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Gal Ben-Josef

Researcher at National Institutes of Health

Publications -  6
Citations -  388

Gal Ben-Josef is an academic researcher from National Institutes of Health. The author has contributed to research in topics: Immunotoxin & Pseudomonas exotoxin. The author has an hindex of 5, co-authored 6 publications receiving 350 citations. Previous affiliations of Gal Ben-Josef include University of Michigan & Yale University.

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SIRT1 Promotes the Central Adaptive Response to Diet Restriction through Activation of the Dorsomedial and Lateral Nuclei of the Hypothalamus

TL;DR: It is demonstrated that diet restriction significantly increases SIRT1 protein levels and induces neural activation in the dorsomedial and lateral hypothalamic nuclei, providing insight into the role of the hypothalamus in the regulation of metabolism and aging in mammals.
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Reporting of Results in ClinicalTrials.gov and High-Impact Journals

TL;DR: Trial information and results reported on ClinicalTrials.gov is fairly complete, although there are concerns about its specificity; optional trial registration information is less complete.
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ABT-737 overcomes resistance to immunotoxin-mediated apoptosis and enhances the delivery of pseudomonas exotoxin-based proteins to the cell cytosol.

TL;DR: ABT-737 might be particularly well suited for enhancing the activity of immunotoxins that translocate from the ER to the cell cytosol, because of its activity in the ER, and possible mechanisms of resistance.
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LPS-binding protein mediates LPS-induced liver injury and mortality in the setting of biliary obstruction

TL;DR: The results indicate that the role of L BP signaling in inflammatory conditions is complex and heterogeneous, and elevated levels of LBP are not always protective, and Increased LBP production in the setting of cholestatic liver disease appears to be deleterious and may represent a potential therapeutic target for preventing overwhelming inflammatory responses to LPS in this setting.
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Enhancing immunotoxin cell-killing activity via combination therapy with ABT-737

TL;DR: Combined therapy with the BH3-only mimetic, ABT-737, and immunotoxin–ABT combinations often exhibit greater killing activity than either compound alone and in some instances overcome resistance.