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Electrophysiological deficits in the retina of the DBA/2J mouse.
Harazny J, Scholz M, Buder T, Lausen B, Kremers J. Harazny J, et al. Among authors: kremers j. Doc Ophthalmol. 2009 Dec;119(3):181-97. doi: 10.1007/s10633-009-9194-5. Epub 2009 Sep 17. Doc Ophthalmol. 2009. PMID: 19760280
Ccdc66 null mutation causes retinal degeneration and dysfunction.
Gerding WM, Schreiber S, Schulte-Middelmann T, de Castro Marques A, Atorf J, Akkad DA, Dekomien G, Kremers J, Dermietzel R, Gal A, Rülicke T, Ibrahim S, Epplen JT, Petrasch-Parwez E. Gerding WM, et al. Among authors: kremers j. Hum Mol Genet. 2011 Sep 15;20(18):3620-31. doi: 10.1093/hmg/ddr282. Epub 2011 Jun 16. Hum Mol Genet. 2011. PMID: 21680557
Identification and immunocytochemical characterization of Piccolino, a novel Piccolo splice variant selectively expressed at sensory ribbon synapses of the eye and ear.
Regus-Leidig H, Ott C, Löhner M, Atorf J, Fuchs M, Sedmak T, Kremers J, Fejtová A, Gundelfinger ED, Brandstätter JH. Regus-Leidig H, et al. Among authors: kremers j. PLoS One. 2013 Aug 6;8(8):e70373. doi: 10.1371/journal.pone.0070373. Print 2013. PLoS One. 2013. PMID: 23936420 Free PMC article.
188 results