Berger W - Search Results

1

Systemic gene therapy rescues retinal dysfunction and hearing loss in a model of Norrie disease.

Pauzuolyte V, Patel A, Wawrzynski JR, Ingham NJ, Leong YC, Karda R, Bitner-Glindzicz M, Berger W, Waddington SN, Steel KP, Sowden JC. Pauzuolyte V, et al. Among authors: berger w. EMBO Mol Med. 2023 Oct 11;15(10):e17393. doi: 10.15252/emmm.202317393. Epub 2023 Aug 29. EMBO Mol Med. 2023. PMID: 37642150 Free PMC article.

2

The timing of auditory sensory deficits in Norrie disease has implications for therapeutic intervention.

Bryant D, Pauzuolyte V, Ingham NJ, Patel A, Pagarkar W, Anderson LA, Smith KE, Moulding DA, Leong YC, Jafree DJ, Long DA, Al-Yassin A, Steel KP, Jagger DJ, Forge A, Berger W, Sowden JC, Bitner-Glindzicz M. Bryant D, et al. Among authors: berger w. JCI Insight. 2022 Feb 8;7(3):e148586. doi: 10.1172/jci.insight.148586. JCI Insight. 2022. PMID: 35132964 Free PMC article.

3

Fetal loss in homozygous mutant Norrie disease mice: a new role of Norrin in reproduction.

Luhmann UF, Meunier D, Shi W, Lüttges A, Pfarrer C, Fundele R, Berger W. Luhmann UF, et al. Among authors: berger w. Genesis. 2005 Aug;42(4):253-62. doi: 10.1002/gene.20141. Genesis. 2005. PMID: 16035034

4

Development of a genotyping microarray for Usher syndrome.

Cremers FP, Kimberling WJ, Külm M, de Brouwer AP, van Wijk E, te Brinke H, Cremers CW, Hoefsloot LH, Banfi S, Simonelli F, Fleischhauer JC, Berger W, Kelley PM, Haralambous E, Bitner-Glindzicz M, Webster AR, Saihan Z, De Baere E, Leroy BP, Silvestri G, McKay GJ, Koenekoop RK, Millan JM, Rosenberg T, Joensuu T, Sankila EM, Weil D, Weston MD, Wissinger B, Kremer H. Cremers FP, et al. Among authors: berger w. J Med Genet. 2007 Feb;44(2):153-60. doi: 10.1136/jmg.2006.044784. Epub 2006 Sep 8. J Med Genet. 2007. PMID: 16963483 Free PMC article.

5

Long-term consequences of developmental vascular defects on retinal vessel homeostasis and function in a mouse model of Norrie disease.

Beck SC, Feng Y, Sothilingam V, Garcia Garrido M, Tanimoto N, Acar N, Shan S, Seebauer B, Berger W, Hammes HP, Seeliger MW. Beck SC, et al. Among authors: berger w. PLoS One. 2017 Jun 2;12(6):e0178753. doi: 10.1371/journal.pone.0178753. eCollection 2017. PLoS One. 2017. PMID: 28575130 Free PMC article.

6

An animal model for Norrie disease (ND): gene targeting of the mouse ND gene.

Berger W, van de Pol D, Bächner D, Oerlemans F, Winkens H, Hameister H, Wieringa B, Hendriks W, Ropers HH. Berger W, et al. Hum Mol Genet. 1996 Jan;5(1):51-9. doi: 10.1093/hmg/5.1.51. Hum Mol Genet. 1996. PMID: 8789439 Free article.

7

Differential gene expression in Ndph-knockout mice in retinal development.

Schäfer NF, Luhmann UF, Feil S, Berger W. Schäfer NF, et al. Among authors: berger w. Invest Ophthalmol Vis Sci. 2009 Feb;50(2):906-16. doi: 10.1167/iovs.08-1731. Epub 2008 Oct 31. Invest Ophthalmol Vis Sci. 2009. PMID: 18978344 Free article.

8

Norrin stimulates cell proliferation in the superficial retinal vascular plexus and is pivotal for the recruitment of mural cells.

Zuercher J, Fritzsche M, Feil S, Mohn L, Berger W. Zuercher J, et al. Among authors: berger w. Hum Mol Genet. 2012 Jun 15;21(12):2619-30. doi: 10.1093/hmg/dds087. Epub 2012 Mar 6. Hum Mol Genet. 2012. PMID: 22394677 Free article.

9

Isolation of a candidate gene for Norrie disease by positional cloning.

Berger W, Meindl A, van de Pol TJ, Cremers FP, Ropers HH, Döerner C, Monaco A, Bergen AA, Lebo R, Warburg M, et al. Berger W, et al. Nat Genet. 1992 Jun;1(3):199-203. doi: 10.1038/ng0692-199. Nat Genet. 1992. PMID: 1303235

10

Mutations in the candidate gene for Norrie disease.

Berger W, van de Pol D, Warburg M, Gal A, Bleeker-Wagemakers L, de Silva H, Meindl A, Meitinger T, Cremers F, Ropers HH. Berger W, et al. Hum Mol Genet. 1992 Oct;1(7):461-5. doi: 10.1093/hmg/1.7.461. Hum Mol Genet. 1992. PMID: 1307245 Review.

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