Merely presenting one’s own name along with target items is insufficient to produce a memory advantage for the items: A critical role of relational processing von Kim, Kyungmi, Johnson, Jenne D., Rothschild, Danielle J., Johnson, Marcia K.

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Numerical simulation of fluid flow through random packs of ellipses von Matsumura, Y., Jenne, D., Jackson, T. L.

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Antibodies to MOG are transient in childhood acute disseminated encephalomyelitis von Pröbstel, A K, Dornmair, K, Bittner, R, Sperl, P, Jenne, D, Magalhaes, S, Villalobos, A, Breithaupt, C, Weissert, R, Jacob, U, Krumbholz, M, Kuempfel, T, Blaschek, A, Stark, W, Gärtner, J, Pohl, D, Rostasy, K, Weber, F, Forne, I, Khademi, M, Olsson, T, Brilot, F, Tantsis, E, Dale, R C, Wekerle, H, Hohlfeld, R, Banwell, B, Bar-Or, A, Meinl, E, Derfuss, T

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High Frequency of Mosaicism among Patients with Neurofibromatosis Type 1 (NF1) with Microdeletions Caused by Somatic Recombination of the JJAZ1 Gene von Kehrer-Sawatzki, H., Kluwe, L., Sandig, C., Kohn, M., Wimmer, K., Krammer, U., Peyrl, A., Jenne, D.E., Hansmann, I., Mautner, V.-F.

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Autoprocessing of neutrophil elastase near its active site reduces the efficiency of natural and synthetic elastase inhibitors von Dau, T., Sarker, R. S. J., Yildirim, A. O., Eickelberg, O., Jenne, D. E.

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Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase von JENNE, D. E, REIMANN, H, NEZU, J.-I, FRIEDEL, W, LOFF, S, JESCHKE, R, MÜLLER, O, BACK, W, ZIMMER, M

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Regulation of Cysteine-Protease Activity Prevents Graft Dysfunction during Ischemia-Lung Reperfusion von Morrone, C., Rehm, S., Smirnova, N., Doryab, A., Schmid, O., Eickelberg, O., Yildirim, A., Jenne, D.

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Antibodies to MOG are transient in childhood acute disseminated encephalomyelitis von PRÖBSTEL, A. K, DORNMAIR, K, KRUMBHOLZ, M, KUEMPFEL, T, BLASCHEK, A, STARK, W, GÄRTNER, J, POHL, D, ROSTASY, K, WEBER, F, FORNE, I, KHADEMI, M, BITTNER, R, OLSSON, T, BRILOT, F, TANTSIS, E, DALE, R. C, WEKERLE, H, HOHLFELD, R, BANWELL, B, BAR-OR, A, MEINL, E, DERFUSS, T, SPERL, P, JENNE, D, MAGALHAES, S, VILLALOBOS, A, BREITHAUPT, C, WEISSERT, R, JACOB, U

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Cleavage of La protein by granzyme H induces cytoplasmic translocation and interferes with La-mediated HCV-IRES translational activity von Romero, V, Fellows, E, Jenne, D E, Andrade, F

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Quantitative analysis of protease recognition by inhibitors in plasma using microscale thermophoresis von Dau, T., Edeleva, E. V., Seidel, S. A. I., Stockley, R. A., Braun, D., Jenne, D. E.

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Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin von Reeves, Roger, Faulkner, Georgine, Wiltshire, Tim J, Vainzof, Mariz, Valle, Giorgio, Moreira, Eloisa S, Nilforoushan, Antje, Passos-Bueno, M. R, Suzuki, Oscar T, Jenne, Dieter E, Zatz, Mayana

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Induction of MHC Class I Genes in Neurons von Neumann, Harald, Cavalié, Adolfo, Jenne, Dieter E., Wekerle, Hartmut

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Migratory Activity and Functional Changes of Green Fluorescent Effector Cells before and during Experimental Autoimmune Encephalomyelitis von Flügel, Alexander, Berkowicz, Tomasz, Ritter, Thomas, Labeur, Marta, Jenne, Dieter E, Li, Zhaoxia, Ellwart, Joachim W, Willem, Michael, Lassmann, Hans, Wekerle, Hartmut

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Molecular Structure and Functional Characterization of a Human Complement Cytolysis Inhibitor Found in Blood and Seminal Plasma: Identity to Sulfated Glycoprotein 2, a Constituent... von Jenne, Dieter E., Tschopp, J.

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Mitotic recombination mediated by the JJAZF1 (KIAA0160) gene causing somatic mosaicism and a new type of constitutional NF1 microdeletion in two children of a mosaic female with on... von Petek, E, Jenne, D E, Smolle, J, Binder, B, Lasinger, W, Windpassinger, C, Wagner, K, Kroisel, P M, Kehrer-Sawatzki, H

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Major histocompatibility complex (MHC) class I gene expression in single neurons of the central nervous system: differential regulation by interferon (IFN)-gamma and tumor necrosis... von Neumann, H, Schmidt, H, Cavalié, A, Jenne, D, Wekerle, H

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Heterogeneity of breakpoints in non-LCR-mediated large constitutional deletions of the 17q11.2 NF1 tumour suppressor region von Kehrer-Sawatzki, H, Tinschert, S, Jenne, D E

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γ-secretase directly sheds the survival receptor BCMA from plasma cells von Laurent, Sarah A., Hoffmann, Franziska S., Kuhn, Peer-Hendrik, Cheng, Qingyu, Chu, Yuanyuan, Schmidt-Supprian, Marc, Hauck, Stefanie M., Schuh, Elisabeth, Krumbholz, Markus, Rübsamen, Heike, Wanngren, Johanna, Khademi, Mohsen, Olsson, Tomas, Alexander, Tobias, Hiepe, Falk, Pfister, Hans-Walter, Weber, Frank, Jenne, Dieter, Wekerle, Hartmut, Hohlfeld, Reinhard, Lichtenthaler, Stefan F., Meinl, Edgar

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Molecular Characterization and Gene Content of Breakpoint Boundaries in Patients with Neurofibromatosis Type 1 with 17q11.2 Microdeletions von Jenne, Dieter E., Tinschert, Sigrid, Reimann, Heike, Lasinger, Wolfgang, Thiel, Gundula, Hameister, Horst, Kehrer-Sawatzki, Hildegard

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Segmental neurofibromatosis is caused by somatic mutation of the neurofibromatosis type 1 (NF1) gene von Tinschert, S, Naumann, I, Stegmann, E, Buske, A, Kaufmann, D, Thiel, G, Jenne, D E

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