نتائج البحث - Martini, Rudolf
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Non-invasive assessment of retinal alterations in mouse models of infantile and juvenile neuronal ceroid lipofuscinosis by spectral domain optical coherence tomography حسب Groh, Janos, Stadler, David, Buttmann, Mathias, Martini, Rudolf
منشور في 2014نص -
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Loss of Distal Axons and Sensory Merkel Cells and Features Indicative of Muscle Denervation in Hindlimbs of P0-Deficient Mice حسب Frei, Regula, Mötzing, Sandra, Kinkelin, Ilka, Schachner, Melitta, Koltzenburg, Martin, Martini, Rudolf
منشور في 1999نص -
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Triple Knock-Out of CNTF, LIF, and CT-1 Defines Cooperative and Distinct Roles of these Neurotrophic Factors for Motoneuron Maintenance and Function حسب Holtmann, Bettina, Wiese, Stefan, Samsam, Mohtashem, Grohmann, Katja, Pennica, Diane, Martini, Rudolf, Sendtner, Michael
منشور في 2005نص -
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The Wld(s) Mutation Delays Robust Loss of Motor and Sensory Axons in a Genetic Model for Myelin-Related Axonopathy حسب Samsam, Mohtashem, Mi, Weiqian, Wessig, Carsten, Zielasek, Jürgen, Toyka, Klaus V., Coleman, Michael P., Martini, Rudolf
منشور في 2003نص -
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The Role of Macrophages in Demyelinating Peripheral Nervous System of Mice Heterozygously Deficient in P0 حسب Carenini, Stefano, Mäurer, Mathias, Werner, Alexander, Blazyca, Heinrich, Toyka, Klaus V., Schmid, Christoph D., Raivich, Gennadij, Martini, Rudolf
منشور في 2001نص -
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Pathology of a mouse mutation in peripheral myelin protein P0 is characteristic of a severe and early onset form of human Charcot-Marie-Tooth type 1B disorder حسب Rünker, Annette E., Kobsar, Igor, Fink, Torsten, Loers, Gabriele, Tilling, Thomas, Putthoff, Peggy, Wessig, Carsten, Martini, Rudolf, Schachner, Melitta
منشور في 2004نص