-
1
-
-
71549124948
-
Novel targets for anti-retroviral therapy
-
Bhattacharya S, Osman H. 2009. Novel targets for anti-retroviral therapy. J. Infect. 59:377-386.
-
(2009)
J. Infect
, vol.59
, pp. 377-386
-
-
Bhattacharya, S.1
Osman, H.2
-
2
-
-
33747046408
-
Targeting the HIV-1RNAleader sequence with synthetic oligonucleotides and siRNA: Chemistry and cell delivery
-
Turner JJ, Fabani M, Arzumanov AA, Ivanova G, Gait MJ. 2006. Targeting the HIV-1RNAleader sequence with synthetic oligonucleotides and siRNA: chemistry and cell delivery. Biochim. Biophys. Acta 1758: 290-300.
-
(2006)
Biochim. Biophys. Acta
, vol.1758
, pp. 290-300
-
-
Turner, J.J.1
Fabani, M.2
Arzumanov, A.A.3
Ivanova, G.4
Gait, M.J.5
-
3
-
-
84855833706
-
PEGylated poly(ethylene imine) copolymer-delivered siRNA inhibits HIV replication in vitro
-
Weber ND, Merkel OM, Kissel T, Muñoz-Fernández MÁ. 2012. PEGylated poly(ethylene imine) copolymer-delivered siRNA inhibits HIV replication in vitro. J. Control Release 157:55- 63.
-
(2012)
J. Control Release
, vol.157
, pp. 55-63
-
-
Weber, N.D.1
Merkel, O.M.2
Kissel, T.3
Muñoz-Fernández, M.Á.4
-
4
-
-
79958716788
-
Dual functional RNA nanoparticles containing phi29 motor pRNA and anti-gp120 aptamer for cell-type specific delivery and HIV-1 inhibition
-
Zhou J, Shu Y, Guo P, Smith DD, Rossi JJ. 2011. Dual functional RNA nanoparticles containing phi29 motor pRNA and anti-gp120 aptamer for cell-type specific delivery and HIV-1 inhibition. Methods 54:284-294.
-
(2011)
Methods
, vol.54
, pp. 284-294
-
-
Zhou, J.1
Shu, Y.2
Guo, P.3
Smith, D.D.4
Rossi, J.J.5
-
5
-
-
33646916634
-
Silencing of HIV by hairpin-loop-structured DNA oligonucleotide
-
Moelling K, Abels S, Jendis J, Matskevich A, Heinrich J. 2006. Silencing of HIV by hairpin-loop-structured DNA oligonucleotide. FEBS Lett. 580: 3545-3550.
-
(2006)
FEBS Lett
, vol.580
, pp. 3545-3550
-
-
Moelling, K.1
Abels, S.2
Jendis, J.3
Matskevich, A.4
Heinrich, J.5
-
6
-
-
58749093598
-
Novel bimodular DNA aptamers with guanosine quadruplexes inhibit phylogenetically diverse HIV-1 reverse transcriptases
-
Michalowski D, Chitima-Matsiga R, Held DM, Burke DH. 2008. Novel bimodular DNA aptamers with guanosine quadruplexes inhibit phylogenetically diverse HIV-1 reverse transcriptases. Nucleic Acids Res. 36: 7124-7135.
-
(2008)
Nucleic Acids Res
, vol.36
, pp. 7124-7135
-
-
Michalowski, D.1
Chitima-Matsiga, R.2
Held, D.M.3
Burke, D.H.4
-
7
-
-
33646125429
-
Delivery of double-stranded DNA thioaptamers into HIV-1 infected cells for antiviral activity
-
Ferguson MR, Rojo DR, Somasunderam A, Thiviyannathan V, Ridley BD, Yang XB, Gorenstein DG. 2006. Delivery of double-stranded DNA thioaptamers into HIV-1 infected cells for antiviral activity. Biochem. Biophys. Res. Commun. 344:792-797.
-
(2006)
Biochem. Biophys. Res. Commun
, vol.344
, pp. 792-797
-
-
Ferguson, M.R.1
Rojo, D.R.2
Somasunderam, A.3
Thiviyannathan, V.4
Ridley, B.D.5
Yang, X.B.6
Gorenstein, D.G.7
-
8
-
-
13444283855
-
Diversity-oriented solidphase synthesis and biological evaluation of oligonucleotide hairpins as HIV-1 RT RNase H inhibitors
-
Hannoush RN, Min KL, Damha MJ. 2004. Diversity-oriented solidphase synthesis and biological evaluation of oligonucleotide hairpins as HIV-1 RT RNase H inhibitors. Nucleic Acids Res. 32:6164-6175.
