Publications by authors named "Hongrong Lin"

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A CD3G homozygous pathogenic variant in a Chinese child with lupus-like disease, autoimmune thyroiditis and immunodeficiency.
Hongrong Lin, Shuai Chu, Cui Tang, Sijin Wang, Yong Cai

Clin Chim Acta· September 2024

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Identification of renal cyst cells of type I Nephronophthisis by single-nucleus RNA sequencing.
Qianying Wang, Baojuan Zou, Xiaoya Wei, Hongrong Lin, Changmiao Pang, Jinglin Zhong

Front Cell Dev Biol· July 2023

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Reducing GEF-H1 Expression Inhibits Renal Cyst Formation, Inflammation, and Fibrosis via RhoA Signaling in Nephronophthisis.
Qiulei Hu, Jiayong Lai, Huamu Chen, Yong Cai, Zhihui Yue, Hongrong Lin

Int J Mol Sci· February 2023

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mutation associated isolated nephropathy in two siblings from a Chinese pedigree.
Min Li, Zhihui Yue, Hongrong Lin, Haiyan Wang, Huamu Chen

Ren Fail· December 2021

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An Nphp1 knockout mouse model targeting exon 2-20 demonstrates characteristic phenotypes of human nephronophthisis.
Dantong Li, Miaoyue Hu, Huamu Chen, Xiaohong Wu, Xiaoya Wei, Hongrong Lin

Hum Mol Genet· December 2021

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Overexpression of smad7 inhibits the TGF-β/Smad signaling pathway and EMT in NPHP1-defective MDCK cells.
Xiaohong Wu, Haiyan Wang, Huamu Chen, Hongrong Lin, Min Li

Biochem Biophys Res Commun· December 2021

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A novel ITGA3 homozygous splice mutation in an ILNEB syndrome child with slow progression.
Yaqing Liu, Zhihui Yue, Haiyan Wang, Min Li, Xiaohong Wu, Hongrong Lin, Shuling Lan

Clin Chim Acta· December 2021

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Cyclosporine A relieved proteinuria and hypoproteinemia in DGKE nephropathy.
Wenjun Fu, Min Li, Hongrong Lin, Youjing Xu, Wei Han

Clin Chim Acta· July 2021

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Clinical and pathological features and varied mutational spectra of pathogenic genes in 55 Chinese patients with nephronophthisis.
Zhihui Yue, Hongrong Lin, Min Li, Haiyan Wang, Ting Liu

Clin Chim Acta· July 2020

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A new therapy in Epstein-Barr virus-associated lymphoproliferative disease: a case report and a revision of the literature.
Lingling Xu, Hongjun Ba, Hongrong Lin, Liangying Zhong, Suping Li

Ital J Pediatr· November 2019

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Two Chinese nephronophthisis pedigrees harbored a compound heterozygous deletion with a point mutation in .
Huamu Chen, Hongrong Lin, Zhihui Yue, Haiyan Wang, Junhui Yang

Int J Mol Epidemiol Genet· August 2019

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WT1 mutation-associated nephropathy: a single-center experience
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Zhihui Yue, Haiyan Wang, Hongrong Lin, Juan Yang, Ting Liu, Yulin Liu

Clin Nephrol· May 2017

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[Clinical and pathological features and the misdiagnosis of childhood Alport syndrome: a retrospective analysis of 91 cases].
Yan-Zhen Chen, Liang-Zhong Sun, Hai-Yan Wang, Xiao-Yun Jiang, Ying Mo, Hong-Rong Lin

Zhongguo Dang Dai Er Ke Za Zhi· April 2017

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High mutation rate of NPHP3 in 18 Chinese infantile nephronophthisis patients.
Liangzhong Sun, Huajuan Tong, Haiyan Wang, Zhihui Yue, Ting Liu, Hongrong Lin

Nephrology (Carlton)· March 2016

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