Publications of Dieter E. Jenne

Bade, B.; Boettcher, H. E.; Lohrmann, J.; Hink-Schauer, C.; Bratke, K.; Jenne, D. E.; Virchow, J. C.; Luttmann, W.: Differential expression of the granzymes A, K and M and perforin in human peripheral blood lymphocytes. International Immunology 17 (11), pp. 1419 - 1428 (2005)

Jenne, D. E.; Kley, R. A.; Vorgerd, M.; Schroder, J. M.; Weis, J.; Reimann, H.; Albrecht, B.; Nurnberg, P.; Thiele, H.; Muller, C. R. et al.; Meng, G.; Witt, C. C.; Labeit, S.: Limb girdle muscular dystrophy in a sibling pair with a homozygous Ser606Leu mutation in the alternatively spliced IS2 region of calpain 3. Biological Chemistry 386 (1), pp. 61 - 67 (2005)

Krumbholz, M.; Specks, U.; Wick, M.; Kalled, S. L.; Jenne, D. E.; Meinl, E.: BAFF is elevated in serum of patients with Wegener's granulomatosis. Journal of Autoimmunity 25 (4), pp. 298 - 302 (2005)

Kurschus, F. C.; Bruno, R.; Fellows, E.; Falk, C. S.; Jenne, D. E.: Membrane receptors are not required to deliver granzyme B during killer cell attack. Blood 105 (5), pp. 2049 - 2058 (2005)

Schuller, M.; Jenne, D. E.; Voltz, R.: The human PNMA family: Novel neuronal proteins implicated in paraneoplastic neurological disease. Journal of Neuroimmunology 169 (1-2), pp. 172 - 176 (2005)

Spiegel, M.; Oexle, K.; Horn, D.; Windt, E.; Buske, A.; Albrecht, B.; Prott, E. C.; Seemanova, E.; Seidel, J.; Rosenbaum, T. et al.; Jenne, D. E.; Kehrer-Sawatzki, H. K.; Tinschert, S.: Childhood overgrowth in patients with common NF1 microdeletions. European Journal of Human Genetics 13 (7), pp. 883 - 888 (2005)

Wiesner, O.; Litwiller, R. D.; Hummel, A. M.; Viss, M. A.; McDonald, C. J.; Jenne, D. E.; Fass, D. N.; Specks, U.: Differences between human proteinase 3 and neutrophil elastase and their murine homologues are relevant for murine model experiments. FEBS Letters 579 (24), pp. 5305 - 5312 (2005)

Kehrer-Sawatzki, H.; Kluwe, L.; Sandig, C.; Kohn, M.; Wimmer, K.; Krammer, U.; Peyrl, A.; Jenne, D. E.; Hansmann, I.; Mautner, V. F.: High frequency of mosaicism among patients with neurofibromatosis type 1 (NF1) with microdeletions caused by somatic recombination of the JJAZ1 gene. American Journal of Human Genetics 75 (3), pp. 410 - 423 (2004)

Kurschus, F. C.; Kleinschmidt, M.; Fellows, E.; Dornmair, K.; Rudolph, R.; Lilie, H.; Jenne, D. E.: Killing of target cells by redirected granzyme B in the absence of perforin. FEBS Letters 562 (1-3), pp. 87 - 92 (2004)

Pfister, H.; Ollert, M.; Fröhlich, L. O.; Quintanilla-Fend, L.; Colby, T. V.; Specks, U.; Jenne, D. E.: Autoantibodies against the murine homolog of Wegener’s autoantigen (proteinase 3) are pathogenic in vivo. Blood 104, pp. 1411 - 1418 (2004)

Pfister, H.; Ollert, M.; Fröhlich, L. F.; Quintanilla-Martinez, L.; Colby, T. V.; Specks, U.; Jenne, D. E.: Antineutrophil cytoplasmic autoantibodies against the murine homolog of proteinase 3 (Wegener autoantigen) are pathogenic in vivo. Blood 104 (5), pp. 1411 - 1418 (2004)

Wiesner, O.; Russell, K. A.; Lee, A. S.; Jenne, D. E.; Trimarchi, M.; Gregorini, G.; Specks, U.: Antineutrophil cytoplasmic antibodies reacting with human neutrophil elastase as a diagnostic marker for cocaine-induced midline destructive lesions but not autoimmune vasculitis. Arthritis and Rheumatism 50 (9), pp. 2954 - 2965 (2004)

Hink-Schauer, C.; Estebanez-Perpina, E.; Kurschus, F. C.; Bode, W.; Jenne, D. E.: Crystal structure of the apoptosis-inducing human granzyme A dimer. Nature Structural Biology 10 (7), pp. 535 - 540 (2003)

Jenne, D. E.; Tinschert, S.; Dorschner, M. O.; Hameister, H.; Stephens, K.; Kehrer-Sawatzki, H.: Complete physical map and gene content of the human NFI tumor suppressor region in human and mouse. Genes Chromosomes & Cancer 37 (2), pp. 111 - 120 (2003)

Kehrer-Sawatzki, H.; Tinschert, S.; Jenne, D. E.: Heterogeneity of breakpoints in non-LCR-mediated large constitutional deletions of the 17q11.2 NF1 tumour suppressor region. Journal of Medical Genetics 40 (10), e116 (2003)

Petek, E.; Jenne, D. E.; Smolle, J.; Binder, B.; Lasinger, W.; Windpassinger, C.; Wagner, K.; Kroisel, P. M.; Kehrer-Sawatzki, H.: 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 only few manifestations. Journal of Medical Genetics 40 (7), pp. 520 - 525 (2003)

Burger, B.; Uhlhaas, S.; Mangold, E.; Propping, P.; Friedl, W.; Jenne, D. E.; Dockter, G.; Back, W.: Novel de novo mutation of MADH4/SMAD4 in a patient with juvenile polyposis. American Journal of Medical Genetics 110 (3), pp. 289 - 291 (2002)

Campbell, P. K.; Waymire, K. G.; Heier, R. L.; Sharer, C.; Day, D. E.; Reimann, H.; Jaje, J. M.; Friedrich, G. A.; Burmeister, M.; Bartness, T. J. et al.; Russell, L. D.; Young, L. J.; Zimmer, M.; Jenne, D. E.; MacGregor, G. R.: Mutation of a novel gene results in abnormal development of spermatid flagella, loss of intermale aggression and reduced body fat in mice. Genetics 162 (1), pp. 307 - 320 (2002)

Hink-Schauer, C.; Estebanez-Perpina, E.; Wilharm, E.; Fuentes-Prior, P.; Klinkert, W. E. F.; Bode, W.; Jenne, D. E.: The 2.2-angstrom crystal structure of human pro-granzyme K reveals a rigid zymogen with unusual features. Journal of Biological Chemistry 277 (52), pp. 50923 - 50933 (2002)

Jishage, K.; Nezu, J.; Kawase, Y.; Iwata, T.; Watanabe, M.; Miyoshi, A.; Ose, A.; Habu, K.; Kake, T.; Kamada, N. et al.; Ueda, O.; Kinoshita, M.; Jenne, D. E.; Shimane, M.; Suzuki, H.: Role of Lkb1, the causative gene of Peutz-Jegher's syndrome, in embryogenesis and polyposis. Proceedings of the National Academy of Sciences of the United States of America 99 (13), pp. 8903 - 8908 (2002)