| scholarly article | Q13442814 |
| P2093 | author name string | Woan-Yuh Tarn | |
| Ruei-Min Lu | |||
| Hung-Hsi Chen | |||
| Jan-Growth Chang | |||
| Tsui-Yi Peng | |||
| P2860 | cites work | A novel function for SMN, the spinal muscular atrophy disease gene product, in pre-mRNA splicing | Q22008514 |
| Exon selection in alpha-tropomyosin mRNA is regulated by the antagonistic action of RBM4 and PTB. | Q24293215 | ||
| Primary structure and binding activity of the hnRNP U protein: binding RNA through RGG box | Q24294777 | ||
| hnRNP-G promotes exon 7 inclusion of survival motor neuron (SMN) via direct interaction with Htra2-beta1 | Q24303882 | ||
| SMN interacts with a novel family of hnRNP and spliceosomal proteins | Q24535803 | ||
| Transportin-SR2 mediates nuclear import of phosphorylated SR proteins | Q24555219 | ||
| Spinal muscular atrophy and therapeutic prospects | Q79318646 | ||
| The WW domain-containing proteins interact with the early spliceosome and participate in pre-mRNA splicing in vivo | Q24561427 | ||
| Mechanisms of alternative pre-messenger RNA splicing | Q28131822 | ||
| A mechanism for translationally coupled mRNA turnover: interaction between the poly(A) tail and a c-fos RNA coding determinant via a protein complex | Q28142236 | ||
| Protein-protein interaction among hnRNPs shuttling between nucleus and cytoplasm | Q28142391 | ||
| SRp30c-dependent stimulation of survival motor neuron (SMN) exon 7 inclusion is facilitated by a direct interaction with hTra2 beta 1 | Q28204721 | ||
| Evidence for a modifying pathway in SMA discordant families: reduced SMN level decreases the amount of its interacting partners and Htra2-beta1 | Q28206060 | ||
| Specific interaction of Smn, the spinal muscular atrophy determining gene product, with hnRNP-R and gry-rbp/hnRNP-Q: a role for Smn in RNA processing in motor axons? | Q28214361 | ||
| Correction of SMN2 Pre-mRNA splicing by antisense U7 small nuclear RNAs | Q28277159 | ||
| Smn, the spinal muscular atrophy-determining gene product, modulates axon growth and localization of beta-actin mRNA in growth cones of motoneurons | Q28576647 | ||
| Identification and characterization of a spinal muscular atrophy-determining gene | Q29547495 | ||
| A single nucleotide in the SMN gene regulates splicing and is responsible for spinal muscular atrophy | Q29617367 | ||
| Mass spectrometric identification of proteins from silver-stained polyacrylamide gel: a method for the removal of silver ions to enhance sensitivity | Q30674918 | ||
| Enhancement of SMN2 exon 7 inclusion by antisense oligonucleotides targeting the exon | Q33278100 | ||
| Incidence, prevalence, and gene frequency studies of chronic childhood spinal muscular atrophy | Q33588368 | ||
| A single nucleotide difference that alters splicing patterns distinguishes the SMA gene SMN1 from the copy gene SMN2. | Q33864982 | ||
| Mechanisms of fidelity in pre-mRNA splicing | Q33912887 | ||
| Treatment of spinal muscular atrophy by sodium butyrate | Q33933841 | ||
| Quantitative Analyses of SMN1 and SMN2 Based on Real-Time LightCycler PCR: Fast and Highly Reliable Carrier Testing and Prediction of Severity of Spinal Muscular Atrophy | Q34353103 | ||
| Splicing of a critical exon of human Survival Motor Neuron is regulated by a unique silencer element located in the last intron | Q34353625 | ||
| Htra2-beta 1 stimulates an exonic splicing enhancer and can restore full-length SMN expression to survival motor neuron 2 (SMN2) | Q35210565 | ||
| SMN mutants of spinal muscular atrophy patients are defective in binding to snRNP proteins. | Q35641208 | ||
| An intronic element contributes to splicing repression in spinal muscular atrophy. | Q35652570 | ||
| The RGG box motif of the herpes simplex virus ICP27 protein mediates an RNA-binding activity and determines in vivo methylation. | Q35871646 | ||
| A mouse model for spinal muscular atrophy | Q38316939 | ||
| Origins of binding specificity of the A1 heterogeneous nuclear ribonucleoprotein. | Q38360280 | ||
| Modulating role of RNA structure in alternative splicing of a critical exon in the spinal muscular atrophy genes. | Q40196235 | ||
| Disruption of an SF2/ASF-dependent exonic splicing enhancer in SMN2 causes spinal muscular atrophy in the absence of SMN1. | Q40741164 | ||
