ENDE

Veröffentlichungen

  1. Hauck SM, von Toerne C, Ueffing M (2014). The neuroprotective potential of retinal Müller glial cells. Advances in Experimental and Medicinal Biology 801:381-7.
  2. Kucharska J, Río PD, Arango-Gonzalez B, Gorza M, Feuchtinger A, Hauck SM, Ueffing M (2014). Cyr61 activates retinal cells and prolongs photoreceptor survival in rd1 mouse model of retinitis pigmentosa. Journal of Neurochemistry Mar 4. doi: 10.1111/jnc.12704. [Epub] [pdf]
  3. Bauss K, Knapp B, Jores P, Roepman R, Kremer H, v. Wijk E, Maerker T, Wolfrum U (2014). Phosphorylation of the Usher syndrome protein SANS controls Magi2-mediated endocytosis. Hum Mol Genet, doi: 10.1093/hmg/ddu104. [pdf]
  4. Arango-Gonzalez B, Leitritz MA, Fischer D, Gerberding M, Paquet-Durand F, Ueffing M (2014) Therapieansätze für Erbliche Netzhauterkrankungen: Von den Genen bis zum Chip [Current therapeutic approaches in inherited retinal degeneration: from genes to chip]. Klinische Monatsblätter für Augenheilkunde 231(3): 222-31. [pdf]
  5. Wahl V, Vogler S, Grosche A, Pannicke T, Ueffing M, Wiedemann P, Reichenbach A, Hauck SM and Bringmann A (2013). Osteopontin Inhibits Osmotic Swelling of Retinal Glial (Müller) Cells by Inducing Release of VEGF. Neuroscience. 246:59-72. [pdf]
  6. Roosing S, Rohrschneider K, Beryozkin A, Sharon D, Weisschuh N, Staller J, Kohl S, Zelinger L, Peters TA, Neveling K, Strom TM; European Retinal Disease Consortium, van den Born LI, Hoyng CB, Klaver CC, Roepman R, Wissinger B, Banin E, Cremers FP, den Hollander AI (2013). Mutations in RAB28, Encoding a Farnesylated Small GTPase, Are Associated with Autosomal-Recessive Cone-Rod Dystrophy. Am J Hum Genet. 93(1):110-7. [pdf]
  7. Glöckle N, Kohl S, Mohr J, Scheurenbrand T, Sprecher A, Weisschuh N, Bernd A, Rudolph G, Schubach M, Poloschek C, Zrenner E, Biskup S, Berger W, Wissinger B, Neidhardt J (2013). Panel-based Next Generation Sequencing as a reliable and efficient technique to detect mutations in unselected patients with retinal dystrophies. Eur J Hum Genet 2013 Apr 17. doi: 10.1038/ejhg.2013.72. [Epub ahead of print]. [pdf]
  8. Pach J, Kohl S, Gekeler F, Zobor D (2013). Identification of a novel mutation in the PRCD gene causing autosomal recessive retinitis pigmentosa in a Turkish family. Mol Vis. 19:1350-5. [pdf]
  9. Fischer MD, Goldmann T, Wallrapp C, Mühlfriedel R, Beck SC, Stern-Schneider G, Ueffing M, Wolfrum U, Seeliger MW (2013). Successful subretinal delivery and monitoring of MicroBeads in mice". PLoS One. 8(1):e55173. [pdf]
  10. Merl J, Ueffing M, Hauck SM, von Toerne C (2012). Direct comparison of MS-based label-free and SILAC quantitative proteome profiling strategies in primary retinal Müller cells. Proteomics. 12:1902-11. [pdf]
  11. Prokofyeva E, Zrenner E (2012). Epidemiology of major eye diseases leading to blindness in Europe: a literature review. Ophthalmic Res. 47(4):171-88. [pdf]
  12. Prokofyeva E, Troeger E, Bernd A, Zrenner E (2012). Visual acuity changes in cone and cone-rod dystrophies. Ophthal Physiol Opt. 32:53-59. [pdf]
  13. Prokofyeva E, Troeger E, Zrenner E (2012). The Special Electrophysiological Signs of Inherited Retinal Dystrophies. Open Ophthalmol J. 6:86-97. [pdf]
  14. Kellner U, Renner AB, Herbst SM, Kellner S, Weinitz S, Weber BH (2012). Hereditäre Netzhautdystrophien. Klin Monatsbl Augenheilkd. 229:171-196. [pdf]
  15. Schatz A, Wilke R, Strasser T, Gekeler F, Messias A, Zrenner E (2012). Assessment of "non-recordable" electroretinograms by 9 Hz flicker stimulation under scotopic conditions. Doc Ophthalmol. 124(1):27-39. [pdf]
  16. Schroeder C, Stutzmann F, Weber BH, Riess O, Bonin M (2012). High-throughput resequencing in the diagnosis of BRCA1/2 mutations using oligonucleotide resequencing microarrays. Breast Cancer Res Treat. 122:287-97. [pdf]
  17. Sliesoraityte I, Troeger E, Bernd A, Kurtenbach A, Zrenner E (2012). Correlation between spectral domain OCT retinal nerve fibre layer thickness and multifocal pattern electroretinogram in advanced retinitis pigmentosa. Adv Exp Med Biol. 723:471-8. [pdf]
  18. Schatz A, Willmann G, Enderle H, Sliesoraityte I, Messias A, Bartz-Schmidt KU, Zrenner E, Gekeler F (2011). A new DTL-electrode holder for recording of electroretinograms in animals. J Neurosci Methods. 195(2):128-34. [pdf]
  19. Del Río P, Irmler M, Arango-González B, Favor J, Bobe C, Bartsch U, Vecino E, Beckers J, Hauck SM, Ueffing M (2011). GDNF-induced osteopontin from Müller glial cells promotes photoreceptor survival in the Pde6brd1 mouse model of retinal degeneration. Glia. 59:821-32. [pdf]
  20. Schimpf-Linzenbold S, Balendran S, Wissinger B (2010). Biased allelic expression in retinal expressed genes. Cold Spring Harbor Meeting: Systems Biology - Global Regulation of Gene Expression; 23.-27.03.2010, Cold Spring Harbor, USA [pdf]
  21. Troeger E, Sliesoraityte I, Charbel Issa P, Scholl HN, Zrenner E, Wilke R (2010). An integrated software solution for multi-modal mapping of morphological and functional ocular data. Conf Proc IEEE Eng Med Biol Soc. 2010: 6280-3. [pdf]
  22. Kellner U, Kellner S, Renner AB, Fiebig BS, Weinitz S, Weber BH (2009). Evidence-based diagnostic approach to inherited retinal dystrophies. Klin Monbl Augenheilkd. 226:999-1011. [pdf]