Riess O - Search Results

1

Predominant neuronal expression of the gene responsible for dentatorubral-pallidoluysian atrophy (DRPLA) in rat.

Schmitt I, Epplen JT, Riess O. Schmitt I, et al. Among authors: riess o. Hum Mol Genet. 1995 Sep;4(9):1619-24. doi: 10.1093/hmg/4.9.1619. Hum Mol Genet. 1995. PMID: 8541849

2

Trinucleotide expansion within the MJD1 gene presents clinically as spinocerebellar ataxia and occurs most frequently in German SCA patients.

Schöls L, Vieira-Saecker AM, Schöls S, Przuntek H, Epplen JT, Riess O. Schöls L, et al. Among authors: riess o. Hum Mol Genet. 1995 Jun;4(6):1001-5. doi: 10.1093/hmg/4.6.1001. Hum Mol Genet. 1995. PMID: 7655453

3

Toward the complete genomic map and molecular pathology of human chromosome 4.

Riess O, Winkelmann B, Epplen JT. Riess O, et al. Hum Genet. 1994 Jul;94(1):1-18. doi: 10.1007/BF02272834. Hum Genet. 1994. PMID: 8034286 Review.

4

Chromosomal assignment of the human smg GDP dissociation stimulator gene to human chromosome 4q21-q25.

Riess O, Epplen C, Siedlaczck I, Epplen JT. Riess O, et al. Hum Genet. 1993 Dec;92(6):629-30. doi: 10.1007/BF00420952. Hum Genet. 1993. PMID: 8262526

5

Improved PCR conditions for the stretch of (CAG)n repeats causing Huntington's disease.

Riess O, Noerremoelle A, Soerensen SA, Epplen JT. Riess O, et al. Hum Mol Genet. 1993 Jun;2(6):637. doi: 10.1093/hmg/2.6.637. Hum Mol Genet. 1993. PMID: 8353483 No abstract available.

6

Expression of the Huntington disease gene in rodents: cloning the rat homologue and evidence for downregulation in non-neuronal tissues during development.

Schmitt I, Bächner D, Megow D, Henklein P, Hameister H, Epplen JT, Riess O. Schmitt I, et al. Among authors: riess o. Hum Mol Genet. 1995 Jul;4(7):1173-82. doi: 10.1093/hmg/4.7.1173. Hum Mol Genet. 1995. PMID: 8528205

7

cDNA cloning and expression of rsca1, the rat counterpart of the human spinocerebellar ataxia type 1 gene.

Gossen M, Schmitt I, Obst K, Wahle P, Epplen JT, Riess O. Gossen M, et al. Among authors: riess o. Hum Mol Genet. 1996 Mar;5(3):381-9. doi: 10.1093/hmg/5.3.381. Hum Mol Genet. 1996. PMID: 8852664

8

Transmission distortion of the mutant alleles in spinocerebellar ataxia.

Riess O, Epplen JT, Amoiridis G, Przuntek H, Schöls L. Riess O, et al. Hum Genet. 1997 Feb;99(2):282-4. doi: 10.1007/s004390050355. Hum Genet. 1997. PMID: 9048937

9

Characterization of the rat spinocerebellar ataxia type 3 gene.

Schmitt I, Brattig T, Gossen M, Riess O. Schmitt I, et al. Among authors: riess o. Neurogenetics. 1997 Sep;1(2):103-12. doi: 10.1007/s100480050015. Neurogenetics. 1997. PMID: 10732811

10

Genetic background of apparently idiopathic sporadic cerebellar ataxia.

Schöls L, Szymanski S, Peters S, Przuntek H, Epplen JT, Hardt C, Riess O. Schöls L, et al. Among authors: riess o. Hum Genet. 2000 Aug;107(2):132-7. doi: 10.1007/s004390000346. Hum Genet. 2000. PMID: 11030410

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