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A single carbocyclic nucleotide substitution in a 12mer DNA gives a Hoogsteen basepaired duplex (till 38 degrees C) and a hairpin (till 65 degrees C). A 600 MHZ NMR spectroscopic study.
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- Isaksson, J (author)
- Uppsala universitet
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- Maltseva, T (author)
- Uppsala universitet
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- Agback, P (author)
- Uppsala universitet
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- MARCEL DEKKER INC, 1999
- 1999
- English.
- In: NUCLEOSIDES & NUCLEOTIDES. - : MARCEL DEKKER INC. - 0732-8311. ; 18:6-7, s. 1593-1596
- Journal article (other academic/artistic)
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- The impact of intramolecular stereoelectronic effects has been examined by comparison of the solution structures of natural oligo-DNA duplex, 5'((1)C(2)G(3)C(4)G(5)A(6)A(7)T(8)T(9)C(10)G(11)C(12)G)(2)(3'), and its carbocyclic-nucleotide analogues in which
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- Isaksson, J
- Maltseva, T
- Agback, P
- Luo, X
- Kumar, A
- Zamaratski, E
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