| review article | Q7318358 |
| scholarly article | Q13442814 |
| P50 | author | Adrian Robert Krainer | Q40473018 |
| Xavier Roca | Q42177767 | ||
| Ian C Eperon | Q55137400 | ||
| P2860 | cites work | The SR protein family | Q21183897 |
| The apoptosis-promoting factor TIA-1 is a regulator of alternative pre-mRNA splicing | Q24290594 | ||
| Structural basis of G-tract recognition and encaging by hnRNP F quasi-RRMs | Q24317191 | ||
| Functional expression of cloned human splicing factor SF2: homology to rna-binding proteins, U1 70K, and drosophila splicing regulators | Q24317722 | ||
| The splicing regulator TIA-1 interacts with U1-C to promote U1 snRNP recruitment to 5' splice sites | Q24337164 | ||
| Phosphorylation-dephosphorylation differentially affects activities of splicing factor ASF/SF2. | Q24533375 | ||
| Prp5 bridges U1 and U2 snRNPs and enables stable U2 snRNP association with intron RNA | Q24535910 | ||
| Congenital end-plate acetylcholinesterase deficiency caused by a nonsense mutation and an A-->G splice-donor-site mutation at position +3 of the collagenlike-tail-subunit gene (COLQ): how does G at position +3 result in aberrant splicing? | Q24540131 | ||
| Spliced segments at the 5′ terminus of adenovirus 2 late mRNA | Q24561528 | ||
| Functional domains of the human splicing factor ASF/SF2 | Q24564249 | ||
| The human splicing factors ASF/SF2 and SC35 possess distinct, functionally significant RNA binding specificities | Q24598907 | ||
| Identification of functional exonic splicing enhancer motifs recognized by individual SR proteins | Q24600148 | ||
| The spliceosome assembly pathway in mammalian extracts | Q24601223 | ||
| RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression | Q24633499 | ||
| Splicing factor SFRS1 recognizes a functionally diverse landscape of RNA transcripts | Q24651972 | ||
| SR proteins in vertical integration of gene expression from transcription to RNA processing to translation | Q24654094 | ||
| General and specific functions of exonic splicing silencers in splicing control | Q24673220 | ||
| Extended base pair complementarity between U1 snRNA and the 5' splice site does not inhibit splicing in higher eukaryotes, but rather increases 5' splice site recognition | Q24812684 | ||
| Genetic variation of pre-mRNA alternative splicing in human populations | Q26858897 | ||
| Crystal structure of human spliceosomal U1 snRNP at 5.5 Å resolution | Q27654469 | ||
| Expanded sequence dependence of thermodynamic parameters improves prediction of RNA secondary structure | Q27860806 | ||
| Functional mammalian spliceosomal complex E contains SMN complex proteins in addition to U1 and U2 snRNPs. | Q27865260 | ||
| The U1 snRNP protein U1C recognizes the 5' splice site in the absence of base pairing | Q27933790 | ||
| Interaction of the U1 snRNP with nonconserved intronic sequences affects 5' splice site selection. | Q27936014 | ||
| Genetic therapies for RNA mis-splicing diseases | Q28235690 | ||
| Comparative analysis identifies exonic splicing regulatory sequences--The complex definition of enhancers and silencers | Q28247879 | ||
| 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 | ||
| Splicing of a rare class of introns by the U12-dependent spliceosome | Q28275293 | ||
| Are snRNPs involved in splicing? | Q28281898 | ||
| Role of the snRNAs in spliceosomal active site | Q28282063 | ||
| Short/branched-chain acyl-CoA dehydrogenase deficiency due to an IVS3+3A>G mutation that causes exon skipping | Q28284385 | ||
| The RNA-binding protein TIA-1 is a novel mammalian splicing regulator acting through intron sequences adjacent to a 5' splice site | Q28609616 | ||
| Global control of aberrant splice-site activation by auxiliary splicing sequences: evidence for a gradient in exon and intron definition | Q40078319 | ||
| In vitro and in silico analysis reveals an efficient algorithm to predict the splicing consequences of mutations at the 5' splice sites | Q40088295 | ||
| A novel approach to describe a U1 snRNA binding site. | Q40315328 | ||
| HMGA1a trapping of U1 snRNP at an authentic 5' splice site induces aberrant exon skipping in sporadic Alzheimer's disease | Q40334418 | ||
