The Role of Epigenetics
Author:
Publisher
Springer International Publishing
Link
http://link.springer.com/content/pdf/10.1007/978-3-319-55865-3_3
Reference117 articles.
1. Adkins, R. M., Krushkal, J., Tylavsky, F. A., & Thomas, F. (2011). Racial differences in gene-specific DNA methylation levels are present at birth. Birth Defects Research Part A: Clinical and Molecular Teratology, 91(8), 728–736. Available from: PM:21308978.
2. Almen, M. S., Jacobsson, J. A., Moschonis, G., Benedict, C., Chrousos, G. P., Fredriksson, R., et al. (2012). Genome wide analysis reveals association of a FTO gene variant with epigenetic changes. Genomics, 99(3), 132–137. Available from: PM:22234326.
3. Alvarez-Garcia, I., & Miska, E. A. (2005). MicroRNA functions in animal development and human disease. Development, 132(21), 4653–4662. Available from: PM:16224045.
4. Ambrosone, C. B., Young, A. C., Sucheston, L. E., Wang, D., Yan, L., Liu, S., et al. (2014). Genome-wide methylation patterns provide insight into differences in breast tumor biology between American women of African and European ancestry. Oncotarget, 5(1), 237–248. Available from: PM:24368439.
5. Amir, R. E., Van den Veyver, I. B., Wan, M., Tran, C. Q., Francke, U., & Zoghbi, H. Y. (1999). Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nature Genetics, 23(2), 185–188. Available from: PM:10508514.
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