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

B G Winchester

Showing results (11-20 of 55) with videos related to

Pageof 6
Sort By:
Journal of Inherited Metabolic Disease|January 1, 1992
Hypertrophic obstructive cardiomyopathy in a neonate with the carbohydrate-deficient glycoprotein syndromeP T Clayton, B G Winchester, G Keir
The Biochemical Journal|March 1, 1976
Characterization of human liver alpha-D-mannosidase purified by affinity chromatographyN C Phillips, D Robinson, B G Winchester
Human Molecular Genetics|July 1, 1993
Mutation analysis in patients with the typical form of Anderson-Fabry diseaseJ P Davies, B G Winchester, S Malcolm
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 30, 1974
Human liver alpha-D-mannosidase activityN C Phillips, D Robinson, B G Winchester
FEBS Letters|July 15, 1978
Evidence that the mutant enzyme in fibroblasts of a patient with mannosidosis does not crossreact with antiserum raised against normal acidic alpha-D-mannosidaseL J Burditt, K A Chotai, B G Winchester
The Biochemical Journal|April 1, 1970
Study of the thermal denaturation of ribonuclease A by differential thermal analysis and susceptibility to proteolysisB G Winchester, A P Mathias, B R Rabin
Brain Pathology (Zurich, Switzerland)|February 11, 1998
Prenatal diagnosis of lysosomal storage diseasesB D Lake, E P Young, B G Winchester
Biochemical Medicine|June 1, 1976
Mannosidosis--use of reference enzymes in heterozygote detectionK G Thompson, R D Jolly, B G Winchester
Birth Defects Original Article Series|January 1, 1975
Bovine mannosidosis--a model lysosomal storage diseaseR D Jolly, K G Thompson, B G Winchester
Genetical Research|October 1, 1978
Strain variation in spermatozoal glycosidases in inbred miceS J Self, B G Winchester, J R Archer
Pageof 6

Showing results (11-20 of 55) with videos related to

Sort By:
Pageof 6
Journal of Inherited Metabolic Disease|January 1, 1992
Hypertrophic obstructive cardiomyopathy in a neonate with the carbohydrate-deficient glycoprotein syndromeP T Clayton, B G Winchester, G Keir
The Biochemical Journal|March 1, 1976
Characterization of human liver alpha-D-mannosidase purified by affinity chromatographyN C Phillips, D Robinson, B G Winchester
Human Molecular Genetics|July 1, 1993
Mutation analysis in patients with the typical form of Anderson-Fabry diseaseJ P Davies, B G Winchester, S Malcolm
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 30, 1974
Human liver alpha-D-mannosidase activityN C Phillips, D Robinson, B G Winchester
FEBS Letters|July 15, 1978
Evidence that the mutant enzyme in fibroblasts of a patient with mannosidosis does not crossreact with antiserum raised against normal acidic alpha-D-mannosidaseL J Burditt, K A Chotai, B G Winchester
The Biochemical Journal|April 1, 1970
Study of the thermal denaturation of ribonuclease A by differential thermal analysis and susceptibility to proteolysisB G Winchester, A P Mathias, B R Rabin
Brain Pathology (Zurich, Switzerland)|February 11, 1998
Prenatal diagnosis of lysosomal storage diseasesB D Lake, E P Young, B G Winchester
Biochemical Medicine|June 1, 1976
Mannosidosis--use of reference enzymes in heterozygote detectionK G Thompson, R D Jolly, B G Winchester
Birth Defects Original Article Series|January 1, 1975
Bovine mannosidosis--a model lysosomal storage diseaseR D Jolly, K G Thompson, B G Winchester
Genetical Research|October 1, 1978
Strain variation in spermatozoal glycosidases in inbred miceS J Self, B G Winchester, J R Archer
Pageof 6