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Article
Beitrag zur Kenntnis der Bindungsverhältnisse bei der Vereinigung von Diphtheriegift und Antiserum.
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Year: 1904 Publisher: Leipzig : Georg Thieme,

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Dissertation
Ueber das Verhalten des Klebs-Löffler'schen Diphtheriebacillus in der Milch nebst einigen Bemerkungen zur Sterilisation derselben
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Year: 1897 Publisher: Berlin : L. Schumacher,

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Dissertation
Relevance of the cell cycle status of leukemic cells in the treatment of acute myeloid leukemia
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Year: 2003 Publisher: Leiden s.n.


Book
Corynebacterium diphtheriae and Related Toxigenic Species : Genomics, Pathogenicity and Applications
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ISBN: 9400776233 9400776241 Year: 2014 Publisher: Dordrecht : Springer Netherlands : Imprint: Springer,

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Corynebacterium diphtheriae is the classical etiological agent of diphtheria and the type strain of the genus Corynebacterium. While diphtheria of the respiratory tract became rare with the introduction of vaccination programs in industrialized countries, even today several thousand cases per year are reported to the World Health Organization. This shows that diphtheria is not completely eradicated and that reservoirs exist. The book summarizes the latest advances made in understanding C. diphtheriae and the closely related species Corynebacterium ulcerans and Corynebacterium pseudotuberculosis. Topics addressed are genomics of toxigenic corynebacteria, host-pathogen-interaction, detection, surveillance and treatment as well as application aspects.

Clinical applications of immunotoxins
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ISBN: 3540640975 3642721559 3642721532 Year: 1998 Volume: 234 Publisher: Berlin : Springer,

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1 2 D. FITZGERALDI, I. PASTAN , and J. ROBERTUS Introduction . . . . . . . . . . . . . I 2 Toxin Structure-Function Properties 2 2. 1 Functions. . . . . . . . . . . . . . . . . . . . . . . . 2 2. 2 Binding. . . . . . . . . . . . . . . . . . . . . . . . . 3 3 Intracellular Processing - Cleavage and Reduction . . . . . . 4 3. 1 Cytosolic Activity . . . . . . . . . . . . . . . . 5 4 Immunotoxin Design and Testing. 6 5 Conclusion. . 8 References. . . . . 8 1 Introduction While various treatment approaches for cancer include reversal of the transformed phenotype, stimulation of immune responses, inhibition of metastatic spread and deprivation of key nutrients, the goal of immunotoxin treatment is the direct killing of malignant cells. Because they are enzymatic proteins that act catalytically to kill cells, bacterial and plant toxins are often employed as the cell-killing component of immunotoxins. Here we provide background information into the structure-func­ tion relationships of toxins and discuss how they can be combined with cell-binding antibodies or other ligands to generate immunotoxins. Bacterial and plant toxins (e. g. , diphtheria toxin, Pseudomonas exotoxin and ricin) are among the most toxic substances known. However, because they bind to cell surface receptors that are present on most normal cells, unmodified toxins are generally useless as anti-cancer agents. To convert toxins into more selective agents, their binding domains are either eliminated or disabled and replaceq with cell­ binding antibodies that are tumor-selective.

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