Complete haematological and cytogenetic response to interferon alpha-2a of a myeloproliferative disorder with eosinophilia associated with a unique t(4;7) aberration

Autor: B Gaede, Bernd Hertenstein, Guntram Büsche, Patrick Schöffski, Arnold Ganser, U Pascheberg

Publikováno v: Annals of Hematology. 79:95-98

A female patient with eosinophilia and cardiac symptoms was found to have a unique chromosomal aberration [t(4;7)(q11;p13)] of bone-marrow precursors. The disorder was classified as a chronic myeloproliferative syndrome with eosinophilia. Due to a si

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c77daf1ba4fe3140a3f6b857a752a43
https://doi.org/10.1007/s002770050018

Supplement II: Abstracts of the international symposium on Skin Carcinogenesis in man and in experimental models. Heidelberg, 29–31 October 1991 (pp S61–S88)

Autor: C. J. Kemp, G. Stingl, C. Caulín, E. G. Jung, H. Tanooka, J. Lassus, E. F. Griffin, Douglas R. Lowy, J. L. Jorcano, J. C. Wang, L. Weber, R. Kato, Paul Janiaud, S. Ohno, A. Schwaaf, R. Gollhausen, N. Sönnichsen, H. Hug, Toshio Kuroki, M. Yaar, J. R. Schlehofer, K. Krasagakis, PE Purkis, Monika M. Gross, H. Heine, H. Mukhtar, J. A. Newton, G. Reisbach, C. Bauer, A. Winter, K. M. Niemi, S. Yamamoto, Bernd L. Sorg, V. A. DeLeo, S. Bruvers, P. Navarro, A. Ootsuyama, G. Tadini, Bert J. Vermeer, D. English, A. B. Bianchi, S. Feil, A. Lehmus, H. Winter, P. T. Strickland, C. Proby, J. M. Foidart, R. Eckert, R. E. Albert, N. E. Fusenig, E. Lee, R. D. Granstein, P. Bums, E. Berti, J. Jürgensmeier, H. Roeser, J. Nährig, A. Anders, F. R. de Gruijl, C. S. Baxter, R. Mailhammer, H. van Weelden, Y. Fujiwara, E. Filvaroff, E. Weber, S. Froschermaier, G. Graf, J. C. Barrett, J. Weiss, H. Weber, B. Hennig, M. Miller, F. Urbach, K. Yamamura, E. Pâques, A. Hülsen, Seymour Garte, B. A. Gilchrest, S. Neill, K. Thalmeier, C. Zechel, Jan P. Vandenbroucke, B. Epe, P. Höfler, B. Przybilla, A. Markey, C. Gilles, C. Bauluz, I. B. Weinstein, U. Van der Piepen, Fokko J. Van Der Woude, T. Jimbo, A. Cano, P. Tomakidi, M. Quintanilla, A. Real, T. Grande, G. T. Bowden, H. Friesel, Y. Mishima, Jan N. Bouwes Bavinck, D. Breitkreutz, Stanley J. Miller, M. Piette, E. Wagner, M. Buček, A. Kopp-Schneider, C. A. Afshari, A. Ranki, M. Garmyn, Margaret L. Kripke, C. Baxter, E. Hecker, Hiroshi Tanooka, F. Harks, E. Lopez-Bran, P. A. Futreal, H. Wei, M. B. Abdel-Naser, A. Diugosz, S. Altmeier, J. Macejewski, Uwe Wollina, J. Römisch, B. Eberlein, E. B. Broecker, Y. Funasaka, M. Glover, M. Haas, S. Gruner, T. Bishop, J. Leers, G. Picht, A. Gilani, W. Diezel, D. S. Silvers, A. Glick, R. Krauß, H. Harris, Anne Østerlind, J. Levy, A. Cerri, E. Danen, K. Schiess, E. Viesel, H. Gröger, B. C. Bastian, K. Hayashibe, K. H. Richter, K. Frenkel, Odilia Popanda, M. Gómez, I. Moll, U. Schleenbecker, M. Ueda, Fritz Anders, H. D. Volk, K. Möller, M. Ichihashi, M. Martín, G. Krauter, S. Krüger-Krasagakes, D. J. Ruiter, J. C. van der Leun, M. Götschl, R. Niedner, Sylvia A. Sedman, T. M. Rünqer, Akira Ootsuyama, Judith P. Johnson, A. Montes, A. G. Ushmorov, G. Bauer, R. Schnapke, S. Kahn, B. Kempkes, C. Garbe, B. Steinbauer, B. K. Armstrong, P. Plein, T. Schneider, C. Missero, B. Schlatterer, M. Schara, P. J. Heenan, M. Stephan, B. A. Burkhart, A. J. P. Klein-Szanto, Eva-B. Bröcker, R. Halaban, S. Grabbe, G. N. P. van Muijen, E. Azizi, D. Schaefer, A. A. Hartmann, C. Ballestin, P. Klein-Bauernschmitt, R. Shukla, G. Kelfkens, M. Nelson, Friedrich Rippmann, M. Kaszkin, S. G. Zubova, Bruce D. Cohen, T. Cody, A. Kricker, V. B. Okulov, P. Fuchs, V. Kinzel, S. Osada, A. Balmain, A. B. Stoler, T. T. Sun, J. Svetek, W. D. Lehmann, F. Larcher, P. Krieg, Jürgen Schweizer, M. Hergenhahn, A. Faissner, G. P. Dotto, C. J. Conti, U. Burcin, L. Hültner, V. Bataille, G. Fürstenberger, EB Lane, A. Smith, D. Jahrens, K. Elgjo, Walter Troll, A. Gandarillas, M. Schön, R. D. Owen, S. Ramón y Cajal, Heinz Walter Thielmann, A. O. Danilov, S. H. Yuspa, J. Cuzick, P. L. Randell, Sylvia Unger, J. A. Boyd, C. Sutter, N. M. Navone, IM Leigh, H. J. Stark, L. A. Annab, R. Gitto, James M. Spencer, C. E. Orfanos, R. M. Lavker, W. Tilgen, R. Albert, H. L. Moses, Eric J. Stanbridge, R. Kosters, Rainer Schmidt, P. Boukamp, E. Schöpf, U. Pascheberg, Yuichi Hashimoto, A. Robledo, F. Marks, J. Sherman, J. Richards, C. E. Klein, Frans H.J. Claas, S. Pečar, Bernard M. Mechler, Doris Rueß, B. Fiebich, Lutz Edler, John T. Schiller, H. Fujiki

