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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/s13238-012-2083-9.

Title:
New components of the necroptotic pathway | Protein & Cell
Description:
Programmed necrosis, also known as necroptosis, has recently drawn great attention. As an important cellular regulation mechanism, knowledge of its signaling components is expanding. Necroptosisis demonstrated to be regulated by the RIP1 and RIP3 kinases, and its pathophysiological importance has been confirmed in a number of disease models. Here we review the new members of this necroptosis pathway, MLKL, PGAM5, Drp1 and DAI, and discuss some of their possible applications according to recent findings.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {๐Ÿ“š}

  • Education
  • Telecommunications
  • Health & Fitness

Content Management System {๐Ÿ“}

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 {๐Ÿ“ˆ}

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

๐ŸŒ  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? {๐Ÿ’ธ}

We can't see how the site brings in money.

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 secretly minting cash, but we can't detect the process.

Keywords {๐Ÿ”}

article, google, scholar, cell, necrosis, apoptosis, death, necroptosis, mitochondrial, protein, rip, wang, han, mol, biol, nature, signaling, nat, complex, programmed, kinase, induces, necrotic, vandenabeele, van, cells, caspase, zhang, receptor, privacy, cookies, cellular, inflammation, immunol, fadd, sci, chen, fission, differ, tumor, content, publish, search, pathway, download, zhou, regulated, kinases, prevents, regulates,

Topics {โœ’๏ธ}

prevent bax/bak-dependent apoptosis protein serine/threonine phosphatase tnf-r1 signaling complex nf-kappab activation [corrected] bak-induced mitochondrial fission victor hanย &ย jiahuai han rip3-driven regulated necrosis caspase-independent cell death tnf-mediated gene induction rip1/rip3 necrosome forms phosphorylation-driven assembly mitochondrial death/life regulator rip3-dependent necrosis caspase-dependent necrosis tumor necrosis factor tnf-alpha induces death domain protein bcl-xl block apoptosis tnf-induced necrosis tnf induced necroptosis tnf-induced necroptosis prevents skin inflammation dynamin-related protein 1 articleย  google scholar interferon induces necroptosis multiple tnfr1 complex dai/zbp1/dlm-1 complexes virus-induced inflammation privacy choices/manage cookies specific cellular target caspase-8 protects mice innate immune response mammalian mitochondrial fission mitochondrial fission machinery grim-19 mediated translocation promote rip1 ubiquitination sequential signaling complexes ordered cellular explosion inflammation-related hepatocarcinogenesis cellular stress biology caspase-8-deficient mice rip3 kinases main content log therapeutic potential energy metabolism regulator nonapoptotic cell death cell death subroutines cell death differ chronic intestinal inflammation european economic area

Questions {โ“}

  • Necrostatin: a potentially novel cardioprotective agent?

