Auburger G - Search Results

1

Hereditary early-onset Parkinson's disease caused by mutations in PINK1.

Valente EM, Abou-Sleiman PM, Caputo V, Muqit MM, Harvey K, Gispert S, Ali Z, Del Turco D, Bentivoglio AR, Healy DG, Albanese A, Nussbaum R, González-Maldonado R, Deller T, Salvi S, Cortelli P, Gilks WP, Latchman DS, Harvey RJ, Dallapiccola B, Auburger G, Wood NW. Valente EM, et al. Among authors: auburger g. Science. 2004 May 21;304(5674):1158-60. doi: 10.1126/science.1096284. Epub 2004 Apr 15. Science. 2004. PMID: 15087508

2

Neurodegeneration in the polyglutamine diseases: Act 1, Scene 1.

Nussbaum R, Auburger G. Nussbaum R, et al. Among authors: auburger g. Nat Neurosci. 2000 Feb;3(2):103-4. doi: 10.1038/72042. Nat Neurosci. 2000. PMID: 10649562 No abstract available.

3

Transgenic mice expressing mutant A53T human alpha-synuclein show neuronal dysfunction in the absence of aggregate formation.

Gispert S, Del Turco D, Garrett L, Chen A, Bernard DJ, Hamm-Clement J, Korf HW, Deller T, Braak H, Auburger G, Nussbaum RL. Gispert S, et al. Among authors: auburger g. Mol Cell Neurosci. 2003 Oct;24(2):419-29. doi: 10.1016/s1044-7431(03)00198-2. Mol Cell Neurosci. 2003. PMID: 14572463

4

Exacerbated synucleinopathy in mice expressing A53T SNCA on a Snca null background.

Cabin DE, Gispert-Sanchez S, Murphy D, Auburger G, Myers RR, Nussbaum RL. Cabin DE, et al. Among authors: auburger g. Neurobiol Aging. 2005 Jan;26(1):25-35. doi: 10.1016/j.neurobiolaging.2004.02.026. Neurobiol Aging. 2005. PMID: 15585343

5

Failure to find alpha-synuclein gene dosage changes in 190 patients with familial Parkinson disease.

Gispert S, Trenkwalder C, Mota-Vieira L, Kostic V, Auburger G. Gispert S, et al. Among authors: auburger g. Arch Neurol. 2005 Jan;62(1):96-8. doi: 10.1001/archneur.62.1.96. Arch Neurol. 2005. PMID: 15642855

6

Clinical and positron emission tomography of Parkinson's disease caused by LRRK2.

Hernandez DG, Paisán-Ruíz C, McInerney-Leo A, Jain S, Meyer-Lindenberg A, Evans EW, Berman KF, Johnson J, Auburger G, Schäffer AA, Lopez GJ, Nussbaum RL, Singleton AB. Hernandez DG, et al. Among authors: auburger g. Ann Neurol. 2005 Mar;57(3):453-6. doi: 10.1002/ana.20401. Ann Neurol. 2005. PMID: 15732108

7

Dopaminergic function in a family with the PARK6 form of autosomal recessive Parkinson's syndrome.

Kessler KR, Hamscho N, Morales B, Menzel C, Barrero F, Vives F, Gispert S, Auburger G. Kessler KR, et al. Among authors: auburger g. J Neural Transm (Vienna). 2005 Oct;112(10):1345-53. doi: 10.1007/s00702-005-0281-9. Epub 2005 Mar 23. J Neural Transm (Vienna). 2005. PMID: 15785866

8

Mitochondrial dysfunction, peroxidation damage and changes in glutathione metabolism in PARK6.

Hoepken HH, Gispert S, Morales B, Wingerter O, Del Turco D, Mülsch A, Nussbaum RL, Müller K, Dröse S, Brandt U, Deller T, Wirth B, Kudin AP, Kunz WS, Auburger G. Hoepken HH, et al. Among authors: auburger g. Neurobiol Dis. 2007 Feb;25(2):401-11. doi: 10.1016/j.nbd.2006.10.007. Epub 2006 Nov 30. Neurobiol Dis. 2007. PMID: 17141510

9

Mitochondrial translation initiation factor 3 gene polymorphism associated with Parkinson's disease.

Abahuni N, Gispert S, Bauer P, Riess O, Krüger R, Becker T, Auburger G. Abahuni N, et al. Among authors: auburger g. Neurosci Lett. 2007 Mar 6;414(2):126-9. doi: 10.1016/j.neulet.2006.12.053. Epub 2007 Jan 11. Neurosci Lett. 2007. PMID: 17267121

10

Loss-of-function of human PINK1 results in mitochondrial pathology and can be rescued by parkin.

Exner N, Treske B, Paquet D, Holmström K, Schiesling C, Gispert S, Carballo-Carbajal I, Berg D, Hoepken HH, Gasser T, Krüger R, Winklhofer KF, Vogel F, Reichert AS, Auburger G, Kahle PJ, Schmid B, Haass C. Exner N, et al. Among authors: auburger g. J Neurosci. 2007 Nov 7;27(45):12413-8. doi: 10.1523/JNEUROSCI.0719-07.2007. J Neurosci. 2007. PMID: 17989306 Free PMC article.

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