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Biochimica Et Biophysica Acta
|
June 9, 1995
Cloning and sequence analysis of caprine N-acetylglucosamine 6-sulfatase cDNA
K Friderici, K T Cavanagh, J R Leipprandt, et al.
Molecular Biology & Medicine
|
February 1, 1987
Towards gene therapy for hemophilia B
D S Anson, R A Hock, D Austen, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 1, 1991
Human alpha-L-iduronidase: cDNA isolation and expression
H S Scott, D S Anson, A M Orsborn, et al.
The Biochemical Journal
|
April 15, 1995
Two site-directed mutations abrogate enzyme activity but have different effects on the conformation and cellular content of the N-acetylgalactosamine 4-sulphatase protein
D A Brooks, D A Robertson, C Bindloss, et al.
Lancet (London, England)
|
February 4, 1984
Characterisation and use of an intragenic polymorphic marker for detection of carriers of haemophilia B (factor IX deficiency)
F Giannelli, D S Anson, K H Choo, et al.
Neuromuscular Disorders : NMD
|
July 1, 1997
Canine fucosidosis: a model for retroviral gene transfer into haematopoietic stem cells
M L Ferrara, T Occhiodoro, M Fuller, et al.
Gene Therapy
|
May 1, 1997
In vitro correction of iduronate-2-sulfatase deficiency by adenovirus-mediated gene transfer
C Di Francesco, C Cracco, R Tomanin, et al.
Gene Therapy
|
February 16, 2007
Lentivirus-mediated gene transfer to the rat, ovine and human cornea
D G A Parker, C Kaufmann, H M Brereton, et al.
The Journal of Clinical Investigation
|
April 15, 1996
Enzyme replacement therapy in a feline model of Maroteaux-Lamy syndrome
A C Crawley, D A Brooks, V J Muller, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 5, 1996
Long-term in vitro correction of alpha-L-iduronidase deficiency (Hurler syndrome) in human bone marrow
L J Fairbairn, L S Lashford, E Spooncer, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 51) with videos related to
Sort By:
Page
of 6
Biochimica Et Biophysica Acta
|
June 9, 1995
Cloning and sequence analysis of caprine N-acetylglucosamine 6-sulfatase cDNA
K Friderici, K T Cavanagh, J R Leipprandt, et al.
Molecular Biology & Medicine
|
February 1, 1987
Towards gene therapy for hemophilia B
D S Anson, R A Hock, D Austen, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 1, 1991
Human alpha-L-iduronidase: cDNA isolation and expression
H S Scott, D S Anson, A M Orsborn, et al.
The Biochemical Journal
|
April 15, 1995
Two site-directed mutations abrogate enzyme activity but have different effects on the conformation and cellular content of the N-acetylgalactosamine 4-sulphatase protein
D A Brooks, D A Robertson, C Bindloss, et al.
Lancet (London, England)
|
February 4, 1984
Characterisation and use of an intragenic polymorphic marker for detection of carriers of haemophilia B (factor IX deficiency)
F Giannelli, D S Anson, K H Choo, et al.
Neuromuscular Disorders : NMD
|
July 1, 1997
Canine fucosidosis: a model for retroviral gene transfer into haematopoietic stem cells
M L Ferrara, T Occhiodoro, M Fuller, et al.
Gene Therapy
|
May 1, 1997
In vitro correction of iduronate-2-sulfatase deficiency by adenovirus-mediated gene transfer
C Di Francesco, C Cracco, R Tomanin, et al.
Gene Therapy
|
February 16, 2007
Lentivirus-mediated gene transfer to the rat, ovine and human cornea
D G A Parker, C Kaufmann, H M Brereton, et al.
The Journal of Clinical Investigation
|
April 15, 1996
Enzyme replacement therapy in a feline model of Maroteaux-Lamy syndrome
A C Crawley, D A Brooks, V J Muller, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 5, 1996
Long-term in vitro correction of alpha-L-iduronidase deficiency (Hurler syndrome) in human bone marrow
L J Fairbairn, L S Lashford, E Spooncer, et al.
Page
of 6