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  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
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We are analyzing https://link.springer.com/article/10.1007/s00403-013-1410-1.

Title:
The role of microRNAs in skin fibrosis | Archives of Dermatological Research
Description:
Fibrotic skin disorders may be debilitating and impair quality of life. There are few effective treatment options for cutaneous fibrotic diseases. In this review, we discuss our current understanding of the role of microRNAs (miRNAs) in skin fibrosis. miRNAs are a class of small, non-coding RNAs involved in skin fibrosis. These small RNAs range from 18 to 25 nucleotides in length and modify gene expression by binding to target messenger RNA (mRNA), causing degradation of the target mRNA or inhibiting the translation into proteins. We present an overview of the biogenesis, maturation and function of miRNAs. We highlight miRNA’s role in key skin fibrotic processes including: transforming growth factor-beta signaling, extracellular matrix deposition, and fibroblast proliferation and differentiation. Some miRNAs are profibrotic and their upregulation favors these processes contributing to fibrosis, while anti-fibrotic miRNAs inhibit these processes and may be reduced in fibrosis. Finally, we describe the diagnostic and therapeutic significance of miRNAs in the management of skin fibrosis. The discovery that miRNAs are detectable in serum, plasma, and other bodily fluids, and are relatively stable, suggests that miRNAs may serve as valuable biomarkers to monitor disease progression and response to treatment. In the treatment of skin fibrosis, anti-fibrotic miRNAs may be upregulated using mimics and viral vectors. Conversely, profibrotic miRNAs may be downregulated by employing anti-miRNAs, sponges, erasers and masks. We believe that miRNA-based therapies hold promise as important treatments and may transform the management of fibrotic skin diseases by physicians.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
  • Science
  • Health & Fitness

Content Management System {📝}

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 {📈}

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? {💸}

We find it hard to spot revenue streams.

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 secretly minting cash, but we can't detect the process.

Keywords {🔍}

article, google, scholar, pubmed, cas, micrornas, skin, fibrosis, microrna, wang, expression, makino, mirnas, scleroderma, zhang, dermatol, res, fibroblasts, therapeutic, cell, sci, biol, systemic, diseases, collagen, jinnin, honda, kajihara, fukushima, ihn, usa, function, role, treatment, cutaneous, disease, dermatology, wound, doi, cancer, xiao, sclerosis, content, research, target, growth, access, mirna, healing, curr,

Topics {✒️}

inhibiting wnt/beta-catenin pathway month download article/chapter wnt/beta-catenin signaling tgf-beta-mediated downregulation precursor-mirna pri-mirna circulating mir-29a levels circulating mir-142-3p levels late-gestational fetal skin therapeutic cardiac-targeted delivery mirna-based therapeutic strategies adenovirus-mediated mutant smad4 stable blood-based markers mir-196a downregulation increases anti-fibrotic mirnas inhibit full article pdf jared jagdeo coding rnas involved privacy choices/manage cookies lev-tov nuclear factor-kappa acad sci bohemoslov small rnas range dermatological research aims gene-specific interference award number r33ai080604 related subjects mirna expression profiles tumor-released microvesicles scarless wound healing primary-mirna pten article archives extracellular matrix deposition extracellular thrombospondin-2 due normal skin tissue european economic area engrav lh nana-sinkam sp attenuates pathological remodeling hildebrandt-eriksen es pogosova-agadjanyan el vazquez del-mercado severe burn injury advancing translational sciences albert einstein school cutaneous fibrotic diseases fibrotic skin diseases dermal fibroblasts increases mesenchymal–epithelial transitions microrna-targeted drug pleiotropically acting microrna

Questions {❓}

  • Sonkoly E, Wei T, Janson PC, Saaf A, Lundeberg L, Tengvall-Linder M, Norstedt G, Alenius H, Homey B, Scheynius A, Stahle M, Pivarcsi A (2007) MicroRNAs: novel regulators involved in the pathogenesis of psoriasis?

