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

C R Scriver

Showing results (181-190 of 317) with videos related to

Pageof 32
Sort By:
Kidney International|February 1, 1976
Genetic aspects of renal tubular transport: diversity and topology of carriersC R Scriver, R W Chesney, R R McInnes
Canadian Medical Association Journal|April 5, 1975
Letter: Screening for hereditary metabolic diseaseC R Scriver, J C Haworth, J R Miller
Molecular Genetics and Metabolism|July 20, 2001
Homomeric and heteromeric interactions between wild-type and mutant phenylalanine hydroxylase subunits: evaluation of two-hybrid approaches for functional analysis of mutations causing hyperphenylalaninemiaP J Waters, C R Scriver, M A Parniak
European Journal of Human Genetics : EJHG|January 1, 1993
'Celtic' phenylketonuria chromosomes found? Evidence in two regions of Quebec ProvinceE Treacy, S Byck, C Clow, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|January 1, 1991
The thalassemias and health care in Canada: a place for genetics in medicineD H Chui, S C Wong, C R Scriver
Biomedical & Environmental Mass Spectrometry|October 1, 1986
Stable isotope dilution assay for branched chain alpha-hydroxy-and alpha-ketoacids: serum concentrations for normal childrenO A Mamer, N S Laschic, C R Scriver
Nucleic Acids Research|January 1, 1997
The PAH mutation analysis consortium database: update 1996P Nowacki, S Byck, L Prevost, et al.
Biochemical Society Transactions|October 10, 1998
Degradation rates differ between mutant and wild-type forms of phenylalanine hydroxylase expressed in vitroP J Waters, C R Scriver, M A Parniak
Ciba Foundation Symposium|January 1, 1996
The phenylalanine hydroxylase locus: a marker for the history of phenylketonuria and human genetic diversity. PAH Mutation Analysis ConsortiumC R Scriver, S Byck, L Prevost, et al.
The Journal of Clinical Investigation|December 1, 1983
Metabolism of methylmalonic acid in rats. Is methylmalonyl-coenzyme a racemase deficiency symptomatic in man?J A Montgomery, O A Mamer, C R Scriver
Pageof 32

Showing results (181-190 of 317) with videos related to

Sort By:
Pageof 32
Kidney International|February 1, 1976
Genetic aspects of renal tubular transport: diversity and topology of carriersC R Scriver, R W Chesney, R R McInnes
Canadian Medical Association Journal|April 5, 1975
Letter: Screening for hereditary metabolic diseaseC R Scriver, J C Haworth, J R Miller
Molecular Genetics and Metabolism|July 20, 2001
Homomeric and heteromeric interactions between wild-type and mutant phenylalanine hydroxylase subunits: evaluation of two-hybrid approaches for functional analysis of mutations causing hyperphenylalaninemiaP J Waters, C R Scriver, M A Parniak
European Journal of Human Genetics : EJHG|January 1, 1993
'Celtic' phenylketonuria chromosomes found? Evidence in two regions of Quebec ProvinceE Treacy, S Byck, C Clow, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|January 1, 1991
The thalassemias and health care in Canada: a place for genetics in medicineD H Chui, S C Wong, C R Scriver
Biomedical & Environmental Mass Spectrometry|October 1, 1986
Stable isotope dilution assay for branched chain alpha-hydroxy-and alpha-ketoacids: serum concentrations for normal childrenO A Mamer, N S Laschic, C R Scriver
Nucleic Acids Research|January 1, 1997
The PAH mutation analysis consortium database: update 1996P Nowacki, S Byck, L Prevost, et al.
Biochemical Society Transactions|October 10, 1998
Degradation rates differ between mutant and wild-type forms of phenylalanine hydroxylase expressed in vitroP J Waters, C R Scriver, M A Parniak
Ciba Foundation Symposium|January 1, 1996
The phenylalanine hydroxylase locus: a marker for the history of phenylketonuria and human genetic diversity. PAH Mutation Analysis ConsortiumC R Scriver, S Byck, L Prevost, et al.
The Journal of Clinical Investigation|December 1, 1983
Metabolism of methylmalonic acid in rats. Is methylmalonyl-coenzyme a racemase deficiency symptomatic in man?J A Montgomery, O A Mamer, C R Scriver
Pageof 32