Hochschulschrift
Structural insights into the mechanism of pore-forming toxin alpha-Xenorhabdolysin
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Maße
-
30 cm
- Umfang
-
IX, 153 Seiten
- Sprache
-
Englisch
- Anmerkungen
-
Illustrationen
Technische Universität Dortmund, Dissertation, 2020
- Klassifikation
-
Biowissenschaften, Biologie
Landwirtschaft, Veterinärmedizin
- Inhaltsverzeichnis
- Rechteinformation
-
Bei diesem Objekt liegt nur das Inhaltsverzeichnis digital vor. Der Zugriff darauf ist unbeschränkt möglich.
- Letzte Aktualisierung
-
11.03.2025, 11:42 MEZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Objekttyp
- Hochschulschrift
Beteiligte
Entstanden
- [2020?]
Ähnliche Objekte (12)
Role for caspase-2 during pore-forming toxin-mediated apoptosis
Characterization and pharmacological inhibition of the pore-forming clostridioides difficile CDTb toxin
Single Particle Tracking to Characterize the Mechanism of Pore Formation by Pore Forming Proteins
Structural and biochemical characterization of the YaxAB pore-forming toxin from Yersinia enterocolitica
Pore forming toxins : with 1 table
Analysis of pore-forming proteins in lipid membranes
Structural and functional characterization of pore-forming proteins
The pore-forming subunit C2IIa of the binary clostridium botulinum C2 toxin reduces the chemotactic translocation of human polymorphonuclear leukocytes
Tailored cyclodextrin pore blocker protects mammalian cells from Clostridium difficile binary toxin CDT
Structural studies on the pore-forming mitochondrial membrane proteins Bak and MPV17
Characterization of the cellular uptake mechanism and cytotoxic effects of pertussis toxin, Clostridium botulinum C2 toxin, and Clostridioides difficile toxins: Pathways to novel pharmacological inhibitors against toxin-mediated diseases
pore
Role for caspase-2 during pore-forming toxin-mediated apoptosis
Characterization and pharmacological inhibition of the pore-forming clostridioides difficile CDTb toxin
Single Particle Tracking to Characterize the Mechanism of Pore Formation by Pore Forming Proteins
Structural and biochemical characterization of the YaxAB pore-forming toxin from Yersinia enterocolitica
Pore forming toxins : with 1 table
Analysis of pore-forming proteins in lipid membranes
Structural and functional characterization of pore-forming proteins
The pore-forming subunit C2IIa of the binary clostridium botulinum C2 toxin reduces the chemotactic translocation of human polymorphonuclear leukocytes
Tailored cyclodextrin pore blocker protects mammalian cells from Clostridium difficile binary toxin CDT
Structural studies on the pore-forming mitochondrial membrane proteins Bak and MPV17
Characterization of the cellular uptake mechanism and cytotoxic effects of pertussis toxin, Clostridium botulinum C2 toxin, and Clostridioides difficile toxins: Pathways to novel pharmacological inhibitors against toxin-mediated diseases
pore
Role for caspase-2 during pore-forming toxin-mediated apoptosis
Characterization and pharmacological inhibition of the pore-forming clostridioides difficile CDTb toxin
Single Particle Tracking to Characterize the Mechanism of Pore Formation by Pore Forming Proteins
Structural and biochemical characterization of the YaxAB pore-forming toxin from Yersinia enterocolitica
Pore forming toxins : with 1 table
Analysis of pore-forming proteins in lipid membranes
Structural and functional characterization of pore-forming proteins
The pore-forming subunit C2IIa of the binary clostridium botulinum C2 toxin reduces the chemotactic translocation of human polymorphonuclear leukocytes
Tailored cyclodextrin pore blocker protects mammalian cells from Clostridium difficile binary toxin CDT
Structural studies on the pore-forming mitochondrial membrane proteins Bak and MPV17
Characterization of the cellular uptake mechanism and cytotoxic effects of pertussis toxin, Clostridium botulinum C2 toxin, and Clostridioides difficile toxins: Pathways to novel pharmacological inhibitors against toxin-mediated diseases