Ekiert, Robert
Wellcome Centre for Cell Biology · University of Edinburgh
2 papers on CoChatORCID 0000-0002-8879-0646
Most cited papers
- Verified
Rett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressor
Lyst, M. J., Ekiert, R., Ebert, D. H., Merusi, C., Nowak, J., Selfridge, J., Guy, J., Kastan, N. R., Robinson, N. D., de Lima Alves, F., et al. (2013) · Nature Neuroscience
Genetics and Neurodevelopmental DisordersEpigenetics and DNA Methylation
Cited by 410
- Verified
Activity-dependent phosphorylation of MeCP2 threonine 308 regulates interaction with NCoR
Ebert, D. H., Gabel, H. W., Robinson, N. D., Kastan, N. R., Hu, L. S., Cohen, S., Navarro, A. J., Lyst, M. J., Ekiert, R., Bird, A. P., et al. (2013) · Nature
Genetics and Neurodevelopmental DisordersNeuroscience and Neuropharmacology Research
Cited by 227
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