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B Fehse

Showing results (1-10 of 49) with videos related to

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Gene Therapy|November 2, 2007
Insertional mutagenesis and clonal dominance: biological and statistical considerationsB Fehse, I Roeder
Gene Therapy|March 28, 2014
TALEN-mediated editing of endogenous T-cell receptors facilitates efficient reprogramming of T lymphocytes by lentiviral gene transferB Berdien, U Mock, D Atanackovic, et al.
Current Gene Therapy|July 12, 2002
T lymphocytes as targets of gene transfer with Moloney-type retroviral vectorsF A Ayuk, A R Zander, B Fehse
Nucleic Acids Research|December 24, 1998
Rapid and efficient cloning of proviral flanking fragments by kanamycin resistance gene complementationB Fehse, K Kühlcke, A Langer, et al.
Gene Therapy|December 18, 2009
Lentiviral gene ontology (LeGO) vectors equipped with novel drug-selectable fluorescent proteins: new building blocks for cell marking and multi-gene analysisK Weber, U Mock, B Petrowitz, et al.
Journal of Hematotherapy & Stem Cell Research|February 20, 2003
Molecular methods for detection and quantification of myeloma cells after bone marrow transplantation: comparison between real-time quantitative and nested PCRF Tögel, N Kröger, F Korioth, et al.
British Journal of Haematology|July 11, 2000
Efficient depletion of alloreactive donor T lymphocytes based on expression of two activation-induced antigens (CD25 and CD69)B Fehse, O Frerk, M Goldmann, et al.
Bone Marrow Transplantation|August 10, 2000
Depletion of alloreactive donor T cells using immunomagnetic cell selectionB Fehse, M Goldmann, O Frerk, et al.
Nucleic Acids Research|November 11, 1995
Excision of specific DNA-sequences from integrated retroviral vectors via site-specific recombinationJ Bergemann, K Kühlcke, B Fehse, et al.
Cytotherapy|July 26, 2005
Improving the ex vivo retroviral-mediated suicide-gene transfer process in T lymphocytes to preserve immune functionE Robinet, B Fehse, S Ebeling, et al.
Pageof 5

Showing results (1-10 of 49) with videos related to

Sort By:
Pageof 5
Gene Therapy|November 2, 2007
Insertional mutagenesis and clonal dominance: biological and statistical considerationsB Fehse, I Roeder
Gene Therapy|March 28, 2014
TALEN-mediated editing of endogenous T-cell receptors facilitates efficient reprogramming of T lymphocytes by lentiviral gene transferB Berdien, U Mock, D Atanackovic, et al.
Current Gene Therapy|July 12, 2002
T lymphocytes as targets of gene transfer with Moloney-type retroviral vectorsF A Ayuk, A R Zander, B Fehse
Nucleic Acids Research|December 24, 1998
Rapid and efficient cloning of proviral flanking fragments by kanamycin resistance gene complementationB Fehse, K Kühlcke, A Langer, et al.
Gene Therapy|December 18, 2009
Lentiviral gene ontology (LeGO) vectors equipped with novel drug-selectable fluorescent proteins: new building blocks for cell marking and multi-gene analysisK Weber, U Mock, B Petrowitz, et al.
Journal of Hematotherapy & Stem Cell Research|February 20, 2003
Molecular methods for detection and quantification of myeloma cells after bone marrow transplantation: comparison between real-time quantitative and nested PCRF Tögel, N Kröger, F Korioth, et al.
British Journal of Haematology|July 11, 2000
Efficient depletion of alloreactive donor T lymphocytes based on expression of two activation-induced antigens (CD25 and CD69)B Fehse, O Frerk, M Goldmann, et al.
Bone Marrow Transplantation|August 10, 2000
Depletion of alloreactive donor T cells using immunomagnetic cell selectionB Fehse, M Goldmann, O Frerk, et al.
Nucleic Acids Research|November 11, 1995
Excision of specific DNA-sequences from integrated retroviral vectors via site-specific recombinationJ Bergemann, K Kühlcke, B Fehse, et al.
Cytotherapy|July 26, 2005
Improving the ex vivo retroviral-mediated suicide-gene transfer process in T lymphocytes to preserve immune functionE Robinet, B Fehse, S Ebeling, et al.
Pageof 5