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Gene Therapy
|
October 20, 2006
Lentiviral vectors targeting WASp expression to hematopoietic cells, efficiently transduce and correct cells from WAS patients
S Charrier, L Dupré, S Scaramuzza, et al.
Blood
|
April 15, 1996
gamma-c gene transfer into SCID X1 patients' B-cell lines restores normal high-affinity interleukin-2 receptor expression and function
H Hacein-Bey, M Cavazzana-Calvo, F Le Deist, et al.
The Journal of Gene Medicine
|
March 30, 2000
Selective uptake and sustained expression of AAV vectors following subcutaneous delivery
B A Donahue, J G McArthur, S K Spratt, et al.
Experimental Cell Research
|
July 30, 2005
Abnormal ion content, hydration and granule expansion of the secretory granules from cystic fibrosis airway glandular cells
S Baconnais, F Delavoie, J M Zahm, et al.
Nature Biotechnology
|
August 14, 1998
Regulation of gene expression in vivo following transduction by two separate rAAV vectors
K G Rendahl, S E Leff, G R Otten, et al.
Human Gene Therapy
|
May 6, 2005
Adeno-associated virus pseudotype 5 vector improves gene transfer in arthritic joints
F Apparailly, M Khoury, M J B Vervoordeldonk, et al.
The Journal of General Virology
|
April 11, 2006
Relationship between retroviral vector membrane and vector stability
M Carmo, T Q Faria, H Falk, et al.
Nature Genetics
|
July 1, 1997
Persistent and therapeutic concentrations of human factor IX in mice after hepatic gene transfer of recombinant AAV vectors
R O Snyder, C H Miao, G A Patijn, et al.
Current Gene Therapy
|
November 9, 2010
Relevance of an academic GMP Pan-European vector infra-structure (PEVI)
O Cohen-Haguenauer, N Creff, P Cruz, et al.
Page
of 11
Search research articles
Search
Showing results (101-110 of 109) with videos related to
Sort By:
Page
of 11
You have reached the last page of results.
This site can display upto 109 results.
Gene Therapy
|
October 20, 2006
Lentiviral vectors targeting WASp expression to hematopoietic cells, efficiently transduce and correct cells from WAS patients
S Charrier, L Dupré, S Scaramuzza, et al.
Blood
|
April 15, 1996
gamma-c gene transfer into SCID X1 patients' B-cell lines restores normal high-affinity interleukin-2 receptor expression and function
H Hacein-Bey, M Cavazzana-Calvo, F Le Deist, et al.
The Journal of Gene Medicine
|
March 30, 2000
Selective uptake and sustained expression of AAV vectors following subcutaneous delivery
B A Donahue, J G McArthur, S K Spratt, et al.
Experimental Cell Research
|
July 30, 2005
Abnormal ion content, hydration and granule expansion of the secretory granules from cystic fibrosis airway glandular cells
S Baconnais, F Delavoie, J M Zahm, et al.
Nature Biotechnology
|
August 14, 1998
Regulation of gene expression in vivo following transduction by two separate rAAV vectors
K G Rendahl, S E Leff, G R Otten, et al.
Human Gene Therapy
|
May 6, 2005
Adeno-associated virus pseudotype 5 vector improves gene transfer in arthritic joints
F Apparailly, M Khoury, M J B Vervoordeldonk, et al.
The Journal of General Virology
|
April 11, 2006
Relationship between retroviral vector membrane and vector stability
M Carmo, T Q Faria, H Falk, et al.
Nature Genetics
|
July 1, 1997
Persistent and therapeutic concentrations of human factor IX in mice after hepatic gene transfer of recombinant AAV vectors
R O Snyder, C H Miao, G A Patijn, et al.
Current Gene Therapy
|
November 9, 2010
Relevance of an academic GMP Pan-European vector infra-structure (PEVI)
O Cohen-Haguenauer, N Creff, P Cruz, et al.
Page
of 11