메뉴 건너뛰기




Volumn 43, Issue 6, 2015, Pages 2993-3011

Erratum: Identification of metabolically stable 5'-phosphate analogs that support single-stranded siRNA activity (Nucleic Acids Res (2015) 43:6 (2993–3011) (DOI:10.1093/nar/gkv162));Identification of metabolically stable 5′-phosphate analogs that support single-stranded siRNA activity

Author keywords

[No Author keywords available]

Indexed keywords

APOLIPOPROTEIN C3; ARGONAUTE 2 PROTEIN; LOW DENSITY LIPOPROTEIN CHOLESTEROL; MESSENGER RNA; PHOSPHATE; SINGLE STRANDED SMALL INTERFERING RNA; SMALL INTERFERING RNA; TRIACYLGLYCEROL; UNCLASSIFIED DRUG; ARGONAUTE PROTEIN; EIF2C2 PROTEIN, HUMAN; RECOMBINANT PROTEIN;

EID: 84942279838     PISSN: 03051048     EISSN: 13624962     Source Type: Journal    
DOI: 10.1093/nar/gkx381     Document Type: Erratum
Times cited : (66)

References (40)
  • 1
    • 0035863097 scopus 로고    scopus 로고
    • RNA interference is mediated by 21- and 22-nucleotide RNAs
    • Elbashir,S.M., Lendeckel,W. and Tuschl,T. (2001) RNA interference is mediated by 21- and 22-nucleotide RNAs. Genes Dev., 15, 188-200.
    • (2001) Genes Dev. , vol.15 , pp. 188-200
    • Elbashir, S.M.1    Lendeckel, W.2    Tuschl, T.3
  • 2
    • 0035942736 scopus 로고    scopus 로고
    • Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells
    • Elbashir,S.M., Harborth,J., Lendeckel,W., Yalcin,A., Weber,K. and Tuschl,T. (2001) Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells. Nature, 411, 494-498.
    • (2001) Nature , vol.411 , pp. 494-498
    • Elbashir, S.M.1    Harborth, J.2    Lendeckel, W.3    Yalcin, A.4    Weber, K.5    Tuschl, T.6
  • 7
    • 77949512140 scopus 로고    scopus 로고
    • RNA targeting therapeutics: Molecular mechanisms of antisense oligonucleotides as a therapeutic platform
    • Bennett,C.F. and Swayze,E.E. (2010) RNA targeting therapeutics: molecular mechanisms of antisense oligonucleotides as a therapeutic platform. Annu. Rev. Pharmacol. Toxicol., 50, 259-293.
    • (2010) Annu. Rev. Pharmacol. Toxicol. , vol.50 , pp. 259-293
    • Bennett, C.F.1    Swayze, E.E.2
  • 8
    • 59049105558 scopus 로고    scopus 로고
    • Human Dicer binds short single-strand and double-strand RNA with high affinity and interacts with different regions of the nucleic acids
    • Lima,W.F., Murray,H., Nichols,J.G., Wu,H., Sun,H., Prakash,T.P., Berdeja,A.R., Gaus,H.J. and Crooke,S.T. (2009) Human Dicer binds short single-strand and double-strand RNA with high affinity and interacts with different regions of the nucleic acids. J. Biol. Chem., 284, 2535-2548.
    • (2009) J. Biol. Chem. , vol.284 , pp. 2535-2548
    • Lima, W.F.1    Murray, H.2    Nichols, J.G.3    Wu, H.4    Sun, H.5    Prakash, T.P.6    Berdeja, A.R.7    Gaus, H.J.8    Crooke, S.T.9
  • 12
    • 84861451595 scopus 로고    scopus 로고
    • The crystal structure of human Argonaute2
    • Schirle,N.T. and MacRae,I.J. (2012) The crystal structure of human Argonaute2. Science, 336, 1037-1040.
    • (2012) Science , vol.336 , pp. 1037-1040
    • Schirle, N.T.1    MacRae, I.J.2
  • 14
    • 57749206034 scopus 로고    scopus 로고
    • Structure of an argonaute silencing complex with a seed-containing guide DNA and target RNA duplex
    • Wang,Y., Juranek,S., Li,H., Sheng,G., Tuschl,T. and Patel,D.J. (2008) Structure of an argonaute silencing complex with a seed-containing guide DNA and target RNA duplex. Nature, 456, 921-926.
    • (2008) Nature , vol.456 , pp. 921-926
    • Wang, Y.1    Juranek, S.2    Li, H.3    Sheng, G.4    Tuschl, T.5    Patel, D.J.6
  • 15
    • 70349961432 scopus 로고    scopus 로고
    • Nucleation, propagation and cleavage of target RNAs in Ago silencing complexes
