Pretsch W - Search Results

1

Electroretinography as a screening method for mutations causing retinal dysfunction in mice.

Dalke C, Löster J, Fuchs H, Gailus-Durner V, Soewarto D, Favor J, Neuhäuser-Klaus A, Pretsch W, Gekeler F, Shinoda K, Zrenner E, Meitinger T, Hrabé de Angelis M, Graw J. Dalke C, et al. Among authors: pretsch w. Invest Ophthalmol Vis Sci. 2004 Feb;45(2):601-9. doi: 10.1167/iovs.03-0561. Invest Ophthalmol Vis Sci. 2004. PMID: 14744904

2

Three novel Pax6 alleles in the mouse leading to the same small-eye phenotype caused by different consequences at target promoters.

Graw J, Löster J, Puk O, Münster D, Haubst N, Soewarto D, Fuchs H, Meyer B, Nürnberg P, Pretsch W, Selby P, Favor J, Wolf E, Hrabé de Angelis M. Graw J, et al. Among authors: pretsch w. Invest Ophthalmol Vis Sci. 2005 Dec;46(12):4671-83. doi: 10.1167/iovs.04-1407. Invest Ophthalmol Vis Sci. 2005. PMID: 16303964

3

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.

Graw J, Pretsch W, Löster J. Graw J, et al. Among authors: pretsch w. Genetics. 2003 Jul;164(3):1035-41. doi: 10.1093/genetics/164.3.1035. Genetics. 2003. PMID: 12871913 Free PMC article.

4

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

Pretsch W, Favor J. Pretsch W, et al. Mamm Genome. 2007 Oct;18(10):686-92. doi: 10.1007/s00335-007-9055-z. Epub 2007 Sep 17. Mamm Genome. 2007. PMID: 17874335

5

Molecular analysis of two new Steel mutations in mice shows a transversion or an insertion.

Graw J, Löster J, Neuhäuser-Klaus A, Pretsch W, Schmitt-John T. Graw J, et al. Among authors: pretsch w. Mamm Genome. 1996 Nov;7(11):843-6. doi: 10.1007/s003359900247. Mamm Genome. 1996. PMID: 8875893 No abstract available.

6

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

Pretsch W, Favor J. Pretsch W, et al. Mamm Genome. 1997 Apr;8(4):296-7. doi: 10.1007/s003359900421. Mamm Genome. 1997. PMID: 9096122 No abstract available.

7

Detection of a point mutation (A to G) in exon 5 of the murine Mgf gene defines a novel allele at the Steel locus with a weak phenotype.

Graw J, Neuhäuser-Klaus A, Pretsch W. Graw J, et al. Among authors: pretsch w. Mutat Res. 1997 Sep;382(1-2):75-8. doi: 10.1016/s1383-5726(97)00005-8. Mutat Res. 1997. PMID: 9360640

8

Three murine cataract mutants (Cat2) are defective in different gamma-crystallin genes.

Klopp N, Favor J, Löster J, Lutz RB, Neuhäuser-Klaus A, Prescott A, Pretsch W, Quinlan RA, Sandilands A, Vrensen GF, Graw J. Klopp N, et al. Among authors: pretsch w. Genomics. 1998 Sep 1;52(2):152-8. doi: 10.1006/geno.1998.5417. Genomics. 1998. PMID: 9782080

9

Towards an understanding of the nature and fitness of induced mutations in germ cells of mice: homozygous viability and heterozygous fitness effects of induced specific-locus, dominant cataract and enzyme-activity mutations.

Favor J, Neuhäuser-Klaus A, Kratochvilova J, Pretsch W. Favor J, et al. Among authors: pretsch w. Mutat Res. 1989 May;212(1):67-75. doi: 10.1016/0027-5107(89)90023-7. Mutat Res. 1989. PMID: 2725543

10

Estimates of the radiation-induced mutation frequencies to recessive visible, dominant cataract and enzyme-activity alleles in germ cells of AKR, BALB/c, DBA/2 and (102xC3H)F1 mice.

Pretsch W, Favor J, Lehmacher W, Neuhäuser-Klaus A. Pretsch W, et al. Mutagenesis. 1994 Jul;9(4):289-94. doi: 10.1093/mutage/9.4.289. Mutagenesis. 1994. PMID: 7968568

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