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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/s00018-018-2959-9.

Title:
How toll-like receptors reveal monocyte plasticity: the cutting edge of antiinflammatory therapy | Cellular and Molecular Life Sciences
Description:
Toll-like receptors (TLR)s are central in immune response by recognizing pathogen-associated molecular patterns (PAMP)s. If they are essential to eliminate pathogens in earlier stages of infection, they also might play a role in homeostasis and tissue repair. TLR versatility parallels the plasticity of monocytes, which represent an heterogeneous population of immune cells. They are rapidly recruited to sites of infection and involved in clearance of pathogens and in tissue healing. This review underlines how TLRs have proved to be an interesting tool to study the properties of monocytes and why different therapeutic strategies exploring monocyte plasticity may be relevant in the context of chronic inflammatory disorders.
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 7,642,828 visitors per month in the current month.

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

We can't figure out the monetization strategy.

Not all websites are made for profit; some exist to inform or educate users. Or any other reason why people make websites. And this might be the case. Link.springer.com might be earning cash quietly, but we haven't detected the monetization method.

Keywords {🔍}

pubmed, article, google, scholar, cas, central, tlr, immunol, tolllike, receptors, monocytes, receptor, monocyte, httpsdoiorgjimmunol, infection, immunity, akira, signaling, nat, innate, blood, ropert, immune, cells, rev, cell, role, disease, inflammation, macrophages, httpsdoiorgnri, subsets, signalling, essential, human, httpsdoiorgjimmuni, httpsdoiorgs, sci, dendritic, responses, biol, expression, mouse, gazzinelli, myd, activation, privacy, cookies, content, response,

Topics {✒️}

month download article/chapter selective irak4 inhibition attenuates disease tlr-driven creb-mediated mechanism pi3 k-mediated inside ziegler-heitbrock hw trif-related adaptor molecule mitogen-activated protein kinases serum tnf-α levels myd88-irak4-irak2 complex tlr4-mediated signaling pathways full article pdf de nardo cm cd14+/cd16+ blood monocytes tlr/il-1r signalling kagan jc progenitor cells occurs innate immune system privacy choices/manage cookies receptors—redefining innate immunity signal transduction system human kawasaki disease adaptor molecule tirap receptor-induced inflammation transcription factor irf5 chemokine receptor ccr2 proinflammatory cytokines synthesis article cellular monocyte-mediated defense impair wound healing central player innate immune responses chronic chagas disease article ropert therapeutic sirna silencing coronary artery disease signalling cascade shared innate immune defence receptor-mediated stimulation irf transcription factors innate immune signalling blood monocytes consist article log innate immune signaling hematopoietic stem european economic area cytokine pro duction guzmán pruneda fa porphyromonas gingivalis fimbriae sense nucleic acids large arteries intensified

Schema {🗺️}

WebPage:
      mainEntity:
         headline:How toll-like receptors reveal monocyte plasticity: the cutting edge of antiinflammatory therapy
         description:Toll-like receptors (TLR)s are central in immune response by recognizing pathogen-associated molecular patterns (PAMP)s. If they are essential to eliminate pathogens in earlier stages of infection, they also might play a role in homeostasis and tissue repair. TLR versatility parallels the plasticity of monocytes, which represent an heterogeneous population of immune cells. They are rapidly recruited to sites of infection and involved in clearance of pathogens and in tissue healing. This review underlines how TLRs have proved to be an interesting tool to study the properties of monocytes and why different therapeutic strategies exploring monocyte plasticity may be relevant in the context of chronic inflammatory disorders.
         datePublished:2018-11-09T00:00:00Z
         dateModified:2018-11-09T00:00:00Z
         pageStart:745
         pageEnd:755
         sameAs:https://doi.org/10.1007/s00018-018-2959-9
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            Life Sciences
            Biochemistry
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         isPartOf:
            name:Cellular and Molecular Life Sciences
            issn:
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      headline:How toll-like receptors reveal monocyte plasticity: the cutting edge of antiinflammatory therapy
      description:Toll-like receptors (TLR)s are central in immune response by recognizing pathogen-associated molecular patterns (PAMP)s. If they are essential to eliminate pathogens in earlier stages of infection, they also might play a role in homeostasis and tissue repair. TLR versatility parallels the plasticity of monocytes, which represent an heterogeneous population of immune cells. They are rapidly recruited to sites of infection and involved in clearance of pathogens and in tissue healing. This review underlines how TLRs have proved to be an interesting tool to study the properties of monocytes and why different therapeutic strategies exploring monocyte plasticity may be relevant in the context of chronic inflammatory disorders.
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         Biomedicine
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         Biochemistry
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                     name:Departamento de Bioquímica e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil
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               name:Departamento de Bioquímica e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil
               type:PostalAddress
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External Links {🔗}(431)

Analytics and Tracking {📊}

  • Google Tag Manager

Libraries {📚}

  • Clipboard.js
  • Prism.js

CDN Services {📦}

  • Crossref

4.57s.