Thioltransferase (glutaredoxin) is a member of the family of thiol-disulfide oxido-reductases that maintain the sulfhydryl homeostasis in cells by catalyzing thiol-disulfide interchange reactions. One of the major consequences of oxidative stress in brain is formation of protein-glutathione mixed disulfide (through oxidation of protein thiols) which can be reversed by thioltransferase during recovery of brain from oxidative stress. Here we have visualized the location of thioltransferase in brain regions from seven human tissues obtained at autopsy. Constitutively expressed thioltransferase activity was detectable in all human brains examined although inter-individual variations were seen. The enzyme activity was significantly higher in hip...
AbstractPCR primers were designed from the known amino acid (aa) sequence for human red blood cell t...
Sulfur containing molecules such as thiols, disulfides, sulfoxides, sulfonic acids, and sulfates may...
Redox regulation of proteins through oxidation and S-thiolation are important regulatory processes, ...
Thioltransferase (TTase) is a member of the family of thiol-disulfide oxidoreductases that are invol...
Mitochondrial dysfunction involving electron transport components is implicated in the pathogenesis ...
The physiological and pathological roles of reactive oxygen species (ROS) in the brain are still unc...
The immunoreactivity for thioredoxin, which catalyzes protein disulfide reductions, has previously b...
Production of reactive oxygen species (ROS) has long been regarded as a side effect of oxygen metabo...
The significance of pro-oxidative pathways for normal brain function remains uncertain. Reactive oxy...
The status of glutathione (GSH) and protein thiol homeostasis was examined in rat brain regions duri...
Oxidative stress has been implicated in the pathogenesis and progression of many neurodegenerative d...
Glutathione (GSH) was discovered in yeast cells in 1888. Studies of GSH in mammalian cells before th...
Glutathione (GSH) was discovered in yeast cells in 1888. Studies of GSH in mammalian cells before th...
Aims: The human branched-chain aminotransferase proteins (hBCATm and hBCATc) are regulated through o...
Aims: The human branched-chain aminotransferase proteins (hBCATm and hBCATc) are regulated through o...
AbstractPCR primers were designed from the known amino acid (aa) sequence for human red blood cell t...
Sulfur containing molecules such as thiols, disulfides, sulfoxides, sulfonic acids, and sulfates may...
Redox regulation of proteins through oxidation and S-thiolation are important regulatory processes, ...
Thioltransferase (TTase) is a member of the family of thiol-disulfide oxidoreductases that are invol...
Mitochondrial dysfunction involving electron transport components is implicated in the pathogenesis ...
The physiological and pathological roles of reactive oxygen species (ROS) in the brain are still unc...
The immunoreactivity for thioredoxin, which catalyzes protein disulfide reductions, has previously b...
Production of reactive oxygen species (ROS) has long been regarded as a side effect of oxygen metabo...
The significance of pro-oxidative pathways for normal brain function remains uncertain. Reactive oxy...
The status of glutathione (GSH) and protein thiol homeostasis was examined in rat brain regions duri...
Oxidative stress has been implicated in the pathogenesis and progression of many neurodegenerative d...
Glutathione (GSH) was discovered in yeast cells in 1888. Studies of GSH in mammalian cells before th...
Glutathione (GSH) was discovered in yeast cells in 1888. Studies of GSH in mammalian cells before th...
Aims: The human branched-chain aminotransferase proteins (hBCATm and hBCATc) are regulated through o...
Aims: The human branched-chain aminotransferase proteins (hBCATm and hBCATc) are regulated through o...
AbstractPCR primers were designed from the known amino acid (aa) sequence for human red blood cell t...
Sulfur containing molecules such as thiols, disulfides, sulfoxides, sulfonic acids, and sulfates may...
Redox regulation of proteins through oxidation and S-thiolation are important regulatory processes, ...