Poths S - Search Results

1

Mayer-Rokitansky-Küster-Hauser syndrome discordance in monozygotic twins: matrix metalloproteinase 14, low-density lipoprotein receptor-related protein 10, extracellular matrix, and neoangiogenesis genes identified as candidate genes in a tissue-specific mosaicism.

Rall K, Eisenbeis S, Barresi G, Rückner D, Walter M, Poths S, Wallwiener D, Riess O, Bonin M, Brucker S. Rall K, et al. Among authors: poths s. Fertil Steril. 2015 Feb;103(2):494-502.e3. doi: 10.1016/j.fertnstert.2014.10.053. Epub 2014 Dec 6. Fertil Steril. 2015. PMID: 25492683 Free article.

2

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: poths s. 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.

3

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: poths s. Neurogenetics. 2008 May;9(2):83-94. doi: 10.1007/s10048-007-0114-0. Epub 2007 Dec 21. Neurogenetics. 2008. PMID: 18097693

4

Utilization of AFFX spike-in control probes to monitor sample identity throughout Affymetrix GeneChip Array processing.

Walter M, Honegger A, Schweizer R, Poths S, Bonin M. Walter M, et al. Among authors: poths s. Biotechniques. 2010 May;48(5):371-8. doi: 10.2144/000113421. Biotechniques. 2010. PMID: 20569210 Free article.

5

Whole genome expression analyses of single- and double-knock-out mice implicate partially overlapping functions of alpha- and gamma-synuclein.

Kuhn M, Haebig K, Bonin M, Ninkina N, Buchman VL, Poths S, Riess O. Kuhn M, et al. Among authors: poths s. Neurogenetics. 2007 Apr;8(2):71-81. doi: 10.1007/s10048-007-0079-z. Epub 2007 Feb 22. Neurogenetics. 2007. PMID: 17318638 Free PMC article.

6

Gene expression changes in a transgenic mouse model overexpressing human wildtype and mutant torsinA.

Grundmann K, Hübener J, Häbig K, Reischmann B, Poths S, Hauser TK, Magg J, Riess O, Bonin M, Nguyen HP. Grundmann K, et al. Among authors: poths s. Proteomics Clin Appl. 2008 May;2(5):720-36. doi: 10.1002/prca.200780053. Proteomics Clin Appl. 2008. PMID: 21136869

7

UPDtool: a tool for detection of iso- and heterodisomy in parent-child trios using SNP microarrays.

Schroeder C, Sturm M, Dufke A, Mau-Holzmann U, Eggermann T, Poths S, Riess O, Bonin M. Schroeder C, et al. Among authors: poths s. Bioinformatics. 2013 Jun 15;29(12):1562-4. doi: 10.1093/bioinformatics/btt174. Epub 2013 Apr 14. Bioinformatics. 2013. PMID: 23589652

8

Microarray expression analysis of gad mice implicates involvement of Parkinson's disease associated UCH-L1 in multiple metabolic pathways.

Bonin M, Poths S, Osaka H, Wang YL, Wada K, Riess O. Bonin M, et al. Among authors: poths s. Brain Res Mol Brain Res. 2004 Jul 5;126(1):88-97. doi: 10.1016/j.molbrainres.2004.03.025. Brain Res Mol Brain Res. 2004. PMID: 15207921

9

Nuclear localization of ataxin-3 is required for the manifestation of symptoms in SCA3: in vivo evidence.

Bichelmeier U, Schmidt T, Hübener J, Boy J, Rüttiger L, Häbig K, Poths S, Bonin M, Knipper M, Schmidt WJ, Wilbertz J, Wolburg H, Laccone F, Riess O. Bichelmeier U, et al. Among authors: poths s. J Neurosci. 2007 Jul 11;27(28):7418-28. doi: 10.1523/JNEUROSCI.4540-06.2007. J Neurosci. 2007. PMID: 17626202 Free PMC article.

10

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. Among authors: poths s. 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

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