Topology of the human and mouse m6A RNA methylomes revealed by m6A-seq
By D. Dominissini, S. Moshitch-Moshkovitz, Schraga Schwartz, M. Salmon-Divon, L. Ungar, Sivan Osenberg, K. Cesarkas, J. Jacob-Hirsch, N. Amariglio, M. Kupiec and 2 more. Nature, 2012
4,382 citations recorded by the source corpus.
Subfields: Cancer Research, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/715852403fb0d8cd839f0ee3d98b9e61b08ca149
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Cancer Research
In Molecular Biology
- Chuan He
- Samie R. Jaffrey
- P. He
- Kate D. Meyer
- Howard Y. Chang
- Hailing Shi
- Pedro J. Batista
- Jiangbo W
Citations in the corpus
- FMRP Modulates Neural Differentiation through m6A-Dependent mRNA Nuclear Export (2019, background): “RNAmethylation on N(6)-adenosine is emerging as a vital mechanism regulating RNAmetabolism and function (Dominissini et al., 2012; Meyer et al., 2012; Peer et al., 2017).”
- m6A RNA Methylation Regulates the Self-Renewal and Tumorigenesis of Glioblastoma Stem Cells (2017, methodology): “Peak distribution analysis revealed strong enrichment of m6A peaks near the stop codon (Figure 7F) as previously described (Dominissini et al., 2012; Meyer et al., 2012).”
- YTHDC1 mediates nuclear export of N6-methyladenosine methylated mRNAs (2017, background): “YTHDC1 affects subcellular mRNA localization independent of premRNA splicing Both m6A and YTHDC1 have been shown to affect alternative splicing patterns in mRNA (Alarcón et al., 2015; Dominissini et al., 2012; Liu et al., 2015; Xiao et al., 2016).”
- YTH Domain: A Family of N6-methyladenosine (m6A) Readers (2018, methodology): “Although YTH domaincontaining proteins are putative RBPs, their exact binding ligands had remained unknown until two reports discovered that mammalian YTH family members are the candidates of m(6)A readers [36,37].”
- SRAMP: prediction of mammalian N6-methyladenosine (m6A) sites based on sequence-derived features (2016, background): “MCC = TP × TN − FP × FN √ (TP + FP) × (TP + FN) × (TN + FP) × (TN + FN) (6)”