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Genetic spectrum of CAKUT and risk factors for kidney failure: a pediatric multicenter cohort study.
Liu JL, Wang XW, Liu CH, Gao DMX, Jiang XY, Mao JH, Zhu GH, Zhang AH, Wang M, Dang XQ, Zhuang JQ, Li YF, Bai HT, Zhang RF, Shen T, Bi YL, Sun YB, Wang X, Wu BB, Chen J, Rao J, Tang XS, Shen Q, Xu H; Chinese Children Genetic Kidney Disease Database (CCGKDD), “Internet Plus” Nephrology Alliance of the National Center for Children's Care Department of Nephrology, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China. Liu JL, et al. Among authors: wu bb. Nephrol Dial Transplant. 2022 Dec 22;38(9):1981-91. doi: 10.1093/ndt/gfac338. Online ahead of print. Nephrol Dial Transplant. 2022. PMID: 36549658 Free PMC article.
Clinical and genetic features of Prader-Willi syndrome in China.
Lu W, Qi Y, Cui B, Chen XL, Wu BB, Chen C, Cao Y, Zhou WH, Xu H, Luo FH. Lu W, et al. Among authors: wu bb. Eur J Pediatr. 2014 Jan;173(1):81-6. doi: 10.1007/s00431-013-2124-2. Epub 2013 Aug 11. Eur J Pediatr. 2014. PMID: 23933672
Responsible genes in children with primary vesicoureteral reflux: findings from the Chinese Children Genetic Kidney Disease Database.
Liu JL, Shen Q, Wu MY, Zhu GH, Li YF, Wang XW, Tang XS, Bi YL, Gong YN, Chen J, Fang XY, Zhai YH, Wu BB, Li GM, Sun YB, Gao XJ, Liu CH, Jiang XY, Hao S, Kang YL, Gong YL, Rong LP, Li D, Wang S, Ma D, Rao J, Xu H; for Chinese Children Genetic Kidney Disease Database (CCGKDD), “Internet Plus” Nephrology Alliance of the National Center for Children’s Care. Liu JL, et al. Among authors: wu bb, wu my. World J Pediatr. 2021 Aug;17(4):409-418. doi: 10.1007/s12519-021-00428-x. Epub 2021 May 31. World J Pediatr. 2021. PMID: 34059960
Genetic Architecture of Childhood Kidney and Urological Diseases in China.
Fang Y, Shi H, Xiang T, Liu J, Liu J, Tang X, Fang X, Chen J, Zhai Y, Shen Q, Li G, Sun L, Bi Y, Wang X, Qian Y, Wu B, Wang H, Zhou W, Ma D, Mao J, Jiang X, Sun S, Shen Y, Liu X, Zhang A, Wang X, Huang W, Li Q, Wang M, Gao X, Wu Y, Deng F, Zhang R, Liu C, Yu L, Zhuang J, Sun Q, Dang X, Bai H, Zhu Y, Lu S, Zhang B, Shao X, Liu X, Han M, Zhao L, Liu Y, Gao J, Bao Y, Zhang D, Ma Q, Zhao L, Xia Z, Lu B, Wang Y, Zhao M, Zhang J, Jian S, He G, Zhang H, Zhao B, Li X, Wang F, Li Y, Zhu H, Luo X, Li J, Rao J, Xu H. Fang Y, et al. Phenomics. 2021 Jul 15;1(3):91-104. doi: 10.1007/s43657-021-00014-1. eCollection 2021 Jun. Phenomics. 2021. PMID: 36939782 Free PMC article.
Genetic Spectrum of Congenital Anomalies of the Kidney and Urinary Tract in Chinese Newborn Genome Project.
Huang Z, Shen Q, Wu B, Wang H, Dong X, Lu Y, Cheng G, Wang L, Lu W, Chen L, Kang W, Li L, Pan X, Wei Q, Zhuang D, Chen D, Yin Z, Yang L, Ni Q, Liu R, Li G, Zhang P, Qian Y, Peng X, Wang Y, Cao Y, Xu H, Hu L, Yang L, Zhou W. Huang Z, et al. Kidney Int Rep. 2023 Aug 14;8(11):2376-2384. doi: 10.1016/j.ekir.2023.08.005. eCollection 2023 Nov. Kidney Int Rep. 2023. PMID: 38025242 Free PMC article.
A Cohort Study on Deficiency of ADA2 from China.
Li GM, Han X, Wu Y, Wang W, Tang HX, Lu MP, Tang XM, Lin Y, Deng F, Yang J, Wang XN, Liu CC, Zheng WJ, Wu BB, Zhou F, Luo H, Zhang L, Liu HM, Guan WZ, Wang SH, Tao PF, Jin TJ, Fang R, Wu Y, Zhang J, Zhang Y, Zhang TN, Yin W, Guo L, Tang WJ, Chang H, Zhang QY, Li XZ, Li JG, Zhou ZX, Yang SR, Yang KK, Xu H, Song HM, Deuitch NT, Lee PY, Zhou Q, Sun L. Li GM, et al. Among authors: wu y, wu bb. J Clin Immunol. 2023 May;43(4):835-845. doi: 10.1007/s10875-023-01432-8. Epub 2023 Feb 18. J Clin Immunol. 2023. PMID: 36807221 Free PMC article.
131 results