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Frontiers in Immunology
|
September 6, 2024
Functional evaluation of rare variants in complement factor I using a minigene assay
Cobey 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 syndrome
Fengxiao Bu, Nicole C Meyer, Yuzhou Zhang, et al.
Molecular Immunology
|
August 5, 2016
Familial C3 glomerulonephritis caused by a novel CFHR5-CFHR2 fusion gene
Xue 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 Glomerulopathy
Jill J Hauer, Yuzhou Zhang, Renee Goodfellow, et al.
Frontiers in Immunology
|
January 1, 2021
Factor H Autoantibodies and Complement-Mediated Diseases
Yuzhou 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 Syndrome
Fengxiao 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 syndrome
Yuzhou Zhang, Robin A Kremsdorf, C John Sperati, et al.
Frontiers in Immunology
|
May 27, 2022
Complement Factor I Variants in Complement-Mediated Renal Diseases
Yuzhou 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 Glomerulopathies
Fengxiao 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 glomerulopathy
Amanda K Slagle, Nicolo Ghiringhelli Borsa, Kai Wang, et al.
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of 2
Search research articles
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Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
Frontiers in Immunology
|
September 6, 2024
Functional evaluation of rare variants in complement factor I using a minigene assay
Cobey 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 syndrome
Fengxiao Bu, Nicole C Meyer, Yuzhou Zhang, et al.
Molecular Immunology
|
August 5, 2016
Familial C3 glomerulonephritis caused by a novel CFHR5-CFHR2 fusion gene
Xue 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 Glomerulopathy
Jill J Hauer, Yuzhou Zhang, Renee Goodfellow, et al.
Frontiers in Immunology
|
January 1, 2021
Factor H Autoantibodies and Complement-Mediated Diseases
Yuzhou 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 Syndrome
Fengxiao 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 syndrome
Yuzhou Zhang, Robin A Kremsdorf, C John Sperati, et al.
Frontiers in Immunology
|
May 27, 2022
Complement Factor I Variants in Complement-Mediated Renal Diseases
Yuzhou 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 Glomerulopathies
Fengxiao 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 glomerulopathy
Amanda K Slagle, Nicolo Ghiringhelli Borsa, Kai Wang, et al.
Page
of 2