| U1 snRNP-ASF/SF2 interaction and 5' splice site recognition: characterization of required elements. | Q40395456 | ||
| Stabilization of RNA stacking by pseudouridine | Q40397122 | ||
| The SR protein family: pleiotropic functions in pre-mRNA splicing | Q41083714 | ||
| A U1 snRNA:pre-mRNA base pairing interaction is required early in yeast spliceosome assembly but does not uniquely define the 5' cleavage site. | Q41107145 | ||
| U1 snRNA promotes the selection of nearby 5' splice sites by U6 snRNA in mammalian cells | Q41235244 | ||
| Evidence against a scanning model of RNA splicing | Q41454583 | ||
| An RNA switch at the 5' splice site requires ATP and the DEAD box protein Prp28p | Q41607972 | ||
| hnRNP A/B proteins are required for inhibition of HIV-1 pre-mRNA splicing | Q41679293 | ||
| A protein factor, ASF, controls cell-specific alternative splicing of SV40 early pre-mRNA in vitro | Q41728182 | ||
| Comparative analysis detects dependencies among the 5' splice-site positions | Q41807332 | ||
| Features of 5'-splice-site efficiency derived from disease-causing mutations and comparative genomics | Q41824436 | ||
| DExD/H-box Prp5 protein is in the spliceosome during most of the splicing cycle | Q41870184 | ||
| hnRNP A1 and hnRNP H can collaborate to modulate 5' splice site selection | Q41873390 | ||
| Cis-acting elements distinct from the 5' splice site promote U1-independent pre-mRNA splicing | Q41898179 | ||
| Dynamic regulation of alternative splicing by silencers that modulate 5' splice site competition | Q41984492 | ||
| High-affinity hnRNP A1 binding sites and duplex-forming inverted repeats have similar effects on 5' splice site selection in support of a common looping out and repression mechanism | Q41993441 | ||
| Overexpression of the SR proteins ASF/SF2 and SC35 influences alternative splicing in vivo in diverse ways | Q42000836 | ||
| Widespread recognition of 5' splice sites by noncanonical base-pairing to U1 snRNA involving bulged nucleotides | Q42177704 | ||
| Quantitative evaluation of all hexamers as exonic splicing elements | Q42181233 | ||
| The transition in spliceosome assembly from complex E to complex A purges surplus U1 snRNPs from alternative splice sites | Q42264162 | ||
| The SR protein SC35 is responsible for aberrant splicing of the E1alpha pyruvate dehydrogenase mRNA in a case of mental retardation with lactic acidosis | Q42709929 | ||
| Ordered and dynamic assembly of single spliceosomes | Q42726090 | ||
| Stoichiometry of a regulatory splicing complex revealed by single-molecule analyses | Q42730959 | ||
| Ab initio identification of functionally interacting pairs of cis-regulatory elements | Q43012647 | ||
| U1-like snRNAs lacking complementarity to canonical 5' splice sites. | Q43054877 | ||
| U1-independent pre-mRNA splicing contributes to the regulation of alternative splicing | Q43150426 | ||
| Electrophoretic separation of complexes involved in the splicing of precursors to mRNAs | Q43517287 | ||
| Early organization of pre-mRNA during spliceosome assembly. | Q44046358 | ||
| 5' splice site selection in yeast: genetic alterations in base-pairing with U1 reveal additional requirements | Q44055786 | ||
| An ATP-independent complex commits pre-mRNA to the mammalian spliceosome assembly pathway | Q44540184 | ||
| Purification and characterization of pre-mRNA splicing factor SF2 from HeLa cells | Q44744396 | ||
| Influences of separation and adjacent sequences on the use of alternative 5′ splice sites | Q45103471 | ||
| A pathway of sequential arginine-serine-rich domain-splicing signal interactions during mammalian spliceosome assembly | Q45138449 | ||
| RBM5/Luca-15/H37 regulates Fas alternative splice site pairing after exon definition. | Q46050971 | ||
| Mutations in U6 snRNA that alter splice site specificity: implications for the active site | Q46572305 | ||
| A splicing enhancer complex controls alternative splicing of doublesex pre-mRNA. | Q47070080 | ||
| Single base-pair substitutions in exon-intron junctions of human genes: nature, distribution, and consequences for mRNA splicing | Q48084485 | ||
| Prediction of human mRNA donor and acceptor sites from the DNA sequence | Q48219047 | ||
