Here's how DOI.ORG makes money* and how much!

*Please read our disclaimer before using our estimates.
Loading...

DOI . ORG {}

  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. Schema
  9. External Links
  10. Analytics And Tracking
  11. Libraries
  12. Hosting Providers
  13. CDN Services

We began analyzing https://link.springer.com/article/10.1007/BF02603118, but it redirected us to https://link.springer.com/article/10.1007/BF02603118. The analysis below is for the second page.

Title[redir]:
An evaluation of the molecular clock hypothesis using mammalian DNA sequences | Journal of Molecular Evolution
Description:
A statistical analysis of extensive DNA sequence data from primates, rodents, and artiodacytls clearly indicates that no global molecular clock exists in mammals. Rates of nucleotide subsitution in rodents are estimated to be four to eight times higher than those in higher primates and two to four times higher than those in artiodactyls. There is strong evidence for lower substitution rates in apes and humans than in monkeys, supporting the hominoid slowdown hypothesis. There is also evidence for lower rates in humans than in apes, suggesting a further rate slowdown in the human lineage after the separation of humans from apes. By contrast, substitution rates are nearly equal in mouse and rat. These results suggest that differences in generation time or, more precisely, in the number of germline DNA replications per year are the primary cause of rate differences in mammals. Further, these differences are more in line with the neutral mutation hypothesis than if the rates are the same for short-and long-living mammals.

Matching Content Categories {📚}

  • Education
  • Science
  • Animals & Wildlife

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?

🌠 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.

check SE Ranking
check Ahrefs
check Similarweb
check Ubersuggest
check Semrush

How Does Doi.org Make Money? {💸}

We see no obvious way the site makes money.

Websites don't always need to be profitable; some serve as platforms for education or personal expression. Websites can serve multiple purposes. And this might be one of them. Doi.org has a revenue plan, but it's either invisible or we haven't found it.

Keywords {🔍}

google, scholar, article, cas, pubmed, evolution, gene, molecular, sequence, nucleotide, human, mol, evol, dna, biol, genes, sequences, nature, cdna, usa, rates, mouse, sci, evolutionary, proc, natl, acad, clock, structure, globin, expression, analysis, rate, cell, res, goodman, evidence, substitution, hominoid, rat, cloning, biochem, chem, science, βglobin, press, slightom, aldolase, content, apes,

Topics {✒️}

k-atpase β-chain gene month download article/chapter human β-globin gene time-dependent effect late oligocene-early miocene goat β-globin locus k-atpase β-subunit chimpanzee α-globin mrnas hominoid slowdown hypothesis neutral theory muscle acetylcholine receptor γ subunit precursor generation time human α-globin dna molecular clock human ∈-globin gene full article pdf ��4 β-globin genes bovine globin locus fetal globin gene βγ-crystallin superfamily multiple gene conversions related subjects molecular clock hypothesis molecular clock runs fossil-based divergence dates neutral mutation hypothesis rate slowdown human cholecystokinin gene privacy choices/manage cookies early paromomyid primate primate dna sequences mitochondrial genes dna-dna hybridization immunological time scale alu-type repeats βa-globin genes placental cdna encoding schimenti jc evolutionarily related enzymes mammalian dna sequences insulin gene family article li rat interleukin-3 gene germline dna replications check access instant access mouse aldolase genes dna repair genes van santen vl

