-
1
-
-
0343065617
-
LNA (locked nucleic acids): Synthesis and high-affinity nucleic acid recognition
-
Singh SK, Nielsen P, Koshkin AA, Wengel J. LNA (locked nucleic acids): synthesis and high-affinity nucleic acid recognition. Chem Commun (Camb) 1998; 4:455-6; http://dx.doi.org/10.1039/a708608c
-
(1998)
Chem Commun (Camb)
, vol.4
, pp. 455-456
-
-
Singh, S.K.1
Nielsen, P.2
Koshkin, A.A.3
Wengel, J.4
-
2
-
-
0032473890
-
LNA (locked nucleic acids): Synthesis of the adenine, cytosine, guanine, 5-methylcytosine, thymine and uracil bicyclonucleoside monomers, oligomerization, and unprecedented nucleic acid recognition
-
Koshkin AA, Singh SK, Nielsen P, Rajwanshi VK, Kumar R, Meldgaard M, et al. LNA (locked nucleic acids): synthesis of the adenine, cytosine, guanine, 5-methylcytosine, thymine and uracil bicyclonucleoside monomers, oligomerization, and unprecedented nucleic acid recognition. Tetrahedron 1998; 54:3607-30; http://dx.doi.org/10.1016/S0040-4020(98)00094-5
-
(1998)
Tetrahedron
, vol.54
, pp. 3607-3630
-
-
Koshkin, A.A.1
Singh, S.K.2
Nielsen, P.3
Rajwanshi, V.K.4
Kumar, R.5
Meldgaard, M.6
-
3
-
-
0032560835
-
Stability and structural features of the duplexes containing nucleoside analogs with a fixed N-type conformation, 2′-O,4′-C-methyleneribonucleosides
-
Obika S, Nanbu D, Hari Y, Andoh J, Morio K, Doi T, et al. Stability and structural features of the duplexes containing nucleoside analogs with a fixed N-type conformation, 2′-O,4′-C-methyleneribonucleosides. Tetrahedron Lett 1998; 39:5401-4; http://dx.doi.org/10.1016/S0040-4039(98)01084-3
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 5401-5404
-
-
Obika, S.1
Nanbu, D.2
Hari, Y.3
Andoh, J.4
Morio, K.5
Doi, T.6
-
4
-
-
0038212048
-
LNA stereoisomers: Xylo-LNA (β-D-xylo configured locked nucleic acid) and a-L-LNA (a-L-ribo configured locked nucleic acid)
-
Rajwanshi VK, Håkansson AE, Dahl BM, Wengel J. LNA stereoisomers: xylo-LNA (β-D-xylo configured locked nucleic acid) and α-L-LNA (α-L-ribo configured locked nucleic acid). Chem Commun (Camb) 1999; 15:1395-6; http://dx.doi.org/10.1039/a903189h
-
(1999)
Chem Commun (Camb)
, vol.15
, pp. 1395-1396
-
-
Rajwanshi, V.K.1
Håkansson, A.E.2
Dahl, B.M.3
Wengel, J.4
-
5
-
-
0038550867
-
High-affinity nucleic acid recognition using 'LNA' (locked nucleic acid, β-D-ribo configured LNA), 'xylo-LNA' (β-D-xylo configured LNA) or 'α-L-LNA' (α-L-ribo configured LNA)
-
Rajwanshi VK, Håkansson AE, Babu R, Wengel J. High-affinity nucleic acid recognition using 'LNA' (locked nucleic acid, β-D-ribo configured LNA), 'xylo-LNA' (β-D-xylo configured LNA) or 'α-L-LNA' (α-L-ribo configured LNA). Chem Commun (Camb) 1999; 20:2073-4; http://dx.doi.org/10.1039/a906713b
-
(1999)
Chem Commun (Camb)
, vol.20
, pp. 2073-2074
-
-
Rajwanshi, V.K.1
Håkansson, A.E.2
Babu, R.3
Wengel, J.4
-
6
-
-
0034595242
-
The eight stereoisomers of LNA (locked nucleic acid): A remarkable family of strong RNA binding molecules
-
39:9,1656::AID-ANIE1656.3.0. CO;2-Q, PMID:10820467
-
