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Hongrong Lin

Showing results (1-10 of 13) with videos related to

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Clinica Chimica Acta; International Journal of Clinical Chemistry|August 2, 2024
A CD3G homozygous pathogenic variant in a Chinese child with lupus-like disease, autoimmune thyroiditis and immunodeficiencyHongrong Lin, Shuai Chu, Cui Tang, et al.
Renal Failure|January 5, 2021
<i>COQ2</i> mutation associated isolated nephropathy in two siblings from a Chinese pedigreeMin Li, Zhihui Yue, Hongrong Lin, et al.
International Journal of Molecular Epidemiology and Genetics|September 17, 2019
Two Chinese nephronophthisis pedigrees harbored a compound heterozygous deletion with a point mutation in <i>NPHP1</i>Huamu Chen, Hongrong Lin, Zhihui Yue, et al.
International Journal of Molecular Sciences|February 25, 2023
Reducing GEF-H1 Expression Inhibits Renal Cyst Formation, Inflammation, and Fibrosis via RhoA Signaling in NephronophthisisQiulei Hu, Jiayong Lai, Huamu Chen, et al.
Biochemical and Biophysical Research Communications|October 24, 2021
Overexpression of smad7 inhibits the TGF-β/Smad signaling pathway and EMT in NPHP1-defective MDCK cellsXiaohong Wu, Haiyan Wang, Huamu Chen, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 20, 2021
Cyclosporine A relieved proteinuria and hypoproteinemia in DGKE nephropathyWenjun Fu, Min Li, Hongrong Lin, et al.
Clinical Nephrology|March 4, 2017
WT1 mutation-associated nephropathy: a single-center experience
Zhihui Yue, Haiyan Wang, Hongrong Lin, et al.
Nephrology (Carlton, Vic.)|July 18, 2015
High mutation rate of NPHP3 in 18 Chinese infantile nephronophthisis patientsLiangzhong Sun, Huajuan Tong, Haiyan Wang, et al.
Italian Journal of Pediatrics|November 6, 2019
A new therapy in Epstein-Barr virus-associated lymphoproliferative disease: a case report and a revision of the literatureLingling Xu, Hongjun Ba, Hongrong Lin, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 17, 2020
Clinical and pathological features and varied mutational spectra of pathogenic genes in 55 Chinese patients with nephronophthisisZhihui Yue, Hongrong Lin, Min Li, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 2, 2024
A CD3G homozygous pathogenic variant in a Chinese child with lupus-like disease, autoimmune thyroiditis and immunodeficiencyHongrong Lin, Shuai Chu, Cui Tang, et al.
Renal Failure|January 5, 2021
<i>COQ2</i> mutation associated isolated nephropathy in two siblings from a Chinese pedigreeMin Li, Zhihui Yue, Hongrong Lin, et al.
International Journal of Molecular Epidemiology and Genetics|September 17, 2019
Two Chinese nephronophthisis pedigrees harbored a compound heterozygous deletion with a point mutation in <i>NPHP1</i>Huamu Chen, Hongrong Lin, Zhihui Yue, et al.
International Journal of Molecular Sciences|February 25, 2023
Reducing GEF-H1 Expression Inhibits Renal Cyst Formation, Inflammation, and Fibrosis via RhoA Signaling in NephronophthisisQiulei Hu, Jiayong Lai, Huamu Chen, et al.
Biochemical and Biophysical Research Communications|October 24, 2021
Overexpression of smad7 inhibits the TGF-β/Smad signaling pathway and EMT in NPHP1-defective MDCK cellsXiaohong Wu, Haiyan Wang, Huamu Chen, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 20, 2021
Cyclosporine A relieved proteinuria and hypoproteinemia in DGKE nephropathyWenjun Fu, Min Li, Hongrong Lin, et al.
Clinical Nephrology|March 4, 2017
WT1 mutation-associated nephropathy: a single-center experience
Zhihui Yue, Haiyan Wang, Hongrong Lin, et al.
Nephrology (Carlton, Vic.)|July 18, 2015
High mutation rate of NPHP3 in 18 Chinese infantile nephronophthisis patientsLiangzhong Sun, Huajuan Tong, Haiyan Wang, et al.
Italian Journal of Pediatrics|November 6, 2019
A new therapy in Epstein-Barr virus-associated lymphoproliferative disease: a case report and a revision of the literatureLingling Xu, Hongjun Ba, Hongrong Lin, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 17, 2020
Clinical and pathological features and varied mutational spectra of pathogenic genes in 55 Chinese patients with nephronophthisisZhihui Yue, Hongrong Lin, Min Li, et al.
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