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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
  13. CDN Services

We are analyzing https://link.springer.com/article/10.1186/s13059-017-1347-3.

Title:
Rewriting the transcriptome: adenosine-to-inosine RNA editing by ADARs | Genome Biology
Description:
One of the most prevalent forms of post-transcritpional RNA modification is the conversion of adenosine nucleosides to inosine (A-to-I), mediated by the ADAR family of enzymes. The functional requirement and regulatory landscape for the majority of A-to-I editing events are, at present, uncertain. Recent studies have identified key in vivo functions of ADAR enzymes, informing our understanding of the biological importance of A-to-I editing. Large-scale studies have revealed how editing is regulated both in cis and in trans. This review will explore these recent studies and how they broaden our understanding of the functions and regulation of ADAR-mediated RNA editing.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Photography
  • Movies
  • Video & Online Content

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? {💸}

The income method remains a mystery to us.

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. Link.springer.com has a secret sauce for making money, but we can't detect it yet.

Keywords {🔍}

editing, pubmed, adar, rna, article, google, scholar, cas, central, atoi, cell, human, adenosine, sites, regulation, adars, biol, activity, nat, sequence, expression, function, genome, deaminase, identified, dsrna, drosophila, specific, protein, analysis, transcriptome, gene, identification, proteins, mammalian, studies, species, levels, cis, regions, mutations, cancer, science, res, site, functions, doublestranded, sequencing, important, phenotypes,

Topics {✒️}

double-stranded-rna-specific adenosine deaminase cdc14b/skp2/p21/p27 axis rna-editing-mediated exon evolution editing activity/catalytic domain double-stranded rna substrate disrupting mir-30b-3p article download pdf central nervous system lps-stimulated immune cells innate immune/interferon response jin billy li post-transcritpional rna modification rna-editing enzyme adar1 double-stranded rna rna-editing enzyme adar2 direct interferon-stimulated gene post-transcriptional gene regulation rna editing/interacting potential rna-induced gene silencing high-throughput sequencing technologies innate immune sensing adar1-mediated editing leads adar-mediated rna editing adar-mediated rna-editing george cx quantitative trait locus full size image transcription factor period human cell line cis-acting regulatory elements innate immune system adar1-mediated rna editing query rna-editing sites adar2-mediated rna editing exclude context-specific functions innate immune response stress-induced apoptosis demonstrated catalytic activity adar1-related neurological disease adar-mediated editing resulting dadar-dependent rna editing rna-interacting proteins act antisense rna injections adenosine deaminase acting putative double-strandedness privacy choices/manage cookies dyschromatosis symmetrica hereditaria cytosolic dna metabolism identify hyper-editing sites adar protein activity/levels

Questions {❓}

  • ADARs, editing, and disease: what happens when editing goes awry?

