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Seminars in Hematology
|
October 28, 2004
New paradigms for gene transfer: RNA trans-splicing and small interfering RNA as therapeutic strategies
Christopher E Walsh
Gene Therapy
|
May 31, 2003
Gene therapy progress and prospects: gene therapy for the hemophilias
Christopher E Walsh
Current Opinion in Pediatrics
|
March 7, 2002
Gene therapy for the hemophilias
Christopher E Walsh
Expert Review of Hematology
|
May 7, 2016
Current and future prospects for hemophilia gene therapy
Peter Ward, Christopher E Walsh
Expert Reviews in Molecular Medicine
|
January 13, 2006
RNA repair for haemophilia A
Hengjun Chao, Christopher E Walsh
The Mount Sinai Journal of Medicine, New York
|
November 16, 2004
AAV vectors for hemophilia B gene therapy
Hengjun Chao, Christopher E Walsh
Current Opinion in Molecular Therapeutics
|
November 19, 2002
Hemophilia gene therapy: novel rAAV vectors and RNA repair strategy
Hengjun Chao, Christopher E Walsh
Virology
|
February 24, 2009
Chimeric AAV Cap sequences alter gene transduction
Peter Ward, Christopher E Walsh
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
October 18, 2005
Spliceosome-mediated RNA trans-splicing
Yanping Yang, Christopher E Walsh
Virology
|
September 18, 2012
Targeted integration of a rAAV vector into the AAVS1 region
Peter Ward, Christopher E Walsh
Page
of 4
Search research articles
Search
Showing results (1-10 of 32) with videos related to
Sort By:
Page
of 4
Seminars in Hematology
|
October 28, 2004
New paradigms for gene transfer: RNA trans-splicing and small interfering RNA as therapeutic strategies
Christopher E Walsh
Gene Therapy
|
May 31, 2003
Gene therapy progress and prospects: gene therapy for the hemophilias
Christopher E Walsh
Current Opinion in Pediatrics
|
March 7, 2002
Gene therapy for the hemophilias
Christopher E Walsh
Expert Review of Hematology
|
May 7, 2016
Current and future prospects for hemophilia gene therapy
Peter Ward, Christopher E Walsh
Expert Reviews in Molecular Medicine
|
January 13, 2006
RNA repair for haemophilia A
Hengjun Chao, Christopher E Walsh
The Mount Sinai Journal of Medicine, New York
|
November 16, 2004
AAV vectors for hemophilia B gene therapy
Hengjun Chao, Christopher E Walsh
Current Opinion in Molecular Therapeutics
|
November 19, 2002
Hemophilia gene therapy: novel rAAV vectors and RNA repair strategy
Hengjun Chao, Christopher E Walsh
Virology
|
February 24, 2009
Chimeric AAV Cap sequences alter gene transduction
Peter Ward, Christopher E Walsh
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
October 18, 2005
Spliceosome-mediated RNA trans-splicing
Yanping Yang, Christopher E Walsh
Virology
|
September 18, 2012
Targeted integration of a rAAV vector into the AAVS1 region
Peter Ward, Christopher E Walsh
Page
of 4