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Volumn 1, Issue 2, 2012, Pages

Intracerebral infusion of antisense oligonucleotides into prion-infected mice

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EID: 84868351310     PISSN: None     EISSN: 21622531     Source Type: Journal    
DOI: 10.1038/mtna.2011.6     Document Type: Article
Times cited : (43)

References (23)
  • 2
    • 0038783253 scopus 로고    scopus 로고
    • Specific inhibition of pathological prion protein accumulation by small interfering RNAs
    • DOI 10.1242/jcs.00494
    • Daude, N, Marella, M and Chabry, J (2003). Specific inhibition of pathological prion protein accumulation by small interfering RNAs. J Cell Sci 116(Pt 13): 2775-2779. (Pubitemid 36857228)
    • (2003) Journal of Cell Science , vol.116 , Issue.13 , pp. 2775-2779
    • Daude, N.1    Marella, M.2    Chabry, J.3
  • 4
    • 48249108696 scopus 로고    scopus 로고
    • Single treatment with RNAi against prion protein rescues early neuronal dysfunction and prolongs survival in mice with prion disease
    • White, MD, Farmer, M, Mirabile, I, Brandner, S, Collinge, J and Mallucci, GR (2008). Single treatment with RNAi against prion protein rescues early neuronal dysfunction and prolongs survival in mice with prion disease. Proc Natl Acad Sci USA 105: 10238-10243.
    • (2008) Proc Natl Acad Sci USA , vol.105 , pp. 10238-10243
    • White, M.D.1    Farmer, M.2    Mirabile, I.3    Brandner, S.4    Collinge, J.5    Mallucci, G.R.6
  • 7
    • 0242363656 scopus 로고    scopus 로고
    • Depleting neuronal prp in prion infection prevents disease and reverses spongiosis
    • DOI 10.1126/science.1090187
    • Mallucci, G, Dickinson, A, Linehan, J, Klöhn, PC, Brandner, S and Collinge, J (2003). Depleting neuronal PrP in prion infection prevents disease and reverses spongiosis. Science 302: 871-874. (Pubitemid 37339628)
    • (2003) Science , vol.302 , Issue.5646 , pp. 871-874
    • Mallucci, G.1    Dickinson, A.2    Linehan, J.3    Klohn, P.-C.4    Brandner, S.5    Collinge, J.6
  • 9
    • 77949512140 scopus 로고    scopus 로고
    • RNA targeting therapeutics: Molecular mechanisms of antisense oligonucleotides as a therapeutic platform
    • Bennett, CF and Swayze, EE (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
  • 10
    • 2342427578 scopus 로고    scopus 로고
    • Determination of the role of the human rnase h1 in the pharmacology of dna-like antisense drugs
    • DOI 10.1074/jbc.M311683200
    • Wu, H, Lima, WF, Zhang, H, Fan, A, Sun, H and Crooke, ST (2004). Determination of the role of the human RNase H1 in the pharmacology of DNA-like antisense drugs. J Biol Chem 279: 17181-17189. (Pubitemid 38560475)
    • (2004) Journal of Biological Chemistry , vol.279 , Issue.17 , pp. 17181-17189
    • Wu, H.1    Lima, W.F.2    Zhang, H.3    Fan, A.4    Sun, H.5    Crooke, S.T.6
  • 12
    • 0037143011 scopus 로고    scopus 로고
    • Postexposure prophylaxis against prion disease with a stimulator of innate immunity
    • DOI 10.1016/S0140-6736(02)09513-2
    • Sethi, S, Lipford, G, Wagner, H and Kretzschmar, H (2002). Postexposure prophylaxis against prion disease with a stimulator of innate immunity. Lancet 360: 229-230. (Pubitemid 34804655)
    • (2002) Lancet , vol.360 , Issue.9328 , pp. 229-230
    • Sethi, S.1    Lipford, G.2    Wagner, H.3    Kretzschmar, H.4
  • 15
    • 0028535880 scopus 로고
    • High prion and PrPSc levels but delayed onset of disease in scrapie-inoculated mice heterozygous for a disrupted PrP gene
