Genomic profiling of DNA methyltransferases reveals a role for DNMT3B in genic methylation
By T. Baubec, Daniele F Colombo, C. Wirbelauer, Juliane Schmidt, Lukas Burger, A. Krebs, Altuna Akalin, Dirk Schübeler. Nature, 2015
651 citations recorded by the source corpus.
Subfields: Genetics, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/1ad4f4b685260b5a6a89d4a8a4a3c7710d1db3a3
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Genetics
- Andrew E. Teschendorff
- Alexander Meissner
- Stephan Beck
- Trey Ideker
- Steve Horvath
- Brock C. Christensen
- Caroline Relton
- Jean-Pierre Issa
In Molecular Biology
- Andrea A. Baccarelli
- Andrew E. Teschendorff
- Alexander Meissner
- Steve Horvath
- Stephan Beck
- Leonard C. Schalkwyk
- Trey Ideker
- Jordana T. Bell
Citations in the corpus
- DNA methylation: a historical perspective. (2022, positive): “A few years later, the Schübeler lab showed that while both DNMT3A and -B are generally recruited to CpG-dense regions, DNMT3B is specifically recruited to the bodies of actively transcribed genes through its PWWP domain interacting withH3K36me3 [242] (Figure 6E).”
- DNA methylation aging clocks: challenges and recommendations (2019, background): “Additionally, the influence of H3K36me3, which recruits DNMT3B to gene bodies [69], is an independent factor that can act to counter this decrease in DNA methylation.”