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We are analyzing https://link.springer.com/article/10.1007/s11064-006-9254-0.

Title:
Mitochondrial OXPHOS Functions in R1H Rhabdomyosarcoma and Skeletal Muscles of the Rat | Neurochemical Research
Description:
The aim of the study was to determinate mitochondrial oxidative phosphorylation (OXPHOS) functions in rat rhabdomyosarcoma R1H (R1H) and rat skeletal muscles. For that purpose skinned fiber technique and multiple substrate inhibitor titration were adapted to tumor samples. In our animal tumor model (R1H) functional abnormalities of OXPHOS were found compared to skeletal muscles. In R1H the state 3 respiration of pyruvate + malate was decreased: 0.56 Â± 0.28 nmol O2/mg/min versus 2.32 Â± 1.19 nmol O2/mg/min, P < 0.001, whereas the state 3 respiration of succinate + rotenone was increased: 36 Â± 14% versus 19 Â± 11%, P < 0.001. In R1H the rotenone-insensitive respiration reached higher levels than the antimycin A-insensitive respiration, whereas in normal muscles the converse was observed. Additionally, the obvious difference between the CAT- and the antimycin A-independent respiration indicates an increased part of leak respiration in R1H. By now, the high feasibility of these techniques is appreciated for the investigation of muscles and prospectively for tumors, too.
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

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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? {💾}

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Keywords {🔍}

google, scholar, article, pubmed, cas, mitochondrial, cancer, respiration, respiratory, rat, res, muscle, cell, rhabdomyosarcoma, skeletal, oxidative, human, tumor, mitochondria, cells, biochem, content, research, oxphos, muscles, gellerich, phosphorylation, access, complex, biol, privacy, cookies, functions, kuhnt, pyruvate, metabolism, chain, biophys, acta, studies, mol, fibers, publish, search, thomas, succinate, tumors, biochim, germany, function,

Topics {✒}

high resolution respirometry 28 nmol o2/mg/min versus 2 otto-von-guericke-university magdeburg month download article/chapter martin-luther-universitĂ€t halle-wittenberg 19 nmol o2/mg/min saponin-skinned fibers mitochondrial oxphos functions von hippel-lindau disease antimycin a-insensitive respiration rat liver mitochondria mitochondrial dna-encoded subunits antimycin a-independent respiration permeabilized muscle fibers rat rhabdomyosarcoma r1h full article pdf electron transfer system related subjects privacy choices/manage cookies rat skeletal muscles richard cw 3rd martin-luther-university check access instant access rhabdomyosarcoma tumor cells mitochondrial oxidative phosphorylation mitochondrial respiratory parameters high feasibility renal cell carcinoma modulating metabolism mitochondrial dna damage mitochondrial membrane potential respiratory nadh dehydrogenase human cell line skeletal muscle van der mey p53-independent proliferation cell population kinetics human colorectal tumours malignant human gliomas mitochondrial genome instability mitochondrial respiratory function mitochondrial respiratory rates article kuhnt mitochondrial myopathy studies european economic area septic icu patients hif−1alpha regulation willett-brozick je beck-bornholdt hp

Questions {❓}

  • Hobermann HD (1975) Is there a role for mitochondrial genes in carcinogenesis?

