Krause S - Search Results

1

Vascular endothelial growth factor antisense pretreatment of bladder cancer cells significantly enhances the cytotoxicity of mitomycin C, gemcitabine and Cisplatin.

Krause S, Förster Y, Kraemer K, Fuessel S, Kotzsch M, Schmidt U, Wirth MP, Meye A, Schwenzer B. Krause S, et al. J Urol. 2005 Jul;174(1):328-31. doi: 10.1097/01.ju.0000161588.94827.27. J Urol. 2005. PMID: 15947684

2

Antisense-mediated VEGF suppression in bladder and breast cancer cells.

Förster Y, Meye A, Krause S, Schwenzer B. Förster Y, et al. Among authors: krause s. Cancer Lett. 2004 Aug 20;212(1):95-103. doi: 10.1016/j.canlet.2004.02.020. Cancer Lett. 2004. PMID: 15246565

3

Distinctive differences in DNA double-strand break repair between normal urothelial and urothelial carcinoma cells.

Windhofer F, Krause S, Hader C, Schulz WA, Florl AR. Windhofer F, et al. Among authors: krause s. Mutat Res. 2008 Feb 1;638(1-2):56-65. doi: 10.1016/j.mrfmmm.2007.08.016. Epub 2007 Sep 5. Mutat Res. 2008. PMID: 17928011

4

Pathological consequences of VCP mutations on human striated muscle.

Hübbers CU, Clemen CS, Kesper K, Böddrich A, Hofmann A, Kämäräinen O, Tolksdorf K, Stumpf M, Reichelt J, Roth U, Krause S, Watts G, Kimonis V, Wattjes MP, Reimann J, Thal DR, Biermann K, Evert BO, Lochmüller H, Wanker EE, Schoser BG, Noegel AA, Schröder R. Hübbers CU, et al. Among authors: krause s. Brain. 2007 Feb;130(Pt 2):381-93. doi: 10.1093/brain/awl238. Epub 2006 Sep 19. Brain. 2007. PMID: 16984901 Free article.

5

The phenotypic spectrum of neutral lipid storage myopathy due to mutations in the PNPLA2 gene.

Reilich P, Horvath R, Krause S, Schramm N, Turnbull DM, Trenell M, Hollingsworth KG, Gorman GS, Hans VH, Reimann J, MacMillan A, Turner L, Schollen A, Witte G, Czermin B, Holinski-Feder E, Walter MC, Schoser B, Lochmüller H. Reilich P, et al. Among authors: krause s. J Neurol. 2011 Nov;258(11):1987-97. doi: 10.1007/s00415-011-6055-4. Epub 2011 May 5. J Neurol. 2011. PMID: 21544567

6

Brain imaging and neuropsychology in late-onset dementia due to a novel mutation (R93C) of valosin-containing protein.

Krause S, Göhringer T, Walter MC, Schoser BG, Reilich P, Linn J, Pöpperl GE, Frölich L, Hentschel F, Lochmüller H, Danek A. Krause S, et al. Clin Neuropathol. 2007 Sep-Oct;26(5):232-40. doi: 10.5414/npp26232. Clin Neuropathol. 2007. PMID: 17907600

7

A novel mutation in the myotilin gene (MYOT) causes a severe form of limb girdle muscular dystrophy 1A (LGMD1A).

Reilich P, Krause S, Schramm N, Klutzny U, Bulst S, Zehetmayer B, Schneiderat P, Walter MC, Schoser B, Lochmüller H. Reilich P, et al. Among authors: krause s. J Neurol. 2011 Aug;258(8):1437-44. doi: 10.1007/s00415-011-5953-9. Epub 2011 Feb 20. J Neurol. 2011. PMID: 21336781

8

Analysis of HLA class I and II alleles in sporadic inclusion-body myositis.

Lampe JB, Gossrau G, Kempe A, Füssel M, Schwurack K, Schröder R, Krause S, Kohnen R, Walter MC, Reichmann H, Lochmüller H. Lampe JB, et al. Among authors: krause s. J Neurol. 2003 Nov;250(11):1313-7. doi: 10.1007/s00415-003-0204-3. J Neurol. 2003. PMID: 14648147

9

CHRND mutation causes a congenital myasthenic syndrome by impairing co-clustering of the acetylcholine receptor with rapsyn.

Müller JS, Baumeister SK, Schara U, Cossins J, Krause S, von der Hagen M, Huebner A, Webster R, Beeson D, Lochmüller H, Abicht A. Müller JS, et al. Among authors: krause s. Brain. 2006 Oct;129(Pt 10):2784-93. doi: 10.1093/brain/awl188. Epub 2006 Aug 17. Brain. 2006. PMID: 16916845

10

The p.G154S mutation of the alpha-B crystallin gene (CRYAB) causes late-onset distal myopathy.

Reilich P, Schoser B, Schramm N, Krause S, Schessl J, Kress W, Müller-Höcker J, Walter MC, Lochmuller H. Reilich P, et al. Among authors: krause s. Neuromuscul Disord. 2010 Apr;20(4):255-9. doi: 10.1016/j.nmd.2010.01.012. Epub 2010 Feb 19. Neuromuscul Disord. 2010. PMID: 20171888

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