Gruppe Clemen  
Publikationen


  1. Rijal R, Arhzaouy K, Strucksberg K-H, Cross M, Hofmann A, Schröder R, Clemen* CS , Eichinger* L.
    Mutant p97 exhibits species-specific changes of its ATPase activity and compromises the UBXD9-mediated monomerisation of p97 hexamers.
    Eur J Cell Biol. 2016 95:195-207. *Co-senior authors

  2. Heckmann M, Bauer R, Jungmann A, Winter L, Rapti K, Strucksberg K-H, Clemen CS, Li Z, Schröder R, Katus H, Müller O.
    AAV9-mediated gene transfer of desmin ameliorates cardiomyopathy in desmin-deficient mice.
    Gene Ther 2016 23:673-679.

  3. Durmus H, Ayhan O, Cirak S, Deymeer F, Parman Y, Franke A, Eiber N, Chevessier F, Schlötzer-Schrehardt U, Clemen CS, Hashemolhosseini S, Schröder R, Hemmrich-Stanisak G, Tolun A, Serdaroglu-Oflazer P.
    Neuromuscular endplate pathology in recessive desminopathies: Lessons from man and mice.
    Neurology 2016 87:799-805.

  4. Winter L, Wittig I, Peeva V, Eggers B, Heidler J, Chevessier F, Kley RA, Barkovits K, Strecker V, Berwanger C, Herrmann H, Marcus K, Kornblum C, Kunz WS, Schröder R, Clemen CS.
    Mutant desmin substantially perturbs mitochondrial morphology, function and maintenance in skeletal muscle tissue.
    Acta Neuropathol 2016 132:453-473.

  5. Hosseinibarkooie S, Peters M, Torres-Benito L, Rastetter RH, Hupperich K, Hoffmann A, Mendoza-Ferreira N, Kaczmarek A, Janzen E, Milbradt J, Lamkemeyer T, Rigo F, Bennett F, Guschlbauer C, Büschges A, Hammerschmidt M, Riessland M, Kye MJ, Clemen CS, Wirth B.
    The power of human protective modifiers: PLS3 and CORO1C unravel impaired endocytosis in spinal muscular atrophy and rescue SMA phenotype.
    Am J Hum Genet 2016 99:647-665.

  6. Behrens J, Ziemann A, Solga R, Rastetter RH, Berwanger C, Herrmann H, Noegel AA, Clemen CS.
    Knock-out of CRN2 (coronin 1C) causes multiple cytoskeletal alterations and mitochondrial dysfunction.
    Eur. J. Cell Biol. 2016 95:239-251.

  7. Bhattacharya K, Swaminathan K, Peche VS, Clemen CS, Knyphausen P, Lammers M, Noegel AA, Rastetter RH.
    Novel Coronin7 interactions with Cdc42 and N-WASP regulate actin organization and Golgi morphology.
    Sci Rep. 6:25411 (2016)

  8. Rastetter RH, Blömacher M, Drebber U, Marko M, Behrens J, Solga R, Hojeili S, Bhattacharya K, Wunderlich CM, Wunderlich FT, Odenthal M, Ziemann A, Eichinger L, Clemen CS.
    Coronin 2A (CRN5) expression is associated with colorectal adenoma-adenocarcinoma sequence and oncogenic signalling.
    BMC Cancer 2015; 15, 638

  9. Clemen CS, Marko M, Strucksberg KH, Behrens J, Wittig I, Gärtner L, Winter L, Chevessier F, Matthias J, Türk M, Tangavelou K, Schütz J, Arhzaouy K, Klopffleisch K, Hanisch FG, Rottbauer W, Blümcke I, Just S, Eichinger L, Hofmann A, Schröder R.
    VCP and PSMF1: Antagonistic regulators of proteasome activity.
    Biochem Bioph Res Co 2015; 463:1210-1217

  10. Pesch M, Schultheiß I, Klopffleisch K, Uhrig JF, Koegl M, Clemen CS, Simon R, Weidtkamp-Peters S, Hülskamp M.
    TRANSPARENT TESTA GLABRA1 and GLABRA1 Compete for Binding to GLABRA3 in Arabidopsis.
    Plant Physiol 2015; 168:584-597

  11. Bührdel JB, Hirth S, Keßler M, Westphal S, Forster M, Manta L, Wiche G, Schoser B, Schessl J, Schröder R, Clemen CS, Eichinger L, Fürst DO, van der Ven PFM, Rottbauer W, Just S.
    In vivo characterization of human myofibrillar myopathy genes in zebrafish.
    Biochem Bioph Res Co 2015; 461:217-223

