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- Antzutkin, Oleg
(author)
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Polymorphism of Alzheimer´s A-beta Amyloid Fibrils
- 2006
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In: Modern Magnetic Resonance. - Dordrecht : Encyclopedia of Global Archaeology/Springer Verlag. - 9781402038945 - 9781402039102 ; , s. 15-23
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Book chapter (other academic/artistic)abstract
- An overview of the strategy and experimental solid-state NMR, STEM, and AFM methods useful for obtaining structural constraints on Alzheimer’s amyloid-β peptide fibrils is presented. Polymorphism of amyloid fibrils and the relevance to neurotoxicity is discussed.
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3. |
- Antzutkin, Oleg
(author)
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Polymorphism of Alzheimer´s A-beta Amyloid Fibrils and Oligomers
- 2017
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In: Modern Magnetic Resonance. - Cham : Springer International Publishing. - 9783319282756 - 9783319282756 ; , s. 1-15
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Book chapter (other academic/artistic)abstract
- An overview of the strategy and experimental solid-state NMR, STEM, and AFM methods useful for obtaining structural constraints on Alzheimer’s amyloid-β peptide fibrils is presented. Polymorphism of amyloid fibrils and the relevance to neurotoxicity is discussed.
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4. |
- Antzutkin, Oleg
(author)
-
Polymorphism of Alzheimer’s Aβ Amyloid Fibrils and Oligomers
- 2018
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In: Modern Magnetic Resonance. - Cham : Springer. - 9783319283876 - 9783319283883 ; , s. 333-347
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Book chapter (peer-reviewed)abstract
- An overview of the strategy and experimental solid-state NMR, TEM, STEM, and AFM methods useful for obtaining atomic-level-resolution structural models of Alzheimer’s amyloid-β peptide fibrils and oligomers is presented. Polymorphism of amyloid fibrils and oligomers and the relevance to neurotoxicity is discussed.
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5. |
- Ivanov, Alexander V., et al.
(author)
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Natural abundance 15N and 13C CP/MAS NMR of dialkyldithiocarbamate compounds with Ni(II) and Zn(II)
- 2005
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In: New techniques in solid-state NMR. - Berlin : Encyclopedia of Global Archaeology/Springer Verlag. - 3540221689 ; , s. 271-337
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Book chapter (other academic/artistic)abstract
- Different symmetrically substituted and cyclic dialkydithiocarbamate (R=CH3, C2H5, C3H7, i-C3H7, C4H9, i-C4H9 and R2=(CH2)5, (CH2)6, (CH2)4O) compounds, such as tetraalkylthiuram disulfides, mononuclear nickel(II), binuclear zinc(II) and heteropolynuclear complexes and their adducts (both non-solvated and solvated forms) with planar and non-planar N-donor organic bases, have been prepared and studied by means of natural abundance 13C and 15N CP/MAS NMR spectroscopy. Useful correlations between molecular structures and 13C and 15N chemical shifts in these compounds have been established and assignments to carbon and nitrogen sites in resolved molecular structures have been suggested. A combination of the mesomeric effect of dithiocarbamate groups and the (+)inductive effect of alkyl substituents at the nitrogen atoms has been discussed in interpretations of 13C and 15N chemical shifts of the studied compounds. A high sensitivity of 15N chemical shift to the subtle structural differences of both dithiocarbamate groups and N-donor molecules has been revealed. Several remarkable cases of conformational isomerism have been recognized for both dithiocarbamate complexes and their adducts.
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