| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A splice-site mutation causing ovine McArdle's disease
|
Tan, P
|
|
1997
|
7 |
5 |
p. 336-342
7 p.
|
artikel
|
| 2 |
Canine fucosidosis: a model for retroviral gene transfer into haematopoietic stem cells
|
Ferrara, Margaret L
|
|
1997
|
7 |
5 |
p. 361-366
6 p.
|
artikel
|
| 3 |
Cell vehicles for gene transfer to the brain
|
Taylor, Rosanne
|
|
1997
|
7 |
5 |
p. 343-351
9 p.
|
artikel
|
| 4 |
Gene therapy for murine mucopolysaccharidosis type VII
|
Sands, Mark S
|
|
1997
|
7 |
5 |
p. 352-360
9 p.
|
artikel
|
| 5 |
Gene transfer to muscle using herpes simplex virus-based vectors
|
Huard, Johnny
|
|
1997
|
7 |
5 |
p. 299-313
15 p.
|
artikel
|
| 6 |
Improved adenoviral vectors for gene therapy of Duchenne muscular dystrophy
|
Hauser, M.A
|
|
1997
|
7 |
5 |
p. 277-283
7 p.
|
artikel
|
| 7 |
Naked DNA transport and expression in mammalian cells
|
Wolff, Jon A
|
|
1997
|
7 |
5 |
p. 314-318
5 p.
|
artikel
|
| 8 |
Problems and potential for gene therapy in Duchenne muscular dystrophy
|
Kakulas, B.A
|
|
1997
|
7 |
5 |
p. 319-324
6 p.
|
artikel
|
| 9 |
Revertant fibres: a possible genetic therapy for Duchenne muscular dystrophy?
|
Wilton, Stephen D
|
|
1997
|
7 |
5 |
p. 329-335
7 p.
|
artikel
|
| 10 |
Strategies to accomplish targeted gene delivery to muscle cells employing tropism-modified adenoviral vectors
|
Douglas, Joanne T
|
|
1997
|
7 |
5 |
p. 284-298
15 p.
|
artikel
|
| 11 |
The scope of gene therapy in humans: scientific, safety and ethical considerations
|
Karpati, George
|
|
1997
|
7 |
5 |
p. 273-276
4 p.
|
artikel
|
| 12 |
Use of the dog model for Duchenne muscular dystrophy in gene therapy trials
|
McC. Howell, J
|
|
1997
|
7 |
5 |
p. 325-328
4 p.
|
artikel
|
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