Exome sequencing identifies somatic mutations of DNA methyltransferase gene DNMT3A in acute monocytic leukemia
By Xiao-jing Yan, Jie Xu, Zhao-hui Gu, Chun-ming Pan, G. Lu, Yang Shen, Jing-yi Shi, Yong-mei Zhu, L. Tang, Xiao-Wei Zhang and 6 more. Nature Genetics, 2011
815 citations recorded by the source corpus.
Subfields: Cancer Research, Hematology, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/bf9d28fdd83d24750fbc4c8e9c956ab3fff0f01c
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Citations in the corpus
- The role of mutations in epigenetic regulators in myeloid malignancies (2012, background): “Clinical and molecular characterization of a rare syndrome of acute promyelocytic leukemia associated with translocation (11;17).”
- Epigenetic Determinants of Cancer. (2016, background): “…(Kanai et al. 2003) Overexpression (Wu et al. 2007) DNMT3A DNA methyltransferase MDS; AML Mutation (Ley et al. 2010; Yamashita et al. 2010; Yan et al. 2011) DNMT3B DNA methyltransferase ICF syndrome, SNPs in breast and lung adenoma Mutation (Wijmenga et al. 2000) Mutation (Shen et al.…”
- Cancer Genetics and Epigenetics: Two Sides of the Same Coin? (2012, background): “All known DNMT3A mutations are related to poor survival in AML (Ley et al., 2010; Yan et al., 2011), suggesting that these mutations prevent differentiation and have an important role in the progression of disease.”
- Maftools: efficient and comprehensive analysis of somatic variants in cancer (2018, neutral): “5E; Yan et al. 2011).”
- Mechanisms and functions of Tet protein-mediated 5-methylcytosine oxidation. (2011, background): “The founding member of the Tet family of DNA hydroxylases, the TET1 gene, was initially identified in acute myeloid leukemia (AML) as a fusion partner of the histone H3 Lys 4 (H3K4) methyltransferase MLL (mixed-lineage leukemia) (Ono et al. 2002; Lorsbach et al. 2003).”
- Epigenomic profiling of young and aged HSCs reveals concerted changes during aging that reinforce self-renewal (2014, background): “Finally, we showed that the edges of DNA methylation canyons are highly dynamic in a manner concordant with loss of Dnmt3a function (Jeong et al., 2014; Challen et al., 2012), the mutation of which is associated with hematologic malignancies (Ley et al., 2010; Yan et al., 2011).”