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Mouse genetics suggests cell-context dependency for Myc-regulated metabolic enzymes during tumorigenesis

PLoS genetics, 2012-03, Vol.8 (3), p.e1002573

2012

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Relationship of Pax6 Activity Levels to the Extent of Eye Development in the Mouse, Mus musculus

Genetics (Austin), 2008-07, Vol.179 (3), p.1345-1355

2008

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Electroretinography as a Screening Method for Mutations Causing Retinal Dysfunction in Mice

Investigative ophthalmology & visual science, 2004-02, Vol.45 (2), p.601-609

2004

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Enzyme-activity mutants in Mus musculus. I. Phenotypic description and genetic characterization of ethylnitrosourea-induced mutations

Mammalian genome, 2000-07, Vol.11 (7), p.537-542

Pretsch, W

2000

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Type IV Procollagen Missense Mutations Associated With Defects of the Eye, Vascular Stability, the Brain, Kidney Function and Embryonic or Postnatal Viability in the Mouse, Mus musculus: An Extension of the Col4a1 Allelic Series and the Identification of the First Two Col4a2 Mutant Alleles

Genetics (Austin), 2007-02, Vol.175 (2), p.725-736

2007

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A 76-bp Deletion in the Mip Gene Causes Autosomal Dominant Cataract in Hfi Mice

Genomics (San Diego, Calif.), 2001-06, Vol.74 (3), p.313-319

2001

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Genetic, biochemical, and molecular characterization of nine glyceraldehyde-3-phosphate dehydrogenase mutants with reduced enzyme activity in Mus musculus

Mammalian genome, 2007-10, Vol.18 (10), p.686-692

2007

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Analysis of Pax6 Contiguous Gene Deletions in the Mouse, Mus musculus, Identifies Regions Distinct from Pax6 Responsible for Extreme Small-Eye and Belly-Spotting Phenotypes

Genetics (Austin), 2009-08, Vol.182 (4), p.1077-1088

2009

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The mouse Pax2(1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney

Proceedings of the National Academy of Sciences - PNAS, 1996-11, Vol.93 (24), p.13870-13875

1996

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Triosephosphate isomerase activity-deficient mice show haemolytic anaemia in homozygous condition

Genetics Research, 2009-02, Vol.91 (1), p.1-4

PRETSCH, WALTER

2009

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Three Novel Pax6 Alleles in the Mouse Leading to the Same Small-Eye Phenotype Caused by Different Consequences at Target Promoters

Investigative ophthalmology & visual science, 2005-12, Vol.46 (12), p.4671-4683

2005

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Mutation in Intron 6 of the Hamster Mitf Gene Leads to Skipping of the Subsequent Exon and Creates a Novel Animal Model for the Human Waardenburg Syndrome Type II

Genetics (Austin), 2003-07, Vol.164 (3), p.1035-1041

2003

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An ENU-induced mutation in Rs1h causes disruption of retinal structure and function

Molecular vision, 2005-07, Vol.11, p.569

2005

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The mouse Pax21Neu mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney

Proceedings of the National Academy of Sciences - PNAS, 1996-11, Vol.93 (24), p.13870-13875

1996

Volltextzugriff (PDF)

Moderate hypermutability of a transgenic lacZ reporter gene in Myc-dependent inflammation-induced plasma cell tumors in mice

Cancer research (Chicago, Ill.), 2004-01, Vol.64 (2), p.530-537

2004

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Moderate G6PD deficiency increases mutation rates in the brain of mice

Free radical biology & medicine, 2002-04, Vol.32 (7), p.663-673

2002

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Redox imbalance and mutagenesis in spleens of mice harboring a hypomorphic allele of Gpdx(a) encoding glucose 6-phosphate dehydrogenase

Free radical biology & medicine, 2003-01, Vol.34 (2), p.226-232

2003

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Redox imbalance and mutagenesis in spleens of mice harboring a hypomorphic allele of Gpdxa encoding glucose 6-phosphate dehydrogenase

Free radical biology & medicine, 2003, Vol.34 (2), p.226-232

2003

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Three Murine Cataract Mutants (Cat2) Are Defective in Different γ-Crystallin Genes

Genomics (San Diego, Calif.), 1998-09, Vol.52 (2), p.152-158

1998

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Glucose-6-Phosphate Isomerase Deficiency Associated With Nonspherocytic Hemolytic Anemia in the Mouse: An Animal Model for the Human Disease

