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The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.

The microRNA miR-34 modulates ageing and neurodegeneration in Drosophila

Liu, Nan, Landreh, Michael, Cao, Kajia, Abe, Masashi, Hendriks, Gert-Jan, Kennerdell, Jason R., Zhu, Yongqing, Wang, Li-San, Bonini, Nancy M.·2012·Nature
DOI 10.1038/nature10810PMC PMC3326599
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Crossref · 10.1038/nature10810

Cites

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  • Gain- and loss-of-function studies have confirmed the capacity of several miRNAs to modulate longevity in Drosophila melanogaster and C. elegans.

    “Gain- and loss-of-function studies have confirmed the capacity of several miRNAs to modulate longevity in Drosophila melanogaster and C. elegans (Liu et al., 2012; Shen et al., 2012; Smith-Vikos and Slack, 2012).”

    From The Hallmarks of Aging (2013) · cites this paper as Liu et al., 2012

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Research works printed but not linked: 31

  1. Amaducci, L. & Tesco, G. Aging as a major risk for degenerative diseases of the central nervous system. Curr. Opin. Neurol. 7, 283–286 (1994) · DOI
  2. Eacker, S. M., Dawson, T. M. & Dawson, V. L. Understanding microRNAs in neurodegeneration. Nature Rev. Neurosci. 10, 837–841 (2009) · DOI · Paper page
  3. Bilen, J., Liu, N., Burnett, B. G., Pittman, R. N. & Bonini, N. M. MicroRNA pathways modulate polyglutamine-induced neurodegeneration. Mol. Cell 24, 157–163 (2006) · DOI
  4. Jiang, F. et al. Dicer-1 and R3D1-L catalyze microRNA maturation in Drosophila. Genes Dev. 19, 1674–1679 (2005) · DOI
  5. Liu, N. et al. The exoribonuclease Nibbler controls 3′ end processing of microRNAs in Drosophila. Curr. Biol. 21, 1888–1893 (2011) · DOI
  6. Han, B. W. H. u. n. g. J. H., Weng, Z., Zamore, P. D. & Ameres, S. L. The 3′-to-5′ exoribonuclease Nibbler shapes the 3′ ends of microRNAs bound to Drosophila Argonaute1. Curr. Biol. 21, 1878–1887 (2011) · DOI
  7. Chung, W. J., Okamura, K., Martin, R. & Lai, E. C. Endogenous RNA interference provides a somatic defense against Drosophila transposons. Curr. Biol. 18, 795–802 (2008) · DOI
  8. Kretzschmar, D., Hasan, G., Sharma, S., Heisenberg, M. & Benzer, S. The swiss cheese mutant causes glial hyperwrapping and brain degeneration in Drosophila. J. Neurosci. 17, 7425–7432 (1997) · DOI
  9. Cao, K., Chen-Plotkin, A. S., Plotkin, J. B. & Wang, L. S. Age-correlated gene expression in normal and neurodegenerative human brain tissues. PLoS ONE 5, (2010) · DOI
  10. Simon, A. F., Shih, C., Mack, A. & Benzer, S. Steroid control of longevity in Drosophila melanogaster. Science 299, 1407–1410 (2003) · DOI
  11. Fletcher, J. C. & Thummel, C. S. The Drosophila E74 gene is required for the proper stage- and tissue-specific transcription of ecdysone-regulated genes at the onset of metamorphosis. Development 121, 1411–1421 (1995) · DOI
  12. Fletcher, J. C., D’Avino, P. P. & Thummel, C. S. A steroid-triggered switch in E74 transcription factor isoforms regulates the timing of secondary-response gene expression. Proc. Natl Acad. Sci. USA 94, 4582–4586 (1997) · DOI
  13. Morimoto, R. I. Proteotoxic stress and inducible chaperone networks in neurodegenerative disease and aging. Genes Dev. 22, 1427–1438 (2008) · DOI · Paper page
