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Analysis of gene expression using gene sets discriminates cancer patients with and without late radiation toxicity

PLoS medicine, 2006-10, Vol.3 (10), p.e422

2006

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Gene expression profiling of minimally differentiated acute myeloid leukemia: M0 is a distinct entity subdivided by RUNX1 mutation status

Blood, 2009-10, Vol.114 (14), p.3001-3007

2009

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Trisomy 13 correlates with RUNX1 mutation and increased FLT3 expression in AML-M0 patients

Haematologica (Roma), 2007-08, Vol.92 (8), p.1123-1126

2007

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Identification of RUNX1/AML1 as a classical tumor suppressor gene

Oncogene, 2003-01, Vol.22 (4), p.538-547

2003

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Hemizygous deletions in the HLA region account for loss of heterozygosity in the majority of diffuse large B-cell lymphomas of the testis and the central nervous system

Genes chromosomes & cancer, 2002-09, Vol.35 (1), p.38-48

2002

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Genome wide molecular analysis of minimally differentiated acute myeloid leukemia

Haematologica (Roma), 2009-11, Vol.94 (11), p.1546-1554

2009

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A portrait of cisplatin-induced transcriptional changes in mouse embryonic stem cells reveals a dominant p53-like response

Mutation Research-Fundamental and Molecular Mechanisms of Mutagenesis, 2007-04, Vol.617 (1), p.58-70

2007

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Lack of genetic and epigenetic changes in meningiomas without NF2 loss

The Journal of pathology, 2006-03, Vol.208 (4), p.564-573

2006

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Dissecting systems-wide data using mixture models: application to identify affected cellular processes

BMC bioinformatics, 2005-07, Vol.6 (1), p.177-177, Article 177

2005

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Chromosome loss with concomitant duplication and recombination both contribute most to loss of heterozygosity in vitro

Genes chromosomes & cancer, 1998-01, Vol.21 (1), p.30-38

1998

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Intrinsic genetic instability of normal human lymphocytes and its implication for loss of heterozygosity

Genes chromosomes & cancer, 2001-04, Vol.30 (4), p.323-335

2001

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Heterozygous Aprt mouse model: Detection and study of a broad range of autosomal somatic mutations in vivo

Environmental and molecular mutagenesis, 1999, Vol.34 (2-3), p.84-89

1999

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Amplification of the 11q13 region in human carcinoma cell lines: A mechanistic view

Genes chromosomes & cancer, 1993-06, Vol.7 (2), p.74-84

1993

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No threshold for the induction of chromosomal damage at clinically relevant low doses of X rays

Radiation research, 2012-05, Vol.177 (5), p.602

2012

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Invertible DNA determines host specificity of bacteriophage Mu

Nature (London), 1980-07, Vol.286 (5770), p.218-222

1980

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Structural polypeptides and products of late genes of bacteriophage Mu: Characterization and functional aspects

Journal of molecular biology, 1981-01, Vol.145 (1), p.139-163

1981

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Trisomy 13 correlates with RUNX1 mutation and increased FLT3 expression in AML-MO patients

Haematologica (Roma), 2007, Vol.92 (8), p.1123-1126

2007

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Both the rate and spectrum of loss of heterozygosity differ between human lymphoblastoid cells derived from various donors

Mutation research, 1999-01, Vol.423 (1), p.1-10

1999

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Genomic position influences spontaneous mutagenesis of an integrated retroviral vector containing the hprt cDNA as target for mutagenesis

Human molecular genetics, 1993-02, Vol.2 (2), p.173-182

1993

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Spontaneous mutation spectrum in the hprt gene in human lymphoblastoid TK6 cells

Mutagenesis, 1995-03, Vol.10 (2), p.137-143

1995

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Genome wide spontaneous mutation in human cells determined by the spectrum of mutations in hprt cDNA genes

Mutagenesis, 1993-05, Vol.8 (3), p.207-220

1993

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Site-specific analysis of UV-induced cyclobutane pyrimidine dimers in nucleotide excision repair-proficient and -deficient hamster cells: Lack of correlation with mutational spectra

Mutation research, 2009-04, Vol.663 (1), p.7-14

2009

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The ability of the restriction endonuclease EcoRI to digest hemi-methylated versus fully cytosine-methylated DNA of the herpes tk promoter region

Gene, 1988-12, Vol.74 (1), p.147-149

1988

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HeterozygousAprt mouse model: Detection and study of a broad range of autosomal somatic mutations in vivo

Environmental and molecular mutagenesis, 1999, Vol.34 (2-3), p.84-89

1999

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Mutation induction by UV light in retroviral hprt cDNA integrated at various chromosomal positions in repair-deficient hamster cells

Mutagenesis, 1993-09, Vol.8 (5), p.399-406

1993

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Analysis of gene expression using gene sets discriminates cancer patients with and without late radiation toxicity

Gene expression profiling of minimally differentiated acute myeloid leukemia: M0 is a distinct entity subdivided by RUNX1 mutation status

Trisomy 13 correlates with RUNX1 mutation and increased FLT3 expression in AML-M0 patients

Identification of RUNX1/AML1 as a classical tumor suppressor gene

Hemizygous deletions in the HLA region account for loss of heterozygosity in the majority of diffuse large B-cell lymphomas of the testis and the central nervous system

Genome wide molecular analysis of minimally differentiated acute myeloid leukemia

A portrait of cisplatin-induced transcriptional changes in mouse embryonic stem cells reveals a dominant p53-like response

Lack of genetic and epigenetic changes in meningiomas without NF2 loss

Dissecting systems-wide data using mixture models: application to identify affected cellular processes

Chromosome loss with concomitant duplication and recombination both contribute most to loss of heterozygosity in vitro

Intrinsic genetic instability of normal human lymphocytes and its implication for loss of heterozygosity

Heterozygous Aprt mouse model: Detection and study of a broad range of autosomal somatic mutations in vivo

Amplification of the 11q13 region in human carcinoma cell lines: A mechanistic view

No threshold for the induction of chromosomal damage at clinically relevant low doses of X rays

Invertible DNA determines host specificity of bacteriophage Mu

Structural polypeptides and products of late genes of bacteriophage Mu: Characterization and functional aspects

Trisomy 13 correlates with RUNX1 mutation and increased FLT3 expression in AML-MO patients

Both the rate and spectrum of loss of heterozygosity differ between human lymphoblastoid cells derived from various donors

Genomic position influences spontaneous mutagenesis of an integrated retroviral vector containing the hprt cDNA as target for mutagenesis

Spontaneous mutation spectrum in the hprt gene in human lymphoblastoid TK6 cells

Genome wide spontaneous mutation in human cells determined by the spectrum of mutations in hprt cDNA genes

Site-specific analysis of UV-induced cyclobutane pyrimidine dimers in nucleotide excision repair-proficient and -deficient hamster cells: Lack of correlation with mutational spectra

The ability of the restriction endonuclease EcoRI to digest hemi-methylated versus fully cytosine-methylated DNA of the herpes tk promoter region

HeterozygousAprt mouse model: Detection and study of a broad range of autosomal somatic mutations in vivo

Mutation induction by UV light in retroviral hprt cDNA integrated at various chromosomal positions in repair-deficient hamster cells

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