DNA Methylation and Its Basic Function
Author:
Publisher
Springer Science and Business Media LLC
Subject
Psychiatry and Mental health,Pharmacology
Link
http://www.nature.com/articles/npp2012112.pdf
Reference210 articles.
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2. Aapola U, Lyle R, Krohn K, Antonarakis SE, Peterson P (2001). Isolation and initial characterization of the mouse Dnmt3l gene. Cytogenet Cell Genet 92: 122–126.
3. Achour M, Jacq X, Ronde P, Alhosin M, Charlot C, Chataigneau T et al (2008). The interaction of the SRA domain of ICBP90 with a novel domain of DNMT1 is involved in the regulation of VEGF gene expression. Oncogene 27: 2187–2197.
4. Amir RE, Van den Veyver IB, Wan M, Tran CQ, Francke U, Zoghbi HY (1999). Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat Genet 23: 185–188. Discovered MECP2 mutation as the cause of Rett Syndrome and paved way for further study of MECP2 protein role in the nervous system.
5. Aran D, Toperoff G, Rosenberg M, Hellman A (2011). Replication timing-related and gene body-specific methylation of active human genes. Hum Mol Genet 20: 670–680.
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