  14. Warrick, J. M. et al. Expanded polyglutamine protein forms nuclear inclusions and causes neural degeneration in Drosophila. Cell 93, 939–949 (1998) · DOI
  15. Hirth, F. Drosophila melanogaster in the study of human neurodegeneration. CNS Neurol. Disord. Drug Targets 9, 504–523 (2010) · DOI
  16. Williams, G. C. Pleitropy, natural selection and the evolution of senescence. Evolution 11, 398–411 (1957) · DOI · Paper page
  17. Kirkwood, T. B. Understanding the odd science of aging. Cell 120, 437–447 (2005) · DOI · Paper page
  18. Boehm, M. & Slack, F. A developmental timing microRNA and its target regulate life span in C. elegans. Science 310, 1954–1957 (2005) · DOI
  19. de Lencastre, A. et al. MicroRNAs both promote and antagonize longevity in C. elegans. Curr. Biol. 20, 2159–2168 (2010) · DOI
  20. Ibanez-Ventoso, C. et al. Modulated microRNA expression during adult lifespan in Caenorhabditis elegans. Aging Cell 5, 235–246 (2006) · DOI
  21. Zovoilis, A. et al. microRNA-34c is a novel target to treat dementias. EMBO J. 30, 4299–4308 (2011) · DOI · Paper page
  22. Minones-Moyano, E. et al. MicroRNA profiling of Parkinson’s disease brains identifies early downregulation of miR-34b/c which modulate mitochondrial function. Hum. Mol. Genet. 20, 3067–3078 (2011) · DOI
  23. Li, X., Khanna, A., Li, N. & Wang, E. Circulatory miR34a as an RNA based, noninvasive biomarker for brain aging. Aging 3, 985–1002 (2011) · DOI
  24. Khanna, A., Muthusamy, S., Liang, R., Sarojini, H. & Wang, E. Gain of survival signaling by down-regulation of three key miRNAs in brain of calorie-restricted mice. Aging 3, 223–236 (2011) · DOI
  25. Gaughwin, P. M. et al. Hsa-miR-34b is a plasma-stable microRNA that is elevated in pre-manifest Huntington’s disease. Hum. Mol. Genet. 20, 2225–2237 (2011) · DOI · Paper page
  26. Yang, J. et al. MiR-34 modulates Caenorhabditis elegans lifespan via repressing the autophagy gene atg9. Age 10.1007/s11357-011-9324-3 (2011) · DOI
  27. Parks, A. L. et al. Systematic generation of high-resolution deletion coverage of the Drosophila melanogaster genome. Nature Genet. 36, 288–292 (2004) · DOI
  28. Dockendorff, T. C. et al. Drosophila lacking dfmr1 activity show defects in circadian output and fail to maintain courtship interest. Neuron 34, 973–984 (2002) · DOI
  29. Lewis, B. P., Shih, I. H., Jones-Rhoades, M. W., Bartel, D. P. & Burge, C. B. Prediction of mammalian microRNA targets. Cell 115, 787–798 (2003) · DOI · Paper page
  30. Grün, D., Wang, Y. L., Langenberger, D., Gunsalus, K. C. & Rajewsky, N. microRNA target predictions across seven Drosophila species and comparison to mammalian targets. PLOS Comput. Biol. 1, e13 (2005) · DOI
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Metadata

Authors
Liu, N., Landreh, M., Cao, K., Abe, M., Hendriks, G.-J., Kennerdell, J. R., Zhu, Y., Wang, L.-S., & Bonini, N. M.
Venue
Nature
Publisher
Springer Science and Business Media LLC
Published
2012-02
Volume
482
Issue
7386
Pages
519-523
ISSN
  • 0028-0836
  • 1476-4687
DOI
10.1038/nature10810
PMC
PMC3326599
Cited by
356
References
3
Language
en
Licence
www.springer.com/tdm (tdm)

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