-
(2004)
Nucleic Acids Res
, vol.32
, pp. 6164-6175
-
-
Hannoush, R.N.1
Min, K.L.2
Damha, M.J.3
-
9
-
-
0033291626
-
Structural study of an RNA aptamer for a Tat protein complexed with ligands
-
Katahira M, Kobayashi S, Matsugami A, Ouhashi K, Uesugi S, Yamamoto R, Taira K, Nishikawa S, Kumar P. 1999. Structural study of an RNA aptamer for a Tat protein complexed with ligands. Nucleic Acids Symp. Ser. 42:269-270.
-
(1999)
Nucleic Acids Symp. Ser
, vol.42
, pp. 269-270
-
-
Katahira, M.1
Kobayashi, S.2
Matsugami, A.3
Ouhashi, K.4
Uesugi, S.5
Yamamoto, R.6
Taira, K.7
Nishikawa, S.8
Kumar, P.9
-
10
-
-
0034647554
-
Mechanism of inhibition of HIV-1 integrase by G-tetrad-forming oligonucleotides in vitro
-
Jing N, Marchand C, Liu J, Mitra R, Hogan ME, Pommier Y. 2000. Mechanism of inhibition of HIV-1 integrase by G-tetrad-forming oligonucleotides in vitro. J. Biol. Chem. 275:21460-21467.
-
(2000)
J. Biol. Chem
, vol.275
, pp. 21460-21467
-
-
Jing, N.1
Marchand, C.2
Liu, J.3
Mitra, R.4
Hogan, M.E.5
Pommier, Y.6
-
12
-
-
79955465915
-
HIV-integrase aptamer folds into a parallel quadruplex: A thermodynamic study
-
Kelley S, Boroda S, Musier-Forsyth K, Kankia BI. 2011. HIV-integrase aptamer folds into a parallel quadruplex: a thermodynamic study. Biophys. Chem. 155:82-88.
-
(2011)
Biophys. Chem
, vol.155
, pp. 82-88
-
-
Kelley, S.1
Boroda, S.2
Musier-Forsyth, K.3
Kankia, B.I.4
-
13
-
-
80455129678
-
HIV-1 integrase inhibitor T30177 forms a stacked dimeric G-quadruplex structure containing bulges
-
Mukundan VT, Do NQ, Phan AT. 2011. HIV-1 integrase inhibitor T30177 forms a stacked dimeric G-quadruplex structure containing bulges. Nucleic Acids Res. 39:8984-8991.
-
(2011)
Nucleic Acids Res
, vol.39
, pp. 8984-8991
-
-
Mukundan, V.T.1
Do, N.Q.2
Phan, A.T.3
-
14
-
-
0027983025
-
Combinatorially selected guanosine-quartet structure is a potent inhibitor of human immunodeficiency virus envelope-mediated cell fusion
-
Wyatt JR, Vickers TA, Roberson JL, Buckheit RW, Jr, Klimkait T, DeBaets E, Davis PW, Rayner B, Imbach JL, Ecker DJ. 1994. Combinatorially selected guanosine-quartet structure is a potent inhibitor of human immunodeficiency virus envelope-mediated cell fusion. Proc. Natl. Acad. Sci. U. S. A. 91:1356-1360.
-
(1994)
Proc. Natl. Acad. Sci. U. S. A
, vol.91
, pp. 1356-1360
-
-
Wyatt, J.R.1
Vickers, T.A.2
Roberson, J.L.3
Buckheit Jr., R.W.4
Klimkait, T.5
Debaets, E.6
Davis, P.W.7
Rayner, B.8
Imbach, J.L.9
Ecker, D.J.10
-
15
-
-
66249129385
-
Selection, characterization and application of new RNA HIV gp 120 aptamers for facile delivery of Dicer substrate siRNAs into HIV infected cells
-
Zhou J, Swiderski P, Li H, Zhang J, Neff CP, Akkina R, Rossi JJ. 2009. Selection, characterization and application of new RNA HIV gp 120 aptamers for facile delivery of Dicer substrate siRNAs into HIV infected cells. Nucleic Acids Res. 37:3094-3109.
