Riess O - Search Results

1

Gene expression changes in a transgenic mouse model overexpressing human wildtype and mutant torsinA.

Grundmann K, Hübener J, Häbig K, Reischmann B, Poths S, Hauser TK, Magg J, Riess O, Bonin M, Nguyen HP. Grundmann K, et al. Among authors: riess o. Proteomics Clin Appl. 2008 May;2(5):720-36. doi: 10.1002/prca.200780053. Proteomics Clin Appl. 2008. PMID: 21136869

2

Transgenic rat model of Huntington's disease.

von Hörsten S, Schmitt I, Nguyen HP, Holzmann C, Schmidt T, Walther T, Bader M, Pabst R, Kobbe P, Krotova J, Stiller D, Kask A, Vaarmann A, Rathke-Hartlieb S, Schulz JB, Grasshoff U, Bauer I, Vieira-Saecker AM, Paul M, Jones L, Lindenberg KS, Landwehrmeyer B, Bauer A, Li XJ, Riess O. von Hörsten S, et al. Among authors: riess o. Hum Mol Genet. 2003 Mar 15;12(6):617-24. doi: 10.1093/hmg/ddg075. Hum Mol Genet. 2003. PMID: 12620967

3

Frequency and phenotypic variability of the GAG deletion of the DYT1 gene in an unselected group of patients with dystonia.

Grundmann K, Laubis-Herrmann U, Bauer I, Dressler D, Vollmer-Haase J, Bauer P, Stuhrmann M, Schulte T, Schöls L, Topka H, Riess O. Grundmann K, et al. Among authors: riess o. Arch Neurol. 2003 Sep;60(9):1266-70. doi: 10.1001/archneur.60.9.1266. Arch Neurol. 2003. PMID: 12975293

4

Lack of mutations in the epsilon-sarcoglycan gene in patients with different subtypes of primary dystonias.

Grundmann K, Laubis-Herrmann U, Dressler D, Vollmer-Haase J, Bauer P, Stuhrmann M, Schulte T, Schöls L, Topka H, Riess O. Grundmann K, et al. Among authors: riess o. Mov Disord. 2004 Nov;19(11):1294-7. doi: 10.1002/mds.20128. Mov Disord. 2004. PMID: 15390016

5

Mutation at the SCA17 locus is not a common cause of primary dystonia.

Grundmann K, Laubis-Herrmann U, Dressler D, Vollmer-Haase J, Bauer P, Stuhrmann M, Schulte T, Schöls L, Topka H, Riess O. Grundmann K, et al. Among authors: riess o. J Neurol. 2004 Oct;251(10):1232-4. doi: 10.1007/s00415-004-0520-2. J Neurol. 2004. PMID: 15503103

6

A rapid microarray based whole genome analysis for detection of uniparental disomy.

Altug-Teber O, Dufke A, Poths S, Mau-Holzmann UA, Bastepe M, Colleaux L, Cormier-Daire V, Eggermann T, Gillessen-Kaesbach G, Bonin M, Riess O. Altug-Teber O, et al. Among authors: riess o. Hum Mutat. 2005 Aug;26(2):153-9. doi: 10.1002/humu.20198. Hum Mutat. 2005. PMID: 15968682

7

Progression-specific genes identified by expression profiling of matched ductal carcinomas in situ and invasive breast tumors, combining laser capture microdissection and oligonucleotide microarray analysis.

Schuetz CS, Bonin M, Clare SE, Nieselt K, Sotlar K, Walter M, Fehm T, Solomayer E, Riess O, Wallwiener D, Kurek R, Neubauer HJ. Schuetz CS, et al. Among authors: riess o. Cancer Res. 2006 May 15;66(10):5278-86. doi: 10.1158/0008-5472.CAN-05-4610. Cancer Res. 2006. PMID: 16707453

8

Behavioral abnormalities precede neuropathological markers in rats transgenic for Huntington's disease.

Nguyen HP, Kobbe P, Rahne H, Wörpel T, Jäger B, Stephan M, Pabst R, Holzmann C, Riess O, Korr H, Kántor O, Petrasch-Parwez E, Wetzel R, Osmand A, von Hörsten S. Nguyen HP, et al. Among authors: riess o. Hum Mol Genet. 2006 Nov 1;15(21):3177-94. doi: 10.1093/hmg/ddl394. Epub 2006 Sep 19. Hum Mol Genet. 2006. PMID: 16984963

9

Whole genome expression analyses of single- and double-knock-out mice implicate partially overlapping functions of alpha- and gamma-synuclein.

Kuhn M, Haebig K, Bonin M, Ninkina N, Buchman VL, Poths S, Riess O. Kuhn M, et al. Among authors: riess o. Neurogenetics. 2007 Apr;8(2):71-81. doi: 10.1007/s10048-007-0079-z. Epub 2007 Feb 22. Neurogenetics. 2007. PMID: 17318638 Free PMC article.

10

Nuclear localization of ataxin-3 is required for the manifestation of symptoms in SCA3: in vivo evidence.

Bichelmeier U, Schmidt T, Hübener J, Boy J, Rüttiger L, Häbig K, Poths S, Bonin M, Knipper M, Schmidt WJ, Wilbertz J, Wolburg H, Laccone F, Riess O. Bichelmeier U, et al. Among authors: riess o. J Neurosci. 2007 Jul 11;27(28):7418-28. doi: 10.1523/JNEUROSCI.4540-06.2007. J Neurosci. 2007. PMID: 17626202 Free PMC article.

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