1. He, Xue, Bai, Mei, Liu, Ming, Yuan, Dongya, Jin, Tianbo. 2019. Genetic variants in the ITPR2 gene are associated with Kashin-Beck Disease in Tibetan. In Molecular genetics & genomic medicine, 7, e00715. doi:10.1002/mgg3.715. https://pubmed.ncbi.nlm.nih.gov/31066235/
2. Zeisel, Amit, Muñoz-Manchado, Ana B, Codeluppi, Simone, Hjerling-Leffler, Jens, Linnarsson, Sten. 2015. Brain structure. Cell types in the mouse cortex and hippocampus revealed by single-cell RNA-seq. In Science (New York, N.Y.), 347, 1138-42. doi:10.1126/science.aaa1934. https://pubmed.ncbi.nlm.nih.gov/25700174/
3. van Es, Michael A, Van Vught, Paul W, Blauw, Hylke M, Ophoff, Roel A, van den Berg, Leonard H. . ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study. In The Lancet. Neurology, 6, 869-77. doi:. https://pubmed.ncbi.nlm.nih.gov/17827064/
4. Zhang, Feng, Wen, Yan, Guo, Xiong, Tian, Qing, Deng, Hong-Wen. . Genome-wide association study identifies ITPR2 as a susceptibility gene for Kashin-Beck disease in Han Chinese. In Arthritis & rheumatology (Hoboken, N.J.), 67, 176-81. doi:10.1002/art.38898. https://pubmed.ncbi.nlm.nih.gov/25303641/
5. Zhang, Yixin, Wang, Yikang, Yang, Yaozu, Li, Sihong, Zhang, Xiuying. 2023. Proteomic analysis of ITPR2 as a new therapeutic target for curcumin protection against AFB1-induced pyroptosis. In Ecotoxicology and environmental safety, 260, 115073. doi:10.1016/j.ecoenv.2023.115073. https://pubmed.ncbi.nlm.nih.gov/37257342/
6. Zhao, Sen, Zhao, Hengqiang, Zhao, Lina, Zhang, Jianguo, Wu, Nan. 2024. Unraveling the genetic architecture of congenital vertebral malformation with reference to the developing spine. In Nature communications, 15, 1125. doi:10.1038/s41467-024-45442-5. https://pubmed.ncbi.nlm.nih.gov/38321032/
7. Fernández-Santiago, Rubén, Sharma, Manu, Berg, Daniela, Ludolph, Albert, Gasser, Thomas. 2009. No evidence of association of FLJ10986 and ITPR2 with ALS in a large German cohort. In Neurobiology of aging, 32, 551.e1-4. doi:10.1016/j.neurobiolaging.2009.04.018. https://pubmed.ncbi.nlm.nih.gov/19464757/
8. Molitor, Anne, Lederle, Alexandre, Radosavljevic, Mirjana, Bertoli-Avella, Aida, Bahram, Seiamak. 2024. A pleiotropic recurrent dominant ITPR3 variant causes a complex multisystemic disease. In Science advances, 10, eado5545. doi:10.1126/sciadv.ado5545. https://pubmed.ncbi.nlm.nih.gov/39270020/
9. Wiel, Clotilde, Lallet-Daher, Hélène, Gitenay, Delphine, Vindrieux, David, Bernard, David. 2014. Endoplasmic reticulum calcium release through ITPR2 channels leads to mitochondrial calcium accumulation and senescence. In Nature communications, 5, 3792. doi:10.1038/ncomms4792. https://pubmed.ncbi.nlm.nih.gov/24797322/
10. Shi, Jin-long, Fu, Lin, Wang, Wei-dong. . High expression of inositol 1,4,5-trisphosphate receptor, type 2 (ITPR2) as a novel biomarker for worse prognosis in cytogenetically normal acute myeloid leukemia. In Oncotarget, 6, 5299-309. doi:. https://pubmed.ncbi.nlm.nih.gov/25779662/
智鼠故事 
