Association of mutations in mannose binding protein gene with childhood infection in consecutive hospital series.
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Mannose-binding lectin-deficient mice are susceptible to infection with Staphylococcus aureusBeta-defensin genomic copy number is not a modifier locus for cystic fibrosis.Genetics of susceptibility to human infectious diseaseMannose-binding lectin and maladies of the bowel and liverCISH and susceptibility to infectious diseasesLectin complement pathway gene profile of donor and recipient determine the risk of bacterial infections after orthotopic liver transplantationPolymorphisms of the mannose binding lectin gene in patients with Sjögren's syndromeThe mannose binding lectin gene influences the severity of chronic liver disease in cystic fibrosisRecurrent miscarriage and variant alleles of mannose binding lectin, tumour necrosis factor and lymphotoxin alpha genesDifferential recognition of obligate anaerobic bacteria by human mannose-binding lectinMannose-binding lectin binds to a range of clinically relevant microorganisms and promotes complement depositionMannose-binding lectin contributes to deleterious inflammatory response in pandemic H1N1 and avian H9N2 infection.Deficient serum mannose-binding lectin levels and MBL2 polymorphisms increase the risk of single and recurrent Cryptosporidium infections in young children.Conformation of a trimannoside bound to mannose-binding protein by nuclear magnetic resonance and molecular dynamics simulations.Direct Fmoc/tert-Bu solid phase synthesis of octamannosyl polylysine dendrimer-peptide conjugates.Mannan-binding lectin in children with Escherichia coli O157:H7 haemmorrhagic colitis and haemolytic uraemic syndrome.Characterization of the cytokine immune response in children who have experienced an episode of typical hemolytic-uremic syndrome.Genetic and other factors determining mannose-binding lectin levels in American Indians: the Strong Heart Study.Mannose-binding lectin genotypes: lack of association with susceptibility to thoracic empyema.Genetic polymorphisms associated with acute lung injury.Association of mannose-binding lectin gene heterogeneity with severity of lung disease and survival in cystic fibrosis.Clinical and genetic risk factors for pneumonia in systemic lupus erythematosus.Human SP-A protein variants derived from one or both genes stimulate TNF-alpha production in the THP-1 cell line.Recombinant form of human wild type mannan-binding lectin (MBL/A) but not its structural variant (MBL/C) promotes phagocytosis of zymosan by activating complement.Human serum mannose-binding lectin senses wall teichoic acid Glycopolymer of Staphylococcus aureus, which is restricted in infancy.Enhancement of protective efficacy following intranasal immunization with vaccine plus a nontoxic LTK63 mutant delivered with nanoparticlesNeutrophil disorders and their management.Disseminated candidiasis and hepatic malarial infection in mannose-binding-lectin-A-deficient mice.Protective molecules--C-reactive protein (CRP), serum amyloid P (SAP), pentraxin3 (PTX3), mannose-binding lectin (MBL), and apolipoprotein A1 (Apo A1), and their autoantibodies: prevalence and clinical significance in autoimmunity.Mannose-binding lectin in innate immunity: past, present and future.Mannan-binding lectin and its role in innate immunity.Assay of locus-specific genetic load implicates rare Toll-like receptor 4 mutations in meningococcal susceptibilityThe immunopathogenesis of meningococcal disease.Invasive pneumococcal disease in Oxford, 1985-2001: a retrospective case series.Mannan binding lectin deficiency and concomitant immunodefects.MBL2 genotypes and their associations with MBL levels and NICU morbidity in a cohort of Greek neonates.Mannan binding lectin in febrile adults: no correlation with microbial infection and complement activationDeficiency of functional mannose-binding lectin is not associated with infections in patients with systemic lupus erythematosusA population-based study of morbidity and mortality in mannose-binding lectin deficiency.The effect of weight loss on serum mannose-binding lectin levels.
P2860
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P2860
Association of mutations in mannose binding protein gene with childhood infection in consecutive hospital series.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
1997年论文
@zh
1997年论文
@zh-cn
name
Association of mutations in ma ...... n consecutive hospital series.
@ast
Association of mutations in ma ...... n consecutive hospital series.
@en
type
label
Association of mutations in ma ...... n consecutive hospital series.
@ast
Association of mutations in ma ...... n consecutive hospital series.
@en
prefLabel
Association of mutations in ma ...... n consecutive hospital series.
@ast
Association of mutations in ma ...... n consecutive hospital series.
@en
P2093
P1433
P1476
Association of mutations in ma ...... n consecutive hospital series.
@en
P2093
Summerfield JA
P304
P356
10.1136/BMJ.314.7089.1229
P407
P577
1997-04-01T00:00:00Z