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CFHR1
Modulation of the Alternative Pathway of Complement by Murine Factor H–Related Proteins
Complement Factor H Deficiency and Endocapillary Glomerulonephritis Due to Paternal Isodisomy and a Novel Factor H Mutation
Mai Muudatuntuu Ti on Man Mini
A Hybrid CFHR3-1 Gene Causes Familial C3 Glomerulopathy
Cell-Deposited Matrix Improves Retinal Pigment Epithelium Survival on Aged Submacular Human Bruch’S Membrane
Genetic Analysis of 400 Patients Refines Understanding And
Integrated Functional Genomic Analysis Enables Annotation of Kidney Genome-Wide Association Study Loci
Rare Variants in the Complement Factor H–Related Protein 5 Gene Contribute to Genetic Susceptibility to Iga Nephropathy
Routine Use of Clinical Exome-Based Next-Generation Sequencing for Evaluation of Patients with Thrombotic Microangiopathies
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CFHR Gene Variations Provide Insights in the Pathogenesis of the Kidney Diseases Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy
CFHR1 Monoclonal Antibody (M01), Clone 4D7
Downloaded in October 2016) Were Retained for The
Curriculum Vitae
Positive Association of Common Variants in CD36 with Neovascular Age-Related Macular Degeneration
Sequence and Expression of Complement Factor H Gene Cluster Variants and Their Roles in Age-Related Macular Degeneration Risk
UNIVERSITY of CALIFORNIA, SAN DIEGO Compressing and Querrying the Human Genome a Dissertation Submitted in Partial Satisfaction
Structural Insight on CFHR1 Deficiency in AI-Ahus the Major Autoantibody Epitope on Factor H in Atypical Hemolytic Uremic Syndro
Top View
Variation of Complement Factor H and Mannan Binding Lectin in Human
Microsatellite Scanning of the Immunogenome for Associations with Graft-Versus-Host Disease Following Haematopoietic Stem Cell Transplantation
The 15Q11.2 BP1-BP2 Microdeletion
A Hybrid CFHR3-1 Gene Causes Familial C3 Glomerulopathy
A Genome-Wide Association Study Identifies Key Modulators of Complement Factor H Binding to Malondialdehyde-Epitopes
Complement Factor H C-Terminus and Its Significance
Deletions in Genes Participating in Innate Immune Response Modify the Clinical Course of Andes Orthohantavirus Infection
View of Epidermal Growth Factor Receptor/HER2 In- 11
Statistical Validation of Rare Complement Variants Provides
Mouse Genetics and Proteomic Analyses Demonstrate a Critical Role for Complement in a Model of DHRD/ML, an Inherited Macular Degeneration
A Mega-Analysis of Expression Quantitative Trait Loci (Eqtl) Provides Insight Into the Regulatory Architecture of Gene Expressio
Abstracts from the 51St European Society of Human Genetics Conference: Oral Presentations
CFHR Gene Variations Provide Insights in the Pathogenesis of the Kidney Diseases Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy