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Ira Pastan

Researcher at Laboratory of Molecular Biology

Publications -  1304
Citations -  113191

Ira Pastan is an academic researcher from Laboratory of Molecular Biology. The author has contributed to research in topics: Immunotoxin & Pseudomonas exotoxin. The author has an hindex of 160, co-authored 1286 publications receiving 110069 citations. Previous affiliations of Ira Pastan include Heidelberg University & National Institutes of Health.

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Immunotoxins containing Pseudomonas exotoxin that target LeY damage human endothelial cells in an antibody-specific mode: relevance to vascular leak syndrome.

TL;DR: Investigation of the effects of several PE-based ITs on different human endothelial cell lines suggests that VLS in patients is due to capillary damage caused by prolonged exposure to high concentrations of LMB-1, and evidence that the cytotoxicity of B3-containing ITs isdue to specific B3 binding to endothelial cells can be blocked by excess free MAb B3 is found.
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Targeted disruption of the mouse mdr1b gene reveals that steroid hormones enhance mdr gene expression.

TL;DR: Kinetic analyses of vinblastine and daunomycin accumulation in both the wild-type and the mutant cell lines during ACTH-stimulated steroidogenesis show that in the mutant cells both drugs accumulated to higher levels than in Y1 cells, suggesting that the remaining mdr1b allele in the Mutant cells is relatively inactive as an exporter of steroids.
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Antitumor effects of an immunotoxin made with Pseudomonas exotoxin in a nude mouse model of human ovarian cancer

TL;DR: It is suggested that intraperitoneal injection of immunotoxins may have a role in the treatment of ovarian cancer.
Journal Article

Regional treatment of epidermal growth factor receptor vIII-expressing neoplastic meningitis with a single-chain immunotoxin, MR-1.

TL;DR: In this article, a single-chain antibody specific for the EGFRvIII mutation was expressed with a modified form of the Pseudomonas exotoxin to form the immunotoxin MR1scFvPE38KDEL (MR-1).
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Isolation and characterization of a highly enriched preparation of receptosomes (endosomes) from a human cell line.

TL;DR: Receptor-mediated endocytosis proceeds by transfer of receptor-ligand complexes from clathrin-coated pits at the cell surface to uncoated endocytic vesicles termed receptosomes (or endosomes), which have now been purified more than 37-fold based on their content of newly internalized epidermal growth factor.