Cubn-flox 基因敲除小鼠

1. Yang, Jing, Xu, Yongli, Deng, Linxia, Zhang, Yu, Zhou, Jianhua. 2022. CUBN gene mutations may cause focal segmental glomerulosclerosis (FSGS) in children. In BMC nephrology, 23, 15. doi:10.1186/s12882-021-02654-x. https://pubmed.ncbi.nlm.nih.gov/34979989/

2. Bedin, Mathilda, Boyer, Olivia, Servais, Aude, Antignac, Corinne, Simons, Matias. . Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function. In The Journal of clinical investigation, 130, 335-344. doi:10.1172/JCI129937. https://pubmed.ncbi.nlm.nih.gov/31613795/

3. Ran, Jingyang, Chen, Qingsong, Hu, Yudong, Liao, Xiaohui, Lei, Jianrong. 2023. Isolated Proteinuria Caused by CUBN Gene Mutations: A Case Report and Review of the Literature. In Case reports in nephrology and dialysis, 13, 27-35. doi:10.1159/000530466. https://pubmed.ncbi.nlm.nih.gov/37384121/

4. Park, Han Sung, Kim, In Jai, Kim, Eun Gyo, Sung, Jung Hoon, Kim, Nam Keun. 2020. A study of associations between CUBN, HNF1A, and LIPC gene polymorphisms and coronary artery disease. In Scientific reports, 10, 16294. doi:10.1038/s41598-020-73048-6. https://pubmed.ncbi.nlm.nih.gov/33004870/

5. Tsekmekidou, Xanthippi, Tsetsos, Fotis, Koufakis, Theocharis, Paschou, Peristera, Kotsa, Kalliopi. 2019. Association between CUBN gene variants, type 2 diabetes and vitamin D concentrations in an elderly Greek population. In The Journal of steroid biochemistry and molecular biology, 198, 105549. doi:10.1016/j.jsbmb.2019.105549. https://pubmed.ncbi.nlm.nih.gov/31770575/

6. Böger, Carsten A, Chen, Ming-Huei, Tin, Adrienne, Fox, Caroline S, Kao, W H L. . CUBN is a gene locus for albuminuria. In Journal of the American Society of Nephrology : JASN, 22, 555-70. doi:10.1681/ASN.2010060598. https://pubmed.ncbi.nlm.nih.gov/21355061/

7. Drögemüller, Michaela, Jagannathan, Vidhya, Howard, Judith, Leeb, Tosso, Kook, Peter H. 2013. A frameshift mutation in the cubilin gene (CUBN) in Beagles with Imerslund-Gräsbeck syndrome (selective cobalamin malabsorption). In Animal genetics, 45, 148-50. doi:10.1111/age.12094. https://pubmed.ncbi.nlm.nih.gov/24164695/

8. Ma, Jun, Guan, Meijian, Bowden, Donald W, Palmer, Nicholette D, Freedman, Barry I. 2016. Association Analysis of the Cubilin (CUBN) and Megalin (LRP2) Genes with ESRD in African Americans. In Clinical journal of the American Society of Nephrology : CJASN, 11, 1034-1043. doi:10.2215/CJN.12971215. https://pubmed.ncbi.nlm.nih.gov/27197912/

9. Katsa, Maria Efthymia, Gil, Andrea Paola Rojas. . Vitamin B-related Gene Polymorphisms and Cardiovascular Disease. In Endocrine, metabolic & immune disorders drug targets, 22, 979-984. doi:10.2174/1381612828666220328115605. https://pubmed.ncbi.nlm.nih.gov/35346016/

10. Choi, Yun Young, Ahn, Yo Han, Park, Eujin, Kang, Hee Gyung, Lee, Hyun Kyung. 2024. To treat or not to treat: CUBN-associated persistent proteinuria. In Kidney research and clinical practice, 43, 663-670. doi:10.23876/j.krcp.23.258. https://pubmed.ncbi.nlm.nih.gov/39390623/