q52466521 | ||
Splicing of Balbiani ring 1 gene pre-mRNA occurs simultaneously with transcription. | Q52544550 | ||
A nuclear cap-binding complex facilitates association of U1 snRNP with the cap-proximal 5' splice site. | Q55066526 | ||
Characteristics of genomic breakpoints in TLS-CHOP translocations in liposarcomas suggest the involvement of Translin and topoisomerase II in the process of translocation | Q57033225 | ||
What If There Are Only 30,000 Human Genes? | Q57986035 | ||
Diffusion mechanisms in metallic supercooled liquids and glasses | Q59058749 | ||
Localization of pre-mRNA splicing in mammalian nuclei | Q59083697 | ||
In vivo evidence that transcription and splicing are coordinated by a recruiting mechanism | Q64377799 | ||
U1 snRNP targets an essential splicing factor, U2AF65, to the 3' splice site by a network of interactions spanning the exon | Q67469400 | ||
In vitro polyadenylation is stimulated by the presence of an upstream intron | Q67676618 | ||
Positive patches and negative noodles: linking RNA processing to transcription? | Q70716691 | ||
Human beta-globin pre-mRNA synthesized in vitro is accurately spliced in Xenopus oocyte nuclei | Q70821733 | ||
The addition of 5' cap structures occurs early in hnRNA synthesis and prematurely terminated molecules are capped | Q71140403 | ||
Alternative splicing of fibroblast growth factor receptor 2 (FGF-R2) in human prostate cancer | Q74098948 | ||
EWS.Fli-1 fusion protein interacts with hyperphosphorylated RNA polymerase II and interferes with serine-arginine protein-mediated RNA splicing | Q74303777 | ||
The cellular organization of gene expression | Q74701351 | ||
RNA polymerase II targets pre-mRNA splicing factors to transcription sites in vivo | Q77962891 | ||
A yeast intronic splicing enhancer and Nam8p are required for Mer1p-activated splicing. | Q27939445 | ||
Different phosphorylated forms of RNA polymerase II and associated mRNA processing factors during transcription | Q28131686 | ||
Direct coupling of transcription and mRNA processing through the thermogenic coactivator PGC-1 | Q28138472 | ||
Transcription of eukaryotic protein-coding genes | Q28138540 | ||
Identification of an RNA binding specificity for the potential splicing factor TLS | Q28138875 | ||
The splicing factor U1C represses EWS/FLI-mediated transactivation | Q28145198 | ||
Pre-mRNA splicing: the discovery of a new spliceosome doubles the challenge | Q28238029 | ||
Protein-protein interactions and 5'-splice-site recognition in mammalian mRNA precursors | Q28251112 | ||
Specific interactions between proteins implicated in splice site selection and regulated alternative splicing | Q28257351 | ||
The transcription factor Spi-1/PU.1 interacts with the potential splicing factor TLS | Q28262912 | ||
The general transcription factors of RNA polymerase II | Q28298663 | ||
The C-terminal domain of RNA polymerase II couples mRNA processing to transcription | Q28301744 | ||
A nuclear matrix protein interacts with the phosphorylated C-terminal domain of RNA polymerase II. | Q28509334 | ||
The C-terminal domain of the largest subunit of RNA polymerase II interacts with a novel set of serine/arginine-rich proteins | Q28570708 | ||
The RNA-binding protein TIA-1 is a novel mammalian splicing regulator acting through intron sequences adjacent to a 5' splice site | Q28609616 | ||
An intronic splicing silencer causes skipping of the IIIb exon of fibroblast growth factor receptor 2 through involvement of polypyrimidine tract binding protein | Q28609617 | ||
Multiple interdependent sequence elements control splicing of a fibroblast growth factor receptor 2 alternative exon | Q28609655 | ||
hnRNP A1 recruited to an exon in vivo can function as an exon splicing silencer | Q28609663 | ||
5'-Capping enzymes are targeted to pre-mRNA by binding to the phosphorylated carboxy-terminal domain of RNA polymerase II | Q28623635 | ||
Control of elongation by RNA polymerase II | Q28646668 | ||
Dynamic association of capping enzymes with transcribing RNA polymerase II | Q29614771 | ||
Exon recognition in vertebrate splicing | Q29615088 | ||
