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- 2010
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Mark
Homozygosity For a Novel Mutation in the C1q C Chain Gene in a Turkish Family With Hereditary C1q Deficiency
(
- Contribution to journal › Article
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Mark
A 3 '-Untranslated Region Variant Is Associated With Impaired Expression of CD226 in T and Natural Killer T Cells and Is Associated With Susceptibility to Systemic Lupus Erythematosus
(
- Contribution to journal › Article
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Mark
Expression of activation markers on eosinophils in patients with systemic sclerosis
(
- Contribution to journal › Published meeting abstract
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Mark
Toll-Like Receptor 4 Promoter Polymorphisms: Common TLR4 Variants May Protect against Severe Urinary Tract Infection.
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- Contribution to journal › Article
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Mark
Recombinant human complement component C2 produced in a human cell line restores the classical complement pathway activity in-vitro: an alternative treatment for C2 deficiency diseases
(
- Contribution to journal › Article
- 2009
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Mark
C1q inhibits immune complex induced IFN-alpha production in plasmacytoid dendritic cells-A novel link between C1q deficiency and SLE pathogenesis
2009) 12th European Meeting on Complement in Human Disease In Molecular Immunology 46(14). p.2857-2857(
- Contribution to journal › Published meeting abstract
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Mark
Influence of IgG allotypes on defense against Haemophilus influenzae type b in children-A complement-dependent mechanism?
2009) 12th European Meeting on Complement in Human Disease In Molecular Immunology 46(14). p.2867-2868(
- Contribution to journal › Published meeting abstract
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Mark
Additive effects of the major risk alleles of IRF5 and STAT4 in primary Sjogren's syndrome
(
- Contribution to journal › Article
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Mark
Neutrophil degranulation and complement release in ANCA-associated vasculitis: an in vitro study
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- Contribution to journal › Published meeting abstract
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Mark
Mannose-binding lectin as a risk factor for acute coronary syndromes.
(
- Contribution to journal › Article