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

F Neufeld

Showing results (11-20 of 124) with videos related to

Pageof 13
Sort By:
Upsala Journal of Medical Sciences|January 19, 2010
Genetic diseases of mucopolysaccharide catabolism; single-enzyme deficiency disordersE F Neufeld
The Journal of Biological Chemistry|July 5, 1989
Natural history and inherited disorders of a lysosomal enzyme, beta-hexosaminidaseE F Neufeld
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|December 4, 2013
Unexpected observations--a tribute to Christian de Duve (1917-2013)Elizabeth F Neufeld
Advances in Genetics|October 13, 2001
Biosynthesis of normal and mutant beta-hexosaminidasesE F Neufeld, A d'Azzo
Biochemical and Biophysical Research Communications|April 15, 1983
Synthesis and maturation of cross-reactive glycoprotein in fibroblasts deficient in arylsulfatase A activityG Bach, E F Neufeld
The Journal of Biological Chemistry|March 25, 1981
Maturation of alpha-L-iduronidase in cultured human fibroblastsR Myerowitz, E F Neufeld
Biochemical and Biophysical Research Communications|November 15, 1972
A hypothesis for I-cell disease: defective hydrolases that do not enter lysosomesS Hickman, E F Neufeld
The Journal of Biological Chemistry|April 10, 1972
The Sanfilippo A corrective factor. Purification and mode of actionH Kresse, E F Neufeld
Methods in Enzymology|January 1, 1982
Iduronate sulfatase from human plasmaA Wasteson, E F Neufeld
Biochemical and Biophysical Research Communications|April 14, 1982
Is there a mechanism for introducing acid hydrolases into liver lysosomes that is independent of mannose 6-phosphate recognition? Evidence from I-cell diseaseM Owada, E F Neufeld
Pageof 13

Showing results (11-20 of 124) with videos related to

Sort By:
Pageof 13
Upsala Journal of Medical Sciences|January 19, 2010
Genetic diseases of mucopolysaccharide catabolism; single-enzyme deficiency disordersE F Neufeld
The Journal of Biological Chemistry|July 5, 1989
Natural history and inherited disorders of a lysosomal enzyme, beta-hexosaminidaseE F Neufeld
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|December 4, 2013
Unexpected observations--a tribute to Christian de Duve (1917-2013)Elizabeth F Neufeld
Advances in Genetics|October 13, 2001
Biosynthesis of normal and mutant beta-hexosaminidasesE F Neufeld, A d'Azzo
Biochemical and Biophysical Research Communications|April 15, 1983
Synthesis and maturation of cross-reactive glycoprotein in fibroblasts deficient in arylsulfatase A activityG Bach, E F Neufeld
The Journal of Biological Chemistry|March 25, 1981
Maturation of alpha-L-iduronidase in cultured human fibroblastsR Myerowitz, E F Neufeld
Biochemical and Biophysical Research Communications|November 15, 1972
A hypothesis for I-cell disease: defective hydrolases that do not enter lysosomesS Hickman, E F Neufeld
The Journal of Biological Chemistry|April 10, 1972
The Sanfilippo A corrective factor. Purification and mode of actionH Kresse, E F Neufeld
Methods in Enzymology|January 1, 1982
Iduronate sulfatase from human plasmaA Wasteson, E F Neufeld
Biochemical and Biophysical Research Communications|April 14, 1982
Is there a mechanism for introducing acid hydrolases into liver lysosomes that is independent of mannose 6-phosphate recognition? Evidence from I-cell diseaseM Owada, E F Neufeld
Pageof 13