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. Questions
  9. Schema
  10. External Links
  11. Analytics And Tracking
  12. Libraries

We are analyzing https://link.springer.com/article/10.1007/s10555-023-10149-4.

Title:
Clonal tracking in cancer and metastasis | Cancer and Metastasis Reviews
Description:
The eradication of many cancers has proven challenging due to the presence of functionally and genetically heterogeneous clones maintained by rare cancer stem cells (CSCs), which contribute to disease progression, treatment refractoriness, and late relapse. The characterization of functional CSC activity has necessitated the development of modern clonal tracking strategies. This review describes viral-based and CRISPR-Cas9-based cellular barcoding, lineage tracing, and imaging-based approaches. DNA-based cellular barcoding technology is emerging as a powerful and robust strategy that has been widely applied to in vitro and in vivo model systems, including patient-derived xenograft models. This review also highlights the potential of these methods for use in the clinical and drug discovery contexts and discusses the important insights gained from such approaches. Graphical Abstract
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 8,170,236 visitors per month in the current month.

check SE Ranking
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How Does Link.springer.com Make Money? {πŸ’Έ}

We see no obvious way the site makes money.

Earning money isn't the goal of every website; some are designed to offer support or promote social causes. People have different reasons for creating websites. This might be one such reason. Link.springer.com might be plotting its profit, but the way they're doing it isn't detectable yet.

Keywords {πŸ”}

pubmed, article, google, scholar, cas, central, cancer, nature, cell, stem, cells, clonal, barcoding, lineage, human, singlecell, analysis, van, tracking, cellular, medicine, science, molecular, dynamics, nguyen, tracing, breast, dna, sequencing, tumor, evolution, wang, reviews, methods, leukemia, reveals, therapy, kannan, vivo, genetic, growth, gene, mice, states, blood, data, journal, research, heterogeneity, hematopoietic,

Topics {βœ’οΈ}

crispr/cas9/cas12/cas13/cas14 proteins utilized cd40-based immuno-chemotherapy combination crispr/cas9-based genome editing crispr-cas9-based cellular barcoding month download article/chapter human colon-cancer-initiating cells cre-recombinase-driven polylox barcoding crispr-cas9-induced genetic scars review describes viral-based fluorescent multi-clonal tracking long-term multilineage engraftment plasma cell-free dna tumor clone-initiating cells lineage-specific gene expression reversible transcriptomic profile single-stem-cell level single-cell analyses define single-cell cancer genomes double-strand breaks induced sequential small-molecule fluorescent single-cell lineage tracing single-clone tracking gene expression profiles imaging-based approaches pre-existing functional heterogeneity simultaneous single-cell profiling long viet nguyen single-cell lineages reveal high dna specificity cell-free dna minute chromosome human glioblastoma reveals full article pdf cancer stem cells initiating tumour growth cellular barcoding tool single-cell sequencing early haematopoietic progenitors single-cell resolution nagarajan kannan studying clonal dynamics decipher clonal dynamics acute myeloid leukemia crispr-cas9 leads crispr-cas9 nucleases counting stem cells crispra-inducible reporters primitive hematopoietic cell cell stem cell article aalam

Questions {❓}

  • Tackling the cancer stem cells - what challenges do they pose?

