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LINK . SPRINGER . COM {}

  1. Analyzed Page
  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Link.springer.com Make Money
  6. Keywords
  7. Topics
  8. Questions
  9. Schema
  10. External Links
  11. Analytics And Tracking
  12. Libraries
  13. CDN Services

We are analyzing https://link.springer.com/article/10.1007/s10495-010-0478-8.

Title:
Inefficient clearance of dying cells in patients with SLE: anti-dsDNA autoantibodies, MFG-E8, HMGB-1 and other players | Apoptosis
Description:
Systemic lupus erythematosus (SLE) is a complex disease resulting from inflammatory responses of the immune system against several autoantigens. Inflammation is conditioned by the continuous presence of autoantibodies and leaked autoantigens, e.g. from not properly cleared dying and dead cells. Various soluble molecules and biophysical properties of the surface of apoptotic cells play significant roles in the appropriate recognition and further processing of dying and dead cells. We exemplarily discuss how Milk fat globule epidermal growth factor 8 (MFG-E8), biophysical membrane alterations, High mobility group box 1 (HMGB1), C-reactive protein (CRP), and anti-nuclear autoantibodies may contribute to the etiopathogenesis of the disease. Up to date knowledge about these key elements may provide new insights that lead to the development of new treatment strategies of the disease.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
  • Science
  • Health & Fitness

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
However, some sources were not loaded, we suggest to reload the page to get complete results.

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How Does Link.springer.com Make Money? {💸}

We're unsure how the site profits.

Websites don't always need to be profitable; some serve as platforms for education or personal expression. Websites can serve multiple purposes. And this might be one of them. Link.springer.com could be secretly minting cash, but we can't detect the process.

Keywords {🔍}

google, scholar, pubmed, protein, lupus, creactive, cells, immunol, systemic, erythematosus, hmgb, apoptotic, rheum, human, arthritis, herrmann, cell, kalden, voll, disease, med, antibodies, group, exp, expression, dna, bianchi, immune, binding, mice, article, patients, autoantibodies, mfge, high, proteins, clin, apoptosis, mobility, biochem, hmg, nuclear, wang, gaipl, nagata, activity, van, university, clearance, sle,

Topics {✒️}

anti-double-stranded dna antibodies anti-double-stranded dna autoantibodies milk-fat globule protein c-reactive protein mediates month download article/chapter modified c-reactive protein experimentally uv-induced lesions human c-reactive protein c-reactive protein reacts targeting c-reactive protein monomeric c-reactive protein neutrophil-endothelial cell adhesion transforming growth factor-beta c-reactive protein levels multiply o-glycosylated domain anti-chromatin autoantibody production c-reactive protein expression nk/idc interaction results /ebp-beta complex formation anti-nucleosome antibodies complexed anti-ds dna antibodies interferon-alpha production c-reactive protein binds high mobility group serum autoantibody profiles biophysical membrane alterations vesicle-mediated secretory pathway plasma membrane constituents tlr9-mediated inflammatory responses mfg-e8-deficient mice epidermal growth factor necrotic cell-derived chromatin systemic autoimmune diseases nucleic acid released c-reactive protein chromosomal protein hmg1 peripheral membrane protein major milk protein du clos tw macrophage cytokine production apoptotic cell death weaning-induced expression developmental endothelial locus-1 phosphatidylserine-binding activity systemic rheumatic diseases cytomix-induced hyperpermeability hmgb1 chromosomal protein induces autoantibody production privacy choices/manage cookies disrupt cell growth

Questions {❓}

  • Frisoni L, McPhie L, Colonna L, Sriram U, Monestier M, Gallucci S, Caricchio R (2005) Nuclear autoantigen translocation and autoantibody opsonization lead to increased dendritic cell phagocytosis and presentation of nuclear antigens: a novel pathogenic pathway for autoimmunity?
  • Isenberg DA, Manson JJ, Ehrenstein MR, Rahman A (2007) Fifty years of anti-ds DNA antibodies: are we approaching journey’s end?