Schema {๐Ÿ—บ๏ธ}

WebPage:
      mainEntity:
         headline:New components of the necroptotic pathway
         description:Programmed necrosis, also known as necroptosis, has recently drawn great attention. As an important cellular regulation mechanism, knowledge of its signaling components is expanding. Necroptosisis demonstrated to be regulated by the RIP1 and RIP3 kinases, and its pathophysiological importance has been confirmed in a number of disease models. Here we review the new members of this necroptosis pathway, MLKL, PGAM5, Drp1 and DAI, and discuss some of their possible applications according to recent findings.
         datePublished:2012-10-17T00:00:00Z
         dateModified:2012-10-17T00:00:00Z
         pageStart:811
         pageEnd:817
         sameAs:https://doi.org/10.1007/s13238-012-2083-9
         keywords:
            necrosis
            necroptosis
            necrosome
            Biochemistry
            general
            Protein Science
            Cell Biology
            Stem Cells
            Human Genetics
            Developmental Biology
         image:
         isPartOf:
            name:Protein & Cell
            issn:
               1674-8018
               1674-800X
            volumeNumber:3
            type:
               Periodical
               PublicationVolume
         publisher:
            name:Higher Education Press
            logo:
               url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
               type:ImageObject
            type:Organization
         author:
               name:Zhenru Zhou
               affiliation:
                     name:Xiamen University
                     address:
                        name:State Key Laboratory of Cellular Stress Biology and School of Life Sciences, Xiamen University, Xiamen, China
                        type:PostalAddress
                     type:Organization
               type:Person
               name:Victor Han
               affiliation:
                     name:Xiamen University
                     address:
                        name:State Key Laboratory of Cellular Stress Biology and School of Life Sciences, Xiamen University, Xiamen, China
                        type:PostalAddress
                     type:Organization
               type:Person
               name:Jiahuai Han
               affiliation:
                     name:Xiamen University
                     address:
                        name:State Key Laboratory of Cellular Stress Biology and School of Life Sciences, Xiamen University, Xiamen, China
                        type:PostalAddress
                     type:Organization
               email:[email protected]
               type:Person
         isAccessibleForFree:1
         type:ScholarlyArticle
      context:https://schema.org
ScholarlyArticle:
      headline:New components of the necroptotic pathway
      description:Programmed necrosis, also known as necroptosis, has recently drawn great attention. As an important cellular regulation mechanism, knowledge of its signaling components is expanding. Necroptosisis demonstrated to be regulated by the RIP1 and RIP3 kinases, and its pathophysiological importance has been confirmed in a number of disease models. Here we review the new members of this necroptosis pathway, MLKL, PGAM5, Drp1 and DAI, and discuss some of their possible applications according to recent findings.
      datePublished:2012-10-17T00:00:00Z
      dateModified:2012-10-17T00:00:00Z
      pageStart:811
      pageEnd:817
      sameAs:https://doi.org/10.1007/s13238-012-2083-9
      keywords:
         necrosis
         necroptosis
         necrosome
         Biochemistry
         general
         Protein Science
         Cell Biology
         Stem Cells
         Human Genetics
         Developmental Biology
      image:
      isPartOf:
         name:Protein & Cell
         issn:
            1674-8018
            1674-800X
         volumeNumber:3
         type:
            Periodical
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      publisher:
         name:Higher Education Press
         logo:
            url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
            type:ImageObject
         type:Organization
      author:
            name:Zhenru Zhou
            affiliation:
                  name:Xiamen University
                  address:
                     name:State Key Laboratory of Cellular Stress Biology and School of Life Sciences, Xiamen University, Xiamen, China
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Victor Han
            affiliation:
                  name:Xiamen University
                  address:
                     name:State Key Laboratory of Cellular Stress Biology and School of Life Sciences, Xiamen University, Xiamen, China
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Jiahuai Han
            affiliation:
                  name:Xiamen University
                  address:
                     name:State Key Laboratory of Cellular Stress Biology and School of Life Sciences, Xiamen University, Xiamen, China
                     type:PostalAddress
                  type:Organization
            email:[email protected]
            type:Person
      isAccessibleForFree:1
["Periodical","PublicationVolume"]:
      name:Protein & Cell
      issn:
         1674-8018
         1674-800X
      volumeNumber:3
Organization:
      name:Higher Education Press
      logo:
         url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
         type:ImageObject
      name:Xiamen University
      address:
         name:State Key Laboratory of Cellular Stress Biology and School of Life Sciences, Xiamen University, Xiamen, China
         type:PostalAddress
      name:Xiamen University
      address:
         name:State Key Laboratory of Cellular Stress Biology and School of Life Sciences, Xiamen University, Xiamen, China
         type:PostalAddress
      name:Xiamen University
      address:
         name:State Key Laboratory of Cellular Stress Biology and School of Life Sciences, Xiamen University, Xiamen, China
         type:PostalAddress
ImageObject:
      url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
Person:
      name:Zhenru Zhou
      affiliation:
            name:Xiamen University
            address:
               name:State Key Laboratory of Cellular Stress Biology and School of Life Sciences, Xiamen University, Xiamen, China
               type:PostalAddress
            type:Organization
      name:Victor Han
      affiliation:
            name:Xiamen University
            address:
               name:State Key Laboratory of Cellular Stress Biology and School of Life Sciences, Xiamen University, Xiamen, China
               type:PostalAddress
            type:Organization
      name:Jiahuai Han
      affiliation:
            name:Xiamen University
            address:
               name:State Key Laboratory of Cellular Stress Biology and School of Life Sciences, Xiamen University, Xiamen, China
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:State Key Laboratory of Cellular Stress Biology and School of Life Sciences, Xiamen University, Xiamen, China
      name:State Key Laboratory of Cellular Stress Biology and School of Life Sciences, Xiamen University, Xiamen, China
      name:State Key Laboratory of Cellular Stress Biology and School of Life Sciences, Xiamen University, Xiamen, China

External Links {๐Ÿ”—}(158)

Analytics and Tracking {๐Ÿ“Š}

  • Google Tag Manager

Libraries {๐Ÿ“š}

  • Clipboard.js
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CDN Services {๐Ÿ“ฆ}

  • Crossref

5.02s.