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CCR2-Dependent Recruitment of Macrophages by Tumor-Educated Mesenchymal Stromal Cells Promotes Tumor Development and Is Mimicked by TNFα

Cell stem cell, 2012-12, Vol.11 (6), p.812-824

2012

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Methylome-wide comparison of human genomic DNA extracted from whole blood and from EBV-transformed lymphocyte cell lines

European journal of human genetics : EJHG, 2012-09, Vol.20 (9), p.953-955

2012

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Mitotic recombination is suppressed by chromosomal divergence in hybrids of distantly related mouse strains

Nature genetics, 2001-06, Vol.28 (2), p.169-172

2001

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X-rays induce distinct patterns of somatic mutation in fetal versus adult hematopoietic cells

DNA repair, 2007-09, Vol.6 (9), p.1380-1385

2007

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Association of NFKB1, which encodes a subunit of the transcription factor NF-κB, with alcohol dependence

Human molecular genetics, 2008-04, Vol.17 (7), p.963-970

2008

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Mlh1 mediates tissue-specific regulation of mitotic recombination

Oncogene, 2004-12, Vol.23 (56), p.9017-9024

2004

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Loss of Heterozygosity or: How I Learned to Stop Worrying and Love Mitotic Recombination

American journal of human genetics, 1997-11, Vol.61 (5), p.995-999

Tischfield, Jay A.

1997

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Loss of heterozygosity and point mutation at Aprt locus in T cells and fibroblasts of Pms2-/- mice

Oncogene, 2002-04, Vol.21 (18), p.2840-2845

2002

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Linkage and linkage disequilibrium of evoked EEG oscillations with CHRM2 receptor gene polymorphisms: implications for human brain dynamics and cognition

International journal of psychophysiology, 2004-07, Vol.53 (2), p.75-90

2004

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A novel signature mutation for oxidative damage resembles a mutational pattern found commonly in human cancers

Cancer research (Chicago, Ill.), 1999-04, Vol.59 (8), p.1837-1839

1999

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Biallelic methylation and silencing of mouse Aprt in normal kidney cells

Cancer research (Chicago, Ill.), 2000-07, Vol.60 (13), p.3404-3408

2000

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A systematic gene-based screen of chr4q22–q32 identifies association of a novel susceptibility gene, DKK2, with the quantitative trait of alcohol dependence symptom counts

Human molecular genetics, 2010-06, Vol.19 (12), p.2497-2506

2010

Volltextzugriff (PDF)

High frequency in vivo loss of heterozygosity is primarily a consequence of mitotic recombination

Cancer research (Chicago, Ill.), 1997-03, Vol.57 (6), p.1188-1193

1997

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A regulatory variation in OPRK1, the gene encoding the K-opioid receptor, is associated with alcohol dependence

Human molecular genetics, 2008, Vol.17 (12), p.1783-1789

2008

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Low-molecular-weight, calcium-dependent phospholipase A2 genes are linked and map to homologous chromosome regions in mouse and human

Genomics (San Diego, Calif.), 1996-03, Vol.32 (3), p.328-333

1996

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In vivo loss of heterozygosity in T-cells of B6C3F1 Aprt+/− mice

Environmental and molecular mutagenesis, 2000, Vol.35 (2), p.150-157

2000

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Human Chromosomes 6 and 21 are Required for Sensitivity to Human Interferon γ

Proceedings of the National Academy of Sciences - PNAS, 1987-06, Vol.84 (12), p.4151-4155

1987

Volltextzugriff (PDF)

Radiation-induced genetic instability in vivo depends on p53 status

Mutation research. Fundamental and molecular mechanisms of mutagenesis, 2002, Vol.502 (1-2), p.69-80

2002

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Nucleotide Sequence and Organization of the Mouse Adenine Phosphoribosyltransferase Gene: Presence of a Coding Region Common to Animal and Bacterial Phosphoribosyltransferases That Has a Variable Intron/Exon Arrangement

Proceedings of the National Academy of Sciences - PNAS, 1985-05, Vol.82 (9), p.2731-2735

