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The Journal of Pediatrics
|
December 1, 1972
Infantile (type II) Gaucher's disease: in utero diagnosis and fetal pathology
E L Schneider, W G Ellis, R O Brady, et al.
Kidney International
|
January 29, 2000
Glycosphingolipid depletion in fabry disease lymphoblasts with potent inhibitors of glucosylceramide synthase
A Abe, L J Arend, L Lee, et al.
Human Gene Therapy
|
July 1, 1995
Retroviral coexpression of a multidrug resistance gene (MDR1) and human alpha-galactosidase A for gene therapy of Fabry disease
Y Sugimoto, I Aksentijevich, G J Murray, et al.
FEBS Letters
|
July 15, 1978
The uptake of agalacto-glucocerebrosidase by rat hepatocytes and Kupffer cells
C J Steer, F S Furbish, J A Barranger, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 14, 2010
Induced pluripotent stem cells derived from mouse models of lysosomal storage disorders
Xing-Li Meng, Jin-Song Shen, Shiho Kawagoe, et al.
Progress in Clinical and Biological Research
|
January 1, 1982
Glucocerebroside-beta-glucosidase isozymes
E I Ginns, R O Brady, D W Stowens, et al.
Progress in Clinical and Biological Research
|
January 1, 1982
Prospects for enzyme replacement therapy in Gaucher disease
R O Brady, J A Barranger, F S Furbish, et al.
Pediatric Research
|
June 1, 1995
Cultured skin fibroblasts derived from patients with mucolipidosis 4 are auto-fluorescent
E Goldin, E J Blanchette-Mackie, N K Dwyer, et al.
Analytical Biochemistry
|
May 1, 1979
The distribution of glucocerebroside in the liver of patients with Gaucher's disease
A E Gal, P G Pentchev, J A Barranger, et al.
Journal of Immunological Methods
|
March 1, 1991
Gaucher's disease: lack of antibody response in 12 patients following repeated intravenous infusions of mannose terminal glucocerebrosidase
G J Murray, K D Howard, S M Richards, et al.
Page
of 54
Search research articles
Search
Showing results (291-300 of 536) with videos related to
Sort By:
Page
of 54
The Journal of Pediatrics
|
December 1, 1972
Infantile (type II) Gaucher's disease: in utero diagnosis and fetal pathology
E L Schneider, W G Ellis, R O Brady, et al.
Kidney International
|
January 29, 2000
Glycosphingolipid depletion in fabry disease lymphoblasts with potent inhibitors of glucosylceramide synthase
A Abe, L J Arend, L Lee, et al.
Human Gene Therapy
|
July 1, 1995
Retroviral coexpression of a multidrug resistance gene (MDR1) and human alpha-galactosidase A for gene therapy of Fabry disease
Y Sugimoto, I Aksentijevich, G J Murray, et al.
FEBS Letters
|
July 15, 1978
The uptake of agalacto-glucocerebrosidase by rat hepatocytes and Kupffer cells
C J Steer, F S Furbish, J A Barranger, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 14, 2010
Induced pluripotent stem cells derived from mouse models of lysosomal storage disorders
Xing-Li Meng, Jin-Song Shen, Shiho Kawagoe, et al.
Progress in Clinical and Biological Research
|
January 1, 1982
Glucocerebroside-beta-glucosidase isozymes
E I Ginns, R O Brady, D W Stowens, et al.
Progress in Clinical and Biological Research
|
January 1, 1982
Prospects for enzyme replacement therapy in Gaucher disease
R O Brady, J A Barranger, F S Furbish, et al.
Pediatric Research
|
June 1, 1995
Cultured skin fibroblasts derived from patients with mucolipidosis 4 are auto-fluorescent
E Goldin, E J Blanchette-Mackie, N K Dwyer, et al.
Analytical Biochemistry
|
May 1, 1979
The distribution of glucocerebroside in the liver of patients with Gaucher's disease
A E Gal, P G Pentchev, J A Barranger, et al.
Journal of Immunological Methods
|
March 1, 1991
Gaucher's disease: lack of antibody response in 12 patients following repeated intravenous infusions of mannose terminal glucocerebrosidase
G J Murray, K D Howard, S M Richards, et al.
Page
of 54