Berger W - Search Results

1

Identification and Characterization of ATOH7-Regulated Target Genes and Pathways in Human Neuroretinal Development.

Atac D, Maggi K, Feil S, Maggi J, Cuevas E, Sowden JC, Koller S, Berger W. Atac D, et al. Among authors: berger w. Cells. 2024 Jul 3;13(13):1142. doi: 10.3390/cells13131142. Cells. 2024. PMID: 38994994 Free PMC article.

2

Global gene expression analysis in a mouse model for Norrie disease: late involvement of photoreceptor cells.

Lenzner S, Prietz S, Feil S, Nuber UA, Ropers HH, Berger W. Lenzner S, et al. Among authors: berger w. Invest Ophthalmol Vis Sci. 2002 Sep;43(9):2825-33. Invest Ophthalmol Vis Sci. 2002. PMID: 12202498

3

NYX (nyctalopin on chromosome X), the gene mutated in congenital stationary night blindness, encodes a cell surface protein.

Zeitz C, Scherthan H, Freier S, Feil S, Suckow V, Schweiger S, Berger W. Zeitz C, et al. Among authors: berger w. Invest Ophthalmol Vis Sci. 2003 Oct;44(10):4184-91. doi: 10.1167/iovs.03-0251. Invest Ophthalmol Vis Sci. 2003. PMID: 14507859 Free article.

4

Novel mutations in CACNA1F and NYX in Dutch families with X-linked congenital stationary night blindness.

Zeitz C, Minotti R, Feil S, Mátyás G, Cremers FP, Hoyng CB, Berger W. Zeitz C, et al. Among authors: berger w. Mol Vis. 2005 Mar 2;11:179-83. Mol Vis. 2005. PMID: 15761389 Free article.

5

Role of the Norrie disease pseudoglioma gene in sprouting angiogenesis during development of the retinal vasculature.

Luhmann UF, Lin J, Acar N, Lammel S, Feil S, Grimm C, Seeliger MW, Hammes HP, Berger W. Luhmann UF, et al. Among authors: berger w. Invest Ophthalmol Vis Sci. 2005 Sep;46(9):3372-82. doi: 10.1167/iovs.05-0174. Invest Ophthalmol Vis Sci. 2005. PMID: 16123442

6

Structural and functional abnormalities of retinal ribbon synapses due to Cacna2d4 mutation.

Wycisk KA, Budde B, Feil S, Skosyrski S, Buzzi F, Neidhardt J, Glaus E, Nürnberg P, Ruether K, Berger W. Wycisk KA, et al. Among authors: berger w. Invest Ophthalmol Vis Sci. 2006 Aug;47(8):3523-30. doi: 10.1167/iovs.06-0271. Invest Ophthalmol Vis Sci. 2006. PMID: 16877424

7

Mutation in the auxiliary calcium-channel subunit CACNA2D4 causes autosomal recessive cone dystrophy.

Wycisk KA, Zeitz C, Feil S, Wittmer M, Forster U, Neidhardt J, Wissinger B, Zrenner E, Wilke R, Kohl S, Berger W. Wycisk KA, et al. Among authors: berger w. Am J Hum Genet. 2006 Nov;79(5):973-7. doi: 10.1086/508944. Epub 2006 Sep 27. Am J Hum Genet. 2006. PMID: 17033974 Free PMC article.

8

Night blindness-associated mutations in the ligand-binding, cysteine-rich, and intracellular domains of the metabotropic glutamate receptor 6 abolish protein trafficking.

Zeitz C, Forster U, Neidhardt J, Feil S, Kälin S, Leifert D, Flor PJ, Berger W. Zeitz C, et al. Among authors: berger w. Hum Mutat. 2007 Aug;28(8):771-80. doi: 10.1002/humu.20499. Hum Mutat. 2007. PMID: 17405131

9

Vascular changes in the cerebellum of Norrin /Ndph knockout mice correlate with high expression of Norrin and Frizzled-4.

Luhmann UF, Neidhardt J, Kloeckener-Gruissem B, Schäfer NF, Glaus E, Feil S, Berger W. Luhmann UF, et al. Among authors: berger w. Eur J Neurosci. 2008 May;27(10):2619-28. doi: 10.1111/j.1460-9568.2008.06237.x. Eur J Neurosci. 2008. PMID: 18547247 Free article.

10

Overexpression of RPGR leads to male infertility in mice due to defects in flagellar assembly.

Brunner S, Colman D, Travis AJ, Luhmann UF, Shi W, Feil S, Imsand C, Nelson J, Grimm C, Rülicke T, Fundele R, Neidhardt J, Berger W. Brunner S, et al. Among authors: berger w. Biol Reprod. 2008 Oct;79(4):608-17. doi: 10.1095/biolreprod.107.067454. Epub 2008 Jun 25. Biol Reprod. 2008. PMID: 18579752

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