Auburger G - Search Results

1

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

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

Search for the chromosomal location of autosomal dominant cerebellar ataxia from Holguin, Cuba: exclusion from candidate regions on chromosome 4 and 11q.

Gispert S, Nothers C, Orozco G, Auburger G. Gispert S, et al. Among authors: auburger g. Hum Hered. 1993 Jan-Feb;43(1):12-20. doi: 10.1159/000154107. Hum Hered. 1993. PMID: 8514320

6

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

7

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

8

Absence of mutation in the beta- and gamma-synuclein genes in familial autosomal dominant Parkinson's disease.

Lavedan C, Buchholtz S, Auburger G, Albin RL, Athanassiadou A, Blancato J, Burguera JA, Ferrell RE, Kostic V, Leroy E, Leube B, Mota-Vieira L, Papapetropoulos T, Pericak-Vance MA, Pinkus J, Scott WK, Ulm G, Vasconcelos J, Vilchez JJ, Nussbaum RL, Polymeropoulos MH. Lavedan C, et al. Among authors: auburger g. DNA Res. 1998 Dec 31;5(6):401-2. doi: 10.1093/dnares/5.6.401. DNA Res. 1998. PMID: 10048491 Free article. No abstract available.

9

SCA2 trinucleotide expansion in German SCA patients.

Riess O, Laccone FA, Gispert S, Schöls L, Zühlke C, Vieira-Saecker AM, Herlt S, Wessel K, Epplen JT, Weber BH, Kreuz F, Chahrokh-Zadeh S, Meindl A, Lunkes A, Aguiar J, Macek M Jr, Krebsová A, Macek M Sr, Bürk K, Tinschert S, Schreyer I, Pulst SM, Auburger G. Riess O, et al. Among authors: auburger g. Neurogenetics. 1997 May;1(1):59-64. doi: 10.1007/s100480050009. Neurogenetics. 1997. PMID: 10735276

10

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

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