-
(2009)
Nucleic Acids Res
, vol.37
, pp. 3094-3109
-
-
Zhou, J.1
Swiderski, P.2
Li, H.3
Zhang, J.4
Neff, C.P.5
Akkina, R.6
Rossi, J.J.7
-
16
-
-
0028340635
-
Biologically active oligodeoxyribonucleotides-II: Structure activity relationships of anti-HIV-1 pentadecadeoxyribonucleotides bearing 5=-end-modifications
-
Hotoda H, Momota K, Furukawa H, Nakamura T, Kaneko M, Kimura S, Shimade K. 1994. Biologically active oligodeoxyribonucleotides-II: structure activity relationships of anti-HIV-1 pentadecadeoxyribonucleotides bearing 5=-end-modifications. Nucleosides Nucleotides Nucleic Acids 13:1375-1395.
-
(1994)
Nucleosides Nucleotides Nucleic Acids
, vol.13
, pp. 1375-1395
-
-
Hotoda, H.1
Momota, K.2
Furukawa, H.3
Nakamura, T.4
Kaneko, M.5
Kimura, S.6
Shimade, K.7
-
17
-
-
0031439074
-
Biologically active oligodeoxyribonucleotides IX. Synthesis and anti-HIV-1 activity of hexadeoxyribonucleotides, TGGGAG, bearing 3=and 5=-end-modification
-
Koizumi M, Koga R, Hotoda H, Momota K, Ohmine T, Furukawa H, Agatsuma T, Nishigaki T, Abe K, Kosaka T, Tsutsumi S, Sone J, Kaneko M, Kimura S, Shimada K. 1997. Biologically active oligodeoxyribonucleotides. IX. Synthesis and anti-HIV-1 activity of hexadeoxyribonucleotides, TGGGAG, bearing 3=and 5=-end-modification. Bioorg. Med. Chem. 5:2235-2243.
-
(1997)
Bioorg. Med. Chem
, vol.5
, pp. 2235-2243
-
-
Koizumi, M.1
Koga, R.2
Hotoda, H.3
Momota, K.4
Ohmine, T.5
Furukawa, H.6
Agatsuma, T.7
Nishigaki, T.8
Abe, K.9
Kosaka, T.10
Tsutsumi, S.11
Sone, J.12
Kaneko, M.13
Kimura, S.14
Shimada, K.15
-
18
-
-
15644384134
-
5=-End-substituted d(TGGGAG) possesses anti-human immunodeficiency virus type 1 activity by forming a G-quadruplex structure
-
Hotoda H, Koizumi M, Koga R, Kaneko M, Momota K, Ohmine T, Furukawa H, Agatsuma T, Nishigaki T, Sone J, Tsutsumi S, Kosaka T, Abe K, Kimura S, Shimada K 5=-End-substituted d(TGGGAG) possesses anti-human immunodeficiency virus type 1 activity by forming a G-quadruplex structure. J. Med. Chem. 41:3655-3663.
-
(1998)
J. Med. Chem
, vol.41
, pp. 3655-3663
-
-
Hotoda, H.1
Koizumi, M.2
Koga, R.3
Kaneko, M.4
Momota, K.5
Ohmine, T.6
Furukawa, H.7
Agatsuma, T.8
Nishigaki, T.9
Sone, J.10
Tsutsumi, S.11
Kosaka, T.12
Abe, K.13
Kimura, S.14
Shimada, K.15
-
19
-
-
34547227651
-
5=-Modified G-quadruplex forming oligonucleotides endowed with anti-HIV activity: Synthesis and biophysical properties
-
D'Onofrio J, Petraccone L, Erra E, Martino L, Fabio GD, Napoli LD, Giancola C, Montesarchio D. 2007. 5=-Modified G-quadruplex forming oligonucleotides endowed with anti-HIV activity: synthesis and biophysical properties. Bioconjug Chem. 18:1194-1204.
-
(2007)
Bioconjug Chem
, vol.18
, pp. 1194-1204
-
-
D'onofrio, J.1
Petraccone, L.2
Erra, E.3
Martino, L.4
Fabio, G.D.5
Napoli, L.D.6
Giancola, C.7
Montesarchio, D.8
-
20
-
-
79751512787
-
Discovery of novel anti-HIV active G-quadruplex-forming oligonucleotides
-
Di Fabio G, D'Onofrio J, Chiapparelli M, Hoorelbeke B, Montesarchio D, Balzarini J, De Napoli L. 2011. Discovery of novel anti-HIV active G-quadruplex-forming oligonucleotides. Chem. Commun. 47:2363- 2365.
