Lyst, Matthew J.

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

Rett syndrome: a complex disorder with simple roots

Lyst, M. J., & Bird, A. (2015) · Nature Reviews Genetics

Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases

Cited by 353

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

Structure of the MeCP2–TBLR1 complex reveals a molecular basis for Rett syndrome and related disorders

Kruusvee, V., Lyst, M. J., Taylor, C., Tarnauskaitė, Ž., Bird, A. P., & Cook, A. G. (2017) · Proceedings of the National Academy of Sciences

Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases

Cited by 82

Dysfunction of a SET3-like complex underlies a family of related neurological disorders

Paton, K. M., Alexander-Howden, B., Hare, J. I., Guy, J., Chhatbar, K., Yudina, M., Morris, S. T., Walls, R., Mathieson, T., Spanos, C., et al. (2026) · Nature Communications

Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases

Cited by 0