1985

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Comparative Anatomy of the Human APRT Gene and Enzyme: Nucleotide Sequence Divergence and Conservation of a Nonrandom CpG Dinucleotide Arrangement

Proceedings of the National Academy of Sciences - PNAS, 1987-05, Vol.84 (10), p.3349-3353

1987

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The Gene for the Human Immune Interferon Receptor is Located on Chromosome 6

Proceedings of the National Academy of Sciences - PNAS, 1986-01, Vol.83 (2), p.384-388

1986

Volltextzugriff (PDF)

Loss of heterozygosity: The most frequent cause of recessive phenotype expression at the heterozygous human adenine phosphoribosyltransferase locus

Molecular carcinogenesis, 1993, Vol.8 (3), p.138-144

1993

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Identification of DNA sequences required for mouse APRT gene expression

Nucleic acids research, 1988-09, Vol.16 (17), p.8509-8524

1988

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Use of two different deoxyribonucleic acid probes to detect Y chromosome deoxyribonucleic acid in subjects with normal and altered Y chromosomes

American journal of obstetrics and gynecology, 1986-04, Vol.154 (4), p.737-745

1986

Volltextzugriff (PDF)

Reconstitution of an episomal mouse aprt gene as a consequence of recombination

Molecular & general genetics, 1992-03, Vol.232 (1), p.24-32

1992

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CCR2-Dependent Recruitment of Macrophages by Tumor-Educated Mesenchymal Stromal Cells Promotes Tumor Development and Is Mimicked by TNFα

Methylome-wide comparison of human genomic DNA extracted from whole blood and from EBV-transformed lymphocyte cell lines

Mitotic recombination is suppressed by chromosomal divergence in hybrids of distantly related mouse strains

X-rays induce distinct patterns of somatic mutation in fetal versus adult hematopoietic cells

Association of NFKB1, which encodes a subunit of the transcription factor NF-κB, with alcohol dependence

Mlh1 mediates tissue-specific regulation of mitotic recombination

Loss of Heterozygosity or: How I Learned to Stop Worrying and Love Mitotic Recombination

Loss of heterozygosity and point mutation at Aprt locus in T cells and fibroblasts of Pms2-/- mice

Linkage and linkage disequilibrium of evoked EEG oscillations with CHRM2 receptor gene polymorphisms: implications for human brain dynamics and cognition

A novel signature mutation for oxidative damage resembles a mutational pattern found commonly in human cancers

Biallelic methylation and silencing of mouse Aprt in normal kidney cells

A systematic gene-based screen of chr4q22–q32 identifies association of a novel susceptibility gene, DKK2, with the quantitative trait of alcohol dependence symptom counts

High frequency in vivo loss of heterozygosity is primarily a consequence of mitotic recombination

A regulatory variation in OPRK1, the gene encoding the K-opioid receptor, is associated with alcohol dependence

Low-molecular-weight, calcium-dependent phospholipase A2 genes are linked and map to homologous chromosome regions in mouse and human

In vivo loss of heterozygosity in T-cells of B6C3F1 Aprt+/− mice

Human Chromosomes 6 and 21 are Required for Sensitivity to Human Interferon γ

Radiation-induced genetic instability in vivo depends on p53 status

Nucleotide Sequence and Organization of the Mouse Adenine Phosphoribosyltransferase Gene: Presence of a Coding Region Common to Animal and Bacterial Phosphoribosyltransferases That Has a Variable Intron/Exon Arrangement

Comparative Anatomy of the Human APRT Gene and Enzyme: Nucleotide Sequence Divergence and Conservation of a Nonrandom CpG Dinucleotide Arrangement

The Gene for the Human Immune Interferon Receptor is Located on Chromosome 6

Loss of heterozygosity: The most frequent cause of recessive phenotype expression at the heterozygous human adenine phosphoribosyltransferase locus

Identification of DNA sequences required for mouse APRT gene expression

Use of two different deoxyribonucleic acid probes to detect Y chromosome deoxyribonucleic acid in subjects with normal and altered Y chromosomes

Reconstitution of an episomal mouse aprt gene as a consequence of recombination

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