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

L C Brody

Showing results (11-20 of 63) with videos related to

Pageof 7
Sort By:
Analytical Chemistry|November 18, 2000
Effective capillary electrophoresis-based heteroduplex analysis through optimization of surface coating and polymer networksH Tian, L C Brody, D Mao, et al.
Human Mutation|August 3, 2000
The breast cancer information core: database design, structure, and scopeC Szabo, A Masiello, J F Ryan, et al.
Human Molecular Genetics|September 1, 1996
KVLQT1 mutations in three families with familial or sporadic long QT syndromeM W Russell, M Dick, F S Collins, et al.
Human Molecular Genetics|November 1, 1993
Expression and processing of human ornithine-delta-aminotransferase in Saccharomyces cerevisiaeK M Dougherty, D A Swanson, L C Brody, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1997
Cloning of the human NADH: ubiquinone oxidoreductase subunit B13: localization to chromosome 7q32 and identification of a pseudogene on 11p15M W Russell, S du Manoir, F S Collins, et al.
Clinical Chemistry|February 13, 2001
Capillary and microchip electrophoresis for rapid detection of known mutations by combining allele-specific DNA amplification with heteroduplex analysisH Tian, L C Brody, S Fan, et al.
The Journal of Biological Chemistry|August 1, 1997
Defects in auxiliary redox proteins lead to functional methionine synthase deficiencyS Gulati, Z Chen, L C Brody, et al.
Biochimica Et Biophysica Acta|January 8, 1999
Molecular cloning of the human HAND2 geneM W Russell, P Kemp, L Wang, et al.
Public Health Genomics|September 5, 2009
Considerations for designing a prototype genetic test for use in translational researchC H Wade, C M McBride, S L R Kardia, et al.
Nucleic Acids Research|April 25, 1991
A polymorphic synonymous mutation in human ornithine-delta-aminotransferase (N378N)L S Martin, G A Mitchell, J Michaud, et al.
Pageof 7

Showing results (11-20 of 63) with videos related to

Sort By:
Pageof 7
Analytical Chemistry|November 18, 2000
Effective capillary electrophoresis-based heteroduplex analysis through optimization of surface coating and polymer networksH Tian, L C Brody, D Mao, et al.
Human Mutation|August 3, 2000
The breast cancer information core: database design, structure, and scopeC Szabo, A Masiello, J F Ryan, et al.
Human Molecular Genetics|September 1, 1996
KVLQT1 mutations in three families with familial or sporadic long QT syndromeM W Russell, M Dick, F S Collins, et al.
Human Molecular Genetics|November 1, 1993
Expression and processing of human ornithine-delta-aminotransferase in Saccharomyces cerevisiaeK M Dougherty, D A Swanson, L C Brody, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1997
Cloning of the human NADH: ubiquinone oxidoreductase subunit B13: localization to chromosome 7q32 and identification of a pseudogene on 11p15M W Russell, S du Manoir, F S Collins, et al.
Clinical Chemistry|February 13, 2001
Capillary and microchip electrophoresis for rapid detection of known mutations by combining allele-specific DNA amplification with heteroduplex analysisH Tian, L C Brody, S Fan, et al.
The Journal of Biological Chemistry|August 1, 1997
Defects in auxiliary redox proteins lead to functional methionine synthase deficiencyS Gulati, Z Chen, L C Brody, et al.
Biochimica Et Biophysica Acta|January 8, 1999
Molecular cloning of the human HAND2 geneM W Russell, P Kemp, L Wang, et al.
Public Health Genomics|September 5, 2009
Considerations for designing a prototype genetic test for use in translational researchC H Wade, C M McBride, S L R Kardia, et al.
Nucleic Acids Research|April 25, 1991
A polymorphic synonymous mutation in human ornithine-delta-aminotransferase (N378N)L S Martin, G A Mitchell, J Michaud, et al.
Pageof 7