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We are analyzing https://link.springer.com/article/10.1007/s00395-012-0316-y.

Title:
Mapping genetic determinants of coronary microvascular remodeling in the spontaneously hypertensive rat | Basic Research in Cardiology
Description:
The mechanisms underlying coronary microvascular remodeling and dysfunction, which are critical determinants of abnormal myocardial blood flow regulation in human hypertension, are poorly understood. The spontaneously hypertensive rat (SHR) exhibits many features of human hypertensive cardiomyopathy. We demonstrate that remodeling of intramural coronary arterioles is apparent in the SHR already at 4 weeks of age, i.e. before the onset of systemic hypertension. To uncover possible genetic determinants of coronary microvascular remodeling, we carried out detailed histological and histomorphometric analysis of the heart and coronary vasculature in 30 weeks old SHR, age-matched Brown Norway (BN-Lx) parentals and BXH/HXB recombinant inbred (RI) strains. Using previously mapped expression quantitative trait loci (eQTLs), we carried out a genome-wide association analysis between genetic determinants of cardiac gene expression and histomorphometric traits. This identified 36 robustly mapped eQTLs in the heart which were associated with medial area of intramural coronary arterioles [false discovery rate (FDR) ~5 %]. Transcripts, which were both under cis-acting genetic regulation and significantly correlated with medial area (FDR <5 %), but not with blood pressure indices, were prioritized and four candidate genes were identified (Rtel1, Pla2g5, Dnaja4 and Rcn2) according to their expression levels and biological functions. Our results demonstrate that genetic factors play a role in the development of coronary microvascular remodeling and suggest blood pressure independent candidate genes for further functional experiments.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
  • Health & Fitness
  • Science

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.
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How Does Link.springer.com Make Money? {💸}

The income method remains a mystery to us.

Many websites are intended to earn money, but some serve to share ideas or build connections. Websites exist for all kinds of purposes. This might be one of them. Link.springer.com could be secretly minting cash, but we can't detect the process.

Keywords {🔍}

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Topics {✒️}

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Questions {❓}

  • Mulvany MJ (1999) Vascular remodelling of resistance vessels: can we define this?

