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FEBS Letters
|
April 28, 1997
Immune responses, not promoter inactivation, are responsible for decreased long-term expression following plasmid gene transfer into skeletal muscle
K E Wells, J Maule, R Kingston, et al.
Experimental Cell Research
|
August 2, 2005
Mutated fukutin-related protein (FKRP) localises as wild type in differentiated muscle cells
N F Dolatshad, M Brockington, S Torelli, et al.
Human Gene Therapy
|
December 16, 1998
Insertion of two independent enhancers in the long terminal repeat of a self-inactivating vector results in high-titer retroviral vectors with tissue-specific expression
A Fassati, A Bardoni, M Sironi, et al.
The Journal of Clinical Investigation
|
August 1, 1997
Genetic correction of dystrophin deficiency and skeletal muscle remodeling in adult MDX mouse via transplantation of retroviral producer cells
A Fassati, D J Wells, P A Sgro Serpente, et al.
Human Molecular Genetics
|
August 1, 1995
Expression of human full-length and minidystrophin in transgenic mdx mice: implications for gene therapy of Duchenne muscular dystrophy
D J Wells, K E Wells, E A Asante, et al.
Human Molecular Genetics
|
April 1, 1992
Human dystrophin expression corrects the myopathic phenotype in transgenic mdx mice
D J Wells, K E Wells, F S Walsh, et al.
Bone
|
June 23, 2004
Bone biomechanical properties in LRP5 mutant mice
M P Akhter, D J Wells, S J Short, et al.
Laboratory Animals
|
April 8, 2006
Assessing the welfare of genetically altered mice
D J Wells, L C Playle, W E J Enser, et al.
Page
of 6
Search research articles
Search
Showing results (51-60 of 58) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 58 results.
FEBS Letters
|
April 28, 1997
Immune responses, not promoter inactivation, are responsible for decreased long-term expression following plasmid gene transfer into skeletal muscle
K E Wells, J Maule, R Kingston, et al.
Experimental Cell Research
|
August 2, 2005
Mutated fukutin-related protein (FKRP) localises as wild type in differentiated muscle cells
N F Dolatshad, M Brockington, S Torelli, et al.
Human Gene Therapy
|
December 16, 1998
Insertion of two independent enhancers in the long terminal repeat of a self-inactivating vector results in high-titer retroviral vectors with tissue-specific expression
A Fassati, A Bardoni, M Sironi, et al.
The Journal of Clinical Investigation
|
August 1, 1997
Genetic correction of dystrophin deficiency and skeletal muscle remodeling in adult MDX mouse via transplantation of retroviral producer cells
A Fassati, D J Wells, P A Sgro Serpente, et al.
Human Molecular Genetics
|
August 1, 1995
Expression of human full-length and minidystrophin in transgenic mdx mice: implications for gene therapy of Duchenne muscular dystrophy
D J Wells, K E Wells, E A Asante, et al.
Human Molecular Genetics
|
April 1, 1992
Human dystrophin expression corrects the myopathic phenotype in transgenic mdx mice
D J Wells, K E Wells, F S Walsh, et al.
Bone
|
June 23, 2004
Bone biomechanical properties in LRP5 mutant mice
M P Akhter, D J Wells, S J Short, et al.
Laboratory Animals
|
April 8, 2006
Assessing the welfare of genetically altered mice
D J Wells, L C Playle, W E J Enser, et al.
Page
of 6