Löster J - Search Results

1

Mutually regulated expression of Pax6 and Six3 and its implications for the Pax6 haploinsufficient lens phenotype.

Goudreau G, Petrou P, Reneker LW, Graw J, Löster J, Gruss P. Goudreau G, et al. Among authors: loster j. Proc Natl Acad Sci U S A. 2002 Jun 25;99(13):8719-24. doi: 10.1073/pnas.132195699. Epub 2002 Jun 18. Proc Natl Acad Sci U S A. 2002. PMID: 12072567 Free PMC article.

2

Developmental genetics in ophthalmology.

Graw J, Löster J. Graw J, et al. Among authors: loster j. Ophthalmic Genet. 2003 Mar;24(1):1-33. doi: 10.1076/opge.24.1.1.13888. Ophthalmic Genet. 2003. PMID: 12660863 Review.

3

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: loster j. Invest Ophthalmol Vis Sci. 2005 Dec;46(12):4671-83. doi: 10.1167/iovs.04-1407. Invest Ophthalmol Vis Sci. 2005. PMID: 16303964

4

Aphakia (ak), a mouse mutation affecting early eye development: fine mapping, consideration of candidate genes and altered Pax6 and Six3 gene expression pattern.

Grimm C, Chatterjee B, Favor J, Immervoll T, Löster J, Klopp N, Sandulache R, Graw J. Grimm C, et al. Among authors: loster j. Dev Genet. 1998;23(4):299-316. doi: 10.1002/(SICI)1520-6408(1998)23:4<299::AID-DVG5>3.0.CO;2-G. Dev Genet. 1998. PMID: 9883582

5

Crygf(Rop): the first mutation in the Crygf gene causing a unique radial lens opacity.

Graw J, Klopp N, Neuhäuser-Klaus A, Favor J, Löster J. Graw J, et al. Among authors: loster j. Invest Ophthalmol Vis Sci. 2002 Sep;43(9):2998-3002. Invest Ophthalmol Vis Sci. 2002. PMID: 12202521

6

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: loster j. Genetics. 2003 Jul;164(3):1035-41. doi: 10.1093/genetics/164.3.1035. Genetics. 2003. PMID: 12871913 Free PMC article.

7

Characterization of a 1-bp deletion in the gammaE-crystallin gene leading to a nuclear and zonular cataract in the mouse.

Klopp N, Löster J, Graw J. Klopp N, et al. Among authors: loster j. Invest Ophthalmol Vis Sci. 2001 Jan;42(1):183-7. Invest Ophthalmol Vis Sci. 2001. PMID: 11133865

8

Mutation in a novel connexin-like gene (Gjf1) in the mouse affects early lens development and causes a variable small-eye phenotype.

Puk O, Löster J, Dalke C, Soewarto D, Fuchs H, Budde B, Nürnberg P, Wolf E, de Angelis MH, Graw J. Puk O, et al. Among authors: loster j. Invest Ophthalmol Vis Sci. 2008 Apr;49(4):1525-32. doi: 10.1167/iovs.07-1033. Invest Ophthalmol Vis Sci. 2008. PMID: 18385072

9

A 6-bp deletion in the Crygc gene leading to a nuclear and radial cataract in the mouse.

Graw J, Neuhäuser-Klaus A, Löster J, Favor J. Graw J, et al. Among authors: loster j. Invest Ophthalmol Vis Sci. 2002 Jan;43(1):236-40. Invest Ophthalmol Vis Sci. 2002. PMID: 11773036

10

A new Fgf10 mutation in the mouse leads to atrophy of the harderian gland and slit-eye phenotype in heterozygotes: a novel model for dry-eye disease?

Puk O, Esposito I, Söker T, Löster J, Budde B, Nürnberg P, Michel-Soewarto D, Fuchs H, Wolf E, Hrabé de Angelis M, Graw J. Puk O, et al. Among authors: loster j. Invest Ophthalmol Vis Sci. 2009 Sep;50(9):4311-8. doi: 10.1167/iovs.09-3451. Epub 2009 Apr 30. Invest Ophthalmol Vis Sci. 2009. PMID: 19407009

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