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  3. CMS
  4. Monthly Traffic Estimate
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We began analyzing https://link.springer.com/chapter/10.1007/978-1-4614-8289-5_1, but it redirected us to https://link.springer.com/chapter/10.1007/978-1-4614-8289-5_1. The analysis below is for the second page.

Title[redir]:
Gadd45 in Stress Signaling, Cell Cycle Control, and Apoptosis | SpringerLink
Description:
The first identified Gadd45 gene, Gadd45a, encodes a ubiquitously expressed protein that is often induced by DNA damage and other stress signals associated with growth arrest and apoptosis. This protein and the other two members of this small gene family, Gadd45b and...

Matching Content Categories {📚}

  • Education
  • Telecommunications
  • Science

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 98,426,998 visitors per month in the current month.

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How Does Doi.org Make Money? {💸}

We don’t know how the website earns money.

Not all websites are made for profit; some exist to inform or educate users. Or any other reason why people make websites. And this might be the case. Doi.org has a secret sauce for making money, but we can't detect it yet.

Keywords {🔍}

google, scholar, pubmed, cas, article, cell, fornace, gadd, dna, gadda, cancer, biol, protein, wang, stress, signaling, gene, hollander, expression, chapter, cycle, res, mol, pmid, repair, activation, kinase, zhang, ajj, zhan, genes, apoptosis, salvador, arrest, chen, park, kim, chem, cells, usa, growth, gaddb, proteins, gaddg, mapk, immunol, huang, oncogene, pathway, damage,

Topics {✒️}

c-jun n-terminal kinase stress-responsive mtk1/mekk4 mapkkk nf-kappa b-mediated repression dna-damage-inducible proteins 45alpha month download article/chapter n-terminal autoinhibitory domain mtk1/mekk4 kinase activity dna damage-inducible transcripts mk2-mediated rna stabilization cell-type-specific differences jnk2-foxo3-gadd45 pathway p53-responsive stress protein p53-regulated protein gadd45 cell cycle checkpoint repair-mediated dna demethylation {beta}-catenin cellular localization anti-tumor immune responses p38 mapk-mediated control cell cycle checkpoints gadd45-gamma methylation levels hormone receptor dependent methylation-mediated repression reactive oxygen production privacy choices/manage cookies estrogen receptor beta modifies dna accessibility stress-inducible gadd45 device instant download cell cycle control atf-2 controls transcription gadd45-factor deficiency p50 nf-kappab apc complex activation smad-dependent expression van vugt ma p38 map kinase p38 map kinase inactivating gadd45 pathway dna damage response dna damage activates mtor/stat3 pathway modulating jnk signaling rrna genes leading p38 mapk signal cell growth arrest information-intensive approach editor information editors receptor pxr activates primary sex determination peripheral nerve injury

Questions {❓}

  • Karger S, Weidinger C, Krause K, Sheu SY, Aigner T, Gimm O, Schmid KW, Dralle H, Fuhrer D (2009) FOXO3a: a novel player in thyroid carcinogenesis?
  • Snyder AR, Morgan WF (2004) Gene expression profiling after irradiation: clues to understanding acute and persistent responses?

Schema {🗺️}

ScholarlyArticle:
      headline:Gadd45 in Stress Signaling, Cell Cycle Control, and Apoptosis
      pageEnd:19
      pageStart:1
      image:https://media.springernature.com/w153/springer-static/cover/book/978-1-4614-8289-5.jpg
      genre:
         Biomedical and Life Sciences
         Biomedical and Life Sciences (R0)
      isPartOf:
         name:Gadd45 Stress Sensor Genes
         isbn:
            978-1-4614-8289-5
            978-1-4614-8288-8
         type:Book
      publisher:
         name:Springer New York
         logo:
            url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
            type:ImageObject
         type:Organization
      author:
            name:Jesús M. Salvador
            affiliation:
                  name:Centro Nacional de Biotecnología
                  address:
                     name:Department of Immunology and Oncology, Centro Nacional de Biotecnología, Madrid, Spain
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Joshua D. Brown-Clay
            affiliation:
                  name:Georgetown University
                  address:
                     name:Department of Biochemistry and Molecular and Cellular Biology, Georgetown University, Washington, DC, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Albert J. Fornace
            affiliation:
                  name:Georgetown University
                  address:
                     name:Department of Biochemistry and Molecular and Cellular Biology, Georgetown University, Washington, DC, USA
                     type:PostalAddress
                  type:Organization
                  name:Georgetown University
                  address:
                     name:Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA
                     type:PostalAddress
                  type:Organization
            email:[email protected]
            type:Person
      keywords:Proliferate Cell Nuclear Antigen, Ionize Radiation, Adenomatous Polyposis Coli, Nucleotide Excision Repair, Genotoxic Stress
      description:The first identified Gadd45 gene, Gadd45a, encodes a ubiquitously expressed protein that is often induced by DNA damage and other stress signals associated with growth arrest and apoptosis. This protein and the other two members of this small gene family, Gadd45b and Gadd45g, have been implicated in a variety of the responses to cell injury including cell cycle checkpoints, apoptosis, and DNA repair. In vivo, many of the prominent roles for the Gadd45 proteins are associated with signaling mediated by p38 mitogen-activated protein kinases (MAPK). Gadd45 proteins can contribute to p38 activation either by activation of upstream kinase(s) or by direct interaction. In vivo, there are important tissue and cell-type-specific differences in the roles for Gadd45 in MAPK signaling. In addition to being p53-regulated, Gadd45a has been found to contribute to p53 activation via p38. Like other stress and signaling proteins, Gadd45 proteins show complex regulation and numerous effectors.
      datePublished:2013
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Book:
      name:Gadd45 Stress Sensor Genes
      isbn:
         978-1-4614-8289-5
         978-1-4614-8288-8
Organization:
      name:Springer New York
      logo:
         url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
         type:ImageObject
      name:Centro Nacional de Biotecnología
      address:
         name:Department of Immunology and Oncology, Centro Nacional de Biotecnología, Madrid, Spain
         type:PostalAddress
      name:Georgetown University
      address:
         name:Department of Biochemistry and Molecular and Cellular Biology, Georgetown University, Washington, DC, USA
         type:PostalAddress
      name:Georgetown University
      address:
         name:Department of Biochemistry and Molecular and Cellular Biology, Georgetown University, Washington, DC, USA
         type:PostalAddress
      name:Georgetown University
      address:
         name:Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA
         type:PostalAddress
ImageObject:
      url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
Person:
      name:Jesús M. Salvador
      affiliation:
            name:Centro Nacional de Biotecnología
            address:
               name:Department of Immunology and Oncology, Centro Nacional de Biotecnología, Madrid, Spain
               type:PostalAddress
            type:Organization
      name:Joshua D. Brown-Clay
      affiliation:
            name:Georgetown University
            address:
               name:Department of Biochemistry and Molecular and Cellular Biology, Georgetown University, Washington, DC, USA
               type:PostalAddress
            type:Organization
      name:Albert J. Fornace
      affiliation:
            name:Georgetown University
            address:
               name:Department of Biochemistry and Molecular and Cellular Biology, Georgetown University, Washington, DC, USA
               type:PostalAddress
            type:Organization
            name:Georgetown University
            address:
               name:Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:Department of Immunology and Oncology, Centro Nacional de Biotecnología, Madrid, Spain
      name:Department of Biochemistry and Molecular and Cellular Biology, Georgetown University, Washington, DC, USA
      name:Department of Biochemistry and Molecular and Cellular Biology, Georgetown University, Washington, DC, USA
      name:Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA
WebPageElement:
      isAccessibleForFree:
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