-
(2011)
Chem. Commun
, vol.47
, pp. 2363-2365
-
-
Di Fabio, G.1
D'onofrio, J.2
Chiapparelli, M.3
Hoorelbeke, B.4
Montesarchio, D.5
Balzarini, J.6
De Napoli, L.7
-
21
-
-
41149164708
-
Synthesis, biophysical characterization, and anti-HIV activity of glyco-conjugated G-quadruplex-forming oligonucleotides
-
D'Onofrio J, Petraccone L, Martino L, Di Fabio G, Iadonisi A, Balzarini J, Giancola C, Montesarchio D. 2008. Synthesis, biophysical characterization, and anti-HIV activity of glyco-conjugated G-quadruplex-forming oligonucleotides. Bioconjug. Chem. 19:607-616.
-
(2008)
Bioconjug. Chem
, vol.19
, pp. 607-616
-
-
D'onofrio, J.1
Petraccone, L.2
Martino, L.3
Di Fabio, G.4
Iadonisi, A.5
Balzarini, J.6
Giancola, C.7
Montesarchio, D.8
-
22
-
-
0034597025
-
Biologically active oligodeoxyribonucleotides. Part. N2-methylation of 2=-deoxyguanosines enhances stability of parallel G-quadruplex and anti-HIV-1 activity
-
Koizumi M, Akahori K, Ohmine T, Tsutsumi S, Sone J, Kosaka T, Kaneko M, Kimura S, Shimada K 2000. Biologically active oligodeoxyribonucleotides. Part. N2-methylation of 2=-deoxyguanosines enhances stability of parallel G-quadruplex and anti-HIV-1 activity. Bioorg. Med. Chem. Lett. 10:2213-2216.
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 2213-2216
-
-
Koizumi, M.1
Akahori, K.2
Ohmine, T.3
Tsutsumi, S.4
Sone, J.5
Kosaka, T.6
Kaneko, M.7
Kimura, S.8
Shimada, K.9
-
23
-
-
79953700299
-
Enhanced anti-HIV-1 activity of G-quadruplexes comprising locked nucleic acids and intercalating nucleic acids
-
Pedersen EB, Nielsen JT, Nielsen C, Filichev VV. 2011. Enhanced anti-HIV-1 activity of G-quadruplexes comprising locked nucleic acids and intercalating nucleic acids. Nucleic Acid Res. 39:2470-2481.
-
(2011)
Nucleic Acid Res
, vol.39
, pp. 2470-2481
-
-
Pedersen, E.B.1
Nielsen, J.T.2
Nielsen, C.3
Filichev, V.V.4
-
24
-
-
13044297059
-
Biologically active oligodeoxyribonucleotides. Part The least phosphate-modification of quadruplex-forming hexadeoxyribonucleotide TGGGAG, bearing 3-and 5-end-modification, with anti-HIV-1 activity
-
Koizumi M, Koga R, Hotoda H, Ohmine T, Furukawa H, Agatsuma T, Nishigaki T, Abe K, Kosaka T, Tsutsumi S, Sone J, Kaneko M, Kimura S, Shimada K.1998. Biologically active oligodeoxyribonucleotides. Part The least phosphate-modification of quadruplex-forming hexadeoxyribonucleotide TGGGAG, bearing 3-and 5-end-modification, with anti-HIV-1 activity. Bioorg. Med. Chem. 6:2469-2475.
-
(1998)
Bioorg. Med. Chem
, vol.6
, pp. 2469-2475
-
-
Koizumi, M.1
Koga, R.2
Hotoda, H.3
Ohmine, T.4
Furukawa, H.5
Agatsuma, T.6
Nishigaki, T.7
Abe, K.8
Kosaka, T.9
Tsutsumi, S.10
Sone, J.11
Kaneko, M.12
Kimura, S.13
Shimada, K.14
-
25
-
-
0028607441
-
Mechanism of inhibition of HIV-1 infection in vitro by guanine-rich oligonucleotides modified at the 5= terminal by dimethoxytrityl residue
-
Furukawa H, Momota K, Agatsuma T, Yamamoto I, Kimura S, Shimada K. 1994. Mechanism of inhibition of HIV-1 infection in vitro by guanine-rich oligonucleotides modified at the 5= terminal by dimethoxytrityl residue. Nucleic Acids Res. 22:5621-5627.
