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Nicolo Ghiringhelli Borsa

Showing results (1-10 of 11) with videos related to

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Frontiers in Immunology|September 6, 2024
Functional evaluation of rare variants in complement factor I using a minigene assayCobey J H Donelson, Nicolo Ghiringhelli Borsa, Amanda O Taylor, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 31, 2015
Soluble c5b-9 as a biomarker for complement activation in atypical hemolytic uremic syndromeFengxiao Bu, Nicole C Meyer, Yuzhou Zhang, et al.
Molecular Immunology|August 5, 2016
Familial C3 glomerulonephritis caused by a novel CFHR5-CFHR2 fusion geneXue Xiao, Cybele Ghossein, Agustín Tortajada, et al.
Kidney International Reports|February 12, 2024
Defining Nephritic Factors as Diverse Drivers of Systemic Complement Dysregulation in C3 GlomerulopathyJill J Hauer, Yuzhou Zhang, Renee Goodfellow, et al.
Frontiers in Immunology|January 1, 2021
Factor H Autoantibodies and Complement-Mediated DiseasesYuzhou Zhang, Nicolo Ghiringhelli Borsa, Dingwu Shao, et al.
Journal of the American Society of Nephrology : JASN|November 1, 2018
Genetic Analysis of 400 Patients Refines Understanding and Implicates a New Gene in Atypical Hemolytic Uremic SyndromeFengxiao Bu, Yuzhou Zhang, Kai Wang, et al.
Kidney International|June 17, 2020
Mutation of complement factor B causing massive fluid-phase dysregulation of the alternative complement pathway can result in atypical hemolytic uremic syndromeYuzhou Zhang, Robin A Kremsdorf, C John Sperati, et al.
Frontiers in Immunology|May 27, 2022
Complement Factor I Variants in Complement-Mediated Renal DiseasesYuzhou Zhang, Renee X Goodfellow, Nicolo Ghiringhelli Borsa, et al.
Journal of the American Society of Nephrology : JASN|August 19, 2015
High-Throughput Genetic Testing for Thrombotic Microangiopathies and C3 GlomerulopathiesFengxiao Bu, Nicolo Ghiringhelli Borsa, Michael B Jones, et al.
Frontiers in Immunology|June 2, 2025
Factor H-related 1 and heparan sulfate architecture contribute to complement dysregulation in C3 glomerulopathyAmanda K Slagle, Nicolo Ghiringhelli Borsa, Kai Wang, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Frontiers in Immunology|September 6, 2024
Functional evaluation of rare variants in complement factor I using a minigene assayCobey J H Donelson, Nicolo Ghiringhelli Borsa, Amanda O Taylor, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 31, 2015
Soluble c5b-9 as a biomarker for complement activation in atypical hemolytic uremic syndromeFengxiao Bu, Nicole C Meyer, Yuzhou Zhang, et al.
Molecular Immunology|August 5, 2016
Familial C3 glomerulonephritis caused by a novel CFHR5-CFHR2 fusion geneXue Xiao, Cybele Ghossein, Agustín Tortajada, et al.
Kidney International Reports|February 12, 2024
Defining Nephritic Factors as Diverse Drivers of Systemic Complement Dysregulation in C3 GlomerulopathyJill J Hauer, Yuzhou Zhang, Renee Goodfellow, et al.
Frontiers in Immunology|January 1, 2021
Factor H Autoantibodies and Complement-Mediated DiseasesYuzhou Zhang, Nicolo Ghiringhelli Borsa, Dingwu Shao, et al.
Journal of the American Society of Nephrology : JASN|November 1, 2018
Genetic Analysis of 400 Patients Refines Understanding and Implicates a New Gene in Atypical Hemolytic Uremic SyndromeFengxiao Bu, Yuzhou Zhang, Kai Wang, et al.
Kidney International|June 17, 2020
Mutation of complement factor B causing massive fluid-phase dysregulation of the alternative complement pathway can result in atypical hemolytic uremic syndromeYuzhou Zhang, Robin A Kremsdorf, C John Sperati, et al.
Frontiers in Immunology|May 27, 2022
Complement Factor I Variants in Complement-Mediated Renal DiseasesYuzhou Zhang, Renee X Goodfellow, Nicolo Ghiringhelli Borsa, et al.
Journal of the American Society of Nephrology : JASN|August 19, 2015
High-Throughput Genetic Testing for Thrombotic Microangiopathies and C3 GlomerulopathiesFengxiao Bu, Nicolo Ghiringhelli Borsa, Michael B Jones, et al.
Frontiers in Immunology|June 2, 2025
Factor H-related 1 and heparan sulfate architecture contribute to complement dysregulation in C3 glomerulopathyAmanda K Slagle, Nicolo Ghiringhelli Borsa, Kai Wang, et al.
Pageof 2