Publikationen

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  • Characterization of the protein components of Nephila clavipes dragline silk.
    Sponner A, Schlott B, Vollrath F, Unger E, Grosse F, Weisshart K
    Biochemistry 2005, 44(12), 4727-36 published as IMB
  • Differential polymerization of the two main protein components of dragline silk during fibre spinning.
    Sponner A, Unger E, Grosse F, Weisshart K
    Nat Mater 2005, 4(10), 772-5
  • The conserved C-termini contribute to the properties of spider silk fibroins.
    Sponner A, Vater W, Rommerskirch W, Vollrath F, Unger E, Grosse F, Weisshart K
    Biochem Biophys Res Commun 2005, 338(2), 897-902
  • Hereditary lattice corneal dystrophy is associated with corneal amyloid deposits enclosing C-terminal fragments of keratoepithelin.
    Stix B, Leber M, Bingemer P, Gross C, Rüschoff J, Fändrich M, Schorderet DF, Vorwerk CK, Zacharias M, Roessner A, Röcken C
    Invest Ophthalmol Vis Sci 2005, 46(4), 1133-9
  • Stable chromosomal association of MSL2 defines a dosage-compensated nuclear compartment.
    Straub T, Neumann MF, Prestel M, Kremmer E, Kaether C, Haass C, Becker PB
    Chromosoma 2005, 114(5), 352-64 published during change of institution
  • Gene organization features in A/T-rich organisms.
    Szafranski K, Lehmann R, Parra G, Guigo R, Glöckner G
    J Mol Evol 2005, 60(1), 90-8
  • Insights into human Lck SH3 domain binding specificity: different binding modes of artificial and native ligands.
    Tran T, Hoffmann S, Wiesehan K, Jonas E, Luge C, Aladag A, Willbold D
    Biochemistry 2005, 44(45), 15042-52
  • Molecular mechanisms of glucocorticoids in the control of inflammation and lymphocyte apoptosis.
    Tuckermann JP, Kleiman A, McPherson KG, Reichardt HM
    Crit Rev Clin Lab Sci 2005, 42(1), 71-104
  • Microtubules in electric fields.
    Unger E, Stracke R, Michette A, Mavromatos N, Tuszynski JA, Böhm KJ
    In: Proceedings of Coherence and Electric Fields in Biological Systems, CEFBIOS July 1-4, 2005 (edited by Pokorný J), Fröhlich Centenary International Symposium 2005, 23-25, Neoset, Praha
  • Sarcoidosis is associated with a truncating splice site mutation in BTNL2.
    Valentonyte R, Hampe J, Huse K, Rosenstiel P, Albrecht M, Stenzel A, Nagy M, Gaede KI, Franke A, Haesler R, Koch A, Lengauer T, Seegert D, Reiling N, Ehlers S, Schwinger E, Platzer M, Krawczak M, Müller-Quernheim J, Schürmann M, Schreiber S
    Nat Genet 2005, 37(4), 357-64