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Effects of cysteamine onPseudomonas infections in mice [PDF]
Antonie van Leeuwenhoek, 1964 A non-lethal dose of cysteamine — a radioprotective agent — when administered intraperitoneally was demonstrated to increase the susceptibility of mice to infection byPseudomonas aeruginosa. At numbers of cells (about 106) which killed 30–40 per cent of the untreated mice, the intraperitoneal treatment with 5 mg per day of cysteamine raised the ...
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ACS Applied Nano Materials, 2019
Despite the significant therapeutic use of cysteamine as drug in cystinosis, it also has some serious health issues such as idiopathic intracranial hypertension (IIH), Ehlers–Danlos syndrome, and eye related problems including blurred or loss of vision ...
Gagandeep Singh +4 more
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Despite the significant therapeutic use of cysteamine as drug in cystinosis, it also has some serious health issues such as idiopathic intracranial hypertension (IIH), Ehlers–Danlos syndrome, and eye related problems including blurred or loss of vision ...
Gagandeep Singh +4 more
semanticscholar +1 more source
Steroid derivatives of cysteamine and cysteine
Canadian Journal of Chemistry, 1969A number of androstenone, estrone, and pregnenone derivatives of cysteamine have been prepared by reacting the steroid amines with ethylene monothiolcarbonate. The amides of androstenone carboxylic acid with mercaptoethylamine and cysteine have also been prepared.
Cesar Reyes-Zamora, Owen H. Wheeler
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High Energy Chemistry, 2002
5-S-Cysteaminemethyluracil (the product of cysteamine attachment to the methyl group of thymine) was isolated from irradiated solutions containing thymine and cysteamine and identified. This compound was formed in the reaction of thiyl radicals with 5-methyleneuracil-5-yl radicals formed by H-atom abstraction from the methyl group of thymine.
G. I. Litvyakova +2 more
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5-S-Cysteaminemethyluracil (the product of cysteamine attachment to the methyl group of thymine) was isolated from irradiated solutions containing thymine and cysteamine and identified. This compound was formed in the reaction of thiyl radicals with 5-methyleneuracil-5-yl radicals formed by H-atom abstraction from the methyl group of thymine.
G. I. Litvyakova +2 more
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Particle & Particle Systems Characterization, 2018
Sonodynamic therapy (SDT), as a newly emerging and promising modality for cancer treatment, has been extensively investigated but with limited therapeutic outcome because of the absence of highly efficient sonosensitizer.
Pan Wang +9 more
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Sonodynamic therapy (SDT), as a newly emerging and promising modality for cancer treatment, has been extensively investigated but with limited therapeutic outcome because of the absence of highly efficient sonosensitizer.
Pan Wang +9 more
semanticscholar +1 more source
Journal of Molecular Recognition, 2019
In this study, a novel electroconductive interface was prepared based on Fe3O4 magnetic nanoparticle and cysteamine functionalized gold nanoparticle. The engineered interface was used as signal amplification substrate in the electrochemical analysis of ...
Fatemeh Farshchi +2 more
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In this study, a novel electroconductive interface was prepared based on Fe3O4 magnetic nanoparticle and cysteamine functionalized gold nanoparticle. The engineered interface was used as signal amplification substrate in the electrochemical analysis of ...
Fatemeh Farshchi +2 more
semanticscholar +1 more source
Inhibitory effects of cysteamine on neuroendocrine function
Regulatory Peptides, 1983The action of cysteamine on anterior pituitary hormone secretion was studied in vivo using conscious, freely moving male rats and in vitro using anterior pituitary cells in monolayer culture. Administration of 500 micrograms cysteamine into the lateral cerebral ventricles of normal rats caused the complete inhibition of pulsatile GH secretion for a ...
Roger Guillemin +3 more
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The Journal of Pharmacology and Experimental Therapeutics, 1957
R A, SALVADOR, C, DAVISON, P K, SMITH
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R A, SALVADOR, C, DAVISON, P K, SMITH
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