| Saccharomyces cerevisiae has a U1-like small nuclear RNA with unexpected properties | Q48338318 | ||
| Pseudouridine residues in the 5′-terminus of uridine-rich nuclear RNA I (U1 RNA) | Q48410567 | ||
| Maximum entropy modeling of short sequence motifs with applications to RNA splicing signals | Q48531006 | ||
| Using information content and base frequencies to distinguish mutations from genetic polymorphisms in splice junction recognition sites. | Q49947386 | ||
| Properties of a U1/mRNA 5' splice site duplex containing pseudouridine as measured by thermodynamic and NMR methods | Q50136284 | ||
| hnRNP A1 recruited to an exon in vivo can function as an exon splicing silencer | Q28609663 | ||
| A compensatory base change in U1 snRNA suppresses a 5' splice site mutation | Q29618292 | ||
| The SR protein family of splicing factors: master regulators of gene expression | Q29619935 | ||
| Regulation of alternative pre-mRNA splicing by hnRNP A1 and splicing factor SF2 | Q29620278 | ||
| Exon Identity Established through Differential Antagonism between Exonic Splicing Silencer-Bound hnRNP A1 and Enhancer-Bound SR Proteins | Q30040281 | ||
| A mutation in a rare type of intron in a sodium-channel gene results in aberrant splicing and causes myotonia | Q30584867 | ||
| Defining a 5' splice site by functional selection in the presence and absence of U1 snRNA 5' end. | Q30827740 | ||
| Deletion of the N-terminus of SF2/ASF permits RS-domain-independent pre-mRNA splicing | Q33297016 | ||
| Selection of alternative 5' splice sites: role of U1 snRNP and models for the antagonistic effects of SF2/ASF and hnRNP A1. | Q33605355 | ||
| FragSeq: transcriptome-wide RNA structure probing using high-throughput sequencing | Q33740599 | ||
| Competing upstream 5' splice sites enhance the rate of proximal splicing | Q33769266 | ||
| A systematic analysis of the factors that determine the strength of pre-mRNA splicing enhancers. | Q33890073 | ||
| Serine/arginine-rich protein-dependent suppression of exon skipping by exonic splicing enhancers | Q33935979 | ||
| Identification of a bidirectional splicing enhancer: differential involvement of SR proteins in 5' or 3' splice site activation | Q33959923 | ||
| Deciphering the splicing code | Q34022324 | ||
| An amazing sequence arrangement at the 5' ends of adenovirus 2 messenger RNA. | Q34064140 | ||
| Functional analysis of pre-mRNA splicing factor SF2/ASF structural domains | Q34070174 | ||
| Determination of the RNA binding specificity of the heterogeneous nuclear ribonucleoprotein (hnRNP) H/H'/F/2H9 family | Q34092482 | ||
| Splice junctions, branch point sites, and exons: sequence statistics, identification, and applications to genome project | Q34311043 | ||
| In vivo selection reveals combinatorial controls that define a critical exon in the spinal muscular atrophy genes | Q34365948 | ||
| Splicing defects in the ataxia-telangiectasia gene, ATM: underlying mutations and consequences | Q34389747 | ||
| Distinct functions of SR proteins in recruitment of U1 small nuclear ribonucleoprotein to alternative 5' splice sites | Q34487822 | ||
| G Run-mediated recognition of proteolipid protein and DM20 5' splice sites by U1 small nuclear RNA is regulated by context and proximity to the splice site. | Q34575659 | ||
| Cryptic splice site usage in exon 7 of the human fibrinogen Bbeta-chain gene is regulated by a naturally silent SF2/ASF binding site within this exon | Q34625741 | ||
| RS domains contact splicing signals and promote splicing by a common mechanism in yeast through humans | Q34863401 | ||
| Ab initio prediction of mutation-induced cryptic splice-site activation and exon skipping. | Q34921189 | ||
| Interaction between the RNA binding domains of Ser-Arg splicing factor 1 and U1-70K snRNP protein determines early spliceosome assembly | Q35002838 | ||
| Comprehensive splice-site analysis using comparative genomics | Q35013128 | ||
| Pre-mRNA splicing in the absence of an SR protein RS domain | Q35209029 | ||
| The A1 and A1B proteins of heterogeneous nuclear ribonucleoparticles modulate 5' splice site selection in vivo | Q35604494 | ||
