-
7
-
-
0034626769
-
-
R. A. DePinho Nature 2000 408 248 254
-
(2000)
Nature
, vol.408
, pp. 248-254
-
-
Depinho, R.A.1
-
16
-
-
84893303932
-
-
Compounds that bind and stabilize G-quadruplex structures can be potential anticancer agents
-
A. Henderson Y. Wu Y. C. Huang E. A. Chavez J. Platt F. B. Johnson R. M. Brosh Jr D. Sen P. M. Lansdrop Nucleic Acids Res. 2013 42 860 869
-
(2013)
Nucleic Acids Res.
, vol.42
, pp. 860-869
-
-
Henderson, A.1
Wu, Y.2
Huang, Y.C.3
Chavez, E.A.4
Platt, J.5
Johnson, F.B.6
Brosh Jr., R.M.7
Sen, D.8
Lansdrop, P.M.9
-
18
-
-
79954570122
-
-
See ref. 12 for recent examples
-
Y. Xu Chem. Soc. Rev. 2011 40 2719 2740
-
(2011)
Chem. Soc. Rev.
, vol.40
, pp. 2719-2740
-
-
Xu, Y.1
-
24
-
-
84887447149
-
-
K. Iida T. Nakamura W. Yoshida M. Tera K. Nakabayashi K. Hata K. Ikebukuro K. Nagasawa Angew. Chem., Int. Ed. 2013 52 12052 12055
-
(2013)
Angew. Chem., Int. Ed.
, vol.52
, pp. 12052-12055
-
-
Iida, K.1
Nakamura, T.2
Yoshida, W.3
Tera, M.4
Nakabayashi, K.5
Hata, K.6
Ikebukuro, K.7
Nagasawa, K.8
-
29
-
-
79751503987
-
-
M. Kimura R. C. Stone S. C. Hunt J. Skurnick X. Lu X. Cao C. B. Harley A. Aviv Nat. Protoc. 2010 5 1596 1607
-
(2010)
Nat. Protoc.
, vol.5
, pp. 1596-1607
-
-
Kimura, M.1
Stone, R.C.2
Hunt, S.C.3
Skurnick, J.4
Lu, X.5
Cao, X.6
Harley, C.B.7
Aviv, A.8
-
34
-
-
0029939848
-
-
G-quadruplex forming sequences, which are prevalent in human genome, play an important role in replication, transcriptional regulation and telomere maintenance.
-
P. M. Lansdorp N. P. Verwoerd F. M. van de Rijke V. Dragowska M.-T. Little R. W. Dirks A. K. Raap H. J. Tanke Hum. Mol. Genet. 1996 5 685 691
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 685-691
-
-
Lansdorp, P.M.1
Verwoerd, N.P.2
Van De Rijke, F.M.3
Dragowska, V.4
Little, M.-T.5
Dirks, R.W.6
Raap, A.K.7
Tanke, H.J.8
-
35
-
-
79953313413
-
-
Quarfloxin is the only G-quadruplex-binding ligand that reached the phase II clinical trials for the treatment of neuroendocrine and carcinoid tumors.
-
S. Balasubramanian L. H. Hurley S. Neidle Nat. Rev. Drug Discovery 2011 10 261 275
-
(2011)
Nat. Rev. Drug Discovery
, vol.10
, pp. 261-275
-
-
Balasubramanian, S.1
Hurley, L.H.2
Neidle, S.3
-
36
-
-
70350220557
-
-
D. Drygin A. Siddiqui-Jain S. O'Brien M. Schwaebe A. Lin J. Bliesath C. B. Ho C. Proffitt K. Trent J. P. Whitten J. K. C. Lim D. Von Hoff K. Anderes W. G. Rice Cancer Res. 2009 69 7653 7661
-
(2009)
Cancer Res.
, vol.69
, pp. 7653-7661
-
-
Drygin, D.1
Siddiqui-Jain, A.2
O'Brien, S.3
Schwaebe, M.4
Lin, A.5
Bliesath, J.6
Ho, C.B.7
Proffitt, C.8
Trent, K.9
Whitten, J.P.10
Lim, J.K.C.11
Von Hoff, D.12
Anderes, K.13
Rice, W.G.14
-
40
-
-
76149090494
-
-
S. He B. Song D. Li C. Zhu W. Qi Y. Wen L. Wang S. Song H. Fang C. Fan Adv. Funct. Mater. 2010 20 453 459
-
(2010)
Adv. Funct. Mater.
