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There are 3518 results for: content related to: Microarray-based genomic profiling as a diagnostic tool in acute lymphoblastic leukemia

  1. Comprehensive cytogenetic and molecular cytogenetic analysis of 44 Burkitt lymphoma cell lines: Secondary chromosomal changes characterization, karyotypic evolution, and comparison with primary samples

    Genes, Chromosomes and Cancer

    Volume 53, Issue 6, June 2014, Pages: 497–515, Eva Maria Murga Penas, Georgia Schilling, Petra Behrmann, Marianne Klokow, Eik Vettorazzi, Carsten Bokemeyer and Judith Dierlamm

    Article first published online : 4 MAR 2014, DOI: 10.1002/gcc.22161

  2. Definitive molecular cytogenetic characterization of 15 colorectal cancer cell lines

    Genes, Chromosomes and Cancer

    Volume 49, Issue 3, March 2010, Pages: 204–223, Turid Knutsen, Hesed M. Padilla-Nash, Danny Wangsa, Linda Barenboim-Stapleton, Jordi Camps, Nicole McNeil, Michael J. Difilippantonio and Thomas Ried

    Article first published online : 19 NOV 2009, DOI: 10.1002/gcc.20730

  3. Novel evidence of a role for chromosome 1 pericentric heterochromatin in the pathogenesis of B-cell lymphoma and multiple myeloma

    Genes, Chromosomes and Cancer

    Volume 32, Issue 3, November 2001, Pages: 250–264, Patricia Le Baccon, Dominique Leroux, Christina Dascalescu, Samuel Duley, Danielle Marais, Eliane Esmenjaud, Jean Jacques Sotto and Mary Callanan

    Article first published online : 25 SEP 2001, DOI: 10.1002/gcc.1189

  4. High frequency of BTG1 deletions in acute lymphoblastic leukemia in children with down syndrome

    Genes, Chromosomes and Cancer

    Volume 51, Issue 2, February 2012, Pages: 196–206, Catarina Lundin, Lars Hjorth, Mikael Behrendtz, Ann Nordgren, Lars Palmqvist, Mette Klarskov Andersen, Andrea Biloglav, Erik Forestier, Kajsa Paulsson and Bertil Johansson

    Article first published online : 10 NOV 2011, DOI: 10.1002/gcc.20944

  5. You have free access to this content
    Follicular lymphoma lacking the t(14;18)(q32;q21): identification of two disease subtypes

    British Journal of Haematology

    Volume 120, Issue 3, February 2003, Pages: 424–433, Douglas E. Horsman, Ichiro Okamoto, Olga Ludkovski, Nhu Le, Lana Harder, Stefan Gesk, Reiner Siebert, Mukesh Chhanabhai, Laurie Sehn, Joseph M. Connors and Randy D. Gascoyne

    Article first published online : 6 FEB 2003, DOI: 10.1046/j.1365-2141.2003.04086.x

  6. Spectral karyotyping in patients with acute myeloid leukemia and a complex karyotype shows hidden aberrations, including recurrent overrepresentation of 21q, 11q, and 22q

    Genes, Chromosomes and Cancer

    Volume 34, Issue 2, June 2002, Pages: 137–153, Krzysztof Mrózek, Kristiina Heinonen, Karl S. Theil and Clara D. Bloomfield

    Article first published online : 15 FEB 2002, DOI: 10.1002/gcc.10027

  7. Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 8, August 2009, Pages: 1661–1677, Margaret J. Wat, Oleg A. Shchelochkov, Ashley M. Holder, Amy M. Breman, Aditi Dagli, Carlos Bacino, Fernando Scaglia, Roberto T. Zori, Sau Wai Cheung, Daryl A. Scott and Sung-Hae Lee Kang

    Article first published online : 15 JUL 2009, DOI: 10.1002/ajmg.a.32896

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    Multicolour fluorescence in situ hybridization analysis of t(14;18)-positive follicular lymphoma and correlation with gene expression data and clinical outcome

