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Cited by in F6Publishing
For: Yue Z, Lin H, Li M, Wang H, Liu T, Hu M, Chen H, Tong H, Sun L. Clinical and pathological features and varied mutational spectra of pathogenic genes in 55 Chinese patients with nephronophthisis. Clin Chim Acta 2020;506:136-44. [PMID: 32173348 DOI: 10.1016/j.cca.2020.03.015] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
Number Citing Articles
1 Wang X, Xiao H, Yao Y, Xu K, Liu X, Su B, Zhang H, Guan N, Zhong X, Zhang Y, Ding J, Wang F. Spectrum of Mutations in Pediatric Non-glomerular Chronic Kidney Disease Stages 2-5. Front Genet 2021;12:697085. [PMID: 34295353 DOI: 10.3389/fgene.2021.697085] [Reference Citation Analysis]
2 Li D, Hu M, Chen H, Wu X, Wei X, Lin H, Gao X, Wang H, Li M, Ong ACM, Yue Z, Sun L. An Nphp1 knockout mouse model targeting exon 2-20 demonstrates characteristic phenotypes of human Nephronophthisis. Hum Mol Genet 2021:ddab239. [PMID: 34415307 DOI: 10.1093/hmg/ddab239] [Reference Citation Analysis]
3 Wu X, Wang H, Chen H, Lin H, Li M, Yue Z, Sun L. Overexpression of smad7 inhibits the TGF-β/Smad signaling pathway and EMT in NPHP1-defective MDCK cells. Biochem Biophys Res Commun 2021;582:57-63. [PMID: 34689106 DOI: 10.1016/j.bbrc.2021.10.037] [Reference Citation Analysis]