Schmidt T - 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: schmidt t. 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. Ann Neurol. 2002 Mar;51(3):302-10. doi: 10.1002/ana.10101. Ann Neurol. 2002. PMID: 11891825

3

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: schmidt t. Hum Mol Genet. 2003 Mar 15;12(6):617-24. doi: 10.1093/hmg/ddg075. Hum Mol Genet. 2003. PMID: 12620967

4

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: schmidt t. Lancet Neurol. 2004 May;3(5):291-304. doi: 10.1016/S1474-4422(04)00737-9. Lancet Neurol. 2004. PMID: 15099544 Review.

5

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: schmidt wj, schmidt t. J Neurosci. 2007 Jul 11;27(28):7418-28. doi: 10.1523/JNEUROSCI.4540-06.2007. J Neurosci. 2007. PMID: 17626202 Free PMC article.

6

Neurodegeneration and motor dysfunction in a conditional model of Parkinson's disease.

Nuber S, Petrasch-Parwez E, Winner B, Winkler J, von Hörsten S, Schmidt T, Boy J, Kuhn M, Nguyen HP, Teismann P, Schulz JB, Neumann M, Pichler BJ, Reischl G, Holzmann C, Schmitt I, Bornemann A, Kuhn W, Zimmermann F, Servadio A, Riess O. Nuber S, et al. Among authors: schmidt t. J Neurosci. 2008 Mar 5;28(10):2471-84. doi: 10.1523/JNEUROSCI.3040-07.2008. J Neurosci. 2008. PMID: 18322092 Free PMC article.

7

Identification and functional dissection of localization signals within ataxin-3.

Antony PM, Mäntele S, Mollenkopf P, Boy J, Kehlenbach RH, Riess O, Schmidt T. Antony PM, et al. Among authors: schmidt t. Neurobiol Dis. 2009 Nov;36(2):280-92. doi: 10.1016/j.nbd.2009.07.020. Epub 2009 Aug 4. Neurobiol Dis. 2009. PMID: 19660550

8

Reversibility of symptoms in a conditional mouse model of spinocerebellar ataxia type 3.

Boy J, Schmidt T, Wolburg H, Mack A, Nuber S, Böttcher M, Schmitt I, Holzmann C, Zimmermann F, Servadio A, Riess O. Boy J, et al. Among authors: schmidt t. Hum Mol Genet. 2009 Nov 15;18(22):4282-95. doi: 10.1093/hmg/ddp381. Epub 2009 Aug 10. Hum Mol Genet. 2009. PMID: 19666958

9

A transgenic mouse model of spinocerebellar ataxia type 3 resembling late disease onset and gender-specific instability of CAG repeats.

Boy J, Schmidt T, Schumann U, Grasshoff U, Unser S, Holzmann C, Schmitt I, Karl T, Laccone F, Wolburg H, Ibrahim S, Riess O. Boy J, et al. Among authors: schmidt t. Neurobiol Dis. 2010 Feb;37(2):284-93. doi: 10.1016/j.nbd.2009.08.002. Epub 2009 Aug 20. Neurobiol Dis. 2010. PMID: 19699305

10

Atlas of transgenic Tet-Off Ca2+/calmodulin-dependent protein kinase II and prion protein promoter activity in the mouse brain.

Odeh F, Leergaard TB, Boy J, Schmidt T, Riess O, Bjaalie JG. Odeh F, et al. Among authors: schmidt t. Neuroimage. 2011 Feb 14;54(4):2603-11. doi: 10.1016/j.neuroimage.2010.11.032. Epub 2010 Nov 18. Neuroimage. 2011. PMID: 21093594

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