Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

P G Pentchev

Showing results (51-60 of 120) with videos related to

Pageof 12
Sort By:
Birth Defects Original Article Series|January 1, 1980
Status of enzyme replacement therapy for Gaucher diseaseR 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 diseaseP 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-9944N 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 diseaseR 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 geneJ 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 acidE 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 cholesterolP 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 miceH Weintraub, A Abramovici, D Amichai, et al.
Lancet (London, England)|May 6, 1989
Diagnosis of Niemann-Pick disease type C on chorionic villus cellsM 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 studiesH Weintraub, J Alroy, R DeGasperi, et al.
Pageof 12

Showing results (51-60 of 120) with videos related to

Sort By:
Pageof 12
Birth Defects Original Article Series|January 1, 1980
Status of enzyme replacement therapy for Gaucher diseaseR 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 diseaseP 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-9944N 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 diseaseR 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 geneJ 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 acidE 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 cholesterolP 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 miceH Weintraub, A Abramovici, D Amichai, et al.
Lancet (London, England)|May 6, 1989
Diagnosis of Niemann-Pick disease type C on chorionic villus cellsM 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 studiesH Weintraub, J Alroy, R DeGasperi, et al.
Pageof 12