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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. Social Networks
  10. External Links
  11. Analytics And Tracking
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  14. CDN Services

We began analyzing https://stemcellres.biomedcentral.com/articles/10.1186/s13287-024-04127-y, but it redirected us to https://stemcellres.biomedcentral.com/articles/10.1186/s13287-024-04127-y. The analysis below is for the second page.

Title[redir]:
Mesenchymal stem cell therapy as a game-changer in liver diseases: review of current clinical trials | Stem Cell Research & Therapy | Full Text
Description:
Chronic liver diseases, including cirrhosis and liver failure, remain formidable challenges due to their complex progression and limited therapeutic options. Mesenchymal stem cell (MSC) therapy has emerged as a game-changing approach, leveraging its potent immunomodulatory, anti-fibrotic, and regenerative capabilities, along with the ability to transdifferentiate into hepatocytes. This review delves into the latest advances in MSC-based treatments for chronic and end-stage liver diseases, as highlighted in current clinical trials. MSCs derived from bone marrow and umbilical cord have shown remarkable promise in reversing liver damage, improving liver function, and providing hope for patients who do not respond to conventional therapies. When administered through hepatic, portal, or peripheral veins, MSCs have significantly improved liver histology, reduced fibrosis, and restored functional capacity. Furthermore, MSC-derived materials, such as extracellular vesicles and exosomes, are emerging as cutting-edge tools for treating liver failure and mitigating post-transplant complications. While autologous MSC-derived hepatocytes hold promise for non-fatal cirrhosis, allogeneic MSCs are being applied in more severe conditions, including liver failure and transplantation cases. Despite these promising early outcomes, larger trials and long-term studies are essential to fully harness MSCs as a transformative, off-the-shelf alternative to liver transplantation, heralding a new era in regenerative liver therapies.

Matching Content Categories {📚}

  • Science
  • Education
  • Health & Fitness

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?

🚀 Good Traffic: 50k - 100k visitors per month


Based on our best estimate, this website will receive around 50,019 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 Doi.org Make Money? {💸}

We can't tell how the site generates income.

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 revenue plan, but it's either invisible or we haven't found it.

Keywords {🔍}

liver, pubmed, cells, article, google, scholar, stem, mesenchymal, cell, trials, cas, mscs, trial, cirrhosis, diseases, central, clinical, therapy, transplantation, failure, disease, patients, chen, msc, hepatic, wang, autologous, fibrosis, including, liu, zhang, allogeneic, treatment, chronic, million, human, function, hepatitis, ucmscs, bmmscs, table, immune, therapeutic, stromal, growth, phase, current, treating, complications, acute,

Topics {✒️}

adipose-derived stromal/stem cells decreasing tlr2/nf-kappab signaling myeloid-derived suppressor cell myeloid-derived suppressor cells hepatocyte growth factor/c-met umbilical cord-derived sources mesenchymal stromal/stem cells drug-induced liver injury end-stage liver disease mesenchymal stem cell-mediated end-stage liver diseases α-smooth muscle actin myeloid-derived suppressive phenotype placenta-derived multipotent cells monocyte-derived dendritic cells placenta-derived stem cells downregulating t-bet expression tri-service general hospital kynurenine-ahr-nrf2 pathway induce cd4 + cd25highfoxp3 + regulatory pi3k/akt/mtor pathway transforming growth factor-β1 utilizing cell-free products including anti-inflammatory cytokines biliary-specific inflammatory disease disease-related liver injury abo-incompatible liver transplantation cd4 + cd25 + foxp3 + regulatory mesenchymal stromal cells growth-regulated oncogene-γ [69] growth-regulated oncogene-γ inflammation-mediated liver diseases mesenchymal stem cell msc-derived prostaglandin e2 additional information publisher including bone marrow multipotent stromal cells growth-regulated oncogene chemokines vitro msc-mediated inhibition interleukin-1 receptor antagonist mesenchymal stem cells mesenchymal stem cells standard liver-supportive treatment increase il-10-expressing regulatory neutrophil-mediated tissue damage cell stem cell allogenic msc-based trials heme oxygenase-1-mediated induction egyptian hcv-positive patients hepatic transdifferentiation

Schema {🗺️}

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         headline:Mesenchymal stem cell therapy as a game-changer in liver diseases: review of current clinical trials
         description:Chronic liver diseases, including cirrhosis and liver failure, remain formidable challenges due to their complex progression and limited therapeutic options. Mesenchymal stem cell (MSC) therapy has emerged as a game-changing approach, leveraging its potent immunomodulatory, anti-fibrotic, and regenerative capabilities, along with the ability to transdifferentiate into hepatocytes. This review delves into the latest advances in MSC-based treatments for chronic and end-stage liver diseases, as highlighted in current clinical trials. MSCs derived from bone marrow and umbilical cord have shown remarkable promise in reversing liver damage, improving liver function, and providing hope for patients who do not respond to conventional therapies. When administered through hepatic, portal, or peripheral veins, MSCs have significantly improved liver histology, reduced fibrosis, and restored functional capacity. Furthermore, MSC-derived materials, such as extracellular vesicles and exosomes, are emerging as cutting-edge tools for treating liver failure and mitigating post-transplant complications. While autologous MSC-derived hepatocytes hold promise for non-fatal cirrhosis, allogeneic MSCs are being applied in more severe conditions, including liver failure and transplantation cases. Despite these promising early outcomes, larger trials and long-term studies are essential to fully harness MSCs as a transformative, off-the-shelf alternative to liver transplantation, heralding a new era in regenerative liver therapies.
         datePublished:2025-01-06T00:00:00Z
         dateModified:2025-01-06T00:00:00Z
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      headline:Mesenchymal stem cell therapy as a game-changer in liver diseases: review of current clinical trials
      description:Chronic liver diseases, including cirrhosis and liver failure, remain formidable challenges due to their complex progression and limited therapeutic options. Mesenchymal stem cell (MSC) therapy has emerged as a game-changing approach, leveraging its potent immunomodulatory, anti-fibrotic, and regenerative capabilities, along with the ability to transdifferentiate into hepatocytes. This review delves into the latest advances in MSC-based treatments for chronic and end-stage liver diseases, as highlighted in current clinical trials. MSCs derived from bone marrow and umbilical cord have shown remarkable promise in reversing liver damage, improving liver function, and providing hope for patients who do not respond to conventional therapies. When administered through hepatic, portal, or peripheral veins, MSCs have significantly improved liver histology, reduced fibrosis, and restored functional capacity. Furthermore, MSC-derived materials, such as extracellular vesicles and exosomes, are emerging as cutting-edge tools for treating liver failure and mitigating post-transplant complications. While autologous MSC-derived hepatocytes hold promise for non-fatal cirrhosis, allogeneic MSCs are being applied in more severe conditions, including liver failure and transplantation cases. Despite these promising early outcomes, larger trials and long-term studies are essential to fully harness MSCs as a transformative, off-the-shelf alternative to liver transplantation, heralding a new era in regenerative liver therapies.
      datePublished:2025-01-06T00:00:00Z
      dateModified:2025-01-06T00:00:00Z
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External Links {🔗}(624)

Analytics and Tracking {📊}

  • Google Tag Manager

Libraries {📚}

  • 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

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