| The SRSF1 linker induces semi-conservative ESE binding by cooperating with the RRMs | Q35620904 | ||
| A U1-U2 snRNP interaction network during intron definition | Q35665670 | ||
| Three RNA recognition motifs participate in RNA recognition and structural organization by the pro-apoptotic factor TIA-1. | Q35764716 | ||
| Broad specificity of SR (serine/arginine) proteins in the regulation of alternative splicing of pre-messenger RNA. | Q35813276 | ||
| Suppression of mammalian 5' splice-site defects by U1 small nuclear RNAs from a distance | Q35857085 | ||
| Low U1 snRNP dependence at the NF1 exon 29 donor splice site. | Q51764906 | ||
| Correlation of hnRNP structure and nascent transcript cleavage | Q52516604 | ||
| Extensive in silico analysis of NF1 splicing defects uncovers determinants for splicing outcome upon 5' splice-site disruption. | Q52577158 | ||
| Alternative splicing caused by RNA secondary structure. | Q54198854 | ||
| Mutations affecting mRNA splicing are the most common molecular defects in patients with neurofibromatosis type 1. | Q55476319 | ||
| Resolving the functions of overlapping viral genes by site-specific mutagenesis at a mRNA splice site | Q58451157 | ||
| Complexities of 5'splice site definition: Implications in clinical analyses | Q58454175 | ||
| Structural and functional defects in beta-thalassemia | Q58485020 | ||
| An RNA Splicing Enhancer that Does Not Act by Looping | Q58830805 | ||
| Effects of RNA secondary structure on alternative splicing of Pre-mRNA: Is folding limited to a region behind the transcribing RNA polymerase? | Q58830817 | ||
| The role of nucleotide sequences in splice site selection in eukaryotic pre-messenger RNA | Q58830821 | ||
| Interactions of small nuclear RNA's with precursor messenger RNA during in vitro splicing | Q64378031 | ||
| SR proteins can compensate for the loss of U1 snRNP functions in vitro | Q64383400 | ||
| Unusual splice sites revealed by mutagenic inactivation of an authentic splice site of the rabbit β-globin gene | Q67260093 | ||
| A role for exon sequences and splice-site proximity in splice-site selection | Q68970669 | ||
| Sequence requirements for splicing of higher eukaryotic nuclear pre-mRNA | Q69660486 | ||
| Splice site selection and ribonucleoprotein complex assembly during in vitro pre-mRNA splicing | Q69829038 | ||
| Mammalian heterogeneous ribonucleoprotein A1 and its constituent domains. Nucleic acid interaction, structural stability and self-association | Q70591313 | ||
| 3' splice site recognition in S. cerevisiae does not require base pairing with U1 snRNA | Q70732949 | ||
| A functional association between the 5' and 3' splice site is established in the earliest prespliceosome complex (E) in mammals | Q70744375 | ||
| hnRNP A1 selectively interacts through its Gly-rich domain with different RNA-binding proteins | Q71176264 | ||
| A U6 snRNA:pre-mRNA interaction can be rate-limiting for U1-independent splicing | Q71738198 | ||
| Complementation by SR proteins of pre-mRNA splicing reactions depleted of U1 snRNP | Q72202030 | ||
| A splicing enhancer in the human fibronectin alternate ED1 exon interacts with SR proteins and stimulates U2 snRNP binding | Q72638665 | ||
| Involvement of U6 snRNA in 5' splice site selection | Q72669455 | ||
| The 5′ terminus of the RNA moiety of U1 small nuclear ribonucleoprotein particles is required for the splicing of messenger RNA precursors | Q72821863 | ||
| The 5' end of U2 snRNA is in close proximity to U1 and functional sites of the pre-mRNA in early spliceosomal complexes | Q79749517 | ||
| An exonic splicing silencer represses spliceosome assembly after ATP-dependent exon recognition | Q80336614 | ||
| Role of the modular domains of SR proteins in subnuclear localization and alternative splicing specificity | Q36268125 | ||
| A mechanism for RNA splicing | Q36362761 | ||
| Position-dependent splicing activation and repression by SR and hnRNP proteins rely on common mechanisms. | Q36481243 | ||
| G triplets located throughout a class of small vertebrate introns enforce intron borders and regulate splice site selection | Q36570227 | ||
| Differentially expressed, variant U1 snRNAs regulate gene expression in human cells | Q36580574 | ||
