Pallasaho S, Gondane A, Kutz J, et al. Compromised CDK12 activity causes dependency on the high activity of O-GlcNAc transferase. Glycobiology. 2024. doi:10.1093/glycob/cwae081
Senn KA, Lipinski KA, Zeps NJ, Griffin AF, Wilkinson ME, Hoskins AA. Control of 3’ splice site selection by the yeast splicing factor Fyv6. bioRxiv : the preprint server for biology. 2024. doi:10.1101/2024.05.04.592262
Engal E, Oja KT, Maroofian R, et al. Bi-allelic loss-of-function variants in WBP4, encoding a spliceosome protein, result in a variable neurodevelopmental syndrome. American journal of human genetics. 2023;110(12):2112-2119. doi:10.1016/j.ajhg.2023.10.013
Engal E, Oja KT, Maroofian R, et al. Biallelic loss of function variants in , encoding a spliceosome protein, result in a variable neurodevelopmental delay syndrome. medRxiv : the preprint server for health sciences. 2023. doi:10.1101/2023.06.19.23291425
Engal E, Oja KT, Maroofian R, et al. Biallelic loss of function variants in , encoding a spliceosome protein, result in a variable neurodevelopmental delay syndrome. medRxiv : the preprint server for health sciences. 2023. doi:10.1101/2023.06.19.23291425
Lazear MR, Remsberg JR, Jaeger MG, et al. Proteomic discovery of chemical probes that perturb protein complexes in human cells. Molecular cell. 2023. doi:10.1016/j.molcel.2023.03.026