Schema {🗺️}

WebPage:
      mainEntity:
         headline:Rewriting the transcriptome: adenosine-to-inosine RNA editing by ADARs
         description:One of the most prevalent forms of post-transcritpional RNA modification is the conversion of adenosine nucleosides to inosine (A-to-I), mediated by the ADAR family of enzymes. The functional requirement and regulatory landscape for the majority of A-to-I editing events are, at present, uncertain. Recent studies have identified key in vivo functions of ADAR enzymes, informing our understanding of the biological importance of A-to-I editing. Large-scale studies have revealed how editing is regulated both in cis and in trans. This review will explore these recent studies and how they broaden our understanding of the functions and regulation of ADAR-mediated RNA editing.
         datePublished:2017-10-30T00:00:00Z
         dateModified:2017-10-30T00:00:00Z
         pageStart:1
         pageEnd:13
         license:http://creativecommons.org/publicdomain/zero/1.0/
         sameAs:https://doi.org/10.1186/s13059-017-1347-3
         keywords:
            Adenosine Deaminase Acting On RNA (ADAR)
            ADAR Family
            ADAR Enzymes
            Editing Events
            ADAR Proteins
            Animal Genetics and Genomics
            Human Genetics
            Plant Genetics and Genomics
            Microbial Genetics and Genomics
            Bioinformatics
            Evolutionary Biology
         image:
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         isPartOf:
            name:Genome Biology
            issn:
               1474-760X
            volumeNumber:18
            type:
               Periodical
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            name:BioMed Central
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         author:
               name:Carl R. Walkley
               affiliation:
                     name:St Vincent’s Institute of Medical Research
                     address:
                        name:St Vincent’s Institute of Medical Research, Fitzroy, Australia
                        type:PostalAddress
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                     name:University of Melbourne
                     address:
                        name:Department of Medicine, St Vincent’s Hospital, University of Melbourne, Fitzroy, Australia
                        type:PostalAddress
                     type:Organization
               email:[email protected]
               type:Person
               name:Jin Billy Li
               affiliation:
                     name:Stanford University
                     address:
                        name:Department of Genetics, Stanford University, Stanford, USA
                        type:PostalAddress
                     type:Organization
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ScholarlyArticle:
      headline:Rewriting the transcriptome: adenosine-to-inosine RNA editing by ADARs
      description:One of the most prevalent forms of post-transcritpional RNA modification is the conversion of adenosine nucleosides to inosine (A-to-I), mediated by the ADAR family of enzymes. The functional requirement and regulatory landscape for the majority of A-to-I editing events are, at present, uncertain. Recent studies have identified key in vivo functions of ADAR enzymes, informing our understanding of the biological importance of A-to-I editing. Large-scale studies have revealed how editing is regulated both in cis and in trans. This review will explore these recent studies and how they broaden our understanding of the functions and regulation of ADAR-mediated RNA editing.
      datePublished:2017-10-30T00:00:00Z
      dateModified:2017-10-30T00:00:00Z
      pageStart:1
      pageEnd:13
      license:http://creativecommons.org/publicdomain/zero/1.0/
      sameAs:https://doi.org/10.1186/s13059-017-1347-3
      keywords:
         Adenosine Deaminase Acting On RNA (ADAR)
         ADAR Family
         ADAR Enzymes
         Editing Events
         ADAR Proteins
         Animal Genetics and Genomics
         Human Genetics
         Plant Genetics and Genomics
         Microbial Genetics and Genomics
         Bioinformatics
         Evolutionary Biology
      image:
         https://media.springernature.com/lw1200/springer-static/image/art%3A10.1186%2Fs13059-017-1347-3/MediaObjects/13059_2017_1347_Fig1_HTML.gif
         https://media.springernature.com/lw1200/springer-static/image/art%3A10.1186%2Fs13059-017-1347-3/MediaObjects/13059_2017_1347_Fig2_HTML.gif
      isPartOf:
         name:Genome Biology
         issn:
            1474-760X
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            Periodical
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      publisher:
         name:BioMed Central
         logo:
            url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
            type:ImageObject
         type:Organization
      author:
            name:Carl R. Walkley
            affiliation:
                  name:St Vincent’s Institute of Medical Research
                  address:
                     name:St Vincent’s Institute of Medical Research, Fitzroy, Australia
                     type:PostalAddress
                  type:Organization
                  name:University of Melbourne
                  address:
                     name:Department of Medicine, St Vincent’s Hospital, University of Melbourne, Fitzroy, Australia
                     type:PostalAddress
                  type:Organization
            email:[email protected]
            type:Person
            name:Jin Billy Li
            affiliation:
                  name:Stanford University
                  address:
                     name:Department of Genetics, Stanford University, Stanford, USA
                     type:PostalAddress
                  type:Organization
            email:[email protected]
            type:Person
      isAccessibleForFree:1
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      name:Genome Biology
      issn:
         1474-760X
      volumeNumber:18
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      name:BioMed Central
      logo:
         url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
         type:ImageObject
      name:St Vincent’s Institute of Medical Research
      address:
         name:St Vincent’s Institute of Medical Research, Fitzroy, Australia
         type:PostalAddress
      name:University of Melbourne
      address:
         name:Department of Medicine, St Vincent’s Hospital, University of Melbourne, Fitzroy, Australia
         type:PostalAddress
      name:Stanford University
      address:
         name:Department of Genetics, Stanford University, Stanford, USA
         type:PostalAddress
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      url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
Person:
      name:Carl R. Walkley
      affiliation:
            name:St Vincent’s Institute of Medical Research
            address:
               name:St Vincent’s Institute of Medical Research, Fitzroy, Australia
               type:PostalAddress
            type:Organization
            name:University of Melbourne
            address:
               name:Department of Medicine, St Vincent’s Hospital, University of Melbourne, Fitzroy, Australia
               type:PostalAddress
            type:Organization
      email:[email protected]
      name:Jin Billy Li
      affiliation:
            name:Stanford University
            address:
               name:Department of Genetics, Stanford University, Stanford, USA
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:St Vincent’s Institute of Medical Research, Fitzroy, Australia
      name:Department of Medicine, St Vincent’s Hospital, University of Melbourne, Fitzroy, Australia
      name:Department of Genetics, Stanford University, Stanford, USA

External Links {🔗}(567)

Analytics and Tracking {📊}

  • Google Tag Manager

Libraries {📚}

  • Backbone.js
  • Clipboard.js
  • Prism.js

CDN Services {📦}

  • Crossref

5.2s.