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Ralf Gerhard

Showing results (21-30 of 70) with videos related to

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Cellular Microbiology|December 23, 2014
Human neutrophils are activated by a peptide fragment of Clostridium difficile toxin B presumably via formyl peptide receptorSebastian D Goy, Alexandra Olling, Detlef Neumann, et al.
Toxins|January 20, 2023
CDT of <i>Clostridioides difficile</i> Induces MLC-Dependent Intestinal Barrier Dysfunction in HT-29/B6 Epithelial Cell MonolayersLucas Heils, Martina Schneemann, Ralf Gerhard, et al.
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.
Plos One|March 30, 2011
The repetitive oligopeptide sequences modulate cytopathic potency but are not crucial for cellular uptake of Clostridium difficile toxin AAlexandra Olling, Sebastian Goy, Florian Hoffmann, 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.
Toxins|December 1, 2020
Receptor Binding Domains of TcdB from <i>Clostridioides difficile</i> for Chondroitin Sulfate Proteoglycan-4 and Frizzled Proteins Are Functionally Independent and AdditiveDaniel Henkel, Helma Tatge, Dennis Schöttelndreier, et al.
Toxicology|December 16, 2014
Clostridium difficile toxin B inhibits the secretory response of human mast cell line-1 (HMC-1) cells stimulated with high free-Ca²⁺ and GTPγSAndrea Balletta, Dorothea Lorenz, Andreas Rummel, et al.
Proteomics|June 15, 2017
Glucosyltransferase-dependent and -independent effects of TcdB on the proteome of HEp-2 cellsJelena Erdmann, Johannes Junemann, Anke Schröder, et al.
Toxins|April 27, 2026
Interference of Large Clostridial Glucosyltransferases with the Endolysosomal Pathway: Toxin-Induced Imbalance of Early Endosomes, Functional Lysosomes and AutophagosomesAnna Langejürgen, Gudula Schmidt, Leon Unsöld, et al.
Pageof 7

Showing results (21-30 of 70) with videos related to

Sort By:
Pageof 7
Cellular Microbiology|December 23, 2014
Human neutrophils are activated by a peptide fragment of Clostridium difficile toxin B presumably via formyl peptide receptorSebastian D Goy, Alexandra Olling, Detlef Neumann, et al.
Toxins|January 20, 2023
CDT of <i>Clostridioides difficile</i> Induces MLC-Dependent Intestinal Barrier Dysfunction in HT-29/B6 Epithelial Cell MonolayersLucas Heils, Martina Schneemann, Ralf Gerhard, et al.
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.
Plos One|March 30, 2011
The repetitive oligopeptide sequences modulate cytopathic potency but are not crucial for cellular uptake of Clostridium difficile toxin AAlexandra Olling, Sebastian Goy, Florian Hoffmann, 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.
Toxins|December 1, 2020
Receptor Binding Domains of TcdB from <i>Clostridioides difficile</i> for Chondroitin Sulfate Proteoglycan-4 and Frizzled Proteins Are Functionally Independent and AdditiveDaniel Henkel, Helma Tatge, Dennis Schöttelndreier, et al.
Toxicology|December 16, 2014
Clostridium difficile toxin B inhibits the secretory response of human mast cell line-1 (HMC-1) cells stimulated with high free-Ca²⁺ and GTPγSAndrea Balletta, Dorothea Lorenz, Andreas Rummel, et al.
Proteomics|June 15, 2017
Glucosyltransferase-dependent and -independent effects of TcdB on the proteome of HEp-2 cellsJelena Erdmann, Johannes Junemann, Anke Schröder, et al.
Toxins|April 27, 2026
Interference of Large Clostridial Glucosyltransferases with the Endolysosomal Pathway: Toxin-Induced Imbalance of Early Endosomes, Functional Lysosomes and AutophagosomesAnna Langejürgen, Gudula Schmidt, Leon Unsöld, et al.
Pageof 7