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Chapter 2a: Virology


          36.  Proutski V, Gould EA, Holmes EC. Secondary   45.  Asghar N, Lee YP, Nilsson E, et al. The role of
              structure of the 3′ untranslated region of   the poly(A) tract in the replication and
              flaviviruses: similarities and differences. Nucl   virulence of tick-borne encephalitis virus. Sci
              Acid Res. 1997;25:1194-202.                 Rep. 2016;6:39265.

          37.  Gritsun TS, Gould EA. Origin and evolution of   46.  Sakai M, Yoshii K, Sunden Y, et al. Variable
              flavivirus 5’UTRs and panhandles: trans-    region of the 3′ UTR is a critical virulence
              terminal duplications? Virology. 2007;366:8-  factor in the Far-Eastern subtype of tick-borne
              15.                                         encephalitis virus in a mouse model. J Gen
                                                          Virol. 2014;95:823-35.
          38.  Wallner G, Mandl CW, Kunz C, Heinz FX. The
              flavivirus 3′- noncoding region: extensive size   47.  Gritsun TS, Gould EA. The 3′ untranslated
              heterogeneity independent of evolutionary   region of tick-borne flaviviruses originated by
              relationships among strains of tick-borne   the duplication of long repeat sequences
              encephalitis virus. Virology. 1995;213:169-78.   within the open reading frame. Virology.
                                                          2006;354:217-23.
          39.  Lindenbach BD, Rice CM. Molecular biology of
              flaviviruses. Adv Virus Res. 2003;59:23-61.   48.  Gritsun TS, Gould EA. Origin and evolution of
                                                          3’UTR of flaviviruses: long direct repeats as a
          40.  Mandl CW, Kunz C, Heinz FX. Presence of poly  basis for the formation of secondary structures
              (A) in a flavivirus: significant differences   and their significance for virus transmission.
              between the 3′ noncoding regions of the     Adv Virus Res. 2007;69:203-48.
              genomic RNAs of tick-borne encephalitis virus
              strains. J Virol. 1991;65:4070-7.       49.  Roby JA, Pijlman GP, Wilusz J, Khromykh AA.
                                                          Noncoding subgenomic flavivirus RNA:
          41.  Formanová P, Černý J, Bolfíková BČ, et al. Full   multiple functions in West Nile virus
              genome sequences and molecular              pathogenesis and modulation of host
              characterization of tick-borne encephalitis   responses. Viruses. 2014;6:404-27.
              virus strains isolated from human patients.
              Ticks Tick Borne Dis. 2015;6:38-46.     50.  Khromykh AA, Westaway EG. RNA binding
                                                          properties of core protein of the flavivirus
          42.  Leonova GN, Belikov SI, Kondratov IG,      Kunjin. Arch Virol. 1996;141:685-99.
              Takashima I. Comprehensive assessment of
              the genetics and virulence of tick-borne   51.  Samsa MM, Mondotte JA, Iglesias NG, et al.
              encephalitis virus strains isolated from    Dengue virus capsid protein usurps lipid
              patients with inapparent and clinical forms of   droplets for viral particle formation. PLoS
              the infection in the Russian Far East. Virology.   Pathog. 2009;5:e1000632.
              2013;443:89-98.
                                                      52.  Kofler RM, Heinz FX, Mandl CW. Capsid
          43.  Mandl CW, Holzmann H, Meixner T, et al.    protein C of tick- borne encephalitis virus
              Spontaneous and engineered deletions in the   tolerates large internal deletions and is a
              3′ noncoding region of tick- borne encephalitis   favorable target for attenuation of virulence.
              virus: construction of highly attenuated     J Virol. 2002;76:3534-43.
              mutants of a flavivirus. J Virol. 1998;72:2132-
              40.                                     53.  Kofler RM, Leitner A, O’Riordain G, Heinz FX,
                                                          Mandl CW. Spontaneous mutations restore
          44.  Sakai M, Muto M, Hirano M, Kariwa H, Yoshii   the viability of tick-borne encephalitis virus
              K. Virulence of tick-borne encephalitis virus is   mutants with large deletions in protein C.
              associated with intact conformational viral   J Virol. 2003;77:443-51.
              RNA structures in the variable region of the 3′-
              UTR. Virus Res. 2015;203:36-40.



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