Rajwanshi VK, Håkansson AE, Sørensen MD, Pitsch S, Singh SK, Kumar R, et al. The eight stereoisomers of LNA (locked nucleic acid): a remarkable family of strong RNA binding molecules. Angew Chem Int Ed Engl 2000; 39:1656-9; PMID:10820467; http://dx.doi.org/10.1002/(SICI)1521-3773(20000502) 39:9,1656::AID-ANIE1656.3.0.CO;2-Q
-
(2000)
Angew Chem Int Ed Engl
, vol.39
, pp. 1656-1659
-
-
Rajwanshi, V.K.1
Håkansson, A.E.2
Sørensen, M.D.3
Pitsch, S.4
Singh, S.K.5
Kumar, R.6
-
7
-
-
0037892646
-
Convenient syntheses of 7-hydroxy-1-(hydroxymethyl)-3-(thymin-1-yl)-2,5-dioxabicyclo
-
PMID:10993341
-
Håkansson AE, Koshkin AA, Sørensen MD, Wengel J. Convenient syntheses of 7-hydroxy-1-(hydroxymethyl)-3-(thymin-1-yl)-2,5-dioxabicyclo. J Org Chem 2000; 65:5161-6; PMID:10993341; http://dx.doi.org/10. 1021/jo000232g
-
(2000)
J Org Chem
, vol.65
, pp. 5161-5166
-
-
Håkansson, A.E.1
Koshkin, A.A.2
Sørensen, M.D.3
Wengel, J.4
-
8
-
-
0035832098
-
The adenine derivative of α-L-LNA (α-L-ribo configured locked nucleic acid): Synthesis and high-affinity hybridization towards DNA, RNA, LNA and α-L-LNA complementary sequences
-
PMID:11294395
-
Håkansson AE, Wengel J. The adenine derivative of α-L-LNA (α-L-ribo configured locked nucleic acid): synthesis and high-affinity hybridization towards DNA, RNA, LNA and α-L-LNA complementary sequences. Bioorg Med Chem Lett 2001; 11:935-8; PMID:11294395; http://dx.doi.org/10.1016/S0960-894X(01)00110-X
-
(2001)
Bioorg Med Chem Lett
, vol.11
, pp. 935-938
-
-
Håkansson, A.E.1
Wengel, J.2
-
9
-
-
0038230095
-
α-L-ribo-configured locked nucleic acid (α-L-LNA): Synthesis and properties
-
PMID: 11878970
-
Sørensen MD, Kvaernø L, Bryld T, Håkansson AE, Verbeure B, Gaubert G, et al. α-L-ribo-configured locked nucleic acid (α-L-LNA): synthesis and properties. J Am Chem Soc 2002; 124:2164-76; PMID: 11878970; http://dx.doi.org/10.1021/ja0168763
-
(2002)
J Am Chem Soc
, vol.124
, pp. 2164-2176
-
-
Sørensen, M.D.1
Kvaernø, L.2
Bryld, T.3
Håkansson, A.E.4
Verbeure, B.5
Gaubert, G.6
-
10
-
-
0141708061
-
Synthesis of a base-protected α-L-LNA guanine nucleoside
-
PMID:14565368
-
Gaubert G, Wengel J. Synthesis of a base-protected α-L-LNA guanine nucleoside. Nucleosides Nucleotides Nucleic Acids 2003; 22:1155-7; PMID:14565368; http://dx.doi.org/10.1081/NCN-120022824
-
(2003)
Nucleosides Nucleotides Nucleic Acids
, vol.22
, pp. 1155-1157
-
-
Gaubert, G.1
Wengel, J.2
-
11
-
-
0037310844
-
LNA: A versatile tool for therapeutics and genomics
-
PMID:12573856
-
Petersen M, Wengel J. LNA: a versatile tool for therapeutics and genomics. Trends Biotechnol 2003; 21:74-81; PMID:12573856; http://dx.doi.org/10. 1016/S0167-7799(02)00038-0
-
(2003)
Trends Biotechnol
, vol.21
, pp. 74-81
-
-
Petersen, M.1
Wengel, J.2
-
12
-
-
6344277190
-
LNA (locked nucleic acid): Highaffinity targeting of complementary RNA and DNA
-
PMID:15491130
-
Vester B, Wengel J. LNA (locked nucleic acid): highaffinity targeting of complementary RNA and DNA. Biochemistry 2004; 43:13233-41; PMID:15491130; http://dx.doi.org/10.1021/bi0485732
-
(2004)
Biochemistry
, vol.43
, pp. 13233-13241
-
-
Vester, B.1
Wengel, J.2
-
13
-
-
3342961686
