Relativistic Calculation of Hyperfine Parameters of Mercury Compounds

Die Speicherung von 197Hg-Quecksilbercysteinide wurde in vier Arten von experimentellen Tumoren untersucht. Die Ergebnisse zeigten keine höhere Tumorspeicherung im Vergleich zum 197Hg-Quecksilbertetracycline oder 197Hg-Quecksilberazetat. Die Möglichkeit einer Verwendung von 197Hg-cysteinid zur Diagnose eines Herzinfarktes wurde bestätigt.

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Stationary source emissions. Sampling and determination of mercury compounds in flue gas using gold amalgamation trap

10.3403/30349188 ◽

2020 ◽

Keyword(s):

Flue Gas ◽

Mercury Compounds ◽

Stationary Source

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Toolbox approach for quasi-relativistic calculation of molecular properties for precision tests of fundamental physics

The Journal of Chemical Physics ◽

10.1063/1.5121483 ◽

2020 ◽

Vol 152 (4) ◽

pp. 044101 ◽

Cited By ~ 4

Author(s):

Konstantin Gaul ◽

Robert Berger

Keyword(s):

Molecular Properties ◽

Fundamental Physics ◽

Relativistic Calculation

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ORGANIC MERCURY COMPOUNDS PREPARED FROM ORTHO-CHLOROMERCURI-PARA-NITROBENZOYL CHLORIDE1

Journal of the American Chemical Society ◽

10.1021/ja01428a023 ◽

1922 ◽

Vol 44 (7) ◽

pp. 1546-1551 ◽

Cited By ~ 1

Author(s):

Frank C. Whitmore ◽

Edmund Burrus Middleton

Keyword(s):

Organic Mercury ◽

Mercury Compounds

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In Vitro Methods as a Tool in Neurotoxicity Studies

Alternatives to Laboratory Animals ◽

10.1177/026119299502300412 ◽

1995 ◽

Vol 23 (4) ◽

pp. 491-496

Author(s):

Hanna Tähti ◽

Leila Vaalavirta ◽

Tarja Toimela

Keyword(s):

Risk Evaluation ◽

Toxicity Testing ◽

In Vitro Models ◽

In Vitro Tests ◽

Industrial Chemicals ◽

Mercury Compounds ◽

Toxicological Data ◽

In Vivo Tests

— There are several hundred industrial chemicals with neurotoxic potential. The neurotoxic risks of most of these chemicals are unknown. Additional methods are needed to assess the risks more effectively and to elucidate the mechanisms of neurotoxicity more accurately than is possible with the conventional methods. This paper deals with general tasks concerning the use of in vitro models in the evaluation of neurotoxic risks. It is based on our previous studies with various in vitro models and on recent literature. The induction of glial fibrillary acidic protein in astrocyte cultures after treatment with known neurotoxicants (mercury compounds and aluminium) is discussed in more detail as an important response which can be detected in vitro. When used appropriately with in vivo tests and with previous toxicological data, in vitro neurotoxicity testing considerably improves risk assessment. The incorporation of in vitro tests into the early stages of risk evaluation can reduce the number of animals used in routine toxicity testing, by identifying chemicals with high neurotoxic potential.

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