Hanisch FG - Search Results

1

Novel recessive myotilin mutation causes severe myofibrillar myopathy.

Schessl J, Bach E, Rost S, Feldkirchner S, Kubny C, Müller S, Hanisch FG, Kress W, Schoser B. Schessl J, et al. Among authors: hanisch fg. Neurogenetics. 2014 Aug;15(3):151-6. doi: 10.1007/s10048-014-0410-4. Epub 2014 Jun 14. Neurogenetics. 2014. PMID: 24928145

2

Patient-specific protein aggregates in myofibrillar myopathies: laser microdissection and differential proteomics for identification of plaque components.

Feldkirchner S, Schessl J, Müller S, Schoser B, Hanisch FG. Feldkirchner S, et al. Among authors: hanisch fg. Proteomics. 2012 Dec;12(23-24):3598-609. doi: 10.1002/pmic.201100559. Epub 2012 Nov 5. Proteomics. 2012. PMID: 23044792

3

Proteomic characterization of aggregate components in an intrafamilial variable FHL1-associated myopathy.

Feldkirchner S, Walter MC, Müller S, Kubny C, Krause S, Kress W, Hanisch FG, Schoser B, Schessl J. Feldkirchner S, et al. Among authors: hanisch fg. Neuromuscul Disord. 2013 May;23(5):418-26. doi: 10.1016/j.nmd.2013.02.006. Epub 2013 Mar 13. Neuromuscul Disord. 2013. PMID: 23489660

4

Analysis of methylated O-glycan alditols by reversed-phase NanoLC coupled CAD-ESI mass spectrometry.

Hanisch FG, Müller S. Hanisch FG, et al. Methods Mol Biol. 2009;534:107-15. doi: 10.1007/978-1-59745-022-5_8. Methods Mol Biol. 2009. PMID: 19277532 Review.

5

Recombinant MUC1 probe authentically reflects cell-specific O-glycosylation profiles of endogenous breast cancer mucin. High density and prevalent core 2-based glycosylation.

Müller S, Hanisch FG. Müller S, et al. Among authors: hanisch fg. J Biol Chem. 2002 Jul 19;277(29):26103-12. doi: 10.1074/jbc.M202921200. Epub 2002 May 8. J Biol Chem. 2002. PMID: 12000758 Free article.

6

Proteomic analysis of Dictyostelium discoideum.

Roth U, Müller S, Hanisch FG. Roth U, et al. Among authors: hanisch fg. Methods Mol Biol. 2006;346:95-109. doi: 10.1385/1-59745-144-4:95. Methods Mol Biol. 2006. PMID: 16957286

7

MUC1: the polymorphic appearance of a human mucin.

Hanisch FG, Müller S. Hanisch FG, et al. Glycobiology. 2000 May;10(5):439-49. doi: 10.1093/glycob/10.5.439. Glycobiology. 2000. PMID: 10764832 Review. No abstract available.

8

Strumpellin is a novel valosin-containing protein binding partner linking hereditary spastic paraplegia to protein aggregation diseases.

Clemen CS, Tangavelou K, Strucksberg KH, Just S, Gaertner L, Regus-Leidig H, Stumpf M, Reimann J, Coras R, Morgan RO, Fernandez MP, Hofmann A, Müller S, Schoser B, Hanisch FG, Rottbauer W, Blümcke I, von Hörsten S, Eichinger L, Schröder R. Clemen CS, et al. Among authors: hanisch fg. Brain. 2010 Oct;133(10):2920-41. doi: 10.1093/brain/awq222. Epub 2010 Sep 9. Brain. 2010. PMID: 20833645

9

Porcine gastric TFF2 is a mucus constituent and differs from pancreatic TFF2.

Stürmer R, Müller S, Hanisch FG, Hoffmann W. Stürmer R, et al. Among authors: hanisch fg. Cell Physiol Biochem. 2014;33(4):895-904. doi: 10.1159/000358662. Epub 2014 Mar 28. Cell Physiol Biochem. 2014. PMID: 24713603 Free article.

10

Autosomal Tubulointerstitial Kidney Disease-MUC1 Type: Differential Proteomics Suggests that Mutated MUC1 (insC) Affects Vesicular Transport in Renal Epithelial Cells.

Staubach S, Wenzel A, Beck BB, Rinschen MM, Müller S, Hanisch FG. Staubach S, et al. Among authors: hanisch fg. Proteomics. 2018 Apr;18(7):e1700456. doi: 10.1002/pmic.201700456. Epub 2018 Mar 13. Proteomics. 2018. PMID: 29436780

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