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Reviews on non-enzymatic scission of DNA
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Reviews on non-enzymatic scission of DNA:
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3
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0032839614
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b) N. H. Williams, B. Takasaki, M. Wall, J. Chin, Acc. Chem. Res. 1999, 32, 485 - 493;
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Acc. Chem. Res
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Williams, N.H.1
Takasaki, B.2
Wall, M.3
Chin, J.4
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6
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0038506966
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e) J. Suh, Acc. Chem. Res. 2003, 36, 562-570;
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(2003)
Acc. Chem. Res
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, pp. 562-570
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Suh, J.1
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8
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20444439223
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g) F. Mancin, P. Scrimin, P. Tecilla, U. Tonellato, Chem. Commun. 2005, 2540-2548;
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(2005)
Chem. Commun
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Mancin, F.1
Scrimin, P.2
Tecilla, P.3
Tonellato, U.4
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11
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DNA scission by using the combination of enzymes and sequence- recognizing molecules
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DNA scission by using the combination of enzymes and sequence- recognizing molecules:
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12
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0025673895
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a) D. H. Pei, D. R. Corey, P. G. Schultz, Proc. Natl. Acad. Sci. USA 1990, 87, 9858-9862;
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Proc. Natl. Acad. Sci. USA
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Pei, D.H.1
Corey, D.R.2
Schultz, P.G.3
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16
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0001332952
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a) M. Komiyama, T. Shiiba, T. Kodama, N. Takeda, J. Sumaoka, M. Yashiro, Chem. Lett. 1994, 1025-1028;
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(1994)
Chem. Lett
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Komiyama, M.1
Shiiba, T.2
Kodama, T.3
Takeda, N.4
Sumaoka, J.5
Yashiro, M.6
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18
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0030776410
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c) K. Bracken, R. A. Moss, K. G. Ragunathan, J. Am. Chem. Soc. 1997, 119, 9323-9324;
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(1997)
J. Am. Chem. Soc
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, pp. 9323-9324
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Bracken, K.1
Moss, R.A.2
Ragunathan, K.G.3
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19
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75249104218
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M. Komiyama, N. Takeda, H. Shigekawa, Chem. Commun. 1999, 14431451
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d) M. Komiyama, N. Takeda, H. Shigekawa, Chem. Commun. 1999, 14431451
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21
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f) H. B. Shen, J. F. Xia, H. F. Yang, Y. M. Luo, Sci. China Ser. B: Chem. 2001, 44, 169-174;
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Sci. China Ser. B: Chem
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Shen, H.B.1
Xia, J.F.2
Yang, H.F.3
Luo, Y.M.4
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23
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0002421061
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a) M. Komiyama, T. Shiiba, Y. Takahashi, N. Takeda, K. Matsumura, T. Kodama, Supramol. Chem. 1994, 4, 31-34;
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(1994)
Supramol. Chem
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, pp. 31-34
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Komiyama, M.1
Shiiba, T.2
Takahashi, Y.3
Takeda, N.4
Matsumura, K.5
Kodama, T.6
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24
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b) H. B. Shen, W.J. Zhou, Y.T. Yang, F. Zhang, Sci. China Ser. B: Chem. 2004, 47, 7579;
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(2004)
Sci. China Ser. B: Chem
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Shen, H.B.1
Zhou, W.J.2
Yang, Y.T.3
Zhang, F.4
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25
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33745021346
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c) H. B. Shen, F. Wang, Y.T. Yang, Chin. Chem. Lett. 2005, 16, 1663-1666.
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Chin. Chem. Lett
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Shen, H.B.1
Wang, F.2
Yang, Y.T.3
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26
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4143153938
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6 and EDTA, and used for selective scission of single-stranded DNA at gap-sites. The scission was greatly promoted by attaching monophosphate groups to the ODNs and placing them near the gap site; W. Chen, Y. Kitamura, J. M. Zhou, J. Sumaoka, M. Komiyama, J. Am. Chem. Soc. 2004, 126, 1028510291.
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6 and EDTA, and used for selective scission of single-stranded DNA at gap-sites. The scission was greatly promoted by attaching monophosphate groups to the ODNs and placing them near the gap site; W. Chen, Y. Kitamura, J. M. Zhou, J. Sumaoka, M. Komiyama, J. Am. Chem. Soc. 2004, 126, 1028510291.
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27
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42049106385
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IV solutions in reference were also used for site-selective scission of double-stranded DNA in the presence of two peptide nucleic acid strands: M. Komiyama, Y. Aiba, Y. Yamamoto, J. Sumao- ka, Nat. Protoc. 2008, 3, 655 -662.
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IV solutions in reference were also used for site-selective scission of double-stranded DNA in the presence of two peptide nucleic acid strands: M. Komiyama, Y. Aiba, Y. Yamamoto, J. Sumao- ka, Nat. Protoc. 2008, 3, 655 -662.
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29
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b) J. X. Meng, H. J. Wu, D. X. Feng, Spectrochim. Acta Part A 2000, 56, 1925-1928.
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(2000)
Spectrochim. Acta Part A
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Meng, J.X.1
Wu, H.J.2
Feng, D.X.3
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30
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52149096527
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T. Lönnberg, Y. Suzuki, M. Komiyama, Org. Biomol. Chem. 2008, 6, 3580-3587.
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(2008)
Org. Biomol. Chem
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Lönnberg, T.1
Suzuki, Y.2
Komiyama, M.3
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31
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IV species at neutral pH:
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IV species at neutral pH:
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32
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a) S. A. Hayes, P. Yu, T. J. O'Keefe, M. J. O'Keefe, J. O. Stoffer, J. Electrochem. Soc. 2002, 149, C623-C630;
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J. Electrochem. Soc
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Hayes, S.A.1
Yu, P.2
O'Keefe, T.J.3
O'Keefe, M.J.4
Stoffer, J.O.5
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b) P. Yu, S. A. Hayes, T. J. O'Keefe, M. J. O'Keefe, J. O. Stoffer, J. Electrochem. Soc. 2006, 153, C74-C79.
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J. Electrochem. Soc
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Yu, P.1
Hayes, S.A.2
O'Keefe, T.J.3
O'Keefe, M.J.4
Stoffer, J.O.5
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34
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75249083052
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When one-base gap system was formed by using two EDTP- attached oligonucleotides and treated with CeIV/EDTA, only one phosphodiester linkage at the gap site was selectively hydrolyzed see Figure S1 in the Supporting Information, Apparently, the strong CeIV binding by EDTP is very effective to hydrolyze smaller gaps
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IV binding by EDTP is very effective to hydrolyze smaller gaps.
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35
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Attempts to determine the composition of the catalytically active species of the present DNA cutters through the analysis of the rate, CeNO 3] dependence, have so far been unsuccessful
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3] dependence, have so far been unsuccessful.
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Consistent with this result, no oxidation product was observed when 2'-deoxyadenosine, 2′-deoxcytidine, or thymidine was used instead
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Consistent with this result, no oxidation product was observed when 2'-deoxyadenosine, 2′-deoxcytidine, or thymidine was used instead.
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