    • Wang,Y., Juranek,S., Li,H., Sheng,G., Wardle,G.S., Tuschl,T. and Patel,D.J. (2009) Nucleation, propagation and cleavage of target RNAs in Ago silencing complexes. Nature, 461, 754-761.
    • (2009) Nature , vol.461 , pp. 754-761
    • Wang, Y.1    Juranek, S.2    Li, H.3    Sheng, G.4    Wardle, G.S.5    Tuschl, T.6    Patel, D.J.7
  • 16
    • 73349086270 scopus 로고    scopus 로고
    • Off-target and a portion of target-specific siRNA mediated mRNA degradation is Ago2 'Slicer' independent and can be mediated by Ago1
    • Vickers,T.A., Lima,W.F., Wu,H., Nichols,J.G., Linsley,P.S. and Crooke,S.T. (2009) Off-target and a portion of target-specific siRNA mediated mRNA degradation is Ago2 'Slicer' independent and can be mediated by Ago1. Nucleic Acids Res., 37, 6927-6941.
    • (2009) Nucleic Acids Res. , vol.37 , pp. 6927-6941
    • Vickers, T.A.1    Lima, W.F.2    Wu, H.3    Nichols, J.G.4    Linsley, P.S.5    Crooke, S.T.6
  • 18
    • 84878637167 scopus 로고    scopus 로고
    • Antisense oligonucleotide inhibition of apolipoprotein C-III reduces plasma triglycerides in rodents, nonhuman primates, and humans
    • Graham,M.J., Lee,R.G., Bell,T.A. III, Fu,W., Mullick,A.E., Alexander,V.J., Singleton,W., Viney,N., Geary,R., Su,J. et al. (2013) Antisense oligonucleotide inhibition of apolipoprotein C-III reduces plasma triglycerides in rodents, nonhuman primates, and humans. Circ. Res., 112, 1479-1490.
    • (2013) Circ. Res. , vol.112 , pp. 1479-1490
    • Graham, M.J.1    Lee, R.G.2    Bell, T.A.3    Fu, W.4    Mullick, A.E.5    Alexander, V.J.6    Singleton, W.7    Viney, N.8    Geary, R.9    Su, J.10
  • 20
  • 23
    • 0029005062 scopus 로고
    • Synthesis of 5′-deoxy-5′-difluoromethyl phosphonate nucleotide analogs
    • Matulic-Adamic,J., Haeberli,P. and Usman,N. (1995) Synthesis of 5″-deoxy-5′-difluoromethyl phosphonate nucleotide analogs. J. Org. Chem., 60, 2563-2569.
    • (1995) J. Org. Chem. , vol.60 , pp. 2563-2569
    • Matulic-Adamic, J.1    Haeberli, P.2    Usman, N.3
  • 24
    • 1542690351 scopus 로고
    • Phosphonates as analogues of natural phosphates
    • Engel,R. (1977) Phosphonates as analogues of natural phosphates. Chem. Rev., 77, 349-367.
    • (1977) Chem. Rev. , vol.77 , pp. 349-367
    • Engel, R.1
  • 25
    • 37049106807 scopus 로고
    • The dealkylation of phosphate and phosphonate esters by iodotrimethylsilane: A mild and selective procedure
    • Blackburn,G.M. and Ingleson,D. (1980) The dealkylation of phosphate and phosphonate esters by iodotrimethylsilane: a mild and selective procedure. J. Chem. Soc. , 1, 1150-1153.
    • (1980) J. Chem. Soc. , vol.1 , pp. 1150-1153
    • Blackburn, G.M.1    Ingleson, D.2
  • 26
    • 37049087186 scopus 로고
    • Synthesis of α- and γ-fluoroalkylphosphonates
    • Blackburn,G.M. and Kent,D.E. (1986) Synthesis of α- and γ-fluoroalkylphosphonates. J. Chem. Soc., 1, 913-917.
    • (1986) J. Chem. Soc. , vol.1 , pp. 913-917
    • Blackburn, G.M.1    Kent, D.E.2
  • 27
    • 0029975902 scopus 로고    scopus 로고
    • Stannyl radical-mediated cleavage of π-deficient heterocyclic sulfones. Synthesis of α-fluoro esters and the first homonucleoside α-fluoromethylene phosphonate1
    • Wnuk,S.F. and Robins,M.J. (1996) Stannyl radical-mediated cleavage of π-deficient heterocyclic sulfones. Synthesis of α-fluoro esters and the first homonucleoside α-fluoromethylene phosphonate1. J. Am. Chem. Soc., 118, 2519-2520.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 2519-2520
    • Wnuk, S.F.1    Robins, M.J.2
  • 31
    • 0003028599 scopus 로고
    • Phosphonic acid analogs of nucleoside phosphates. III. The synthesis of adenosine 5′-methylenediphosphonate, a phosphonic acid analog of adenosine 5′-diphosphate
