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There are 6707 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

    Version of Record online : 4 MAR 2014, DOI: 10.1002/gcc.22161

  2. 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

    Version of Record online : 15 FEB 2002, DOI: 10.1002/gcc.10027

  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

    Version of Record online : 25 SEP 2001, DOI: 10.1002/gcc.1189

  4. 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

    Version of Record online : 24 SEP 2003, DOI: 10.1002/gcc.10291

  5. 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

    Version of Record online : 19 NOV 2009, DOI: 10.1002/gcc.20730

  6. ETV6/RUNX1 fusion at diagnosis and relapse: Some prognostic indications

    Genes, Chromosomes and Cancer

    Volume 43, Issue 1, May 2005, Pages: 54–71, Mary Martineau, G. Reza Jalali, Kerry E. Barber, Zoë J. Broadfield, Kan Luk Cheung, John Lilleyman, Anthony V. Moorman, Sue Richards, Hazel M. Robinson, Fiona Ross and Christine J. Harrison

    Version of Record online : 9 FEB 2005, DOI: 10.1002/gcc.20158

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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

    Version of Record online : 21 AUG 2003, DOI: 10.1046/j.1365-2141.2003.04502.x

  8. 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

    Version of Record online : 4 SEP 2003, DOI: 10.1002/gcc.10275

  9. 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

    Version of Record online : 8 FEB 2010, DOI: 10.1002/gcc.20754

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    The prognostic impact of karyotypic subgroups in myelodysplastic syndromes is strongly modified by sex

    British Journal of Haematology

    Volume 113, Issue 2, May 2001, Pages: 347–356, N. Mauritzson, B. Johansson, L. Rylander, M. Albin, U. Strömberg, R. Billström, T. Ahlgren, Z. Mikoczy, F. Mitelman, L. Hagmar and P. G. Nilsson

    Version of Record online : 12 JAN 2002, DOI: 10.1046/j.1365-2141.2001.02750.x

  11. 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

    Version of Record online : 8 NOV 2001, DOI: 10.1002/gcc.1212

  12. 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

    Version of Record online : 11 JAN 2005, DOI: 10.1002/gcc.20145

  13. Analysis of myelodysplastic syndromes with complex karyotypes by high-resolution comparative genomic hybridization and subtelomeric CGH array

    Genes, Chromosomes and Cancer

    Volume 42, Issue 3, March 2005, Pages: 287–298, Angel Martínez-Ramírez, Miguel Urioste, Lorenzo Melchor, David Blesa, Laura Valle, Sara Alvarez de Andrés, Klaas Kok, Maria José Calasanz, Juan Cruz Cigudosa and Javier Benítez

    Version of Record online : 20 DEC 2004, DOI: 10.1002/gcc.20154

  14. 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

    Version of Record online : 30 JAN 2003, DOI: 10.1002/gcc.10180

  15. Characterization of karyotypic events and evolution in neuroblastoma

    Pediatric Blood & Cancer

    Volume 44, Issue 2, February 2005, Pages: 147–157, David R. Betts, Ninette Cohen, Kurt E. Leibundgut, Thomas Kühne, Ueli Caflisch, Jeanette Greiner, Luba Traktenbrot and Felix K. Niggli

    Version of Record online : 24 AUG 2004, DOI: 10.1002/pbc.20179

  16. GAB2 is a novel target of 11q amplification in AML/MDS

    Genes, Chromosomes and Cancer

    Volume 45, Issue 9, September 2006, Pages: 798–807, Andrea Zatkova, Claudia Schoch, Frank Speleman, Bruce Poppe, Christine Mannhalter, Christa Fonatsch and Katharina Wimmer

    Version of Record online : 30 MAY 2006, DOI: 10.1002/gcc.20344

  17. 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

    Version of Record online : 9 NOV 2005, DOI: 10.1002/gcc.20285

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    Del (9q) AML: clinical and cytological characteristics and prognostic implications

    British Journal of Haematology

    Volume 129, Issue 2, April 2005, Pages: 210–220, Andrew Peniket, James Wainscoat, Lucy Side, Sarah Daly, Rajko Kusec, Georgina Buck, Keith Wheatley, Helen Walker, Steve Chatters, Christine Harrison, Jacqueline Boultwood, Anthony Goldstone and Alan Burnett

    Version of Record online : 6 APR 2005, DOI: 10.1111/j.1365-2141.2005.05445.x

  19. 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

    Version of Record online : 5 SEP 2002, DOI: 10.1002/gcc.10132

  20. Characterization of chromosome aberrations associated with soft-tissue leiomyosarcomas by twenty-four-color karyotyping and comparative genomic hybridization analysis

    Genes, Chromosomes and Cancer

    Volume 31, Issue 1, May 2001, Pages: 54–64, Rubin Wang, Yong-Jie Lu, Cyril Fisher, Julia A. Bridge and Janet Shipley

    Version of Record online : 7 MAR 2001, DOI: 10.1002/gcc.1118