| The activity of the spinal muscular atrophy protein is regulated during development and cellular differentiation. | Q42485526 | ||
| Optimized sample-processing time and peptide recovery for the mass spectrometric analysis of protein digests | Q44897200 | ||
| The effect of hydroxyurea in spinal muscular atrophy cells and patients | Q46827709 | ||
| Mildly affected patients with spinal muscular atrophy are partially protected by an increased SMN2 copy number | Q46969503 | ||
| HRP-2, a heterogeneous nuclear ribonucleoprotein, is essential for embryogenesis and oogenesis in Caenorhabditis elegans | Q47068799 | ||
| Thermodynamics of the fragile X mental retardation protein RGG box interactions with G quartet forming RNA. | Q51915247 | ||
| Characterization of an RNA granule from developing brain | Q54626978 | ||
| An exonic enhancer is required for inclusion of an essential exon in the SMA-determining gene SMN | Q73295491 | ||
| Analysis of the mRNA transcripts of the survival motor neuron (SMN) gene in the tissue of an SMA fetus and the peripheral blood mononuclear cells of normals, carriers and SMA patients | Q73450673 | ||
| A negative element in SMN2 exon 7 inhibits splicing in spinal muscular atrophy | Q73588971 | ||
| SMN oligomerization defect correlates with spinal muscular atrophy severity | Q74557706 | ||
| An extended inhibitory context causes skipping of exon 7 of SMN2 in spinal muscular atrophy | Q75431784 | ||
| P433 | issue | 22 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | cell biology | Q7141 |
| P304 | page(s) | 6929-38 | |
| P577 | publication date | 2008-11-01 | |
| P1433 | published in | Molecular and Cellular Biology | Q3319478 |
| P1476 | title | The RNA binding protein hnRNP Q modulates the utilization of exon 7 in the survival motor neuron 2 (SMN2) gene | |
| P478 | volume | 28 |
| Q53063077 | 3' Splice site sequences of spinal muscular atrophy related SMN2 pre-mRNA include enhancers for nearby exons |
| Q50334595 | A cryptic RNA-binding domain mediates Syncrip recognition and exosomal partitioning of miRNA targets. |
| Q34341178 | A feedback loop regulates splicing of the spinal muscular atrophy-modifying gene, SMN2. |
| Q34184793 | A humanized Smn gene containing the SMN2 nucleotide alteration in exon 7 mimics SMN2 splicing and the SMA disease phenotype |
| Q28244480 | A short antisense oligonucleotide masking a unique intronic motif prevents skipping of a critical exon in spinal muscular atrophy |
| Q35578535 | Alternative splicing in spinal muscular atrophy underscores the role of an intron definition model |
| Q93089125 | Computational analysis of non-coding RNAs in Alzheimer's disease |
| Q34734843 | Control of translation and miRNA-dependent repression by a novel poly(A) binding protein, hnRNP-Q. |
| Q38318922 | Design principles for bifunctional targeted oligonucleotide enhancers of splicing |
| Q39092025 | Diverse role of survival motor neuron protein |
| Q34240890 | Drosophila Syncrip modulates the expression of mRNAs encoding key synaptic proteins required for morphology at the neuromuscular junction |
| Q28730280 | Evaluation of SMN protein, transcript, and copy number in the biomarkers for spinal muscular atrophy (BforSMA) clinical study |
| Q37783316 | Functional diversity of the hnRNPs: past, present and perspectives |
| Q51903481 | Genome-wide identification and evaluation of novel internal control genes for Q-PCR based transcript normalization in wheat. |
| Q37431043 | HRP-2, the Caenorhabditis elegans homolog of mammalian heterogeneous nuclear ribonucleoproteins Q and R, is an alternative splicing factor that binds to UCUAUC splicing regulatory elements |
| Q38086752 | Hepatitis C Virus RNA Translation |
| Q64237309 | Heterogeneous nuclear ribonucleoproteins R and Q accumulate in pathological inclusions in FTLD-FUS |
| Q27311317 | High expression level of Tra2-β1 is responsible for increased SMN2 exon 7 inclusion in the testis of SMA mice |
| Q52684010 | High expression of hnRNPA1 promotes cell invasion by inducing EMT in gastric cancer |
| Q33937593 | Intron 7 conserved sequence elements regulate the splicing of the SMN genes |
| Q38260614 | Invited review: decoding the pathophysiological mechanisms that underlie RNA dysregulation in neurodegenerative disorders: a review of the current state of the art. |
