De novo erythroleukemia chromosome features include multiple rearrangements, with special involvement of chromosomes 11 and 19 (English)
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- New search for: Odero, Maria D.
- New search for: Calasanz, M. José
- New search for: Solé, Francesc
- New search for: Salido, Marta
- New search for: Arranz, Eva
- New search for: Martínez‐Ramirez, Angel
- New search for: Urioste, Miguel
- New search for: Alvarez, Sara
- New search for: Cervera, Jose V.
- New search for: MacGrogan, Donald
- New search for: Sanz, Miguel A.
- New search for: Nimer, Stephen D.
- New search for: Benitez, Javier
- New search for: Cigudosa, Juan C.
- New search for: Odero, Maria D.
- New search for: Calasanz, M. José
- New search for: Solé, Francesc
- New search for: Salido, Marta
- New search for: Arranz, Eva
- New search for: Martínez‐Ramirez, Angel
- New search for: Urioste, Miguel
- New search for: Alvarez, Sara
- New search for: Cervera, Jose V.
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In:
Genes, Chromosomes and Cancer
;
36
, 4
;
406-412
;
2003
- Article (Journal) / Electronic Resource
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Title:De novo erythroleukemia chromosome features include multiple rearrangements, with special involvement of chromosomes 11 and 19
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Contributors:Cigudosa, Juan C. ( author ) / Odero, Maria D. ( author ) / Calasanz, M. José ( author ) / Solé, Francesc ( author ) / Salido, Marta ( author ) / Arranz, Eva ( author ) / Martínez‐Ramirez, Angel ( author ) / Urioste, Miguel ( author ) / Alvarez, Sara ( author ) / Cervera, Jose V. ( author )
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Published in:Genes, Chromosomes and Cancer ; 36, 4 ; 406-412
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Publisher:
- New search for: Wiley Subscription Services, Inc., A Wiley Company
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Publication date:2003-04-01
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Size:7 pages
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ISSN:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
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Source:
Table of contents – Volume 36, Issue 4
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 317
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Deletion of Brca2 exon 27 causes hypersensitivity to DNA crosslinks, chromosomal instability, and reduced life span in miceDonoho, Greg / Brenneman, Mark A. / Cui, Tracy X. / Donoviel, Dorit / Vogel, Hannes / Goodwin, Edwin H. / Chen, David J. / Hasty, Paul et al. | 2003
- 318
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Letter to the editorLima, Jorge / Máximo, Valdemar / Soares, Paula / Sobrinho‐Simões, Manuel et al. | 2003
- 319
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RxFISH karyotype and MYC amplification in the HT‐29 colon adenocarcinoma cell lineCorzo, Cristina / Petzold, Miriam / Mayol, Xavier / Espinet, Blanca / Salido, Marta / Serrano, Sergi / Real, Francisco X. / Solé, Francesc et al. | 2003
- 332
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Prostate cancer aggressiveness locus on chromosome segment 19q12–q13.1 identified by linkage and allelic imbalance studiesNeville, Phillippa J. / Conti, David V. / Krumroy, Lisa M. / Catalona, William J. / Suarez, Brian K. / Witte, John S. / Casey, Graham et al. | 2003
- 340
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Pancreatic carcinoma cell lines with SMAD4 inactivation show distinct expression responses to TGFB1Jonson, Tord / Heidenblad, Markus / Håkansson, Petra / Gorunova, Ludmila / Johansson, Bertil / Fioretos, Thoas / Höglund, Mattias et al. | 2003
- 353
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Genomic deletions on other chromosomes involved in variant t(9;22) chronic myeloid leukemia casesAlbano, Francesco / Specchia, Giorgina / Anelli, Luisa / Zagaria, Antonella / Storlazzi, Clelia Tiziana / Buquicchio, Caterina / Roberti, Maria Grazia / Liso, Vincenzo / Rocchi, Mariano et al. | 2003
- 361
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DNA microarrays for comparative genomic hybridization based on DOP‐PCR amplification of BAC and PAC clonesFiegler, Heike / Carr, Philippa / Douglas, Eleanor J. / Burford, Deborah C. / Hunt, Sarah / Smith, James / Vetrie, David / Gorman, Patricia / Tomlinson, Ian P.M. / Carter, Nigel P. et al. | 2003
- 375
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Characterization of the recurrent translocation t(1;1)(p36.3;q21.1–2) in non‐Hodgkin lymphoma by multicolor banding and fluorescence in situ hybridization analysisLestou, Valia S. / Ludkovski, Olga / Connors, Joseph M. / Gascoyne, Randy D. / Lam, Wan L. / Horsman, Douglas E. et al. | 2003
- 382
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Detailed gene copy number and RNA expression analysis of the 17q12–23 region in primary breast cancersWillis, Simon / Hutchins, Anne‐Marie / Hammet, Fleur / Ciciulla, John / Soo, Wee‐Kheng / White, David / van der Spek, Peter / Henderson, Michael A. / Gish, Kurt / Venter, Deon J. et al. | 2003
- 393
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Analysis of t(9;11) chromosomal breakpoint sequences in childhood acute leukemia: Almost identical MLL breakpoints in therapy‐related AML after treatment without etoposidesLanger, Thorsten / Metzler, Markus / Reinhardt, Dirk / Viehmann, Susanne / Borkhardt, Arndt / Reichel, Martin / Stanulla, Martin / Schrappe, Martin / Creutzig, Ursula / Ritter, Jörg et al. | 2003
- 402
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t(10;16)(q22;p13) and MORF‐CREBBP fusion is a recurrent event in acute myeloid leukemiaVizmanos, José L. / Larráyoz, María J. / Lahortiga, Idoya / Floristán, Filomena / Álvarez, Carmen / Odero, María D. / Novo, Francisco J. / Calasanz, María J. et al. | 2003
- 406
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De novo erythroleukemia chromosome features include multiple rearrangements, with special involvement of chromosomes 11 and 19Cigudosa, Juan C. / Odero, Maria D. / Calasanz, M. José / Solé, Francesc / Salido, Marta / Arranz, Eva / Martínez‐Ramirez, Angel / Urioste, Miguel / Alvarez, Sara / Cervera, Jose V. et al. | 2003
- 413
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Rearrangement of the MOZ gene in pediatric therapy‐related myelodysplastic syndrome with a novel chromosomal translocation t(2;8)(p23;p11)Imamura, Toshihiko / Kakazu, Naoki / Hibi, Shigeyoshi / Morimoto, Akira / Fukushima, Yoko / Ijuin, Ikuko / Hada, Satoshi / Kitabayashi, Issei / Abe, Tatsuo / Imashuku, Shinsaku et al. | 2003
- 420
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Human homeobox gene HOXC13 is the partner of NUP98 in adult acute myeloid leukemia with t(11;12)(p15;q13)La Starza, Roberta / Trubia, Maurizio / Crescenzi, Barbara / Matteucci, Caterina / Negrini, Massimo / Martelli, Massimo F. / Pelicci, Pier Giuseppe / Mecucci, Cristina et al. | 2003