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2. Qian, Zhaoyang, Liang, Junbo, Huang, Rong, Bao, Li, Zhao, Hong. 2024. HBV integrations reshaping genomic structures promote hepatocellular carcinoma. In Gut, 73, 1169-1182. doi:10.1136/gutjnl-2023-330414. https://pubmed.ncbi.nlm.nih.gov/38395437/
3. Carraro, Massimo, Hendriks, Ivo A, Hammond, Colin M, Nielsen, Michael L, Groth, Anja. 2023. DAXX adds a de novo H3.3K9me3 deposition pathway to the histone chaperone network. In Molecular cell, 83, 1075-1092.e9. doi:10.1016/j.molcel.2023.02.009. https://pubmed.ncbi.nlm.nih.gov/36868228/
4. Liang, Anru, Wu, Zuotao, Zhuo, Ting, Tan, Xiang, Chen, Mingwu. 2024. TONSL promotes lung adenocarcinoma progression, immune escape and drug sensitivity. In Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 27, 518-533. doi:10.1007/s12094-024-03627-w. https://pubmed.ncbi.nlm.nih.gov/39097545/
5. Wang, Peng, Yang, Xi, Zhao, Liang, Liu, Junmao, Ding, Yongbin. 2019. A novel long non-coding RNA TONSL-AS1 regulates progression of gastric cancer via activating TONSL. In Experimental cell research, 382, 111453. doi:10.1016/j.yexcr.2019.05.034. https://pubmed.ncbi.nlm.nih.gov/31158361/
6. Chang, Hae Ryung, Cho, Sung Yoon, Lee, Jae Hoon, Kim, Yonghwan, Cho, Tae-Joon. 2019. Hypomorphic Mutations in TONSL Cause SPONASTRIME Dysplasia. In American journal of human genetics, 104, 439-453. doi:10.1016/j.ajhg.2019.01.009. https://pubmed.ncbi.nlm.nih.gov/30773278/
7. Yu, Bin, Ding, Youming, Liao, Xiaofeng, Wang, Bin, Chen, Xiaoyan. 2019. Overexpression of TONSL might be an independent unfavorable prognostic indicator in hepatocellular carcinoma. In Pathology, research and practice, 215, 939-945. doi:10.1016/j.prp.2019.01.044. https://pubmed.ncbi.nlm.nih.gov/30723051/
8. Burrage, Lindsay C, Reynolds, John J, Baratang, Nissan Vida, Campeau, Philippe M, Lee, Brendan. 2019. Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes. In American journal of human genetics, 104, 422-438. doi:10.1016/j.ajhg.2019.01.007. https://pubmed.ncbi.nlm.nih.gov/30773277/
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