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1
Human telomerase and Cajal body ribonucleoproteins share a unique specificity of Sm protein association.
Genes Dev. 2006 Mar 1;20(5):531-6. doi: 10.1101/gad.1390306. Epub 2006 Feb 15.
2
snRNP protein expression enhances the formation of Cajal bodies containing p80-coilin and SMN.
J Cell Sci. 2001 Dec;114(Pt 24):4407-19. doi: 10.1242/jcs.114.24.4407.
3
A role for Cajal bodies in the final steps of U2 snRNP biogenesis.
J Cell Sci. 2004 Sep 1;117(Pt 19):4423-33. doi: 10.1242/jcs.01308. Epub 2004 Aug 17.
4
Human telomerase RNA and box H/ACA scaRNAs share a common Cajal body-specific localization signal.
J Cell Biol. 2004 Mar 1;164(5):647-52. doi: 10.1083/jcb.200310138. Epub 2004 Feb 23.
8
Towards an understanding of regulating Cajal body activity by protein modification.
RNA Biol. 2017 Jun 3;14(6):761-778. doi: 10.1080/15476286.2016.1243649. Epub 2016 Oct 7.
10
A human telomerase holoenzyme protein required for Cajal body localization and telomere synthesis.
Science. 2009 Jan 30;323(5914):644-8. doi: 10.1126/science.1165357.

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Molecular and Evolutionary Analysis of RNA-Protein Interactions in Telomerase Regulation.
Noncoding RNA. 2024 Jun 18;10(3):36. doi: 10.3390/ncrna10030036.
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A contemporary review of snoRNAs in cardiovascular health: RNA modification and beyond.
Mol Ther Nucleic Acids. 2023 Dec 5;35(1):102087. doi: 10.1016/j.omtn.2023.102087. eCollection 2024 Mar 12.
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NHP2 downregulation counteracts hTR-mediated activation of the DNA damage response at ALT telomeres.
EMBO J. 2021 Mar 15;40(6):e106336. doi: 10.15252/embj.2020106336. Epub 2021 Feb 17.
4
Regulation of human telomerase RNA biogenesis and localization.
RNA Biol. 2021 Mar;18(3):305-315. doi: 10.1080/15476286.2020.1809196. Epub 2020 Sep 2.
5
Core spliceosomal Sm proteins as constituents of cytoplasmic mRNPs in plants.
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6
Loss of Human TGS1 Hypermethylase Promotes Increased Telomerase RNA and Telomere Elongation.
Cell Rep. 2020 Feb 4;30(5):1358-1372.e5. doi: 10.1016/j.celrep.2020.01.004.
8
Telomerase Mechanism of Telomere Synthesis.
Annu Rev Biochem. 2017 Jun 20;86:439-460. doi: 10.1146/annurev-biochem-061516-045019. Epub 2017 Jan 30.
9
Dynamics of Human Telomerase Holoenzyme Assembly and Subunit Exchange across the Cell Cycle.
J Biol Chem. 2015 Aug 28;290(35):21320-35. doi: 10.1074/jbc.M115.659359. Epub 2015 Jul 13.
10
Diverse mechanisms for spliceosome-mediated 3' end processing of telomerase RNA.
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本文引用的文献

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Cajal bodies: a long history of discovery.
Annu Rev Cell Dev Biol. 2005;21:105-31. doi: 10.1146/annurev.cellbio.20.010403.103738.
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LSm proteins form heptameric rings that bind to RNA via repeating motifs.
Trends Biochem Sci. 2005 Sep;30(9):522-8. doi: 10.1016/j.tibs.2005.07.006.
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RNA structure and function in C/D and H/ACA s(no)RNPs.
Curr Opin Struct Biol. 2004 Jun;14(3):335-43. doi: 10.1016/j.sbi.2004.05.006.
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Can telomerase be put in its place?
J Cell Biol. 2004 Mar 1;164(5):637-9. doi: 10.1083/jcb.200401152.
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Human telomerase RNA and box H/ACA scaRNAs share a common Cajal body-specific localization signal.
J Cell Biol. 2004 Mar 1;164(5):647-52. doi: 10.1083/jcb.200310138. Epub 2004 Feb 23.
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The centennial of the Cajal body.
Nat Rev Mol Cell Biol. 2003 Dec;4(12):975-80. doi: 10.1038/nrm1262.
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Telomerase RNA accumulates in Cajal bodies in human cancer cells.
Mol Biol Cell. 2004 Jan;15(1):81-90. doi: 10.1091/mbc.e03-07-0525. Epub 2003 Oct 3.
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A common sequence motif determines the Cajal body-specific localization of box H/ACA scaRNAs.
EMBO J. 2003 Aug 15;22(16):4283-93. doi: 10.1093/emboj/cdg394.
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Distinct biogenesis pathways for human telomerase RNA and H/ACA small nucleolar RNAs.
Mol Cell. 2003 May;11(5):1361-72. doi: 10.1016/s1097-2765(03)00196-5.

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