-
(1994)
Nucleic Acids Res
, vol.22
, pp. 5621-5627
-
-
Furukawa, H.1
Momota, K.2
Agatsuma, T.3
Yamamoto, I.4
Kimura, S.5
Shimada, K.6
-
26
-
-
0030200369
-
Guaninerich oligonucleotide modified at the 5= terminal by dimethoxytrityl residue inhibits HIV-1 replication by specific interaction with the envelope glycoprotein
-
Agatsuma T, Yamamoto I, Furukawa H, Nishigaki T. 1996. Guaninerich oligonucleotide modified at the 5= terminal by dimethoxytrityl residue inhibits HIV-1 replication by specific interaction with the envelope glycoprotein. Antiviral Res. 31:137-148.
-
(1996)
Antiviral Res
, vol.31
, pp. 137-148
-
-
Agatsuma, T.1
Yamamoto, I.2
Furukawa, H.3
Nishigaki, T.4
-
27
-
-
80052567537
-
D(TGGGAG) with 5=-nucleobase-attached large hydrophobic groups as potent inhibitors for HIV-1 envelop proteins mediated cell-cell fusion
-
Chen W, Xu L, Cai L, Zheng B, Wang K, He J, Liu K. 2011. d(TGGGAG) with 5=-nucleobase-attached large hydrophobic groups as potent inhibitors for HIV-1 envelop proteins mediated cell-cell fusion. Bioorg. Med. Chem. Lett. 21:5762-5764.
-
(2011)
Bioorg. Med. Chem. Lett
, vol.21
, pp. 5762-5764
-
-
Chen, W.1
Xu, L.2
Cai, L.3
Zheng, B.4
Wang, K.5
He, J.6
Liu, K.7
-
28
-
-
77958005892
-
Hydroxylfunctionalized DNAs with different linkers and their complementary duplex stability
-
Zhang D, Li Y, Xu L, Cheng M, Zhou Y, He J, Liu K. 2010. Hydroxylfunctionalized DNAs with different linkers and their complementary duplex stability. Nucleosides Nucleotides Nucleic Acids 29:734-747.
-
(2010)
Nucleosides Nucleotides Nucleic Acids
, vol.29
, pp. 734-747
-
-
Zhang, D.1
Li, Y.2
Xu, L.3
Cheng, M.4
Zhou, Y.5
He, J.6
Liu, K.7
-
30
-
-
0036090585
-
Emergence of resistant human immunodeficiency virus type 1 in patients receiving fusion inhibitor (T-20) monotherapy
-
Wei X, Decker JM, Liu H, Zhang Z, Arani RB, Kilby JM, Saag MS, Wu X, Shaw GM, Kappes JC. 2002. Emergence of resistant human immunodeficiency virus type 1 in patients receiving fusion inhibitor (T-20) monotherapy. Antimicrob. Agents Chemother. 46:1896-1905.
-
(2002)
Antimicrob. Agents Chemother
, vol.46
, pp. 1896-1905
-
-
Wei, X.1
Decker, J.M.2
Liu, H.3
Zhang, Z.4
Arani, R.B.5
Kilby, J.M.6
Saag, M.S.7
Wu, X.8
Shaw, G.M.9
Kappes, J.C.10
-
31
-
-
55549105768
-
Conserved salt bridge between the N-and C-terminal heptad repeat regions of the human immunodeficiency virus type 1 gp41 core structure is critical for virus entry and inhibition
-
He Y, Liu S, Li J, Lu H, Qi Z, Liu Z, Debnath AK, Jiang S. 2008. Conserved salt bridge between the N-and C-terminal heptad repeat regions of the human immunodeficiency virus type 1 gp41 core structure is critical for virus entry and inhibition. J. Virol. 82:11129-11139.
-
(2008)
J. Virol
, vol.82
, pp. 11129-11139
-
-
He, Y.1
Liu, S.2
Li, J.3
Lu, H.4
Qi, Z.5
Liu, Z.6
Debnath, A.K.7
Jiang, S.8
-
32
-
-
34548481743
-
Conserved residue Lys574 in the cavity of HIV-1 Gp41 coiled-coil domain is critical for six-helix bundle stability and virus entry
-
He Y, Liu S, Jing W, Lu H, Cai D, Chin DJ, Debnath AK, Kirchhoff F, Jiang S. 2007. Conserved residue Lys574 in the cavity of HIV-1 Gp41 coiled-coil domain is critical for six-helix bundle stability and virus entry. J. Biol. Chem. 282:25631-25639.
