1. Chang, Jingjia, Wu, Hao, Wu, Jin, Yu, Pengfei, Zhu, Jianjun. 2023. Constructing a novel mitochondrial-related gene signature for evaluating the tumor immune microenvironment and predicting survival in stomach adenocarcinoma. In Journal of translational medicine, 21, 191. doi:10.1186/s12967-023-04033-6. https://pubmed.ncbi.nlm.nih.gov/36915111/
2. Liu, Ren, Zou, Zhihao, Chen, Lingwu, Wang, Zongren, Zhong, Weide. 2024. FKBP10 promotes clear cell renal cell carcinoma progression and regulates sensitivity to the HIF2α blockade by facilitating LDHA phosphorylation. In Cell death & disease, 15, 64. doi:10.1038/s41419-024-06450-x. https://pubmed.ncbi.nlm.nih.gov/38233415/
3. Merkuryeva, Elena S, Markova, Tatiana V, Kenis, Vladimir M, Dadali, Elena L, Kutsev, Sergey I. 2024. Presentation of Rare Phenotypes Associated with the FKBP10 Gene. In Genes, 15, . doi:10.3390/genes15060674. https://pubmed.ncbi.nlm.nih.gov/38927610/
4. Cai, Hong-Qing, Zhang, Min-Jie, Cheng, Zhi-Jian, Wang, Ming-Rong, Wan, Jing-Hai. 2021. FKBP10 promotes proliferation of glioma cells via activating AKT-CREB-PCNA axis. In Journal of biomedical science, 28, 13. doi:10.1186/s12929-020-00705-3. https://pubmed.ncbi.nlm.nih.gov/33557829/
5. Tauseef, Usman, Ibrahim, Mohsina, Noor, Noshaba, Hanif, Misbah. . Mutation In Fkbp10 Gene Cause Bruck Syndrome 1 (Brks1) In A Pakistani Family Of Pashtun Origin. In Journal of Ayub Medical College, Abbottabad : JAMC, 35, 341-347. doi:10.55519/JAMC-02-11056. https://pubmed.ncbi.nlm.nih.gov/37422836/
6. Megarbane, Andre, Bizzari, Sami, Deepthi, Asha, Delague, Valérie, Urtizberea, J Andoni. . A 20-year Clinical and Genetic Neuromuscular Cohort Analysis in Lebanon: An International Effort. In Journal of neuromuscular diseases, 9, 193-210. doi:10.3233/JND-210652. https://pubmed.ncbi.nlm.nih.gov/34602496/
7. Tan, Zhijia, Shek, Hiu Tung, Chen, Peikai, Gao, Bo, To, Michael Kai Tsun. 2023. Clinical features and molecular characterization of Chinese patients with FKBP10 variants. In Molecular genetics & genomic medicine, 11, e2122. doi:10.1002/mgg3.2122. https://pubmed.ncbi.nlm.nih.gov/36655627/
8. Li, Lulu, Mao, Bin, Li, Shan, Zhao, Xiuli, Zhang, Xue. 2019. Genotypic and phenotypic characterization of Chinese patients with osteogenesis imperfecta. In Human mutation, 40, 588-600. doi:10.1002/humu.23718. https://pubmed.ncbi.nlm.nih.gov/30715774/