Tbc1d8b-KO 基因敲除小鼠

1. Milosavljevic, Julian, Lempicki, Camille, Lang, Konrad, Pollak, Martin R, Hermle, Tobias. 2022. Nephrotic Syndrome Gene TBC1D8B Is Required for Endosomal Maturation and Nephrin Endocytosis in Drosophila. In Journal of the American Society of Nephrology : JASN, 33, 2174-2193. doi:10.1681/ASN.2022030275. https://pubmed.ncbi.nlm.nih.gov/36137753/

2. Kampf, Lina L, Schneider, Ronen, Gerstner, Lea, Hildebrandt, Friedhelm, Hermle, Tobias. 2019. TBC1D8B Mutations Implicate RAB11-Dependent Vesicular Trafficking in the Pathogenesis of Nephrotic Syndrome. In Journal of the American Society of Nephrology : JASN, 30, 2338-2353. doi:10.1681/ASN.2019040414. https://pubmed.ncbi.nlm.nih.gov/31732614/

3. Fang, Zhengying, Zhang, Chunli, Jin, Yuanmeng, Pan, Xiaoxia, Xie, Jingyuan. 2022. Adult-Onset Focal Segmental Glomerulosclerosis With Steroid-Dependent Nephrotic Syndrome Caused by a Novel TBC1D8B Variant: A Case Report and Literature Review. In American journal of kidney diseases : the official journal of the National Kidney Foundation, 81, 240-244. doi:10.1053/j.ajkd.2022.06.012. https://pubmed.ncbi.nlm.nih.gov/35970429/

4. Okada, Junichi, Matsumoto, Shunichi, Yamada, Eijiro, Ohshima, Kihachi, Okada, Shuichi. . TBC1D8B, a GTPase-activating protein, is a novel apoptosis inducer. In Biomedical research (Tokyo, Japan), 42, 95-102. doi:10.2220/biomedres.42.95. https://pubmed.ncbi.nlm.nih.gov/34092754/

5. Zhao, Hui, Liu, Lin-Lin, Sun, Jian, Chen, Ce-Shi, Zhang, Ya-Ping. 2023. A human-specific insertion promotes cell proliferation and migration by enhancing TBC1D8B expression. In Science China. Life sciences, 67, 765-777. doi:10.1007/s11427-023-2442-3. https://pubmed.ncbi.nlm.nih.gov/38110796/

6. Hou, Ling, Yin, Lu, Wu, Yubin, Zhao, Chengguang, Du, Yue. 2021. Novel TBC1D8B Variant in a 6-Month-Old Boy With Steroid-Sensitive Nephrotic Syndrome: A Case Report. In Frontiers in pediatrics, 9, 732512. doi:10.3389/fped.2021.732512. https://pubmed.ncbi.nlm.nih.gov/34858901/

7. Dorval, Guillaume, Kuzmuk, Valeryia, Gribouval, Olivier, Saleem, Moin A, Antignac, Corinne. 2019. TBC1D8B Loss-of-Function Mutations Lead to X-Linked Nephrotic Syndrome via Defective Trafficking Pathways. In American journal of human genetics, 104, 348-355. doi:10.1016/j.ajhg.2018.12.016. https://pubmed.ncbi.nlm.nih.gov/30661770/

8. Xu, Yuanyuan, Dai, Chao, He, Jing, Wang, Chang, Jin, Danqun. 2024. Novel TBC1D8B variant causes neonatal nephrotic syndrome combined with acute kidney injury. In Italian journal of pediatrics, 50, 222. doi:10.1186/s13052-024-01790-y. https://pubmed.ncbi.nlm.nih.gov/39468641/

9. Florentinus-Mefailoski, Angelique, Bowden, Peter, Scheltens, Philip, Teunissen, Charlotte, Marshall, John G. 2021. The plasma peptides of Alzheimer's disease. In Clinical proteomics, 18, 17. doi:10.1186/s12014-021-09320-2. https://pubmed.ncbi.nlm.nih.gov/34182925/

10. Lan, Wanwen, Hou, Aihua, Lakshminarayanan, Rajamani, Lim, Yoon-Pin, Tong, Louis. 2018. Linc-9432 is a novel pterygium lincRNA which regulates differentiation of fibroblasts. In FEBS letters, 592, 1173-1184. doi:10.1002/1873-3468.13027. https://pubmed.ncbi.nlm.nih.gov/29513395/