Auburger G - Search Results

1

Primary skin fibroblasts as a model of Parkinson's disease.

Auburger G, Klinkenberg M, Drost J, Marcus K, Morales-Gordo B, Kunz WS, Brandt U, Broccoli V, Reichmann H, Gispert S, Jendrach M. Auburger G, et al. Mol Neurobiol. 2012 Aug;46(1):20-7. doi: 10.1007/s12035-012-8245-1. Epub 2012 Feb 19. Mol Neurobiol. 2012. PMID: 22350618 Free PMC article. Review.

2

Genetic mapping of the spinocerebellar ataxia 2 (SCA2) locus on chromosome 12q23-q24.1.

Hernández A, Magariño C, Gispert S, Santos N, Lunkes A, Orozco G, Heredero L, Beckmann J, Auburger G. Hernández A, et al. Among authors: auburger g. Genomics. 1995 Jan 20;25(2):433-5. doi: 10.1016/0888-7543(95)80043-l. Genomics. 1995. PMID: 7789976

3

Autosomal dominant familial spastic paraplegia: reduction of the FSP1 candidate region on chromosome 14q to 7 cM and locus heterogeneity.

Gispert S, Santos N, Damen R, Voit T, Schulz J, Klockgether T, Orozco G, Kreuz F, Weissenbach J, Auburger G. Gispert S, et al. Among authors: auburger g. Am J Hum Genet. 1995 Jan;56(1):183-7. Am J Hum Genet. 1995. PMID: 7825576 Free PMC article.

4

Molecular heterogeneity of autosomal dominant cerebellar ataxia: analysis of flanking microsatellites of the spinocerebellar ataxia 1 locus in a northern European family unequivocally demonstrates non-linkage.

Lunkes A, Gispert S, Enczmann J, Auburger G. Lunkes A, et al. Among authors: auburger g. Hum Genet. 1993 May;91(4):362-6. doi: 10.1007/BF00217357. Hum Genet. 1993. PMID: 8099059

5

Spinocerebellar ataxia type 2. Genotype and phenotype in German kindreds.

Schöls L, Gispert S, Vorgerd M, Menezes Vieira-Saecker AM, Blanke P, Auburger G, Amoiridis G, Meves S, Epplen JT, Przuntek H, Pulst SM, Riess O. Schöls L, et al. Among authors: auburger g. Arch Neurol. 1997 Sep;54(9):1073-80. doi: 10.1001/archneur.1997.00550210011007. Arch Neurol. 1997. PMID: 9311350

6

Identification of the physiological promoter for spinocerebellar ataxia 2 gene reveals a CpG island for promoter activity situated into the exon 1 of this gene and provides data about the origin of the nonmethylated state of these types of islands.

Aguiar J, Santurlidis S, Nowok J, Alexander C, Rudnicki D, Gispert S, Schulz W, Auburger G. Aguiar J, et al. Among authors: auburger g. Biochem Biophys Res Commun. 1999 Jan 19;254(2):315-8. doi: 10.1006/bbrc.1998.9929. Biochem Biophys Res Commun. 1999. PMID: 9918835

7

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

8

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

9

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

10

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

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