-
Locked nucleic acid: A potent nucleic acid analog in therapeutics and biotechnology
-
PMID:15294076
-
Jepsen JS, Sørensen MD, Wengel J. Locked nucleic acid: a potent nucleic acid analog in therapeutics and biotechnology. Oligonucleotides 2004; 14:130-46; PMID:15294076; http://dx.doi.org/10.1089/1545457041526317
-
(2004)
Oligonucleotides
, vol.14
, pp. 130-146
-
-
Jepsen, J.S.1
Sørensen, M.D.2
Wengel, J.3
-
14
-
-
36849035783
-
Perspectives on chemistry and therapeutic applications of Locked Nucleic Acid (LNA)
-
PMID: 17944519
-
Kaur H, Babu BR, Maiti S. Perspectives on chemistry and therapeutic applications of Locked Nucleic Acid (LNA). Chem Rev 2007; 107:4672-97; PMID: 17944519; http://dx.doi.org/10.1021/cr050266u
-
(2007)
Chem Rev
, vol.107
, pp. 4672-4697
-
-
Kaur, H.1
Babu, B.R.2
Maiti, S.3
-
15
-
-
36849021637
-
In vitro incorporation of LNA nucleotides
-
PMID:18058567
-
Veedu RN, Vester B, Wengel J. In vitro incorporation of LNA nucleotides. Nucleosides Nucleotides Nucleic Acids 2007; 26:1207-10; PMID:18058567; http://dx. doi.org/10.1080/15257770701527844
-
(2007)
Nucleosides Nucleotides Nucleic Acids
, vol.26
, pp. 1207-1210
-
-
Veedu, R.N.1
Vester, B.2
Wengel, J.3
-
16
-
-
34447623217
-
Enzymatic incorporation of LNA nucleotides into DNA strands
-
PMID:17315250
-
Veedu RN, Vester B, Wengel J. Enzymatic incorporation of LNA nucleotides into DNA strands. Chembiochem 2007; 8:490-2; PMID:17315250; http://dx.doi.org/10.1002/cbic.200600501
-
(2007)
Chembiochem
, vol.8
, pp. 490-492
-
-
Veedu, R.N.1
Vester, B.2
Wengel, J.3
-
17
-
-
46049121018
-
Polymerase chain reaction and transcription using locked nucleic acid nucleotide triphosphates
-
PMID:18533656
-
Veedu RN, Vester B, Wengel J. Polymerase chain reaction and transcription using locked nucleic acid nucleotide triphosphates. J Am Chem Soc 2008; 130: 8124-5; PMID:18533656; http://dx.doi.org/10.1021/ja801389n
-
(2008)
J Am Chem Soc
, vol.130
, pp. 8124-8125
-
-
Veedu, R.N.1
Vester, B.2
Wengel, J.3
-
18
-
-
67649329663
-
Efficient enzymatic synthesis of LNA-modified DNA duplexes using KOD DNA polymerase
-
PMID:19300826
-
Veedu RN, Vester B, Wengel J. Efficient enzymatic synthesis of LNA-modified DNA duplexes using KOD DNA polymerase. Org Biomol Chem 2009; 7:1404-9; PMID:19300826; http://dx.doi.org/10.1039/b819946a
-
(2009)
Org Biomol Chem
, vol.7
, pp. 1404-1409
-
-
Veedu, R.N.1
Vester, B.2
Wengel, J.3
-
19
-
-
48349115007
-
Systematic analysis of enzymatic DNA polymerization using oligo-DNA templates and triphosphate analogs involving 2′,4′-bridged nucleosides
-
PMID: 18583360
-
Kuwahara M, Obika S, Nagashima J-I, Ohta Y, Suto Y, Ozaki H, et al. Systematic analysis of enzymatic DNA polymerization using oligo-DNA templates and triphosphate analogs involving 2′,4′-bridged nucleosides. Nucleic Acids Res 2008; 36:4257-65; PMID: 18583360; http://dx.doi.org/10.1093/nar/gkn404
-
(2008)
Nucleic Acids Res
, vol.36
, pp. 4257-4265
-
-
Kuwahara, M.1
Obika, S.2
Nagashima, J-I.3
Ohta, Y.4
Suto, Y.5
Ozaki, H.6
-
20
-
-
70349342914
-
