Redox-Dependent HMGB1 Isoforms as Pivotal Co-Ordinators of Drug-Induced Liver Injury: Mechanistic Biomarkers and Therapeutic Targets-Reference-Cited by-同舟云学术

Redox-Dependent HMGB1 Isoforms as Pivotal Co-Ordinators of Drug-Induced Liver Injury: Mechanistic Biomarkers and Therapeutic Targets

Published:2016-04-20 Issue:12 Volume:24 Page:652-665
ISSN:1523-0864
Container-title:Antioxidants & Redox Signaling
language:en
Short-container-title:Antioxidants & Redox Signaling

Author:

Lea Jonathan D.¹,Clarke Joanna I.¹,McGuire Niamh¹,Antoine Daniel J.¹

Affiliation:

1. Department of Molecular and Clinical Pharmacology, MRC Centre for Drug Safety Science, University of Liverpool, Liverpool, United Kingdom.

Publisher

Mary Ann Liebert Inc

Subject

Cell Biology,Clinical Biochemistry,Molecular Biology,Physiology,Biochemistry,Cell Biology,Clinical Biochemistry,Molecular Biology,Physiology,Biochemistry

Link

http://www.liebertpub.com/doi/pdf/10.1089/ars.2015.6406

Reference102 articles.

1. Expression of Concern: The functions of HMGB 1 depend on molecular localization and post‐translational modifications

2. Drug-Induced Liver Injury: An Analysis of 461 Incidences Submitted to the Spanish Registry Over a 10-Year Period

3. Mechanistic biomarkers provide early and sensitive detection of acetaminophen‐induced acute liver injury at first presentation to hospital

4. Safety biomarkers for drug-induced liver injury – current status and future perspectives

5. A Systematic Nomenclature for the Redox States of High Mobility Group Box (HMGB) Proteins

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