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Microbial Pathogenesis|March 8, 2005
Comparison of wild type with recombinant Clostridium difficile toxin ARalf Gerhard, Silke Burger, Helma Tatge, et al.
Biochemical and Biophysical Research Communications|August 2, 2003
Expression of recombinant Clostridium difficile toxin A using the Bacillus megaterium systemSilke Burger, Helma Tatge, Fred Hofmann, et al.
The Journal of Biological Chemistry|November 9, 2004
Clostridium difficile toxin A induces expression of the stress-induced early gene product RhoBRalf Gerhard, Helma Tatge, Harald Genth, et al.
FEBS Letters|May 30, 2006
Cellular stability of Rho-GTPases glucosylated by Clostridium difficile toxin BHarald Genth, Johannes Huelsenbeck, Birgit Hartmann, et al.
Infection and Immunity|September 22, 2006
Application of mutated Clostridium difficile toxin A for determination of glucosyltransferase-dependent effectsMatthias Teichert, Helma Tatge, Janett Schoentaube, et al.
Cellular Microbiology|August 28, 2009
Serine-71 phosphorylation of Rac1/Cdc42 diminishes the pathogenic effect of Clostridium difficile toxin AJanett Schoentaube, Alexandra Olling, Helma Tatge, et al.
Journal of Medical Microbiology|May 16, 2008
Glucosylation of Rho GTPases by Clostridium difficile toxin A triggers apoptosis in intestinal epithelial cellsRalf Gerhard, Stefanie Nottrott, Janett Schoentaube, et al.
The Journal of Biological Chemistry|March 29, 2007
Neogenin-RGMa signaling at the growth cone is bone morphogenetic protein-independent and involves RhoA, ROCK, and PKCSabine Conrad, Harald Genth, Fred Hofmann, et al.
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