Locked nucleic acid nucleoside triphosphates and polymerases: On the way towards evolution of LNA aptamers
-
PMID:19603111
-
Veedu RN, Wengel J. Locked nucleic acid nucleoside triphosphates and polymerases: on the way towards evolution of LNA aptamers. Mol Biosyst 2009; 5:787-92; PMID:19603111; http://dx.doi.org/10.1039/b905513b
-
(2009)
Mol Biosyst
, vol.5
, pp. 787-792
-
-
Veedu, R.N.1
Wengel, J.2
-
21
-
-
77952573711
-
Polymerase directed incorporation studies of LNA-G nucleoside 5′-triphosphate and primer extension involving all four LNA nucleotides
-
Veedu RN, Vester B, Wengel J. Polymerase directed incorporation studies of LNA-G nucleoside 5′-triphosphate and primer extension involving all four LNA nucleotides. New J Chem 2010; 34:877-9; http://dx. doi.org/10.1039/b9nj00628a
-
(2010)
New J Chem
, vol.34
, pp. 877-879
-
-
Veedu, R.N.1
Vester, B.2
Wengel, J.3
-
22
-
-
0141819348
-
Nuclease stability of LNA oligonucleotides and LNA-DNA chimeras
-
PMID:14565339
-
Frieden M, Hansen HF, Koch T. Nuclease stability of LNA oligonucleotides and LNA-DNA chimeras. Nucleosides Nucleotides Nucleic Acids 2003; 22: 1041-3; PMID:14565339; http://dx.doi.org/10.1081/NCN-120022731
-
(2003)
Nucleosides Nucleotides Nucleic Acids
, vol.22
, pp. 1041-1043
-
-
Frieden, M.1
Hansen, H.F.2
Koch, T.3
-
23
-
-
0344011088
-
Expanding the design horizon of antisense oligonucleotides with a-L-LNA
-
PMID:14576324
-
FriedenM, Christensen SM, Mikkelsen ND, Rosenbohm C, Thrue CA, Westergaard M, et al. Expanding the design horizon of antisense oligonucleotides with a-L-LNA. Nucleic Acids Res 2003; 31:6365-72; PMID:14576324; http://dx.doi.org/10.1093/nar/gkg820
-
(2003)
Nucleic Acids Res
, vol.31
, pp. 6365-6372
-
-
Frieden, M.1
Christensen, S.M.2
Mikkelsen, N.D.3
Rosenbohm, C.4
Thrue, C.A.5
Westergaard, M.6
-
24
-
-
0037007910
-
a-L-LNA (a-L-ribo configured locked nucleic acid) recognition of DNA: An NMR spectroscopic study
-
PMID:12489231
-
Nielsen KME, Petersen M, Håkansson AE, Wengel J, Jacobsen JP. a-L-LNA (a-L-ribo configured locked nucleic acid) recognition of DNA: an NMR spectroscopic study. Chemistry 2002; 8:3001-9; PMID:12489231; http://dx.doi.org/10.1002/1521-3765(20020703)8:13,3001::AID-CHEM3001.3.0. CO;2-1
-
(2002)
Chemistry
, vol.8
, pp. 3001-3009
-
-
Nielsen, K.M.E.1
Petersen, M.2
Håkansson, A.E.3
Wengel, J.4
Jacobsen, J.P.5
-
25
-
-
0345305429
-
NMR structure of an α-L-LNA:RNA hybrid: Structural implications for RNase H recognition
-
PMID:14530434
-
Nielsen JT, Stein PC, Petersen M. NMR structure of an α-L-LNA:RNA hybrid: structural implications for RNase H recognition. Nucleic Acids Res 2003; 31: 5858-67; PMID:14530434; http://dx.doi.org/10.1093/nar/gkg800
-
(2003)
Nucleic Acids Res
, vol.31
, pp. 5858-5867
-
-
Nielsen, J.T.1
Stein, P.C.2
Petersen, M.3
-
26
-
-
22444448397
-
Investigation of the DNA-dependent cyclohexenyl nucleic acid polymerization and the cyclohexenyl nucleic acid-dependent DNA polymerization
-
PMID:16027107
-
Kempeneers V, Renders M, Froeyen M, Herdewijn P. Investigation of the DNA-dependent cyclohexenyl nucleic acid polymerization and the cyclohexenyl nucleic acid-dependent DNA polymerization. Nucleic Acids Res 2005; 33:3828-36; PMID:16027107; http://dx.doi.org/10.1093/nar/gki695
