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Cancer Genetics and Cytogenetics
Volume 169, Issue 1, Pages 1-88 (August 2006)
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Editorial board
page CO2
Full-Text PDF (39 KB)

Original Articles


Establishment of a myeloid leukemia cell line, TRL-01, with MLL-ENL fusion gene
Manabu Ninomiya, Akihiro Abe, Toshiya Yokozawa, Kazutaka Ozeki, Kazuhito Yamamoto, Mamoru Ito, Masafumi Ito, Hitoshi Kiyoi, Nobuhiko Emi, Tomoki Naoe
pages 1-11
Abstract | Full Text | Full-Text PDF (598 KB) | Add-Ons


Brain-derived neurotrophic factor promotes growth and migration of multiple myeloma cells
Yu Hu, Chun-yan Sun, Hua-fang Wang, Tao Guo, Wen-ning Wei, Ya-dan Wang, Wen-juan He, Tao Wu, Hao Tan, Tang-chun Wu
pages 12-20
Abstract | Full Text | Full-Text PDF (1534 KB)


Fluorescence in situ hybridization patterns in newly diagnosed superficial bladder lesions and corresponding bladder washings
Daniela V. Frau, Paolo Usai, Tinuccia Dettori, Paola Caria, Antonello De Lisa, Roberta Vanni
pages 21-26
Abstract | Full Text | Full-Text PDF (227 KB)


Polymorphism of the DNA repair gene ERCC2 Lys751Gln and risk of lung cancer in a northeastern Chinese population
Jiaoyang Yin, Ulla Vogel, Yegang Ma, Li Guo, Huiwen Wang, Rong Qi
pages 27-32
Abstract | Full Text | Full-Text PDF (121 KB)


The I1307K APC polymorphism in Ashkenazi Jews with colorectal cancer: clinical and pathologic features
Gershon Y. Locker, Karen Kaul, David S. Weinberg, Zoran Gatalica, Gordon Gong, Amy Peterman, Jane Lynch, Lucy Klatzco, Olufunmilayo I. Olopade, Charles A. Bomzer, Anna Newlin, Eileen Keenan, Mohammed Tajuddin, Joseph Knezetic, Stephanie Coronel, Henry T. Lynch
pages 33-38
Abstract | Full Text | Full-Text PDF (118 KB)


Single nucleotide polymorphisms of the TGFB1 gene and lung cancer risk in a Korean population
Kyong Hwa Park, Sle Gi Lo Han, Young Mi Whang, Hyo Jung Lee, Young Do Yoo, Jae Won Lee, Sang Won Shin, Yeul Hong Kim
pages 39-44
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Numerical aberrations of chromosome 8 detected by conventional cytogenetics and fluorescence in situ hybridization in individuals from northern Brazil with gastric adenocarcinoma
Paulo Pimentel Assumpção, Geraldo Ishak, Elizabeth Suchi Chen, Sylvia Satomi Takeno, Mariana Ferreira Leal, Adriana Costa Guimarães, Danielle Queiroz Calcagno, André Salim Khayat, Samia Demachki, Marília de Arruda Cardoso Smith, Rommel Rodríguez Burbano
pages 45-49
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Near-triploidy and near-tetraploidy in childhood acute lymphoblastic leukemia: association with B-lineage blast cells carrying the ETV6–RUNX1 fusion, T-lineage immunophenotype, and favorable outcome
Susana C. Raimondi, Yinmei Zhou, Sheila A. Shurtleff, Jeffrey E. Rubnitz, Ching-Hon Pui, Frederick G. Behm
pages 50-57
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Short Communications


Down syndrome with low hypodiploidy in precursor B-cell acute lymphoblastic leukemia
Jennifer J.D. Morrissette, Gregory E. Halligan, Hope H. Punnett, Ann Shoemaker McKenzie, Felicula Guerrero, J.P. de Chadarévian
pages 58-61
Abstract | Full Text | Full-Text PDF (123 KB)


Twenty-three novel BRCA1 and BRCA2 sequence variations identified in a cohort of Swiss breast and ovarian cancer families
Philippe Maillet, Pierre Olivier Chappuis, Mary Khoshbeen-Boudal, Véronique Sciretta, André-Pascal Sappino, on behalf of the SIAK Network for Cancer Predisposition Testing and Counseling
pages 62-68
Abstract | Full Text | Full-Text PDF (109 KB)


Deletion (20q) as the sole abnormality in Waldenström macroglobulinemia suggests distinct pathogenesis of 20q11 anomaly
Yi-Chang Liu, Keisuke Miyazawa, Goro Sashida, Atsushi Kodama, Kazuma Ohyashiki
pages 69-72
Abstract | Full Text | Full-Text PDF (178 KB)


Trisomy 1q in a patient with severe aplastic anemia
Prodromos Angelidis, Kiarash Kojouri, Jiyun Lee, William Kern, John J. Mulvihill, Shibo Li
pages 73-75
Abstract | Full Text | Full-Text PDF (141 KB)

Letters to the Editor


Childhood CML in India: b2a2 transcript is more common than b3a2
Syed Khizer Hasan, Sudha Sazawal, Bijender Kumar, Rekha Chaubey, Pravas Mishra, Rashid Mir, Ved Prakash Chaudhry, Renu Saxena
pages 76-77
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Cytogenetic findings of a primary Merkel cell carcinoma
Esther Manor, Eric Bellaiche, Lipa Bodner
pages 78-80
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PML/RARA rearrangement associated with a t(15;19;17) in a case of acute myeloid leukemia with abundant myelocytes with salmon-pink cytoplasm
In-Suk Kim, Hee-Jin Kim, Hee-Suk Choung, Chul-Won Jung, Jong-Won Kim, Sun-Hee Kim
pages 81-82
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Secondary acute myeloid leukemia with a t(1;11)(q23;p15) in an adolescent treated for testicular sarcoma
Eliane Maria Azevedo Soares, Neide Santos, Bethânia de Araújo Silva Amaral, Maria Luiza Macedo Silva, Ednalva Pereira Leite, Mariluze Oliveira Silva, Maria Tereza Cartaxo Muniz, Raul C. Ribeiro, Vera Lúcia Lins de Morais, Terezinha de Jesus Marques Salles
pages 83-85
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Trisomy 22 as sole cytogenetic abnormality in acute monoblastic leukemia (M5b)
Alessandro Gozzetti, Simona Calabrese, Rosaria Crupi, Daniela Tozzuoli, Monica Bocchia, Alberto Fabbri, Maria Teresa Pirrotta, Simona Sammassimo, Marzia Defina, Francesco Lauria
page 86
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Erratum free full text
page 87
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Frontmatter


Table of contents
pages A1-A2
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