Systemic Lupus Erythematosus and Deficiencies of Early Components of the Complement Classical Pathway
about
Type I interferonopathies in pediatric rheumatologyLupus pathobiology based on genomics.New milestones ahead in complement-targeted therapy.Can Cell Bound Complement Activation Products Predict Inherited Complement Deficiency in Systemic Lupus Erythematosus?Keeping It All Going-Complement Meets MetabolismThe complement system as a potential therapeutic target in rheumatic disease.Production of complement components by cells of the immune system.Old dogs-new tricks: immunoregulatory properties of C3 and C5 cleavage fragments.Viral-derived complement inhibitors: current status and potential role in immunomodulation.The many ways tissue phagocytes respond to dying cells.Pathogenesis of Human Systemic Lupus Erythematosus: A Cellular Perspective.C1q Deficiency and Neuropsychiatric Systemic Lupus ErythematosusImmunodeficiency and autoimmunity coming together: a nearly missed diagnosis.Circadian clock cryptochrome proteins regulate autoimmunity.Approach to a Child with Primary Immunodeficiency Made Simple.Monogenic interferonopathies: Phenotypic and genotypic findings of CANDLE syndrome and its overlap with C1q deficient SLE.Complement-activation fragment C4a mediates effector functions by binding as untethered agonist to protease-activated receptors 1 and 4.Complement Immune Evasion by Spirochetes.Systemic lupus erythematosus with C1q deficiency: treatment with fresh frozen plasma.Coagulation cascade and complement system in systemic lupus erythematosus.Role of Murine Complement Component C5 in Acute in Vivo Infection by Pathogenic Leptospira interrogans.The Complement System and C1q in Chronic Hepatitis C Virus Infection and Mixed Cryoglobulinemia.Insights Gained From the Study of Pediatric Systemic Lupus Erythematosus.Complement deficiency in pediatric-onset systemic lupus erythematosus.Investigation of C1-complex regions reveals new C1Q variants associated with protection from systemic lupus erythematosus, and affect its transcript abundance.Cutaneous Vasculitis and Digital Ischaemia Caused by Heterozygous Gain-of-Function Mutation inMonogenic Lupus: A Developing Paradigm of Disease
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P2860
Systemic Lupus Erythematosus and Deficiencies of Early Components of the Complement Classical Pathway
description
2016 nî lūn-bûn
@nan
2016 թուականին հրատարակուած գիտական յօդուած
@hyw
2016 թվականին հրատարակված գիտական հոդված
@hy
2016年の論文
@ja
2016年学术文章
@wuu
2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
name
Systemic Lupus Erythematosus a ...... e Complement Classical Pathway
@ast
Systemic Lupus Erythematosus a ...... e Complement Classical Pathway
@en
Systemic Lupus Erythematosus a ...... e Complement Classical Pathway
@nl
type
label
Systemic Lupus Erythematosus a ...... e Complement Classical Pathway
@ast
Systemic Lupus Erythematosus a ...... e Complement Classical Pathway
@en
Systemic Lupus Erythematosus a ...... e Complement Classical Pathway
@nl
prefLabel
Systemic Lupus Erythematosus a ...... e Complement Classical Pathway
@ast
Systemic Lupus Erythematosus a ...... e Complement Classical Pathway
@en
Systemic Lupus Erythematosus a ...... e Complement Classical Pathway
@nl
P2860
P3181
P356
P1476
Systemic Lupus Erythematosus a ...... e Complement Classical Pathway
@en
P2093
Ana Catarina Lunz Macedo
P2860
P3181
P356
10.3389/FIMMU.2016.00055
P407
P577
2016-01-01T00:00:00Z