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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.
The Journal of Biological Chemistry
|
February 25, 1986
The cholesterol storage disorder of the mutant BALB/c mouse. A primary genetic lesion closely linked to defective esterification of exogenously derived cholesterol and its relationship to human type C Niemann-Pick disease
P G Pentchev, M E Comly, H S Kruth, et al.
Science (New York, N.Y.)
|
April 15, 1977
Niemann-Pick disease experimental model: sphingomyelinase reduction induced by AY-9944
N Sakuragawa, M Sakuragaw, T Kuwabara, 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.
Biochemical and Biophysical Research Communications
|
July 30, 1999
The genomic organization and polymorphism analysis of the human Niemann-Pick C1 gene
J A Morris, D Zhang, K G Coleman, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1994
Mucolipidosis IV fibroblasts synthesize normal amounts of hyaluronic acid
E Goldin, Y Imai, C R Kaneski, et al.
The Journal of Biological Chemistry
|
May 10, 1984
A genetic storage disorder in BALB/C mice with a metabolic block in esterification of exogenous cholesterol
P G Pentchev, A D Boothe, H S Kruth, et al.
Journal of Cell Science
|
May 1, 1992
Morphometric studies of pancreatic acinar granule formation in NCTR-Balb/c mice
H Weintraub, A Abramovici, D Amichai, et al.
Lancet (London, England)
|
May 6, 1989
Diagnosis of Niemann-Pick disease type C on chorionic villus cells
M T Vanier, R M Rousson, G Mandon, et al.
Virchows Archiv. B, Cell Pathology Including Molecular Pathology
|
January 1, 1992
Storage of glycoprotein in NCTR-Balb/C mouse. Lectin histochemistry, and biochemical studies
H Weintraub, J Alroy, R DeGasperi, et al.
Page
of 12
Search research articles
Search
Showing results (51-60 of 120) with videos related to
Sort By:
Page
of 12
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.
The Journal of Biological Chemistry
|
February 25, 1986
The cholesterol storage disorder of the mutant BALB/c mouse. A primary genetic lesion closely linked to defective esterification of exogenously derived cholesterol and its relationship to human type C Niemann-Pick disease
P G Pentchev, M E Comly, H S Kruth, et al.
Science (New York, N.Y.)
|
April 15, 1977
Niemann-Pick disease experimental model: sphingomyelinase reduction induced by AY-9944
N Sakuragawa, M Sakuragaw, T Kuwabara, 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.
Biochemical and Biophysical Research Communications
|
July 30, 1999
The genomic organization and polymorphism analysis of the human Niemann-Pick C1 gene
J A Morris, D Zhang, K G Coleman, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1994
Mucolipidosis IV fibroblasts synthesize normal amounts of hyaluronic acid
E Goldin, Y Imai, C R Kaneski, et al.
The Journal of Biological Chemistry
|
May 10, 1984
A genetic storage disorder in BALB/C mice with a metabolic block in esterification of exogenous cholesterol
P G Pentchev, A D Boothe, H S Kruth, et al.
Journal of Cell Science
|
May 1, 1992
Morphometric studies of pancreatic acinar granule formation in NCTR-Balb/c mice
H Weintraub, A Abramovici, D Amichai, et al.
Lancet (London, England)
|
May 6, 1989
Diagnosis of Niemann-Pick disease type C on chorionic villus cells
M T Vanier, R M Rousson, G Mandon, et al.
Virchows Archiv. B, Cell Pathology Including Molecular Pathology
|
January 1, 1992
Storage of glycoprotein in NCTR-Balb/C mouse. Lectin histochemistry, and biochemical studies
H Weintraub, J Alroy, R DeGasperi, et al.
Page
of 12