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High prevalence of immunoglobulin light chain gene aberrations as revealed by FISH in multiple myeloma and MGUS.
Tuerkmen, S. and Binder, A. and Gerlach, A. and Niehage, S. and Melissari, M.T. and Inandiklioglu, N. and Doerken, B. and Burmeister, T.
Genes Chromosomes & Cancer 53 (8): 650-656. August 2014


Stepwise accumulation of distinct genomic aberrations in a patient with progressively metastasizing ependymoma.
Milde, T. and Pfister, S. and Korshunov, K. and Deubzer, H.E. and Oehme, I. and Ernst, A. and Starzinski-Powitz, A. and Seitz, A. and Lichter, P. and von Deimling, A. and Witt, O.
Genes Chromosomes & Cancer 48 (3): 229-238. March 2009


Genetic background of different cancer cell lines influences the gene set involved in chromosome 8 mediated breast tumor suppression.
Seitz, S. and Korsching, E. and Weimer, J. and Jacobsen, A. and Arnold, N. and Meindl, A. and Arnold, W. and Gustavus, D. and Klebig, C. and Petersen, I. and Scherneck, S.
Genes Chromosomes & Cancer 45 (6): 612-627. June 2006


Profile of differentially expressed genes after transfer of chromosome 17 into the breast cancer cell line CAl51.
Klebig, C. and Seitz, S. and Korsching, E. and Kristiansen, G. and Gustavus, D. and Scherneck, S. and Petersen, I.
Genes Chromosomes & Cancer 44 (3): 233-246. 27 July 2005


Identification of microsatellite instability and mismatch repair gene mutations in breast cancer cell lines.
Seitz, S. and Wassmuth, P. and Plaschke, J. and Schackert, H.K. and Karsten, U. and Santibanez-Koref, M.F. and Schlag, P.M. and Scherneck, S.
Genes Chromosomes & Cancer 37 (1): 29-35. May 2003


Loss of heterozygosity at 11q23.1 and survival in breast cancer: Results of a large European study.
Laake, K. and Launonen, V. and Niederacher, D. and Gudlaugsdottir, S. and Seitz, S. and Rio, P. and Champeme, M.H. and Bieche, I. and Birnbaum, D. and White, G. and Sztan, M. and Sever, N. and Plummer, S. and Osorio, A. and Broeks, A. and Huusko, P. and Spurr, N. and Borg, A. and Cleton-Jansen, A.M. and Veer, L. and Benitez, J. and Casey, G. and Peterlin, B. and Olah, E. and Varley, J. and Bignon, Y.J. and Scherneck, S. and Sigurdardottir, V. and Lidereau, R. and Eyfjord, J. and Beckmann, M.W. and Winqvist, R. and Skovlund, E. and Borresen-Dale, A.L.
Genes Chromosomes & Cancer 25 : 212-221. 1 July 1999


Loss of heterozygosity at 7q31 in breast cancer: results from an international collaborative study group.
Devilee, P. and Hermans, J. and Eyfjoerd, J. and Borresen, A.L. and Liderau, R. and Sobol, H. and Borg, A. and Cleton-Jansen, A.M. and Olah, E. and Cohen, B. and Scherneck, S. and Hamann, U. and Peterlin, B. and Caligo, M. and Bignon, Y.L. and Maugard, C. and Andersen, T.I. and Odegand, A.E.M. and Bieche, I. and Birnbaum, D. and Cornelisse, C.J. and Sztan, M. and Steel, M.R. and Seitz, S. and Logar, N. and Golouh, R. and Ghimenti, C. and Bruelle, S. and Joalland, M.P.
Genes Chromosomes & Cancer 18 : 193-199. 1 January 1997


TP53 mutations and breast cancer prognosis - particularly poor survival rates for cases with mutations in the zinc-binding domains.
Borresen, A.L. and Andersen, T.I. and Eyfjord, J.E. and Cornelis, R.S. and Thorlacius, S. and Borg, A. and Johansson, U. and Theillet, C. and Scherneck, S. and Hartman, S. and Cornelisse, C.J. and Hovig, E. and Devilee, P.
Genes Chromosomes & Cancer 14 (1): 71-75. September 1995

High allele loss rates at 17q12-q21 in breast and ovarian tumors from BRCA1-linked families.
Cornelis, R.S. and Neuhausen, S.L. and Johansson, O. and Arason, A. and Kelsell, D. and Ponder, B.A.J. and Tonin, P. and Hamann, U. and Lindblom, A. and Lalle, P. and Longy, M. and Olah, E. and Scherneck, S. and Bignon, Y.J. and Sobol, H. and Chang-Claude, J. and Larsson, C. and Spurr, N. and Borg, A. and Barkardottir, R.B. and Narod, S. and Devilee, P.
Genes Chromosomes & Cancer 13 (3): 203-210. 1 July 1995

dic(9;20): a new recurrent chromosome abnormality in adult acute lymphoblastic leukemia.
Rieder, H. and Schnittger, S. and Bodenstein, H. and Schwonzen, M. and Woermann, B. and Berkovic, D. and Ludwig, W.D. and Hoelzer, D. and Fonatsch, C.
Genes Chromosomes & Cancer 13 : 54-61. 1 January 1995


Breakpoints of Burkitt`s lymphoma t(8;22) translocations map within a distance of 300 kb downstream of MYC.
Zeidler, R. and Joos, S. and Delecluse, H.J. and Klobeck, G. and Vuillaume, M. and Lenoir, G.M. and Bornkamm, G.W. and Lipp, M.
Genes Chromosomes & Cancer 9 : 282-287. 1 January 1994


Specific metaphase and interphase detection of the breakpoint region in 8q24 of Burkitt lymphoma cells by triple-color fluorescence in situ hybridization.
Ried, T. and Lengauer, C. and Cremer, T. and Wiegant, J. and Raap, A.K. and van der Ploeg, M. and Groitl, P. and Lipp, M.
Genes Chromosomes & Cancer 4 (1): 69-74. 1 January 1992

Deletions in the short arm of chromosome 8 are present in up to 90% of human colorectal cancer cell lines.
van der Bosch, K. and Becker, I. and Savelyeva, L. and Bruederlein, S. and Schlag, P.M. and Schwab, M.
Genes Chromosomes & Cancer 5 : 91-95. 1 January 1992

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