Blood, 1993-01, Vol.81 (1), p.206-213

1993

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A second locus encoding elevated phosphoglycerate mutase activity (Pgam2e) maps to mouse chromosome 4

Mammalian genome, 1997-04, Vol.8 (4), p.296-297

1997

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Molecular, genetic and biochemical characterization of lactate dehydrogenase-A enzyme activity mutations in Mus musculus

Mammalian genome, 1998-02, Vol.9 (2), p.144-149

1998

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A comparison of enzyme activity mutation frequencies in germ cells of mice (Mus musculus) and golden hamsters (Mesocricetus auratus) after exposure to 2 + 2 Gy γ-irradiation

Mutagenesis, 2000-01, Vol.15 (1), p.39-43

2000

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Mapping of the autosomal dominant cataract mutation (Coc) on mouse chromosome 16

Investigative ophthalmology & visual science, 1997-11, Vol.38 (12), p.2502-2507

1997

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Characterization of two electrophoretic lactate dehydrogenase-A mutants inMus musculus

Biochemical genetics, 1992-02, Vol.30 (1-2), p.49-59

1992

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Mouse genetics suggests cell-context dependency for Myc-regulated metabolic enzymes during tumorigenesis

Relationship of Pax6 Activity Levels to the Extent of Eye Development in the Mouse, Mus musculus

Electroretinography as a Screening Method for Mutations Causing Retinal Dysfunction in Mice

Enzyme-activity mutants in Mus musculus. I. Phenotypic description and genetic characterization of ethylnitrosourea-induced mutations

Type IV Procollagen Missense Mutations Associated With Defects of the Eye, Vascular Stability, the Brain, Kidney Function and Embryonic or Postnatal Viability in the Mouse, Mus musculus: An Extension of the Col4a1 Allelic Series and the Identification of the First Two Col4a2 Mutant Alleles

A 76-bp Deletion in the Mip Gene Causes Autosomal Dominant Cataract in Hfi Mice

Genetic, biochemical, and molecular characterization of nine glyceraldehyde-3-phosphate dehydrogenase mutants with reduced enzyme activity in Mus musculus

Analysis of Pax6 Contiguous Gene Deletions in the Mouse, Mus musculus, Identifies Regions Distinct from Pax6 Responsible for Extreme Small-Eye and Belly-Spotting Phenotypes

The mouse Pax2(1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney

Triosephosphate isomerase activity-deficient mice show haemolytic anaemia in homozygous condition

Three Novel Pax6 Alleles in the Mouse Leading to the Same Small-Eye Phenotype Caused by Different Consequences at Target Promoters

Mutation in Intron 6 of the Hamster Mitf Gene Leads to Skipping of the Subsequent Exon and Creates a Novel Animal Model for the Human Waardenburg Syndrome Type II

An ENU-induced mutation in Rs1h causes disruption of retinal structure and function

The mouse Pax21Neu mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney

Moderate hypermutability of a transgenic lacZ reporter gene in Myc-dependent inflammation-induced plasma cell tumors in mice

Moderate G6PD deficiency increases mutation rates in the brain of mice

Redox imbalance and mutagenesis in spleens of mice harboring a hypomorphic allele of Gpdx(a) encoding glucose 6-phosphate dehydrogenase

Redox imbalance and mutagenesis in spleens of mice harboring a hypomorphic allele of Gpdxa encoding glucose 6-phosphate dehydrogenase

Three Murine Cataract Mutants (Cat2) Are Defective in Different γ-Crystallin Genes

Glucose-6-Phosphate Isomerase Deficiency Associated With Nonspherocytic Hemolytic Anemia in the Mouse: An Animal Model for the Human Disease

A second locus encoding elevated phosphoglycerate mutase activity (Pgam2e) maps to mouse chromosome 4

Molecular, genetic and biochemical characterization of lactate dehydrogenase-A enzyme activity mutations in Mus musculus

A comparison of enzyme activity mutation frequencies in germ cells of mice (Mus musculus) and golden hamsters (Mesocricetus auratus) after exposure to 2 + 2 Gy γ-irradiation

Mapping of the autosomal dominant cataract mutation (Coc) on mouse chromosome 16

Characterization of two electrophoretic lactate dehydrogenase-A mutants inMus musculus

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