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Cancer-causing karyotypes: chromosomal equilibria between destabilizing aneuploidy and stabilizing selection for oncogenic function

Bioorganic & medicinal chemistry, 2009-01, Vol.188 (1), p.1-25

2009

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Molecular cytogenetic characterization of variant Philadelphia translocations in chronic myeloid leukemia: genesis and deletion of derivative chromosome 9

Cancer genetics and cytogenetics, 2009-10, Vol.194 (1), p.30-37

2009

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Intercellular centrosome number is correlated with the copy number of chromosomes in bladder cancer

Cancer genetics and cytogenetics, 2009-05, Vol.191 (1), p.38-42

2009

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Leiomyoma of the urinary bladder: a cytogenetic study of a case

Cancer genetics and cytogenetics, 2007-09, Vol.177 (2), p.147-148

2007

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Genetic abnormalities in chronic lymphocytic leukemia and their clinical and prognostic implications

Cancer genetics and cytogenetics, 1997-03, Vol.94 (1), p.27-35

1997

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Differential expression of TCL1 during pre–B-cell acute lymphoblastic leukemia progression

Cancer genetics and cytogenetics, 2002-06, Vol.135 (2), p.110-119

2002

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Infantile and adult testicular germ cell tumors: a different pathogenesis?

Cancer genetics and cytogenetics, 2002-05, Vol.135 (1), p.57-62

2002

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Cytogenetic findings in two new cases of hepatoblastoma

Cancer genetics and cytogenetics, 2002-03, Vol.133 (2), p.179-182

2002

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COLIA1-PDGFB gene fusion in dermatofibrosarcoma protuberans. molecular analysis of a case with an unusual large marker containing sequences from chromosomes 7, 8, 17, 21, and 22

Cancer genetics and cytogenetics, 2002-06, Vol.135 (2), p.197-199

2002

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Multiple chromosomal mechanisms generate an EWS/FLI1 or an EWS/ERG fusion gene in Ewing tumors

Cancer genetics and cytogenetics, 1997-08, Vol.97 (1), p.12-19

1997

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Genetic imbalances in pT2 breast cancers of southern Chinese women

Cancer genetics and cytogenetics, 2001, Vol.124 (1), p.56-61

2001

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Heterogeneity of PLAG1 gene rearrangements in pleomorphic adenoma

Cancer genetics and cytogenetics, 2007-08, Vol.177 (1), p.1-5

2007

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Specific patterns of chromosomal gains and losses associate with t(3;14), t(8;14), and t(14;18) in diffuse large B-cell lymphoma

Cancer genetics and cytogenetics, 2009-10, Vol.194 (1), p.48-52

2009

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Investigation of bone marrow involvement in malignant lymphoma using fluorescence in situ hybridization: possible utility in the detection of micrometastasis

Cancer genetics and cytogenetics, 2008-10, Vol.186 (1), p.1-5

2008

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Cryptic insertion into 11q23 of MLLT10 not involved in t(1;15;11;10)(p36;q11;q23;q24) in infant acute biphenotypic leukemia

Cancer genetics and cytogenetics, 2009-04, Vol.190 (2), p.113-120

2009

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Comparative genomic hybridization analysis of benign and invasive male breast neoplasms

Cancer genetics and cytogenetics, 2002-04, Vol.134 (2), p.123-126

2002

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Cytogenetic characterization of Ewing tumors using fine needle aspiration samples: a 10-year experience and review of the literature

Cancer genetics and cytogenetics, 2001-05, Vol.127 (1), p.42-48

2001

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Chromosome Changes in a Metastasis of a Chromophobe Renal Cell Tumor

Cancer genetics and cytogenetics, 1998-08, Vol.105 (1), p.86-89

1998

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Philadelphia chromosome of a constitutional der(22)t(Y;22)(q11.2;p11) with a variant t(1;9;22)(p36;q34;q11) in a case of chronic myelogenous leukemia

Cancer genetics and cytogenetics, 2006-07, Vol.168 (1), p.80-82

2006

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Acute myeloid leukemia (AML) with t(8;21)(q22;q22) relapsing as AML with t(3;21)(q26;q22)

