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Complement regulator CD46: genetic variants and disease associations

Complement regulator CD46: genetic variants and disease associations

http://www.wikidata.org/entity/Q28263110

about

HUS and atypical HUS.Dysregulation of mCD46 and sCD46 contribute to the pathogenesis of bullous pemphigoid.Minocycline modulates NFκB phosphorylation and enhances antimicrobial activity against Staphylococcus aureus in mesenchymal stromal/stem cells.Complement Dysregulation and Disease: Insights from Contemporary Genetics.Case report - atypical hemolytic uremic syndrome triggered by influenza B Regulators of complement activity mediate inhibitory mechanisms through a common C3b-binding mode.Comprehensive genetic testing for primary immunodeficiency disorders in a tertiary hospital: 10-year experience in Auckland, New Zealand Regulation of Complement-Dependent Cytotoxicity by MicroRNAs miR-200b, miR-200c, and miR-217.Utilizing complement evasion strategies to design complement-based antibacterial immunotherapeutics: Lessons from the pathogenic Neisseriae.Immune Cell Metabolism in Systemic Lupus Erythematosus.Endothelial cells: source, barrier, and target of defensive mediators.Complementopathies.The role of complement inhibitors beyond controlling inflammation.A teleost CD46 is involved in the regulation of complement activation and pathogen infection.Use of Defibrotide to help prevent post-transplant endothelial injury in a genetically predisposed infant with metachromatic leukodystrophy undergoing hematopoietic stem cell gene therapy.Measles Virus Persistent Infection of Human Induced Pluripotent Stem Cells.Mutations in membrane cofactor protein (CD46) gene in Indian children with hemolytic uremic syndrome.

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Complement regulator CD46: genetic variants and disease associations

http://www.wikidata.org/entity/Q28263110

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2015 nî lūn-bûn

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2015 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2015年の論文

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2015年学术文章

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Complement regulator CD46: genetic variants and disease associations

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Complement regulator CD46: genetic variants and disease associations

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Complement regulator CD46: genetic variants and disease associations

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Complement regulator CD46: genetic variants and disease associations

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Complement regulator CD46: genetic variants and disease associations

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Complement regulator CD46: genetic variants and disease associations

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Complement regulator CD46: genetic variants and disease associations

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Complement regulator CD46: genetic variants and disease associations

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Complement regulator CD46: genetic variants and disease associations

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Atypical hemolytic uremic syndrome

Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype

Four viruses, two bacteria, and one receptor: membrane cofactor protein (CD46) as pathogens' magnet

Membrane cofactor protein mutations in atypical hemolytic uremic syndrome (aHUS), fatal Stx-HUS, C3 glomerulonephritis, and the HELLP syndrome

Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome

Genetic variants in the complement system predisposing to age-related macular degeneration: a review

Complement. First of two parts

Are complement deficiencies really rare? Overview on prevalence, clinical importance and modern diagnostic approach

Epidemiological approach to identifying genetic predispositions for atypical hemolytic uremic syndrome

Genetic disorders in complement (regulating) genes in patients with atypical haemolytic uraemic syndrome (aHUS)

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