1. Selinger, Martin, Věchtová, Pavlína, Tykalová, Hana, Štěrba, Ján, Grubhoffer, Libor. 2022. Integrative RNA profiling of TBEV-infected neurons and astrocytes reveals potential pathogenic effectors. In Computational and structural biotechnology journal, 20, 2759-2777. doi:10.1016/j.csbj.2022.05.052. https://pubmed.ncbi.nlm.nih.gov/35685361/
2. Huang, Shanzhou, Ma, Zuyi, Zhou, Qi, Hou, Baohua, Zhang, Chuanzhao. 2022. Genome-Wide CRISPR/Cas9 Library Screening Identified that DUSP4 Deficiency Induces Lenvatinib Resistance in Hepatocellular Carcinoma. In International journal of biological sciences, 18, 4357-4371. doi:10.7150/ijbs.69969. https://pubmed.ncbi.nlm.nih.gov/35864956/
3. Delgado, Camila, Bu, Lei, Zhang, Jie, Furley, Andrew J, Fishman, Glenn I. 2021. Neural cell adhesion molecule is required for ventricular conduction system development. In Development (Cambridge, England), 148, . doi:10.1242/dev.199431. https://pubmed.ncbi.nlm.nih.gov/34100064/
4. Stogmann, Elisabeth, Reinthaler, Eva, Eltawil, Salwa, Strom, Tim M, Zimprich, Alexander. 2013. Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2. In Brain : a journal of neurology, 136, 1155-60. doi:10.1093/brain/awt068. https://pubmed.ncbi.nlm.nih.gov/23518707/
5. Chen, Wenjie, Chen, Fei, Shen, Yiping, Yang, Zhixian, Qin, Jiong. 2021. Case Report: A Case of Epileptic Disorder Associated With a Novel CNTN2 Frameshift Variant in Homozygosity due to Maternal Uniparental Disomy. In Frontiers in genetics, 12, 743833. doi:10.3389/fgene.2021.743833. https://pubmed.ncbi.nlm.nih.gov/34691156/
智鼠故事 
