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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/10.1186/1478-811x-7-13.

Title:
Crk and CrkL adaptor proteins: networks for physiological and pathological signaling | Cell Communication and Signaling
Description:
The Crk adaptor proteins (Crk and CrkL) constitute an integral part of a network of essential signal transduction pathways in humans and other organisms that act as major convergence points in tyrosine kinase signaling. Crk proteins integrate signals from a wide variety of sources, including growth factors, extracellular matrix molecules, bacterial pathogens, and apoptotic cells. Mounting evidence indicates that dysregulation of Crk proteins is associated with human diseases, including cancer and susceptibility to pathogen infections. Recent structural work has identified new and unusual insights into the regulation of Crk proteins, providing a rationale for how Crk can sense diverse signals and produce a myriad of biological responses.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {πŸ“š}

  • Education
  • Science
  • Telecommunications

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 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? {πŸ’Έ}

We don't see any clear sign of profit-making.

Some websites aren't about earning revenue; they're built to connect communities or raise awareness. There are numerous motivations behind creating websites. This might be one of them. Link.springer.com could be getting rich in stealth mode, or the way it's monetizing isn't detectable.

Keywords {πŸ”}

crk, pubmed, cas, google, scholar, article, cell, cells, phosphorylation, tyrosine, pcas, proteins, signaling, biol, domain, central, activation, abl, studies, dock, kinase, crkl, protein, binding, src, rac, figure, chem, human, cancer, domains, adhesion, role, growth, pathway, complex, adaptor, signal, vcrk, activity, shn, region, shc, interaction, oncogene, migration, hanafusa, family, transformation, rap,

Topics {βœ’οΈ}

pro-x-x-pro-x-lys/arg unc-73/trio-mig-2/rhog signaling module e-cadherin-based cell-cell contacts x1-p2-p3-x4-p5 notch-dependent t-cell leukemia uanine-nucleotide releasing factor pubmed search combining ptyr-asp-x-pro c-src-crk-c3g-rap1 signaling analyze crk-phosphotyrosine-dependent interactions proto-oncogenic protein c-cbl chronic myelogenous leukemia c-crk link c-abl mediates rap1-induced adhesion v-crk-induced cell transformation crk-ii/tc10 signaling pathway fine-tune signals related article download pdf p130cas/crk/c3g ternary complex dock1/elmo rac-gef argues prolyl cis-trans isomerization p130cas/crk/dock180 ternary complex c-terminal src kinase achieve cis-trans isomerization c-abl kinase regulates src-dependent tyrosine phosphorylation transgenic mmtv-p130cas mouse proto-oncogene product p120cbl p130cas/crk/c3g-induced activation organized protein-protein networks ezrin-radixin-moesin proteins ras-induced cell transformations c-abl tyrosine kinase tyrosine phosphorylation-dependent manner jun nh2-terminal kinase met-induced cell motility preosteoblastic mc3t3-e1 cells src-family tyrosine kinases abl-dependent tyrosine phosphorylation conserved c-terminal region classic c-terminal region cytoskeleton-dependent tyrosine phosphorylation phosphoinositide 3-kinase/akt pathway adhesion-dependent actin reorganization regulated rho-dependent phosphorylation c-src activity requires proto-oncogene products abl aeruginosa adp-ribosylates crk c-terminal sh3 domain nerve growth factor

Questions {❓}

  • Cote JF, Vuori K: GEF what?

