Zobrazeno 1 - 10
of 74
pro vyhledávání: '"Karl Kremser"'
Publikováno v:
Zeitschrift für Hochschulentwicklung, Iss 1 (2011)
Fragestellung: Berichtet wird über die Evaluation der Effektivität des supportiven Unterrichtsangebotes "self organized learning" (SOL), das seit 2002 in den ersten Wochen des Medizinstudiums in Wien eingerichtet wurde. Ziel ist, die Grund-kenntnis
Externí odkaz:
https://doaj.org/article/0220c50366b54d808026a7284a456b18
l-Carnitine alters nitric oxide synthase activity in fibroblasts depending on the peroxisomal status
Autor:
Karl Kremser, Thomas Koeck
Publikováno v:
The International Journal of Biochemistry & Cell Biology. 35:149-156
Fibroblast cellular models are widely used for research on fatty acid metabolism. Due to the importance of l -carnitine in intermediary metabolism we studied the effects of l -carnitine on healthy human skin fibroblasts and fibroblasts without functi
Publikováno v:
Journal of Neurochemistry. 67:2373-2378
Peroxisomal disorders are a newly described group of inherited neurological diseases. In disorders of peroxisomal biogenesis, e.g., Zellweger syndrome, owing to the lack of peroxisomes, catalase, a peroxisomal enzyme, is found to be present in the cy
Autor:
Karl Kremser, Thomas Koeck
Publikováno v:
Nitric Oxide. 5:213-218
As shown recently, in human skin fibroblasts both a constitutively expressed and the inducible nitric oxide synthase (NOS) isoform are present. To identify the NOS isoforms expressed under standard conditions in healthy human skin fibroblasts and fib
Fragestellung: Berichtet wird uber die Evaluation der Effektivitat des supportiven Unterrichtsangebotes "self organized learning" (SOL), das seit 2002 in den ersten Wochen des Medizinstudiums in Wien eingerichtet wurde. Ziel ist, die Grund-kenntnisse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::290d850cc0ae1b78702b70363f4efa55
Publikováno v:
Biochemical and Molecular Medicine. 61:198-207
The peroxisomal disorders represent a group of inherited metabolic disorders that derive from defects of peroxisomal biogenesis and/or from dysfunction of single or multiple peroxisomal enzymes. We described earlier an 8 1/2 year-old with a history o
Autor:
Maria Nemethova, Karl Kremser, Nigel J. Cairns, Marianne Hayn, Gert Lubec, Barbara Lubec, Nicolas Singewald
Publikováno v:
Life Sciences. 59:537-544
It has been proposed that the pathogenesis of Down's Syndrome (DS) involves reactive oxygen species (ROS) arising from a gene dosage effect that disproportionately elevates Superoxide dismutase (SOD1) activity. It was also suggested that generation o
Publikováno v:
Life Sciences. 58:2317-2325
The effects of arginine on tumor growth, antitumor mechanisms and a potential therapeutic role have been reviewed recently. In these studies, however controversial they were, high dose protocols for arginine treatment have been applied. Based upon ow
Publikováno v:
cclm. 33:775-784
Human (HepG2) and rat (MH1C1) hepatoblastoma cells were incubated with different concentrations of the hypolipidaemics cetaben, clofibrate and thyroxine. The enzymatic activities of catalase, peroxisomal bifunctional enzyme, succinate dehydrogenase,
Publikováno v:
Free Radical Research. 22:39-46
To delineate the role of peroxisomes in the pathophysiology of hypoxia-reoxygenation we examined the functions of peroxisomes and mitochondria in cultured skin fibroblasts from controls and from patients with cells lacking peroxisomes (Zellweger cell