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  • Renate Frei, Sandra Mötzing, Ilka Kinkelin, Melitta Schachner, Martin Koltzenburg, Rudolf Martini
  • Biology, Medicine
  • The Journal of neuroscience : the official…
  • 1999 (First Publication: 15 July 1999)
  • Mice lacking the major Schwann cell myelin component P0 show a severe dysmyelination with pathological features reminiscent of the Déjérine-Sottas syndrome in humans. Previous morphological andContinue Reading
  • Vivianne I Otto, Eugen Damoc, +8 authors Michael Przybylski
  • Medicine, Chemistry
  • Glycobiology
  • 2006 (First Publication: 1 November 2006)
  • Intercellular adhesion molecule-1 (ICAM-1) is a heavily N-glycosylated transmembrane protein comprising five extracellular Ig-like domains. The soluble isoform of ICAM-1 (sICAM-1), consisting of itsContinue Reading
  • Willem Haasnoot, Robert Schilt, +4 authors Udo A. T. Brinkman
  • Chemistry, Medicine
  • Journal of chromatography
  • 1989 (First Publication: 1 April 1989)
  • An immunoaffinity precolumn (immuno precolumn) packed with Sepharose-immobilized polyclonal antibodies against the anabolic hormone 17 beta-19-nortestosterone (beta-19-NT) was used for the selectiveContinue Reading
  • Katrin Adlkofer, Renate Frei, D H Neuberg, Jurgen Zielasek, K. V. Toyka, Ueli Suter
  • Biology, Medicine
  • The Journal of neuroscience : the official…
  • 1997 (First Publication: 15 June 1997)
  • Hereditary neuropathy with liability to pressure palsy (HNPP) is associated with a heterozygous 1.5 megabase deletion on chromosome 17 that includes the peripheral myelin protein (PMP) gene PMP22. WeContinue Reading
  • Mohtashem Samsam, Renate Frei, Martin Marziniak, Rina Martini, Claudia L Sommer
  • Medicine, Biology
  • Journal of neuroscience research
  • 2002 (First Publication: 15 January 2002)
  • Mice heterozygously deficient in the major myelin component P0 are an established model of an inherited neuropathy and show signs of myelin degeneration in motor nerves. Unlike the case in patients,Continue Reading