SR proteins and splicing control | Q29619936 | ||
P-TEFb, a cyclin-dependent kinase controlling elongation by RNA polymerase II | Q29620167 | ||
Regulation of alternative splicing in vivo by overexpression of antagonistic splicing factors | Q29620283 | ||
The structure and function of proteins involved in mammalian pre-mRNA splicing | Q29620286 | ||
The RNA polymerase II holoenzyme and its implications for gene regulation | Q29622942 | ||
Splice site selection, rate of splicing, and alternative splicing on nascent transcripts | Q30461752 | ||
Polypyrimidine tract binding protein antagonizes exon definition | Q33558440 | ||
mRNA polyadenylation and its coupling to other RNA processing reactions and to transcription | Q33680787 | ||
Coupling RNA polymerase II transcription with pre-mRNA processing | Q33680813 | ||
Mechanism and regulation of transcriptional elongation by RNA polymerase II. | Q33680820 | ||
HIV-1 Tat: coping with negative elongation factors | Q33711447 | ||
Exonic splicing enhancers: mechanism of action, diversity and role in human genetic diseases | Q33850031 | ||
Transcription elongation factor SII. | Q33866716 | ||
Huntingtin's WW domain partners in Huntington's disease post-mortem brain fulfill genetic criteria for direct involvement in Huntington's disease pathogenesis | Q33915109 | ||
The ends of the affair: capping and polyadenylation. | Q33920085 | ||
Connecting transcription to messenger RNA processing | Q33934155 | ||
Transcription elongation and human disease | Q33953565 | ||
Protein diversity from alternative splicing: a challenge for bioinformatics and post-genome biology | Q34084341 | ||
Quality control of mRNA function | Q34156109 | ||
Preferential excision of the 5' proximal intron from mRNA precursors with two introns as mediated by the cap structure | Q34332907 | ||
The KH domain of the branchpoint sequence binding protein determines specificity for the pre-mRNA branchpoint sequence | Q34361494 | ||
The exon sequence TAGG can inhibit splicing | Q34597789 | ||
The nuclear matrix phosphoprotein p255 associates with splicing complexes as part of the [U4/Y6.U5]tri-snRNP particle | Q34767752 | ||
Phosphorylated RNA polymerase II stimulates pre-mRNA splicing | Q35197241 | ||
Intron-dependent recruitment of pre-mRNA splicing factors to sites of transcription | Q36236894 | ||
A functional interaction between the carboxy-terminal domain of RNA polymerase II and pre-mRNA splicing | Q36254478 | ||
Exon and Intron Sequences, Respectively, Repress and Activate Splicing of a Fibroblast Growth Factor Receptor 2 Alternative Exon | Q36554345 | ||
Conserved intron elements repress splicing of a neuron-specific c-src exon in vitro | Q36555950 | ||
Functional association between promoter structure and transcript alternative splicing. | Q36597450 | ||
Control of BEK and K-SAM splice sites in alternative splicing of the fibroblast growth factor receptor 2 pre-mRNA. | Q36699418 | ||
Exon definition may facilitate splice site selection in RNAs with multiple exons | Q36713104 | ||
Inhibition by SR proteins of splicing of a regulated adenovirus pre-mRNA. | Q36799268 | ||
Transcription of herpes simplex virus tk sequences under the control of wild-type and mutant human RNA polymerase I promoters | Q36885592 | ||
Specificity of RNA maturation pathways: RNAs transcribed by RNA polymerase III are not substrates for splicing or polyadenylation | Q36922600 | ||
Splicing of adenovirus RNA in a cell-free transcription system | Q37347164 | ||
Coupling of transcription with alternative splicing: RNA pol II promoters modulate SF2/ASF and 9G8 effects on an exonic splicing enhancer | Q38320513 | ||
Participation of the C-terminal domain of RNA polymerase II in exon definition during pre-mRNA splicing | Q38499037 | ||
Evidence for substrate-specific requirement of the splicing factor U2AF(35) and for its function after polypyrimidine tract recognition by U2AF(65). | Q39449313 | ||
An intronic sequence element mediates both activation and repression of rat fibroblast growth factor receptor 2 pre-mRNA splicing | Q39631167 | ||
