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Cancer Genetics and Cytogenetics
Volume 162, Issue 1, Pages 1-94 (01 October 2005)
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Editorial board
page CO2
Full-Text PDF (48 KB)

Original articles


Chromosome abnormalities in 10 lung cancer cell lines of the NCI-H series analyzed with spectral karyotyping
Mira Grigorova, Rachel C. Lyman, Carlos Caldas, Paul A.W. Edwards
pages 1-9
Abstract | Full Text | Full-Text PDF (488 KB)


Polymorphisms of the GSTM1, GSTP1, MPO, XRCC1, and NQO1 genes in Chinese patients with non-small cell lung cancers: relationship with aberrant promoter methylation of the CDKN2A and RARB genes
Eunice C. Chan, Shui Y. Lam, Kin H. Fu, Yok L. Kwong
pages 10-20
Abstract | Full Text | Full-Text PDF (374 KB)


Genetic abnormalities associated with the t(12;21) and their impact in the outcome of 56 patients with B-precursor acute lymphoblastic leukemia
Y. Alvarez, M.D. Coll, J.J. Ortega, P. Bastida, N. Dastugue, A. Robert, J. Cervera, A. Verdeguer, M. Tasso, A. Aventín, M. Guitart, M.R. Caballín
pages 21-29
Abstract | Full Text | Full-Text PDF (420 KB)


9q34 Rearrangements in BCR/ABL fusion-negative acute lymphoblastic leukemia
Bhavana J. Dave, Michele Wiggins, Christine M. Higgins, Diane L. Pickering, Deborah Perry, Patricia Aoun, Minnie Abromowich, Marcel DeVetten, Warren G. Sanger
pages 30-37
Abstract | Full Text | Full-Text PDF (304 KB)


Chromosomal imbalances in a recurrent solitary fibrous tumor of the orbit
Gro Oddveig Ness, Helle Lybæk, Jarle Arnes, Eyvind Rødahl
pages 38-44
Abstract | Full Text | Full-Text PDF (713 KB)


Leukemic recombinations involving heterochromatin in myeloproliferative disorders with t(1;9)
Constantina Sambani, Roberta La Starza, Valentina Pierini, Peter Vandenberghe, Juan J. Gonzales-Aguilera, Helen Rigana, Daphne Koumbi, Kalliopi N. Manola, Chryssa Stavropoulou, Vasileios N. Georgakakos, Maria Pagoni, Iwona Wlodarska, Cristina Mecucci
pages 45-49
Abstract | Full Text | Full-Text PDF (375 KB)


Epithelioid sarcoma with SYT-SSX1 fusion gene expression: molecular and cytogenetic analysis
Carmen de Torres, Teresa M. Cardesa, Sandra Rodríguez-Perales, Juan C. Cigudosa, Jaume Mora
pages 50-56
Abstract | Full Text | Full-Text PDF (574 KB)


Quantitative molecular monitoring of BCR-ABL and MDR1 transcripts in patients with chronic myeloid leukemia during Imatinib treatment
Sara Galimberti, Giulia Cervetti, Francesca Guerrini, Rossana Testi, Simone Pacini, Rita Fazzi, Paolo Simi, Mario Petrini
pages 57-62
Abstract | Full Text | Full-Text PDF (293 KB)


GADD45A and EPB41 as tumor suppressor genes in meningioma pathogenesis
S. Piaskowski, P. Rieske, M. Szybka, K. Wozniak, A. Bednarek, E. Płuciennik, D. Jaskolski, B. Sikorska, Pawel Piotr Liberski
pages 63-67
Abstract | Full Text | Full-Text PDF (244 KB)


Who takes the lead in the development of ulcerative colitis–associated colorectal cancers: mutator, suppressor, or methylator pathway?
Lara Maia, Joana Dinis, Marília Cravo, Isabel Claro, Célia Baltazar, Isabel Fonseca, Tavarela Veloso, Ana F. Capelinha, Fátima Carneiro, Carlos Nobre-Leitão
pages 68-73
Abstract | Full Text | Full-Text PDF (198 KB)


Cytogenetic findings in clear cell chondrosarcoma
Jun Nishio, John D. Reith, Akira Ogose, Gary Maale, James R. Neff, Julia A. Bridge
pages 74-77
Abstract | Full Text | Full-Text PDF (390 KB)


Random aneuploidy in neoplastic and pre-neoplastic diseases, multiple myeloma, and monoclonal gammopathy
A. Amiel, N. Gronich, M. Yukla, S. Suliman, G. Josef, E. Gaber, G. Drori, M.D. Fejgin, M. Lishner
pages 78-81
Abstract | Full Text | Full-Text PDF (147 KB)

Short communications


HOXA gene cluster rearrangement in a t(7;9)(p15;q34) in a child with MDS
Bruce Poppe, Nurten Yigit, Barbara De Moerloose, Anne De Paepe, Yves Benoit, Frank Speleman
pages 82-84
Abstract | Full Text | Full-Text PDF (183 KB)


Deletion 6q is not a characteristic marker of nodal lymphoplasmacytic lymphoma
James R. Cook, Nadine Ives Aguilera, Shalini Reshmi, Xin Huang, Zhisheng Yu, Susanne M. Gollin, Susan L. Abbondanzo, Steven H. Swerdlow
pages 85-88
Abstract | Full Text | Full-Text PDF (265 KB)

Letters to the editor


Isochromosome of a deleted 20q may be a relatively common abnormality in myeloid malignancies
Azra H. Ligon, Daniel J. DeAngelo, Leonard Atkins, Paola Dal Cin
pages 89-91
Full Text | Full-Text PDF (197 KB)


A novel interstitial deletion on the long arm of chromosome 16 in a patient with chronic myelomonocytic leukemia
Lukasz K. Kozon, Deborah L. Wesley, John Van Brunt, Marilyn M. Li
pages 92-94
Full Text | Full-Text PDF (219 KB)

Frontmatter


Table of contents
pages A1-A2
Full-Text PDF (36 KB)

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