    • Büeler, H, Raeber, A, Sailer, A, Fischer, M, Aguzzi, A and Weissmann, C (1994). High prion and PrPSc levels but delayed onset of disease in scrapie-inoculated mice heterozygous for a disrupted PrP gene. Mol Med 1: 19-30.
    • (1994) Mol Med , vol.1 , pp. 19-30
    • Büeler, H.1    Raeber, A.2    Sailer, A.3    Fischer, M.4    Aguzzi, A.5    Weissmann, C.6
  • 16
    • 79952167224 scopus 로고    scopus 로고
    • Prion propagation and toxicity in vivo occur in two distinct mechanistic phases
    • Sandberg, MK, Al-Doujaily, H, Sharps, B, Clarke, AR and Collinge, J (2011). Prion propagation and toxicity in vivo occur in two distinct mechanistic phases. Nature 470: 540-542.
    • (2011) Nature , vol.470 , pp. 540-542
    • Sandberg, M.K.1    Al-Doujaily, H.2    Sharps, B.3    Clarke, A.R.4    Collinge, J.5
  • 17
    • 0037212852 scopus 로고    scopus 로고
    • A novel solid support for synthesis of oligonucleotide 3′-phosphorothioate monoesters
    • DOI 10.1016/S0960-894X(02)00922-8, PII S0960894X02009228
    • Cheruvallath, ZS, Cole, DL and Ravikumar, VT (2003). A novel solid support for synthesis of oligonucleotide 3'-phosphorothioate monoesters. Bioorg Med Chem Lett 13: 281-284. (Pubitemid 35441352)
    • (2003) Bioorganic and Medicinal Chemistry Letters , vol.13 , Issue.2 , pp. 281-284
    • Cheruvallath, Z.S.1    Cole, D.L.2    Ravikumar, V.T.3
  • 18
    • 0033555551 scopus 로고    scopus 로고
    • Characterization of a potent and specific class of antisense oligonucleotide inhibitor of human protein kinase C-alpha expression
    • McKay, RA, Miraglia, LJ, Cummins, LL, Owens, SR, Sasmor, H and Dean, NM (1999). Characterization of a potent and specific class of antisense oligonucleotide inhibitor of human protein kinase C-alpha expression. J Biol Chem 274: 1715-1722.
    • (1999) J Biol Chem , vol.274 , pp. 1715-1722
    • McKay, R.A.1    Miraglia, L.J.2    Cummins, L.L.3    Owens, S.R.4    Sasmor, H.5    Dean, N.M.6
  • 19
    • 13544257472 scopus 로고    scopus 로고
    • Sequence-dependent cytotoxicity of secondgeneration oligonucleotides
    • Drygin, D, Barone, S and Bennett, CF (2004). Sequence-dependent cytotoxicity of secondgeneration oligonucleotides. Nucleic Acids Res 32: 6585-6594.
    • (2004) Nucleic Acids Res , vol.32 , pp. 6585-6594
    • Drygin, D.1    Barone, S.2    Bennett, C.F.3
  • 22
    • 0026651376 scopus 로고
    • The sequential development of abnormal prion protein accumulation in mice with Creutzfeldt-Jakob disease
    • Muramoto, T, Kitamoto, T, Tateishi, J and Goto, I (1992). The sequential development of abnormal prion protein accumulation in mice with Creutzfeldt-Jakob disease. Am J Pathol 140: 1411-1420.
    • (1992) Am J Pathol , vol.140 , pp. 1411-1420
    • Muramoto, T.1    Kitamoto, T.2    Tateishi, J.3    Goto, I.4
  • 23
    • 0030811015 scopus 로고    scopus 로고
    • Heritable disorder resembling neuronal storage disease in mice expressing prion protein with deletion of an α-helix
    • DOI 10.1038/nm0797-750
    • Muramoto, T, DeArmond, SJ, Scott, M, Telling, GC, Cohen, FE and Prusiner, SB (1997). Heritable disorder resembling neuronal storage disease in mice expressing prion protein with deletion of an alpha-helix. Nat Med 3: 750-755. (Pubitemid 27298718)
    • (1997) Nature Medicine , vol.3 , Issue.7 , pp. 750-755
    • Muramoto, T.1    DeArmond, S.J.2    Scott, M.3    Telling, G.C.4    Cohen, F.E.5    Prusiner, S.B.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.