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  1. Analyzed Page
  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Doi.org Make Money
  6. Keywords
  7. Topics
  8. Questions
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We began analyzing https://link.springer.com/article/10.1007/s10014-013-0149-x, but it redirected us to https://link.springer.com/article/10.1007/s10014-013-0149-x. The analysis below is for the second page.

Title[redir]:
Pathological features of highly invasive glioma stem cells in a mouse xenograft model | Brain Tumor Pathology
Description:
Glioma stem cells (GSCs) may be a source of tumor progression and recurrence after multimodal therapy, because of their high invasive potential. The purpose of this study was to compare the invasive and migratory properties of GSCs and non-GSCs and examine the distribution of these cells in a mouse xenograft model. Three GSC lines, G144, Y02, and Y10, cultured from human glioblastoma, were used in the study. Matrigel-invasion assays of infiltration and time-lapse studies of migration were performed for comparison of the GSCs with the corresponding differentiated non-GSC lines. Cells were also transplanted into mouse brain and the different distribution of GSCs and non-GSCs was examined in the tumor xenograft model. All 3 GSC lines had greater invasion and migration ability than the corresponding non-GSCs. In vivo, GSCs infiltrated more widely than non-GSCs and reached the contralateral hemisphere via the corpus callosum in the early stage of tumorigenesis. GSCs also primarily penetrated the subventricular zone (SVZ). GSCs have high invasive potential and tend to be present in the outer tumor bulk and infiltrate the contralateral hemisphere via the corpus callosum, in addition to penetrating the SVZ.

Matching Content Categories {📚}

  • Science
  • Education
  • Telecommunications

Content Management System {📝}

What CMS is doi.org built with?

Custom-built

No common CMS systems were detected on Doi.org, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of doi.org audience?

🏙️ Massive Traffic: 50M - 100M visitors per month


Based on our best estimate, this website will receive around 80,904,851 visitors per month in the current month.

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How Does Doi.org Make Money? {💸}

We find it hard to spot revenue streams.

While profit motivates many websites, others exist to inspire, entertain, or provide valuable resources. Websites have a variety of goals. And this might be one of them. Doi.org might be making money, but it's not detectable how they're doing it.

Keywords {🔍}

article, pubmed, stem, cells, google, scholar, cas, cell, tumor, glioma, glioblastoma, cancer, brain, central, invasive, gscs, mouse, access, yamaguchi, privacy, cookies, content, research, yoshikawa, lines, human, migration, invasion, dirks, huang, publish, search, xenograft, model, sadahiro, nongscs, clarke, res, bao, rich, nature, data, information, log, journal, pathology, highly, hirokazu, ideguchi, potential,

Topics {✒️}

pten/pi3k/akt pathway regulates month download article/chapter n-cadherin signaling pathway patched-1-deficient mouse medulloblastoma glioma stem cells glioma tumor stem tumor stem cells cancer stem cells cancer stem cell central nervous system tumor-initiating cells matrigel-invasion assays glioblastoma stem cells stem cell markers full article pdf subventricular zone pathological features cell migration tumor xenograft model privacy choices/manage cookies glioblastoma—molecular signaling mouse xenograft model human brain tumors outer tumor bulk tumor-specific phenotypes specialized vascular niche yamaguchi university school high invasive potential elevated invasive potential increased akt activation van der veken migration ability corpus callosum cancer stem greater invasion european economic area time-lapse studies article sadahiro cancer cell 17 cancer cell 11 cancer cell 15 conditions privacy policy check access garcia-verdugo jm instant access article log ludwin sk accepting optional cookies aya ishii eiji ikeda

Questions {❓}

  • Dong J, Huang Q (2011) Targeting glioma stem cells: enough to terminate gliomagenesis?

Schema {🗺️}

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         headline:Pathological features of highly invasive glioma stem cells in a mouse xenograft model
         description:Glioma stem cells (GSCs) may be a source of tumor progression and recurrence after multimodal therapy, because of their high invasive potential. The purpose of this study was to compare the invasive and migratory properties of GSCs and non-GSCs and examine the distribution of these cells in a mouse xenograft model. Three GSC lines, G144, Y02, and Y10, cultured from human glioblastoma, were used in the study. Matrigel-invasion assays of infiltration and time-lapse studies of migration were performed for comparison of the GSCs with the corresponding differentiated non-GSC lines. Cells were also transplanted into mouse brain and the different distribution of GSCs and non-GSCs was examined in the tumor xenograft model. All 3 GSC lines had greater invasion and migration ability than the corresponding non-GSCs. In vivo, GSCs infiltrated more widely than non-GSCs and reached the contralateral hemisphere via the corpus callosum in the early stage of tumorigenesis. GSCs also primarily penetrated the subventricular zone (SVZ). GSCs have high invasive potential and tend to be present in the outer tumor bulk and infiltrate the contralateral hemisphere via the corpus callosum, in addition to penetrating the SVZ.
         datePublished:2013-05-14T00:00:00Z
         dateModified:2013-05-14T00:00:00Z
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      headline:Pathological features of highly invasive glioma stem cells in a mouse xenograft model
      description:Glioma stem cells (GSCs) may be a source of tumor progression and recurrence after multimodal therapy, because of their high invasive potential. The purpose of this study was to compare the invasive and migratory properties of GSCs and non-GSCs and examine the distribution of these cells in a mouse xenograft model. Three GSC lines, G144, Y02, and Y10, cultured from human glioblastoma, were used in the study. Matrigel-invasion assays of infiltration and time-lapse studies of migration were performed for comparison of the GSCs with the corresponding differentiated non-GSC lines. Cells were also transplanted into mouse brain and the different distribution of GSCs and non-GSCs was examined in the tumor xenograft model. All 3 GSC lines had greater invasion and migration ability than the corresponding non-GSCs. In vivo, GSCs infiltrated more widely than non-GSCs and reached the contralateral hemisphere via the corpus callosum in the early stage of tumorigenesis. GSCs also primarily penetrated the subventricular zone (SVZ). GSCs have high invasive potential and tend to be present in the outer tumor bulk and infiltrate the contralateral hemisphere via the corpus callosum, in addition to penetrating the SVZ.
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         Cancer Research
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External Links {🔗}(192)

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Mail Servers:

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Name Servers:

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