  12. Clemen CS, Stöckigt F, Strucksberg KH, Chevessier F, Winter L, Schütz J, Bauer R, Thorweihe JM, Wenzel D, Schlötzer-Schrehardt U, Rasche V, Krsmanovic P, Katus HA, Rottbauer W, Just S, Müller OJ, Friedrich O, Meyer R, Herrmann H, Schrickel JW, Schröder R.
    The toxic effect of R350P mutant desmin in striated muscle of man and mouse.
    Acta Neuropathol. 2015; 129:297-315

  13. Vu LH, Araki T, Na J, Clemen CS, Williams JG and Eichinger L.
    Identification of the protein kinases Pyk3 and Phg2 as regulators of the STATc mediated response to hyperosmolarity.
    PLoS ONE 2014; 9:e90025

  14. Ziemann A, Hess S, Bhuwania R, Linder S, Kloppenburg P, Noegel AA, Clemen CS.
    CRN2 enhances the invasiveness of glioblastoma cells,
    Neuro Oncol. 2013; 15:548-61.

  15. Clemen CS, Herrmann H, Strelkov SV, Schröder R.,
    Desminopathies: pathology and mechanisms,
    Acta Neuropathol. 2013; 125:47-75.

  16. Arhzaouy K, Strucksberg KH, Tung SM, Tangavelou K, Stumpf M, Faix J, Schröder R, Clemen CS, Eichinger L.,
    Heteromeric p97/p97R155C complexes induce dominant negative changes in wild-type and autophagy 9-deficient Dictyostelium strains,
    PLoS One. 2012; 7:e46879

  17. Xavier CP, Rastetter RH, Blömacher M, Stumpf M, Himmel M, Morgan RO, Fernandez MP, Wang C, Osman A, Miyata Y, Gjerset RA, Eichinger L, Hofmann A, Linder S, Noegel AA, Clemen CS.
    Phosphorylation of CRN2 by CK2 regulates F-actin and Arp2/3 interaction and inhibits cell migration.
    Sci Rep. 2012; 2:241.

  18. Sprinkart AM, Block W, Träber F, Meyer R, Paulin D, Clemen CS, Schröder R, Gieseke J, Schild H, Thomas D.
    Characterization of the failing murine heart in a desmin knock-out model using a clinical 3 T MRI scanner.
    Int J Cardiovasc Imaging 2012; 28:1699-1705.

  19. Clemen CS, Eichinger L and Schröder R.
    Reply: Hereditary spastic paraplegia caused by a mutation in the VCP gene - VCP: A jack of all trades in neuro- and myodegeneration?
    Brain 2012; 135:1-3.

  20. Arhzaouy K, Strucksberg KH, Tung SM, Tangavelou K, Stumpf M, Faix J, Schröder R, Clemen CS, and Eichinger L.
    Heteromeric p97/p97R155C complexes induce dominant negative changes in wild-type and autophagy 9-deficient Dictyostelium strains.
    PLoS ONE 201; 2 10, e46879.

  21. Kalbe E, Onur OA, Minnerop M, Reimann J, Althaus A, Ahmadzadehfar H, Dodel R, Strach K, Clemen CS, Herholz K, Haense C, Fink GR, Schröder R.
    Early signs of VCP-related frontotemporal dementia: a neuropsychological, FDG-PET and fMRI study.
    J. Neurol. 2011; 258:515-518.

  22. Clemen, C.S., K. Tangavelou, K-H. Strucksberg, S. Just, L. Gaertner, H. Regus-Leidig, M. Stumpf, J. Reimann, R. Coras, R.O. Morgan, M-P. Fernandez, A. Hofmann, S. Müller, B. Schoser, F-G. Hanisch, W. Rottbauer, I. Blümcke, S. von Hörsten, L. Eichinger, and R. Schröder.
    Strumpellin is a novel valosin-containing protein binding partner linking hereditary spastic paraplegia to protein aggregation diseases
    Brain 2010; 133:2920-2941.

  23. Lang E, Lang PA, Shumilina E, Qadri SM, Kucherenko Y, Kempe DS, Föller M, Capasso A, Wieder T, Gulbins E, Clemen CS, Herr C, Noegel AA, Huber SM, Lang F.
    Enhanced eryptosis of erythrocytes from gene-targeted mice lacking annexin A7.
    Pflugers Arch. 2010; May 20.

