Reverse genetics systems for non-segmented negative-strand RNA viruses rely on co-transfection of a plasmid containing the full-length viral cDNA and helper plasmids encoding essential viral replication proteins. Here, a system is presented in which virus can be rescued from a single plasmid without the need for helper plasmids in cells infected with a host-restricted recombinant poxvirus that expresses T7 RNA polymerase. This approach relies on the insertion of T7 promoter sequences in the viral cDNA at positions that allow transcription of sub-genomic RNAs encoding essential viral replication proteins.</p
AbstractIn this study we report the development and optimization of two minigenome rescue systems fo...
AbstractBunyaviruses are trisegmented, negative-sense RNA viruses. Previously, we described a rescue...
Since 1999, plasmid-based reverse genetics (RG) systems have revolutionized the way influenza viruse...
Reverse genetics systems for non-segmented negative-strand RNA viruses rely on co-transfection of a ...
We have rescued influenza A virus by transfection of 12 plasmids into Vero cells. The eight individu...
The invention relates to an in vitro method ofrescuing negative RNA virus from low virulent virus st...
Within paramyxoviruses, conventional reverse genetics require the transfection of a minimum of four ...
Reverse genetics is a technology that allows the production of a virus from its complementary DNA (c...
Within paramyxoviruses, conventional reverse genetics require the transfection of a minimum of four ...
Within paramyxoviruses, conventional reverse genetics require the transfection of a minimum of four ...
We report the establishment of a reverse-genetics system for the rescue of recombinant influenza C/J...
SummaryMammalian orthoreoviruses (reoviruses) are highly tractable experimental models for studies o...
A reverse genetics system is the only available method to introduce specific mutations into the AMP...
We describe here the development of a reverse genetics system for the phlebovirus Uukuniemi virus, a...
<div><p>Since 1999, plasmid-based reverse genetics (RG) systems have revolutionized the way influenz...
AbstractIn this study we report the development and optimization of two minigenome rescue systems fo...
AbstractBunyaviruses are trisegmented, negative-sense RNA viruses. Previously, we described a rescue...
Since 1999, plasmid-based reverse genetics (RG) systems have revolutionized the way influenza viruse...
Reverse genetics systems for non-segmented negative-strand RNA viruses rely on co-transfection of a ...
We have rescued influenza A virus by transfection of 12 plasmids into Vero cells. The eight individu...
The invention relates to an in vitro method ofrescuing negative RNA virus from low virulent virus st...
Within paramyxoviruses, conventional reverse genetics require the transfection of a minimum of four ...
Reverse genetics is a technology that allows the production of a virus from its complementary DNA (c...
Within paramyxoviruses, conventional reverse genetics require the transfection of a minimum of four ...
Within paramyxoviruses, conventional reverse genetics require the transfection of a minimum of four ...
We report the establishment of a reverse-genetics system for the rescue of recombinant influenza C/J...
SummaryMammalian orthoreoviruses (reoviruses) are highly tractable experimental models for studies o...
A reverse genetics system is the only available method to introduce specific mutations into the AMP...
We describe here the development of a reverse genetics system for the phlebovirus Uukuniemi virus, a...
<div><p>Since 1999, plasmid-based reverse genetics (RG) systems have revolutionized the way influenz...
AbstractIn this study we report the development and optimization of two minigenome rescue systems fo...
AbstractBunyaviruses are trisegmented, negative-sense RNA viruses. Previously, we described a rescue...
Since 1999, plasmid-based reverse genetics (RG) systems have revolutionized the way influenza viruse...