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Items: 18

1.

Analysis of blood-based gene expression in idiopathic Parkinson disease.

Shamir R, Klein C, Amar D, Vollstedt EJ, Bonin M, Usenovic M, Wong YC, Maver A, Poths S, Safer H, Corvol JC, Lesage S, Lavi O, Deuschl G, Kuhlenbaeumer G, Pawlack H, Ulitsky I, Kasten M, Riess O, Brice A, Peterlin B, Krainc D.

Neurology. 2017 Oct 17;89(16):1676-1683. doi: 10.1212/WNL.0000000000004516. Epub 2017 Sep 15.

PMID:
28916538
2.

Molecular Signatures of Primary Human Spermatogonial Progenitors and Its Neighboring Peritubular Stromal Compartment.

Harichandan A, Sivasubramaniyan K, Hennenlotter J, Poths S, Bedke J, Kruck S, Stenzl A, Bühring HJ.

Stem Cells Dev. 2017 Feb 15;26(4):263-273. doi: 10.1089/scd.2016.0042. Epub 2016 Dec 16.

PMID:
27821019
3.

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.

Fertil Steril. 2015 Feb;103(2):494-502.e3. doi: 10.1016/j.fertnstert.2014.10.053. Epub 2014 Dec 6.

PMID:
25492683
4.

Genome-wide UPD screening in patients with intellectual disability.

Schroeder C, Ekici AB, Moog U, Grasshoff U, Mau-Holzmann U, Sturm M, Vosseler V, Poths S, Rappold G, Riess A, Riess O, Dufke A, Bonin M.

Eur J Hum Genet. 2014 Oct;22(10):1233-5. doi: 10.1038/ejhg.2014.63. Epub 2014 May 7.

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.

Bioinformatics. 2013 Jun 15;29(12):1562-4. doi: 10.1093/bioinformatics/btt174. Epub 2013 Apr 14.

PMID:
23589652
6.

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.

Neurogenetics. 2012 Aug;13(3):215-27. doi: 10.1007/s10048-012-0329-6. Epub 2012 May 3.

PMID:
22552817
7.

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.

Orphanet J Rare Dis. 2011 May 28;6:32. doi: 10.1186/1750-1172-6-32.

8.

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.

Biotechniques. 2010 May;48(5):371-8. doi: 10.2144/000113421.

9.

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.

Neurobiol Dis. 2010 May;38(2):192-200. doi: 10.1016/j.nbd.2009.12.019. Epub 2010 Jan 4.

PMID:
20053375
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.

Int J Oncol. 2010 Feb;36(2):491-500.

PMID:
20043085
11.

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.

Proteomics Clin Appl. 2008 May;2(5):720-36. doi: 10.1002/prca.200780053.

PMID:
21136869
12.

Array-based resequencing assay for mutations causing hypertrophic cardiomyopathy.

Waldmüller S, Müller M, Rackebrandt K, Binner P, Poths S, Bonin M, Scheffold T.

Clin Chem. 2008 Apr;54(4):682-7. doi: 10.1373/clinchem.2007.099119. Epub 2008 Feb 7.

13.

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

Häbig K, Walter M, Poths S, Riess O, Bonin M.

Neurogenetics. 2008 May;9(2):83-94. Epub 2007 Dec 21.

PMID:
18097693
14.

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.

J Neurosci. 2007 Jul 11;27(28):7418-28.

15.

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.

Neurogenetics. 2007 Apr;8(2):71-81. Epub 2007 Feb 22.

16.

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.

Invest Ophthalmol Vis Sci. 2007 Feb;48(2):891-900.

PMID:
17251492
17.

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.

Hum Mutat. 2005 Aug;26(2):153-9.

PMID:
15968682
18.

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.

Brain Res Mol Brain Res. 2004 Jul 5;126(1):88-97.

PMID:
15207921

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