Disease-causing mutations in genes of the complement system.
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Non-synonymous polymorphisms in the FCN1 gene determine ligand-binding ability and serum levels of M-ficolinStructural basis for activation of the complement system by component C4 cleavageComplement in Lupus Nephritis: New PerspectivesMannose-binding lectin and the balance between immune protection and complicationPhenotypic expansion of DGKE-associated diseasesThe role of CRP and inflammation in the pathogenesis of age-related macular degeneration.Comparison of human blood concentrations of collectin kidney 1 and mannan-binding lectin.Complement in animal development: unexpected roles of a highly conserved pathway.Genome-wide association studies: getting to pathogenesis, the role of inflammation/complement in age-related macular degenerationPolymorphisms in the MASP1 gene are associated with serum levels of MASP-1, MASP-3, and MAp44The lectin pathway of complement and rheumatic heart disease.Genetic factors regulating lung vasculature and immune cell functions associate with resistance to pneumococcal infectionMannose binding lectin and susceptibility to rheumatoid arthritis in Brazilian patients and their relatives.Rare loss-of-function mutation in complement component C3 provides insight into molecular and pathophysiological determinants of complement activityLectin complement protein Collectin 11 (CL-K1) and susceptibility to urinary schistosomiasis.Complement-mediated neutralization of dengue virus requires mannose-binding lectinRole of complement and complement regulatory proteins in the complications of diabetesCollectin CL-LK Is a Novel Soluble Pattern Recognition Receptor for Mycobacterium tuberculosisNovel MASP1 mutations are associated with an expanded phenotype in 3MC1 syndromeLow level of MAp44, an inhibitor of the lectin complement pathway, and long-term graft and patient survival; a cohort study of 382 kidney recipientsComplement factor I deficiency: a not so rare immune defect: characterization of new mutations and the first large gene deletionSusceptibility to advanced age-related macular degeneration and alleles of complement factor H, complement factor B, complement component 2, complement component 3, and age-related maculopathy susceptibility 2 genes in a Mexican population.Complement defects in patients with chronic rhinosinusitis.Progress and Trends in Complement TherapeuticsMannose-binding lectin protein and its association to clinical outcomes in COPD: a longitudinal study.Complement genetics, deficiencies, and disease associations.Association between endogenous complement inhibitor and myocardial salvage in patients with myocardial infarction.The complement system in ischemia-reperfusion injuriesFamilial Recurrence of 3MC Syndrome in Consanguineous Families: A Clinical and Molecular Diagnostic Approach With Review of the Literature.The emerging roles of mannose-binding lectin-associated serine proteases (MASPs) in the lectin pathway of complement and beyond.Complement regulation and kidney diseases: recent knowledge of the double-edged roles of complement activation in nephrology.[Primary immunodeficiency].Mannose binding lectin and ficolin-2 polymorphisms are associated with increased risk for bacterial infections in children with B acute lymphoblastic leukemia.Mitochondria and the lectin pathway of complement.Lectin pathway of complement activation and relation with clinical complications in critically ill children.Plasma levels of mannan-binding lectin (MBL)-associated serine proteases (MASPs) and MBL-associated protein in cardio- and cerebrovascular diseases.Endogenous Natural Complement Inhibitor Regulates Cardiac Development.Mannan-binding lectin (MBL)-associated serine protease-1 (MASP-1), a serine protease associated with humoral pattern-recognition molecules: normal and acute-phase levels in serum and stoichiometry of lectin pathway components.Lectin complement pathway proteins in healthy individuals.Cutaneous Vasculitis and Recurrent Infection Caused by Deficiency in Complement Factor I.
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Disease-causing mutations in genes of the complement system.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on June 2011
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Disease-causing mutations in genes of the complement system.
@en
Disease-causing mutations in genes of the complement system.
@nl
type
label
Disease-causing mutations in genes of the complement system.
@en
Disease-causing mutations in genes of the complement system.
@nl
prefLabel
Disease-causing mutations in genes of the complement system.
@en
Disease-causing mutations in genes of the complement system.
@nl
P2860
P1476
Disease-causing mutations in genes of the complement system.
@en
P2093
Jens C Jensenius
P2860
P304
P356
10.1016/J.AJHG.2011.05.011
P407
P577
2011-06-01T00:00:00Z