| scholarly article | Q13442814 |
| P50 | author | Zissimos Mourelatos | Q37383021 |
| P2093 | author name string | G Dreyfuss | |
| L Abel | |||
| N Kataoka | |||
| J Yong | |||
| P2860 | cites work | The double lives of shuttling mRNA binding proteins | Q33913906 |
| Preferential excision of the 5' proximal intron from mRNA precursors with two introns as mediated by the cap structure | Q34332907 | ||
| The survival motor neuron protein in spinal muscular atrophy | Q34435656 | ||
| SMN mutants of spinal muscular atrophy patients are defective in binding to snRNP proteins. | Q35641208 | ||
| The polypyrimidine tract binding protein binds upstream of neural cell-specific c-src exon N1 to repress the splicing of the intron downstream | Q36570481 | ||
| Inactivation of the survival motor neuron gene, a candidate gene for human spinal muscular atrophy, leads to massive cell death in early mouse embryos | Q36578997 | ||
| Isolation of the heterogeneous nuclear RNA-ribonucleoprotein complex (hnRNP): a unique supramolecular assembly | Q37578982 | ||
| Nuclear targeting defect of SMN lacking the C-terminus in a mouse model of spinal muscular atrophy | Q38313528 | ||
| Characterization of the Schizosaccharomyces pombe orthologue of the human survival motor neuron (SMN) protein | Q38313541 | ||
| The Schizosaccharomyces pombe protein Yab8p and a novel factor, Yip1p, share structural and functional similarity with the spinal muscular atrophy-associated proteins SMN and SIP1. | Q38313544 | ||
| A mouse model for spinal muscular atrophy | Q38316939 | ||
| Nucleocytoplasmic transport and snRNP assembly | Q40776319 | ||
| Correlation between severity and SMN protein level in spinal muscular atrophy | Q41102726 | ||
| When is a deletion not a deletion? When it is converted | Q43105061 | ||
| The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn(-/-) mice and results in a mouse with spinal muscular atrophy | Q43569750 | ||
| The Caenorhabditis elegans orthologue of the human gene responsible for spinal muscular atrophy is a maternal product critical for germline maturation and embryonic viability. | Q47068856 | ||
| Immunopurification of heterogeneous nuclear ribonucleoprotein particles reveals an assortment of RNA-binding proteins. | Q54389649 | ||
| Reduced survival motor neuron (Smn) gene dose in mice leads to motor neuron degeneration: an animal model for spinal muscular atrophy type III | Q60215386 | ||
| The survival motor neuron protein of Schizosacharomyces pombe. Conservation of survival motor neuron interaction domains in divergent organisms | Q73804884 | ||
| A novel function for SMN, the spinal muscular atrophy disease gene product, in pre-mRNA splicing | Q22008514 | ||
| A novel heterogeneous nuclear ribonucleoprotein-like protein interacts with NS1 of the minute virus of mice | Q22008520 | ||
| Human step II splicing factor hSlu7 functions in restructuring the spliceosome between the catalytic steps of splicing | Q22009171 | ||
| Gemin3: A novel DEAD box protein that interacts with SMN, the spinal muscular atrophy gene product, and is a component of gems | Q22010941 | ||
| Gemin4. A novel component of the SMN complex that is found in both gems and nucleoli | Q22253358 | ||
| Pre-mRNA splicing imprints mRNA in the nucleus with a novel RNA-binding protein that persists in the cytoplasm | Q24290398 | ||
| Mass spectrometry and EST-database searching allows characterization of the multi-protein spliceosome complex | Q24311408 | ||
| Interaction between the human nuclear cap-binding protein complex and hnRNP F | Q24314610 | ||
| The spinal muscular atrophy disease gene product, SMN, and its associated protein SIP1 are in a complex with spliceosomal snRNP proteins | Q24316085 | ||
| The SMN-SIP1 complex has an essential role in spliceosomal snRNP biogenesis | Q24316121 | ||
| Molecular definition of heterogeneous nuclear ribonucleoprotein R (hnRNP R) using autoimmune antibody: immunological relationship with hnRNP P | Q24318358 | ||
| A novel nuclear structure containing the survival of motor neurons protein | Q24324247 | ||
| A novel heterogeneous nuclear RNP protein with a unique distribution on nascent transcripts | Q24339390 | ||
| hnRNP H is a component of a splicing enhancer complex that activates a c-src alternative exon in neuronal cells | Q24554786 | ||
| Characterization and primary structure of the poly(C)-binding heterogeneous nuclear ribonucleoprotein complex K protein | Q24630724 | ||
| A functional interaction between the survival motor neuron complex and RNA polymerase II | Q24674951 | ||
| Accurate transcription initiation by RNA polymerase II in a soluble extract from isolated mammalian nuclei | Q27860728 | ||
