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Chromosomal Doubling: The Significance of Polyploidization in the Development of Human Tumors: Possibly Relevant Findings on a Lymphoma

Cancer genetics and cytogenetics, 2000, Vol.116 (1), p.81-83

Atkin, Niels B

2000

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Development of a multiplex MethyLight assay for the detection of multigene methylation in human colorectal cancer

Cancer genetics and cytogenetics, 2010-10, Vol.202 (1), p.1-10

2010

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Oncogenes and onco-suppressor genes as prognostic indicators in the development of human tumors

Cancer genetics and cytogenetics, 1992-10, Vol.63 (2), p.112-112

Spandidos, Demetrios A.

1992

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Genetic basis of human prostate cancer development and progression

Cancer genetics and cytogenetics, 1995-10, Vol.84 (2), p.131-131

1995

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The role of genetic changes in the short arm of chromosome 11 in the development of human solid tumors

Cancer genetics and cytogenetics, 1989-04, Vol.38 (2), p.162-162

1989

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Role of the RARRES1 gene in nasopharyngeal carcinoma

Cancer genetics and cytogenetics, 2009-10, Vol.194 (1), p.58-64

2009

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DNA fingerprint analysis in development and progression of human solid tumors

Cancer genetics and cytogenetics, 1994-10, Vol.77 (2), p.183-183

1994

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Characterization of a recurrent t(1;2)(p36;p24) in human uterine leiomyoma

Cancer genetics and cytogenetics, 2009-08, Vol.193 (1), p.54-62

2009

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A unique EBV-negative low-grade lymphoma line (WSU-FSCCL) exhibiting both t(14;18) and t(8;11)

Cancer genetics and cytogenetics, 1993-10, Vol.70 (1), p.62-67

1993

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The tumor suppressor gene FBXW7 is disrupted by a constitutional t(3;4)(q21;q31) in a patient with renal cell cancer

Cancer genetics and cytogenetics, 2009-12, Vol.195 (2), p.105-111

2009

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The role of viral integration in the development of cervical cancer

Cancer genetics and cytogenetics, 2005-04, Vol.158 (1), p.27-34

2005

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MUC1 oncogene amplification correlates with protein overexpression in invasive breast carcinoma cells

Cancer genetics and cytogenetics, 2010-09, Vol.201 (2), p.102-110

2010

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Frequent Loss of 9p21 ( p16INK4A) and Other Genomic Imbalances in Human Malignant Fibrous Histiocytoma

Cancer genetics and cytogenetics, 2000-04, Vol.118 (2), p.89-98

2000

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UOK 262 cell line, fumarate hydratase deficient ( FH− / FH− ) hereditary leiomyomatosis renal cell carcinoma: in vitro and in vivo model of an aberrant energy metabolic pathway in human cancer

Cancer genetics and cytogenetics, 2010, Vol.196 (1), p.45-55

2010

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A functional promoter polymorphism in the TERT gene does not affect inherited susceptibility to breast cancer

Cancer genetics and cytogenetics, 2009-04, Vol.190 (2), p.71-74

2009

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Angiotensin I–converting enzyme gene insertion/deletion polymorphism and endometrial human cancer in normotensive and hypertensive women

Cancer genetics and cytogenetics, 2004-11, Vol.155 (1), p.42-46

2004

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Association between polymorphisms of TP53 and MDM2 and prostate cancer risk in southern Chinese

Cancer genetics and cytogenetics, 2010-10, Vol.202 (2), p.76-81

2010

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Alterations in the ATP2A2 gene in correlation with colon and lung cancer

Cancer genetics and cytogenetics, 2006-12, Vol.171 (2), p.105-111

2006

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Cytogenetics and genetics of human cancer: methods and accomplishments

Cancer genetics and cytogenetics, 2010-12, Vol.203 (2), p.102-126

2010

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Fetal colon cell line FHC exhibits tumorigenic phenotype, complex karyotype, and TP53 gene mutation

Cancer genetics and cytogenetics, 2010-03, Vol.197 (2), p.107-116

2010

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Functional Evidence for Involvement of Multiple Putative Tumor Suppressor Genes on the Short Arm of Chromosome 3 in Human Oral Squamous Cell Carcinogenesis

Cancer genetics and cytogenetics, 1998-12, Vol.107 (2), p.125-131

1998

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Molecular Definition of Chromosome Translocations Involving 10q24 and 19q13 in Human Malignant Glioma Cells

Cancer genetics and cytogenetics, 1998-08, Vol.105 (1), p.60-68

1998

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Minimal regions of chromosomal imbalance in retinoblastoma detected by comparative genomic hybridization

Cancer genetics and cytogenetics, 2001-08, Vol.129 (1), p.57-63

2001

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Structural Alterations of Chromosome 5 in Twelve Human Prostate Cancer Cell Lines

Cancer genetics and cytogenetics, 1998-10, Vol.106 (2), p.105-109

1998

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Analysis of oncogene expression in primary human gliomas: Evidence for increased expression of the ros oncogene

Cancer genetics and cytogenetics, 1994-02, Vol.72 (2), p.130-136

1994

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Chromosomal Doubling: The Significance of Polyploidization in the Development of Human Tumors: Possibly Relevant Findings on a Lymphoma

Development of a multiplex MethyLight assay for the detection of multigene methylation in human colorectal cancer

Oncogenes and onco-suppressor genes as prognostic indicators in the development of human tumors

Genetic basis of human prostate cancer development and progression

The role of genetic changes in the short arm of chromosome 11 in the development of human solid tumors

Role of the RARRES1 gene in nasopharyngeal carcinoma

DNA fingerprint analysis in development and progression of human solid tumors

Characterization of a recurrent t(1;2)(p36;p24) in human uterine leiomyoma

A unique EBV-negative low-grade lymphoma line (WSU-FSCCL) exhibiting both t(14;18) and t(8;11)

The tumor suppressor gene FBXW7 is disrupted by a constitutional t(3;4)(q21;q31) in a patient with renal cell cancer

The role of viral integration in the development of cervical cancer

MUC1 oncogene amplification correlates with protein overexpression in invasive breast carcinoma cells

Frequent Loss of 9p21 ( p16INK4A) and Other Genomic Imbalances in Human Malignant Fibrous Histiocytoma

UOK 262 cell line, fumarate hydratase deficient ( FH− / FH− ) hereditary leiomyomatosis renal cell carcinoma: in vitro and in vivo model of an aberrant energy metabolic pathway in human cancer

A functional promoter polymorphism in the TERT gene does not affect inherited susceptibility to breast cancer

Angiotensin I–converting enzyme gene insertion/deletion polymorphism and endometrial human cancer in normotensive and hypertensive women

Association between polymorphisms of TP53 and MDM2 and prostate cancer risk in southern Chinese

Alterations in the ATP2A2 gene in correlation with colon and lung cancer

Cytogenetics and genetics of human cancer: methods and accomplishments

Fetal colon cell line FHC exhibits tumorigenic phenotype, complex karyotype, and TP53 gene mutation

Functional Evidence for Involvement of Multiple Putative Tumor Suppressor Genes on the Short Arm of Chromosome 3 in Human Oral Squamous Cell Carcinogenesis

Molecular Definition of Chromosome Translocations Involving 10q24 and 19q13 in Human Malignant Glioma Cells

Minimal regions of chromosomal imbalance in retinoblastoma detected by comparative genomic hybridization

Structural Alterations of Chromosome 5 in Twelve Human Prostate Cancer Cell Lines

Analysis of oncogene expression in primary human gliomas: Evidence for increased expression of the ros oncogene

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