Riess O - Search Results

1

Expression mapping of tetracycline-responsive prion protein promoter: digital atlasing for generating cell-specific disease models.

Boy J, Leergaard TB, Schmidt T, Odeh F, Bichelmeier U, Nuber S, Holzmann C, Wree A, Prusiner SB, Bujard H, Riess O, Bjaalie JG. Boy J, et al. Among authors: riess o. Neuroimage. 2006 Nov 1;33(2):449-62. doi: 10.1016/j.neuroimage.2006.05.055. Epub 2006 Aug 23. Neuroimage. 2006. PMID: 16931059

2

Protein surveillance machinery in brains with spinocerebellar ataxia type 3: redistribution and differential recruitment of 26S proteasome subunits and chaperones to neuronal intranuclear inclusions.

Schmidt T, Lindenberg KS, Krebs A, Schöls L, Laccone F, Herms J, Rechsteiner M, Riess O, Landwehrmeyer GB. Schmidt T, et al. Among authors: riess o. Ann Neurol. 2002 Mar;51(3):302-10. doi: 10.1002/ana.10101. Ann Neurol. 2002. PMID: 11891825

3

Neurofilament L gene is not a genetic factor of sporadic and familial Parkinson's disease.

Rahner N, Holzmann C, Krüger R, Schöls L, Berger K, Riess O. Rahner N, et al. Among authors: riess o. Brain Res. 2002 Sep 27;951(1):82-6. doi: 10.1016/s0006-8993(02)03138-4. Brain Res. 2002. PMID: 12231460

4

14-3-3 protein is a component of Lewy bodies in Parkinson's disease-mutation analysis and association studies of 14-3-3 eta.

Ubl A, Berg D, Holzmann C, Krüger R, Berger K, Arzberger T, Bornemann A, Riess O. Ubl A, et al. Among authors: riess o. Brain Res Mol Brain Res. 2002 Dec;108(1-2):33-9. doi: 10.1016/s0169-328x(02)00510-7. Brain Res Mol Brain Res. 2002. PMID: 12480176

5

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

6

Identification and functional characterization of a novel R621C mutation in the synphilin-1 gene in Parkinson's disease.

Marx FP, Holzmann C, Strauss KM, Li L, Eberhardt O, Gerhardt E, Cookson MR, Hernandez D, Farrer MJ, Kachergus J, Engelender S, Ross CA, Berger K, Schöls L, Schulz JB, Riess O, Krüger R. Marx FP, et al. Among authors: riess o. Hum Mol Genet. 2003 Jun 1;12(11):1223-31. doi: 10.1093/hmg/ddg134. Hum Mol Genet. 2003. PMID: 12761037

7

14-3-3 proteins in the nervous system.

Berg D, Holzmann C, Riess O. Berg D, et al. Among authors: riess o. Nat Rev Neurosci. 2003 Sep;4(9):752-62. doi: 10.1038/nrn1197. Nat Rev Neurosci. 2003. PMID: 12951567 Review. No abstract available.

8

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.

Schöls L, Bauer P, Schmidt T, Schulte T, Riess O. Schöls L, et al. Among authors: riess o. Lancet Neurol. 2004 May;3(5):291-304. doi: 10.1016/S1474-4422(04)00737-9. Lancet Neurol. 2004. PMID: 15099544 Review.

9

Regional and subtype selective changes of neurotransmitter receptor density in a rat transgenic for the Huntington's disease mutation.

Bauer A, Zilles K, Matusch A, Holzmann C, Riess O, von Hörsten S. Bauer A, et al. Among authors: riess o. J Neurochem. 2005 Aug;94(3):639-50. doi: 10.1111/j.1471-4159.2005.03169.x. J Neurochem. 2005. PMID: 16033418 Free article.

10

Selective striatal neuron loss and alterations in behavior correlate with impaired striatal function in Huntington's disease transgenic rats.

Kántor O, Temel Y, Holzmann C, Raber K, Nguyen HP, Cao C, Türkoglu HO, Rutten BP, Visser-Vandewalle V, Steinbusch HW, Blokland A, Korr H, Riess O, von Hörsten S, Schmitz C. Kántor O, et al. Among authors: riess o. Neurobiol Dis. 2006 Jun;22(3):538-47. doi: 10.1016/j.nbd.2005.12.014. Epub 2006 Feb 9. Neurobiol Dis. 2006. PMID: 16480885

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