The 5' and 3' splice sites come together via a three dimensional diffusion mechanism | Q39716206 | ||
Common themes in assembly and function of eukaryotic transcription complexes | Q40422045 | ||
Regulation of transcriptional elongation by RNA polymerase II. | Q40445607 | ||
Role of RNA polymerase II carboxy-terminal domain in coordinating transcription with RNA processing | Q40945481 | ||
A novel isoform ratio switch of the polypyrimidine tract binding protein | Q40951842 | ||
Reciprocal effects of splicing and polyadenylation on human immunodeficiency virus type 1 pre-mRNA processing | Q41158512 | ||
RNA polymerase slides home: pause and termination site recognition | Q41444690 | ||
A comparison of mammalian and yeast pre-mRNA 3'-end processing | Q41477066 | ||
Basic mechanisms of transcript elongation and its regulation | Q41550178 | ||
Transcription units as RNA processing units | Q41667132 | ||
P433 | issue | 1-2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | alternative mRNA splicing, via spliceosome | Q21114084 |
P304 | page(s) | 31-47 | |
P577 | publication date | 2001-10-01 | |
P1433 | published in | Gene | Q5531065 |
P1476 | title | Co-transcriptional splicing of pre-messenger RNAs: considerations for the mechanism of alternative splicing | |
P478 | volume | 277 |
Q34365389 | 5' exon replacement and repair by spliceosome-mediated RNA trans-splicing |
Q36800469 | A DNA damage signal activates and derepresses exon inclusion in Drosophila TAF1 alternative splicing |
Q44863809 | A contemporary, laboratory-intensive course on messenger RNA transcription and processing |
Q33855473 | A mutation in a splicing factor that causes retinitis pigmentosa has a transcriptome-wide effect on mRNA splicing. |
Q81639777 | A mutation-created novel intra-exonic pre-mRNA splice site causes constitutive activation of KIT in human gastrointestinal stromal tumors |
Q43058032 | A novel mutation (c.951C>T) in an exonic splicing enhancer results in exon 10 skipping in the human mitochondrial acetoacetyl-CoA thiolase gene |
Q36167380 | A subset of nuclear receptor coregulators act as coupling proteins during synthesis and maturation of RNA transcripts |
Q45919172 | Agonists of fibroblast growth factor receptor induce neurite outgrowth and survival of cerebellar granule neurons. |
Q29618540 | Alternative pre-mRNA splicing and proteome expansion in metazoans |
Q44879918 | Alternative splicing in disease and therapy |
Q34762634 | Alternative splicing in multiple sclerosis and other autoimmune diseases |
Q33393896 | Alternative splicing of exon 10 in the tau gene as a target for treatment of tauopathies |
Q46632156 | Alternative splicing of type II procollagen exon 2 is regulated by the combination of a weak 5' splice site and an adjacent intronic stem-loop cis element |
Q34310398 | Alternative splicing regulation of telomerase: a new paradigm? |
Q33911993 | An exonic splicing silencer downstream of the 3' splice site A2 is required for efficient human immunodeficiency virus type 1 replication |
Q29547273 | An extensive network of coupling among gene expression machines |
Q64066199 | Analysis by RNA-seq of transcriptomic changes elicited by heat shock in Leishmania major |
Q34586190 | Analysis of genetic interaction networks shows that alternatively spliced genes are highly versatile |
Q73489672 | Asymmetric distribution of nuclear pore complexes and the cytoplasmic localization of beta2-tubulin mRNA in Chlamydomonas reinhardtii |
Q35813276 | Broad specificity of SR (serine/arginine) proteins in the regulation of alternative splicing of pre-messenger RNA. |
Q24303611 | CDK12 is a transcription elongation-associated CTD kinase, the metazoan ortholog of yeast Ctk1 |
Q79964123 | Case study for identification of potentially indel-caused alternative expression isoforms in the rice subspecies japonica and indica by integrative genome analysis |
Q40287167 | Cellular splicing and transcription regulatory protein p32 represses adenovirus major late transcription and causes hyperphosphorylation of RNA polymerase II. |
