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Showing results (131-140 of 137) with videos related to

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Journal of Immunology (Baltimore, Md. : 1950)|March 4, 2018
Statistical Validation of Rare Complement Variants Provides Insights into the Molecular Basis of Atypical Hemolytic Uremic Syndrome and C3 GlomerulopathyAmy J Osborne, Matteo Breno, Nicolo Ghiringhelli Borsa, et al.
Clinical Journal of the American Society of Nephrology : CJASN|September 23, 2021
C3 Glomerulopathy and Related Disorders in Children: Etiology-Phenotype Correlation and OutcomesEdwin K S Wong, Kevin J Marchbank, Hannah Lomax-Browne, et al.
Blood|September 18, 2008
Mutations in complement C3 predispose to development of atypical hemolytic uremic syndromeVeronique Frémeaux-Bacchi, Elizabeth C Miller, M Kathryn Liszewski, et al.
Kidney International|June 18, 2004
Lack of major involvement of human uroplakin genes in vesicoureteral reflux: implications for disease heterogeneitySongshan Jiang, Jordan Gitlin, Fang-Ming Deng, et al.
American Journal of Human Genetics|August 4, 2015
Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter DevelopmentAsaf Vivante, Marc-Jens Kleppa, Julian Schulz, et al.
Journal of the American Society of Nephrology : JASN|August 23, 2014
Urinary tract effects of HPSE2 mutationsHelen M Stuart, Neil A Roberts, Emma N Hilton, et al.
Plos Genetics|June 4, 2011
Association of genetic variants in complement factor H and factor H-related genes with systemic lupus erythematosus susceptibilityJian Zhao, Hui Wu, Melanie Khosravi, et al.
Pageof 14

Showing results (131-140 of 137) with videos related to

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Pageof 14
You have reached the last page of results.This site can display upto 137 results.
Journal of Immunology (Baltimore, Md. : 1950)|March 4, 2018
Statistical Validation of Rare Complement Variants Provides Insights into the Molecular Basis of Atypical Hemolytic Uremic Syndrome and C3 GlomerulopathyAmy J Osborne, Matteo Breno, Nicolo Ghiringhelli Borsa, et al.
Clinical Journal of the American Society of Nephrology : CJASN|September 23, 2021
C3 Glomerulopathy and Related Disorders in Children: Etiology-Phenotype Correlation and OutcomesEdwin K S Wong, Kevin J Marchbank, Hannah Lomax-Browne, et al.
Blood|September 18, 2008
Mutations in complement C3 predispose to development of atypical hemolytic uremic syndromeVeronique Frémeaux-Bacchi, Elizabeth C Miller, M Kathryn Liszewski, et al.
Kidney International|June 18, 2004
Lack of major involvement of human uroplakin genes in vesicoureteral reflux: implications for disease heterogeneitySongshan Jiang, Jordan Gitlin, Fang-Ming Deng, et al.
American Journal of Human Genetics|August 4, 2015
Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter DevelopmentAsaf Vivante, Marc-Jens Kleppa, Julian Schulz, et al.
Journal of the American Society of Nephrology : JASN|August 23, 2014
Urinary tract effects of HPSE2 mutationsHelen M Stuart, Neil A Roberts, Emma N Hilton, et al.
Plos Genetics|June 4, 2011
Association of genetic variants in complement factor H and factor H-related genes with systemic lupus erythematosus susceptibilityJian Zhao, Hui Wu, Melanie Khosravi, et al.
Pageof 14