Low neurotoxicity of ONX-0914 supports the idea of specific immunoproteasome inhibition as a side-effect-limiting, therapeutic strategy-Reference-Cited by-同舟云学术

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Low neurotoxicity of ONX-0914 supports the idea of specific immunoproteasome inhibition as a side-effect-limiting, therapeutic strategy

Published:2017-09 Issue:3 Volume:7 Page:234-245
ISSN:2062-8633
Container-title:European Journal of Microbiology and Immunology
language:en
Short-container-title:European Journal of Microbiology and Immunology

Author:

von Brzezinski Laura¹,Säring Paula¹,Landgraf Peter¹,Cammann Clemens²,Seifert Ulrike²,Dieterich Daniela C.¹³

Affiliation:

1. Neural Plasticity and Communication, Institute for Pharmacology and Toxicology, Otto-von-Guericke-University Magdeburg, Magdeburg, Germany

2. Friedrich Loeffler Institute for Medical Microbiology, Greifswald, Germany

3. Center for Behavioral Brain Sciences, Magdeburg, Germany

Publisher

Akademiai Kiado Zrt.

Link

https://www.akademiai.com/doi/pdf/10.1556/1886.2017.00025

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2. Interplay between proteasome function and inflammatory responses in e-cig vapor condensate-challenged lung epithelial cells;Archives of Toxicology;2023-06-22

3. PR-957 Suppresses Th1 and Th17 Cell Differentiation via Inactivating PI3K/AKT Pathway in Alzheimer’s Disease;Neuroscience;2023-02

4. Improved Scalable Synthesis of Clinical Candidate KZR‐616, a Selective Immunoproteasome Inhibitor;ChemistrySelect;2021-11-25

5. A Nut for Every Bolt: Subunit-Selective Inhibitors of the Immunoproteasome and Their Therapeutic Potential;Cells;2021-07-29

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