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@ARTICLE{Engeland:128621,
author = {C. Engeland$^*$ and S. Bossow$^*$ and A. W. Hudacek and B.
Hoyler$^*$ and J. Förster$^*$ and R. Veinalde$^*$ and D.
Jäger$^*$ and R. Cattaneo and G. Ungerechts$^*$ and C.
Springfeld},
title = {{A} {T}upaia paramyxovirus vector system for targeting and
transgene expression.},
journal = {Journal of general virology},
volume = {98},
number = {9},
issn = {1465-2099},
address = {Reading},
publisher = {Soc.},
reportid = {DKFZ-2017-04637},
pages = {2248 - 2257},
year = {2017},
abstract = {Viruses from the diverse family of Paramyxoviridae include
important pathogens and are applied in gene therapy and for
cancer treatment. The Tupaia paramyxovirus (TPMV), isolated
from the kidney of a tree shrew, does not infect human cells
and neutralizing antibodies against other Paramyxoviridae do
not cross-react with TPMV. Here, we present a vector system
for de novo generation of infectious TPMV that allows for
insertion of additional genes as well as targeting using
antibody single-chain variable fragments. We show that the
recombinant TPMV specifically infect cells expressing the
targeted receptor and replicate in human cells. This vector
system provides a valuable tool for both basic research and
therapeutic applications.},
cin = {G100 / G010},
ddc = {570},
cid = {I:(DE-He78)G100-20160331 / I:(DE-He78)G010-20160331},
pnm = {317 - Translational cancer research (POF3-317)},
pid = {G:(DE-HGF)POF3-317},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:28809150},
doi = {10.1099/jgv.0.000887},
url = {https://inrepo02.dkfz.de/record/128621},
}