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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
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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:
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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
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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
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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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