Titlebook: Regulation of Gene Expression in Animal Viruses; Luis Carrasco,Nahum Sonenberg,Eckard Wimmer Book 1993 Springer Science+Business Media New

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Hans-Georg Kräusslichstruments) transfers benefit the recipient country and hurt the donor. Within this neoclassical trade paradigm, however, despite the exogeneity of transfers and the existence of Walrasian stability, it has been shown that in several cases, mainly due to transfer induced changes in the terms of trade

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Adolfo García-Sastre,Peter Palesestruments) transfers benefit the recipient country and hurt the donor. Within this neoclassical trade paradigm, however, despite the exogeneity of transfers and the existence of Walrasian stability, it has been shown that in several cases, mainly due to transfer induced changes in the terms of trade

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Cascade Regulation of Vaccinia Virus Gene Expression, the newly synthesized transcription complex. Following DNA replication, however, intermediate genes are transcribed. The products of the intermediate genes include three transactivators of late gene expression. In the third phase of the cycle, the late genes are expressed and virion enzymes, early

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Mechanisms Regulating Nucleocapsid Formation of the Hepatitis B Viruses,ell, DNA synthesis in hepadnaviruses commences before release of virus particles. Therefore, retrovirus particles contain an RNA genome, hepadnavirus particles a DNA genome, leading to their classification as pararetroviruses.

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Regulation of Human Immunodeficiency Virus Structural Protein Expression and Virion Formation,ng elements and .-acting factors which regulate gene expression at a transcriptional and/or post-transcriptional level. In contrast to these transcriptional and post-transcriptional control mechanisms which have been scrutinized extensively in recent years, the late stages of assembly and maturation

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Infectious Influenza Viruses from cDNA-Derived RNA: Reverse Genetics,een the vRNA and the viral nucleoprotein (ribonucleoprotein complex, RNP) (Honda et al., 1988). Until the development of an appropriate system of introducing cDNA-derived RNA into viral particles, it has not been posible to use reverse genetics for the study of influenza virus and other negative-str

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Translation Regulation by Reovirus Structural Proteins, decreasing the translation of plasmid-encoded dihydrofolate reductase (DHFR) reporter mRNA in a process that is reversed by co-expression of adenovirus VA1. The reovirus S4 gene similarly stimulated CAT mRNA translation in transfected cells. S4 also replaced the VA1 requirement for transient expres