Schema {πŸ—ΊοΈ}

WebPage:
      mainEntity:
         headline:Crk and CrkL adaptor proteins: networks for physiological and pathological signaling
         description:The Crk adaptor proteins (Crk and CrkL) constitute an integral part of a network of essential signal transduction pathways in humans and other organisms that act as major convergence points in tyrosine kinase signaling. Crk proteins integrate signals from a wide variety of sources, including growth factors, extracellular matrix molecules, bacterial pathogens, and apoptotic cells. Mounting evidence indicates that dysregulation of Crk proteins is associated with human diseases, including cancer and susceptibility to pathogen infections. Recent structural work has identified new and unusual insights into the regulation of Crk proteins, providing a rationale for how Crk can sense diverse signals and produce a myriad of biological responses.
         datePublished:2009-05-10T00:00:00Z
         dateModified:2009-05-10T00:00:00Z
         pageStart:1
         pageEnd:23
         license:http://creativecommons.org/licenses/by/2.0
         sameAs:https://doi.org/10.1186/1478-811X-7-13
         keywords:
            Focal Adhesion Kinase
            Tyrosine Phosphorylation
            Chronic Myelogenous Leukemia
            Noonan Syndrome
            Tyrosine Kinase Oncogene
            Cell Biology
            Protein-Ligand Interactions
            Receptors
            Cytokines and Growth Factors
         image:
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         isPartOf:
            name:Cell Communication and Signaling
            issn:
               1478-811X
            volumeNumber:7
            type:
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         publisher:
            name:BioMed Central
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                     address:
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                        type:PostalAddress
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               affiliation:
                     name:Hokkaido University School of Medicine
                     address:
                        name:Department of Pathology, Division of Medicine, Hokkaido University School of Medicine, Kita-ku, Japan
                        type:PostalAddress
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ScholarlyArticle:
      headline:Crk and CrkL adaptor proteins: networks for physiological and pathological signaling
      description:The Crk adaptor proteins (Crk and CrkL) constitute an integral part of a network of essential signal transduction pathways in humans and other organisms that act as major convergence points in tyrosine kinase signaling. Crk proteins integrate signals from a wide variety of sources, including growth factors, extracellular matrix molecules, bacterial pathogens, and apoptotic cells. Mounting evidence indicates that dysregulation of Crk proteins is associated with human diseases, including cancer and susceptibility to pathogen infections. Recent structural work has identified new and unusual insights into the regulation of Crk proteins, providing a rationale for how Crk can sense diverse signals and produce a myriad of biological responses.
      datePublished:2009-05-10T00:00:00Z
      dateModified:2009-05-10T00:00:00Z
      pageStart:1
      pageEnd:23
      license:http://creativecommons.org/licenses/by/2.0
      sameAs:https://doi.org/10.1186/1478-811X-7-13
      keywords:
         Focal Adhesion Kinase
         Tyrosine Phosphorylation
         Chronic Myelogenous Leukemia
         Noonan Syndrome
         Tyrosine Kinase Oncogene
         Cell Biology
         Protein-Ligand Interactions
         Receptors
         Cytokines and Growth Factors
      image:
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         name:BioMed Central
         logo:
            url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
            type:ImageObject
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      author:
            name:Raymond B Birge
            affiliation:
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                  address:
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                     type:PostalAddress
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            name:Charalampos Kalodimos
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                  address:
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                     type:PostalAddress
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                  address:
                     name:Department of Structural Biology, Graduate School of Pharmaceutical Sciences, Hokkaido University, kita-ku, Japan
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Shinya Tanaka
            affiliation:
                  name:Hokkaido University School of Medicine
                  address:
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      name:UMDNJ-New Jersey Medical School
      address:
         name:Department of Biochemistry & Molecular Biology, UMDNJ-New Jersey Medical School, Newark, USA
         type:PostalAddress
      name:Rutgers University
      address:
         name:Department of Chemistry, Chemical Biology and Biomedical Engineering, Rutgers University, Piscataway, USA
         type:PostalAddress
      name:Hokkaido University
      address:
         name:Department of Structural Biology, Graduate School of Pharmaceutical Sciences, Hokkaido University, kita-ku, Japan
         type:PostalAddress
      name:Hokkaido University School of Medicine
      address:
         name:Department of Pathology, Division of Medicine, Hokkaido University School of Medicine, Kita-ku, Japan
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      affiliation:
            name:UMDNJ-New Jersey Medical School
            address:
               name:Department of Biochemistry & Molecular Biology, UMDNJ-New Jersey Medical School, Newark, USA
               type:PostalAddress
            type:Organization
      email:[email protected]
      name:Charalampos Kalodimos
      affiliation:
            name:Rutgers University
            address:
               name:Department of Chemistry, Chemical Biology and Biomedical Engineering, Rutgers University, Piscataway, USA
               type:PostalAddress
            type:Organization
      name:Fuyuhiko Inagaki
      affiliation:
            name:Hokkaido University
            address:
               name:Department of Structural Biology, Graduate School of Pharmaceutical Sciences, Hokkaido University, kita-ku, Japan
               type:PostalAddress
            type:Organization
      name:Shinya Tanaka
      affiliation:
            name:Hokkaido University School of Medicine
            address:
               name:Department of Pathology, Division of Medicine, Hokkaido University School of Medicine, Kita-ku, Japan
               type:PostalAddress
            type:Organization
PostalAddress:
      name:Department of Biochemistry & Molecular Biology, UMDNJ-New Jersey Medical School, Newark, USA
      name:Department of Chemistry, Chemical Biology and Biomedical Engineering, Rutgers University, Piscataway, USA
      name:Department of Structural Biology, Graduate School of Pharmaceutical Sciences, Hokkaido University, kita-ku, Japan
      name:Department of Pathology, Division of Medicine, Hokkaido University School of Medicine, Kita-ku, Japan

External Links {πŸ”—}(694)

Analytics and Tracking {πŸ“Š}

  • Google Tag Manager

Libraries {πŸ“š}

  • Clipboard.js
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CDN Services {πŸ“¦}

  • Crossref
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