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Retraction Note to: High systemic levels of the cytokine-inducing HMGB1 isoform secreted in severe macrophage activation syndrome

Molecular medicine (Cambridge, Mass.), 2020-12, Vol.26 (1), p.131-131, Article 131

2020

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Retraction Note: The α7 nicotinic acetylcholine receptor agonist GTS-21 improves bacterial clearance in mice by restoring hyperoxia-compromised macrophage function

Molecular medicine (Cambridge, Mass.), 2020-12, Vol.26 (1), p.132-132, Article 132

2020

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Retraction Note to: Redox modification of cysteine residues regulates the cytokine activity of high mobility group box-1 (HMGB1)

Molecular medicine (Cambridge, Mass.), 2020-12, Vol.26 (1), p.133-133, Article 133

2020

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Expression of concern to: High systematic levels of the cytokine-inducing HMGB1 isoform secreted in severe macrophage activation syndrome

Molecular medicine (Cambridge, Mass.), 2020-02, Vol.26 (1), p.1-1, Article 17

2020

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Expression of Concern to: The α7 nicotine acetylcholine receptor agonist GTS-21 improves bacterial clearance in mice by restoring hyperoxia-compromised macrophage function

Molecular medicine (Cambridge, Mass.), 2020-02, Vol.26 (1), p.16-16, Article 16

2020

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Expression of Concern to: Redox modification of cysteine residues regulates the cytokine activity of high mobility group box-1 (HMGB1)

Molecular medicine (Cambridge, Mass.), 2020-02, Vol.26 (1), p.18-18, Article 18

2020

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Aminoglycoside-induced nephrotoxicity in children

Pediatric nephrology (Berlin, West), 2017-11, Vol.32 (11), p.2015-2025

2017

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Sequestering HMGB1 via DNA-conjugated beads ameliorates murine colitis

PloS one, 2014-08, Vol.9 (8), p.e103992-e103992

2014

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Redox modification of cysteine residues regulates the cytokine activity of high mobility group box-1 (HMGB1)

Molecular medicine (Cambridge, Mass.), 2012-03, Vol.18 (1), p.250-259

2012

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Signalling via the osteopontin and high mobility group box-1 axis drives the fibrogenic response to liver injury

Gut, 2017-06, Vol.66 (6), p.1123

2017

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CSF1 Restores Innate Immunity After Liver Injury in Mice and Serum Levels Indicate Outcomes of Patients With Acute Liver Failure

Gastroenterology (New York, N.Y. 1943), 2015-12, Vol.149 (7), p.1896-1909.e14

2015

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Targeting oxidative stress improves disease outcomes in a rat model of acquired epilepsy

Brain (London, England : 1878), 2017-07, Vol.140 (7), p.1885-1899

2017

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Are some people at increased risk of paracetamol-induced liver injury? A critical review of the literature

European journal of clinical pharmacology, 2018-02, Vol.74 (2), p.147-160

2018

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Molecular forms of HMGB1 and keratin-18 as mechanistic biomarkers for mode of cell death and prognosis during clinical acetaminophen hepatotoxicity

Journal of hepatology, 2012-01, Vol.56 (5), p.1070-1079

2012

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Bile acid-induced necrosis in primary human hepatocytes and in patients with obstructive cholestasis

Toxicology and applied pharmacology, 2015-03, Vol.283 (3), p.168-177

2015

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Redox‐dependent regulation of hepatocyte absent in melanoma 2 inflammasome activation in sterile liver injury in mice

Hepatology (Baltimore, Md.), 2017-01, Vol.65 (1), p.253-268

2017

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HMGB1 links chronic liver injury to progenitor responses and hepatocarcinogenesis

The Journal of clinical investigation, 2019-04, Vol.129 (4), p.1803-1803

2019

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Plasma biomarkers of liver injury and inflammation demonstrate a lack of apoptosis during obstructive cholestasis in mice

Toxicology and applied pharmacology, 2013-12, Vol.273 (3), p.524-531

2013

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Target biomarker profile for the clinical management of paracetamol overdose

