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Title
Genetic analysis of the complement pathway in C3 glomerulopathy
Authors
Keywords
-
Journal
NEPHROLOGY DIALYSIS TRANSPLANTATION
Volume -, Issue -, Pages -
Publisher
Oxford University Press (OUP)
Online
2018-02-01
DOI
10.1093/ndt/gfy033
References
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Related references
Note: Only part of the references are listed.- Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference
- (2017) Timothy H.J. Goodship et al. KIDNEY INTERNATIONAL
- A haplotype in CFH family genes confers high risk of rare glomerular nephropathies
- (2017) Yin Ding et al. Scientific Reports
- Comprehensive Analysis of Complement Genes in Patients with Atypical Hemolytic Uremic Syndrome
- (2016) Tao Zhang et al. AMERICAN JOURNAL OF NEPHROLOGY
- Complement gene variants determine the risk of immunoglobulin-associated MPGN and C3 glomerulopathy and predict long-term renal outcome
- (2016) Paraskevas Iatropoulos et al. MOLECULAR IMMUNOLOGY
- ConSurf 2016: an improved methodology to estimate and visualize evolutionary conservation in macromolecules
- (2016) Haim Ashkenazy et al. NUCLEIC ACIDS RESEARCH
- Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
- (2015) Sue Richards et al. GENETICS IN MEDICINE
- High-Throughput Genetic Testing for Thrombotic Microangiopathies and C3 Glomerulopathies
- (2015) F. Bu et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- New functional and structural insights from updated mutational databases for complement factor H, Factor I, membrane cofactor protein and C3
- (2014) Elizabeth Rodriguez et al. BIOSCIENCE REPORTS
- Rapid and cost effective screening of breast and ovarian cancer genes using novel sequence capture method in clinical samples
- (2014) Kristóf Árvai et al. Familial Cancer
- Analysis of patients with atypical hemolytic uremic syndrome treated at the Mie University Hospital: concentration of C3 p.I1157T mutation
- (2014) Takeshi Matsumoto et al. INTERNATIONAL JOURNAL OF HEMATOLOGY
- Guidelines for investigating causality of sequence variants in human disease
- (2014) D. G. MacArthur et al. NATURE
- Genetics and Outcome of Atypical Hemolytic Uremic Syndrome: A Nationwide French Series Comparing Children and Adults
- (2013) V. Fremeaux-Bacchi et al. Clinical Journal of the American Society of Nephrology
- C3 glomerulopathy: consensus report
- (2013) Matthew C. Pickering et al. KIDNEY INTERNATIONAL
- Analysis of genetic and predisposing factors in Japanese patients with atypical hemolytic uremic syndrome
- (2013) Xinping Fan et al. MOLECULAR IMMUNOLOGY
- Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies
- (2012) Aude Servais et al. KIDNEY INTERNATIONAL
- Membranoproliferative Glomerulonephritis — A New Look at an Old Entity
- (2012) Sanjeev Sethi et al. NEW ENGLAND JOURNAL OF MEDICINE
- Membranoproliferative Glomerulonephritis: Pathogenetic Heterogeneity and Proposal for a New Classification
- (2011) Sanjeev Sethi et al. SEMINARS IN NEPHROLOGY
- C3 glomerulopathy: a new classification
- (2010) Fadi Fakhouri et al. Nature Reviews Nephrology
- Mutations in components of complement influence the outcome of Factor I-associated atypical hemolytic uremic syndrome
- (2009) Frank Bienaime et al. KIDNEY INTERNATIONAL
- Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome
- (2008) V. Fremeaux-Bacchi et al. BLOOD
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