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

J J Jonsson

Showing results (1-10 of 15) with videos related to

Pageof 2
Sort By:
Proceedings of the National Academy of Sciences of the United States of America|January 3, 1995
From mutation mapping to phenotype cloningJ J Jonsson, S M Weissman
Analytical Biochemistry|December 1, 1991
Herpes simplex virus thymidine kinase enzymatic assay in transient transfection experiments using thymidine kinase-deficient cellsJ J Jonsson, R S McIvor
Gene|March 25, 1994
An enhancer in the first intron of the human purine nucleoside phosphorylase-encoding geneJ J Jonsson, A Converse, R S McIvor
Human Gene Therapy|May 1, 1995
Retrovirus-mediated transduction of an engineered intron-containing purine nucleoside phosphorylase geneJ J Jonsson, D E Habel, R S McIvor
Nucleic Acids Research|September 25, 1991
Sequence and functional characterization of the human purine nucleoside phosphorylase promoterJ J Jonsson, S R Williams, R S McIvor
Nucleic Acids Research|June 25, 1992
Intron requirement for expression of the human purine nucleoside phosphorylase geneJ J Jonsson, M D Foresman, N Wilson, et al.
American Journal of Human Genetics|March 1, 1995
Molecular diagnosis of mucopolysaccharidosis type II (Hunter syndrome) by automated sequencing and computer-assisted interpretation: toward mutation mapping of the iduronate-2-sulfatase geneJ J Jonsson, E L Aronovich, S E Braun, et al.
Molecular Genetics and Metabolism|August 5, 2000
"Supercharged Cells" for delivery of recombinant human iduronate-2-sulfataseD Pan, J J Jonsson, S E Braun, et al.
Journal of Clinical Epidemiology|January 1, 1991
Prevalence of iron deficiency and iron overload in the adult Icelandic populationJ J Jonsson, G M Johannesson, N Sigfusson, et al.
American Journal of Human Genetics|April 1, 1997
Molecular characterization of patients with 18q23 deletionsG Strathdee, R Sutherland, J J Jonsson, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Proceedings of the National Academy of Sciences of the United States of America|January 3, 1995
From mutation mapping to phenotype cloningJ J Jonsson, S M Weissman
Analytical Biochemistry|December 1, 1991
Herpes simplex virus thymidine kinase enzymatic assay in transient transfection experiments using thymidine kinase-deficient cellsJ J Jonsson, R S McIvor
Gene|March 25, 1994
An enhancer in the first intron of the human purine nucleoside phosphorylase-encoding geneJ J Jonsson, A Converse, R S McIvor
Human Gene Therapy|May 1, 1995
Retrovirus-mediated transduction of an engineered intron-containing purine nucleoside phosphorylase geneJ J Jonsson, D E Habel, R S McIvor
Nucleic Acids Research|September 25, 1991
Sequence and functional characterization of the human purine nucleoside phosphorylase promoterJ J Jonsson, S R Williams, R S McIvor
Nucleic Acids Research|June 25, 1992
Intron requirement for expression of the human purine nucleoside phosphorylase geneJ J Jonsson, M D Foresman, N Wilson, et al.
American Journal of Human Genetics|March 1, 1995
Molecular diagnosis of mucopolysaccharidosis type II (Hunter syndrome) by automated sequencing and computer-assisted interpretation: toward mutation mapping of the iduronate-2-sulfatase geneJ J Jonsson, E L Aronovich, S E Braun, et al.
Molecular Genetics and Metabolism|August 5, 2000
"Supercharged Cells" for delivery of recombinant human iduronate-2-sulfataseD Pan, J J Jonsson, S E Braun, et al.
Journal of Clinical Epidemiology|January 1, 1991
Prevalence of iron deficiency and iron overload in the adult Icelandic populationJ J Jonsson, G M Johannesson, N Sigfusson, et al.
American Journal of Human Genetics|April 1, 1997
Molecular characterization of patients with 18q23 deletionsG Strathdee, R Sutherland, J J Jonsson, et al.
Pageof 2