-
(2007)
J. Biol. Chem
, vol.282
, pp. 25631-25639
-
-
He, Y.1
Liu, S.2
Jing, W.3
Lu, H.4
Cai, D.5
Chin, D.J.6
Debnath, A.K.7
Kirchhoff, F.8
Jiang, S.9
-
33
-
-
67649227059
-
Mutation L33M in the HR1 region of HIV-1 gp41 may play a role in T20 resistance
-
Chong H, Xu S, Zhang C, Nie J, Wang Y. 2009. Mutation L33M in the HR1 region of HIV-1 gp41 may play a role in T20 resistance. J. Clin. Virol. 45:255-258.
-
(2009)
J. Clin. Virol
, vol.45
, pp. 255-258
-
-
Chong, H.1
Xu, S.2
Zhang, C.3
Nie, J.4
Wang, Y.5
-
34
-
-
84863116316
-
Broad antiviral activity and crystal structure of HIV-1 fusion inhibitor Sifuvirtide
-
Yao X, Chong H, Zhang C, Waltersperger S, Wang M, Cui S, He Y. 2012. Broad antiviral activity and crystal structure of HIV-1 fusion inhibitor Sifuvirtide. J. Biol. Chem. 287:6788-6799.
-
(2012)
J. Biol. Chem
, vol.287
, pp. 6788-6799
-
-
Yao, X.1
Chong, H.2
Zhang, C.3
Waltersperger, S.4
Wang, M.5
Cui, S.6
He, Y.7
-
35
-
-
34447260888
-
A novel fluorescence intensity screening assay identifies new low-molecular-weight inhibitors of the gp41 coiled-coil domain of human immunodeficiency virus type Antimicrob
-
Cai L, Gochin M. 2007. A novel fluorescence intensity screening assay identifies new low-molecular-weight inhibitors of the gp41 coiled-coil domain of human immunodeficiency virus type Antimicrob. Agents Chemother. 51:2388-2395.
-
(2007)
Agents Chemother
, vol.51
, pp. 2388-2395
-
-
Cai, L.1
Gochin, M.2
-
36
-
-
34248155890
-
HIV gp41 C-terminal heptad repeat contains multifunctional domains relation to mechanisms of action of anti-HIV peptides
-
Liu S, Jing W, Cheung B, Lu H, Sun J, Yan X, Niu J, Farmar J, Wu S, Jiang S. 2007. HIV gp41 C-terminal heptad repeat contains multifunctional domains relation to mechanisms of action of anti-HIV peptides. J. Biol. Chem. 282:9612-9620.
-
(2007)
J. Biol. Chem
, vol.282
, pp. 9612-9620
-
-
Liu, S.1
Jing, W.2
Cheung, B.3
Lu, H.4
Sun, J.5
Yan, X.6
Niu, J.7
Farmar, J.8
Wu, S.9
Jiang, S.10
-
37
-
-
57649155175
-
Rationally designed anti-HIV peptides containing multifunctional domains as molecule probes for studying the mechanisms of action of the first and second generation HIV fusion inhibitors
-
Qi Z, Shi W, Xue N, Pan C, Jing W, Liu K, Jiang S. 2008. Rationally designed anti-HIV peptides containing multifunctional domains as molecule probes for studying the mechanisms of action of the first and second generation HIV fusion inhibitors. J. Biol. Chem. 283:30376-30384.
-
(2008)
J. Biol. Chem
, vol.283
, pp. 30376-30384
-
-
Qi, Z.1
Shi, W.2
Xue, N.3
Pan, C.4
Jing, W.5
Liu, K.6
Jiang, S.7
-
38
-
-
84856389509
-
RNA-based therapeutics: Current progress and future prospects
-
Burnett JC, Rossi JJ. 2012. RNA-based therapeutics: current progress and future prospects. Chem. Biol. 19:60-71.
-
(2012)
Chem. Biol
, vol.19
, pp. 60-71
-
-
Burnett, J.C.1
Rossi, J.J.2
|