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Cell-type-specific molecular characterization of cells from circulation and kidney in IgA nephropathy with nephrotic syndrome.
Chen Q, Jiang H, Ding R, Zhong J, Li L, Wan J, Feng X, Peng L, Yang X, Chen H, Wang A, Jiao J, Yang Q, Chen X, Li X, Shi L, Zhang G, Wang M, Yang H, Li Q. Chen Q, et al. Among authors: jiao j. Front Immunol. 2023 Oct 16;14:1231937. doi: 10.3389/fimmu.2023.1231937. eCollection 2023. Front Immunol. 2023. PMID: 37908345 Free PMC article.
Relationships between the clinical phenotypes and genetic variants associated with the immunological mechanism in childhood idiopathic nephrotic syndrome: protocol for a prospective observational single-centre cohort study.
Chan H, Lee H, Yang X, Wang J, Yang X, Gan C, Xiao H, Li Q, Jiao J, Wu D, Zhang G, Wang M, Yang H, Li Q. Chan H, et al. Among authors: jiao j. BMJ Open. 2019 Aug 28;9(8):e028717. doi: 10.1136/bmjopen-2018-028717. BMJ Open. 2019. PMID: 31467050 Free PMC article.
Whole-exome sequencing of a multicenter cohort identifies genetic changes associated with clinical phenotypes in pediatric nephrotic syndrome.
Jiao J, Wang L, Ni F, Wang M, Feng S, Gao X, Chan H, Yang X, Lee H, Chi H, Chen X, Wu D, Zhang G, Yang B, Wang A, Yang Q, Wan J, Yu S, Li X, Wang M, Chen X, Mai X, Ruan X, Yang H, Li Q. Jiao J, et al. Genes Dis. 2022 May 5;9(6):1662-1673. doi: 10.1016/j.gendis.2022.03.023. eCollection 2022 Nov. Genes Dis. 2022. PMID: 36157477 Free PMC article.
A genomic association study revealing subphenotypes of childhood steroid-sensitive nephrotic syndrome in a larger genomic sequencing cohort.
Chan H, Ni F, Zhao B, Jiang H, Ding J, Wang L, Wang X, Cui J, Feng S, Gao X, Yang X, Chi H, Lee H, Chen X, Li X, Jiao J, Wu D, Zhang G, Wang M, Cun Y, Ruan X, Yang H, Li Q. Chan H, et al. Among authors: jiao j. Genes Dis. 2023 Sep 27;11(4):101126. doi: 10.1016/j.gendis.2023.101126. eCollection 2024 Jul. Genes Dis. 2023. PMID: 38560502 Free PMC article.
3,252 results