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Acta Neuropathologica
|
January 1, 1987
Dysmyelination in NCTR-Balb/C mouse mutant with a lysosomal storage disorder. Morphological survey
H Weintraub, A Abramovici, U Sandbank, et al.
The Journal of Biological Chemistry
|
August 10, 1973
Isolation and characterization of glucocerebrosidase from human placental tissue
P G Pentchev, R O Brady, S R Hibbert, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 1, 1977
Enzyme replacement therapy in Gaucher's disease: large-scale purification of glucocerebrosidase suitable for human administration
F S Furbish, H E Blair, J Shiloach, et al.
Journal of Medical Genetics
|
October 1, 1978
A new form of Niemann-Pick disease characterised by temperature-labile sphingomyelinase
E L Schneider, P G Pentchev, S R Hibbert, et al.
Methods in Enzymology
|
January 1, 1975
Mutarotase (aldose 1-epimerase) from kidney cortex
J F Bailey, P H Fishman, J W Kusiak, et al.
The American Journal of Medicine
|
December 1, 1983
Normolipemic subcutaneous xanthomatosis
R Fleischmajer, E J Schaefer, A E Gal, 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.
Biochimica Et Biophysica Acta
|
April 2, 1990
Abnormal cholesterol metabolism in imipramine-treated fibroblast cultures. Similarities with Niemann-Pick type C disease
C Rodriguez-Lafrasse, R Rousson, J Bonnet, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 1, 1978
Gaucher disease: isolation and comparison of normal and mutant glucocerebrosidase from human spleen tissue
P G Pentchev, R O Brady, H E Blair, et al.
Page
of 12
Search research articles
Search
Showing results (41-50 of 120) with videos related to
Sort By:
Page
of 12
Acta Neuropathologica
|
January 1, 1987
Dysmyelination in NCTR-Balb/C mouse mutant with a lysosomal storage disorder. Morphological survey
H Weintraub, A Abramovici, U Sandbank, et al.
The Journal of Biological Chemistry
|
August 10, 1973
Isolation and characterization of glucocerebrosidase from human placental tissue
P G Pentchev, R O Brady, S R Hibbert, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 1, 1977
Enzyme replacement therapy in Gaucher's disease: large-scale purification of glucocerebrosidase suitable for human administration
F S Furbish, H E Blair, J Shiloach, et al.
Journal of Medical Genetics
|
October 1, 1978
A new form of Niemann-Pick disease characterised by temperature-labile sphingomyelinase
E L Schneider, P G Pentchev, S R Hibbert, et al.
Methods in Enzymology
|
January 1, 1975
Mutarotase (aldose 1-epimerase) from kidney cortex
J F Bailey, P H Fishman, J W Kusiak, et al.
The American Journal of Medicine
|
December 1, 1983
Normolipemic subcutaneous xanthomatosis
R Fleischmajer, E J Schaefer, A E Gal, 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.
Biochimica Et Biophysica Acta
|
April 2, 1990
Abnormal cholesterol metabolism in imipramine-treated fibroblast cultures. Similarities with Niemann-Pick type C disease
C Rodriguez-Lafrasse, R Rousson, J Bonnet, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 1, 1978
Gaucher disease: isolation and comparison of normal and mutant glucocerebrosidase from human spleen tissue
P G Pentchev, R O Brady, H E Blair, et al.
Page
of 12