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Cellular drug resistance in childhood acute myeloid leukemia is related to chromosomal abnormalities

Blood, 2002-11, Vol.100 (9), p.3352-3360

2002

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Detection of Genetic Prognostic Markers in Uveal Melanoma Biopsies Using Fluorescence in Situ Hybridization

Clinical cancer research, 2002-02, Vol.8 (2), p.534-539

2002

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LAF4, an AF4-related gene, is fused to MLL in infant acute lymphoblastic leukemia

Genes chromosomes & cancer, 2002-09, Vol.35 (1), p.92-96

2002

Volltextzugriff (PDF)

Carcinogen-Induced Loss of Heterozygosity at the Aprt Locus in Somatic Cells of the Mouse

Proceedings of the National Academy of Sciences - PNAS, 1998-11, Vol.95 (23), p.13759-13764

1998

Volltextzugriff (PDF)

High EVI1 expression predicts poor survival in acute myeloid leukemia: a study of 319 de novo AML patients

Blood, 2003-02, Vol.101 (3), p.837-845

2003

Volltextzugriff (PDF)

Sensitivity to L-asparaginase is not associated with expression levels of asparagine synthetase in t(12;21)+ pediatric ALL

Blood, 2003-04, Vol.101 (7), p.2743-2747

2003

Volltextzugriff (PDF)

Allelic Loss of Chromosome 1p as a Predictor of Unfavorable Outcome in Patients with Neuroblastoma

The New England journal of medicine, 1996-01, Vol.334 (4), p.225-230

1996

Volltextzugriff (PDF)

Molecular cytogenetic and clinical findings inETV6/ABL1-positive leukemia

Genes chromosomes & cancer, 2001-03, Vol.30 (3), p.274-282

2001

Volltextzugriff (PDF)

21q22 balanced chromosome aberrations in therapy-related hematopoietic disorders: Report from an International Workshop

Genes chromosomes & cancer, 2002-04, Vol.33 (4), p.379-394

2002

Volltextzugriff (PDF)

Fusion of the homeobox gene HLXB9 and the ETV6 gene in infant acute myeloid leukemias with the t(7;12)(q36;p13)

Cancer research (Chicago, Ill.), 2001-07, Vol.61 (14), p.5374-5377

2001

Volltextzugriff (PDF)

Characterization of complex chromosomal abnormalities in uveal melanoma by fluorescence in situ hybridization, spectral karyotyping, and comparative genomic hybridization

Genes chromosomes & cancer, 2001-03, Vol.30 (3), p.267-273

2001

Volltextzugriff (PDF)

Evidence for two tumour suppressor loci on chromosomal bands 1p35–36 involved in neuroblastoma: one probably imprinted, another associated with N-myc amplification

Human molecular genetics, 1995-04, Vol.4 (4), p.535-539

1995

Volltextzugriff (PDF)

Determination of spontaneous loss of heterozygosity mutations in Aprt heterozygous mice

Nucleic acids research, 1998-11, Vol.26 (21), p.4888

1998

Volltextzugriff (PDF)

Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N-myc amplification

Nature genetics, 1993-06, Vol.4 (2), p.187-190

1993

Volltextzugriff (PDF)

DMBA-induced toxic and mutagenic responses vary dramatically between NER-deficient Xpa, Xpc and Csb mice

Carcinogenesis (New York), 2001-07, Vol.22 (7), p.1099-1106

2001

Volltextzugriff (PDF)

Mutation analysis of the PTEN gene in uveal melanoma cell lines

International journal of cancer, 2000-07, Vol.87 (1), p.151-153

2000

Volltextzugriff (PDF)

Maintenance of Vascular Endothelial Cell-Specific Properties after Immortalization with an Amphotrophic Replication-Deficient Retrovirus Containing Human Papilloma Virus 16 E6/E7 DNA

Experimental cell research, 1995-01, Vol.216 (1), p.199-207

1995

Volltextzugriff (PDF)

Centromeric breakage as a major cause of cytogenetic abnormalities in oral squamous cell carcinoma

Genes chromosomes & cancer, 1996-01, Vol.15 (1), p.1-9

1996

Volltextzugriff (PDF)

