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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
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We are analyzing https://link.springer.com/article/10.1007/s10577-006-1030-0.

Title:
Chromatin dynamics and the evolution of alternate promoter states | Chromosome Research
Description:
Eucaryotic gene transcriptional switches utilize changes both in the activity and composition of soluble transcription factor complexes, and epigenetic modifications to the chromatin template. Until recently, alternate states of promoter activity have been associated with the assembly of relatively stable multiprotein complexes on target genes, with transitions in the composition of these complexes occurring on the time scale of minutes or hours. The development of living cell techniques to characterize transcription factor function in real time has led to an alternate view of highly dynamic protein/template interactions. In addition, emerging evidence suggests that energy-dependent processes contribute significantly to the rapid movement of proteins in living cells, and to the exchange of sequence-specific DNA-binding proteins with regulatory elements. Potential mechanisms involved in the unexpectedly rapid flux of factor/template interactions are discussed in the context of a “return-to-template” model for transcription factor function.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
  • Science
  • Telecommunications

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 5,000,019 visitors per month in the current month.
However, some sources were not loaded, we suggest to reload the page to get complete results.

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

We find it hard to spot revenue streams.

While many websites aim to make money, others are created to share knowledge or showcase creativity. People build websites for various reasons. This could be one of them. Link.springer.com might have a hidden revenue stream, but it's not something we can detect.

Keywords {🔍}

google, scholar, cas, pubmed, article, chromatin, transcription, cell, receptor, biol, hager, mol, dynamics, promoter, gene, receptors, glucocorticoid, science, remodeling, nuclear, elbi, nagaich, cells, research, transcriptional, factor, living, dynamic, proteins, steroid, factors, walker, curr, privacy, cookies, content, john, complexes, rapid, access, structure, estrogen, chem, cancer, function, publish, search, alternate, johnson, interactions,

Topics {✒️}

month download article/chapter sequence-specific dna-binding proteins yi qiu & sam john induced alpha-helix structure uv laser cross-linking pre-unfolding resonant oscillations nf-kappab transcription factor steroid–dependent hypersensitive region swi/snf chromatin remodeling regulatory elements saccharomyces cerevisiae snf2/swi2 estrogen receptor-regulated transcription related subjects atp-dependent nucleosome remodeling progesterone receptor-hsp90 complexes full article pdf regulated transcription factors gene expression privacy choices/manage cookies transcription factor dynamics n-terminal domains transcription factor function dynamic regulation signal-mediated transport factor/template interactions atp-dependent mobilization ligand specific dynamics steroid hormone receptors dynamic hp1 binding ligand-dependent interaction transcriptional state transcriptional activation transcription factors rapid periodic binding alternate promoter states p160 coactivator complexes glucocorticoid receptor requires smith cl stable multiprotein complexes nuclear hormone receptors gene targeting european economic area emerging evidence suggests potential mechanisms involved stable heterochromatin domains mammalian rna polymerase archer tk higher education press proteasome-mediated turnover mcnally jg

Questions {❓}

  • Margueron R, Trojer P, Reinberg D (2005) The key to development: interpreting the histone code?

Schema {🗺️}

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         headline:Chromatin dynamics and the evolution of alternate promoter states
         description:Eucaryotic gene transcriptional switches utilize changes both in the activity and composition of soluble transcription factor complexes, and epigenetic modifications to the chromatin template. Until recently, alternate states of promoter activity have been associated with the assembly of relatively stable multiprotein complexes on target genes, with transitions in the composition of these complexes occurring on the time scale of minutes or hours. The development of living cell techniques to characterize transcription factor function in real time has led to an alternate view of highly dynamic protein/template interactions. In addition, emerging evidence suggests that energy-dependent processes contribute significantly to the rapid movement of proteins in living cells, and to the exchange of sequence-specific DNA-binding proteins with regulatory elements. Potential mechanisms involved in the unexpectedly rapid flux of factor/template interactions are discussed in the context of a “return-to-template” model for transcription factor function.
         datePublished:2006-03-03T00:00:00Z
         dateModified:2006-03-03T00:00:00Z
         pageStart:107
         pageEnd:116
         sameAs:https://doi.org/10.1007/s10577-006-1030-0
         keywords:
            chromatin
            DNA methylation
            gene expression
            promoter
            transcription
            Cell Biology
            Human Genetics
            Animal Genetics and Genomics
            Plant Genetics and Genomics
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            issn:
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            volumeNumber:14
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      headline:Chromatin dynamics and the evolution of alternate promoter states
      description:Eucaryotic gene transcriptional switches utilize changes both in the activity and composition of soluble transcription factor complexes, and epigenetic modifications to the chromatin template. Until recently, alternate states of promoter activity have been associated with the assembly of relatively stable multiprotein complexes on target genes, with transitions in the composition of these complexes occurring on the time scale of minutes or hours. The development of living cell techniques to characterize transcription factor function in real time has led to an alternate view of highly dynamic protein/template interactions. In addition, emerging evidence suggests that energy-dependent processes contribute significantly to the rapid movement of proteins in living cells, and to the exchange of sequence-specific DNA-binding proteins with regulatory elements. Potential mechanisms involved in the unexpectedly rapid flux of factor/template interactions are discussed in the context of a “return-to-template” model for transcription factor function.
      datePublished:2006-03-03T00:00:00Z
      dateModified:2006-03-03T00:00:00Z
      pageStart:107
      pageEnd:116
      sameAs:https://doi.org/10.1007/s10577-006-1030-0
      keywords:
         chromatin
         DNA methylation
         gene expression
         promoter
         transcription
         Cell Biology
         Human Genetics
         Animal Genetics and Genomics
         Plant Genetics and Genomics
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            address:
               name:Laboratory of Receptor Biology and Gene Expression, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, USA
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            address:
               name:Laboratory of Receptor Biology and Gene Expression, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, USA
               type:PostalAddress
            type:Organization
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            name:National Cancer Institute, NIH
            address:
               name:Laboratory of Receptor Biology and Gene Expression, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, USA
               type:PostalAddress
            type:Organization
      name:R. Louis Schiltz
      affiliation:
            name:National Cancer Institute, NIH
            address:
               name:Laboratory of Receptor Biology and Gene Expression, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, USA
               type:PostalAddress
            type:Organization
      name:Yi Qiu
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            address:
               name:Laboratory of Receptor Biology and Gene Expression, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, USA
               type:PostalAddress
            type:Organization
      name:Sam John
      affiliation:
            name:National Cancer Institute, NIH
            address:
               name:Laboratory of Receptor Biology and Gene Expression, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, USA
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      name:Laboratory of Receptor Biology and Gene Expression, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, USA
      name:Laboratory of Receptor Biology and Gene Expression, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, USA
      name:Laboratory of Receptor Biology and Gene Expression, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, USA
      name:Laboratory of Receptor Biology and Gene Expression, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, USA
      name:Laboratory of Receptor Biology and Gene Expression, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, USA
      name:Laboratory of Receptor Biology and Gene Expression, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, USA
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External Links {🔗}(178)

Analytics and Tracking {📊}

  • Google Tag Manager

Libraries {📚}

  • Clipboard.js
  • Prism.js

CDN Services {📦}

  • Crossref

4.6s.