, vol.20
, pp. 453-459
-
-
He, S.1
Song, B.2
Li, D.3
Zhu, C.4
Qi, W.5
Wen, Y.6
Wang, L.7
Song, S.8
Fang, H.9
Fan, C.10
-
43
-
-
77949396616
-
-
W. Yang K. R. Ratinac S. P. Ringer P. Thordarson J. J. Gooding F. Braet Angew. Chem., Int. Ed 2010 49 2114 2138
-
(2010)
Angew. Chem., Int. Ed
, vol.49
, pp. 2114-2138
-
-
Yang, W.1
Ratinac, K.R.2
Ringer, S.P.3
Thordarson, P.4
Gooding, J.J.5
Braet, F.6
-
44
-
-
33746344730
-
-
S. Stankovich D. A. Dikin G. H. B. Dommett K. M. Kohlhaas E. J. Zimney E. A. Stach R. D. Piner S. T. Nguyen R. S. Ruoff Nature 2006 442 282 286
-
(2006)
Nature
, vol.442
, pp. 282-286
-
-
Stankovich, S.1
Dikin, D.A.2
Dommett, G.H.B.3
Kohlhaas, K.M.4
Zimney, E.J.5
Stach, E.A.6
Piner, R.D.7
Nguyen, S.T.8
Ruoff, R.S.9
-
76
-
-
84880957749
-
-
Examples
-
L. Cui Y. Song G. Ke Z. Guan H. Zhang Y. Lin Y. Huang Z. Zhu C. J. Yang Chem.-Eur. J. 2013 19 10442 10451
-
(2013)
Chem.-Eur. J.
, vol.19
, pp. 10442-10451
-
-
Cui, L.1
Song, Y.2
Ke, G.3
Guan, Z.4
Zhang, H.5
Lin, Y.6
Huang, Y.7
Zhu, Z.8
Yang, C.J.9
-
78
-
-
79960638579
-
-
H. Wang Q. Zhang X. Chu T. Chen J. Ge R. Yu Angew. Chem., Int. Ed. 2011 50 7065 7069
-
(2011)
Angew. Chem., Int. Ed.
, vol.50
, pp. 7065-7069
-
-
Wang, H.1
Zhang, Q.2
Chu, X.3
Chen, T.4
Ge, J.5
Yu, R.6
-
86
-
-
84880769157
-
-
S.-R. Ryoo J. Lee J. Yeo H.-K. Na Y.-K. Kim H. Jang H. H. Lee S. W. Han Y. Lee V. N. Kim D.-H. Min ACS Nano 2013 7 5882 5891
-
(2013)
ACS Nano
, vol.7
, pp. 5882-5891
-
-
Ryoo, S.-R.1
Lee, J.2
Yeo, J.3
Na, H.-K.4
Kim, Y.-K.5
Jang, H.6
Lee, H.H.7
Han, S.W.8
Lee, Y.9
Kim, V.N.10
Min, D.-H.11
-
89
-
-
84894653282
-
-
Analogous fluorescent DNA oligonucleotides may not be suitable with this GO platform as benzofuran-modified DNA oligonucleotides exhibit drastic quenching in fluorescence intensity upon hybridization with G-rich DNA sequences. See ref. 31b
-
R. K. Koninti A. Sengupta K. Gavvala N. Ballav P. Hazra Nanoscale 2014 6 2937 2944
-
(2014)
Nanoscale
, vol.6
, pp. 2937-2944
-
-
Koninti, R.K.1
Sengupta, A.2
Gavvala, K.3
Ballav, N.4
Hazra, P.5
-
96
-
-
84882685930
-
-
Higher-order G-quadruplex structures could be an important factor in recognition and function of telomeric DNA in vivo.
-
B. Liu Z. Sun X. Zhang J. Liu Anal. Chem. 2013 85 7987 7993
-
(2013)
Anal. Chem.
, vol.85
, pp. 7987-7993
-
-
Liu, B.1
Sun, Z.2
Zhang, X.3
Liu, J.4
|