1. Liu, Qian, Zhu, Chunfu, Dong, Yanfen. . LncRNA TCTN2 Promotes the Malignant Development of Hepatocellular Carcinoma via Regulating mIR-1285-3p/ARF6 Axis. In Recent patents on anti-cancer drug discovery, 18, 517-527. doi:10.2174/1574892818666221019163656. https://pubmed.ncbi.nlm.nih.gov/36278455/
2. Huppke, Peter, Wegener, Eike, Böhrer-Rabel, Helena, Gärtner, Jutta, Bergmann, Carsten. 2014. Tectonic gene mutations in patients with Joubert syndrome. In European journal of human genetics : EJHG, 23, 616-20. doi:10.1038/ejhg.2014.160. https://pubmed.ncbi.nlm.nih.gov/25118024/
3. Fang, Liwei, Wang, Lulu, Yang, Li, Pei, Shanai, Wu, De. 2023. Novel variants identified in five Chinese families with Joubert Syndrome: a case report. In BMC medical genomics, 16, 221. doi:10.1186/s12920-023-01669-7. https://pubmed.ncbi.nlm.nih.gov/37735380/
4. Liu, Jian, Lin, Mingxia, Qiao, Feng, Zhang, Chenghua. 2021. Exosomes Derived from lncRNA TCTN2-Modified Mesenchymal Stem Cells Improve Spinal Cord Injury by miR-329-3p/IGF1R Axis. In Journal of molecular neuroscience : MN, 72, 482-495. doi:10.1007/s12031-021-01914-7. https://pubmed.ncbi.nlm.nih.gov/34623606/
5. Abrams, Shaun R, Reiter, Jeremy F. 2021. Ciliary Hedgehog signaling regulates cell survival to build the facial midline. In eLife, 10, . doi:10.7554/eLife.68558. https://pubmed.ncbi.nlm.nih.gov/34672258/
6. Shaheen, Ranad, Faqeih, Eissa, Seidahmed, Mohammed Z, AlQahtani, Khadijah, Alkuraya, Fowzan S. 2011. A TCTN2 mutation defines a novel Meckel Gruber syndrome locus. In Human mutation, 32, 573-8. doi:10.1002/humu.21507. https://pubmed.ncbi.nlm.nih.gov/21462283/
7. Wang, Chengbing, Li, Jia, Meng, Qing, Wang, Baolin. 2017. Three Tctn proteins are functionally conserved in the regulation of neural tube patterning and Gli3 processing but not ciliogenesis and Hedgehog signaling in the mouse. In Developmental biology, 430, 156-165. doi:10.1016/j.ydbio.2017.08.003. https://pubmed.ncbi.nlm.nih.gov/28800946/
8. Hiraide, Takuya, Shimizu, Kenji, Okumura, Yoshinori, Ogata, Tsutomu, Saitsu, Hirotomo. 2023. A deep intronic TCTN2 variant activating a cryptic exon predicted by SpliceRover in a patient with Joubert syndrome. In Journal of human genetics, 68, 499-505. doi:10.1038/s10038-023-01143-3. https://pubmed.ncbi.nlm.nih.gov/36894704/
智鼠故事 