Cancer genetics and cytogenetics, 2006-07, Vol.168 (2), p.172-174

2006

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Multicolor fluorescence in situ hybridization analysis of a synovial sarcoma of the larynx with a t(X;18)(p11.2;q11.2) and trisomies 2 and 8

Cancer genetics and cytogenetics, 2004-08, Vol.153 (1), p.48-52

2004

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Malignant peripheral nerve sheath tumor with rhabdomyoblastic differentiation (malignant triton tumor) with balanced t(7;9)(q11.2;p24) and unbalanced translocation der(16)t(1;16)(q23;q13)

Cancer genetics and cytogenetics, 2004-02, Vol.149 (1), p.23-27

2004

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Concomitant t(4;11) and t(1;19) in a patient with biphenotypic acute leukemia

Cancer genetics and cytogenetics, 2007-08, Vol.177 (1), p.81-82

2007

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An hsr on chromosome 7 was shown to be an insertion of four copies of the 11q23 MLL gene region in an HIV-related lymphoma

Cancer genetics and cytogenetics, 2001-09, Vol.129 (2), p.107-111

2001

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Loss of heterozygosity at 1p, 8p, 10p, 13q, and 17p in advanced urothelial cancer and lack of relation to chemotherapy response and outcome

Cancer genetics and cytogenetics, 2000-12, Vol.123 (2), p.109-113

2000

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Cancer-causing karyotypes: chromosomal equilibria between destabilizing aneuploidy and stabilizing selection for oncogenic function

Molecular cytogenetic characterization of variant Philadelphia translocations in chronic myeloid leukemia: genesis and deletion of derivative chromosome 9

Intercellular centrosome number is correlated with the copy number of chromosomes in bladder cancer

Leiomyoma of the urinary bladder: a cytogenetic study of a case

Genetic abnormalities in chronic lymphocytic leukemia and their clinical and prognostic implications

Differential expression of TCL1 during pre–B-cell acute lymphoblastic leukemia progression

Infantile and adult testicular germ cell tumors: a different pathogenesis?

Cytogenetic findings in two new cases of hepatoblastoma

COLIA1-PDGFB gene fusion in dermatofibrosarcoma protuberans. molecular analysis of a case with an unusual large marker containing sequences from chromosomes 7, 8, 17, 21, and 22

Multiple chromosomal mechanisms generate an EWS/FLI1 or an EWS/ERG fusion gene in Ewing tumors

Genetic imbalances in pT2 breast cancers of southern Chinese women

Heterogeneity of PLAG1 gene rearrangements in pleomorphic adenoma

Specific patterns of chromosomal gains and losses associate with t(3;14), t(8;14), and t(14;18) in diffuse large B-cell lymphoma

Investigation of bone marrow involvement in malignant lymphoma using fluorescence in situ hybridization: possible utility in the detection of micrometastasis

Cryptic insertion into 11q23 of MLLT10 not involved in t(1;15;11;10)(p36;q11;q23;q24) in infant acute biphenotypic leukemia

Comparative genomic hybridization analysis of benign and invasive male breast neoplasms

Cytogenetic characterization of Ewing tumors using fine needle aspiration samples: a 10-year experience and review of the literature

Chromosome Changes in a Metastasis of a Chromophobe Renal Cell Tumor

Philadelphia chromosome of a constitutional der(22)t(Y;22)(q11.2;p11) with a variant t(1;9;22)(p36;q34;q11) in a case of chronic myelogenous leukemia

Acute myeloid leukemia (AML) with t(8;21)(q22;q22) relapsing as AML with t(3;21)(q26;q22)

Multicolor fluorescence in situ hybridization analysis of a synovial sarcoma of the larynx with a t(X;18)(p11.2;q11.2) and trisomies 2 and 8

Malignant peripheral nerve sheath tumor with rhabdomyoblastic differentiation (malignant triton tumor) with balanced t(7;9)(q11.2;p24) and unbalanced translocation der(16)t(1;16)(q23;q13)

Concomitant t(4;11) and t(1;19) in a patient with biphenotypic acute leukemia

An hsr on chromosome 7 was shown to be an insertion of four copies of the 11q23 MLL gene region in an HIV-related lymphoma

Loss of heterozygosity at 1p, 8p, 10p, 13q, and 17p in advanced urothelial cancer and lack of relation to chemotherapy response and outcome

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