| Conserved structures and diversity of functions of RNA-binding proteins | Q27861066 | ||
| Mechanical devices of the spliceosome: motors, clocks, springs, and things | Q27938081 | ||
| 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 | ||
| Characterization of a nuclear 20S complex containing the survival of motor neurons (SMN) protein and a specific subset of spliceosomal Sm proteins | Q28143590 | ||
| Spinal muscular atrophy | Q28251310 | ||
| Monoclonal antibody characterization of the C proteins of heterogeneous nuclear ribonucleoprotein complexes in vertebrate cells | Q28263029 | ||
| Identification and characterization of a spinal muscular atrophy-determining gene | Q29547495 | ||
| hnRNP proteins and the biogenesis of mRNA | Q29547911 | ||
| hnRNP complexes: composition, structure, and function | Q29619428 | ||
| Protein functions in pre-mRNA splicing | Q29620262 | ||
| Regulation of alternative pre-mRNA splicing by hnRNP A1 and splicing factor SF2 | Q29620278 | ||
| A cell system with targeted disruption of the SMN gene: functional conservation of the SMN protein and dependence of Gemin2 on SMN. | Q30976876 | ||
| A systematic analysis of the factors that determine the strength of pre-mRNA splicing enhancers. | Q33890073 | ||
| Specific sequences of the Sm and Sm-like (Lsm) proteins mediate their interaction with the spinal muscular atrophy disease gene product (SMN). | Q33905442 | ||
| P433 | issue | 19 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | spliceosome | Q915868 |
| P304 | page(s) | 5443-5452 | |
| P577 | publication date | 2001-10-01 | |
| P1433 | published in | The EMBO Journal | Q1278554 |
| P1476 | title | SMN interacts with a novel family of hnRNP and spliceosomal proteins | |
| P478 | volume | 20 |
| Q24563044 | A cellular RNA-binding protein enhances internal ribosomal entry site-dependent translation through an interaction downstream of the hepatitis C virus polyprotein initiation codon |
| 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. |
| Q24298937 | A human, ATP-independent, RISC assembly machine fueled by pre-miRNA |
| Q24539224 | A novel function for human factor C1 (HCF-1), a host protein required for herpes simplex virus infection, in pre-mRNA splicing |
| Q58379271 | A novel function for the survival motoneuron protein as a translational regulator |
| Q44611061 | A proteomic analysis of arginine-methylated protein complexes |
| Q56241303 | Activation of RNA metabolism-related genes in mouse but not human tissues deficient in SMN |
| Q38668630 | Advances in understanding the role of disease-associated proteins in spinal muscular atrophy. |
| Q57243671 | Affinity purification of ARE-binding proteins identifies poly(A)-binding protein 1 as a potential substrate in MK2-induced mRNA stabilization |
| Q28584162 | An RNA-interacting protein, SYNCRIP (heterogeneous nuclear ribonuclear protein Q1/NSAP1) is a component of mRNA granule transported with inositol 1,4,5-trisphosphate receptor type 1 mRNA in neuronal dendrites |
| Q90371997 | An epilepsy-associated mutation in the nuclear import receptor KPNA7 reduces nuclear localization signal binding |
| Q24306727 | An mRNA m7G cap binding-like motif within human Ago2 represses translation |
| Q39665747 | Assisted RNP assembly: SMN and PRMT5 complexes cooperate in the formation of spliceosomal UsnRNPs |
| Q35006728 | C-to-U RNA editing: mechanisms leading to genetic diversity |
| Q33257010 | Caenorhabditis elegans in the study of SMN-interacting proteins: a role for SMI-1, an orthologue of human Gemin2 and the identification of novel components of the SMN complex |
| Q92503341 | Chromatin-associated RNAs as facilitators of functional genomic interactions |
| 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. |
| Q97570201 | Current and emerging treatment options for spinal muscular atrophy |
| Q28203025 | Determinants of the interaction of the spinal muscular atrophy disease protein SMN with the dimethylarginine-modified box H/ACA small nucleolar ribonucleoprotein GAR1 |
| Q39092025 | Diverse role of survival motor neuron protein |
| Q41966606 | Down-regulation of the cancer/testis antigen 45 (CT45) is associated with altered tumor cell morphology, adhesion and migration |
| Q47070454 | Drosophila SMN complex proteins Gemin2, Gemin3, and Gemin5 are components of U bodies. |
| Q58826477 | Drug discovery for spinal muscular atrophy |
| Q42414886 | Dynamic remodelling of human 7SK snRNP controls the nuclear level of active P-TEFb |
| Q28206060 | Evidence for a modifying pathway in SMA discordant families: reduced SMN level decreases the amount of its interacting partners and Htra2-beta1 |
| Q37073200 | Expression of microRNA processing machinery genes in rhesus monkey oocytes and embryos of different developmental potentials |
