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An indo investigation of the structure and bonding in malondialdehyde and lithium malondialdehyde
Journal of Molecular Structure, 1975Abstract The geometries of the enol forms of malondialdehyde and its lithium analog have been investigated using the INDO MO method in its original parametrization. The former molecule is predicted to have a planar, symmetric structure nearly identical with that of acetylacetone.
F.J. Marsh, B.G. Thomas, M.S. Gordon
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Lipofuscin-like fluorophores originated from malondialdehyde
Free Radical Research, 2006The accumulation of fluorescent age pigment or lipofuscin is a frequently observed age-associated cellular alteration in a variety of post-mitotic cells of many species. These pigments are observed within granules composed, in part, of damaged protein and lipid.
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Lipid peroxidation—DNA damage by malondialdehyde
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, 1999Malondialdehyde is a naturally occurring product of lipid peroxidation and prostaglandin biosynthesis that is mutagenic and carcinogenic. It reacts with DNA to form adducts to deoxyguanosine and deoxyadenosine. The major adduct to DNA is a pyrimidopurinone called M1G.
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Some Derivatives of Malondialdehyde
The Journal of Organic Chemistry, 1957T. L. V. ULBRICHT, CHARLES C. PRICE
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Malonaldehyde (malondialdehyde).
IARC monographs on the evaluation of carcinogenic risks to humans, 1999openaire +1 more source