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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. Schema
  9. External Links
  10. Analytics And Tracking
  11. Libraries
  12. CDN Services

We are analyzing https://link.springer.com/article/10.1007/s12016-010-8203-5.

Title:
Estrogen Receptors in Immunity and Autoimmunity | Clinical Reviews in Allergy & Immunology
Description:
Clinical Reviews in Allergy & Immunology - Due to the female predominance of autoimmune diseases, the role of gender and sex hormones in the immune system is of long-term interest....
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.
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How Does Link.springer.com Make Money? {💸}

We find it hard to spot revenue streams.

Some websites aren't about earning revenue; they're built to connect communities or raise awareness. There are numerous motivations behind creating websites. This might be one of them. Link.springer.com could be getting rich in stealth mode, or the way it's monetizing isn't detectable.

Keywords {🔍}

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Topics {✒️}

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Schema {🗺️}

WebPage:
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         headline:Estrogen Receptors in Immunity and Autoimmunity
         description:Due to the female predominance of autoimmune diseases, the role of gender and sex hormones in the immune system is of long-term interest. Estrogen's primary effects are mediated via estrogen receptors alpha and beta (ER α/β) that are expressed on most immune cells. ERs are nuclear hormone receptors that can either directly bind to estrogen response elements in gene promoters or serve as cofactors with other transcription factors (i.e., NFkB/AP1). Cytoplasmic ER and membrane associated ER impact specific kinase signaling pathways. ERs have prominent effects on immune function in both the innate and adaptive immune responses. Genetic deficiency of ERα in murine models of lupus resulted in significantly decreased disease and prolonged survival, while ERβ deficiency had minimal to no effect in autoimmune models. The protective effect of ERα in lupus is multifactoral. In arthritis models, ERα agonists appears to mediate a protective effect. The modulation of ERα function appears to be a potential target for therapy in autoimmunity.
         datePublished:2010-03-30T00:00:00Z
         dateModified:2010-03-30T00:00:00Z
         pageStart:66
         pageEnd:73
         sameAs:https://doi.org/10.1007/s12016-010-8203-5
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            Autoimmunity
            Gender prevalence
            Allergology
            Immunology
            Internal Medicine
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            name:Clinical Reviews in Allergy & Immunology
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         author:
               name:Melissa Cunningham
               affiliation:
                     name:Medical University of South Carolina
                     address:
                        name:Medical Research Service, Ralph H. Johnson VAMC and the Department of Medicine, Division of Rheumatology, Medical University of South Carolina, Charleston, USA
                        type:PostalAddress
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                     name:Medical University of South Carolina
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      headline:Estrogen Receptors in Immunity and Autoimmunity
      description:Due to the female predominance of autoimmune diseases, the role of gender and sex hormones in the immune system is of long-term interest. Estrogen's primary effects are mediated via estrogen receptors alpha and beta (ER α/β) that are expressed on most immune cells. ERs are nuclear hormone receptors that can either directly bind to estrogen response elements in gene promoters or serve as cofactors with other transcription factors (i.e., NFkB/AP1). Cytoplasmic ER and membrane associated ER impact specific kinase signaling pathways. ERs have prominent effects on immune function in both the innate and adaptive immune responses. Genetic deficiency of ERα in murine models of lupus resulted in significantly decreased disease and prolonged survival, while ERβ deficiency had minimal to no effect in autoimmune models. The protective effect of ERα in lupus is multifactoral. In arthritis models, ERα agonists appears to mediate a protective effect. The modulation of ERα function appears to be a potential target for therapy in autoimmunity.
      datePublished:2010-03-30T00:00:00Z
      dateModified:2010-03-30T00:00:00Z
      pageStart:66
      pageEnd:73
      sameAs:https://doi.org/10.1007/s12016-010-8203-5
      keywords:
         Estrogen receptors
         Autoimmunity
         Gender prevalence
         Allergology
         Immunology
         Internal Medicine
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                  name:Medical University of South Carolina
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                  type:Organization
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                  name:Medical University of South Carolina
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                     name:Medical Research Service, Ralph H. Johnson VAMC and the Department of Medicine, Division of Rheumatology, Medical University of South Carolina, Charleston, USA
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            address:
               name:Medical Research Service, Ralph H. Johnson VAMC and the Department of Medicine, Division of Rheumatology, Medical University of South Carolina, Charleston, USA
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External Links {🔗}(262)

Analytics and Tracking {📊}

  • Google Tag Manager

Libraries {📚}

  • Clipboard.js
  • Prism.js

CDN Services {📦}

  • Crossref

3.98s.