Browse by Journal Title

Article

Reconstruction of rearranged T-cell receptor loci by whole genome and transcriptome sequencing gives insights into the initial steps of T-cell prolymphocytic leukemia.
Patil, P., Cieslak, A., Bernhart, S.H., Toprak, U.H., Wagener, R., López, C., Wiehle, L., Bens, S., Altmüller, J., Franitza, M., Scholz, I., Jayne, S., Ahearne, M.J., Scheffold, A., Jebaraj, B.M.C., Schneider, C., Costa, D., Braun, T., Schrader, A., Campo, E., Dyer, M.J.S., Nürnberg, P., Dürig, J., Johansson, P., Böttcher, S., Schlesner, M., Herling, M., Stilgenbauer, S., Macintyre, E. and Siebert, R.
Genes Chromosomes & Cancer 59 (4): 261-267. April 2020

High prevalence of immunoglobulin light chain gene aberrations as revealed by FISH in multiple myeloma and MGUS.
Tuerkmen, S., Binder, A., Gerlach, A., Niehage, S., Melissari, M.T., Inandiklioglu, N., 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., Pfister, S., Korshunov, K., Deubzer, H.E., Oehme, I., Ernst, A., Starzinski-Powitz, A., Seitz, A., Lichter, P., 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., Korsching, E., Weimer, J., Jacobsen, A., Arnold, N., Meindl, A., Arnold, W., Gustavus, D., Klebig, C., 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., Seitz, S., Korsching, E., Kristiansen, G., Gustavus, D., 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., Wassmuth, P., Plaschke, J., Schackert, H.K., Karsten, U., Santibanez-Koref, M.F., 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., Launonen, V., Niederacher, D., Gudlaugsdottir, S., Seitz, S., Rio, P., Champeme, M.H., Bieche, I., Birnbaum, D., White, G., Sztan, M., Sever, N., Plummer, S., Osorio, A., Broeks, A., Huusko, P., Spurr, N., Borg, A., Cleton-Jansen, A.M., Veer, L., Benitez, J., Casey, G., Peterlin, B., Olah, E., Varley, J., Bignon, Y.J., Scherneck, S., Sigurdardottir, V., Lidereau, R., Eyfjord, J., Beckmann, M.W., Winqvist, R., 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., Hermans, J., Eyfjoerd, J., Borresen, A.L., Liderau, R., Sobol, H., Borg, A., Cleton-Jansen, A.M., Olah, E., Cohen, B., Scherneck, S., Hamann, U., Peterlin, B., Caligo, M., Bignon, Y.L., Maugard, C., Andersen, T.I., Odegand, A.E.M., Bieche, I., Birnbaum, D., Cornelisse, C.J., Sztan, M., Steel, M.R., Seitz, S., Logar, N., Golouh, R., Ghimenti, C., 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., Andersen, T.I., Eyfjord, J.E., Cornelis, R.S., Thorlacius, S., Borg, A., Johansson, U., Theillet, C., Scherneck, S., Hartman, S., Cornelisse, C.J., 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., Neuhausen, S.L., Johansson, O., Arason, A., Kelsell, D., Ponder, B.A.J., Tonin, P., Hamann, U., Lindblom, A., Lalle, P., Longy, M., Olah, E., Scherneck, S., Bignon, Y.J., Sobol, H., Chang-Claude, J., Larsson, C., Spurr, N., Borg, A., Barkardottir, R.B., 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., Schnittger, S., Bodenstein, H., Schwonzen, M., Woermann, B., Berkovic, D., Ludwig, W.D., 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., Joos, S., Delecluse, H.J., Klobeck, G., Vuillaume, M., Lenoir, G.M., 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., Lengauer, C., Cremer, T., Wiegant, J., Raap, A.K., van der Ploeg, M., 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., Becker, I., Savelyeva, L., Bruederlein, S., Schlag, P.M. and Schwab, M.
Genes Chromosomes & Cancer 5 : 91-95. 1 January 1992