Schema {🗺️}

WebPage:
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         headline:Inefficient clearance of dying cells in patients with SLE: anti-dsDNA autoantibodies, MFG-E8, HMGB-1 and other players
         description:Systemic lupus erythematosus (SLE) is a complex disease resulting from inflammatory responses of the immune system against several autoantigens. Inflammation is conditioned by the continuous presence of autoantibodies and leaked autoantigens, e.g. from not properly cleared dying and dead cells. Various soluble molecules and biophysical properties of the surface of apoptotic cells play significant roles in the appropriate recognition and further processing of dying and dead cells. We exemplarily discuss how Milk fat globule epidermal growth factor 8 (MFG-E8), biophysical membrane alterations, High mobility group box 1 (HMGB1), C-reactive protein (CRP), and anti-nuclear autoantibodies may contribute to the etiopathogenesis of the disease. Up to date knowledge about these key elements may provide new insights that lead to the development of new treatment strategies of the disease.
         datePublished:2010-03-03T00:00:00Z
         dateModified:2010-03-03T00:00:00Z
         pageStart:1098
         pageEnd:1113
         sameAs:https://doi.org/10.1007/s10495-010-0478-8
         keywords:
            Clearance
            MFG-E8
            Biophysical features
            Plasma membrane
            Phosphatidylserine
            HMGB-1
            CRP
            ANA
            Cancer Research
            Cell Biology
            Oncology
            Biochemistry
            general
            Virology
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                     name:Friedrich-Alexander University of Erlangen-Nuremberg
                     address:
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                     address:
                        name:IZKF Research Group N2, Nikolaus-Fiebiger-Center for Molecular Medicine, University Hospital Erlangen, University of Erlangen-Nuremberg, Erlangen, Germany
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                     name:Friedrich-Alexander University of Erlangen-Nuremberg
                     address:
                        name:Department for Internal Medicine 3, University Hospital Erlangen, Friedrich-Alexander University of Erlangen-Nuremberg, Erlangen, Germany
                        type:PostalAddress
                     type:Organization
               type:Person
               name:Luis E. Muñoz
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                     name:Friedrich-Alexander University of Erlangen-Nuremberg
                     address:
                        name:Department for Internal Medicine 3, University Hospital Erlangen, Friedrich-Alexander University of Erlangen-Nuremberg, Erlangen, Germany
                        type:PostalAddress
                     type:Organization
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               type:Person
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                     name:Friedrich-Alexander University of Erlangen-Nuremberg
                     address:
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      headline:Inefficient clearance of dying cells in patients with SLE: anti-dsDNA autoantibodies, MFG-E8, HMGB-1 and other players
      description:Systemic lupus erythematosus (SLE) is a complex disease resulting from inflammatory responses of the immune system against several autoantigens. Inflammation is conditioned by the continuous presence of autoantibodies and leaked autoantigens, e.g. from not properly cleared dying and dead cells. Various soluble molecules and biophysical properties of the surface of apoptotic cells play significant roles in the appropriate recognition and further processing of dying and dead cells. We exemplarily discuss how Milk fat globule epidermal growth factor 8 (MFG-E8), biophysical membrane alterations, High mobility group box 1 (HMGB1), C-reactive protein (CRP), and anti-nuclear autoantibodies may contribute to the etiopathogenesis of the disease. Up to date knowledge about these key elements may provide new insights that lead to the development of new treatment strategies of the disease.
      datePublished:2010-03-03T00:00:00Z
      dateModified:2010-03-03T00:00:00Z
      pageStart:1098
      pageEnd:1113
      sameAs:https://doi.org/10.1007/s10495-010-0478-8
      keywords:
         Clearance
         MFG-E8
