Poths S - Search Results

1

A high-throughput resequencing microarray for autosomal dominant spastic paraplegia genes.

Dufke C, Schlipf N, Schüle R, Bonin M, Auer-Grumbach M, Stevanin G, Depienne C, Kassubek J, Klebe S, Klimpe S, Klopstock T, Otto S, Poths S, Seibel A, Stolze H, Gal A, Schöls L, Bauer P. Dufke C, et al. Among authors: poths s. Neurogenetics. 2012 Aug;13(3):215-27. doi: 10.1007/s10048-012-0329-6. Epub 2012 May 3. Neurogenetics. 2012. PMID: 22552817

2

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

3

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.

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

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

6

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

7

A rapid microarray based whole genome analysis for detection of uniparental disomy.

Altug-Teber O, Dufke A, Poths S, Mau-Holzmann UA, Bastepe M, Colleaux L, Cormier-Daire V, Eggermann T, Gillessen-Kaesbach G, Bonin M, Riess O. Altug-Teber O, et al. Among authors: poths s. Hum Mutat. 2005 Aug;26(2):153-9. doi: 10.1002/humu.20198. Hum Mutat. 2005. PMID: 15968682

8

Array-based resequencing assay for mutations causing hypertrophic cardiomyopathy.

Waldmüller S, Müller M, Rackebrandt K, Binner P, Poths S, Bonin M, Scheffold T. Waldmüller S, et al. Among authors: poths s. Clin Chem. 2008 Apr;54(4):682-7. doi: 10.1373/clinchem.2007.099119. Epub 2008 Feb 7. Clin Chem. 2008. PMID: 18258667 Free PMC article.

9

Genome-wide expression profiling of the retinoschisin-deficient retina in early postnatal mouse development.

Gehrig A, Langmann T, Horling F, Janssen A, Bonin M, Walter M, Poths S, Weber BH. Gehrig A, et al. Among authors: poths s. Invest Ophthalmol Vis Sci. 2007 Feb;48(2):891-900. doi: 10.1167/iovs.06-0641. Invest Ophthalmol Vis Sci. 2007. PMID: 17251492 Free article.

10

Inhibition of glutathione-S-transferase as a treatment strategy for multidrug resistance in childhood rhabdomyosarcoma.

Seitz G, Bonin M, Fuchs J, Poths S, Ruck P, Warmann SW, Armeanu-Ebinger S. Seitz G, et al. Among authors: poths s. Int J Oncol. 2010 Feb;36(2):491-500. Int J Oncol. 2010. PMID: 20043085

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