Schema {🗺️}

WebPage:
      mainEntity:
         headline:The role of microRNAs in skin fibrosis
         description:Fibrotic skin disorders may be debilitating and impair quality of life. There are few effective treatment options for cutaneous fibrotic diseases. In this review, we discuss our current understanding of the role of microRNAs (miRNAs) in skin fibrosis. miRNAs are a class of small, non-coding RNAs involved in skin fibrosis. These small RNAs range from 18 to 25 nucleotides in length and modify gene expression by binding to target messenger RNA (mRNA), causing degradation of the target mRNA or inhibiting the translation into proteins. We present an overview of the biogenesis, maturation and function of miRNAs. We highlight miRNA’s role in key skin fibrotic processes including: transforming growth factor-beta signaling, extracellular matrix deposition, and fibroblast proliferation and differentiation. Some miRNAs are profibrotic and their upregulation favors these processes contributing to fibrosis, while anti-fibrotic miRNAs inhibit these processes and may be reduced in fibrosis. Finally, we describe the diagnostic and therapeutic significance of miRNAs in the management of skin fibrosis. The discovery that miRNAs are detectable in serum, plasma, and other bodily fluids, and are relatively stable, suggests that miRNAs may serve as valuable biomarkers to monitor disease progression and response to treatment. In the treatment of skin fibrosis, anti-fibrotic miRNAs may be upregulated using mimics and viral vectors. Conversely, profibrotic miRNAs may be downregulated by employing anti-miRNAs, sponges, erasers and masks. We believe that miRNA-based therapies hold promise as important treatments and may transform the management of fibrotic skin diseases by physicians.
         datePublished:2013-09-11T00:00:00Z
         dateModified:2013-09-11T00:00:00Z
         pageStart:763
         pageEnd:776
         sameAs:https://doi.org/10.1007/s00403-013-1410-1
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            MicroRNA
            miRNA
            Collagen
            Therapeutics
            Dermatology
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                        name:Department of Dermatology, Albert Einstein School of Medicine, Bronx, USA
                        type:PostalAddress
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               name:Jared Jagdeo
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                        name:Department of Dermatology, University of California Davis, Sacramento, USA
                        type:PostalAddress
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      headline:The role of microRNAs in skin fibrosis
      description:Fibrotic skin disorders may be debilitating and impair quality of life. There are few effective treatment options for cutaneous fibrotic diseases. In this review, we discuss our current understanding of the role of microRNAs (miRNAs) in skin fibrosis. miRNAs are a class of small, non-coding RNAs involved in skin fibrosis. These small RNAs range from 18 to 25 nucleotides in length and modify gene expression by binding to target messenger RNA (mRNA), causing degradation of the target mRNA or inhibiting the translation into proteins. We present an overview of the biogenesis, maturation and function of miRNAs. We highlight miRNA’s role in key skin fibrotic processes including: transforming growth factor-beta signaling, extracellular matrix deposition, and fibroblast proliferation and differentiation. Some miRNAs are profibrotic and their upregulation favors these processes contributing to fibrosis, while anti-fibrotic miRNAs inhibit these processes and may be reduced in fibrosis. Finally, we describe the diagnostic and therapeutic significance of miRNAs in the management of skin fibrosis. The discovery that miRNAs are detectable in serum, plasma, and other bodily fluids, and are relatively stable, suggests that miRNAs may serve as valuable biomarkers to monitor disease progression and response to treatment. In the treatment of skin fibrosis, anti-fibrotic miRNAs may be upregulated using mimics and viral vectors. Conversely, profibrotic miRNAs may be downregulated by employing anti-miRNAs, sponges, erasers and masks. We believe that miRNA-based therapies hold promise as important treatments and may transform the management of fibrotic skin diseases by physicians.
      datePublished:2013-09-11T00:00:00Z
      dateModified:2013-09-11T00:00:00Z
      pageStart:763
      pageEnd:776
      sameAs:https://doi.org/10.1007/s00403-013-1410-1
      keywords:
         Skin fibrosis
         MicroRNA
         miRNA
         Collagen
         Therapeutics
         Dermatology
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                     type:PostalAddress
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                  name:Sacramento VA Medical Center
                  address:
                     name:Dermatology Service, Sacramento VA Medical Center, Mather, USA
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            name:Andrew Mamalis
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                  address:
                     name:Department of Dermatology, University of California Davis, Sacramento, USA
                     type:PostalAddress
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                  address:
                     name:Dermatology Service, Sacramento VA Medical Center, Mather, USA
                     type:PostalAddress
                  type:Organization