  24. Schrickel JW, Stöckigt F, Krzyzak W, Paulin D, Li Z, Lübkemeier I, Fleischmann B, Sasse P, Linhart M, Lewalter T, Nickenig G, Lickfett L, Schröder R, Clemen CS.
    Cardiac conduction disturbances and differential effects on atrial and ventricular electrophysiological properties in desmin deficient mice.
    J Interv Card Electrophysiol. 2010; Apr 14.

  25. Strucksberg KH, Tangavelou K, Schröder R, Clemen CS.
    Proteasomal activity in skeletal muscle: a matter of assay design, muscle type, and age.
    Anal Biochem. 2010; 399:225-9.

  26. Lang PA, Kasinathan RS, Brand VB, Duranton C, Lang C, Koka S, Shumilina E, Kempe DS, Tanneur V, Akel A, Lang KS, Foller M, Kun JF, Kremsner PG, Wesselborg S, Laufer S, Clemen CS, Herr C, Noegel AA, Wieder T, Gulbins E, Lang F, Huber SM.
    Accelerated clearance of Plasmodium-infected erythrocytes in sickle cell trait and annexin-A7 deficiency.
    Cell Physiol Biochem. 2009; 24:415-28.

  27. Xavier CP, Rastetter RH, Stumpf M, Rosentreter A, Müller R, Reimann J, Cornfine S, Linder S, van Vliet V, Hofmann A, Morgan RO, Fernandez MP, Schröder R, Noegel AA, Clemen CS.
    Structural and functional diversity of novel coronin 1C (CRN2) isoforms in muscle.
    J Mol Biol. 2009; 393:287-99.

  28. Clemen CS, Fischer D, Reimann J, Eichinger L, Müller CR, Müller HD, Goebel HH, Schröder R.
    How much mutant protein is needed to cause a protein aggregate myopathy in vivo? Lessons from an exceptional desminopathy.
    Hum Mutat. 2009; 30:E490-9. Equal contributors.

  29. Roadcap DW, Clemen CS, Bear JE.
    The role of mammalian coronins in development and disease.
    Subcell Biochem. 2008; 48:124-35.

  30. Xavier CP, Eichinger L, Fernandez MP, Morgan RO, Clemen CS.
    Evolutionary and functional diversity of coronin proteins.
    Subcell Biochem. 2008; 48:98-109.

  31. Clemen CS, Rybakin V, Eichinger L.
    The coronin family of proteins.
    Subcell Biochem. 2008; 48:1-5.

  32. Rybakin V, Rastetter RH, Stumpf M, Uetrecht AC, Bear JE, Noegel AA, Clemen CS.
    Molecular mechanism underlying the association of Coronin-7 with Golgi membranes.
    Cell Mol Life Sci 2008; 65:2419-30.

  33. Thal DR, Xavier C-P, Rosentreter A, Waha A, Pietsch T, Stumpf M, Noegel AA, Clemen CS.
    Expression of coronin-3 (coronin-1C) in diffuse gliomas is related to malignancy.
    J Pathol 2008; 214:415-24.

  34. Peche V, Shekar S, Leichter M, Korte H, Schröder R, Schleicher M, Holak TA, Clemen CS, Ramanath-Y. B, Pfitzer G, Karakesisoglou I, Noegel AA.
    CAP2, Cyclase Associated Protein 2, is a dual compartment protein.
    CMLS 2007; 64:2702-15.

  35. Schrickel JW, Brixius K, Herr C, Clemen CS, Sasse P, Reetz K, Grohe C, Meyer R, Tiemann K, Schröder R, Bloch W, Nickenig G, Fleischmann BK, Noegel AA, Schwinger RH, Lewalter T.
    Enhanced heterogeneity of myocardial conduction and severe cardiac electrical instability in annexin A7-deficient mice.
    Cardiovasc Res 2007; 76:257-68.

  36. Rosentreter A, Hofmann A, Xavier C-P, Stumpf M, Noegel AA, Clemen CS.
    Coronin 3 involvement in F-actin dependent processes at the cell cortex.
    Exp Cell Res 2007; 313:878-95.

  37. 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 BGH, Noegel AA, Schröder R. Pathological consequences of VCP-mutations on human striated muscle.
    Brain 2007; 130:381-93. Equal contributors.

  38. Fischer D, Clemen CS, Olive M, Ferrer I, Goudeau B, Roth U, Badorf P, Wattjes MP, Lutterbey G, Kral T, van der Ven PF, Fürst DO, Vicart P, Goldfarb LG, Moza M, Carpen O, Reichelt J, Schröder R.
    Different early pathogenesis in myotilinopathy compared to primary desminopathy.
    Neuromuscul Disord 2006; 16:361-7. Equal contributors.

