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C E Hatton

Showing results (1-10 of 8) with videos related to

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Biophysical Reviews|December 2, 2024
Exploring the dynamics of allostery through multi-dimensional crystallographyC E Hatton, P Mehrabi
Journal of Inherited Metabolic Disease|January 1, 1989
Detection of Fabry's disease carriers by enzyme assay of hair rootsC E Hatton, A Cooper, I B Sardharwalla
Journal of Inherited Metabolic Disease|January 1, 1990
Alpha- and beta-mannosidosesA Cooper, C E Hatton, M Thornley, et al.
Archives of Disease in Childhood|July 1, 1997
Mutation analysis in 46 British and Irish patients with Gaucher's diseaseC E Hatton, A Cooper, C Whitehouse, et al.
Archives of Disease in Childhood|January 6, 1999
Mutation analysis in 57 unrelated patients with MPS II (Hunter's disease)E Vafiadaki, A Cooper, L E Heptinstall, et al.
Gene Therapy|January 1, 1997
Uptake of alpha-(L)-iduronidase produced by retrovirally transduced fibroblasts into neuronal and glial cells in vitroK Stewart, O A Brown, A E Morelli, 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 marrowL J Fairbairn, L S Lashford, E Spooncer, et al.
Casopis Lekaru Ceskych|January 8, 1997
Towards gene therapy of Hurler syndromeL J Fairbairn, L S Lashford, E Spooncer, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Biophysical Reviews|December 2, 2024
Exploring the dynamics of allostery through multi-dimensional crystallographyC E Hatton, P Mehrabi
Journal of Inherited Metabolic Disease|January 1, 1989
Detection of Fabry's disease carriers by enzyme assay of hair rootsC E Hatton, A Cooper, I B Sardharwalla
Journal of Inherited Metabolic Disease|January 1, 1990
Alpha- and beta-mannosidosesA Cooper, C E Hatton, M Thornley, et al.
Archives of Disease in Childhood|July 1, 1997
Mutation analysis in 46 British and Irish patients with Gaucher's diseaseC E Hatton, A Cooper, C Whitehouse, et al.
Archives of Disease in Childhood|January 6, 1999
Mutation analysis in 57 unrelated patients with MPS II (Hunter's disease)E Vafiadaki, A Cooper, L E Heptinstall, et al.
Gene Therapy|January 1, 1997
Uptake of alpha-(L)-iduronidase produced by retrovirally transduced fibroblasts into neuronal and glial cells in vitroK Stewart, O A Brown, A E Morelli, 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 marrowL J Fairbairn, L S Lashford, E Spooncer, et al.
Casopis Lekaru Ceskych|January 8, 1997
Towards gene therapy of Hurler syndromeL J Fairbairn, L S Lashford, E Spooncer, et al.
Pageof 1