Langmann T - Search Results

1

Autosomal recessive retinitis pigmentosa with homozygous rhodopsin mutation E150K and non-coding cis-regulatory variants in CRX-binding regions of SAMD7.

Van Schil K, Karlstetter M, Aslanidis A, Dannhausen K, Azam M, Qamar R, Leroy BP, Depasse F, Langmann T, De Baere E. Van Schil K, et al. Among authors: langmann t. Sci Rep. 2016 Feb 18;6:21307. doi: 10.1038/srep21307. Sci Rep. 2016. PMID: 26887858 Free PMC article.

2

Retinal expression of the X-linked juvenile retinoschisis (RS1) gene is controlled by an upstream CpG island and two opposing CRX-bound regions.

Kraus D, Karlstetter M, Walczak Y, Hilfinger D, Langmann T, Weber BH. Kraus D, et al. Among authors: langmann t. Biochim Biophys Acta. 2011 Apr-Jun;1809(4-6):245-54. doi: 10.1016/j.bbagrm.2011.03.001. Epub 2011 Mar 23. Biochim Biophys Acta. 2011. PMID: 21392589

3

Sterile alpha motif containing 7 (samd7) is a novel crx-regulated transcriptional repressor in the retina.

Hlawatsch J, Karlstetter M, Aslanidis A, Lückoff A, Walczak Y, Plank M, Böck J, Langmann T. Hlawatsch J, et al. Among authors: langmann t. PLoS One. 2013;8(4):e60633. doi: 10.1371/journal.pone.0060633. Epub 2013 Apr 2. PLoS One. 2013. PMID: 23565263 Free PMC article.

4

RETINA-specific expression of Kcnv2 is controlled by cone-rod homeobox (Crx) and neural retina leucine zipper (Nrl).

Aslanidis A, Karlstetter M, Walczak Y, Jägle H, Langmann T. Aslanidis A, et al. Among authors: langmann t. Adv Exp Med Biol. 2014;801:31-41. doi: 10.1007/978-1-4614-3209-8_5. Adv Exp Med Biol. 2014. PMID: 24664678

5

Early-onset autosomal recessive cerebellar ataxia associated with retinal dystrophy: new human hotfoot phenotype caused by homozygous GRID2 deletion.

Van Schil K, Meire F, Karlstetter M, Bauwens M, Verdin H, Coppieters F, Scheiffert E, Van Nechel C, Langmann T, Deconinck N, De Baere E. Van Schil K, et al. Among authors: langmann t. Genet Med. 2015 Apr;17(4):291-9. doi: 10.1038/gim.2014.95. Epub 2014 Aug 14. Genet Med. 2015. PMID: 25122145 Free article.

6

Cystoid edema, neovascularization and inflammatory processes in the murine Norrin-deficient retina.

Beck SC, Karlstetter M, Garcia Garrido M, Feng Y, Dannhausen K, Mühlfriedel R, Sothilingam V, Seebauer B, Berger W, Hammes HP, Seeliger MW, Langmann T. Beck SC, et al. Among authors: langmann t. Sci Rep. 2018 Apr 13;8(1):5970. doi: 10.1038/s41598-018-24476-y. Sci Rep. 2018. PMID: 29654250 Free PMC article.

7

Isolated and Syndromic Retinal Dystrophy Caused by Biallelic Mutations in RCBTB1, a Gene Implicated in Ubiquitination.

Coppieters F, Ascari G, Dannhausen K, Nikopoulos K, Peelman F, Karlstetter M, Xu M, Brachet C, Meunier I, Tsilimbaris MK, Tsika C, Blazaki SV, Vergult S, Farinelli P, Van Laethem T, Bauwens M, De Bruyne M, Chen R, Langmann T, Sui R, Meire F, Rivolta C, Hamel CP, Leroy BP, De Baere E. Coppieters F, et al. Among authors: langmann t. Am J Hum Genet. 2016 Aug 4;99(2):470-80. doi: 10.1016/j.ajhg.2016.06.017. Am J Hum Genet. 2016. PMID: 27486781 Free PMC article.

8

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.

9

Crocin, a plant-derived carotenoid, modulates microglial reactivity.

Yorgun MA, Rashid K, Aslanidis A, Bresgen C, Dannhausen K, Langmann T. Yorgun MA, et al. Among authors: langmann t. Biochem Biophys Rep. 2017 Oct 2;12:245-250. doi: 10.1016/j.bbrep.2017.09.007. eCollection 2017 Dec. Biochem Biophys Rep. 2017. PMID: 29214225 Free PMC article.

10

Microglia Analysis in Retinal Degeneration Mouse Models.

Dannhausen K, Rashid K, Langmann T. Dannhausen K, et al. Among authors: langmann t. Methods Mol Biol. 2018;1753:159-166. doi: 10.1007/978-1-4939-7720-8_10. Methods Mol Biol. 2018. PMID: 29564787

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