  39. Goffart S, Franko A, Clemen CS, Wiesner RJ.
    alpha-actinin 4 interaction with the Cytochrome c promoter upon skeletal muscle
    differentiation. Curr Genet 2006; 49:125-35.

  40. Clemen CS, Fischer D, Roth U, Simon S, Vicart P, Kato K, Kaminska AM, Vorgerd M, Goldfarb LG, Eymard B, Romero NB, Goudeau B, Eggermann T, Zerres K, Noegel AA, Schröder R.
    Hsp27-2D-gel electrophoresis is a diagnostic tool to differentiate primary desminopathies from myofibrillar myopathies.
    FEBS Letters 2005; 579:3777-82.

  41. Bär H, Fischer D, Goudeau B, Kley RA, Clemen CS, Vicart P, Herrmann H, Vorgerd M, Schröder R.
    Pathogenic effects of a novel heterozygous R350P desmin mutation on the assembly of desmin intermediate filaments in vivo and in vitro.
    Hum Mol Genet 2005; 14:1251-60.

  42. Rick M, Ramos Garrido SI, Herr C, Thal DR, Noegel AA, Clemen CS.
    Nuclear localization of Annexin A7 during murine brain development.
    BMC Neurosci 2005; 6:25.

  43. Clemen CS, Spottke EA, Lütjohann D, Urbach H, von Bergmann K, Klockgether T, Dodel R.
    Cerebrotendinous Xanthomatosis-A treatable ataxia.
    Neurology
    2005; 64:1476.

  44. Hasse A, Rosentreter A, Spoerl Z, Stumpf M, Noegel AA, Clemen CS.
    Coronin 3 and its role in murine brain morphogenesis.
    Eur J Neurosci 2005; 21:1155-68.

  45. Clemen CS, Herr C, Hövelmeyer N, Noegel AA.
    The lack of annexin A7 affects functions of primary astrocytes.
    Exp Cell Res 2003; 291:406-14. Equal contributors.

  46. Clemen CS, Herr C, Lehnert G, Kutschkow R, Picker SM, Gathof BS, Zamparelli C, Schleicher M, Noegel AA.
    Function, expression and localization of annexin A7 in platelets and red blood cells: Insights derived from an annexin A7 mutant mouse.
    BMC Biochem 2003; 4:8. Equal contributors.

  47. Schröder R, Reimann J, Salmikangas P, Clemen CS, Hayashi YK, Nonaka I, Arahata K, Carpen O.
    Beyond LGMD1A: myotilin is a component of central core lesions and nemaline rods.
    Neuromuscul Disord 2003; 13:451-5.

  48. Schröder R, Goudeau B, Simon MC, Fischer D, Eggermann T, Clemen CS, Li Z, Reimann J, Xue Z, Rudnik-Schöneborn S, Zerres K, van der Ven PF, Fürst DO, Kunz WS, Vicart P.
    On noxious desmin: functional effects of a novel heterozygous desmin insertion mutation on the extrasarcomeric desmin cytoskeleton and mitochondria.
    Hum Mol Genet 2003; 12:657-69.

  49. Clemen CS, Herr C, Lie AA, Noegel AA, Schröder R.
    Annexin VII: an astroglial protein exhibiting a Ca2+-dependent subcellular distribution.
    Neuroreport 2001; 12:1139-44. Equal contributors.

  50. Clemen CS, Hofmann A, Zamparelli C, Noegel AA.
    Expression and localisation of annexin VII (synexin) isoforms in differentiating myoblasts,
    J Muscle Res Cell Motil 1999; 20:669-79.



Reviews:
  1. Clemen CS, Herr C, Noegel AA. Annexin A7. AfCS-Nature Molecule Pages 2006; doi:10.1038/mp.a003255.01

  2. Rybakin V, Clemen CS. Coronin proteins as multifunctional regulators of the cytoskeleton and membrane trafficking. Bioessays 2005; 27:625-32. If 6,787



Books:
  1. Clemen CS, Eichinger L, Rybakin V (Ed.). The coronin family of proteins. Sub-cellular Biochemistry, Vol. 48. Austin: Landes Bioscience, New York: Springer Science+Business Media, 2008.
    ISBN 978-0-387-09594-3
    http://www.eurekah.com/chapter/3785



07 März 2017
Christoph Clemen
Institut für Biochemie I, Joseph-Stelzmann-Strasse 52, D50931 Köln
Anregungen und Wünsche: Gudrun Konertz
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