    British Journal of Haematology

    Volume 122, Issue 5, September 2003, Pages: 745–759, Valia S. Lestou, Randy D. Gascoyne, Laurie Sehn, Olga Ludkovski, Mukesh Chhanabhai, Richard J. Klasa, Hervé Husson, Arnold S. Freedman, Joseph M. Connors and Douglas E. Horsman

    Article first published online : 21 AUG 2003, DOI: 10.1046/j.1365-2141.2003.04502.x

  9. Spectral karyotyping identifies recurrent complex rearrangements of chromosomes 8, 17, and 20 in osteosarcomas

    Genes, Chromosomes and Cancer

    Volume 36, Issue 1, January 2003, Pages: 7–16, Jane Bayani, Maria Zielenska, Ajay Pandita, Khaldoun Al-Romaih, Jana Karaskova, Karen Harrison, Julia A. Bridge, Poul Sorensen, Paul Thorner and Jeremy A. Squire

    Article first published online : 5 SEP 2002, DOI: 10.1002/gcc.10132

  10. Centromeric breakage and highly rearranged chromosome derivatives associated with mutations of TP53 are common in therapy-related MDS and AML after therapy with alkylating agents: An M-FISH study

    Genes, Chromosomes and Cancer

    Volume 42, Issue 4, April 2005, Pages: 358–371, Mette K. Andersen, Debes H. Christiansen and Jens Pedersen-Bjergaard

    Article first published online : 11 JAN 2005, DOI: 10.1002/gcc.20145

  11. Intrachromosomal amplification of chromosome 21 (iAMP21) may arise from a breakage–fusion–bridge cycle

    Genes, Chromosomes and Cancer

    Volume 46, Issue 4, April 2007, Pages: 318–326, Hazel M. Robinson, Christine J. Harrison, Anthony V. Moorman, Ilse Chudoba and Jonathan C. Strefford

    Article first published online : 22 JAN 2007, DOI: 10.1002/gcc.20412

  12. Frequent amplification and rearrangement of chromosomal bands 6p12-p21 and 17p11.2 in osteosarcoma

    Genes, Chromosomes and Cancer

    Volume 39, Issue 1, January 2004, Pages: 11–21, Ching C. Lau, Charles P. Harris, Xin-Yan Lu, Laszlo Perlaky, Sheila Gogineni, Murali Chintagumpala, John Hicks, Mark E. Johnson, Nelson A. Davino, Andrew G. Huvos, Paul A. Meyers, John H. Healy, Richard Gorlick and Pulivarthi H. Rao

    Article first published online : 24 SEP 2003, DOI: 10.1002/gcc.10291

  13. De novo erythroleukemia chromosome features include multiple rearrangements, with special involvement of chromosomes 11 and 19

    Genes, Chromosomes and Cancer

    Volume 36, Issue 4, April 2003, Pages: 406–412, Juan C. Cigudosa, Maria D. Odero, M. José Calasanz, Francesc Solé, Marta Salido, Eva Arranz, Angel Martínez-Ramirez, Miguel Urioste, Sara Alvarez, Jose V. Cervera, Donald MacGrogan, Miguel A. Sanz, Stephen D. Nimer and Javier Benitez

    Article first published online : 30 JAN 2003, DOI: 10.1002/gcc.10180

  14. Population-based study of cancer among carriers of a constitutional structural chromosomal rearrangement

    Genes, Chromosomes and Cancer

    Volume 45, Issue 3, March 2006, Pages: 231–246, Iben Bache, Henrik Hasle, Niels Tommerup and Jørgen H. Olsen

    Article first published online : 9 NOV 2005, DOI: 10.1002/gcc.20285

  15. Further cytogenetic characterization of multiple myeloma confirms that 14q32 translocations are a very rare event in hyperdiploid cases