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            name:Hadar Lev-Tov
            affiliation:
                  name:University of California Davis
                  address:
                     name:Department of Dermatology, University of California Davis, Sacramento, USA
                     type:PostalAddress
                  type:Organization
                  name:Sacramento VA Medical Center
                  address:
                     name:Dermatology Service, Sacramento VA Medical Center, Mather, USA
                     type:PostalAddress
                  type:Organization
                  name:Albert Einstein School of Medicine
                  address:
                     name:Department of Dermatology, Albert Einstein School of Medicine, Bronx, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Jared Jagdeo
            affiliation:
                  name:University of California Davis
                  address:
                     name:Department of Dermatology, University of California Davis, Sacramento, USA
                     type:PostalAddress
                  type:Organization
                  name:Sacramento VA Medical Center
                  address:
                     name:Dermatology Service, Sacramento VA Medical Center, Mather, USA
                     type:PostalAddress
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         name:Department of Dermatology, University of California Davis, Sacramento, USA
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         name:Dermatology Service, Sacramento VA Medical Center, Mather, USA
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         name:Department of Dermatology, University of California Davis, Sacramento, USA
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         name:Department of Dermatology, University of California Davis, Sacramento, USA
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      address:
         name:Dermatology Service, Sacramento VA Medical Center, Mather, USA
         type:PostalAddress
      name:Albert Einstein School of Medicine
      address:
         name:Department of Dermatology, Albert Einstein School of Medicine, Bronx, USA
         type:PostalAddress
      name:University of California Davis
      address:
         name:Department of Dermatology, University of California Davis, Sacramento, USA
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         name:Dermatology Service, Sacramento VA Medical Center, Mather, USA
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      name:Olubukola Babalola
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            name:University of California Davis
            address:
               name:Department of Dermatology, University of California Davis, Sacramento, USA
               type:PostalAddress
            type:Organization
            name:Sacramento VA Medical Center
            address:
               name:Dermatology Service, Sacramento VA Medical Center, Mather, USA
               type:PostalAddress
            type:Organization
      name:Andrew Mamalis
      affiliation:
            name:University of California Davis
            address:
               name:Department of Dermatology, University of California Davis, Sacramento, USA
               type:PostalAddress
            type:Organization
            name:Sacramento VA Medical Center
            address:
               name:Dermatology Service, Sacramento VA Medical Center, Mather, USA
               type:PostalAddress
            type:Organization
      name:Hadar Lev-Tov
      affiliation:
            name:University of California Davis
            address:
               name:Department of Dermatology, University of California Davis, Sacramento, USA
               type:PostalAddress
            type:Organization
            name:Sacramento VA Medical Center
            address:
               name:Dermatology Service, Sacramento VA Medical Center, Mather, USA
               type:PostalAddress
            type:Organization
            name:Albert Einstein School of Medicine
            address:
               name:Department of Dermatology, Albert Einstein School of Medicine, Bronx, USA
               type:PostalAddress
            type:Organization
      name:Jared Jagdeo
      affiliation:
            name:University of California Davis
            address:
               name:Department of Dermatology, University of California Davis, Sacramento, USA
               type:PostalAddress
            type:Organization
            name:Sacramento VA Medical Center
            address:
               name:Dermatology Service, Sacramento VA Medical Center, Mather, USA
               type:PostalAddress
            type:Organization
      email:[email protected]
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      name:Department of Dermatology, University of California Davis, Sacramento, USA
      name:Dermatology Service, Sacramento VA Medical Center, Mather, USA
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      name:Dermatology Service, Sacramento VA Medical Center, Mather, USA
      name:Department of Dermatology, University of California Davis, Sacramento, USA
      name:Dermatology Service, Sacramento VA Medical Center, Mather, USA
      name:Department of Dermatology, Albert Einstein School of Medicine, Bronx, USA
      name:Department of Dermatology, University of California Davis, Sacramento, USA
      name:Dermatology Service, Sacramento VA Medical Center, Mather, USA
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