Q24336636 | Characterization of sorCS1, an alternatively spliced receptor with completely different cytoplasmic domains that mediate different trafficking in cells |
Q36481216 | Cleavage and polyadenylation specificity factor 1 (CPSF1) regulates alternative splicing of interleukin 7 receptor (IL7R) exon 6. |
Q40376847 | CoAA, a nuclear receptor coactivator protein at the interface of transcriptional coactivation and RNA splicing |
Q40671345 | Complex alternative splicing of the hKLK3 gene coding for the tumor marker PSA (prostate-specific-antigen). |
Q34810332 | Computational prediction of eukaryotic protein-coding genes |
Q41936701 | Concurrent splicing and transcription are not sufficient to enhance splicing efficiency |
Q66829573 | Conserved nucleotides surrounding the trans-splicing acceptor site and the translation initiation codon in Leishmania genes |
Q80143464 | Cotranscriptional coupling of splicing factor recruitment and precursor messenger RNA splicing in mammalian cells |
Q39793431 | Cotranscriptional recruitment of the U1 snRNP to intron-containing genes in yeast |
Q91891000 | DNA methylation directs microRNA biogenesis in mammalian cells |
Q33832763 | Differential effects of sumoylation on transcription and alternative splicing by transcription elongation regulator 1 (TCERG1). |
Q34411106 | Distal regulation of alternative splicing by splicing enhancer in equine beta-casein intron 1. |
Q33325470 | Dynamics of co-transcriptional pre-mRNA folding influences the induction of dystrophin exon skipping by antisense oligonucleotides |
Q40562298 | Early history of circular RNAs, children of splicing |
Q33919195 | Emerging roles of BRCA1 alternative splicing |
Q36344912 | Emetine regulates the alternative splicing of Bcl-x through a protein phosphatase 1-dependent mechanism |
Q39305157 | Emetine regulates the alternative splicing of caspase 9 in tumor cells |
Q60921915 | Epigenetic regulation of alternative splicing |
Q36513924 | Evidence that phosphorylation of the RNA polymerase II carboxyl-terminal repeats is similar in yeast and humans. |
Q24314647 | FGF-10 and its receptor exhibit bidirectional paracrine targeting to urothelial and smooth muscle cells in the lower urinary tract |
Q46805453 | Fibroblast growth factor-derived peptides: functional agonists of the fibroblast growth factor receptor |
Q48251884 | Frequencies of alpha4 A3061G variants and identification of three new variants of the human integrin alpha4-subunit |
Q24796520 | Full-length messenger RNA sequences greatly improve genome annotation |
Q58198726 | Gene Expression: The Close Coupling of Transcription and Splicing |
Q36496484 | HIV-1 infection induces changes in expression of cellular splicing factors that regulate alternative viral splicing and virus production in macrophages |
Q91932239 | Histone H1.5 binds over splice sites in chromatin and regulates alternative splicing |
Q34718231 | Human transcription elongation factor CA150 localizes to splicing factor-rich nuclear speckles and assembles transcription and splicing components into complexes through its amino and carboxyl regions. |
Q28207148 | Hyperphosphorylated C-terminal repeat domain-associating proteins in the nuclear proteome link transcription to DNA/chromatin modification and RNA processing |
Q28238134 | IG20, in contrast to DENN-SV, (MADD splice variants) suppresses tumor cell survival, and enhances their susceptibility to apoptosis and cancer drugs |
Q39600021 | Identification of Tat-SF1 cellular targets by exon array analysis reveals dual roles in transcription and splicing |
Q39646874 | Identification of an intronic splicing enhancer essential for the inclusion of FGFR2 exon IIIc |
Q38294689 | Identification of the cellular targets of the transcription factor TCERG1 reveals a prevalent role in mRNA processing. |
Q38343318 | Influence of heparin mimetics on assembly of the FGF.FGFR4 signaling complex. |
Q28610124 | Integrating mRNA processing with transcription |
Q40559049 | MAZ elements alter transcription elongation and silencing of the fibroblast growth factor receptor 2 exon IIIb |
Q35179872 | Mechanism of alternative splicing and its regulation |
