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The DOI matches its Crossref record; 6 of the 6 references it cites were found in a registry or an index.

AMPK–SKP2–CARM1 signalling cascade in transcriptional regulation of autophagy

Shin, Hi-Jai R., Kim, Hyunkyung, Oh, Sungryong, Lee, Jun-Gi, Kee, Minjung, Ko, Hyun-Jeong, Kweon, Mi-Na, Won, Kyoung-Jae, Baek, Sung Hee·2016·Nature
DOI 10.1038/nature18014PMC PMC5568428
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Research works printed but not linked: 26

  1. Yang, Z. & Klionsky, D. J. Eaten alive: a history of macroautophagy. Nat. Cell Biol. 12, 814–822 (2010) · DOI
  2. Choi, A. M., Ryter, S. W. & Levine, B. Autophagy in human health and disease. N. Engl. J. Med. 368, 651–662 (2013) · DOI · Paper page
  3. Mizushima, N. Autophagy: process and function. Genes Dev. 21, 2861–2873 (2007) · DOI
  4. Klionsky, D. J. Autophagy: from phenomenology to molecular understanding in less than a decade. Nat. Rev. Mol. Cell Biol. 8, 931–937 (2007) · DOI
  5. Mizushima, N., Yoshimori, T. & Levine, B. Methods in mammalian autophagy research. Cell 140, 313–326 (2010) · DOI · Paper page
  6. Bjørkøy, G. et al. Monitoring autophagic degradation of p62/SQSTM1. Methods Enzymol. 452, 181–197 (2009) · DOI · Paper page
  7. Selvi, B. R. et al. Identification of a novel inhibitor of coactivator-associated arginine methyltransferase 1 (CARM1)-mediated methylation of histone H3 Arg-17. J. Biol. Chem. 285, 7143–7152 (2010) · DOI
  8. Carrano, A. C., Eytan, E., Hershko, A. & Pagano, M. SKP2 is required for ubiquitin-mediated degradation of the CDK inhibitor p27. Nat. Cell Biol. 1, 193–199 (1999) · DOI
  9. Hardie, D. G. AMPK and autophagy get connected. EMBO J. 30, 634–635 (2011) · DOI
  10. Inoki, K., Kim, J. & Guan, K.-L. AMPK and mTOR in cellular energy homeostasis and drug targets. Annu. Rev. Pharmacol. Toxicol. 52, 381–400 (2012) · DOI
  11. Salt, I. et al. AMP-activated protein kinase: greater AMP dependence, and preferential nuclear localization, of complexes containing the α2 isoform. Biochem. J. 334, 177–187 (1998) · DOI
  12. Eijkelenboom, A. & Burgering, B. M. FOXOs: signalling integrators for homeostasis maintenance. Nat. Rev. Mol. Cell Biol. 14, 83–97 (2013) · DOI
  13. Greer, E. L. et al. The energy sensor AMP-activated protein kinase directly regulates the mammalian FOXO3 transcription factor. J. Biol. Chem. 282, 30107–30119 (2007) · DOI
  14. Potente, M. et al. Involvement of Foxo transcription factors in angiogenesis and postnatal neovascularization. J. Clin. Invest. 115, 2382–2392 (2005) · DOI
  15. Wang, K. & Li, P.-F. Foxo3a regulates apoptosis by negatively targeting miR-21. J. Biol. Chem. 285, 16958–16966 (2010) · DOI
  16. Yang, Y.-C. et al. DNMT3B overexpression by deregulation of FOXO3a-mediated transcription repression and MDM2 overexpression in lung cancer. J. Thorac. Oncol. 9, 1305–1315 (2014) · DOI
  17. Tsai, K.-L. et al. Crystal structure of the human FOXO3a-DBD/DNA complex suggests the effects of post-translational modification. Nucleic Acids Res. 35, 6984–6994 (2007) · DOI
  18. Sardiello, M. et al. A gene network regulating lysosomal biogenesis and function. Science 325, 473–477 (2009) · DOI · Paper page
  19. Settembre, C. & Medina, D. L. TFEB and the CLEAR network. Methods Cell Biol. 126, 45–62 (2015) · DOI
  20. Kim, I. S. et al. Roles of Mis18α in epigenetic regulation of centromeric chromatin and CENP-A loading. Mol. Cell 46, 260–273 (2012) · DOI
  21. Kim, H. et al. DNA damage-induced RORα is crucial for p53 stabilization and increased apoptosis. Mol. Cell 44, 797–810 (2011) · DOI
  22. Chen, Z., Zhou, Y., Song, J. & Zhang, Z. hCKSAAP_UbSite: improved prediction of human ubiquitination sites by exploiting amino acid pattern and properties. Biochim. Biophys. Acta 1834, 1461–1467 (2013) · DOI
  23. Kim, J. et al. Differential regulation of distinct Vps34 complexes by AMPK in nutrient stress and autophagy. Cell 152, 290–303 (2013) · DOI
  24. Kim, D. et al. TopHat2: accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusions. Genome Biol. 14, R36 (2013) · DOI · Paper page
  25. Robinson, M. D., McCarthy, D. J. & Smyth, G. K. edgeR: a Bioconductor package for differential expression analysis of digital gene expression data. Bioinformatics 26, 139–140 (2010) · DOI · Paper page
  26. Boo, K. et al. Pontin functions as an essential coactivator for Oct4-dependent lincRNA expression in mouse embryonic stem cells. Nat. Commun. 6, 6810 (2015) · DOI

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Metadata

Authors
Shin, H.-J. R., Kim, H., Oh, S., Lee, J.-G., Kee, M., Ko, H.-J., Kweon, M.-N., Won, K.-J., & Baek, S. H.
Venue
Nature
Publisher
Springer Science and Business Media LLC
Published
2016-06-15
Volume
534
Issue
7608
Pages
553-557
ISSN
  • 0028-0836
  • 1476-4687
DOI
10.1038/nature18014
PMC
PMC5568428
Cited by
417
References
6
Language
en
Licence

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CoChat. (2026). Citation check: AMPK–SKP2–CARM1 signalling cascade in transcriptional regulation of autophagy. https://app.cochat.ai/papers/10.1038/nature18014
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Shin, H.-J. R., Kim, H., Oh, S., Lee, J.-G., Kee, M., Ko, H.-J., Kweon, M.-N., Won, K.-J., & Baek, S. H. (2016). AMPK–SKP2–CARM1 signalling cascade in transcriptional regulation of autophagy. Nature. https://doi.org/10.1038/nature18014