1. Krbanjevic, Aleksandar, Lekakh, Olga, Kadkol, Shrihari, Mohapatra, Gayatry, Gushchin, Anna. . Unique Variant of Cerebrotendinous Xanthomatosis Presenting With Eyelid Involvement Due to Heterozygous CYP7A1 and SLC10A1 Gene Mutations. In The American Journal of dermatopathology, 43, 294-297. doi:10.1097/DAD.0000000000001858. https://pubmed.ncbi.nlm.nih.gov/33298707/
2. Ko, Yu-Lin, Tuan, Wei-Lun, Teng, Ming-Sheng, Wu, Semon, Hsu, Lung-An. 2024. SLC10A1 rs2296651 variant (S267F mutation) predicts biochemical traits, hepatitis B virus infection susceptibility and the risk of gallstone disease. In Molecular genetics and genomics : MGG, 299, 62. doi:10.1007/s00438-024-02153-2. https://pubmed.ncbi.nlm.nih.gov/38869622/
3. Wang, Meifen, Chen, Tao, Chen, Rui, Shao, Qi, Li, Jiwei. 2024. Neonatal jaundice caused by compound mutations of SLC10A1 and a novel UGT1A1 gene. In Clinics and research in hepatology and gastroenterology, 48, 102340. doi:10.1016/j.clinre.2024.102340. https://pubmed.ncbi.nlm.nih.gov/38588793/
4. Perea-Jacobo, Ricardo, Muñiz-Salazar, Raquel, Laniado-Laborín, Rafael, Ochoa-Terán, Adrián, Radilla-Chávez, Patricia. 2022. SLCO1B1 and SLC10A1 polymorphism and plasma rifampin concentrations in patients with co-morbidity tuberculosis-diabetes mellitus in Baja California, Mexico. In Tuberculosis (Edinburgh, Scotland), 136, 102248. doi:10.1016/j.tube.2022.102248. https://pubmed.ncbi.nlm.nih.gov/36055153/
5. Schneider, A L, Köhler, H, Röthlisberger, B, Grobholz, R, McLin, V A. 2021. Sodium taurocholate co-transporting polypeptide deficiency. In Clinics and research in hepatology and gastroenterology, 46, 101824. doi:10.1016/j.clinre.2021.101824. https://pubmed.ncbi.nlm.nih.gov/34757153/
6. Ibrahim, Marwa K, Liu, Cheng-Der, Zhang, Liyong, Gao, Shou-Jiang, Guo, Haitao. 2024. The loss of hepatitis B virus receptor NTCP/SLC10A1 in human liver cancer cells is due to epigenetic silencing. In Journal of virology, 98, e0118724. doi:10.1128/jvi.01187-24. https://pubmed.ncbi.nlm.nih.gov/39297647/