         Biophysical features
         Plasma membrane
         Phosphatidylserine
         HMGB-1
         CRP
         ANA
         Cancer Research
         Cell Biology
         Oncology
         Biochemistry
         general
         Virology
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         name:Springer US
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      author:
            name:Kristin Kruse
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                  address:
                     name:Department for Internal Medicine 3, University Hospital Erlangen, Friedrich-Alexander University of Erlangen-Nuremberg, Erlangen, Germany
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Christina Janko
            affiliation:
                  name:Friedrich-Alexander University of Erlangen-Nuremberg
                  address:
                     name:Department for Internal Medicine 3, University Hospital Erlangen, Friedrich-Alexander University of Erlangen-Nuremberg, Erlangen, Germany
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Vilma Urbonaviciute
            affiliation:
                  name:University of Erlangen-Nuremberg
                  address:
                     name:IZKF Research Group N2, Nikolaus-Fiebiger-Center for Molecular Medicine, University Hospital Erlangen, University of Erlangen-Nuremberg, Erlangen, Germany
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Claudia T. Mierke
            affiliation:
                  name:Friedrich-Alexander University of Erlangen-Nuremberg
                  address:
                     name:Center of Medical Physics and Technology, Biophysics Group, Friedrich-Alexander University of Erlangen-Nuremberg, Erlangen, Germany
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Thomas H. Winkler
            affiliation:
                  name:Friedrich-Alexander University of Erlangen-Nuremberg
                  address:
                     name:Hematopoiesis Unit, Department of Biology, Nikolaus-Fiebiger-Center for Molecular Medicine, Friedrich-Alexander University of Erlangen-Nuremberg, Erlangen, Germany
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Reinhard E. Voll
            affiliation:
                  name:University of Erlangen-Nuremberg
                  address:
                     name:IZKF Research Group N2, Nikolaus-Fiebiger-Center for Molecular Medicine, University Hospital Erlangen, University of Erlangen-Nuremberg, Erlangen, Germany
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Georg Schett
            affiliation:
                  name:Friedrich-Alexander University of Erlangen-Nuremberg
                  address:
                     name:Department for Internal Medicine 3, University Hospital Erlangen, Friedrich-Alexander University of Erlangen-Nuremberg, Erlangen, Germany
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Luis E. Muñoz
            affiliation:
                  name:Friedrich-Alexander University of Erlangen-Nuremberg
                  address:
                     name:Department for Internal Medicine 3, University Hospital Erlangen, Friedrich-Alexander University of Erlangen-Nuremberg, Erlangen, Germany
                     type:PostalAddress
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                  name:Friedrich-Alexander University of Erlangen-Nuremberg
                  address:
                     name:Department for Internal Medicine 3, University Hospital Erlangen, Friedrich-Alexander University of Erlangen-Nuremberg, Erlangen, Germany
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      name:Friedrich-Alexander University of Erlangen-Nuremberg
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         type:PostalAddress
      name:Friedrich-Alexander University of Erlangen-Nuremberg
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         type:PostalAddress
      name:Friedrich-Alexander University of Erlangen-Nuremberg
      address:
         name:Department for Internal Medicine 3, University Hospital Erlangen, Friedrich-Alexander University of Erlangen-Nuremberg, Erlangen, Germany
         type:PostalAddress
      name:Friedrich-Alexander University of Erlangen-Nuremberg
      address:
         name:Department for Internal Medicine 3, University Hospital Erlangen, Friedrich-Alexander University of Erlangen-Nuremberg, Erlangen, Germany
         type:PostalAddress
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            name:Friedrich-Alexander University of Erlangen-Nuremberg
