Search Results - "Handrick, R"

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    Activating Akt1 mutations alter DNA double strand break repair and radiosensitivity by Oeck, S., Al-Refae, K., Riffkin, H., Wiel, G., Handrick, R., Klein, D., Iliakis, G., Jendrossek, V.

    Published in Scientific reports (17-02-2017)
    “…The survival kinase Akt has clinical relevance to radioresistance. However, its contributions to the DNA damage response, DNA double strand break (DSB) repair…”
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    Mobilization of poly(3-hydroxybutyrate) in Ralstonia eutropha by Handrick, R, Reinhardt, S, Jendrossek, D

    Published in Journal of bacteriology (01-10-2000)
    “…Ralstonia eutropha H16 degraded (mobilized) previously accumulated poly(3-hydroxybutyrate) (PHB) in the absence of an exogenous carbon source and used the…”
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    additional loss of Bak and not the lack of the protein tyrosine kinase p56/Lck in one JCaM1.6 subclone caused pronounced apoptosis resistance in response to stimuli of the intrinsic pathway by Rudner, J, Mueller, A.-C, Matzner, N, Huber, S. M, Handrick, R, Belka, C, Jendrossek, V

    Published in Apoptosis (London) (01-05-2009)
    “…Ionising radiation, hypoxia, and the cyclooxygenase-2 inhibitor Celecoxib are known agonists of the intrinsic apoptosis pathway that involves mitochondrial…”
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    Bcl-2 mediated inhibition of erucylphosphocholine-induced apoptosis depends on its subcellular localisation by Handrick, R., Rudner, J., Müller, I., Eibl, H., Belka, C., Jendrossek, V.

    Published in Biochemical pharmacology (15-09-2005)
    “…The synthetic phospholipid derivative erucylphosphocholine (ErPC) is a potent inducer of apoptosis in human tumor cell lines. This membrane-targeted drug…”
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    MICROBIAL DEGRADATION OF POLYHYDROXYALKANOATES by Jendrossek, Dieter, Handrick, René

    Published in Annual review of microbiology (01-01-2002)
    “…Polyesters such as poly(3-hydroxybutyrate) (PHB) or other polyhydroxyalkanoates (PHA) have attracted commercial and academic interest as new biodegradable…”
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    Celecoxib activates a novel mitochondrial apoptosis signaling pathway by Jendrossek, Verena, Handrick, René, Belka, Claus

    Published in The FASEB journal (01-08-2003)
    “…ABSTRACT The cyclooxygenase (COX)‐2 inhibitor Celecoxib may inhibit cancer cell growth independently of its capacity to block the COX‐2 enzyme. The growth…”
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    Membrane targeted anticancer drugs: potent inducers of apoptosis and putative radiosensitisers by Jendrossek, V, Handrick, R

    “…In the last two decades, cellular membranes have been identified as novel targets for antineoplastic drugs. Two classes of synthetic phospholipid analogues:…”
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    The “Intracellular” Poly(3-Hydroxybutyrate) (PHB) Depolymerase of Rhodospirillum rubrum Is a Periplasm-Located Protein with Specificity for Native PHB and with Structural Similarity to Extracellular PHB Depolymerases by HANDRICK, René, REINHARDT, Simone, KIMMIG, Philipp, JENDROSSEK, Dieter

    Published in Journal of Bacteriology (01-11-2004)
    “…Article Usage Stats Services JB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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    A New Type of Thermoalkalophilic Hydrolase of Paucimonas lemoignei with High Specificity for Amorphous Polyesters of Short Chain-length Hydroxyalkanoic Acids by Handrick, René, Reinhardt, Simone, Focarete, Maria Letizia, Scandola, Mariastella, Adamus, Grazyna, Kowalczuk, Marek, Jendrossek, Dieter

    Published in The Journal of biological chemistry (28-09-2001)
    “…A novel type of hydrolase was purified from culture fluid of Paucimonas (formerlyPseudomonas) lemoignei. Biochemical characterization revealed an unusual…”
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    Proapoptotic activity of Ukrain is based on Chelidonium majus L. alkaloids and mediated via a mitochondrial death pathway by Habermehl, Daniel, Kammerer, Bernd, Handrick, René, Eldh, Therese, Gruber, Charlotte, Cordes, Nils, Daniel, Peter T, Plasswilm, Ludwig, Bamberg, Michael, Belka, Claus, Jendrossek, Verena

    Published in BMC cancer (17-01-2006)
    “…The anticancer drug Ukrain (NSC-631570) which has been specified by the manufacturer as semisynthetic derivative of the Chelidonium majus L. alkaloid…”
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