Schema {🗺️}

WebPage:
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         headline:Mapping genetic determinants of coronary microvascular remodeling in the spontaneously hypertensive rat
         description:The mechanisms underlying coronary microvascular remodeling and dysfunction, which are critical determinants of abnormal myocardial blood flow regulation in human hypertension, are poorly understood. The spontaneously hypertensive rat (SHR) exhibits many features of human hypertensive cardiomyopathy. We demonstrate that remodeling of intramural coronary arterioles is apparent in the SHR already at 4 weeks of age, i.e. before the onset of systemic hypertension. To uncover possible genetic determinants of coronary microvascular remodeling, we carried out detailed histological and histomorphometric analysis of the heart and coronary vasculature in 30 weeks old SHR, age-matched Brown Norway (BN-Lx) parentals and BXH/HXB recombinant inbred (RI) strains. Using previously mapped expression quantitative trait loci (eQTLs), we carried out a genome-wide association analysis between genetic determinants of cardiac gene expression and histomorphometric traits. This identified 36 robustly mapped eQTLs in the heart which were associated with medial area of intramural coronary arterioles [false discovery rate (FDR) ~5 %]. Transcripts, which were both under cis-acting genetic regulation and significantly correlated with medial area (FDR <5 %), but not with blood pressure indices, were prioritized and four candidate genes were identified (Rtel1, Pla2g5, Dnaja4 and Rcn2) according to their expression levels and biological functions. Our results demonstrate that genetic factors play a role in the development of coronary microvascular remodeling and suggest blood pressure independent candidate genes for further functional experiments.
         datePublished:2012-11-30T00:00:00Z
         dateModified:2012-11-30T00:00:00Z
         pageStart:1
         pageEnd:14
         sameAs:https://doi.org/10.1007/s00395-012-0316-y
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            Arterial hypertension
            Coronary circulation
            Myocardial ischemia
            Spontaneously hypertensive rat
            Candidate genes
            Recombinant inbred strains
            Cardiology
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      headline:Mapping genetic determinants of coronary microvascular remodeling in the spontaneously hypertensive rat
      description:The mechanisms underlying coronary microvascular remodeling and dysfunction, which are critical determinants of abnormal myocardial blood flow regulation in human hypertension, are poorly understood. The spontaneously hypertensive rat (SHR) exhibits many features of human hypertensive cardiomyopathy. We demonstrate that remodeling of intramural coronary arterioles is apparent in the SHR already at 4 weeks of age, i.e. before the onset of systemic hypertension. To uncover possible genetic determinants of coronary microvascular remodeling, we carried out detailed histological and histomorphometric analysis of the heart and coronary vasculature in 30 weeks old SHR, age-matched Brown Norway (BN-Lx) parentals and BXH/HXB recombinant inbred (RI) strains. Using previously mapped expression quantitative trait loci (eQTLs), we carried out a genome-wide association analysis between genetic determinants of cardiac gene expression and histomorphometric traits. This identified 36 robustly mapped eQTLs in the heart which were associated with medial area of intramural coronary arterioles [false discovery rate (FDR) ~5 %]. Transcripts, which were both under cis-acting genetic regulation and significantly correlated with medial area (FDR <5 %), but not with blood pressure indices, were prioritized and four candidate genes were identified (Rtel1, Pla2g5, Dnaja4 and Rcn2) according to their expression levels and biological functions. Our results demonstrate that genetic factors play a role in the development of coronary microvascular remodeling and suggest blood pressure independent candidate genes for further functional experiments.
      datePublished:2012-11-30T00:00:00Z
      dateModified:2012-11-30T00:00:00Z
      pageStart:1
      pageEnd:14
      sameAs:https://doi.org/10.1007/s00395-012-0316-y
      keywords:
         Arterial hypertension
         Coronary circulation
         Myocardial ischemia
         Spontaneously hypertensive rat
         Candidate genes
         Recombinant inbred strains
         Cardiology
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                  address:
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                  address:
                     name:Vita Salute University and Scientific Institute San Raffaele Milan, Milan, Italy
                     type:PostalAddress
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            name:Angela Scavone
            affiliation:
                  name:Vita Salute University and Scientific Institute San Raffaele Milan
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                     name:Vita Salute University and Scientific Institute San Raffaele Milan, Milan, Italy
                     type:PostalAddress
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                  address:
                     name:MRC Clinical Sciences Centre Imperial College, London, UK
                     type:PostalAddress
                  type:Organization
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            name:Stuart Cook
            affiliation:
                  name:MRC Clinical Sciences Centre Imperial College
                  address:
                     name:MRC Clinical Sciences Centre Imperial College, London, UK
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Jan Silhavy
            affiliation:
                  name:Academy of Sciences of the Czech Republic
                  address:
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                     type:PostalAddress
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            name:Vaclav Zidek
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                  name:Academy of Sciences of the Czech Republic
                  address:
                     name:Institute of Physiology, Academy of Sciences of the Czech Republic, Prague, Czech Republic
                     type:PostalAddress
                  type:Organization
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            name:Michal Pravenec
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                  name:Academy of Sciences of the Czech Republic
                  address:
                     name:Institute of Physiology, Academy of Sciences of the Czech Republic, Prague, Czech Republic
                     type:PostalAddress
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      name:Enrico Petretto
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               type:PostalAddress
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      name:Christina Kleinert
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            name:Vita Salute University and Scientific Institute San Raffaele Milan
            address:
               name:Vita Salute University and Scientific Institute San Raffaele Milan, Milan, Italy
               type:PostalAddress
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      name:Angela Scavone
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            name:Vita Salute University and Scientific Institute San Raffaele Milan
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               name:Vita Salute University and Scientific Institute San Raffaele Milan, Milan, Italy
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               name:MRC Clinical Sciences Centre Imperial College, London, UK
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            name:MRC Clinical Sciences Centre Imperial College
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               name:MRC Clinical Sciences Centre Imperial College, London, UK
               type:PostalAddress
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      affiliation:
            name:Academy of Sciences of the Czech Republic
            address:
               name:Institute of Physiology, Academy of Sciences of the Czech Republic, Prague, Czech Republic
               type:PostalAddress
            type:Organization
      name:Giulia d’Amati
      affiliation:
            name:“Sapienza” University of Rome
            address:
               name:Department of Radiology, Oncology and Pathology, “Sapienza” University of Rome, Rome, Italy
               type:PostalAddress
            type:Organization
      name:Paolo G. Camici
      affiliation:
            name:Vita Salute University and Scientific Institute San Raffaele Milan
            address:
               name:Vita Salute University and Scientific Institute San Raffaele Milan, Milan, Italy
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            type:Organization
      email:[email protected]
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      name:Department of Radiology, Oncology and Pathology, “Sapienza” University of Rome, Rome, Italy
      name:MRC Clinical Sciences Centre Imperial College, London, UK
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      name:Vita Salute University and Scientific Institute San Raffaele Milan, Milan, Italy
      name:MRC Clinical Sciences Centre Imperial College, London, UK
      name:MRC Clinical Sciences Centre Imperial College, London, UK
      name:Institute of Physiology, Academy of Sciences of the Czech Republic, Prague, Czech Republic
      name:Institute of Physiology, Academy of Sciences of the Czech Republic, Prague, Czech Republic
      name:Institute of Physiology, Academy of Sciences of the Czech Republic, Prague, Czech Republic
      name:Department of Radiology, Oncology and Pathology, “Sapienza” University of Rome, Rome, Italy
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External Links {🔗}(203)

Analytics and Tracking {📊}

  • Google Tag Manager

Libraries {📚}

  • Clipboard.js
  • Prism.js

CDN Services {📦}

  • Crossref

4.92s.