Metabolism of the β-oxidized intermediates of N-nitrosodi-n-propylamine: N-nitroso-β-hydroxypropylpropylamine and N-nitroso-β-oxopropylpropylamine
Nitroso-urea-cisplatin-based chemotherapy associated with valproate: Increase of haematologic toxicity
Effect of Aromatic Nitroso-Compounds on Superoxide-Generating Activity in Neutrophils
Strong nasal carcinogenicity and genotoxicity of 1-nitroso-4-methylpiperazine after low dose inhalation in rats
Genotoxicity of propoxur and its N-nitroso derivative in mammalian cells.
P644Mechanisms of myocardial nitroso redox imbalance following elective cardiac surgery on cardiopulmonary bypass
Compromised redox homeostasis, altered nitroso–redox balance, and therapeutic possibilities in atrial fibrillation
Genetic toxicity of N-methylcarbamate insecticides and their N-nitroso derivatives
Molecular Signatures of N-nitroso Compounds in Caco-2 Cells: Implications for Colon Carcinogenesis
Mechanisms of Nitroso Compound—Induced Inhibition of Superoxide Generation in Neutrophils: Fluorescence Quenching of Perylene by Nitroso-Compounds in the Membrane Fractions of Neutrophils
Re: Etiology of Pancreatic Cancer, With a Hypothesis Concerning the Role of N-Nitroso Compounds and Excess Gastric Acidity
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The chemical group −NO in a chemical compound.
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