These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

114 related articles for article (PubMed ID: 14675624)

  • 21. An RNA domain within the 5' untranslated region of the tomato bushy stunt virus genome modulates viral RNA replication.
    Wu B; Vanti WB; White KA
    J Mol Biol; 2001 Jan; 305(4):741-56. PubMed ID: 11162089
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Complete sequence of the citrus tristeza virus RNA genome.
    Karasev AV; Boyko VP; Gowda S; Nikolaeva OV; Hilf ME; Koonin EV; Niblett CL; Cline K; Gumpf DJ; Lee RF
    Virology; 1995 Apr; 208(2):511-20. PubMed ID: 7747424
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The SL1 stem-loop structure at the 5'-end of potato virus X RNA is required for efficient binding to host proteins and for viral infectivity.
    Kwon SJ; Kim KH
    Mol Cells; 2006 Feb; 21(1):63-75. PubMed ID: 16511348
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The p23 protein of citrus tristeza virus controls asymmetrical RNA accumulation.
    Satyanarayana T; Gowda S; Ayllón MA; Albiach-Martí MR; Rabindran S; Dawson WO
    J Virol; 2002 Jan; 76(2):473-83. PubMed ID: 11752137
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Unusual sequence relationships between two isolates of citrus tristeza virus.
    Mawassi M; Mietkiewska E; Gofman R; Yang G; Bar-Joseph M
    J Gen Virol; 1996 Sep; 77 ( Pt 9)():2359-64. PubMed ID: 8811037
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The fitness of citrus tristeza virus defective RNAs is affected by the lengths of their 5'- and 3'-termini and by the coding capacity.
    Mawassi M; Satyanarayana T; Albiach-Martí MR; Gowda S; Ayllón MA; Robertson C; Dawson WO
    Virology; 2000 Sep; 275(1):42-56. PubMed ID: 11017786
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Long-distance RNA-RNA interactions and conserved sequence elements affect potato virus X plus-strand RNA accumulation.
    Kim KH; Hemenway CL
    RNA; 1999 May; 5(5):636-45. PubMed ID: 10334334
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Nucleotide sequences and mutations of the 5'-nontranslated region (5'NTR) of natural isolates of an epidemic echovirus 11' (prime).
    Szendrõi A; El-Sageyer M; Takács M; Mezey I; Berencsi G
    Arch Virol; 2000; 145(12):2575-600. PubMed ID: 11205106
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Cellular protein binds to sequences near the 5' terminus of potato virus X RNA that are important for virus replication.
    Kim KH; Kwon SJ; Hemenway C
    Virology; 2002 Sep; 301(2):305-12. PubMed ID: 12359432
    [TBL] [Abstract][Full Text] [Related]  

  • 30. An engineered closterovirus RNA replicon and analysis of heterologous terminal sequences for replication.
    Satyanarayana T; Gowda S; Boyko VP; Albiach-Marti MR; Mawassi M; Navas-Castillo J; Karasev AV; Dolja V; Hilf ME; Lewandowski DJ; Moreno P; Bar-Joseph M; Garnsey SM; Dawson WO
    Proc Natl Acad Sci U S A; 1999 Jun; 96(13):7433-8. PubMed ID: 10377432
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Role of the 5'-proximal stem-loop structure of the 5' untranslated region in replication and translation of hepatitis C virus RNA.
    Luo G; Xin S; Cai Z
    J Virol; 2003 Mar; 77(5):3312-8. PubMed ID: 12584356
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The leader RNA of coronavirus mouse hepatitis virus contains an enhancer-like element for subgenomic mRNA transcription.
    Wang Y; Zhang X
    J Virol; 2000 Nov; 74(22):10571-80. PubMed ID: 11044101
    [TBL] [Abstract][Full Text] [Related]  

  • 33. cis-Acting sequences required for coat protein binding and in vitro assembly of Potato virus X.
    Kwon SJ; Park MR; Kim KW; Plante CA; Hemenway CL; Kim KH
    Virology; 2005 Mar; 334(1):83-97. PubMed ID: 15749125
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Essential role of cyclization sequences in flavivirus RNA replication.
    Khromykh AA; Meka H; Guyatt KJ; Westaway EG
    J Virol; 2001 Jul; 75(14):6719-28. PubMed ID: 11413342
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The bovine leukemia virus encapsidation signal is composed of RNA secondary structures.
    Mansky LM; Wisniewski RM
    J Virol; 1998 Apr; 72(4):3196-204. PubMed ID: 9525645
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Characterization of citrus tristeza virus subgenomic RNAs in infected tissue.
    Hilf ME; Karasev AV; Pappu HR; Gumpf DJ; Niblett CL; Garnsey SM
    Virology; 1995 Apr; 208(2):576-82. PubMed ID: 7747429
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Sequences in the 5' nontranslated region of hepatitis C virus required for RNA replication.
    Friebe P; Lohmann V; Krieger N; Bartenschlager R
    J Virol; 2001 Dec; 75(24):12047-57. PubMed ID: 11711595
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Genetic analysis of sequences in the 3' nontranslated region of hepatitis C virus that are important for RNA replication.
    Friebe P; Bartenschlager R
    J Virol; 2002 Jun; 76(11):5326-38. PubMed ID: 11991961
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Mutations in the 5' nontranslated region of bovine viral diarrhea virus result in altered growth characteristics.
    Becher P; Orlich M; Thiel HJ
    J Virol; 2000 Sep; 74(17):7884-94. PubMed ID: 10933696
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Cell type-specific enhancement of hepatitis C virus internal ribosome entry site-directed translation due to 5' nontranslated region substitutions selected during passage of virus in lymphoblastoid cells.
    Lerat H; Shimizu YK; Lemon SM
    J Virol; 2000 Aug; 74(15):7024-31. PubMed ID: 10888641
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.