Characterization of mRAD18Sc, a Mouse Homolog of the Yeast Postreplication Repair Gene RAD18

Genomics (San Diego, Calif.), 2000-10, Vol.69 (1), p.86-94

2000

Volltextzugriff (PDF)

Chromosome studies on acute nonlymphocytic leukaemia in children

Pediatric research, 1983-05, Vol.17 (5), p.398-405

1983

Volltextzugriff (PDF)

Sensitivity tol-asparaginase is not associated with expression levels of asparagine synthetase in t(12;21)+pediatric ALL

Blood, 2003-04, Vol.101 (7), p.2743-2747

2003

Volltextzugriff (PDF)

Recurrent 1;17 translocations in human neuroblastoma reveal nonhomologous mitotic recombination during the S/G2 phase as a novel mechanism for loss of heterozygosity

American journal of human genetics, 1994-08, Vol.55 (2), p.341-347

1994

Volltextzugriff (PDF)

Allelic loss of the short arm of chromosome 4 in neuroblastoma suggests a novel tumour suppressor gene locus

Human genetics, 1996-06, Vol.97 (6), p.834-837

1996

Volltextzugriff (PDF)

Mutation analysis of thePTEN gene in uveal melanoma cell lines

International journal of cancer, 2000-07, Vol.87 (1), p.151-153

2000

Volltextzugriff (PDF)

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Cellular drug resistance in childhood acute myeloid leukemia is related to chromosomal abnormalities

Detection of Genetic Prognostic Markers in Uveal Melanoma Biopsies Using Fluorescence in Situ Hybridization

LAF4, an AF4-related gene, is fused to MLL in infant acute lymphoblastic leukemia

Carcinogen-Induced Loss of Heterozygosity at the Aprt Locus in Somatic Cells of the Mouse

High EVI1 expression predicts poor survival in acute myeloid leukemia: a study of 319 de novo AML patients

Sensitivity to L-asparaginase is not associated with expression levels of asparagine synthetase in t(12;21)+ pediatric ALL

Overall and event-free survival are not improved by the use of myeloablative therapy following intensified chemotherapy in previously untreated patients with multiple myeloma: a prospective randomized phase 3 study

Allelic Loss of Chromosome 1p as a Predictor of Unfavorable Outcome in Patients with Neuroblastoma

Molecular cytogenetic and clinical findings inETV6/ABL1-positive leukemia

21q22 balanced chromosome aberrations in therapy-related hematopoietic disorders: Report from an International Workshop

Fusion of the homeobox gene HLXB9 and the ETV6 gene in infant acute myeloid leukemias with the t(7;12)(q36;p13)

Characterization of complex chromosomal abnormalities in uveal melanoma by fluorescence in situ hybridization, spectral karyotyping, and comparative genomic hybridization

Evidence for two tumour suppressor loci on chromosomal bands 1p35–36 involved in neuroblastoma: one probably imprinted, another associated with N-myc amplification

Determination of spontaneous loss of heterozygosity mutations in Aprt heterozygous mice

Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N-myc amplification

DMBA-induced toxic and mutagenic responses vary dramatically between NER-deficient Xpa, Xpc and Csb mice

Mutation analysis of the PTEN gene in uveal melanoma cell lines

Maintenance of Vascular Endothelial Cell-Specific Properties after Immortalization with an Amphotrophic Replication-Deficient Retrovirus Containing Human Papilloma Virus 16 E6/E7 DNA

Centromeric breakage as a major cause of cytogenetic abnormalities in oral squamous cell carcinoma

Characterization of mRAD18Sc, a Mouse Homolog of the Yeast Postreplication Repair Gene RAD18

Chromosome studies on acute nonlymphocytic leukaemia in children

Sensitivity tol-asparaginase is not associated with expression levels of asparagine synthetase in t(12;21)+pediatric ALL

Recurrent 1;17 translocations in human neuroblastoma reveal nonhomologous mitotic recombination during the S/G2 phase as a novel mechanism for loss of heterozygosity

Allelic loss of the short arm of chromosome 4 in neuroblastoma suggests a novel tumour suppressor gene locus

Mutation analysis of thePTEN gene in uveal melanoma cell lines

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