-
(2005)
Nucleic Acids Res
, vol.33
, pp. 3828-3836
-
-
Kempeneers, V.1
Renders, M.2
Froeyen, M.3
Herdewijn, P.4
-
27
-
-
40149109548
-
A pre-RNA candidate revisited: Both enantiomers of flexible nucleoside triphosphates are DNA polymerase substrates
-
PMID:18095688
-
Heuberger BD, Switzer C. A pre-RNA candidate revisited: both enantiomers of flexible nucleoside triphosphates are DNA polymerase substrates. J Am Chem Soc 2008; 130:412-3; PMID:18095688; http://dx.doi.org/10.1021/ja0770680
-
(2008)
J Am Chem Soc
, vol.130
, pp. 412-413
-
-
Heuberger, B.D.1
Switzer, C.2
-
28
-
-
66249142689
-
Polymerase-catalysed incorporation of glucose nucleotides into a DNA duplex
-
PMID:19308979
-
Renders M, Abramov M, Froeyen M, Herdewijn P. Polymerase-catalysed incorporation of glucose nucleotides into a DNA duplex. Chemistry 2009; 15:5463-70; PMID:19308979; http://dx.doi.org/10.1002/chem.200801951
-
(2009)
Chemistry
, vol.15
, pp. 5463-5470
-
-
Renders, M.1
Abramov, M.2
Froeyen, M.3
Herdewijn, P.4
-
29
-
-
0033564079
-
Determinants of nucleotide sugar recognition in an archaeon DNA polymerase
-
PMID:10352184
-
Gardner AF, Jack WE. Determinants of nucleotide sugar recognition in an archaeon DNA polymerase. Nucleic Acids Res 1999; 27:2545-53; PMID:10352184; http://dx.doi.org/10.1093/nar/27.12.2545
-
(1999)
Nucleic Acids Res
, vol.27
, pp. 2545-2553
-
-
Gardner, A.F.1
Jack, W.E.2
-
30
-
-
0037079661
-
Acyclic and dideoxy terminator preferences denote divergent sugar recognition by archaeon and Taq DNA polymerases
-
PMID:11788725
-
Gardner AF, Jack WE. Acyclic and dideoxy terminator preferences denote divergent sugar recognition by archaeon and Taq DNA polymerases. Nucleic Acids Res 2002; 30:605-13; PMID:11788725; http://dx.doi. org/10.1093/nar/30.2.605
-
(2002)
Nucleic Acids Res
, vol.30
, pp. 605-613
-
-
Gardner, A.F.1
Jack, W.E.2
-
31
-
-
0043210727
-
TNA synthesis by DNA polymerases
-
PMID:12889939
-
Chaput JC, Szostak JW. TNA synthesis by DNA polymerases. J Am Chem Soc 2003; 125:9274-5; PMID:12889939; http://dx.doi.org/10.1021/ja035917n
-
(2003)
J Am Chem Soc
, vol.125
, pp. 9274-9275
-
-
Chaput, J.C.1
Szostak, J.W.2
-
32
-
-
19744365730
-
Kinetic analysis of an efficient DNAdependent TNA polymerase
-
PMID:15898792
-
Horhota A, Zou K, Ichida JK, Yu B, McLaughlin LW, Szostak JW, et al. Kinetic analysis of an efficient DNAdependent TNA polymerase. J Am Chem Soc 2005; 127:7427-34; PMID:15898792; http://dx.doi.org/10. 1021/ja0428255
-
(2005)
J Am Chem Soc
, vol.127
, pp. 7427-7434
-
-
Horhota, A.1
Zou, K.2
Ichida, J.K.3
Yu, B.4
McLaughlin, L.W.5
Szostak, J.W.6
-
33
-
-
0035419785
-
Reverse transcriptase incorporation of 1,5-anhydrohexitol nucleotides
-
PMID:11470872
-
Vastmans K, Froeyen M, Kerremans L, Pochet S, Herdewijn P. Reverse transcriptase incorporation of 1,5-anhydrohexitol nucleotides. Nucleic Acids Res 2001; 29:3154-63; PMID:11470872; http://dx.doi. org/10.1093/nar/29.15.3154
-
(2001)