Schema {πŸ—ΊοΈ}

WebPage:
      mainEntity:
         headline:Clonal tracking in cancer and metastasis
         description:The eradication of many cancers has proven challenging due to the presence of functionally and genetically heterogeneous clones maintained by rare cancer stem cells (CSCs), which contribute to disease progression, treatment refractoriness, and late relapse. The characterization of functional CSC activity has necessitated the development of modern clonal tracking strategies. This review describes viral-based and CRISPR-Cas9-based cellular barcoding, lineage tracing, and imaging-based approaches. DNA-based cellular barcoding technology is emerging as a powerful and robust strategy that has been widely applied to in vitro and in vivo model systems, including patient-derived xenograft models. This review also highlights the potential of these methods for use in the clinical and drug discovery contexts and discusses the important insights gained from such approaches.
         datePublished:2023-11-01T00:00:00Z
         dateModified:2023-11-01T00:00:00Z
         pageStart:639
         pageEnd:656
         sameAs:https://doi.org/10.1007/s10555-023-10149-4
         keywords:
            Cellular barcoding
            Clonal tracking
            Cancer stem cells
            Clonal dynamics
            Cancer Research
            Oncology
            Biomedicine
            general
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                        type:PostalAddress
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      headline:Clonal tracking in cancer and metastasis
      description:The eradication of many cancers has proven challenging due to the presence of functionally and genetically heterogeneous clones maintained by rare cancer stem cells (CSCs), which contribute to disease progression, treatment refractoriness, and late relapse. The characterization of functional CSC activity has necessitated the development of modern clonal tracking strategies. This review describes viral-based and CRISPR-Cas9-based cellular barcoding, lineage tracing, and imaging-based approaches. DNA-based cellular barcoding technology is emerging as a powerful and robust strategy that has been widely applied to in vitro and in vivo model systems, including patient-derived xenograft models. This review also highlights the potential of these methods for use in the clinical and drug discovery contexts and discusses the important insights gained from such approaches.
      datePublished:2023-11-01T00:00:00Z
      dateModified:2023-11-01T00:00:00Z
      pageStart:639
      pageEnd:656
      sameAs:https://doi.org/10.1007/s10555-023-10149-4
      keywords:
         Cellular barcoding
         Clonal tracking
         Cancer stem cells
         Clonal dynamics
         Cancer Research
         Oncology
         Biomedicine
         general
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                     type:PostalAddress
                  type:Organization
            type:Person
            name:Long Viet Nguyen
            affiliation:
                  name:University Health Network
                  address:
                     name:Princess Margaret Cancer Centre, University Health Network, Toronto, Canada
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                     name:Department of Medicine, University of Toronto, Toronto, Canada
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                     name:Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, USA
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                  address:
                     name:Mayo Clinic Comprehensive Cancer Center, Mayo Clinic, Rochester, USA
                     type:PostalAddress
                  type:Organization
                  name:Mayo Clinic
                  address:
                     name:Center for Regenerative Biotherapeutics, Mayo Clinic, Rochester, USA
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         name:Department of Medicine, University of Toronto, Toronto, Canada
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      name:University of Toronto
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         name:Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, USA
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      address:
         name:Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, USA
         type:PostalAddress
      name:Mayo Clinic
      address:
         name:Mayo Clinic Comprehensive Cancer Center, Mayo Clinic, Rochester, USA
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      address:
         name:Center for Regenerative Biotherapeutics, Mayo Clinic, Rochester, USA
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            address:
               name:Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, USA
               type:PostalAddress
            type:Organization
      name:Long Viet Nguyen
      affiliation:
            name:University Health Network
            address:
               name:Princess Margaret Cancer Centre, University Health Network, Toronto, Canada
               type:PostalAddress
            type:Organization
            name:University of Toronto
            address:
               name:Department of Medicine, University of Toronto, Toronto, Canada
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            name:University of Toronto
            address:
               name:Department of Medical Biophysics, University of Toronto, Toronto, Canada
               type:PostalAddress
            type:Organization
      name:Megan L. Ritting
      affiliation:
            name:Mayo Clinic
            address:
               name:Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, USA
               type:PostalAddress
            type:Organization
      name:Nagarajan Kannan
      url:http://orcid.org/0000-0002-8825-2178
      affiliation:
            name:Mayo Clinic
            address:
               name:Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, USA
               type:PostalAddress
            type:Organization
            name:Mayo Clinic
            address:
               name:Mayo Clinic Comprehensive Cancer Center, Mayo Clinic, Rochester, USA
               type:PostalAddress
            type:Organization
            name:Mayo Clinic
            address:
               name:Center for Regenerative Biotherapeutics, Mayo Clinic, Rochester, USA
               type:PostalAddress
            type:Organization
      email:[email protected]
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      name:Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, USA
      name:Princess Margaret Cancer Centre, University Health Network, Toronto, Canada
      name:Department of Medicine, University of Toronto, Toronto, Canada
      name:Department of Medical Biophysics, University of Toronto, Toronto, Canada
      name:Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, USA
      name:Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, USA
      name:Mayo Clinic Comprehensive Cancer Center, Mayo Clinic, Rochester, USA
      name:Center for Regenerative Biotherapeutics, Mayo Clinic, Rochester, USA
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External Links {πŸ”—}(513)

Analytics and Tracking {πŸ“Š}

  • Google Tag Manager

Libraries {πŸ“š}

  • Clipboard.js
  • Prism.js

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