Schlötzer-Schrehardt U - Search Results

1

Human Cytomegalovirus Nuclear Capsids Associate with the Core Nuclear Egress Complex and the Viral Protein Kinase pUL97.

Milbradt J, Sonntag E, Wagner S, Strojan H, Wangen C, Lenac Rovis T, Lisnic B, Jonjic S, Sticht H, Britt WJ, Schlötzer-Schrehardt U, Marschall M. Milbradt J, et al. Viruses. 2018 Jan 13;10(1):35. doi: 10.3390/v10010035. Viruses. 2018. PMID: 29342872 Free PMC article.

2

Phenotypical Characterization of the Nuclear Egress of Recombinant Cytomegaloviruses Reveals Defective Replication upon ORF-UL50 Deletion but Not pUL50 Phosphosite Mutation.

Häge S, Sonntag E, Svrlanska A, Borst EM, Stilp AC, Horsch D, Müller R, Kropff B, Milbradt J, Stamminger T, Schlötzer-Schrehardt U, Marschall M. Häge S, et al. Viruses. 2021 Jan 22;13(2):165. doi: 10.3390/v13020165. Viruses. 2021. PMID: 33499341 Free PMC article.

3

The Complex Regulatory Role of Cytomegalovirus Nuclear Egress Protein pUL50 in the Production of Infectious Virus.

Häge S, Büscher N, Pakulska V, Hahn F, Adrait A, Krauter S, Borst EM, Schlötzer-Schrehardt U, Couté Y, Plachter B, Marschall M. Häge S, et al. Cells. 2021 Nov 11;10(11):3119. doi: 10.3390/cells10113119. Cells. 2021. PMID: 34831342 Free PMC article.

4

Variants in ASB10 are associated with open-angle glaucoma.

Pasutto F, Keller KE, Weisschuh N, Sticht H, Samples JR, Yang YF, Zenkel M, Schlötzer-Schrehardt U, Mardin CY, Frezzotti P, Edmunds B, Kramer PL, Gramer E, Reis A, Acott TS, Wirtz MK. Pasutto F, et al. Hum Mol Genet. 2012 Mar 15;21(6):1336-49. doi: 10.1093/hmg/ddr572. Epub 2011 Dec 8. Hum Mol Genet. 2012. PMID: 22156576 Free PMC article.

5

Gene dosage-dependent rescue of HSP neurite defects in SPG4 patients' neurons.

Havlicek S, Kohl Z, Mishra HK, Prots I, Eberhardt E, Denguir N, Wend H, Plötz S, Boyer L, Marchetto MC, Aigner S, Sticht H, Groemer TW, Hehr U, Lampert A, Schlötzer-Schrehardt U, Winkler J, Gage FH, Winner B. Havlicek S, et al. Hum Mol Genet. 2014 May 15;23(10):2527-41. doi: 10.1093/hmg/ddt644. Epub 2013 Dec 30. Hum Mol Genet. 2014. PMID: 24381312 Free PMC article.

6

Whole exome sequencing reveals a novel de novo FOXC1 mutation in a patient with unrecognized Axenfeld-Rieger syndrome and glaucoma.

Pasutto F, Mauri L, Popp B, Sticht H, Ekici A, Piozzi E, Bonfante A, Penco S, Schlötzer-Schrehardt U, Reis A. Pasutto F, et al. Gene. 2015 Aug 15;568(1):76-80. doi: 10.1016/j.gene.2015.05.015. Epub 2015 May 9. Gene. 2015. PMID: 25967385

7

Immunohistochemical identification of kynurenine aminotransferases in corpora amylacea in the human retina and optic nerve.

Rejdak R, Rummelt C, Zrenner E, Grieb P, Zarnowski T, Okuno E, Schlötzer-Schrehardt U, Naumann GO, Kruse F, Jünemann AG. Rejdak R, et al. Folia Neuropathol. 2007;45(2):66-71. Folia Neuropathol. 2007. PMID: 17594596 Free article.

8

Expression and regulation of LOXL1 and elastin-related genes in eyes with exfoliation syndrome.

Zenkel M, Schlötzer-Schrehardt U. Zenkel M, et al. J Glaucoma. 2014 Oct-Nov;23(8 Suppl 1):S48-50. doi: 10.1097/IJG.0000000000000120. J Glaucoma. 2014. PMID: 25275906 Review.

9

Characterization of the cleavage plane in DESCemet's membrane endothelial keratoplasty.

Schlötzer-Schrehardt U, Bachmann BO, Laaser K, Cursiefen C, Kruse FE. Schlötzer-Schrehardt U, et al. Ophthalmology. 2011 Oct;118(10):1950-7. doi: 10.1016/j.ophtha.2011.03.025. Epub 2011 Jun 25. Ophthalmology. 2011. PMID: 21705086

10

LOXL1 deficiency in the lamina cribrosa as candidate susceptibility factor for a pseudoexfoliation-specific risk of glaucoma.

Schlötzer-Schrehardt U, Hammer CM, Krysta AW, Hofmann-Rummelt C, Pasutto F, Sasaki T, Kruse FE, Zenkel M. Schlötzer-Schrehardt U, et al. Ophthalmology. 2012 Sep;119(9):1832-43. doi: 10.1016/j.ophtha.2012.03.015. Epub 2012 May 24. Ophthalmology. 2012. PMID: 22633114

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