Search Results - "Lenk, T"

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    Structural Investigation of Molecular Organization in Self-Assembled Monolayers of a Semifluorinated Amidethiol by Lenk, T. J, Hallmark, V. M, Hoffmann, C. L, Rabolt, J. F, Castner, D. G, Erdelen, C, Ringsdorf, H

    Published in Langmuir (01-12-1994)
    “…A new fluorocarbon-chain-containing molecule, CF[sub 3](CF[sub 2])[sub 7]C(O)N(H)CH[sub 2]CH[sub 2]SH, for self-assembly was synthesized using a simple and…”
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    Journal Article
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    Creating Smart Polymer Surfaces with Selective Adhesion Properties by Koberstein, J. T. J., Duch, D. E. D., Hu, W., Lenk, T. J., Bhatia, R., Brown, H. R., Lingelser, J.-P., Gallot, Y.

    Published in The Journal of adhesion (01-03-1998)
    “…A new concept for polymer surface modification is described that employs surface-active ω-functional block copolymers as additives to create polymers with…”
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    Journal Article Conference Proceeding
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    B32Alterations in Mitochondrial Proteome of Brain and Skeletal Muscle in Two Transgenic HD Mouse Models do not Reflect Mitochondrial Respiratory Activity by Barth, E, Fleischer, C, Lenk, T, Lehnert, S, Jahn, O, Otto, M, Calzia, E, Landwehrmeyer, G B, Lindenberg, K S

    “…Metabolic changes in HD pathogenesis and mitochondrial dysfunction are supposed to be closely linked. HD patients lose significantly body weight despite normal…”
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    Journal Article
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    D03Mitochondrial Biogenesis, And Respiratory Chain Assembly And Function, In Skeletal Muscle Of The R6/2 Mouse Model And Human Huntington's Disease by Hering, T, Kojer, K, Birth, N, Lenk, T, Parker, JA, Haider, S, Tabrizi, S J, Taanman, J, Orth, M

    “…BackgroundHuntington's disease (HD) primarily affects the brain. However, Huntingtin (HTT) is expressed in peripheral tissues as well. In skeletal muscle, like…”
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    Journal Article
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    B21Decreased expression and reduced translocation to the sarcolemma of the insulin-sensitive glucose transporter GLUT4 in skeletal muscle of R6/2 MICE by Wackler, P, Lenk, T, Hering, T, Orth, M, Landwehrmeyer, G B, Lindenberg, K S

    “…Background and aimsSeveral observations indicate a catabolic metabolism in HD patients despite sufficient caloric intake. Furthermore, an impaired glucose…”
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    Journal Article
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    Surface characterization of nanostructured metal and ceramic particles by Luo, P., Nieh, T.G., Schwartz, A.J., Lenk, T.J.

    “…In the present study, nanocrystalline Al, TiN and SiC particles produced by different techniques were examined using X-ray diffraction analysis, scanning…”
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    Journal Article
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    B21 Decreased expression and reduced translocation to the sarcolemma of the insulin-sensitive glucose transporter GLUT4 in skeletal muscle of R6/2 MICE by Wackler, P, Lenk, T, Hering, T, Orth, M, Landwehrmeyer, GB, Lindenberg, KS

    “…Background and aimsSeveral observations indicate a catabolic metabolism in HD patients despite sufficient caloric intake. Furthermore, an impaired glucose…”
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    Journal Article
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    A11 Alterations in the PGC-1 α dependent oxidative stress response in the R6/2 mouse model of HD by Sandtner, H C, Fleischer, C, Lenk, T, Landwehrmeyer, G B, Lindenberg, K S

    “…Background In Huntington's disease (HD), alterations in energy metabolism and mitochondrial function may result in oxidative stress. Increased levels of…”
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    Journal Article
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    A11 Alterations in the PGC-1 [alpha] dependent oxidative stress response in the R6/2 mouse model of HD by Sandtner, H C, Fleischer, C, Lenk, T, Landwehrmeyer, G B, Lindenberg, K S

    “…Background In Huntington's disease (HD), alterations in energy metabolism and mitochondrial function may result in oxidative stress. Increased levels of…”
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    Journal Article
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    A20 Interaction of huntingtin and the ryanodine receptor by Lindenberg, K S, Davranche, A, Klein, F, Thomas, A V, Lill, C, Lenk, T, Orlando, L R, Kama, J, Young, A B, Landwehrmeyer, G B, Trottier, Y

    “…Background Alterations in cellular calcium homeostasis have been recognised as one of several pathogenic mechanisms in Huntington's disease (HD). The discovery…”
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    Journal Article
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    Dopamine transporter-mediated cytotoxicity of 6-hydroxydopamine in vitro depends on expression of mutant α-synucleins related to Parkinson's disease by Lehmensiek, Vera, Tan, Eva-Maria, Liebau, Stefan, Lenk, Thomas, Zettlmeisl, Heinz, Schwarz, Johannes, Storch, Alexander

    Published in Neurochemistry international (01-04-2006)
    “…6-Hydroxydopamine (6-OHDA) is widely used to produce animal models of Parkinson's disease (PD) by selectively destroying the nigro-striatal dopaminergic…”
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    Journal Article