Publications by authors named "Walter Pretsch"

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Mouse genetics suggests cell-context dependency for Myc-regulated metabolic enzymes during tumorigenesis.
Lisa M Nilsson, Tacha Zi Plym Forshell, Sara Rimpi, Christiane Kreutzer, Walter Pretsch

PLoS Genet· September 2012

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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.
Jack Favor, Alan Bradley, Nathalie Conte, Dirk Janik, Walter Pretsch

Genetics· August 2009

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

Genet Res (Camb)· February 2009

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Relationship of Pax6 activity levels to the extent of eye development in the mouse, Mus musculus.
Jack Favor, Christian Johannes Gloeckner, Angelika Neuhäuser-Klaus, Walter Pretsch, Rodica Sandulache

Genetics· July 2008

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

Mamm Genome· October 2007

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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.
Jack Favor, Christian Johannes Gloeckner, Dirk Janik, Martina Klempt, Angelika Neuhäuser-Klaus, Walter Pretsch

Genetics· February 2007

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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.
Jochen Graw, Jana Löster, Oliver Puk, Doris Münster, Nicole Haubst, Walter Pretsch

Invest Ophthalmol Vis Sci· December 2005

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An ENU-induced mutation in Rs1h causes disruption of retinal structure and function.
Monica M Jablonski, Claudia Dalke, XiaoFei Wang, Lu Lu, Kenneth F Manly, Walter Pretsch

Mol Vis· July 2005

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Electroretinography as a screening method for mutations causing retinal dysfunction in mice.
Claudia Dalke, Jana Löster, Helmut Fuchs, Valerie Gailus-Durner, Dian Soewarto, Walter Pretsch

Invest Ophthalmol Vis Sci· February 2004

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Moderate hypermutability of a transgenic lacZ reporter gene in Myc-dependent inflammation-induced plasma cell tumors in mice.
Klaus Felix, Axel Polack, Walter Pretsch, Sharon H Jackson, Lionel Feigenbaum

Cancer Res· January 2004

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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.
Jochen Graw, Walter Pretsch, Jana Löster

Genetics· July 2003

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Redox imbalance and mutagenesis in spleens of mice harboring a hypomorphic allele of Gpdx(a) encoding glucose 6-phosphate dehydrogenase.
Klaus Felix, Lynne D Rockwood, Walter Pretsch, Georg Wilhelm Bornkamm, Siegfried Janz

Free Radic Biol Med· January 2003

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Moderate G6PD deficiency increases mutation rates in the brain of mice.
Klaus Felix, Lynne D Rockwood, Walter Pretsch, Jagadeesan Nair, Helmut Bartsch

Free Radic Biol Med· April 2002

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