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NIPA2 located in 15q11.2 is mutated in patients with childhood absence epilepsy.
Jiang Y, Zhang Y, Zhang P, Sang T, Zhang F, Ji T, Huang Q, Xie H, Du R, Cai B, Zhao H, Wang J, Wu Y, Wu H, Xu K, Liu X, Chan P, Wu X. Jiang Y, et al. Among authors: chan p. Hum Genet. 2012 Jul;131(7):1217-24. doi: 10.1007/s00439-012-1149-3. Epub 2012 Feb 26. Hum Genet. 2012. PMID: 22367439
R2DT: a comprehensive platform for visualising RNA secondary structure.
McCann H, Meade CD, Williams LD, Petrov AS, Johnson PZ, Simon AE, Hoksza D, Nawrocki EP, Chan PP, Lowe TM, Ribas CE, Sweeney BA, Madeira F, Anyango S, Appasamy SD, Deshpande M, Varadi M, Velankar S, Zirbel CL, Naiden A, Jossinet F, Petrov AI. McCann H, et al. Among authors: chan pp. bioRxiv [Preprint]. 2024 Sep 30:2024.09.29.611006. doi: 10.1101/2024.09.29.611006. bioRxiv. 2024. PMID: 39803519 Free PMC article. Preprint.
Human TRMT1 and TRMT1L paralogs ensure the proper modification state, stability, and function of tRNAs.
Zhang K, Manning AC, Lentini JM, Howard J, Dalwigk F, Maroofian R, Efthymiou S, Chan P, Eliseev SI, Yang Z, Chang H, Karimiani EG, Bakhshoodeh B, Houlden H, Kaiser SM, Lowe TM, Fu D. Zhang K, et al. Among authors: chan p. Cell Rep. 2025 Jan 8;44(1):115092. doi: 10.1016/j.celrep.2024.115092. Online ahead of print. Cell Rep. 2025. PMID: 39786990 Free article.
5,518 results