Schema {🗺️}

WebPage:
      mainEntity:
         headline:An evaluation of the molecular clock hypothesis using mammalian DNA sequences
         description:A statistical analysis of extensive DNA sequence data from primates, rodents, and artiodacytls clearly indicates that no global molecular clock exists in mammals. Rates of nucleotide subsitution in rodents are estimated to be four to eight times higher than those in higher primates and two to four times higher than those in artiodactyls. There is strong evidence for lower substitution rates in apes and humans than in monkeys, supporting the hominoid slowdown hypothesis. There is also evidence for lower rates in humans than in apes, suggesting a further rate slowdown in the human lineage after the separation of humans from apes. By contrast, substitution rates are nearly equal in mouse and rat. These results suggest that differences in generation time or, more precisely, in the number of germline DNA replications per year are the primary cause of rate differences in mammals. Further, these differences are more in line with the neutral mutation hypothesis than if the rates are the same for short-and long-living mammals.
         datePublished:
         dateModified:
         pageStart:330
         pageEnd:342
         sameAs:https://doi.org/10.1007/BF02603118
         keywords:
            Molecular clock
            Generation-time effect
            Hominoid slowdown
            Hominid slowdown
            Neutral theory
            Evolutionary Biology
            Microbiology
            Plant Sciences
            Plant Genetics and Genomics
            Animal Genetics and Genomics
            Cell Biology
         image:
         isPartOf:
            name:Journal of Molecular Evolution
            issn:
               1432-1432
               0022-2844
            volumeNumber:25
            type:
               Periodical
               PublicationVolume
         publisher:
            name:Springer-Verlag
            logo:
               url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
               type:ImageObject
            type:Organization
         author:
               name:Wen-Hsiung Li
               affiliation:
                     name:University of Texas
                     address:
                        name:Center for Demographic and Population Genetics, University of Texas, Houston, USA
                        type:PostalAddress
                     type:Organization
               type:Person
               name:Masako Tanimura
               affiliation:
                     name:University of Texas
                     address:
                        name:Center for Demographic and Population Genetics, University of Texas, Houston, USA
                        type:PostalAddress
                     type:Organization
               type:Person
               name:Paul M. Sharp
               affiliation:
                     name:University of Texas
                     address:
                        name:Center for Demographic and Population Genetics, University of Texas, Houston, USA
                        type:PostalAddress
                     type:Organization
                     name:Trinity College
                     address:
                        name:Department of Genetics, Trinity College, Dublin, Ireland
                        type:PostalAddress
                     type:Organization
               type:Person
         isAccessibleForFree:
         hasPart:
            isAccessibleForFree:
            cssSelector:.main-content
            type:WebPageElement
         type:ScholarlyArticle
      context:https://schema.org
ScholarlyArticle:
      headline:An evaluation of the molecular clock hypothesis using mammalian DNA sequences
      description:A statistical analysis of extensive DNA sequence data from primates, rodents, and artiodacytls clearly indicates that no global molecular clock exists in mammals. Rates of nucleotide subsitution in rodents are estimated to be four to eight times higher than those in higher primates and two to four times higher than those in artiodactyls. There is strong evidence for lower substitution rates in apes and humans than in monkeys, supporting the hominoid slowdown hypothesis. There is also evidence for lower rates in humans than in apes, suggesting a further rate slowdown in the human lineage after the separation of humans from apes. By contrast, substitution rates are nearly equal in mouse and rat. These results suggest that differences in generation time or, more precisely, in the number of germline DNA replications per year are the primary cause of rate differences in mammals. Further, these differences are more in line with the neutral mutation hypothesis than if the rates are the same for short-and long-living mammals.
      datePublished:
      dateModified:
      pageStart:330
      pageEnd:342
      sameAs:https://doi.org/10.1007/BF02603118
      keywords:
         Molecular clock
         Generation-time effect
         Hominoid slowdown
         Hominid slowdown
         Neutral theory
         Evolutionary Biology
         Microbiology
         Plant Sciences
         Plant Genetics and Genomics
         Animal Genetics and Genomics
         Cell Biology
      image:
      isPartOf:
         name:Journal of Molecular Evolution
         issn:
            1432-1432
            0022-2844
         volumeNumber:25
         type:
            Periodical
            PublicationVolume
      publisher:
         name:Springer-Verlag
         logo:
            url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
            type:ImageObject
         type:Organization
      author:
            name:Wen-Hsiung Li
            affiliation:
                  name:University of Texas
                  address:
                     name:Center for Demographic and Population Genetics, University of Texas, Houston, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Masako Tanimura
            affiliation:
                  name:University of Texas
                  address:
                     name:Center for Demographic and Population Genetics, University of Texas, Houston, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Paul M. Sharp
            affiliation:
                  name:University of Texas
                  address:
                     name:Center for Demographic and Population Genetics, University of Texas, Houston, USA
                     type:PostalAddress
                  type:Organization
                  name:Trinity College
                  address:
                     name:Department of Genetics, Trinity College, Dublin, Ireland
                     type:PostalAddress
                  type:Organization
            type:Person
      isAccessibleForFree:
      hasPart:
         isAccessibleForFree:
         cssSelector:.main-content
         type:WebPageElement
["Periodical","PublicationVolume"]:
      name:Journal of Molecular Evolution
      issn:
         1432-1432
         0022-2844
      volumeNumber:25
Organization:
      name:Springer-Verlag
      logo:
         url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
         type:ImageObject
      name:University of Texas
      address:
         name:Center for Demographic and Population Genetics, University of Texas, Houston, USA
         type:PostalAddress
      name:University of Texas
      address:
         name:Center for Demographic and Population Genetics, University of Texas, Houston, USA
         type:PostalAddress
      name:University of Texas
      address:
         name:Center for Demographic and Population Genetics, University of Texas, Houston, USA
         type:PostalAddress
      name:Trinity College
      address:
         name:Department of Genetics, Trinity College, Dublin, Ireland
         type:PostalAddress
ImageObject:
      url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
Person:
      name:Wen-Hsiung Li
      affiliation:
            name:University of Texas
            address:
               name:Center for Demographic and Population Genetics, University of Texas, Houston, USA
               type:PostalAddress
            type:Organization
      name:Masako Tanimura
      affiliation:
            name:University of Texas
            address:
               name:Center for Demographic and Population Genetics, University of Texas, Houston, USA
               type:PostalAddress
            type:Organization
      name:Paul M. Sharp
      affiliation:
            name:University of Texas
            address:
               name:Center for Demographic and Population Genetics, University of Texas, Houston, USA
               type:PostalAddress
            type:Organization
            name:Trinity College
            address:
               name:Department of Genetics, Trinity College, Dublin, Ireland
               type:PostalAddress
            type:Organization
PostalAddress:
      name:Center for Demographic and Population Genetics, University of Texas, Houston, USA
      name:Center for Demographic and Population Genetics, University of Texas, Houston, USA
      name:Center for Demographic and Population Genetics, University of Texas, Houston, USA
      name:Department of Genetics, Trinity College, Dublin, Ireland
WebPageElement:
      isAccessibleForFree:
      cssSelector:.main-content

External Links {🔗}(347)

Analytics and Tracking {📊}

  • Google Tag Manager

Libraries {📚}

  • Clipboard.js
  • Prism.js

Emails and Hosting {✉️}

Mail Servers:

  • mx.zoho.eu
  • mx2.zoho.eu
  • mx3.zoho.eu

Name Servers:

  • josh.ns.cloudflare.com
  • zita.ns.cloudflare.com

CDN Services {📦}

  • Crossref

4.58s.