Cancer Genetics and Cytogenetics

1

Identification of polymorphisms in the XIAP gene and analysis of association with lung cancer risk in a Korean population

Hyo-Gyoung Kang, Su Jeong Lee, Myung Hwa Chae, Won Kee Lee, Sung Ick Cha, Chang Ho Kim, Sin Kam, Rang-Woon Park, In-San Kim, Dong Sun Kim, Young Chul Kim, Tae Hoon Jung, Jae Yong Park

Journal:

Year:

2008

Language:

english

File:

PDF, 177 KB

english, 2008

2

Concomitant chronic myeloid leukemia and chronic lymphocytic leukemia: a different clonal origin shown by molecular cytogenetics

Alessandro Gozzetti, Monica Bocchia, Rosaria Crupi, Simona Calabrese, M.T. Pirrotta, Donatella Raspadori, Marzia Defina, Renato Algeri, Francesco Lauria

Journal:

Cancer Genetics and Cytogenetics

Year:

2008

Language:

english

File:

PDF, 122 KB

english, 2008

3

TP53 codon 72 polymorphism in susceptibility, overall survival, and adjuvant therapy response of gliomas

Vítor Lima-Ramos, Luís Pacheco-Figueiredo, Sandra Costa, Fernando Pardal, Ana Silva, Júlia Amorim, José Manuel Lopes, Rui Manuel Reis

Journal:

Cancer Genetics and Cytogenetics

Year:

2008

Language:

english

File:

PDF, 232 KB

english, 2008

4

FAS −1377 G/A polymorphism and the risk of lymph node metastasis in cervical cancer

Sokbom Kang, Seung Myung Dong, Sang Soo Seo, Jae Weon Kim, Sang Yoon Park

Journal:

Cancer Genetics and Cytogenetics

Year:

2008

Language:

english

File:

PDF, 128 KB

english, 2008

5

Disruption of the ETV6 gene as a consequence of a rare translocation (12;12)(p13;q13) in treatment-induced acute myeloid leukemia after breast cancer

Kalliopi N. Manola, Vasileios N. Georgakakos, Dimitris Margaritis, Chryssa Stavropoulou, Christos Panos, Ioannis Kotsianidis, Gabriel E. Pantelias, Constantina Sambani

Journal:

Cancer Genetics and Cytogenetics

Year:

2008

Language:

english

File:

PDF, 364 KB

english, 2008

6

NUP98–NSD1 fusion by insertion in acute myeloblastic leukemia

Arnaud Petit, Isabelle Radford, Marie-Christine Waill, Serge Romana, Roland Berger

Journal:

Cancer Genetics and Cytogenetics

Year:

2008

Language:

english

File:

PDF, 361 KB

english, 2008

7

Methylation of PTCH1, the Patched-1 gene, in a panel of primary medulloblastomas

Joel I. Pritchard, James M. Olson

Journal:

Cancer Genetics and Cytogenetics

Year:

2008

Language:

english

File:

PDF, 188 KB

english, 2008

8

Random aneuploidy in chronic hepatitis C patients

Lilach Goldberg-Bittman, Yona Kitay-Cohen, Ruth Hadari, Monayukla Yukla, Moshe D. Fejgin, Aliza Amiel

Journal:

Cancer Genetics and Cytogenetics

Year:

2008

Language:

english

File:

PDF, 111 KB

english, 2008

9

Polycythemia vera transforming to acute myeloid leukemia and complex abnormalities including 9p homogeneously staining region with amplification of MLLT3, JMJD2C, JAK2, and SMARCA2

Catherine Hélias, Stephanie Struski, Carine Gervais, Vincent Leymarie, Laurent Mauvieux, Raoul Herbrecht, Michel Lessard

Journal:

Cancer Genetics and Cytogenetics

Year:

2008

Language:

english

File:

PDF, 325 KB

english, 2008

10

Determination of ancestral allele for possible human cancer-associated polymorphisms

Yuichi Maruta, Naoko Okayama, Mikako Hiura, Yutaka Suehiro, Hirohisa Hirai, Yuji Hinoda

Journal:

Cancer Genetics and Cytogenetics

Year:

2008

Language:

english

File:

PDF, 154 KB

english, 2008

11

Characterization of complex chromosome aberrations in a recurrent meningioma combining standard cytogenetic and array comparative genomic hybridization techniques

Kwang-Sook Woo, Kyung-Soo Sung, Ki-Uk Kim, Lisa G. Shaffer, Jin-Yeong Han

Journal:

Cancer Genetics and Cytogenetics

Year:

2008

Language:

english

File:

PDF, 233 KB

english, 2008

12

CREB3L4, INTS3, and SNAPAP are targets for the 1q21 amplicon frequently detected in hepatocellular carcinoma

Yoshikazu Inagaki, Kohichiroh Yasui, Mio Endo, Tomoaki Nakajima, Keika Zen, Kazuhiro Tsuji, Masahito Minami, Shinji Tanaka, Masafumi Taniwaki, Yoshito Itoh, Shigeki Arii, Takeshi Okanoue

Journal:

Cancer Genetics and Cytogenetics

Year:

2008

Language:

english

File:

PDF, 354 KB

english, 2008

13

Amplification of BCR–ABL and t(3;21) in a patient with blast crisis of chronic myelogenous leukemia

Chin-Lee Phan, Puteri J.N.B. Megat Baharuddin, Lai-Peng Chin, Zubaidah Zakaria, Subramanian Yegappan, Jameela Sathar, Sen-Mui Tan, Visalachy Purushothaman, Kian-Meng Chang

Journal:

Cancer Genetics and Cytogenetics

Year:

2008

Language:

english

File:

PDF, 183 KB

english, 2008

14

A rare tumor and an ethical dilemma in a family with a germline TP53 mutation

Kamila Prochazkova, Lenka Foretova, Zdenek Sedlacek

Journal:

Cancer Genetics and Cytogenetics

Year:

2008

Language:

english

File:

PDF, 201 KB

english, 2008

15

Translocation (8;21)(q22;q22) without rearrangement of RUNX1 and RUNX1T1 genes in a patient with refractory anemia with excess of blasts

Alberto Aguilar, Maria Talavera, Concepción Villalon, Jose M. Garcia-Sagredo, America de Leon, Teresa Sordo, Pablo Cabello, Fernando A. Gonzalez, Eva Garcia-Galloway, Carlos San Roman, Teresa Ferro

Journal:

Cancer Genetics and Cytogenetics

Year:

2008

Language:

english

File:

PDF, 248 KB

english, 2008

16

Fusion of the COL1A1 and USP6 genes in a benign bone tumor

Ioannis Panagopoulos, Fredrik Mertens, Richard Löfvenberg, Nils Mandahl

Journal:

Cancer Genetics and Cytogenetics

Year:

2008

Language:

english

File:

PDF, 279 KB

english, 2008

17

Mutations of GATA1, FLT3, MLL-partial tandem duplication, NRAS, and RUNX1 genes are not found in a 7-year-old Down syndrome patient with acute myeloid leukemia (FAB-M2) having a good prognosis

Machiko Kawamura, Hidefumi Kaku, Takeshi Taketani, Tomohiko Taki, Akira Shimada, Yasuhide Hayashi

Journal:

Cancer Genetics and Cytogenetics

Year:

2008

Language:

english

File:

PDF, 308 KB

english, 2008

18

Loss of the extra chromosome 21 in a patient with Down syndrome and myelodysplasia

Daryl Tan, Lai Ching Lau, Li Min Teng, Swati Sane, Tse Hui Lim, Sim Leng Tien

Journal:

Cancer Genetics and Cytogenetics

Year:

2008

Language:

english

File:

PDF, 257 KB

english, 2008

19

How early to test for a cancer-causing germline mutation

Henry T. Lynch, Jane F. Lynch

Journal:

Cancer Genetics and Cytogenetics

Year:

2008

Language:

english

File:

PDF, 71 KB

english, 2008

20

Editorial board

Journal:

Cancer Genetics and Cytogenetics

Year:

2008

Language:

english

File:

PDF, 47 KB

english, 2008

21

Volume 180; Issue 1

Identification of polymorphisms in the XIAP gene and analysis of association with lung cancer risk in a Korean population

Concomitant chronic myeloid leukemia and chronic lymphocytic leukemia: a different clonal origin shown by molecular cytogenetics

TP53 codon 72 polymorphism in susceptibility, overall survival, and adjuvant therapy response of gliomas

FAS −1377 G/A polymorphism and the risk of lymph node metastasis in cervical cancer

Disruption of the ETV6 gene as a consequence of a rare translocation (12;12)(p13;q13) in treatment-induced acute myeloid leukemia after breast cancer

NUP98–NSD1 fusion by insertion in acute myeloblastic leukemia

Methylation of PTCH1, the Patched-1 gene, in a panel of primary medulloblastomas

Random aneuploidy in chronic hepatitis C patients

Polycythemia vera transforming to acute myeloid leukemia and complex abnormalities including 9p homogeneously staining region with amplification of MLLT3, JMJD2C, JAK2, and SMARCA2

Determination of ancestral allele for possible human cancer-associated polymorphisms

Characterization of complex chromosome aberrations in a recurrent meningioma combining standard cytogenetic and array comparative genomic hybridization techniques

CREB3L4, INTS3, and SNAPAP are targets for the 1q21 amplicon frequently detected in hepatocellular carcinoma

Amplification of BCR–ABL and t(3;21) in a patient with blast crisis of chronic myelogenous leukemia

A rare tumor and an ethical dilemma in a family with a germline TP53 mutation

Translocation (8;21)(q22;q22) without rearrangement of RUNX1 and RUNX1T1 genes in a patient with refractory anemia with excess of blasts

Fusion of the COL1A1 and USP6 genes in a benign bone tumor

Mutations of GATA1, FLT3, MLL-partial tandem duplication, NRAS, and RUNX1 genes are not found in a 7-year-old Down syndrome patient with acute myeloid leukemia (FAB-M2) having a good prognosis

Loss of the extra chromosome 21 in a patient with Down syndrome and myelodysplasia

How early to test for a cancer-causing germline mutation

Editorial board

Table of contents