Here's how LINK.SPRINGER.COM makes money* and how much!

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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

We are analyzing https://link.springer.com/chapter/10.1007/978-1-4020-6554-5_7.

Title:
Trail Receptors: Targets for Cancer Therapy | SpringerLink
Description:
A human tumor cell's ability to avoid the normal regulatory mechanisms of cell growth, division, and death are the hallmarks of transformation and cancer. Numerous novel therapeutic agents currently in preclinical or clinical evaluation aim to revive the normal...
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
  • Health & Fitness
  • Science

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 5,000,016 visitors per month in the current month.

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

We're unsure how the site profits.

The purpose of some websites isn't monetary gain; they're meant to inform, educate, or foster collaboration. Everyone has unique reasons for building websites. This could be an example. Link.springer.com could be secretly minting cash, but we can't detect the process.

Keywords {🔍}

google, scholar, pubmed, cas, article, cancer, apoptosis, cells, death, trail, cell, human, tumor, ligand, apoptosisinducing, necrosis, receptors, factorrelated, receptor, res, biol, expression, trailinduced, clin, oncogene, chem, inhibitor, prostate, oncol, kim, induces, ther, gene, activity, humphreys, carcinoma, sensitizes, caspase, activation, trailr, protein, mol, van, nat, monoclonal, antibody, inhibition, ashkenazi, vivo, int,

Topics {✒️}

tnf-related apoptosis-inducing ligand tnf-related apoptosis-inducing ligand related apoptosis-inducing ligand tumour-necrosis factor superfamily apo2 ligand/trail-induced apoptosis death-inducing signaling complex trail/apo-2l tumour necrosis factor death ligand-mediated apoptosis histone deacetylase inhibitors–development high-resolution x-ray structure enhancing trail-induced apoptosis interleukin-1beta-converting enzyme membrane-targeted death ligand caspase/direct iap-binding protein histone deacetylase inhibitors apo2l/trail-mediated apoptosis trail/apo2l-mediated apoptosis bortezomib-induced cell death trail/apo-2 ligand tnfalpha-mediated cell death death receptor–induced apoptosis activate nf-kappab tnf-family death receptors trail-mediated cell death month download article/chapter apo2l/trail-induced apoptosis regulate agonist-specific mechanisms signal fadd-dependent apoptosis distinct cross-linking requirements small-cell lung cancer anticancer drug-induced apoptosis tumor cell apoptosis ionizing irradiation-induced apoptosis monocyte-mediated tumoricidal activity modulates chemotherapy-induced apoptosis etoposide-induced apoptosis cellular flice-inhibitory protein inhibits tumor growth dr5-mediated apoptosis recombinant apo2l/trail versions ovarian tumor lines apo2l/trail-dependent recruitment chemoresistant bcl-2-overexpressing cells tumor-cell resistance hormone-refractory prostate cancer human tumor cell' apo-2 ligand human tumor cells proteasome inhibitor bortezomib

Schema {🗺️}

ScholarlyArticle:
      headline:Trail Receptors: Targets for Cancer Therapy
      pageEnd:158
      pageStart:127
      image:https://media.springernature.com/w153/springer-static/cover/book/978-1-4020-6554-5.jpg
      genre:
         Biomedical and Life Sciences
         Biomedical and Life Sciences (R0)
      isPartOf:
         name:Programmed Cell Death in Cancer Progression and Therapy
         isbn:
            978-1-4020-6554-5
            978-1-4020-6553-8
         type:Book
      publisher:
         name:Springer Netherlands
         logo:
            url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
            type:ImageObject
         type:Organization
      author:
            name:Robin C. Humphreys
            affiliation:
                  name:Human Genome Sciences
                  address:
                     name:Development Sciences and Research, Human Genome Sciences, Rockville, USA
                     type:PostalAddress
                  type:Organization
                  name:Human Genome Sciences
                  address:
                     name:Oncology Research Department, Human Genome Sciences, Rockville, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Wendy Halpern
            affiliation:
                  name:Human Genome Sciences, Pathology, Pharmacokinetics and Toxicology
                  address:
                     name:Human Genome Sciences, Pathology, Pharmacokinetics and Toxicology, Rockville, USA
                     type:PostalAddress
                  type:Organization
            type:Person
      keywords:apoptosis, monoclonal antibody, agonist, TRAIL, TRAIL receptor
      description:A human tumor cell's ability to avoid the normal regulatory mechanisms of cell growth, division, and death are the hallmarks of transformation and cancer. Numerous novel therapeutic agents currently in preclinical or clinical evaluation aim to revive the normal regulation or evade these regulatory defects and induce growth arrest and cell death. One of the cell death pathways that has garnered significant interest, as a potential target for therapeutic intervention, is the programmed cell death pathway regulated by the tumor necrosis factor-related apoptosis-inducing ligand receptors (TRAIL-RS). Receptor agonist molecules including forms of the native ligand and monoclonal antibodies are being developed and tested as therapeutics in the treatment of human cancer.
      datePublished:2008
      isAccessibleForFree:
      hasPart:
         isAccessibleForFree:
         cssSelector:.main-content
         type:WebPageElement
      context:https://schema.org
Book:
      name:Programmed Cell Death in Cancer Progression and Therapy
      isbn:
         978-1-4020-6554-5
         978-1-4020-6553-8
Organization:
      name:Springer Netherlands
      logo:
         url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
         type:ImageObject
      name:Human Genome Sciences
      address:
         name:Development Sciences and Research, Human Genome Sciences, Rockville, USA
         type:PostalAddress
      name:Human Genome Sciences
      address:
         name:Oncology Research Department, Human Genome Sciences, Rockville, USA
         type:PostalAddress
      name:Human Genome Sciences, Pathology, Pharmacokinetics and Toxicology
      address:
         name:Human Genome Sciences, Pathology, Pharmacokinetics and Toxicology, Rockville, USA
         type:PostalAddress
ImageObject:
      url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
Person:
      name:Robin C. Humphreys
      affiliation:
            name:Human Genome Sciences
            address:
               name:Development Sciences and Research, Human Genome Sciences, Rockville, USA
               type:PostalAddress
            type:Organization
            name:Human Genome Sciences
            address:
               name:Oncology Research Department, Human Genome Sciences, Rockville, USA
               type:PostalAddress
            type:Organization
      name:Wendy Halpern
      affiliation:
            name:Human Genome Sciences, Pathology, Pharmacokinetics and Toxicology
            address:
               name:Human Genome Sciences, Pathology, Pharmacokinetics and Toxicology, Rockville, USA
               type:PostalAddress
            type:Organization
PostalAddress:
      name:Development Sciences and Research, Human Genome Sciences, Rockville, USA
      name:Oncology Research Department, Human Genome Sciences, Rockville, USA
      name:Human Genome Sciences, Pathology, Pharmacokinetics and Toxicology, Rockville, USA
WebPageElement:
      isAccessibleForFree:
      cssSelector:.main-content

External Links {🔗}(600)

Analytics and Tracking {📊}

  • Google Tag Manager

Libraries {📚}

  • Clipboard.js

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