| SR proteins promote the first specific recognition of Pre-mRNA and are present together with the U1 small nuclear ribonucleoprotein particle in a general splicing enhancer complex | Q36670430 | ||
| Modulation of exon skipping and inclusion by heterogeneous nuclear ribonucleoprotein A1 and pre-mRNA splicing factor SF2/ASF. | Q36682707 | ||
| Multiple interactions between the splicing substrate and small nuclear ribonucleoproteins in spliceosomes | Q36833512 | ||
| Amount of RNA secondary structure required to induce an alternative splice | Q36921027 | ||
| Spliceosome assembly pathways for different types of alternative splicing converge during commitment to splice site pairing in the A complex. | Q37099916 | ||
| Heterogeneous nuclear ribonucleoproteins H and F regulate the proteolipid protein/DM20 ratio by recruiting U1 small nuclear ribonucleoprotein through a complex array of G runs | Q37160862 | ||
| Diagnostics of pathogenic splicing mutations: does bioinformatics cover all bases? | Q37175054 | ||
| Recognition of atypical 5' splice sites by shifted base-pairing to U1 snRNA. | Q37285454 | ||
| Splice site strength-dependent activity and genetic buffering by poly-G runs | Q37397927 | ||
| U1 snRNA directly interacts with polypyrimidine tract-binding protein during splicing repression | Q37597322 | ||
| New insights into RNA secondary structure in the alternative splicing of pre-mRNAs | Q37874082 | ||
| Intrinsic U2AF binding is modulated by exon enhancer signals in parallel with changes in splicing activity | Q38298431 | ||
| Pathways for selection of 5' splice sites by U1 snRNPs and SF2/ASF. | Q38316542 | ||
| Modulation of exon skipping by high-affinity hnRNP A1-binding sites and by intron elements that repress splice site utilization | Q38325989 | ||
| Primary structure of the human splicing factor asf reveals similarities with drosophila regulators | Q38334210 | ||
| An intronic splicing enhancer binds U1 snRNPs to enhance splicing and select 5' splice sites | Q39540203 | ||
| Role of SR protein modular domains in alternative splicing specificity in vivo | Q39607577 | ||
| The differential interaction of snRNPs with pre-mRNA reveals splicing kinetics in living cells | Q39648201 | ||
| Efficient use of a 'dead-end' GA 5' splice site in the human fibroblast growth factor receptor genes | Q39744889 | ||
| Cooperative-binding and splicing-repressive properties of hnRNP A1. | Q39814580 | ||
| hnRNP H binding at the 5' splice site correlates with the pathological effect of two intronic mutations in the NF-1 and TSHbeta genes | Q39946083 | ||
| Stabilization of the tau exon 10 stem loop alters pre-mRNA splicing | Q39958205 | ||
| Polypyrimidine tract binding protein controls the transition from exon definition to an intron defined spliceosome | Q40025470 | ||
| P433 | issue | 2 | |
| P921 | main subject | small nuclear RNA | Q284578 |
| P304 | page(s) | 129-144 | |
| P577 | publication date | 2013-01-01 | |
| P1433 | published in | Genes & Development | Q1524533 |
| P1476 | title | Pick one, but be quick: 5' splice sites and the problems of too many choices | |
| P478 | volume | 27 |
| Q90114576 | A Complex of U1 snRNP with Cleavage and Polyadenylation Factors Controls Telescripting, Regulating mRNA Transcription in Human Cells |
| Q61847314 | A Novel Splice Site Mutation in the SERPING1 Gene Leads to Haploinsufficiency by Complete Degradation of the Mutant Allele mRNA in a Case of Familial Hereditary Angioedema |
| Q40562957 | A Splicing Reporter Tuned to Non-AG Acceptor Sites Reveals that Luteolin Enhances the Recognition of Non-canonical Acceptor Sites |
| Q38966017 | A comprehensive survey of non-canonical splice sites in the human transcriptome. |
| Q36809468 | A large family of Dscam genes with tandemly arrayed 5' cassettes in Chelicerata |
| Q47134651 | A mechanism underlying position-specific regulation of alternative splicing. |
| Q38303896 | A targeted oligonucleotide enhancer of SMN2 exon 7 splicing forms competing quadruplex and protein complexes in functional conditions |
| Q47357344 | ATP7B Mutation Detection and Pathogenicity Analysis: One Atypical Case of Wilson's Disease with Adrenocortical Insufficiency |
