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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/s00280-005-0097-1.

Title:
A self-renewal assay for cancer stem cells | Cancer Chemotherapy and Pharmacology
Description:
Cancers of epithelial origin are responsible for the majority of cancer-related deaths in the USA. Unfortunately, although chemotherapy and/or radiation therapy can sometimes shrink tumors, metastatic cancers of epithelial origin are essentially incurable. It is clear that new approaches are needed to treat these diseases. Although cancer cell lines provide invaluable information, their biological properties often differ in crucial ways from de novo cancer cells. Our laboratory has developed a novel mouse model that reliably permits individual cancer cells isolated directly from patients’ tumors to be assayed. This will allow the characterization of crucial signaling pathways involved in processes such as self-renewal that are critical for tumor formation by the cancer cells within de novo tumors. These tools should lead to new insights into the cellular and molecular mechanisms that drive human breast cancer growth and invasion.
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 5,000,016 visitors per month in the current month.

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

We can't tell how the site generates income.

Not all websites focus on profit; some are designed to educate, connect people, or share useful tools. People create websites for numerous reasons. And this could be one such example. Link.springer.com might be making money, but it's not detectable how they're doing it.

Keywords {🔍}

google, scholar, cancer, pubmed, article, cas, cells, cell, stem, human, clarke, selfrenewal, breast, wnt, nature, van, privacy, cookies, content, assay, epithelial, usa, tumor, weissman, blood, mice, information, publish, search, tumors, metastatic, mouse, access, res, phenotype, leukemia, data, log, journal, research, chemotherapy, michael, novo, signaling, growth, chapter, biology, related, discover, morrison,

Topics {✒️}

beta-catenin/tcf-4 complex imposes month download article/chapter increased beta-catenin levels epithelial stem-cell compartments stem cell factor article cancer chemotherapy full article pdf hematopoietic stem cells related subjects cancer stem cells cancer-related deaths breast cancer cells human cancer cells privacy choices/manage cookies truncated beta-catenin human breast tumours haematopoietic stem cells de novo tumors colorectal cancer cells mammary gland hyperplasia anticancer drug discovery van den elsen van der horn van den born michigan medical school scid repopulating cell leukemic cell maturation lymphocytic l1210 cells apc tumor suppressor european economic area york al-hajj clinically active compounds mice lacking tcf-4 bcl-2 inhibits apoptosis tjon-pon-fong bergsagel de downstream wnt signaling wnt signalling pathways conditions privacy policy spleen colony assay oxford university press divergent molecular phenotypes spleen colony studies wnt gene family accepting optional cookies crypt progenitor phenotype article log stem cells human cancer pharmacology article

Schema {🗺️}

WebPage:
      mainEntity:
         headline:A self-renewal assay for cancer stem cells
         description:Cancers of epithelial origin are responsible for the majority of cancer-related deaths in the USA. Unfortunately, although chemotherapy and/or radiation therapy can sometimes shrink tumors, metastatic cancers of epithelial origin are essentially incurable. It is clear that new approaches are needed to treat these diseases. Although cancer cell lines provide invaluable information, their biological properties often differ in crucial ways from de novo cancer cells. Our laboratory has developed a novel mouse model that reliably permits individual cancer cells isolated directly from patients’ tumors to be assayed. This will allow the characterization of crucial signaling pathways involved in processes such as self-renewal that are critical for tumor formation by the cancer cells within de novo tumors. These tools should lead to new insights into the cellular and molecular mechanisms that drive human breast cancer growth and invasion.
         datePublished:2005-11-05T00:00:00Z
         dateModified:2005-11-05T00:00:00Z
         pageStart:64
         pageEnd:68
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            Self-renewal
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            Cancer Research
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         isPartOf:
            name:Cancer Chemotherapy and Pharmacology
            issn:
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         author:
               name:Michael F. Clarke
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                     name:University of Michigan Medical School
                     address:
                        name:University of Michigan Medical School, Ann Arbor, USA
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      headline:A self-renewal assay for cancer stem cells
      description:Cancers of epithelial origin are responsible for the majority of cancer-related deaths in the USA. Unfortunately, although chemotherapy and/or radiation therapy can sometimes shrink tumors, metastatic cancers of epithelial origin are essentially incurable. It is clear that new approaches are needed to treat these diseases. Although cancer cell lines provide invaluable information, their biological properties often differ in crucial ways from de novo cancer cells. Our laboratory has developed a novel mouse model that reliably permits individual cancer cells isolated directly from patients’ tumors to be assayed. This will allow the characterization of crucial signaling pathways involved in processes such as self-renewal that are critical for tumor formation by the cancer cells within de novo tumors. These tools should lead to new insights into the cellular and molecular mechanisms that drive human breast cancer growth and invasion.
      datePublished:2005-11-05T00:00:00Z
      dateModified:2005-11-05T00:00:00Z
      pageStart:64
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         Cancer
         Self-renewal
         Oncology
         Pharmacology/Toxicology
         Cancer Research
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            name:Michael F. Clarke
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                  name:University of Michigan Medical School
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                     name:University of Michigan Medical School, Ann Arbor, USA
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               name:University of Michigan Medical School, Ann Arbor, USA
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      name:University of Michigan Medical School, Ann Arbor, USA
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External Links {🔗}(117)

Analytics and Tracking {📊}

  • Google Tag Manager

Libraries {📚}

  • Clipboard.js
  • Prism.js

CDN Services {📦}

  • Crossref

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