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Items: 1 to 50 of 56

1.

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

Nilsson LM, Forshell TZ, Rimpi S, Kreutzer C, Pretsch W, Bornkamm GW, Nilsson JA.

PLoS Genet. 2012;8(3):e1002573. doi: 10.1371/journal.pgen.1002573. Epub 2012 Mar 15.

2.

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.

Favor J, Bradley A, Conte N, Janik D, Pretsch W, Reitmeir P, Rosemann M, Schmahl W, Wienberg J, Zaus I.

Genetics. 2009 Aug;182(4):1077-88. doi: 10.1534/genetics.109.104562. Epub 2009 May 27.

3.

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

Pretsch W.

Genet Res (Camb). 2009 Feb;91(1):1-4. doi: 10.1017/S0016672308009944.

PMID:
19220926
4.

Relationship of Pax6 activity levels to the extent of eye development in the mouse, Mus musculus.

Favor J, Gloeckner CJ, Neuhäuser-Klaus A, Pretsch W, Sandulache R, Saule S, Zaus I.

Genetics. 2008 Jul;179(3):1345-55. doi: 10.1534/genetics.108.088591. Epub 2008 Jun 18.

7.

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.

Invest Ophthalmol Vis Sci. 2005 Dec;46(12):4671-83.

PMID:
16303964
8.

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

Jablonski MM, Dalke C, Wang X, Lu L, Manly KF, Pretsch W, Favor J, Pardue MT, Rinchik EM, Williams RW, Goldowitz D, Graw J.

Mol Vis. 2005 Jul 27;11:569-81.

9.

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.

Invest Ophthalmol Vis Sci. 2004 Feb;45(2):601-9.

PMID:
14744904
10.

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

Felix K, Polack A, Pretsch W, Jackson SH, Feigenbaum L, Bornkamm GW, Janz S.

Cancer Res. 2004 Jan 15;64(2):530-7.

12.

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

Felix K, Rockwood LD, Pretsch W, Bornkamm GW, Janz S.

Free Radic Biol Med. 2003 Jan 15;34(2):226-32.

PMID:
12521604
13.

Moderate G6PD deficiency increases mutation rates in the brain of mice.

Felix K, Rockwood LD, Pretsch W, Nair J, Bartsch H, Bornkamm GW, Janz S.

Free Radic Biol Med. 2002 Apr 1;32(7):663-73.

PMID:
11909700
14.

A 76-bp deletion in the Mip gene causes autosomal dominant cataract in Hfi mice.

Sidjanin DJ, Parker-Wilson DM, Neuhäuser-Klaus A, Pretsch W, Favor J, Deen PM, Ohtaka-Maruyama C, Lu Y, Bragin A, Skach WR, Chepelinsky AB, Grimes PA, Stambolian DE.

Genomics. 2001 Jun 15;74(3):313-9.

PMID:
11414759
18.

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.

Genomics. 1998 Sep 1;52(2):152-8.

PMID:
9782080
19.

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

Pretsch W, Chatterjee B, Favor J, Merkle S, Sandulache R.

Mamm Genome. 1998 Feb;9(2):144-9.

PMID:
9457676
20.

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

Sidjanin DJ, Grimes PA, Pretsch W, Neuhäuser-Klaus A, Favor J, Stambolian DE.

Invest Ophthalmol Vis Sci. 1997 Nov;38(12):2502-7.

PMID:
9375568
21.
22.

The mouse Cat4 locus maps to chromosome 8 and mutants express lens-corneal adhesion.

Favor J, Grimes P, Neuhäuser-Klaus A, Pretsch W, Stambolian D.

Mamm Genome. 1997 Jun;8(6):403-6. Erratum in: Mamm Genome. 2008 May;19(5):378.

PMID:
9166583
23.

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

Pretsch W, Favor J.

Mamm Genome. 1997 Apr;8(4):296-7. No abstract available.

PMID:
9096122
24.

Genetic mapping of a mouse ocular malformation locus, Tcm, to chromosome 4.