| Q64060780 | Functional Segments on Intrinsically Disordered Regions in Disease-Related Proteins |
| Q24337865 | Functional association of human Ki-1/57 with pre-mRNA splicing events |
| Q37783316 | Functional diversity of the hnRNPs: past, present and perspectives |
| Q27865260 | Functional mammalian spliceosomal complex E contains SMN complex proteins in addition to U1 and U2 snRNPs. |
| Q34931992 | Gene silencing in mammals by small interfering RNAs |
| Q39072801 | Genome-wide identification of mRNAs associated with the protein SMN whose depletion decreases their axonal localization |
| Q47068799 | HRP-2, a heterogeneous nuclear ribonucleoprotein, is essential for embryogenesis and oogenesis in Caenorhabditis elegans |
| 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 |
| Q34002192 | Heterogeneous nuclear ribonucleoproteins (hnRNPs) in cellular processes: Focus on hnRNP E1's multifunctional regulatory roles |
| Q64237309 | Heterogeneous nuclear ribonucleoproteins R and Q accumulate in pathological inclusions in FTLD-FUS |
| Q41591221 | Heterogenous nuclear ribonucleoprotein Q increases protein expression from HIV-1 Rev-dependent transcripts |
| Q24300963 | Heterotrimeric GAIT complex drives transcript-selective translation inhibition in murine macrophages |
| Q28239705 | Human hnRNP Q re-localizes to cytoplasmic granules upon PMA, thapsigargin, arsenite and heat-shock treatments |
| Q28207148 | Hyperphosphorylated C-terminal repeat domain-associating proteins in the nuclear proteome link transcription to DNA/chromatin modification and RNA processing |
| Q24299793 | Identification and characterization of Gemin7, a novel component of the survival of motor neuron complex |
| Q39790727 | Identification of a heterogeneous nuclear ribonucleoprotein-recognition region in the HIV Rev protein |
| Q37328550 | Identification of the RGG box motif in Shadoo: RNA-binding and signaling roles? |
| Q41783290 | Identifying specific protein interaction partners using quantitative mass spectrometry and bead proteomes |
| Q57657576 | Impact of missense mutations in survival motor neuron protein (SMN1) leading to Spinal Muscular Atrophy (SMA): A computational approach |
| Q28116617 | In vitro and in cellulo evidences for association of the survival of motor neuron complex with the fragile X mental retardation protein |
| Q24613087 | Indoprofen upregulates the survival motor neuron protein through a cyclooxygenase-independent mechanism |
| Q55354265 | Interactome analyses revealed that the U1 snRNP machinery overlaps extensively with the RNAP II machinery and contains multiple ALS/SMA-causative proteins. |
| Q61816592 | Key role of SMN/SYNCRIP and RNA-Motif 7 in spinal muscular atrophy: RNA-Seq and motif analysis of human motor neurons |
| Q24671785 | Large-scale proteomic analysis of the human spliceosome |
| Q33695616 | Lymphotropic Herpesvirus saimiri uses the SMN complex to assemble Sm cores on its small RNAs |
| Q83228786 | Mamo decodes hierarchical temporal gradients into terminal neuronal fate |
| Q39868917 | Messenger RNA processing is altered in autosomal dominant leukodystrophy |
| Q29616012 | Messenger-RNA-binding proteins and the messages they carry |
| Q28594614 | Minute virus of mice NS1 interacts with the SMN protein, and they colocalize in novel nuclear bodies induced by parvovirus infection |
| Q34339435 | Minute virus of mice small nonstructural protein NS2 interacts and colocalizes with the Smn protein |
| Q35226376 | Molecular and cellular basis of spinal muscular atrophy |
| Q36924730 | Molecular functions of the SMN complex |
| Q35578251 | Molecular regulation, evolutionary, and functional adaptations associated with C to U editing of mammalian apolipoproteinB mRNA. |
| Q39958784 | Multiple and specific mRNA processing targets for the major human hnRNP proteins |
| Q35891195 | Negative regulation of RhoA translation and signaling by hnRNP-Q1 affects cellular morphogenesis |
| Q38222192 | Nervous translation, do you get the message? A review of mRNPs, mRNA-protein interactions and translational control within cells of the nervous system |
| Q24306776 | Noncanonical function of glutamyl-prolyl-tRNA synthetase: gene-specific silencing of translation |
| Q24540181 | Numerous microRNPs in neuronal cells containing novel microRNAs |
| 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 |
| Q28243993 | Prolactin increases SMN expression and survival in a mouse model of severe spinal muscular atrophy via the STAT5 pathway. |
| Q24292040 | Purification of native survival of motor neurons complexes and identification of Gemin6 as a novel component |
| Q42001219 | RNA-based affinity purification reveals 7SK RNPs with distinct composition and regulation |