| Q41961878 | Alternative spliceosome assembly pathways revealed by single-molecule fluorescence microscopy |
| Q34712097 | Alternative splicing at GYNNGY 5' splice sites: more noise, less regulation. |
| Q33905777 | Alternative splicing of TAF6: downstream transcriptome impacts and upstream RNA splice control elements |
| Q34310398 | Alternative splicing regulation of telomerase: a new paradigm? |
| Q64122336 | Ambiguous splice sites distinguish circRNA and linear splicing in the human genome |
| Q41718522 | An ENU-induced splice site mutation of mouse Col1a1 causing recessive osteogenesis imperfecta and revealing a novel splicing rescue |
| Q41671484 | An Exon-Specific U1snRNA Induces a Robust Factor IX Activity in Mice Expressing Multiple Human FIX Splicing Mutants. |
| Q89834766 | Animal, Fungi, and Plant Genome Sequences Harbor Different Non-Canonical Splice Sites |
| Q34911031 | Antisense Modulation of RNA Processing as a Therapeutic Approach in Cancer Therapy |
| Q89978329 | Arabidopsis RanBP2-Type Zinc Finger Proteins Related to Chloroplast RNA Editing Factor OZ1 |
| Q35591969 | BAP1 missense mutation c.2054 A>T (p.E685V) completely disrupts normal splicing through creation of a novel 5' splice site in a human mesothelioma cell line |
| Q35575811 | Balanced splicing at the Tat-specific HIV-1 3'ss A3 is critical for HIV-1 replication |
| Q36202448 | CDH1 Missense Variant c.1679C>G (p.T560R) Completely Disrupts Normal Splicing through Creation of a Novel 5' Splice Site. |
| Q48219842 | Characterization of a novel germline BRCA1 splice variant, c.5332+4delA. |
| Q40659030 | Characterization of the Regulation of CD46 RNA Alternative Splicing. |
| Q28540051 | Clinical, molecular and functional investigation on an infant with neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD) |
| Q45874943 | Clustered F8 missense mutations cause hemophilia A by combined alteration of splicing and protein biosynthesis/activity |
| Q90671048 | Competing RNA pairings in complex alternative splicing of a 3' variable region |
| Q37243611 | Complete androgen insensitivity syndrome caused by a deep intronic pseudoexon-activating mutation in the androgen receptor gene |
| Q38157823 | Complexity of the alternative splicing landscape in plants. |
| Q89522110 | Concurrent binding to DNA and RNA facilitates the pluripotency reprogramming activity of Sox2 |
| Q28073341 | Control of human papillomavirus gene expression by alternative splicing |
| Q40339014 | Correction of a Cystic Fibrosis Splicing Mutation by Antisense Oligonucleotides. |
| Q40120224 | Correction of a splicing defect in a mouse model of congenital muscular dystrophy type 1A using a homology-directed-repair-independent mechanism |
| Q41808431 | Crystal structure of human U1 snRNP, a small nuclear ribonucleoprotein particle, reveals the mechanism of 5' splice site recognition |
| Q39301532 | Deep intronic mutations and human disease |
| Q38614549 | Dynamics and consequences of spliceosome E complex formation. |
| Q38911508 | Exon-Specific U1s Correct SPINK5 Exon 11 Skipping Caused by a Synonymous Substitution that Affects a Bifunctional Splicing Regulatory Element |
| Q92313549 | First estimate of the scale of canonical 5' splice site GT>GC variants capable of generating wild-type transcripts |
| Q55254725 | HMGA1a Induces Alternative Splicing of the Estrogen Receptor-αlpha Gene by Trapping U1 snRNP to an Upstream Pseudo-5′ Splice Site. |
| Q92020484 | Human PRPF40B regulates hundreds of alternative splicing targets and represses a hypoxia expression signature |
| Q39932759 | Human Papillomavirus E2 Regulates SRSF3 (SRp20) To Promote Capsid Protein Expression in Infected Differentiated Keratinocytes |
| Q34902920 | Improvement of SMN2 pre-mRNA processing mediated by exon-specific U1 small nuclear RNA. |
| Q42343467 | Improving genetic diagnosis in Mendelian disease with transcriptome sequencing |
| Q90057452 | Interplay of primary sequence, position and secondary RNA structure determines alternative splicing of LMNA in a pre-mature aging syndrome |
| Q40466706 | Intron retention is a widespread mechanism of tumor-suppressor inactivation. |
