Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Heike Merget-Millitzer"'
Autor:
Martin Engelstädter, Heike Merget-Millitzer, RA Willemsen, Stefanie Steidl, Maria Bobkova, Klaus Cichutek, Christian J. Buchholz, Jörn Stitz
Publikováno v:
Gene Therapy. 8:1202-1206
In contrast to murine leukaemia virus (MLV)-derived vector systems, vector particles derived from the avian spleen necrosis virus (SNV) have been successfully targeted to subsets of human cells by envelope modification with antibody fragments (scFv).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::131a9a2c6714d6f18c76fc6694acc559
https://doi.org/10.1038/sj.gt.3301500
https://doi.org/10.1038/sj.gt.3301500
Autor:
Martin Engelstädter, Renate König, Frank Nocken, Maria Bobkova, Christian J. Buchholz, Jörn Stitz, Peter Müller, Isabel Schmitt, Stefanie Steidl, Heike Merget-Millitzer, Klaus Cichutek, Reinhard Kurth
Publikováno v:
Virology. 267:229-236
Retroviral vectors derived from amphotropic murine leukemia viruses (MLV) mediate gene transfer into almost all human cells and are thus not suitable for in vivo applications in gene therapy in which cell-specific gene delivery is required. We and ot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3bacfa34e45652ee4a7772d5dd91e956
https://doi.org/10.1006/viro.1999.0121
https://doi.org/10.1006/viro.1999.0121
Autor:
Frank Nocken, Martin Engelstädter, Reinhard Kurth, Jörn Stitz, Klaus Cichutek, Heike Merget-Millitzer, Barbara S. Schnierle, Valerie Bosch, Bernd Groner
Publikováno v:
Proceedings of the National Academy of Sciences. 94:8640-8645
CD4-expressing T cells in lymphoid organs are infected by the primary strains of HIV and represent one of the main sources of virus replication. Gene therapy strategies are being developed that allow the transfer of exogenous genes into CD4 + T lymph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ced81d44ad46b23447a7a13f47717ce7
https://doi.org/10.1073/pnas.94.16.8640
https://doi.org/10.1073/pnas.94.16.8640
Autor:
Marion-Gabriele Ott, Hans Martin, Dieter Hoelzer, Oliver G. Ottmann, Manuel Grez, Heike Bialek, Heike Merget-Millitzer, Reinhard Seger, Johann Peter Hossle, Nicole Brüggenolte
Publikováno v:
Journal of hematotherapystem cell research. 11(4)
As a single-gene defect in phagocytes, the X-linked form of chronic granulomatous disease (X-CGD) is a disorder potentially amenable to gene therapy by transfer of a functional copy of the gp91(phox) gene into hematopoietic stem cells (HSC). Although
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53795e327e71b4b123cff31597b803de
https://pubmed.ncbi.nlm.nih.gov/12201957
https://pubmed.ncbi.nlm.nih.gov/12201957
Publikováno v:
Bundesgesundheitsblatt - Gesundheitsforschung - Gesundheitsschutz; Dec2001, Vol. 44 Issue 12, p1226-1226, 1p