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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
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We are analyzing https://link.springer.com/chapter/10.1007/978-981-10-3233-2_19.

Title:
Roles of RUNX in Solid Tumors | SpringerLink
Description:
All RUNX genes have been implicated in the development of solid tumors, but the role each RUNX gene plays in the different tumor types is complicated by multiple interactions with major signaling pathways and tumor heterogeneity. Moreover, for a given tissue type,...
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {πŸ“š}

  • Education
  • Science
  • Health & Fitness

Content Management System {πŸ“}

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 {πŸ“ˆ}

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? {πŸ’Έ}

We don’t know how the website earns money.

Many websites are intended to earn money, but some serve to share ideas or build connections. Websites exist for all kinds of purposes. 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 {πŸ”}

pubmed, google, scholar, article, runx, cas, cancer, central, ito, cell, research, journal, cells, gastric, expression, transcription, nature, singapore, development, human, protein, lee, biology, gene, tumor, molecular, chapter, chuang, biological, factor, oncogene, breast, national, epithelial, suppressor, levanon, chemistry, medicine, role, mechanisms, factors, van, sciences, growth, science, kim, inoue, privacy, cookies, function,

Topics {βœ’οΈ}

runt-related transcription factor oncogenic tead-yap complex month download article/chapter runx3 attenuates beta-catenin/ tgfbeta1-mediated growth inhibition dna-induced molecular clamp tumor-induced bone disease runx2-smad signaling impacts lineage-specific transcriptional control aml1/runx-1 runt domain subtype-specific breast cancer transcription factor mutated cell-permeable runx3 protein apoptotic pathway induced gastric epithelial cells growth arrest independently mesenchymal progenitor cells potent prognostic factor privacy choices/manage cookies human tissue microarray human hepatocellular carcinoma human colon carcinoma clinical cancer research transcription factors homologous metazoan transcription factors device instant download epithelial tumor formation frequent allelic inactivation drosophila runt gene human gastric cancers runx transcription factors gastric cancer cells normal gastric epithelium inducing precancerous state chief cell differentiation innate lymphoid cells redirect cell fate regulate cell fate hair shape determination dna repair defects chapter runx proteins gastric mucosal hyperplasia biophysical research communications runx2 regulate transcription inflammation-induced expression van der deen primary murine fibroblasts hair follicle development breast cancer cells human pancreatic cancer

Questions {❓}

  • 1p36 tumor suppression – a matter of dosage?
  • Runt-related transcription factors in human carcinogenesis: a friend or foe?

Schema {πŸ—ΊοΈ}

ScholarlyArticle:
      headline:Roles of RUNX in Solid Tumors
      pageEnd:320
      pageStart:299
      image:https://media.springernature.com/w153/springer-static/cover/book/978-981-10-3233-2.jpg
      genre:
         Biomedical and Life Sciences
         Biomedical and Life Sciences (R0)
      isPartOf:
         name:RUNX Proteins in Development and Cancer
         isbn:
            978-981-10-3233-2
            978-981-10-3231-8
         type:Book
      publisher:
         name:Springer Singapore
         logo:
            url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
            type:ImageObject
         type:Organization
      author:
            name:Linda Shyue Huey Chuang
            affiliation:
                  name:National University of Singapore
                  address:
                     name:Cancer Science Institute of Singapore, Center for Translational Medicine, National University of Singapore, Singapore, Singapore
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Kosei Ito
            affiliation:
                  name:Nagasaki University
                  address:
                     name:Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki, Japan
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Yoshiaki Ito
            affiliation:
                  name:National University of Singapore
                  address:
                     name:Cancer Science Institute of Singapore, Center for Translational Medicine, National University of Singapore, Singapore, Singapore
                     type:PostalAddress
                  type:Organization
            email:[email protected]
            type:Person
      keywords:RUNX, Solid tumors, Tumor suppressor, Oncogene, Wnt, TGFΞ², RAS, Senescence, Protein-protein interaction, Stress-inducible gene, Precancerous state, Intestinal metaplasia
      description:All RUNX genes have been implicated in the development of solid tumors, but the role each RUNX gene plays in the different tumor types is complicated by multiple interactions with major signaling pathways and tumor heterogeneity. Moreover, for a given tissue type, the specific role of each RUNX protein is distinct at different stages of differentiation. A regulatory function for RUNX in tissue stem cells points sharply to a causal effect in tumorigenesis. Understanding how RUNX dysregulation in cancer impinges on normal biological processes is important for identifying the molecular mechanisms that lead to malignancy. It will also indicate whether restoration of proper RUNX function to redirect cell fate is a feasible treatment for cancer. With the recent advances in RUNX research, it is time to revisit the many mechanisms/pathways that RUNX engage to regulate cell fate and decide whether cells proliferate, differentiate or die.
      datePublished:2017
      isAccessibleForFree:
      hasPart:
         isAccessibleForFree:
         cssSelector:.main-content
         type:WebPageElement
      context:https://schema.org
Book:
      name:RUNX Proteins in Development and Cancer
      isbn:
         978-981-10-3233-2
         978-981-10-3231-8
Organization:
      name:Springer Singapore
      logo:
         url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
         type:ImageObject
      name:National University of Singapore
      address:
         name:Cancer Science Institute of Singapore, Center for Translational Medicine, National University of Singapore, Singapore, Singapore
         type:PostalAddress
      name:Nagasaki University
      address:
         name:Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki, Japan
         type:PostalAddress
      name:National University of Singapore
      address:
         name:Cancer Science Institute of Singapore, Center for Translational Medicine, National University of Singapore, Singapore, Singapore
         type:PostalAddress
ImageObject:
      url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
Person:
      name:Linda Shyue Huey Chuang
      affiliation:
            name:National University of Singapore
            address:
               name:Cancer Science Institute of Singapore, Center for Translational Medicine, National University of Singapore, Singapore, Singapore
               type:PostalAddress
            type:Organization
      name:Kosei Ito
      affiliation:
            name:Nagasaki University
            address:
               name:Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki, Japan
               type:PostalAddress
            type:Organization
      name:Yoshiaki Ito
      affiliation:
            name:National University of Singapore
            address:
               name:Cancer Science Institute of Singapore, Center for Translational Medicine, National University of Singapore, Singapore, Singapore
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:Cancer Science Institute of Singapore, Center for Translational Medicine, National University of Singapore, Singapore, Singapore
      name:Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki, Japan
      name:Cancer Science Institute of Singapore, Center for Translational Medicine, National University of Singapore, Singapore, Singapore
WebPageElement:
      isAccessibleForFree:
      cssSelector:.main-content

External Links {πŸ”—}(300)

Analytics and Tracking {πŸ“Š}

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5.26s.