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Experimental Cell Research
|
February 1, 1987
Glucocerebrosidase deficiency and lysosomal storage of glucocerebroside induced in cultured macrophages
P K Das, G J Murray, A E Gal, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
March 14, 1980
Diagnosis of adult Gaucher disease: use of a new chromogenic substrate, 2-hexadecanoylamino-4-nitrophenyl-beta-D-glucopyranoside, in cultured skin fibroblasts
W G Johnson, A E Gal, A F Miranda, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
May 21, 1980
The diagnosis of type A and type B Niemann Pick disease and detection of carriers using leukocytes and a chromogenic analogue of sphingomyelin
A E Gal, R O Brady, J A Barranger, et al.
Chemistry and Physics of Lipids
|
December 15, 1986
Animal and cellular models of sphingolipid storage disorders of humans
A E Gal, A L Weis, J M Quirk, 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.
The American Journal of Medicine
|
December 1, 1983
Normolipemic subcutaneous xanthomatosis
R Fleischmajer, E J Schaefer, A E Gal, et al.
The Journal of Biological Chemistry
|
June 10, 1974
Isolation and relationship of human hexosaminidases
J F Tallman, R O Brady, J M Quirk, et al.
Birth Defects Original Article Series
|
January 1, 1980
Status of enzyme replacement therapy for Gaucher disease
R O Brady, J A Barranger, A E Gal, 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.
The New England Journal of Medicine
|
November 7, 1974
Replacement therapy for inherited enzyme deficiency. Use of purified glucocerebrosidase in Gaucher's disease
R O Brady, P G Pentchev, A E Gal, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 28) with videos related to
Sort By:
Page
of 3
Experimental Cell Research
|
February 1, 1987
Glucocerebrosidase deficiency and lysosomal storage of glucocerebroside induced in cultured macrophages
P K Das, G J Murray, A E Gal, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
March 14, 1980
Diagnosis of adult Gaucher disease: use of a new chromogenic substrate, 2-hexadecanoylamino-4-nitrophenyl-beta-D-glucopyranoside, in cultured skin fibroblasts
W G Johnson, A E Gal, A F Miranda, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
May 21, 1980
The diagnosis of type A and type B Niemann Pick disease and detection of carriers using leukocytes and a chromogenic analogue of sphingomyelin
A E Gal, R O Brady, J A Barranger, et al.
Chemistry and Physics of Lipids
|
December 15, 1986
Animal and cellular models of sphingolipid storage disorders of humans
A E Gal, A L Weis, J M Quirk, 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.
The American Journal of Medicine
|
December 1, 1983
Normolipemic subcutaneous xanthomatosis
R Fleischmajer, E J Schaefer, A E Gal, et al.
The Journal of Biological Chemistry
|
June 10, 1974
Isolation and relationship of human hexosaminidases
J F Tallman, R O Brady, J M Quirk, et al.
Birth Defects Original Article Series
|
January 1, 1980
Status of enzyme replacement therapy for Gaucher disease
R O Brady, J A Barranger, A E Gal, 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.
The New England Journal of Medicine
|
November 7, 1974
Replacement therapy for inherited enzyme deficiency. Use of purified glucocerebrosidase in Gaucher's disease
R O Brady, P G Pentchev, A E Gal, et al.
Page
of 3