| Q98387493 | Intron with transgenic marker (InTraM) facilitates high-throughput screening of endogenous gene reporter lines |
| Q38172352 | Make yourself at home: viral hijacking of the PI3K/Akt signaling pathway |
| Q91592890 | Modified U1 snRNA and antisense oligonucleotides rescue splice mutations in SLC26A4 that cause hereditary hearing loss |
| Q92881813 | Molecular Characterization of a Novel Splicing Mutation underlying Mucopolysaccharidosis (MPS) type VI-Indirect Proof of Principle on Its Pathogenicity |
| Q38896235 | Noncanonical registers and base pairs in human 5' splice-site selection |
| Q38257021 | Predominance of spliceosomal complex formation over polyadenylation site selection in TDP-43 autoregulation |
| Q44357084 | Protein-mRNA interactome capture: cartography of the mRNP landscape |
| Q35885200 | Prp4 Kinase Grants the License to Splice: Control of Weak Splice Sites during Spliceosome Activation |
| Q92753261 | RNA Secondary Structure-Based Design of Antisense Peptide Nucleic Acids for Modulating Disease-Associated Aberrant Tau Pre-mRNA Alternative Splicing |
| Q92162442 | RNA Therapeutics: How Far Have We Gone? |
| Q35156851 | Rectifying RNA splicing errors in hereditary neurodegenerative disease. |
| Q38876359 | Regulated Intron Retention and Nuclear Pre-mRNA Decay Contribute to PABPN1 Autoregulation |
| Q38865127 | Regulation of a strong F9 cryptic 5'ss by intrinsic elements and by combination of tailored U1snRNAs with antisense oligonucleotides |
| Q34465902 | Regulation of mRNA abundance by polypyrimidine tract-binding protein-controlled alternate 5' splice site choice |
| Q64236075 | SAM68 interaction with U1A modulates U1 snRNP recruitment and regulates mTor pre-mRNA splicing |
| Q34478749 | SMN2 splice modulators enhance U1-pre-mRNA association and rescue SMA mice |
| Q90102232 | SNRP-27, the C. elegans homolog of the tri-snRNP 27K protein, has a role in 5' splice site positioning in the spliceosome |
| Q26999350 | Single molecule fluorescence approaches shed light on intracellular RNAs |
| Q88548193 | Small nuclear RNA-mediated modulation of splicing reveals a therapeutic strategy for a TREM2 mutation and its post-transcriptional regulation |
| Q38901072 | Species-dependent splice recognition of a cryptic exon resulting from a recurrent intronic CEP290 mutation that causes congenital blindness |
| Q92773892 | Splice-switching small molecules: A new therapeutic approach to modulate gene expression |
| Q93142119 | Splicing dysregulation contributes to the pathogenicity of several F9 exonic point variants |
| Q38288237 | Splicing modulation therapy in the treatment of genetic diseases |
| Q35113616 | Splicing of designer exons informs a biophysical model for exon definition |
| Q37122051 | Structure-function analysis of the 5' end of yeast U1 snRNA highlights genetic interactions with the Msl5*Mud2 branchpoint-binding complex and other spliceosome assembly factors |
| Q55484645 | Synergistic assembly of human pre-spliceosomes across introns and exons. |
| Q96683851 | Targeting the ERG oncogene with splice-switching oligonucleotides as a novel therapeutic strategy in prostate cancer |
| Q47766930 | The conserved AU dinucleotide at the 5' end of nascent U1 snRNA is optimized for the interaction with nuclear cap-binding-complex. |
| Q50211474 | The mechanisms of a mammalian splicing enhancer. |
| Q26741296 | The nuts and bolts of the endogenous spliceosome |
| Q52678183 | The somatic FAH C.1061C>A change counteracts the frequent FAH c.1062+5G>A mutation and permits U1snRNA-based splicing correction. |
| Q44983925 | The thermodynamic patterns of eukaryotic genes suggest a mechanism for intron-exon recognition. |
| Q37304518 | U1 snRNP-Dependent Suppression of Polyadenylation: Physiological Role and Therapeutic Opportunities in Cancer |
| Q35040273 | Unexpected CEP290 mRNA splicing in a humanized knock-in mouse model for Leber congenital amaurosis. |
| Q83228761 | Viral miRNA adaptor differentially recruits miRNAs to target mRNAs through alternative base-pairing |
| Q36016026 | mRNA-Associated Processes and Their Influence on Exon-Intron Structure in Drosophila melanogaster |
Search more.