| scholarly article | Q13442814 |
| review article | Q7318358 |
| P356 | DOI | 10.1016/S0960-9822(01)00517-6 |
| P698 | PubMed publication ID | 11696342 |
| P2093 | author name string | Terns MP | |
| Terns RM | |||
| P2860 | cites work | A novel function for SMN, the spinal muscular atrophy disease gene product, in pre-mRNA splicing | Q22008514 |
| 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 | ||
| Coilin forms the bridge between Cajal bodies and SMN, the spinal muscular atrophy protein | Q24600358 | ||
| A functional interaction between the survival motor neuron complex and RNA polymerase II | Q24674951 | ||
| SMN tudor domain structure and its interaction with the Sm proteins | Q27629094 | ||
| Essential role for the tudor domain of SMN in spliceosomal U snRNP assembly: implications for spinal muscular atrophy | Q28137718 | ||
| Characterization of a nuclear 20S complex containing the survival of motor neurons (SMN) protein and a specific subset of spliceosomal Sm proteins | Q28143590 | ||
| SMN, the product of the spinal muscular atrophy gene, binds preferentially to dimethylarginine-containing protein targets | Q28199238 | ||
| The survival of motor neurons (SMN) protein interacts with the snoRNP proteins fibrillarin and GAR1 | Q28213183 | ||
| Residual Cajal bodies in coilin knockout mice fail to recruit Sm snRNPs and SMN, the spinal muscular atrophy gene product | Q28590925 | ||
| Identification and characterization of a spinal muscular atrophy-determining gene | Q29547495 | ||
| Direct interaction of the spinal muscular atrophy disease protein SMN with the small nucleolar RNA-associated protein fibrillarin | Q31003752 | ||
| Guided tours: from precursor snoRNA to functional snoRNP. | Q33680763 | ||
| Specific sequences of the Sm and Sm-like (Lsm) proteins mediate their interaction with the spinal muscular atrophy disease gene product (SMN). | Q33905442 | ||
| Cajal bodies: the first 100 years | Q34059715 | ||
| SMN mutants of spinal muscular atrophy patients are defective in binding to snRNP proteins. | Q35641208 | ||
| A multiprotein complex mediates the ATP-dependent assembly of spliceosomal U snRNPs | Q43803910 | ||
| P433 | issue | 21 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | macromolecule | Q178593 |
| P304 | page(s) | R862-4 | |
| P577 | publication date | 2001-10-01 | |
| P1433 | published in | Current Biology | Q1144851 |
| P1476 | title | Macromolecular complexes: SMN--the master assembler | |
| P478 | volume | 11 |
| Q38304823 | A nuclear odyssey: fibroblast growth factor-2 (FGF-2) as a regulator of nuclear homeostasis in the nervous system. |
| Q44611061 | A proteomic analysis of arginine-methylated protein complexes |
| Q36323111 | A transgene carrying an A2G missense mutation in the SMN gene modulates phenotypic severity in mice with severe (type I) spinal muscular atrophy. |
| Q48586550 | Active transport of the survival motor neuron protein and the role of exon-7 in cytoplasmic localization. |
| Q24535295 | An ERG (ets-related gene)-associated histone methyltransferase interacts with histone deacetylases 1/2 and transcription co-repressors mSin3A/B |
| Q34701211 | Analysis of human protein replacement stable cell lines established using snoMEN-PR vector |
| Q37733136 | Antisense Oligonucleotides: Treatment Strategies and Cellular Internalization |
| Q36768167 | Biogenesis and intranuclear trafficking of human box C/D and H/ACA RNPs |
| Q28189028 | Cajal body proteins SMN and Coilin show differential dynamic behaviour in vivo |
| Q24540240 | Cell cycle-regulated trafficking of human telomerase to telomeres |
| Q36385395 | Cellular dynamics of small RNAs |
| Q82029139 | Chapter 5 Cytopathology of the motor neuron |
| Q46881366 | Characterization of a short isoform of human Tgs1 hypermethylase associating with small nucleolar ribonucleoprotein core proteins and produced by limited proteolytic processing |
| Q24307701 | Coupled in vitro import of U snRNPs and SMN, the spinal muscular atrophy protein |
| Q58794833 | Defective Neuromuscular Junction Organization and Postnatal Myogenesis in Mice With Severe 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 |
| Q37810374 | Developments in RNA splicing and disease |
| Q28578502 | Differential intranuclear localization of fibroblast growth factor-2 isoforms and specific interaction with the survival of motoneuron protein |
| Q39079803 | Emerging role of SETDB1 as a therapeutic target |
| Q28584703 | Fibrillarin is essential for early development and required for accumulation of an intron-encoded small nucleolar RNA in the mouse |
| Q42182559 | Fibroblast growth factor-2(23) binds directly to the survival of motoneuron protein and is associated with small nuclear RNAs. |
| Q39072801 | Genome-wide identification of mRNAs associated with the protein SMN whose depletion decreases their axonal localization |
| Q79106179 | Genomic structure and expression of the mouse ESET gene encoding an ERG-associated histone methyltransferase with a SET domain |
| Q27640685 | High-resolution X-ray and NMR structures of the SMN Tudor domain: conformational variation in the binding site for symmetrically dimethylated arginine residues |
| Q35567374 | Identification of a novel cyclic AMP-response element (CRE-II) and the role of CREB-1 in the cAMP-induced expression of the survival motor neuron (SMN) gene |
| Q37094802 | Impaired Muscle Mitochondrial Biogenesis and Myogenesis in Spinal Muscular Atrophy. |
| Q36559321 | Implication of the SMN complex in the biogenesis and steady state level of the signal recognition particle |
| Q37218543 | Increased susceptibility of spinal muscular atrophy fibroblasts to camptothecin is p53-independent |
| Q46464188 | Increased susceptibility of spinal muscular atrophy fibroblasts to camptothecin-induced cell death |
| Q50282492 | Inherited motor neuron disease in domestic cats: a model of spinal muscular atrophy |
| Q35567371 | Knockdown of the survival motor neuron (Smn) protein in zebrafish causes defects in motor axon outgrowth and pathfinding. |
| Q36142393 | Low levels of Survival Motor Neuron protein are sufficient for normal muscle function in the SMNΔ7 mouse model of SMA. |
| Q27934771 | Naf1p, an essential nucleoplasmic factor specifically required for accumulation of box H/ACA small nucleolar RNPs |
| Q39521045 | Neuronal SMN expression corrects spinal muscular atrophy in severe SMA mice while muscle-specific SMN expression has no phenotypic effect |
| Q22121992 | Non-coding RNAs: lessons from the small nuclear and small nucleolar RNAs |
| Q36768163 | Noncoding RNAs of the H/ACA family |
| Q36827345 | RNA transport and localized protein synthesis in neurological disorders and neural repair |
| Q34762623 | Repair of pre-mRNA splicing: prospects for a therapy for spinal muscular atrophy. |
| Q41694012 | SECIS-binding protein 2 interacts with the SMN complex and the methylosome for selenoprotein mRNP assembly and translation |
| Q24676334 | SMN, the spinal muscular atrophy protein, forms a pre-import snRNP complex with snurportin1 and importin beta |
| Q34546169 | Small nucleolar RNAs: versatile trans-acting molecules of ancient evolutionary origin. |
| Q33914362 | Specific splicing defects in S. pombe carrying a degron allele of the Survival of Motor Neuron gene |
| Q35340133 | Spinal muscular atrophy: journeying from bench to bedside |
| Q33785933 | Spinal muscular atrophy: why do low levels of survival motor neuron protein make motor neurons sick? |
| Q38629976 | Spliceosomal small nuclear ribonucleoprotein particles repeatedly cycle through Cajal bodies |
| Q35563254 | Splicing changes in SMA mouse motoneurons and SMN-depleted neuroblastoma cells: evidence for involvement of splicing regulatory proteins |
| Q37263631 | Structure of the insect oocyte nucleus with special reference to interchromatin granule clusters and cajal bodies. |
| Q34796882 | TDRD3, a novel Tudor domain-containing protein, localizes to cytoplasmic stress granules |
| Q34785598 | Telomerase RNA Accumulates in Cajal Bodies in Human Cancer Cells |
| Q41967731 | Telomerase RNA biogenesis involves sequential binding by Sm and Lsm complexes |
| Q36854864 | Telomerase reverse transcriptase is required for the localization of telomerase RNA to cajal bodies and telomeres in human cancer cells |
| Q33951245 | Telomerase trafficking and assembly in Xenopus oocytes |
| Q36436723 | The Cajal body: a meeting place for spliceosomal snRNPs in the nuclear maze |
| Q26749166 | The biology of DHX9 and its potential as a therapeutic target |
| Q24306551 | The exonuclease ISG20 mainly localizes in the nucleolus and the Cajal (Coiled) bodies and is associated with nuclear SMN protein-containing complexes |
| Q35038202 | The many facets of H/ACA ribonucleoproteins |
| Q34060945 | The product of the survival of motor neuron (SMN) gene is a human telomerase-associated protein |
| Q54560146 | The spinal muscular atrophy disease protein SMN is linked to the Rho-kinase pathway via profilin. |
| Q80863125 | Unaffected patients with a homozygous absence of the SMN1 gene |
Search more.