Search Results - "KRAUSE, Guido"

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  1. 1

    High frequency of mitochondrial DNA mutations in glioblastoma multiforme identified by direct sequence comparison to blood samples by Kirches, Elmar, Krause, Guido, Warich‐Kirches, Michaela, Weis, Serge, Schneider, Thomas, Meyer‐Puttlitz, Birgit, Mawrin, Christian, Dietzmann, Knut

    Published in International journal of cancer (15-08-2001)
    “…In an earlier study, we showed that heteroplasmy in the mitochondrial genome of gliomas sometimes occurs in a D‐loop polycytosine tract. We extended this study…”
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    Measurement of electrical activity of long-term mammalian neuronal networks on semiconductor neurosensor chips and comparison with conventional microelectrode arrays by Krause, Guido, Lehmann, Stefanie, Lehmann, Mirko, Freund, Ingo, Schreiber, Erik, Baumann, Werner

    Published in Biosensors & bioelectronics (15-01-2006)
    “…Based on complementary metal-oxide semiconductor (CMOS) technology a neurosensor chip with passive palladium electrodes was developed. The CMOS technology…”
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  5. 5

    Region-specific analysis of mitochondrial DNA deletions in neurodegenerative disorders in humans by Mawrin, Christian, Kirches, Elmar, Krause, Guido, Schneider-Stock, Regine, Bogerts, Bernhard, Vorwerk, Christian K., Dietzmann, Knut

    Published in Neuroscience letters (04-03-2004)
    “…Mitochondrial dysfunction caused by mitochondrial DNA (mtDNA) aberrations has been implicated in the neuronal death in neurodegenerative disorders. Significant…”
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  6. 6

    Single-cell analysis of mtDNA deletion levels in sporadic amyotrophic lateral sclerosis by Mawrin, Christian, Kirches, Elmar, Krause, Guido, Wiedemann, Falk R, Vorwerk, Christian K, Bogerts, Bernhard, Schildhaus, Hans-Ulrich, Dietzmann, Knut, Schneider-Stock, Regine

    Published in Neuroreport (29-04-2004)
    “…One possible cause for the neuronal loss in sporadic amyotrophic lateral sclerosis (S-ALS) is an increase of free radicals, which may produce oxidative damage…”
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  7. 7

    Heterogeneous tissue distribution of a mitochondrial DNA polymorphism in heteroplasmic subjects without mitochondrial disorders by Kirches, Elmar, Michael, Matthias, Warich-Kirches, Michaela, Schneider, Thomas, Weis, Serge, Krause, Guido, Mawrin, Christian, Dietzmann, Knut

    Published in Journal of medical genetics (01-05-2001)
    “…CONTEXT Several maternally inherited point mutations of the mitochondrial genome cause mitochondrial disorders, but the correlation between genotype and…”
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  8. 8

    Gliomatosis cerebri: post-mortem molecular and immunohistochemical analyses in a case treated with thalidomide by MAWRIN, Christian, AUMANN, Volker, KIRCHES, Elmar, SCHNEIDER-STOCK, Regine, SCHERLACH, Cordula, VOGEL, Siegfried, MITTLER, Uwe, DIETZMANN, Knut, KRAUSE, Guido, WEIS, Serge

    Published in Journal of neuro-oncology (01-10-2001)
    “…Gliomatosis cerebri (GC) is a rare tumor of the central nervous system (CNS) characterized by widespread diffuse infiltration of the brain and spinal cord by…”
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