Walter M - Search Results

1

Unraveling Molecular Mechanisms of THAP1 Missense Mutations in DYT6 Dystonia.

Cheng F, Walter M, Wassouf Z, Hentrich T, Casadei N, Schulze-Hentrich J, Barbuti P, Krueger R, Riess O, Grundmann-Hauser K, Ott T. Cheng F, et al. Among authors: walter m. J Mol Neurosci. 2020 Jul;70(7):999-1008. doi: 10.1007/s12031-020-01490-2. Epub 2020 Feb 28. J Mol Neurosci. 2020. PMID: 32112337 Free PMC article.

2

Dynamic nuclear envelope phenotype in rats overexpressing mutated human torsinA protein.

Yu-Taeger L, Gaiser V, Lotzer L, Roenisch T, Fabry BT, Stricker-Shaver J, Casadei N, Walter M, Schaller M, Riess O, Nguyen HP, Ott T, Grundmann-Hauser K. Yu-Taeger L, et al. Among authors: walter m. Biol Open. 2018 Jul 23;7(7):bio032839. doi: 10.1242/bio.032839. Biol Open. 2018. PMID: 29739751 Free PMC article.

3

Microarray expression analysis of human dopaminergic neuroblastoma cells after RNA interference of SNCA--a key player in the pathogenesis of Parkinson's disease.

Häbig K, Walter M, Stappert H, Riess O, Bonin M. Häbig K, et al. Among authors: walter m. Brain Res. 2009 Feb 23;1256:19-33. doi: 10.1016/j.brainres.2008.12.020. Epub 2008 Dec 24. Brain Res. 2009. PMID: 19135032

4

RNA interference of LRRK2-microarray expression analysis of a Parkinson's disease key player.

Häbig K, Walter M, Poths S, Riess O, Bonin M. Häbig K, et al. Among authors: walter m. Neurogenetics. 2008 May;9(2):83-94. doi: 10.1007/s10048-007-0114-0. Epub 2007 Dec 21. Neurogenetics. 2008. PMID: 18097693

5

Specific transcriptional changes in human fetuses with autosomal trisomies.

Altug-Teber O, Bonin M, Walter M, Mau-Holzmann UA, Dufke A, Stappert H, Tekesin I, Heilbronner H, Nieselt K, Riess O. Altug-Teber O, et al. Among authors: walter m. Cytogenet Genome Res. 2007;119(3-4):171-84. doi: 10.1159/000112058. Epub 2008 Feb 1. Cytogenet Genome Res. 2007. PMID: 18253026

6

High-throughput homogeneous mass cleave assay technology for the diagnosis of autosomal recessive Parkinson's disease.

Schroeder C, Walter M, Berg D, Leitner P, Bauer P, Kohl Z, Winkler J, Riess O, Bonin M. Schroeder C, et al. Among authors: walter m. J Mol Diagn. 2008 May;10(3):217-24. doi: 10.2353/jmoldx.2008.070100. Epub 2008 Apr 10. J Mol Diagn. 2008. PMID: 18403612 Free PMC article.

7

Expression profiling in peripheral blood reveals signature for penetrance in DYT1 dystonia.

Walter M, Bonin M, Pullman RS, Valente EM, Loi M, Gambarin M, Raymond D, Tinazzi M, Kamm C, Glöckle N, Poths S, Gasser T, Bressman SB, Klein C, Ozelius LJ, Riess O, Grundmann K. Walter M, et al. Neurobiol Dis. 2010 May;38(2):192-200. doi: 10.1016/j.nbd.2009.12.019. Epub 2010 Jan 4. Neurobiol Dis. 2010. PMID: 20053375

8

Identification of a heterozygous genomic deletion in the spatacsin gene in SPG11 patients using high-resolution comparative genomic hybridization.

Bauer P, Winner B, Schüle R, Bauer C, Häfele V, Hehr U, Bonin M, Walter M, Karle K, Ringer TM, Riess O, Winkler J, Schöls L. Bauer P, et al. Among authors: walter m. Neurogenetics. 2009 Feb;10(1):43-8. doi: 10.1007/s10048-008-0144-2. Epub 2008 Sep 12. Neurogenetics. 2009. PMID: 18787847

9

A combination of transcriptome and methylation analyses reveals embryologically-relevant candidate genes in MRKH patients.

Rall K, Barresi G, Walter M, Poths S, Haebig K, Schaeferhoff K, Schoenfisch B, Riess O, Wallwiener D, Bonin M, Brucker S. Rall K, et al. Among authors: walter m. Orphanet J Rare Dis. 2011 May 28;6:32. doi: 10.1186/1750-1172-6-32. Orphanet J Rare Dis. 2011. PMID: 21619687 Free PMC article.

10

Progression-specific genes identified by expression profiling of matched ductal carcinomas in situ and invasive breast tumors, combining laser capture microdissection and oligonucleotide microarray analysis.

Schuetz CS, Bonin M, Clare SE, Nieselt K, Sotlar K, Walter M, Fehm T, Solomayer E, Riess O, Wallwiener D, Kurek R, Neubauer HJ. Schuetz CS, et al. Among authors: walter m. Cancer Res. 2006 May 15;66(10):5278-86. doi: 10.1158/0008-5472.CAN-05-4610. Cancer Res. 2006. PMID: 16707453

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