            address:
               name:Department for Internal Medicine 3, University Hospital Erlangen, Friedrich-Alexander University of Erlangen-Nuremberg, Erlangen, Germany
               type:PostalAddress
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      name:Christina Janko
      affiliation:
            name:Friedrich-Alexander University of Erlangen-Nuremberg
            address:
               name:Department for Internal Medicine 3, University Hospital Erlangen, Friedrich-Alexander University of Erlangen-Nuremberg, Erlangen, Germany
               type:PostalAddress
            type:Organization
      name:Vilma Urbonaviciute
      affiliation:
            name:University of Erlangen-Nuremberg
            address:
               name:IZKF Research Group N2, Nikolaus-Fiebiger-Center for Molecular Medicine, University Hospital Erlangen, University of Erlangen-Nuremberg, Erlangen, Germany
               type:PostalAddress
            type:Organization
      name:Claudia T. Mierke
      affiliation:
            name:Friedrich-Alexander University of Erlangen-Nuremberg
            address:
               name:Center of Medical Physics and Technology, Biophysics Group, Friedrich-Alexander University of Erlangen-Nuremberg, Erlangen, Germany
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            name:Friedrich-Alexander University of Erlangen-Nuremberg
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      name:Reinhard E. Voll
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            name:University of Erlangen-Nuremberg
            address:
               name:IZKF Research Group N2, Nikolaus-Fiebiger-Center for Molecular Medicine, University Hospital Erlangen, University of Erlangen-Nuremberg, Erlangen, Germany
               type:PostalAddress
            type:Organization
      name:Georg Schett
      affiliation:
            name:Friedrich-Alexander University of Erlangen-Nuremberg
            address:
               name:Department for Internal Medicine 3, University Hospital Erlangen, Friedrich-Alexander University of Erlangen-Nuremberg, Erlangen, Germany
               type:PostalAddress
            type:Organization
      name:Luis E. Muñoz
      affiliation:
            name:Friedrich-Alexander University of Erlangen-Nuremberg
            address:
               name:Department for Internal Medicine 3, University Hospital Erlangen, Friedrich-Alexander University of Erlangen-Nuremberg, Erlangen, Germany
               type:PostalAddress
            type:Organization
      email:[email protected]
      name:Martin Herrmann
      affiliation:
            name:Friedrich-Alexander University of Erlangen-Nuremberg
            address:
               name:Department for Internal Medicine 3, University Hospital Erlangen, Friedrich-Alexander University of Erlangen-Nuremberg, Erlangen, Germany
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      name:Department for Internal Medicine 3, University Hospital Erlangen, Friedrich-Alexander University of Erlangen-Nuremberg, Erlangen, Germany
      name:Department for Internal Medicine 3, University Hospital Erlangen, Friedrich-Alexander University of Erlangen-Nuremberg, Erlangen, Germany
      name:IZKF Research Group N2, Nikolaus-Fiebiger-Center for Molecular Medicine, University Hospital Erlangen, University of Erlangen-Nuremberg, Erlangen, Germany
      name:Center of Medical Physics and Technology, Biophysics Group, Friedrich-Alexander University of Erlangen-Nuremberg, Erlangen, Germany
      name:Hematopoiesis Unit, Department of Biology, Nikolaus-Fiebiger-Center for Molecular Medicine, Friedrich-Alexander University of Erlangen-Nuremberg, Erlangen, Germany
      name:IZKF Research Group N2, Nikolaus-Fiebiger-Center for Molecular Medicine, University Hospital Erlangen, University of Erlangen-Nuremberg, Erlangen, Germany
      name:Department for Internal Medicine 3, University Hospital Erlangen, Friedrich-Alexander University of Erlangen-Nuremberg, Erlangen, Germany
      name:Department for Internal Medicine 3, University Hospital Erlangen, Friedrich-Alexander University of Erlangen-Nuremberg, Erlangen, Germany
      name:Department for Internal Medicine 3, University Hospital Erlangen, Friedrich-Alexander University of Erlangen-Nuremberg, Erlangen, Germany
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External Links {🔗}(350)

Analytics and Tracking {📊}

  • Google Tag Manager

Libraries {📚}

  • Clipboard.js
  • Prism.js

CDN Services {📦}

  • Crossref

4.27s.