    Genes, Chromosomes and Cancer

    Volume 38, Issue 3, November 2003, Pages: 234–239, Nicole Véronique Smadja, Dominique Leroux, Jean Soulier, Sylvie Dumont, Catherine Arnould, Sylvie Taviaux, Jean Louis Taillemite and Christian Bastard

    Article first published online : 4 SEP 2003, DOI: 10.1002/gcc.10275

  16. Incidence and prognostic impact of secondary cytogenetic aberrations in a series of 145 patients with mantle cell lymphoma

    Genes, Chromosomes and Cancer

    Volume 49, Issue 5, May 2010, Pages: 439–451, Blanca Espinet, Itziar Salaverria, Sílvia Beà, Neus Ruiz-Xivillé, Olga Balagué, Marta Salido, Dolors Costa, Joaquim Carreras, Ana Eugenia Rodríguez-Vicente, Juan Luís García, Jesús María Hernández-Rivas, María José Calasanz, Reiner Siebert, Ana Ferrer, Antonio Salar, Ana Carrió, Natividad Polo, José Antonio García-Marco, Alicia Domingo, Eva González-Barca, Vicenç Romagosa, Isabel Marugán, Armando López-Guillermo, Fuensanta Millá, José Luís Mate, Elisa Luño, Carmen Sanzo, Rosa Collado, Isabel Oliver, Sebastià Monzó, Antonio Palacín, Teresa González, Francesc Sant, Ramon Salinas, María Teresa Ardanaz, Llorenç Font, Lourdes Escoda, Lourdes Florensa, Sergi Serrano, Elias Campo and Francesc Solé

    Article first published online : 8 FEB 2010, DOI: 10.1002/gcc.20754

  17. Submicroscopic genomic imbalances in burkitt lymphomas/leukemias: Association with age and further evidence that 8q24/MYC translocations are not sufficient for leukemogenesis

    Genes, Chromosomes and Cancer

    Volume 52, Issue 4, April 2013, Pages: 370–377, Catarina Lundin, Lars Hjorth, Mikael Behrendtz, Mats Ehinger, Andrea Biloglav and Bertil Johansson

    Article first published online : 8 DEC 2012, DOI: 10.1002/gcc.22034

  18. Identification of cytogenetic subclasses and recurring chromosomal aberrations in AML and MDS with complex karyotypes using m-FISH

    Genes, Chromosomes and Cancer

    Volume 33, Issue 1, January 2002, Pages: 60–72, Heidi Van Limbergen, Bruce Poppe, Lucienne Michaux, Christian Herens, Jill Brown, Luc Noens, Zwi Berneman, Robrecht De Bock, Anne De Paepe and Frank Speleman

    Article first published online : 8 NOV 2001, DOI: 10.1002/gcc.1212

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    Characterization of chromosomal abnormalities in uroepithelial carcinomas by G-banding, spectral karyotyping and FISH analysis

    International Journal of Cancer

    Volume 92, Issue 6, 15 June 2001, Pages: 824–831, Imad Fadl-elmula, Soili Kytölä, Yi Pan, Weng-Onn Lui, Gaetano Derienzo, Lars Forsberg, Nils Mandahl, Ludmila Gorunova, Ulf S.R. Bergerheim, Sverre Heim and Catharina Larsson

    Article first published online : 3 APR 2001, DOI: 10.1002/ijc.1267

  20. Molecular cytogenetic analysis of genomic instability at the 1q12–22 chromosomal site in B-cell non-Hodgkin lymphoma

    Genes, Chromosomes and Cancer

    Volume 35, Issue 4, December 2002, Pages: 318–328, Takahiro Itoyama, Gouri Nanjungud, Weiyi Chen, Vadim G. Dyomin, Julie Teruya-Feldstein, Suresh C. Jhanwar, Andrew D. Zelenetz and R.S.K. Chaganti

    Article first published online : 23 JUL 2002, DOI: 10.1002/gcc.10120