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Albert-Ludwigs-Universität Freiburg. Institut für Experimentelle und Klinische Pharmakologie und Toxikologie

Freiburg im Breisgau

Name	Albert-Ludwigs-Universität Freiburg. Institut für Experimentelle und Klinische Pharmakologie und Toxikologie
Time	2001- (Bestehen)
Place	Freiburg im Breisgau Baden-Württemberg (Wirkungsraum) Deutschland
Variant	Albert-Ludwigs-Universität Freiburg. Medizinische Fakultät. Institut für Experimentelle und Klinische Pharmakologie und Toxikologie
Predecessor	Albert-Ludwigs-Universität Freiburg. Institut für Pharmakologie und Toxikologie
Hierarchical superior	Albert-Ludwigs-Universität Freiburg Albert-Ludwigs-Universität Freiburg. Medizinische Fakultät
Source	Homepage: https://portal.uni-freiburg.de/pharmakologie
Record type	Organisation
GND-Identifier	108196426X
Record ID	108196426X
Involved in show all Untersuchungen zu den Funktionen des two-pore channel 1 im Zell- und Tiermodell Kontrolle der Genexpression und des vesikulären Transports Einfluss von RhoA und RhoC auf die EGF-abhängige Proliferation von benignen Brustepithelzellen Promotor-Enhancer-Interaktionen in humanen Herzmuskelzellen High affinity binding of Escherichia coli cytotoxic necrotizing Factor 1 (CNF1) to Lu/BCAM adhesion glycoprotein Auranofin inhibits the enzyme activity of Pasteurella multocida toxin PMT in human cells and protects cells from intoxication Bacterial toxins for cancer therapy Targeted delivery of an ADP-ribosylating bacterial toxin into cancer cells EGA protects mammalian cells from Clostridium difficile CDT, Clostridium perfringens iota toxin, and Clostridium botulinum C2 toxin Roles of Asp179 and Glu270 in ADP-ribosylation of Actin by Clostridium perfringens Iota Toxin Lu/BCAM adhesion glycoprotein is a receptor for Escherichia coli Cytotoxic Necrotizing Factor 1 (CNF1) Tailored cyclodextrin pore blocker protects mammalian cells from Clostridium difficile binary toxin CDT Activation of RhoA,B,C by Yersinia Cytotoxic Necrotizing Factor (CNFy) induces Apoptosis in LNCaP prostate cancer cells Clostridium difficile binary toxin CDT induces clustering of the lipolysis-stimulated lipoprotein receptor into lipid rafts Pasteurella multocida toxin prevents osteoblast differentiation by transactivation of the MAP-kinase cascade via the Gaq/11 - p63RhoGEF - RhoA axis Phosphoinositide-3-kinases p110α and p110β mediate S phase entry in astroglial cells in the marginal zone of rat neocortex Tetraspanin-13 modulates voltage-gated Cav2.2 Ca2+ channels

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Albert-Ludwigs-Universität Freiburg. Institut für Experimentelle und Klinische Pharmakologie und Toxikologie

Untersuchungen zu den Funktionen des two-pore channel 1 im Zell- und Tiermodell Kontrolle der Genexpression und des vesikulären Transports

Einfluss von RhoA und RhoC auf die EGF-abhängige Proliferation von benignen Brustepithelzellen

Promotor-Enhancer-Interaktionen in humanen Herzmuskelzellen

High affinity binding of Escherichia coli cytotoxic necrotizing Factor 1 (CNF1) to Lu/BCAM adhesion glycoprotein

Auranofin inhibits the enzyme activity of Pasteurella multocida toxin PMT in human cells and protects cells from intoxication

Bacterial toxins for cancer therapy

Targeted delivery of an ADP-ribosylating bacterial toxin into cancer cells

EGA protects mammalian cells from Clostridium difficile CDT, Clostridium perfringens iota toxin, and Clostridium botulinum C2 toxin

Roles of Asp179 and Glu270 in ADP-ribosylation of Actin by Clostridium perfringens Iota Toxin

Lu/BCAM adhesion glycoprotein is a receptor for Escherichia coli Cytotoxic Necrotizing Factor 1 (CNF1)

Tailored cyclodextrin pore blocker protects mammalian cells from Clostridium difficile binary toxin CDT

Activation of RhoA,B,C by Yersinia Cytotoxic Necrotizing Factor (CNFy) induces Apoptosis in LNCaP prostate cancer cells

Clostridium difficile binary toxin CDT induces clustering of the lipolysis-stimulated lipoprotein receptor into lipid rafts

Pasteurella multocida toxin prevents osteoblast differentiation by transactivation of the MAP-kinase cascade via the Gaq/11 - p63RhoGEF - RhoA axis

Phosphoinositide-3-kinases p110α and p110β mediate S phase entry in astroglial cells in the marginal zone of rat neocortex

Tetraspanin-13 modulates voltage-gated Cav2.2 Ca2+ channels