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Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations.
Van Schil K, Naessens S, Van de Sompele S, Carron M, Aslanidis A, Van Cauwenbergh C, Kathrin Mayer A, Van Heetvelde M, Bauwens M, Verdin H, Coppieters F, Greenberg ME, Yang MG, Karlstetter M, Langmann T, De Preter K, Kohl S, Cherry TJ, Leroy BP; CNV Study Group; De Baere E. Van Schil K, et al. Among authors: langmann t. Genet Med. 2018 Feb;20(2):202-213. doi: 10.1038/gim.2017.97. Epub 2017 Jul 27. Genet Med. 2018. PMID: 28749477 Free PMC article.
Induction of STAP-1 promotes neurotoxic activation of microglia.
Stoecker K, Weigelt K, Ebert S, Karlstetter M, Walczak Y, Langmann T. Stoecker K, et al. Among authors: langmann t. Biochem Biophys Res Commun. 2009 Jan 30;379(1):121-6. doi: 10.1016/j.bbrc.2008.12.021. Epub 2008 Dec 17. Biochem Biophys Res Commun. 2009. PMID: 19100238
CRX ChIP-seq reveals the cis-regulatory architecture of mouse photoreceptors.
Corbo JC, Lawrence KA, Karlstetter M, Myers CA, Abdelaziz M, Dirkes W, Weigelt K, Seifert M, Benes V, Fritsche LG, Weber BH, Langmann T. Corbo JC, et al. Among authors: langmann t. Genome Res. 2010 Nov;20(11):1512-25. doi: 10.1101/gr.109405.110. Epub 2010 Aug 6. Genome Res. 2010. PMID: 20693478 Free PMC article.
Nonsense mutations in FAM161A cause RP28-associated recessive retinitis pigmentosa.
Langmann T, Di Gioia SA, Rau I, Stöhr H, Maksimovic NS, Corbo JC, Renner AB, Zrenner E, Kumaramanickavel G, Karlstetter M, Arsenijevic Y, Weber BH, Gal A, Rivolta C. Langmann T, et al. Am J Hum Genet. 2010 Sep 10;87(3):376-81. doi: 10.1016/j.ajhg.2010.07.018. Epub 2010 Aug 12. Am J Hum Genet. 2010. PMID: 20705278 Free PMC article.
[Immune mechanisms in retinal degeneration].
Karlstetter M, Langmann T. Karlstetter M, et al. Among authors: langmann t. Klin Monbl Augenheilkd. 2012 Mar;229(3):221-6. doi: 10.1055/s-0031-1282050. Epub 2012 Feb 1. Klin Monbl Augenheilkd. 2012. PMID: 22297848 Review. German.
190 results