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Stefan Fruehauf

Showing results (31-40 of 61) with videos related to

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Lung Cancer (Amsterdam, Netherlands)|October 12, 2004
Susceptibility of mesothelioma cell lines to adeno-associated virus 2 vector-based suicide gene therapySimone Berlinghoff, Marlon R Veldwijk, Stephanie Laufs, et al.
AIDS (London, England)|October 21, 2009
Cold spots in hot spots: transcription start sites of active genes are spared from HIV vector integrationFrank A Giordano, Jens Uwe Appelt, Manuela Zucknick, et al.
Human Gene Therapy|January 29, 2002
Multidrug resistance 1 gene transfer can confer chemoprotection to human peripheral blood progenitor cells engrafted in immunodeficient miceBernd Schiedlmeier, Andrea J Schilz, Klaus Kühlcke, et al.
Experimental Hematology|May 23, 2008
Generation of efficient human blood progenitor-targeted recombinant adeno-associated viral vectors (AAV) by applying an AAV random peptide library on primary human hematopoietic progenitor cellsLeopold Sellner, Marius Stiefelhagen, Jürgen A Kleinschmidt, et al.
Stem Cells (Dayton, Ohio)|July 7, 2007
No evidence of clonal dominance in primates up to 4 years following transplantation of multidrug resistance 1 retrovirally transduced long-term repopulating cellsFarastuk Bozorgmehr, Stefanie Laufs, Stephanie E Sellers, et al.
Genetic Vaccines and Therapy|September 16, 2008
Application of a haematopoetic progenitor cell-targeted adeno-associated viral (AAV) vector established by selection of an AAV random peptide library on a leukaemia cell lineMarius Stiefelhagen, Leopold Sellner, Jürgen A Kleinschmidt, et al.
Cytotherapy|November 26, 2009
Pseudotyped recombinant adeno-associated viral vectors mediate efficient gene transfer into primary human CD34(+) peripheral blood progenitor cellsMarlon R Veldwijk, Leopold Sellner, Marius Stiefelhagen, et al.
Stem Cells (Dayton, Ohio)|July 28, 2004
Clonal analysis of individual marrow-repopulating cells after experimental peripheral blood progenitor cell transplantationK Zsuzsanna Nagy, Stephanie Laufs, Bernhard Gentner, et al.
Blood|August 8, 2008
Overnight transduction with foamyviral vectors restores the long-term repopulating activity of Fancc-/- stem cellsYue Si, Anna C Pulliam, Yvonne Linka, et al.
Cytotherapy|October 19, 2010
Unrestricted somatic stem cells: interaction with CD34+ cells in vitro and in vivo, expression of homing genes and exclusion of tumorigenic potentialKathrin Sonja Jeltsch, Teja Falk Radke, Stephanie Laufs, et al.
Pageof 7

Showing results (31-40 of 61) with videos related to

Sort By:
Pageof 7
Lung Cancer (Amsterdam, Netherlands)|October 12, 2004
Susceptibility of mesothelioma cell lines to adeno-associated virus 2 vector-based suicide gene therapySimone Berlinghoff, Marlon R Veldwijk, Stephanie Laufs, et al.
AIDS (London, England)|October 21, 2009
Cold spots in hot spots: transcription start sites of active genes are spared from HIV vector integrationFrank A Giordano, Jens Uwe Appelt, Manuela Zucknick, et al.
Human Gene Therapy|January 29, 2002
Multidrug resistance 1 gene transfer can confer chemoprotection to human peripheral blood progenitor cells engrafted in immunodeficient miceBernd Schiedlmeier, Andrea J Schilz, Klaus Kühlcke, et al.
Experimental Hematology|May 23, 2008
Generation of efficient human blood progenitor-targeted recombinant adeno-associated viral vectors (AAV) by applying an AAV random peptide library on primary human hematopoietic progenitor cellsLeopold Sellner, Marius Stiefelhagen, Jürgen A Kleinschmidt, et al.
Stem Cells (Dayton, Ohio)|July 7, 2007
No evidence of clonal dominance in primates up to 4 years following transplantation of multidrug resistance 1 retrovirally transduced long-term repopulating cellsFarastuk Bozorgmehr, Stefanie Laufs, Stephanie E Sellers, et al.
Genetic Vaccines and Therapy|September 16, 2008
Application of a haematopoetic progenitor cell-targeted adeno-associated viral (AAV) vector established by selection of an AAV random peptide library on a leukaemia cell lineMarius Stiefelhagen, Leopold Sellner, Jürgen A Kleinschmidt, et al.
Cytotherapy|November 26, 2009
Pseudotyped recombinant adeno-associated viral vectors mediate efficient gene transfer into primary human CD34(+) peripheral blood progenitor cellsMarlon R Veldwijk, Leopold Sellner, Marius Stiefelhagen, et al.
Stem Cells (Dayton, Ohio)|July 28, 2004
Clonal analysis of individual marrow-repopulating cells after experimental peripheral blood progenitor cell transplantationK Zsuzsanna Nagy, Stephanie Laufs, Bernhard Gentner, et al.
Blood|August 8, 2008
Overnight transduction with foamyviral vectors restores the long-term repopulating activity of Fancc-/- stem cellsYue Si, Anna C Pulliam, Yvonne Linka, et al.
Cytotherapy|October 19, 2010
Unrestricted somatic stem cells: interaction with CD34+ cells in vitro and in vivo, expression of homing genes and exclusion of tumorigenic potentialKathrin Sonja Jeltsch, Teja Falk Radke, Stephanie Laufs, et al.
Pageof 7