Mutations in CDC45, encoding an essential component of the pre-initiation complex, cause Meier-Gorlin Syndrome and Craniosynostosis by Fenwick, A, Kliszczak, M, Twigg, S, Goriely, A, McGowan, S, Miller, K, Wilkie, A, Niedzwiedz, W, WGS500 Consortium

Loss of FAM111B protease mutated in hereditary fibrosing poikiloderma negatively regulates telomere length by Kliszczak, M, Moralli, D, Jankowska, JD, Bryjka, P, Subha Meem, L, Goncalves, T, Hester, SS, Fischer, R, Clynes, D, Green, CM

Tryptophan-mediated interactions between tristetraprolin and the CNOT9 subunit are required for CCR4-NOT deadenylase complex recruitment by Bulbrook, D, Brazier, H, Mahajan, P, Kliszczak, M, Fedorov, O, Marchese, F, Aubareda, A, Chalk, R, Picaud, S, Strain-Damerell, C, Filippakopoulos, P, Gileadi, O, Clark, A, Yue, W, Burgess-Brown, N, Dean, J