The DOI matches its Crossref record; 34 of the 34 references it cites were found in a registry or an index.
Mitochondria and Epigenetics – Crosstalk in Homeostasis and Stress
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DNA methylation age of human tissues and cell types
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IDH1 and IDH2 Mutations in Gliomas
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Histone demethylation mediated by the nuclear amine oxidase homolog LSD1
Shi, Y., Lan, F., Matson, C., Mulligan, P., Whetstine, J. R., Cole, P. A., Casero, R. A., & Shi, Y. (2004) · Cell · doi:10.1016/j.cell.2004.12.012 · Cited by 4,051
Transcriptional silencing and longevity protein Sir2 is an NAD-dependent histone deacetylase
Imai, S.-I., Armstrong, C. M., Kaeberlein, M., & Guarente, L. (2000) · Nature · doi:10.1038/35001622 · Cited by 3,510
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The molecular hallmarks of epigenetic control
Allis, C. D., & Jenuwein, T. (2016) · Nature Reviews Genetics · doi:10.1038/nrg.2016.59 · Cited by 2,809
Figueroa, M. E., Abdel-Wahab, O., Lu, C., Ward, P. S., Patel, J., Shih, A., Li, Y., Bhagwat, N., Vasanthakumar, A., Fernandez, H. F., et al. (2010) · Cancer Cell · doi:10.1016/j.ccr.2010.11.015 · Cited by 2,766
ATP-citrate lyase links cellular metabolism to histone acetylation
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Histone methylation: a dynamic mark in health, disease and inheritance
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Cited by
Reactive oxygen species (ROS) as pleiotropic physiological signalling agents
Sies, H., & Jones, D. P. (2020) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-020-0230-3 · Cited by 5,335
Quirós, P. M., Prado, M. A., Zamboni, N., D’Amico, D., Williams, R. W., Finley, D., Gygi, S. P., & Auwerx, J. (2017) · Journal of Cell Biology · doi:10.1083/jcb.201702058 · Cited by 832
Self-citationHistory and progress of hypotheses and clinical trials for Alzheimer’s disease
Liu, P.-P., Xie, Y., Meng, X.-Y., & Kang, J.-S. (2019) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-019-0063-8 · Cited by 723
The Peroxisome-Mitochondria Connection: How and Why?
Fransen, M., Lismont, C., & Walton, P. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18061126 · Cited by 351
“In addition, as many of these co-substrates and metabolites can also serve as substrates or inhibitors of DNA methyltransferases, histone (de)methyltransferases, and histone (de)acetylases, changes in peroxisomal or mitochondrial activity are likely to influence the activity of the other organelle through epigenetic r…”
BackgroundMitochondria as a Cellular Hub in Infection and Inflammation
Andrieux, P., Chevillard, C., Cunha-Neto, E., & Nunes, J. P. S. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222111338 · Cited by 346
Metadata
- Authors
- Matilainen, O., Quirós, P. M., & Auwerx, J.
- Venue
- Trends in Cell Biology
- Publisher
- Elsevier BV
- Published
- 2017-06
- Volume
- 27
- Issue
- 6
- Pages
- 453-463
- ISSN
- 0962-8924 (ISSN-L)
- OpenAlex
- W2593784471
- Cited by
- 364
- References
- 34
- FWCI
- 2.15
- Type
- journal article
- Language
- en
- Open access
- green
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- Matilainen, O., Quirós, P. M., & Auwerx, J. (2017). Mitochondria and Epigenetics – Crosstalk in Homeostasis and Stress. Trends in Cell Biology. https://doi.org/10.1016/j.tcb.2017.02.004
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
