- ORCID iD
- 0000-0001-9362-7475
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- Journal Article
- A1
- open access
Osteopontin characterizes bile duct-associated macrophages and correlates with liver fibrosis severity in primary sclerosing cholangitis
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Metallothioneins alter macrophage phenotype and represent novel therapeutic targets for acetaminophen-induced liver injury
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Myeloid IRE1a deletion alters hepatic macrophage phenotype and attenuates experimental non-alcoholic steatohepatitis-related hepatocellular carcinoma
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- PhD Thesis
- open access
Relevance and application of mouse models to study non-viral chronic liver disease
(2020) -
- Journal Article
- A2
- open access
Lighter serum copper isotopic composition in patients with early non-alcoholic fatty liver disease
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Myeloid-specific IRE1alpha deletion reduces tumour development in a diabetic, non-alcoholic steatohepatitis-induced hepatocellular carcinoma mouse model
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Combination of sivelestat and N-acetylcysteine alleviates the inflammatory response and exceeds standard treatment for acetaminophen-induced liver injury
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Body distribution of stable copper isotopes during the progression of cholestatic liver disease induced by common bile duct ligation in mice
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Myeloid-specific IRE1 alpha deletion reduces tumour development in a non-alcoholic steatohepatitis-induced hepatocellular carcinoma mouse model
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Common bile duct ligation as model for secondary biliary cirrhosis
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Angiopoietin-2 promotes pathological angiogenesis and is a therapeutic target in murine nonalcoholic fatty liver disease
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Angiopoietin-2 as therapeutic target for pathological angiogenesis and inflammation in non-alcoholic steatohepatitis
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Angiopoietin-2 as therapeutic target for pathological angiogenesis and inflammation in non-alcoholic steatohepatitis
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- Conference Paper
- C3
- open access
Angiopoietin-2 promotes pathological angiogenesis and is a novel therapeutic target in non-alcoholic fatty liver disease
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Cu isotope ratio shifts in common bile duct ligated mice and correlates with the degree of cholestatic-induced liver disease
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Laser ablation-inductively coupled plasma-mass spectrometry for quantitative mapping of the copper distribution in liver tissue sections from mice with liver disease induced by common bile duct ligation