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DOI . ORG {}

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  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Doi.org Make Money
  6. Keywords
  7. Topics
  8. Questions
  9. Schema
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We began analyzing https://www.tandfonline.com/doi/full/10.1517/17425255.4.7.895, but it redirected us to https://www.tandfonline.com/doi/full/10.1517/17425255.4.7.895. The analysis below is for the second page.

Title[redir]:
The pregnane X receptor: from bench to bedside: Expert Opinion on Drug Metabolism & Toxicology: Vol 4 , No 7 - Get Access
Description:
1. The pregnane X receptor (PXR; NR1I2), identified in 1998 as a member of the nuclear receptor superfamily, is expressed in liver and intestine and in front-line organs involved in the absorption,...

Matching Content Categories {📚}

  • Games
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  • 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?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,420 visitors per month in the current month.

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How Does Doi.org Make Money? {💸}

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. Doi.org might be earning cash quietly, but we haven't detected the monetization method.

Keywords {🔍}

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Topics {✒️}

influence drug–drug interactions humanized mouse models downloaded article pdf francis group including pxr-null downloaded article pdfs pxr-humanized mice limited period nuclear receptor superfamily controlling xenobiotic metabolism receive personalised research journals books bedside xiaochao ma access rights institution access mouse models published online cart search article https register log clinical implications date register read issues volume 4 pxr knockout institution log shibboleth log current review taylor scheduled work md phd phd & frank phd pages 895-908 metabolic enzymes transporters involved chemical environment results/conclusion recent advances vivo tools hepatic steatosis bile acids steroid hormones shared devices purchases made printed usd 104 printed usd 960 contact newsroom email sign england & wales sw1p 1wg

Questions {❓}

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Schema {🗺️}

BreadcrumbList:
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            name:The pregnane X receptor: from bench to b ....
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PublicationIssue:
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      issueNumber:7
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ScholarlyArticle:
      mainEntityOfPage:https://www.tandfonline.com/doi/full/10.1517/17425255.4.7.895
      url:https://www.tandfonline.com/doi/full/10.1517/17425255.4.7.895
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      articleSection:Review
      name:The pregnane X receptor: from bench to bedside
      headline:The pregnane X receptor: from bench to bedside
      abstract:Background: The pregnane X receptor (PXR; NR1I2), a member of the nuclear receptor superfamily, regulates the expression of metabolic enzymes and transporters involved in the response of mammals to their chemical environment. Objective: To summarize the functions and clinical implications of PXR. Methods: In the current review, the clinical implications of PXR are discussed, and the use of genetically engineered PXR mouse models is highlighted. Results/conclusion: Recent advances in mouse models, including Pxr-null and PXR-humanized mice, provide in vivo tools for evaluating the physiological functions of PXR and its role in controlling xenobiotic metabolism and transport. By using the PXR knockout and humanized mouse models, PXR was found to influence drug–drug interactions, hepatic steatosis, and the homeostasis of vitamin D, bile acids, and steroid hormones. PXR was also shown to influence inflammatory bowel diseases.
      description:Background: The pregnane X receptor (PXR; NR1I2), a member of the nuclear receptor superfamily, regulates the expression of metabolic enzymes and transporters involved in the response of mammals to their chemical environment. Objective: To summarize the functions and clinical implications of PXR. Methods: In the current review, the clinical implications of PXR are discussed, and the use of genetically engineered PXR mouse models is highlighted. Results/conclusion: Recent advances in mouse models, including Pxr-null and PXR-humanized mice, provide in vivo tools for evaluating the physiological functions of PXR and its role in controlling xenobiotic metabolism and transport. By using the PXR knockout and humanized mouse models, PXR was found to influence drug–drug interactions, hepatic steatosis, and the homeostasis of vitamin D, bile acids, and steroid hormones. PXR was also shown to influence inflammatory bowel diseases.
      author:
            type:Person
            name:Frank J Gonzalez
            type:Person
            name:Xiaochao Ma
            type:Person
            name:Jeffrey R Idle
      keywords:Pxr-null mouse, PXR-humanized mouse, pregnane X receptor, nuclear receptor, clinical implications
      pageStart:895
      pageEnd:908
      datePublished:2008-07-15
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         name:Taylor & Francis
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      name:Xiaochao Ma
      name:Jeffrey R Idle
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      name:Taylor & Francis
      logo:
         type:ImageObject
         url:https://www.tandfonline.com/pb-assets/Images/Taylor_and_Francis_Group_Logo-1742461082.png
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      url:https://www.tandfonline.com/pb-assets/Images/Taylor_and_Francis_Group_Logo-1742461082.png

External Links {🔗}(108)

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