Area of research
Molecular Biology · Clinical Biochemistry
Research interest
Research interests include Biology, Peroxisome, Cell biology, Biochemistry, Biogenesis, and Mitochondrion.
Oligodendroglial fatty acid metabolism as a central nervous system energy reserve
The essential role of docosahexaenoic acid and its derivatives for retinal integrity
The physiological functions of human peroxisomes
Spatiotemporal contact between peroxisomes and lipid droplets regulates fasting-induced lipolysis via PEX5
Deciphering the potential involvement of PXMP2 and PEX11B in hydrogen peroxide permeation across the peroxisomal membrane reveals a role for PEX11B in protein sorting
Peroxisomes can oxidize medium‐ and long‐chain fatty acids through a pathway involving ABCD3 and HSD17B4
Constitutive IP3 signaling underlies the sensitivity of B-cell cancers to the Bcl-2/IP3 receptor disruptor BIRD-2
Endothelial cell metabolism in health and disease: impact of hypoxia
Increased Expression of Translocator Protein (TSPO) Marks Pro-inflammatory Microglia but Does Not Predict Neurodegeneration
Peroxisomal biogenesis is genetically and biochemically linked to carbohydrate metabolism in Drosophila and mouse
Peroxisomal dysfunctions cause lysosomal storage and axonal Kv1 channel redistribution in peripheral neuropathy
Fatty acid carbon is essential for dNTP synthesis in endothelial cells
Hepatic dysfunction in peroxisomal disorders
Identification of a chronic non‐neurodegenerative microglia activation state in a mouse model of peroxisomal β‐oxidation deficiency
Peroxisomal Disorders: A Review on Cerebellar Pathologies
The oxysterol and cholestenoic acid profile of mouse cerebrospinal fluid
Mitochondria in peroxisome-deficient hepatocytes exhibit impaired respiration, depleted DNA, and PGC-1α independent proliferation
Role of AMACR (α-methylacyl-CoA racemase) and MFE-1 (peroxisomal multifunctional enzyme-1) in bile acid synthesis in mice
Mitochondria are targets for peroxisome-derived oxidative stress in cultured mammalian cells
Peroxisomal multifunctional protein-2 deficiency causes neuroinflammation and degeneration of Purkinje cells independent of very long chain fatty acid accumulation
Peroxisome deficient invertebrate and vertebrate animal models
Gene-Targeting of Phd2 Improves Tumor Response to Chemotherapy and Prevents Side-Toxicity
Peroxisome deficiency but not the defect in ether lipid synthesis causes activation of the innate immune system and axonal loss in the central nervous system
Mouse models for peroxisome biogenesis defects and β-oxidation enzyme deficiencies