Search Results - "Iversen, Line V"

Unique Protein Signature of Circulating Microparticles in Systemic Lupus Erythematosus by Østergaard, Ole, Nielsen, Christoffer T., Iversen, Line V., Tanassi, Julia T., Knudsen, Steen, Jacobsen, Søren, Heegaard, Niels H. H.

“…Objective To characterize the unique qualities of proteins associated with circulating subcellular material in systemic lupus erythematosus (SLE) patients…”
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The circulating cell-free microRNA profile in systemic sclerosis is distinct from both healthy controls and systemic lupus erythematosus by Steen, Samantha O, Iversen, Line V, Carlsen, Anting Liu, Burton, Mark, Nielsen, Christoffer T, Jacobsen, Søren, Heegaard, Niels H H

“…To evaluate the expression profile of cell-free circulating microRNA (miRNA) in systemic sclerosis (SSc), healthy controls (HC), and systemic lupus…”
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Increased antibody levels to stage-specific Epstein-Barr virus antigens in systemic autoimmune diseases reveal a common pathology by Sternbæk, Louise, Draborg, Anette H., Østerlund, Mark T., Iversen, Line V., Troelsen, Lone, Theander, Elke, Nielsen, Christoffer T., Jacobsen, Søren, Houen, Gunnar

“…The immune responses to antigens from different stages of the Epstein-Barr virus (EBV) life cycle were investigated in systemic lupus erythematosus (SLE),…”
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Distinct proteome pathology of circulating microparticles in systemic lupus erythematosus by Østergaard, Ole, Nielsen, Christoffer Tandrup, Tanassi, Julia T, Iversen, Line V, Jacobsen, Søren, Heegaard, Niels H H

“…The pathogenesis of systemic lupus erythematosus (SLE) is poorly understood but has been linked to defective clearance of subcellular particulate material from…”
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Increased IgG on cell-derived plasma microparticles in systemic lupus erythematosus is associated with autoantibodies and complement activation by Nielsen, Christoffer T., Østergaard, Ole, Stener, Line, Iversen, Line V., Truedsson, Lennart, Gullstrand, Birgitta, Jacobsen, Søren, Heegaard, Niels H. H.

“…Objective To quantify immunoglobulin and C1q on circulating cell‐derived microparticles (MPs) in patients with systemic lupus erythematosus (SLE) and to…”
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Quantitative Proteome Profiling of Normal Human Circulating Microparticles by Østergaard, Ole, Nielsen, Christoffer T, Iversen, Line V, Jacobsen, Søren, Tanassi, Julia T, Heegaard, Niels H. H

“…Circulating microparticles (MPs) are produced as part of normal physiology. Their numbers, origin, and composition change in pathology. Despite this, the…”
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Efficient evaluation of humoral immune responses by the use of serum pools by Sternbæk, Louise, Draborg, Anette H., Nielsen, Christoffer T., Jacobsen, Søren, Iversen, Line V., Troelsen, Lone, Theander, Elke, Houen, Gunnar

“…Collection and testing of individual serum samples are often used in research to gain knowledge about e.g. the humoral response against bacteria or virus. This…”
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Cross-sectional study of soluble selectins, fractions of circulating microparticles and their relationship to lung and skin involvement in systemic sclerosis by Iversen, Line V, Ullman, Susanne, Østergaard, Ole, Nielsen, Christoffer T, Halberg, Poul, Karlsmark, Tonny, Heegaard, Niels H H, Jacobsen, Søren

“…Endothelial damage and activation may play central roles in the pathogenesis of systemic sclerosis (SSc) and are reflected by microparticles (MPs) and soluble…”
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A heparin-based method for flow cytometric analysis of microparticles directly from platelet-poor plasma in calcium containing buffer by Iversen, Line V., Østergaard, Ole, Nielsen, Christoffer T., Jacobsen, Søren, Heegaard, Niels H.H.

“…Characterization of circulating microparticles (MPs) is usually performed by flow cytometry. Annexin V, a protein that Ca2+-dependently binds to…”
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Plasma levels of galectin-3-binding protein reflect type I interferon activity and are increased in patients with systemic lupus erythematosus by Nielsen, Christoffer T, Lood, Christian, Østergaard, Ole, Iversen, Line V, Voss, Anne, Bengtsson, Anders, Jacobsen, Søren, Heegaard, Niels H H

“…Objective Simple measures of type I interferon (IFN) activity constitute highly attractive biomarkers in systemic lupus erythematosus (SLE). We explore…”
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