Wolburg H - Search Results

1

Mitochondrial Morphology, Function and Homeostasis Are Impaired by Expression of an N-terminal Calpain Cleavage Fragment of Ataxin-3.

Harmuth T, Prell-Schicker C, Weber JJ, Gellerich F, Funke C, Drießen S, Magg JCD, Krebiehl G, Wolburg H, Hayer SN, Hauser S, Krüger R, Schöls L, Riess O, Hübener-Schmid J. Harmuth T, et al. Among authors: wolburg h. Front Mol Neurosci. 2018 Oct 10;11:368. doi: 10.3389/fnmol.2018.00368. eCollection 2018. Front Mol Neurosci. 2018. PMID: 30364204 Free PMC article.

2

Reduced basal autophagy and impaired mitochondrial dynamics due to loss of Parkinson's disease-associated protein DJ-1.

Krebiehl G, Ruckerbauer S, Burbulla LF, Kieper N, Maurer B, Waak J, Wolburg H, Gizatullina Z, Gellerich FN, Woitalla D, Riess O, Kahle PJ, Proikas-Cezanne T, Krüger R. Krebiehl G, et al. Among authors: wolburg h. PLoS One. 2010 Feb 23;5(2):e9367. doi: 10.1371/journal.pone.0009367. PLoS One. 2010. PMID: 20186336 Free PMC article.

3

N-terminal ataxin-3 causes neurological symptoms with inclusions, endoplasmic reticulum stress and ribosomal dislocation.

Hübener J, Vauti F, Funke C, Wolburg H, Ye Y, Schmidt T, Wolburg-Buchholz K, Schmitt I, Gardyan A, Driessen S, Arnold HH, Nguyen HP, Riess O. Hübener J, et al. Among authors: wolburg h, wolburg buchholz k. Brain. 2011 Jul;134(Pt 7):1925-42. doi: 10.1093/brain/awr118. Epub 2011 Jun 7. Brain. 2011. PMID: 21653538

4

Mitochondrial defects and neurodegeneration in mice overexpressing wild-type or G399S mutant HtrA2.

Casadei N, Sood P, Ulrich T, Fallier-Becker P, Kieper N, Helling S, May C, Glaab E, Chen J, Nuber S, Wolburg H, Marcus K, Rapaport D, Ott T, Riess O, Krüger R, Fitzgerald JC. Casadei N, et al. Among authors: wolburg h. Hum Mol Genet. 2016 Feb 1;25(3):459-71. doi: 10.1093/hmg/ddv485. Epub 2015 Nov 24. Hum Mol Genet. 2016. PMID: 26604148

5

Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease.

Strauss KM, Martins LM, Plun-Favreau H, Marx FP, Kautzmann S, Berg D, Gasser T, Wszolek Z, Müller T, Bornemann A, Wolburg H, Downward J, Riess O, Schulz JB, Krüger R. Strauss KM, et al. Among authors: wolburg h. Hum Mol Genet. 2005 Aug 1;14(15):2099-111. doi: 10.1093/hmg/ddi215. Epub 2005 Jun 16. Hum Mol Genet. 2005. PMID: 15961413

6

Modulation of mitochondrial function and morphology by interaction of Omi/HtrA2 with the mitochondrial fusion factor OPA1.

Kieper N, Holmström KM, Ciceri D, Fiesel FC, Wolburg H, Ziviani E, Whitworth AJ, Martins LM, Kahle PJ, Krüger R. Kieper N, et al. Among authors: wolburg h. Exp Cell Res. 2010 Apr 15;316(7):1213-24. doi: 10.1016/j.yexcr.2010.01.005. Epub 2010 Jan 11. Exp Cell Res. 2010. PMID: 20064504 Free PMC article.

7

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

8

Mitochondrial defects and neurodegeneration in mice overexpressing wild-type or G399S mutant HtrA2.

Casadei N, Sood P, Ulrich T, Fallier-Becker P, Kieper N, Helling S, May C, Glaab E, Chen J, Nuber S, Wolburg H, Marcus K, Rapaport D, Ott T, Riess O, Krüger R, Fitzgerald JC. Casadei N, et al. Among authors: wolburg h. Hum Mol Genet. 2016 Dec 15;25(24):5513. doi: 10.1093/hmg/ddw353. Hum Mol Genet. 2016. PMID: 28031291 No abstract available.

9

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: wolburg h. 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

10

Transgenic overexpression of the alpha-synuclein interacting protein synphilin-1 leads to behavioral and neuropathological alterations in mice.

Nuber S, Franck T, Wolburg H, Schumann U, Casadei N, Fischer K, Calaminus C, Pichler BJ, Chanarat S, Teismann P, Schulz JB, Luft AR, Tomiuk J, Wilbertz J, Bornemann A, Krüger R, Riess O. Nuber S, et al. Among authors: wolburg h. Neurogenetics. 2010 Feb;11(1):107-20. doi: 10.1007/s10048-009-0212-2. Neurogenetics. 2010. PMID: 19760259

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