British journal of clinical pharmacology, 2015-09, Vol.80 (3), p.351-362

2015

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

Antioxidants & redox signaling, 2016-04, Vol.24 (12), p.652

2016

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Stem cell–derived models to improve mechanistic understanding and prediction of human drug‐induced liver injury

Hepatology (Baltimore, Md.), 2017-02, Vol.65 (2), p.710-721

2017

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Urinary Biomarkers of Aminoglycoside-Induced Nephrotoxicity in Cystic Fibrosis: Kidney Injury Molecule-1 and Neutrophil Gelatinase-Associated Lipocalin

Scientific reports, 2018-03, Vol.8 (1), p.5094-9, Article 5094

2018

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Treatment of paracetamol overdose: room for improvement?

The Lancet (British edition), 2014-02, Vol.383 (9918), p.672-674

2014

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Paracetamol metabolism, hepatotoxicity, biomarkers and therapeutic interventions: a perspective

Toxicology research (Cambridge), 2018-05, Vol.7 (3), p.347-357

2018

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Risk stratification after paracetamol overdose using mechanistic biomarkers: results from two prospective cohort studies

The lancet. Gastroenterology & hepatology, 2018-02, Vol.3 (2), p.104-113

2018

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Retraction Note to: High systemic levels of the cytokine-inducing HMGB1 isoform secreted in severe macrophage activation syndrome

Retraction Note: The α7 nicotinic acetylcholine receptor agonist GTS-21 improves bacterial clearance in mice by restoring hyperoxia-compromised macrophage function

Retraction Note to: Redox modification of cysteine residues regulates the cytokine activity of high mobility group box-1 (HMGB1)

Expression of concern to: High systematic levels of the cytokine-inducing HMGB1 isoform secreted in severe macrophage activation syndrome

Expression of Concern to: The α7 nicotine acetylcholine receptor agonist GTS-21 improves bacterial clearance in mice by restoring hyperoxia-compromised macrophage function

Expression of Concern to: Redox modification of cysteine residues regulates the cytokine activity of high mobility group box-1 (HMGB1)

Aminoglycoside-induced nephrotoxicity in children

Sequestering HMGB1 via DNA-conjugated beads ameliorates murine colitis

Redox modification of cysteine residues regulates the cytokine activity of high mobility group box-1 (HMGB1)

Signalling via the osteopontin and high mobility group box-1 axis drives the fibrogenic response to liver injury

CSF1 Restores Innate Immunity After Liver Injury in Mice and Serum Levels Indicate Outcomes of Patients With Acute Liver Failure

Targeting oxidative stress improves disease outcomes in a rat model of acquired epilepsy

Are some people at increased risk of paracetamol-induced liver injury? A critical review of the literature

Molecular forms of HMGB1 and keratin-18 as mechanistic biomarkers for mode of cell death and prognosis during clinical acetaminophen hepatotoxicity

Bile acid-induced necrosis in primary human hepatocytes and in patients with obstructive cholestasis

Redox‐dependent regulation of hepatocyte absent in melanoma 2 inflammasome activation in sterile liver injury in mice

HMGB1 links chronic liver injury to progenitor responses and hepatocarcinogenesis

Plasma biomarkers of liver injury and inflammation demonstrate a lack of apoptosis during obstructive cholestasis in mice

Target biomarker profile for the clinical management of paracetamol overdose

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

Stem cell–derived models to improve mechanistic understanding and prediction of human drug‐induced liver injury

Urinary Biomarkers of Aminoglycoside-Induced Nephrotoxicity in Cystic Fibrosis: Kidney Injury Molecule-1 and Neutrophil Gelatinase-Associated Lipocalin

Treatment of paracetamol overdose: room for improvement?

Paracetamol metabolism, hepatotoxicity, biomarkers and therapeutic interventions: a perspective

Risk stratification after paracetamol overdose using mechanistic biomarkers: results from two prospective cohort studies

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