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Journal Abstract Search

265 related items for PubMed ID: 25678268

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  • 3. The structure and functions of coronavirus genomic 3' and 5' ends.
    Yang D, Leibowitz JL.
    Virus Res; 2015 Aug 03; 206():120-33. PubMed ID: 25736566
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  • 4. The genome of hawaii virus and its relationship with other members of the caliciviridae.
    Pletneva MA, Sosnovtsev SV, Green KY.
    Virus Genes; 2001 Aug 03; 23(1):5-16. PubMed ID: 11556401
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  • 5. Functional analysis of RNA structures present at the 3' extremity of the murine norovirus genome: the variable polypyrimidine tract plays a role in viral virulence.
    Bailey D, Karakasiliotis I, Vashist S, Chung LM, Rees J, McFadden N, Benson A, Yarovinsky F, Simmonds P, Goodfellow I.
    J Virol; 2010 Mar 03; 84(6):2859-70. PubMed ID: 20053745
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  • 6. Positive strand RNA virus replication: It depends on the ends.
    Brinton MA, Miller WA.
    Virus Res; 2015 Aug 03; 206():1-2. PubMed ID: 26094090
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  • 9. Functions of the 5'- and 3'-untranslated regions of tobamovirus RNA.
    Chujo T, Ishibashi K, Miyashita S, Ishikawa M.
    Virus Res; 2015 Aug 03; 206():82-9. PubMed ID: 25683511
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  • 16. [Structure and function of the non-coding regions of hepatitis C viral RNA].
    Dutkiewicz M, Swiqtkowska A, Ciesiołka J.
    Postepy Biochem; 2006 Aug 03; 52(1):62-71. PubMed ID: 16869303
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  • 17. La protein can simultaneously bind to both 3'- and 5'-noncoding regions of Japanese encephalitis virus genome.
    Vashist S, Bhullar D, Vrati S.
    DNA Cell Biol; 2011 Jun 03; 30(6):339-46. PubMed ID: 21294637
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  • 20. Feline calicivirus can tolerate gross changes of its minor capsid protein expression levels induced by changing translation reinitiation frequency or use of a separate VP2-coding mRNA.
    Haβ M, Luttermann C, Meyers G.
    PLoS One; 2014 Jun 03; 9(7):e102254. PubMed ID: 25007260
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