Paramyxovirus RNA synthesis and the requirement for hexamer genome length: the rule of six revisited.
作者信息
Kolakofsky D, Pelet T, Garcin D, Hausmann S, Curran J, Roux L
机构信息
Department of Genetics and Microbiology, University of Geneva School of Medicine, Switzerland.
出版信息
J Virol. 1998 Feb;72(2):891-9. doi: 10.1128/JVI.72.2.891-899.1998.
Abstract
摘要
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1
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Virology. 1985 Sep;145(2):346-9. doi: 10.1016/0042-6822(85)90170-9.
2
RECONSTITUTION OF ACTIVE TOBACCO MOSAIC VIRUS FROM ITS INACTIVE PROTEIN AND NUCLEIC ACID COMPONENTS.
Proc Natl Acad Sci U S A. 1955 Oct 15;41(10):690-8. doi: 10.1073/pnas.41.10.690.
3
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