Q36005683 | Mechanisms of the androgen receptor splicing in prostate cancer cells |
Q33291238 | Mechanistic role of a disease-associated genetic variant within the ADAM33 asthma susceptibility gene |
Q35202462 | Messenger RNA reprogramming by spliceosome-mediated RNA trans-splicing |
Q57807179 | Micro-exons of the cardiac myosin binding protein C gene: flanking introns contain a disproportionately large number of hypertrophic cardiomyopathy mutations |
Q35786108 | Minimal introns are not "junk". |
Q55258538 | Modulation of splicing events in histone deacetylase 3 by various extracellular and signal transduction pathways. |
Q47822116 | Mutation of the major 5' splice site renders a CMV-driven HIV-1 proviral clone Tat-dependent: connections between transcription and splicing. |
Q30391563 | Neuritogenic and neuroprotective properties of peptide agonists of the fibroblast growth factor receptor |
Q41775010 | New way of regulating alternative splicing in retroviruses: the promoter makes a difference |
Q24559995 | Nuclear speckle-associated protein Pnn/DRS binds to the transcriptional corepressor CtBP and relieves CtBP-mediated repression of the E-cadherin gene |
Q60352020 | Overexpression of SR proteins and splice variants modulates chondrogenesis |
Q31018983 | Pancreatic triacylglycerol lipase in a hibernating mammal. I. Novel genomic organization |
Q38263711 | Precision medicine for prostate cancer |
Q36282619 | Protected graft copolymer-formulated fibroblast growth factors mitigate the lethality of partial body irradiation injury |
Q28066910 | Proteomic approaches to uncovering virus-host protein interactions during the progression of viral infection |
Q26780366 | Prp40 and early events in splice site definition |
Q29540749 | RNA Polymerase II C-Terminal Domain: Tethering Transcription to Transcript and Template |
Q24540290 | RNA editing of a miRNA precursor |
Q33909884 | Rare autosomal recessive cardiac valvular form of Ehlers-Danlos syndrome results from mutations in the COL1A2 gene that activate the nonsense-mediated RNA decay pathway. |
Q24676527 | Receptor specificity of the fibroblast growth factor family. The complete mammalian FGF family |
Q38008396 | Spatial Organization and Dynamics of Transcription Elongation and Pre-mRNA Processing in Live Cells. |
Q24807291 | Splicing of human immunodeficiency virus RNA is position-dependent suggesting sequential removal of introns from the 5' end |
Q24294933 | Structural basis by which alternative splicing confers specificity in fibroblast growth factor receptors |
Q24313388 | Structure and function of the two tandem WW domains of the pre-mRNA splicing factor FBP21 (formin-binding protein 21) |
Q40871398 | TCERG1 regulates alternative splicing of the Bcl-x gene by modulating the rate of RNA polymerase II transcription. |
Q37136812 | The Carboxyl-terminal Domain of RNA Polymerase II Is Not Sufficient to Enhance the Efficiency of Pre-mRNA Capping or Splicing in the Context of a Different Polymerase |
Q42087663 | The FF4 and FF5 domains of transcription elongation regulator 1 (TCERG1) target proteins to the periphery of speckles |
Q27929922 | The RNA polymerase II CTD kinase CTDK-I affects pre-mRNA 3' cleavage/polyadenylation through the processing component Pti1p |
Q24561427 | The WW domain-containing proteins interact with the early spliceosome and participate in pre-mRNA splicing in vivo |
Q27935914 | The shuttling protein Npl3 promotes translation termination accuracy in Saccharomyces cerevisiae |
Q42772904 | Total RNA sequencing reveals nascent transcription and widespread co-transcriptional splicing in the human brain |
Q38731065 | Transcriptional Elongation Regulator 1 Affects Transcription and Splicing of Genes Associated with Cellular Morphology and Cytoskeleton Dynamics and Is Required for Neurite Outgrowth in Neuroblastoma Cells and Primary Neuronal Cultures |
Q42133715 | Updating the CTD Story: From Tail to Epic. |
Q51039333 | p210BCR/ABL-induced alteration of pre-mRNA splicing in primary human CD34+ hematopoietic progenitor cells. |
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