Nucleic Acids Res
, vol.29
, pp. 3154-3163
-
-
Vastmans, K.1
Froeyen, M.2
Kerremans, L.3
Pochet, S.4
Herdewijn, P.5
-
35
-
-
0026491206
-
β-L-thymidine 5′-triphosphate analogs as DNA polymerase substrates
-
PMID:1281153
-
Van Draanen NA, Tucker SC, Boyd FL, Trotter BW, Reardon JE. β-L-thymidine 5′-triphosphate analogs as DNA polymerase substrates. J Biol Chem 1992; 267: 25019-24; PMID:1281153
-
(1992)
J Biol Chem
, vol.267
, pp. 25019-25024
-
-
van Draanen, N.A.1
Tucker, S.C.2
Boyd, F.L.3
Trotter, B.W.4
Reardon, J.E.5
-
36
-
-
0029088833
-
L-and D-enantiomers of 2′,3′-dideoxycytidine 5′-triphosphate analogs as substrates for human DNA polymerases. Implications for the mechanism of toxicity
-
PMID:7559445
-
Kukhanova M, Liu S-H, Mozzherin D, Lin T-S, Chu CK, Cheng Y-C. L-and D-enantiomers of 2′,3′-dideoxycytidine 5′-triphosphate analogs as substrates for human DNA polymerases. Implications for the mechanism of toxicity. J Biol Chem 1995; 270:23055-9; PMID:7559445
-
(1995)
J Biol Chem
, vol.270
, pp. 23055-23059
-
-
Kukhanova, M.1
Liu, S-H.2
Mozzherin, D.3
Lin, T-S.4
Chu, C.K.5
Cheng, Y-C.6
-
37
-
-
0028865886
-
The intracellular phosphorylation of (-)-2′-deoxy-3′-thiacytidine (3TC) and the incorporation of 3TC 5′-monophosphate into DNA by HIV-1 reverse transcriptase and human DNA polymerase c
-
PMID:7575660
-
Gray NM, Marr CLP, Penn CR, Cameron JM, Bethell RC. The intracellular phosphorylation of (-)-2′-deoxy-3′-thiacytidine (3TC) and the incorporation of 3TC 5′-monophosphate into DNA by HIV-1 reverse transcriptase and human DNA polymerase c. Biochem Pharmacol 1995; 50:1043-51; PMID:7575660; http://dx.doi.org/10.1016/0006-2952(95)96620-A
-
(1995)
Biochem Pharmacol
, vol.50
, pp. 1043-1051
-
-
Gray, N.M.1
Marr, C.L.P.2
Penn, C.R.3
Cameron, J.M.4
Bethell, R.C.5
-
38
-
-
0029094279
-
Stereospecificity of human DNA polymerases α, β, γ, δ and ε, HIV-reverse transcriptase, HSV-1 DNA polymerase, calf thymus terminal transferase and Escherichia coliDNA polymerase I in recognizing D-and L-thymidine 5′-triphosphate as substrate
-
PMID: 7544886
-
Focher F, Maga G, Bendiscioli A, Capobianco M, Colonna F, Garbesi A, et al. Stereospecificity of human DNA polymerases α, β, γ, δ and ε, HIV-reverse transcriptase, HSV-1 DNA polymerase, calf thymus terminal transferase and Escherichia coliDNA polymerase I in recognizing D-and L-thymidine 5′-triphosphate as substrate. Nucleic Acids Res 1995; 23:2840-7; PMID: 7544886; http://dx.doi.org/10.1093/nar/23.15.2840
-
(1995)
Nucleic Acids Res
, vol.23
, pp. 2840-2847
-
-
Focher, F.1
Maga, G.2
Bendiscioli, A.3
Capobianco, M.4
Colonna, F.5
Garbesi, A.6
-
39
-
-
0030988492
-
Stereoisomers of deoxynucleoside 5′-triphosphates as substrates for template-dependent and-independent DNA polymerases
-
PMID: 9083099
-
Semizarov DG, Arzumanov AA, Dyatkina NB, Meyer A, Vichier-Guerre S, Gosselin G, et al. Stereoisomers of deoxynucleoside 5′-triphosphates as substrates for template-dependent and-independent DNA polymerases. J Biol Chem 1997; 272:9556-60; PMID: 9083099; http://dx.doi.org/10.1074/jbc.272.14.9556
-
(1997)