| Q61816592 | Key role of SMN/SYNCRIP and RNA-Motif 7 in spinal muscular atrophy: RNA-Seq and motif analysis of human motor neurons |
| Q33814282 | Loss of the multifunctional RNA-binding protein RBM47 as a source of selectable metastatic traits in breast cancer. |
| Q55365906 | Mechanism of Splicing Regulation of Spinal Muscular Atrophy Genes. |
| Q90674893 | Molecular Factors Involved in Spinal Muscular Atrophy Pathways as Possible Disease-modifying Candidates |
| Q42218490 | Morpholino antisense oligonucleotides targeting intronic repressor Element1 improve phenotype in SMA mouse models |
| Q36074475 | Multiple effects of curcumin on promoting expression of the exon 7-containing SMN2 transcript. |
| Q35891195 | Negative regulation of RhoA translation and signaling by hnRNP-Q1 affects cellular morphogenesis |
| Q47700020 | Nuclear poly(A) binding protein 1 (PABPN1) and Matrin3 interact in muscle cells and regulate RNA processing |
| Q38843108 | Optimization of Morpholino Antisense Oligonucleotides Targeting the Intronic Repressor Element1 in Spinal Muscular Atrophy |
| Q27312184 | Oxidative Stress Triggers Body-Wide Skipping of Multiple Exons of the Spinal Muscular Atrophy Gene |
| Q35972530 | PSF contacts exon 7 of SMN2 pre-mRNA to promote exon 7 inclusion. |
| Q35095113 | Poly(A) RNA-binding proteins and polyadenosine RNA: new members and novel functions |
| Q47605317 | Posttranscriptional Regulation of HLA-A Protein Expression by Alternative Polyadenylation Signals Involving the RNA-Binding Protein Syncrip. |
| Q34388403 | Presynaptic localization of Smn and hnRNP R in axon terminals of embryonic and postnatal mouse motoneurons |
| Q38755430 | Protein methylation and stress granules: posttranslational remodeler or innocent bystander? |
| Q45404773 | Proteomic analysis of interleukin enhancer binding factor 3 (Ilf3) and nuclear factor 90 (NF90) interactome |
| Q37720436 | RNA processing pathways in amyotrophic lateral sclerosis |
| Q38097516 | Regulation of snoRNAs in Cancer: Close Encounters with Interferon |
| Q91946029 | Role of RNA Binding Proteins with prion-like domains in muscle and neuromuscular diseases |
| Q36149380 | SAM68 is a physiological regulator of SMN2 splicing in spinal muscular atrophy |
| Q47885235 | SMN regulation in SMA and in response to stress: new paradigms and therapeutic possibilities. |
| Q34312156 | SMN-Inducing Compounds For The Treatment Of Spinal Muscular Atrophy |
| Q36528254 | Severe impairment of male reproductive organ development in a low SMN expressing mouse model of spinal muscular atrophy |
| Q54765007 | Solving the puzzle of spinal muscular atrophy: what are the missing pieces? |
| Q33871311 | Spinal muscular atrophy: mechanisms and therapeutic strategies |
| Q38429727 | Splicing arrays reveal novel RBM10 targets, including SMN2 pre-mRNA. |
| Q34065993 | Splicing of the Survival Motor Neuron genes and implications for treatment of SMA |
| Q36297097 | Splicing regulation in spinal muscular atrophy by an RNA structure formed by long-distance interactions |
| Q27009581 | Splicing therapy for neuromuscular disease |
| Q58454162 | Systematic Analysis of Gene Expression Profiles Controlled by hnRNP Q and hnRNP R, Two Closely Related Human RNA Binding Proteins Implicated in mRNA Processing Mechanisms |
| Q34156826 | TIA1 Prevents Skipping of a Critical Exon Associated with Spinal Muscular Atrophy |
| Q34704344 | Targeting SR proteins improves SMN expression in spinal muscular atrophy cells |
| Q34616822 | Tetracyclines that promote SMN2 exon 7 splicing as therapeutics for spinal muscular atrophy |
| Q55428148 | The EGF/hnRNP Q1 axis is involved in tumorigenesis via the regulation of cell cycle-related genes. |
| Q26746566 | The hnRNP family: insights into their role in health and disease |
| Q24301061 | The splicing regulator Sam68 binds to a novel exonic splicing silencer and functions in SMN2 alternative splicing in spinal muscular atrophy |
| Q37744954 | Translational upregulation of Aurora-A by hnRNP Q1 contributes to cell proliferation and tumorigenesis in colorectal cancer. |
| Q38313545 | cis-Acting RNA elements in the hepatitis C virus RNA genome |
| Q36023305 | hnRNP Q Regulates Cdc42-Mediated Neuronal Morphogenesis |
| Q35468111 | hnRNP Q mediates a phase-dependent translation-coupled mRNA decay of mouse Period3 |
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