Publikováno v: Journal of Cancer Research and Clinical Oncology. 117:S61-S83

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::15049a5efeb2b13268d45c2c4c277a20
https://doi.org/10.1007/bf01613300

Detection of karyotypic aberrations in acute myeloblastic leukaemia: a prospective comparison between PCR/FISH and standard cytogenetics in 140 patients with de novo AML

Autor: J, Krauter, W, Peter, U, Pascheberg, B, Heinze, L, Bergmann, D, Hoelzer, M, Lübbert, G, Schlimok, R, Arnold, H, Kirchner, M, Port, A, Ganser, G, Heil

Publikováno v: British journal of haematology. 103(1)

In 140 patients with de novo acute myeloid leukaemia (AML) standard cytogenetics were compared with RT-PCR for the detection of t(8;21), t(15;17) and inv(16) and fluorescence in situ hybridization (FISH) for numerical aberrations of chromosomes 7, 8,

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https://pubmed.ncbi.nlm.nih.gov/9792292

RT-PCR for the Diagnosis of Acute Myeloblastic Leukemia with Inv(16) and Detection of Minimal Residual Disease

Autor: U. Pascheberg, R H Mertelsmann, Jürgen Krauter, G. Schwab, G. Schlimok, Arnold Ganser, F. Herrmann, Dieter Hoelzer, Gerhard Heil

Publikováno v: Haematology and Blood Transfusion / Hämatologie und Bluttransfusion ISBN: 9783642719622

One of the most common structural chromosomal aberrations in acute myeloblastic leukemia (AML) is the pericentric inversion of chromosome 16, inv(16) (p13q22) which results in the rearrangement of the CBFβ- and the MYH11-gene and the transcription o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::483c6694552f99d395d17fdbce72b5f2
https://doi.org/10.1007/978-3-642-71960-8_143

Delineation of genomic regions in chromosome band 7q22 commonly deleted in myeloid leukemias

Autor: K, Fischer, J, Brown, S W, Scherer, P, Schramm, J, Stewart, G, Fugazza, U, Pascheberg, W, Peter, L C, Tsui, P, Lichter, H, Döhner

Publikováno v: Recent results in cancer research. Fortschritte der Krebsforschung. Progres dans les recherches sur le cancer. 144

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::9e566316fb352cbe36a7473b0a6a48f4
https://pubmed.ncbi.nlm.nih.gov/9304706