| Q38111759 | RNA-binding proteins and translational regulation in axons and growth cones |
| Q28572763 | Rhythmic control of AANAT translation by hnRNP Q in circadian melatonin production |
| Q35697781 | Rhythmic interaction between Period1 mRNA and hnRNP Q leads to circadian time-dependent translation |
| Q24520629 | Rhythmic serotonin N-acetyltransferase mRNA degradation is essential for the maintenance of its circadian oscillation |
| Q33300324 | Ribonucleoprotein assembly defects correlate with spinal muscular atrophy severity and preferentially affect a subset of spliceosomal snRNPs |
| Q29013847 | SMN in spinal muscular atrophy and snRNP biogenesis |
| Q31127282 | SYNCRIP, a member of the heterogeneous nuclear ribonucleoprotein family, is involved in mouse hepatitis virus RNA synthesis |
| Q34086103 | Sequence-specific interaction of U1 snRNA with the SMN complex |
| Q28576647 | Smn, the spinal muscular atrophy-determining gene product, modulates axon growth and localization of beta-actin mRNA in growth cones of motoneurons |
| Q34230914 | Specific sequence features, recognized by the SMN complex, identify snRNAs and determine their fate as snRNPs |
| Q37033848 | Spinal muscular atrophy and a model for survival of motor neuron protein function in axonal ribonucleoprotein complexes |
| Q33345749 | Spinal muscular atrophy. |
| Q33785933 | Spinal muscular atrophy: why do low levels of survival motor neuron protein make motor neurons sick? |
| 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 |
| Q55428148 | The EGF/hnRNP Q1 axis is involved in tumorigenesis via the regulation of cell cycle-related genes. |
| Q47387876 | The GAIT translational control system |
| Q24648050 | The RNA binding protein hnRNP Q modulates the utilization of exon 7 in the survival motor neuron 2 (SMN2) gene |
| Q41859114 | The Role of Polypyrimidine Tract-Binding Proteins and Other hnRNP Proteins in Plant Splicing Regulation |
| Q89497713 | The Role of RNA Binding Proteins for Local mRNA Translation: Implications in Neurological Disorders |
| Q28204829 | The SMN complex, an assemblyosome of ribonucleoproteins |
| Q40798716 | The acidic domain is a unique structural feature of the splicing factor SYNCRIP |
| Q36197666 | The adipogenic transcriptional cofactor ZNF638 interacts with splicing regulators and influences alternative splicing |
| Q28572959 | The expression pattern of heterogeneous nuclear ribonucleoprotein R in rat retina |
| Q47073239 | The heterogeneous nuclear ribonucleoprotein-R is necessary for axonal beta-actin mRNA translocation in spinal motor neurons |
| Q26746566 | The hnRNP family: insights into their role in health and disease |
| Q42910421 | The transcription-dependent dissociation of P-TEFb-HEXIM1-7SK RNA relies upon formation of hnRNP-7SK RNA complexes |
| Q24644697 | Three proteins of the U7-specific Sm ring function as the molecular ruler to determine the site of 3'-end processing in mammalian histone pre-mRNA |
| Q34142599 | Transcriptome profiling of spinal muscular atrophy motor neurons derived from mouse embryonic stem cells |
| Q35224421 | Translation-competent 48S complex formation on HCV IRES requires the RNA-binding protein NSAP1. |
| Q37744954 | Translational upregulation of Aurora-A by hnRNP Q1 contributes to cell proliferation and tumorigenesis in colorectal cancer. |
| Q34426427 | Tudor domains bind symmetrical dimethylated arginines |
| Q24301454 | UNR, a new partner of poly(A)-binding protein, plays a key role in translationally coupled mRNA turnover mediated by the c-fos major coding-region determinant |
| Q40727142 | Ultrastructure of nuclear aggregates formed by expressing an expanded polyglutamine |
| Q38647597 | UsnRNP biogenesis: mechanisms and regulation |
| Q33642469 | WHEP domains direct noncanonical function of glutamyl-Prolyl tRNA synthetase in translational control of gene expression |
| Q44208216 | cAMP-dependent reorganization of the Cajal bodies and splicing machinery in cultured Schwann cells |
| Q36023305 | hnRNP Q regulates Cdc42-mediated neuronal morphogenesis |
| Q36574685 | hnRNP-Q1 represses nascent axon growth in cortical neurons by inhibiting Gap-43 mRNA translation |
| Q40024849 | hnRNP-R regulates the PMA-induced c-fos expression in retinal cells. |
| Q49808601 | mRNP assembly, axonal transport, and local translation in neurodegenerative diseases. |
| Q24672368 | miRNPs: a novel class of ribonucleoproteins containing numerous microRNAs |
| Q34995182 | p38 Mitogen-activated protein kinase stabilizes SMN mRNA through RNA binding protein HuR. |
| Q37012661 | snRNAs contain specific SMN-binding domains that are essential for snRNP assembly |
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