Zhou E, Grimes P, Favor J, Koeberlein B, Pretsch W, Neuhauser-Klaus A, Sidjanin D, Stambolian D.

Mamm Genome. 1997 Mar;8(3):178-81.

PMID:
9069117
25.

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.

Favor J, Sandulache R, Neuhäuser-Klaus A, Pretsch W, Chatterjee B, Senft E, Wurst W, Blanquet V, Grimes P, Spörle R, Schughart K.

Proc Natl Acad Sci U S A. 1996 Nov 26;93(24):13870-5.

26.

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.

Mamm Genome. 1996 Nov;7(11):843-6. No abstract available.

PMID:
8875893
27.
28.

Purkinje cell lineage and the topographic organization of the cerebellar cortex: a view from X inactivation mosaics.

Baader SL, Schilling ML, Rosengarten B, Pretsch W, Teutsch HF, Oberdick J, Schilling K.

Dev Biol. 1996 Mar 15;174(2):393-406.

29.

Molecular analysis of four ENU induced triosephosphate isomerase null mutants in Mus musculus.

Zingg BC, Pretsch W, Mohrenweiser HW.

Mutat Res. 1995 May;328(2):163-73.

PMID:
7739600
30.

Molecular analysis of four lactate dehydrogenase-A mutants in the mouse.

Sandulache R, Pretsch W, Chatterjee B, Gimbel W, Graw J, Favor J.

Mamm Genome. 1994 Dec;5(12):777-80.

PMID:
7534515
31.

Close linkage of the dominant cataract mutations (Cat-2) with Idh-1 and cryge on mouse chromosome 1.

Löster J, Pretsch W, Sandulache R, Schmitt-John T, Lyon MF, Graw J.

Genomics. 1994 Sep 1;23(1):240-2.

PMID:
7829079
35.
37.

Characterization of two electrophoretic lactate dehydrogenase-A mutants in Mus musculus.

Merkle S, Pretsch W.

Biochem Genet. 1992 Feb;30(1-2):49-59.

PMID:
1520254
38.

The liver/erythrocyte pyruvate kinase gene complex [Pk-1] in the mouse: regulatory gene mutations.

Fitton LA, Davidson M, Moore KJ, Charles DJ, Pretsch W, Elston RC, Bulfield G.

Genet Res. 1991 Dec;58(3):233-41.

PMID:
1802805
39.

A mutation resulting in increased triosephosphate isomerase activity in Mus musculus.

Merkle S, Reitmeir P, Pretsch W.

Genet Res. 1991 Apr;57(2):139-45.

PMID:
2055457
40.

Tpi-1 and Gapd are linked very closely on mouse chromosome 6.

Pretsch W, Neuhäuser-Klaus A, Merkle S.

Genet Res. 1991 Feb;57(1):37-40.

PMID:
2040452
41.

Genetic localization and phenotypic expression of X-linked cataract (Xcat) in Mus musculus.

Favor J, Pretsch W.

Genet Res. 1990 Oct-Dec;56(2-3):157-62.

PMID:
2272505
42.
43.
46.

The localization of G6pd, glucose-6-phosphate dehydrogenase, and mdx, muscular dystrophy in the mouse X chromosome.

Peters J, Ball ST, Charles DJ, Pretsch W, Bulfield G, Miller D, Chapman VM.

Genet Res. 1988 Dec;52(3):195-201. No abstract available.

PMID:
3243423
47.

X-linked glucose-6-phosphate dehydrogenase deficiency in Mus musculus.

Pretsch W, Charles DJ, Merkle S.

Biochem Genet. 1988 Feb;26(1-2):89-103.

PMID:
3377761
48.

Mechanisms of compensation of hemolytic anemia in a lactate dehydrogenase mouse mutant.

Kremer JP, Datta T, Pretsch W, Charles DJ, Dörmer P.

Exp Hematol. 1987 Jul;15(6):664-70.

PMID:
3595765
49.
50.

Enzyme-activity mutations detected in mice after paternal fractionated irradiation.

Charles DJ, Pretsch W.

Mutat Res. 1986 May;160(3):243-8.

PMID:
3960038

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