Structural basis of RIP2 activation and signaling

由 Gong, Q, Long, Z, Zhong, F.L, Teo, D.E.T, Jin, Y, Yin, Z, Boo, Z.Z, Zhang, Y, Zhang, J, Yang, R, Bhushan, S, Reversade, B, Li, Z, Wu, B
出版 2020

A homozygous loss-of-function camk2a mutation causes growth delay, frequent seizures and severe intellectual disability

由 Chia, P.H, Zhong, F.L, Niwa, S, Bonnard, C, Utami, K.H, Zeng, R, Lee, H, Eskin, A, Nelson, S.F, Xie, W.H, Al-Tawalbeh, S, El-Khateeb, M, Shboul, M, Pouladi, M.A, Al-Raqad, M, Reversade, B
出版 2020