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Gene Therapy
|
November 2, 2007
Insertional mutagenesis and clonal dominance: biological and statistical considerations
B 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 transfer
B Berdien, U Mock, D Atanackovic, et al.
Current Gene Therapy
|
July 12, 2002
T lymphocytes as targets of gene transfer with Moloney-type retroviral vectors
F 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 complementation
B 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 analysis
K 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 PCR
F 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 selection
B 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 recombination
J 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 function
E Robinet, B Fehse, S Ebeling, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 49) with videos related to
Sort By:
Page
of 5
Gene Therapy
|
November 2, 2007
Insertional mutagenesis and clonal dominance: biological and statistical considerations
B 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 transfer
B Berdien, U Mock, D Atanackovic, et al.
Current Gene Therapy
|
July 12, 2002
T lymphocytes as targets of gene transfer with Moloney-type retroviral vectors
F 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 complementation
B 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 analysis
K 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 PCR
F 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 selection
B 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 recombination
J 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 function
E Robinet, B Fehse, S Ebeling, et al.
Page
of 5