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 R Akerman

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

Pageof 2
Sort By:
Molecular Genetics and Metabolism|March 18, 2000
Characterization of phenylketonuria missense substitutions, distant from the phenylalanine hydroxylase active site, illustrates a paradigm for mechanism and potential modulation of phenotypeP J Waters, M A Parniak, B R Akerman, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|January 21, 2000
Population-specific polymorphisms of the human FMO3 gene: significance for detoxicationJ R Cashman, B R Akerman, S M Forrest, et al.
American Journal of Human Genetics|November 1, 1991
Sequence of DNA flanking the exons of the HEXA gene, and identification of mutations in Tay-Sachs diseaseB L Triggs-Raine, B R Akerman, J T Clarke, et al.
Human Mutation|May 25, 1999
Two novel mutations of the FMO3 gene in a proband with trimethylaminuriaB R Akerman, S Forrest, L Chow, et al.
Pharmacogenetics|March 27, 2001
A novel deletion in the flavin-containing monooxygenase gene (FMO3) in a Greek patient with trimethylaminuriaS M Forrest, M Knight, B R Akerman, et al.
American Journal of Medical Genetics|May 1, 1990
Identification of deletion and triple alpha-globin gene haplotypes in the Montreal beta-thalassemia screening program: implications for genetic medicineB R Akerman, T M Fujiwara, G A Lancaster, et al.
American Journal of Human Genetics|May 1, 1997
Novel mutations and DNA-based screening in non-Jewish carriers of Tay-Sachs diseaseB R Akerman, M R Natowicz, M M Kaback, et al.
American Journal of Human Genetics|July 1, 1994
Mutations participating in interallelic complementation in propionic acidemiaR A Gravel, B R Akerman, A M Lamhonwah, et al.
Molecular Genetics and Metabolism|July 20, 2001
In vivo variability of TMA oxidation is partially mediated by polymorphisms of the FMO3 geneD M Lambert, O A Mamer, B R Akerman, et al.
Human Mutation|January 1, 1992
Molecular basis of hexosaminidase A deficiency and pseudodeficiency in the Berks County Pennsylvania DutchE H Mules, S Hayflick, C E Dowling, et al.
Pageof 2

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

Sort By:
Pageof 2
Molecular Genetics and Metabolism|March 18, 2000
Characterization of phenylketonuria missense substitutions, distant from the phenylalanine hydroxylase active site, illustrates a paradigm for mechanism and potential modulation of phenotypeP J Waters, M A Parniak, B R Akerman, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|January 21, 2000
Population-specific polymorphisms of the human FMO3 gene: significance for detoxicationJ R Cashman, B R Akerman, S M Forrest, et al.
American Journal of Human Genetics|November 1, 1991
Sequence of DNA flanking the exons of the HEXA gene, and identification of mutations in Tay-Sachs diseaseB L Triggs-Raine, B R Akerman, J T Clarke, et al.
Human Mutation|May 25, 1999
Two novel mutations of the FMO3 gene in a proband with trimethylaminuriaB R Akerman, S Forrest, L Chow, et al.
Pharmacogenetics|March 27, 2001
A novel deletion in the flavin-containing monooxygenase gene (FMO3) in a Greek patient with trimethylaminuriaS M Forrest, M Knight, B R Akerman, et al.
American Journal of Medical Genetics|May 1, 1990
Identification of deletion and triple alpha-globin gene haplotypes in the Montreal beta-thalassemia screening program: implications for genetic medicineB R Akerman, T M Fujiwara, G A Lancaster, et al.
American Journal of Human Genetics|May 1, 1997
Novel mutations and DNA-based screening in non-Jewish carriers of Tay-Sachs diseaseB R Akerman, M R Natowicz, M M Kaback, et al.
American Journal of Human Genetics|July 1, 1994
Mutations participating in interallelic complementation in propionic acidemiaR A Gravel, B R Akerman, A M Lamhonwah, et al.
Molecular Genetics and Metabolism|July 20, 2001
In vivo variability of TMA oxidation is partially mediated by polymorphisms of the FMO3 geneD M Lambert, O A Mamer, B R Akerman, et al.
Human Mutation|January 1, 1992
Molecular basis of hexosaminidase A deficiency and pseudodeficiency in the Berks County Pennsylvania DutchE H Mules, S Hayflick, C E Dowling, et al.
Pageof 2