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 (101-110 of 120) with videos related to

Pageof 12
Sort By:
Birth Defects Original Article Series|March 1, 1973
Renal transplantation in Type II Gaucher diseaseS J Desnick, R J Desnick, R O Brady, et al.
American Journal of Human Genetics|July 1, 1992
Prenatal diagnosis of Niemann-Pick type C disease: current strategy from an experience of 37 pregnancies at riskM T Vanier, C Rodriguez-Lafrasse, R Rousson, et al.
Experimental Cell Research|February 10, 2000
NPC1-containing compartment of human granulosa-lutein cells: a role in the intracellular trafficking of cholesterol supporting steroidogenesisH Watari, E J Blanchette-Mackie, N K Dwyer, et al.
Acta Neuropathologica|January 1, 1995
Paired helical filament tau (PHFtau) in Niemann-Pick type C disease is similar to PHFtau in Alzheimer's diseaseI A Auer, M L Schmidt, V M Lee, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 1, 1987
Group C Niemann-Pick disease: faulty regulation of low-density lipoprotein uptake and cholesterol storage in cultured fibroblastsP G Pentchev, M E Comly, H S Kruth, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 3, 1999
Niemann-Pick C1 protein: obligatory roles for N-terminal domains and lysosomal targeting in cholesterol mobilizationH Watari, E J Blanchette-Mackie, N K Dwyer, et al.
Neurology|August 1, 1989
Clinical spectrum of Niemann-Pick disease type CJ K Fink, M R Filling-Katz, J Sokol, et al.
Human Molecular Genetics|April 18, 2000
Alleviation of neuronal ganglioside storage does not improve the clinical course of the Niemann-Pick C disease mouseY Liu, Y P Wu, R Wada, et al.
Advances in Experimental Medicine and Biology|January 1, 1976
Enzyme replacement therapy for the sphingolipidosesR O Brady, P G Pentchev, A E Gal, et al.
Endocrinology|December 1, 1993
The murine Niemann-Pick type C lesion affects testosterone productionC F Roff, J F Strauss, E Goldin, et al.
Pageof 12

Showing results (101-110 of 120) with videos related to

Sort By:
Pageof 12
Birth Defects Original Article Series|March 1, 1973
Renal transplantation in Type II Gaucher diseaseS J Desnick, R J Desnick, R O Brady, et al.
American Journal of Human Genetics|July 1, 1992
Prenatal diagnosis of Niemann-Pick type C disease: current strategy from an experience of 37 pregnancies at riskM T Vanier, C Rodriguez-Lafrasse, R Rousson, et al.
Experimental Cell Research|February 10, 2000
NPC1-containing compartment of human granulosa-lutein cells: a role in the intracellular trafficking of cholesterol supporting steroidogenesisH Watari, E J Blanchette-Mackie, N K Dwyer, et al.
Acta Neuropathologica|January 1, 1995
Paired helical filament tau (PHFtau) in Niemann-Pick type C disease is similar to PHFtau in Alzheimer's diseaseI A Auer, M L Schmidt, V M Lee, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 1, 1987
Group C Niemann-Pick disease: faulty regulation of low-density lipoprotein uptake and cholesterol storage in cultured fibroblastsP G Pentchev, M E Comly, H S Kruth, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 3, 1999
Niemann-Pick C1 protein: obligatory roles for N-terminal domains and lysosomal targeting in cholesterol mobilizationH Watari, E J Blanchette-Mackie, N K Dwyer, et al.
Neurology|August 1, 1989
Clinical spectrum of Niemann-Pick disease type CJ K Fink, M R Filling-Katz, J Sokol, et al.
Human Molecular Genetics|April 18, 2000
Alleviation of neuronal ganglioside storage does not improve the clinical course of the Niemann-Pick C disease mouseY Liu, Y P Wu, R Wada, et al.
Advances in Experimental Medicine and Biology|January 1, 1976
Enzyme replacement therapy for the sphingolipidosesR O Brady, P G Pentchev, A E Gal, et al.
Endocrinology|December 1, 1993
The murine Niemann-Pick type C lesion affects testosterone productionC F Roff, J F Strauss, E Goldin, et al.
Pageof 12