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Factor H
Regulation of the Complement System by Pentraxins
Nephrology Clinical Laboratory Research Compendium
O) 2 Platelets Mediated by Properdin and C3(H Complement Activation on Stimulated Identification of a Novel Mode Of
Proteomic Alterations of HDL in Youth with Type 1 Diabetes and Their Associations with Glycemic Control: a Case-Control Study Evgenia Gourgari Georgetown University
Hemolytic Uremic Syndrome: a Factor H Mutation (E1172stop) Causes Defective Complement Control at the Surface of Endothelial Cells
Activation at Cell Surfaces Factor H in Regulating Complement Critical
Antibody Inhibition of Properdin Prevents Complement-Mediated Intravascular and Extravascular Hemolysis
Factor H and Atypical Hemolytic Uremic Syndrome: Mutations in the C-Terminus Cause Structural Changes and Defective Recognition Functions
C1-Esterase Inhibitor
Supplementary Figure 1. Estimation of the Percentage of Volume of Each Population of Extracellular Vesicles by Dynamic Light Scattering
Monoclonal Antibodies: Anti-Human Factor H#2
The Alternative Complement Pathway Is Activated in Protoporphyria Patients During Sun Exposure
Complement As a Therapeutic Target in Systemic Autoimmune Diseases
Protein, and Associates with Lipoprotein Activity, Binds Heparin
Protein Load Impairs Factor H Binding Promoting Complement-Dependent Dysfunction of Proximal Tubular Cells
Monomeric CRP Contributes to Complement Control in Fluid Phase and on Cellular Surfaces and Increases Phagocytosis by Recruiting
Ahus COMPLEMENT PROFILE
Complement and Acute Phase Proteins in Inflammation
Top View
Complement Factor I Deficiency Associated with Recurrent Meningitis Coinciding with Menstruation
Complement Factor H: Solution Structures and Interactions with Ligands
Phospholipase A2 Receptor–Related Membranous Nephropathy and Mannan-Binding Lectin Deficiency
Atypical Hemolytic Uremic Syndrome Associated with Complement Factor H Autoantibodies and CFHR1/CFHR3 Deficiency
Protein H Affects Binding Affinity to C-Reactive Y402H Polymorphism of Complement Factor
Rare Variants in the Complement Factor H–Related Protein 5 Gene Contribute to Genetic Susceptibility to Iga Nephropathy
Complement Factor H Levels Are Decreased and Correlated with Serum C-Reactive Protein in Late-Onset Alzheimer's Disease
C3 Dysregulation Due to Factor H Deficiency Is
Supporting Information
Haemolytic Uraemic Syndrome and Mutations of the Factor H Gene
A Dissertation Entitled Role of Complement Regulatory Proteins
Family and Plasminogen That Binds Three Members of the Factor H Surface-Exposed Immune Evasion Protein Is a Pseudomonas Aerugino
Pathway Function MASP-1
THROMBOTIC MICROANGIOPATHY (Ahus and TTP) TEST REQUISITION All Information Must Be Completed Before Sample Can Be Processed
Factor H–Igg Chimeric Proteins As a Therapeutic Approach Against the Gram-Positive Bacterial Pathogen Streptococcus Pyogenes
Complement Deficiency
Pearls of Laboratory Medicine
COMPLEMENT FACTOR H ELISA DETECTION of Igg ANTIBODIES
Effect of Supraphysiologic Levels of C1-Inhibitor on the Classical, Lectin and Alternative Pathways of Complement
The Story of Complement Factor I T Peter J Lachmann
Variation of Complement Factor H and Mannan Binding Lectin in Human
Structural Basis for the Stabilization of the Complement Alternative Pathway C3 Convertase by Properdin
Recruitment of Human C1 Esterase Inhibitor Controls Complement Activation on Blood Stage Plasmodium Falciparum Merozoites
Potential Influences of Complement Factor H in Autoimmune Inflammatory and Thrombotic Disorders
Erythrocytes Human Complement Receptor 1 on Complement Factor
Identification and Characterisation of Novel Plasma Clot Components
Human Complement Factor H Is a Novel Diagnostic Marker for Lung Adenocarcinoma
Factor H Uptake Regulates Intracellular C3 Activation During Apoptosis and Decreases the Inflammatory Potential of Nucleosomes
High Sensitivity Human C-Reactive Protein (Hscrp)
Serum-Based Proteomics Profiling in Adult Patients with Cystic Fibrosis
Myriad RBM Discoverymap® 250+ V. 1.0
Gain-Of-Function Factor H–Related 5 Protein Impairs Glomerular Complement Regulation Resulting in Kidney Damage
Interlink Between Inflammation and Oxidative Stress in Age-Related Macular Degeneration: Role of Complement Factor H
Complement Proteins As Soluble Pattern Recognition Receptors for Pathogenic Viruses
Combination of Factor H Mutation and Properdin Deficiency Causes Severe C3 Glomerulonephritis
Autoantibodies Against C-Reactive Protein Influence Complement
Factor H Catalog Number: A137 Sizes Available: 250 Μg/Vial Concentration
Methods for Industrial Scale Production of Therapeutic Complement Factor H Preparations from Human Plasma
Direct Activation of the Alternative Complement Pathway by SARS-Cov-2 Spike Proteins Is Blocked by Factor D Inhibition