| scholarly article | Q13442814 |
| P50 | author | Michael D Hebert | Q90425949 |
| P2093 | author name string | Aaron R Poole | |
| P2860 | cites work | WRAP53 is essential for Cajal body formation and for targeting the survival of motor neuron complex to Cajal bodies | Q21145787 |
| The SMN-SIP1 complex has an essential role in spliceosomal snRNP biogenesis | Q24316121 | ||
| A human telomerase holoenzyme protein required for Cajal body localization and telomere synthesis | Q24323178 | ||
| Ongoing U snRNP biogenesis is required for the integrity of Cajal bodies | Q24336921 | ||
| Self-association of coilin reveals a common theme in nuclear body localization | Q24551044 | ||
| Coilin forms the bridge between Cajal bodies and SMN, the spinal muscular atrophy protein | Q24600358 | ||
| Structure, expression and chromosomal localization of human p80-coilin gene | Q24605102 | ||
| Dyskeratosis congenita mutations in the H/ACA domain of human telomerase RNA affect its assembly into a pre-RNP | Q24647530 | ||
| The SMN complex, an assemblyosome of ribonucleoproteins | Q28204829 | ||
| The coilin interactome identifies hundreds of small noncoding RNAs that traffic through Cajal bodies. | Q51502949 | ||
| Classification of spinal muscular atrophies | Q72423037 | ||
| SMN oligomerization defect correlates with spinal muscular atrophy severity | Q74557706 | ||
| Solution structure of the carboxy-terminal Tudor domain from human Coilin | Q85102498 | ||
| Coilin methylation regulates nuclear body formation | Q28205265 | ||
| The survival of motor neurons (SMN) protein interacts with the snoRNP proteins fibrillarin and GAR1 | Q28213183 | ||
| A conserved WD40 protein binds the Cajal body localization signal of scaRNP particles | Q28238122 | ||
| SMN-mediated assembly of RNPs: a complex story | Q28678650 | ||
| SMN in spinal muscular atrophy and snRNP biogenesis | Q29013847 | ||
| Coilin phosphomutants disrupt Cajal body formation, reduce cell proliferation and produce a distinct coilin degradation product | Q31032498 | ||
| Spinal muscular atrophy: why do low levels of survival motor neuron protein make motor neurons sick? | Q33785933 | ||
| The product of the survival of motor neuron (SMN) gene is a human telomerase-associated protein | Q34060945 | ||
| In vitro RNase and nucleic acid binding activities implicate coilin in U snRNA processing | Q34257423 | ||
| Essential role for the SMN complex in the specificity of snRNP assembly | Q34529450 | ||
| Carrier testing for spinal muscular atrophy | Q34778760 | ||
| Human cells lacking coilin and Cajal bodies are proficient in telomerase assembly, trafficking and telomere maintenance | Q34883221 | ||
| SMN mutants of spinal muscular atrophy patients are defective in binding to snRNP proteins. | Q35641208 | ||
| Immunocytochemical analysis of the coiled body in the cell cycle and during cell proliferation | Q36142454 | ||
| Telomerase recruitment requires both TCAB1 and Cajal bodies independently | Q36210861 | ||
| Biogenesis of telomerase ribonucleoproteins | Q36246606 | ||
| Regulated specific proteolysis of the Cajal body marker protein coilin | Q36460273 | ||
| Coilin displays differential affinity for specific RNAs in vivo and is linked to telomerase RNA biogenesis | Q36597868 | ||
| Phosphorylation regulates coilin activity and RNA association | Q36764309 | ||
| Coilin association with Box C/D scaRNA suggests a direct role for the Cajal body marker protein in scaRNP biogenesis | Q37706165 | ||
| Cajal bodies: where form meets function | Q38050096 | ||
| SMA-causing missense mutations in survival motor neuron (Smn) display a wide range of phenotypes when modeled in Drosophila. | Q41835189 | ||
| The domain encoded by exon 2 of the survival motor neuron protein mediates nucleic acid binding. | Q47827629 | ||
| The RNA-binding properties of SMN: deletion analysis of the zebrafish orthologue defines domains conserved in evolution | Q47973518 | ||
| P275 | copyright license | Creative Commons Attribution 3.0 Unported | Q14947546 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 6 | |
| P304 | page(s) | 726-735 | |
| P577 | publication date | 2016-05-23 | |
| P1433 | published in | Biology Open | Q27724268 |
| P1476 | title | SMN and coilin negatively regulate dyskerin association with telomerase RNA. | |
| P478 | volume | 5 |
| Q50052600 | Advances in therapy for spinal muscular atrophy: promises and challenges. |
| Q58766130 | Altered dynamics of scaRNA2 and scaRNA9 in response to stress correlates with disrupted nuclear organization |
| Q30274553 | Consequences of MEGF10 deficiency on myoblast function and Notch1 interactions. |
| Q39092025 | Diverse role of survival motor neuron protein |
| Q104567661 | Pathogenesis and therapeutic targets in spinal muscular atrophy (SMA) |
| Q38624976 | Regulatory RNPs: a novel class of ribonucleoproteins that potentially contribute to ribosome heterogeneity |
| Q28075938 | Telomerase Regulation from Beginning to the End |
| Q93082066 | The Role of Telomerase and Telomeres in Interstitial Lung Diseases: From Molecules to Clinical Implications |
| Q64444095 | The role of survival motor neuron protein (SMN) in protein homeostasis |
| Q38797923 | Towards an understanding of regulating Cajal body activity by protein modification |
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