    • Myers,T.C., Nakamura,K. and Danielzadeh,A.B. (1965) Phosphonic acid analogs of nucleoside phosphates. III. The synthesis of adenosine 5′-methylenediphosphonate, a phosphonic acid analog of adenosine 5′-diphosphate. J. Org. Chem., 30, 1517-1520.
    • (1965) J. Org. Chem. , vol.30 , pp. 1517-1520
    • Myers, T.C.1    Nakamura, K.2    Danielzadeh, A.B.3
  • 34
    • 77949794068 scopus 로고    scopus 로고
    • Structure-activity relationship of (N)-methanocarba phosphonate analogues of 5′-AMP as cardioprotective agents acting through a cardiac P2X receptor
    • Kumar,T.S., Zhou,S.-Y., Joshi,B.V., Balasubramanian,R., Yang,T., Liang,B.T. and Jacobson,K.A. (2010) Structure-activity relationship of (N)-methanocarba phosphonate analogues of 5′-AMP as cardioprotective agents acting through a cardiac P2X receptor. J. Med. Chem., 53, 2562-2576.
    • (2010) J. Med. Chem. , vol.53 , pp. 2562-2576
    • Kumar, T.S.1    Zhou, S.-Y.2    Joshi, B.V.3    Balasubramanian, R.4    Yang, T.5    Liang, B.T.6    Jacobson, K.A.7
  • 35
    • 0033811816 scopus 로고    scopus 로고
    • Synthesis of phosphonate derivatives of uridine, cytidine, and cytosine arabinoside
    • Jung,K.-Y., Hohl,R.J., Wiemer,A.J. and Wiemer,D.F. (2000) Synthesis of phosphonate derivatives of uridine, cytidine, and cytosine arabinoside. Bioorg. Med. Chem., 8, 2501-2509.
    • (2000) Bioorg. Med. Chem. , vol.8 , pp. 2501-2509
    • Jung, K.-Y.1    Hohl, R.J.2    Wiemer, A.J.3    Wiemer, D.F.4
  • 36
    • 67649381823 scopus 로고    scopus 로고
    • Developing an efficient route to the synthesis of nucleoside 1-alkynylphosphonates
    • Meurillon,M., Gallier,F., Peyrottes,S. and Périgaud,C. (2009) Developing an efficient route to the synthesis of nucleoside 1-alkynylphosphonates. Tetrahedron, 65, 6039-6046.
    • (2009) Tetrahedron , vol.65 , pp. 6039-6046
    • Meurillon, M.1    Gallier, F.2    Peyrottes, S.3    Périgaud, C.4
  • 37
    • 79957618143 scopus 로고    scopus 로고
    • 5′,6′-nucleoside phosphonate analogues architecture: Synthesis and comparative evaluation toward metabolic enzymes
    • Gallier,F., Alexandre,J.A.C., El Amri,C., Deville-Bonne,D., Peyrottes,S. and Périgaud,C. (2011) 5′,6′-nucleoside phosphonate analogues architecture: synthesis and comparative evaluation toward metabolic enzymes. ChemMedChem, 6, 1094-1106.
    • (2011) ChemMedChem , vol.6 , pp. 1094-1106
    • Gallier, F.1    Alexandre, J.A.C.2    El Amri, C.3    Deville-Bonne, D.4    Peyrottes, S.5    Périgaud, C.6
  • 38
    • 37049109325 scopus 로고
    • The synthesis and metal binding characteristics of novel, isopolar phosphonate analogs of nucleotidesIssue
    • Blackburn,G.M., Kent,D.E. and Kolkmann,F. (1984) The synthesis and metal binding characteristics of novel, isopolar phosphonate analogs of nucleotidesIssue, J. Chem. Soc., 1, 1119-1125.
    • (1984) J. Chem. Soc. , vol.1 , pp. 1119-1125
    • Blackburn, G.M.1    Kent, D.E.2    Kolkmann, F.3
  • 39
    • 0026032585 scopus 로고
    • 9-(Difluorophosphonoalkyl)guanines as a new class of multisubstrate analog inhibitors of purine nucleoside phosphorylase
    • Halazy,S., Ehrhard,A. and Danzin,C. (1991) 9-(Difluorophosphonoalkyl)guanines as a new class of multisubstrate analog inhibitors of purine nucleoside phosphorylase. J. Am. Chem. Soc., 113, 315-317.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 315-317
    • Halazy, S.1    Ehrhard, A.2    Danzin, C.3
  • 40
    • 0037031576 scopus 로고    scopus 로고
    • Single-stranded antisense SiRNAs guide target RNA cleavage in RNAi
    • Martinez,J., Patkaniowska,A., Urlaub,H., Luhrmann,R. and Tuschl,T. (2002) Single-stranded antisense SiRNAs guide target RNA cleavage in RNAi. Cell, 110, 563-574.
    • (2002) Cell , vol.110 , pp. 563-574
    • Martinez, J.1    Patkaniowska, A.2    Urlaub, H.3    Luhrmann, R.4    Tuschl, T.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.