Schema {đŸ—ș}

WebPage:
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         headline:Mitochondrial OXPHOS Functions in R1H Rhabdomyosarcoma and Skeletal Muscles of the Rat
         description:The aim of the study was to determinate mitochondrial oxidative phosphorylation (OXPHOS) functions in rat rhabdomyosarcoma R1H (R1H) and rat skeletal muscles. For that purpose skinned fiber technique and multiple substrate inhibitor titration were adapted to tumor samples. In our animal tumor model (R1H) functional abnormalities of OXPHOS were found compared to skeletal muscles. In R1H the state 3 respiration of pyruvate + malate was decreased: 0.56 ± 0.28 nmol O2/mg/min versus 2.32 ± 1.19 nmol O2/mg/min, P < 0.001, whereas the state 3 respiration of succinate + rotenone was increased: 36 ± 14% versus 19 ± 11%, P < 0.001. In R1H the rotenone-insensitive respiration reached higher levels than the antimycin A-insensitive respiration, whereas in normal muscles the converse was observed. Additionally, the obvious difference between the CAT- and the antimycin A-independent respiration indicates an increased part of leak respiration in R1H. By now, the high feasibility of these techniques is appreciated for the investigation of muscles and prospectively for tumors, too.
         datePublished:2007-02-02T00:00:00Z
         dateModified:2007-02-02T00:00:00Z
         pageStart:973
         pageEnd:980
         sameAs:https://doi.org/10.1007/s11064-006-9254-0
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            Mitochondria
            OXPHOS functions
            Skinned fiber technique
            High-resolution respirometry
            Multiple substrate inhibitor titration
            Rat rhabdomyosarcoma R1H
            Neurosciences
            Neurochemistry
            Biochemistry
            general
            Cell Biology
            Neurology
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                     name:Key Neurotech, Otto-von-Guericke-University Magdeburg
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      headline:Mitochondrial OXPHOS Functions in R1H Rhabdomyosarcoma and Skeletal Muscles of the Rat
      description:The aim of the study was to determinate mitochondrial oxidative phosphorylation (OXPHOS) functions in rat rhabdomyosarcoma R1H (R1H) and rat skeletal muscles. For that purpose skinned fiber technique and multiple substrate inhibitor titration were adapted to tumor samples. In our animal tumor model (R1H) functional abnormalities of OXPHOS were found compared to skeletal muscles. In R1H the state 3 respiration of pyruvate + malate was decreased: 0.56 ± 0.28 nmol O2/mg/min versus 2.32 ± 1.19 nmol O2/mg/min, P < 0.001, whereas the state 3 respiration of succinate + rotenone was increased: 36 ± 14% versus 19 ± 11%, P < 0.001. In R1H the rotenone-insensitive respiration reached higher levels than the antimycin A-insensitive respiration, whereas in normal muscles the converse was observed. Additionally, the obvious difference between the CAT- and the antimycin A-independent respiration indicates an increased part of leak respiration in R1H. By now, the high feasibility of these techniques is appreciated for the investigation of muscles and prospectively for tumors, too.
      datePublished:2007-02-02T00:00:00Z
      dateModified:2007-02-02T00:00:00Z
      pageStart:973
      pageEnd:980
      sameAs:https://doi.org/10.1007/s11064-006-9254-0
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         Mitochondria
         OXPHOS functions
         Skinned fiber technique
         High-resolution respirometry
         Multiple substrate inhibitor titration
         Rat rhabdomyosarcoma R1H
         Neurosciences
         Neurochemistry
         Biochemistry
         general
         Cell Biology
         Neurology
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                     name:Department of Radiotherapy, Martin-Luther-University, Halle-Wittenberg, Germany
                     type:PostalAddress
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            name:Xiaoying Qu
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                     name:Department of Radiotherapy, Martin-Luther-University, Halle-Wittenberg, Germany
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                     name:Department of Radiotherapy, Martin-Luther-University, Halle-Wittenberg, Germany
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                  address:
                     name:Department of Radiotherapy, University of Schleswig-Holstein, Luebeck, Germany
                     type:PostalAddress
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            name:Frank Norbert Gellerich
            affiliation:
                  name:Key Neurotech, Otto-von-Guericke-University Magdeburg
                  address:
                     name:Institute of Neuropathology, Key Neurotech, Otto-von-Guericke-University Magdeburg, Magdeburg, Germany
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      address:
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      address:
         name:Department of Radiotherapy, University of Schleswig-Holstein, Luebeck, Germany
         type:PostalAddress
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            address:
               name:Department of Radiotherapy, Martin-Luther-University, Halle-Wittenberg, Germany
               type:PostalAddress
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            name:Martin-Luther-UniversitĂ€t Halle-Wittenberg
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      name:Tanja Pelz
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            name:Martin-Luther-University
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               name:Department of Radiotherapy, Martin-Luther-University, Halle-Wittenberg, Germany
               type:PostalAddress
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      name:Xiaoying Qu
      affiliation:
            name:Martin-Luther-University
            address:
               name:Department of Radiotherapy, Martin-Luther-University, Halle-Wittenberg, Germany
               type:PostalAddress
            type:Organization
      name:Gabriele HĂ€nsgen
      affiliation:
            name:Martin-Luther-University
            address:
               name:Department of Radiotherapy, Martin-Luther-University, Halle-Wittenberg, Germany
               type:PostalAddress
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      name:JĂŒrgen Dunst
      affiliation:
            name:University of Schleswig-Holstein
            address:
               name:Department of Radiotherapy, University of Schleswig-Holstein, Luebeck, Germany
               type:PostalAddress
            type:Organization
      name:Frank Norbert Gellerich
      affiliation:
            name:Key Neurotech, Otto-von-Guericke-University Magdeburg
            address:
               name:Institute of Neuropathology, Key Neurotech, Otto-von-Guericke-University Magdeburg, Magdeburg, Germany
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            type:Organization
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      name:Department of Radiotherapy, Martin-Luther-University, Halle-Wittenberg, Germany
      name:UniversitĂ€tsklinik und Poliklinik fĂŒr Strahlentherapie, Martin-Luther-UniversitĂ€t Halle-Wittenberg, Halle/Saale, Germany
      name:Department of Radiotherapy, Martin-Luther-University, Halle-Wittenberg, Germany
      name:Department of Radiotherapy, Martin-Luther-University, Halle-Wittenberg, Germany
      name:Department of Radiotherapy, Martin-Luther-University, Halle-Wittenberg, Germany
      name:Department of Radiotherapy, University of Schleswig-Holstein, Luebeck, Germany
      name:Institute of Neuropathology, Key Neurotech, Otto-von-Guericke-University Magdeburg, Magdeburg, Germany
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