J Biol Chem
, vol.272
, pp. 9556-9560
-
-
Semizarov, D.G.1
Arzumanov, A.A.2
Dyatkina, N.B.3
Meyer, A.4
Vichier-Guerre, S.5
Gosselin, G.6
-
40
-
-
0000497363
-
New modified nucleoside 5′-triphosphates: Synthesis, properties towards DNA polymerases, stability in blood serum and antiviral activity
-
Shipitsin AV, Victorova LS, Shirokova EA, Dyatkina NB, Goryunova LE, Beabealashvilli RS, et al. New modified nucleoside 5′-triphosphates: synthesis, properties towards DNA polymerases, stability in blood serum and antiviral activity. J Chem Soc Perkin 1999; 1:1039-50; http://dx.doi.org/10.1039/a900336c
-
(1999)
J Chem Soc Perkin
, vol.1
, pp. 1039-1050
-
-
Shipitsin, A.V.1
Victorova, L.S.2
Shirokova, E.A.3
Dyatkina, N.B.4
Goryunova, L.E.5
Beabealashvilli, R.S.6
-
41
-
-
5444224668
-
Reading, writing, and modulating genetic information with boranophosphate mimics of nucleotides, DNA, and RNA
-
PMID:14751819
-
Shaw BR, Dobrikov M, Wang X, Wan J, He K, Lin J-L, et al. Reading, writing, and modulating genetic information with boranophosphate mimics of nucleotides, DNA, and RNA. Ann N Y Acad Sci 2003; 1002:12-29; PMID:14751819; http://dx.doi.org/10. 1196/annals.1281.004
-
(2003)
Ann N Y Acad Sci
, vol.1002
, pp. 12-29
-
-
Shaw, B.R.1
Dobrikov, M.2
Wang, X.3
Wan, J.4
He, K.5
Lin, J-L.6
-
42
-
-
33947144816
-
Synthesis and recognition of novel isonucleoside triphosphates by DNA polymerases
-
PMID:17320403
-
Jiang C, Li B, Guan Z, Yang Z, Zhang L, Zhang L. Synthesis and recognition of novel isonucleoside triphosphates by DNA polymerases. Bioorg Med Chem 2007; 15:3019-25; PMID:17320403; http://dx.doi.org/10. 1016/j.bmc.2007.02.003
-
(2007)
Bioorg Med Chem
, vol.15
, pp. 3019-3025
-
-
Jiang, C.1
Li, B.2
Guan, Z.3
Yang, Z.4
Zhang, L.5
Zhang, L.6
-
43
-
-
51149123895
-
Probing DNA polymerase activity with stereoisomeric 2′-fluoro-β-D-arabinose (2′F-araNTPs) and 2′-fluoro-β-D-ribose (2′F-rNTPs) nucleoside 5′-triphosphates
-
Peng CG, Damha MJ. Probing DNA polymerase activity with stereoisomeric 2′-fluoro-β-D-arabinose (2′F-araNTPs) and 2′-fluoro-β-D-ribose (2′F-rNTPs) nucleoside 5′-triphosphates. Can J Chem 2008; 86: 881-91; http://dx.doi.org/10.1139/v08-089
-
(2008)
Can J Chem
, vol.86
, pp. 881-891
-
-
Peng, C.G.1
Damha, M.J.2
-
44
-
-
0019760168
-
A new route to nucleoside 5′-triphosphates
-
PMID:7347985
-
Ludwig J. A new route to nucleoside 5′-triphosphates. Acta Biochim Biophys Acad Sci Hung 1981; 16:131-3; PMID:7347985
-
(1981)
Acta Biochim Biophys Acad Sci Hung
, vol.16
, pp. 131-133
-
-
Ludwig, J.1
-
45
-
-
17344376224
-
The conformations of locked nucleic acids (LNA)
-
PMID:10679896
-
Petersen M, Nielsen CB, Nielsen KE, Jensen GA, Bondensgaard K, Singh SK, et al. The conformations of locked nucleic acids (LNA). J Mol Recognit 2000; 13:44-53; PMID:10679896; http://dx.doi.org/10.1002/(SICI) 1099-1352(200001/02)13:1,44::AID-JMR486.3.0. CO;2-6
-
(2000)
J Mol Recognit
, vol.13
, pp. 44-53
-
-
Petersen, M.1
Nielsen, C.B.2
Nielsen, K.E.3
Jensen, G.A.4
Bondensgaard, K.5
Singh, S.K.6
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