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 Triggs-Raine

Showing results (1-10 of 11) with videos related to

Pageof 2
Sort By:
BMC Medical Genetics|July 25, 2016
Genotyping an immunodeficiency causing c.1624-11G>A ZAP70 mutation in Canadian MennonitesM L Schroeder, B Triggs-Raine, T Zelinski
The Journal of Biological Chemistry|June 6, 1997
Benign HEXA mutations, C739T(R247W) and C745T(R249W), cause beta-hexosaminidase A pseudodeficiency by reducing the alpha-subunit protein levelsZ Cao, E Petroulakis, T Salo, et al.
Molecular Genetics and Metabolism|December 15, 2006
Molecular basis of succinylcholine sensitivity in a prairie Hutterite kindred and genetic characterization of the region containing the BCHE geneT Zelinski, G Coghlan, J Mauthe, et al.
Molecular and Cellular Biochemistry|April 12, 1995
PCR-based analysis of voltage-gated K+ channels in vascular smooth muscleP Zahradka, K D Harris, B Triggs-Raine, et al.
American Journal of Human Genetics|April 1, 1995
Mutational analyses of Tay-Sachs disease: studies on Tay-Sachs carriers of French Canadian background living in New EnglandB Triggs-Raine, M Richard, N Wasel, et al.
Molecular and Cellular Biochemistry|July 1, 1997
Identification of proteins that interact with a protein of interest: applications of the yeast two-hybrid systemR D Gietz, B Triggs-Raine, A Robbins, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 26, 1999
Mutations in HYAL1, a member of a tandemly distributed multigene family encoding disparate hyaluronidase activities, cause a newly described lysosomal disorder, mucopolysaccharidosis IXB Triggs-Raine, T J Salo, H Zhang, et al.
Human Mutation|May 29, 1998
W474C amino acid substitution affects early processing of the alpha-subunit of beta-hexosaminidase A and is associated with subacute G(M2) gangliosidosisE Petroulakis, Z Cao, J T Clarke, et al.
Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire|March 10, 2001
Human growth factor receptor bound 14 binds the activated insulin receptor and alters the insulin-stimulated tyrosine phosphorylation levels of multiple proteinsR Hemming, R Agatep, K Badiani, et al.
Genomics|July 1, 1993
A homoallelic Gly317-->Asp mutation in ALPL causes the perinatal (lethal) form of hypophosphatasia in Canadian mennonitesC R Greenberg, C L Taylor, J C Haworth, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
BMC Medical Genetics|July 25, 2016
Genotyping an immunodeficiency causing c.1624-11G>A ZAP70 mutation in Canadian MennonitesM L Schroeder, B Triggs-Raine, T Zelinski
The Journal of Biological Chemistry|June 6, 1997
Benign HEXA mutations, C739T(R247W) and C745T(R249W), cause beta-hexosaminidase A pseudodeficiency by reducing the alpha-subunit protein levelsZ Cao, E Petroulakis, T Salo, et al.
Molecular Genetics and Metabolism|December 15, 2006
Molecular basis of succinylcholine sensitivity in a prairie Hutterite kindred and genetic characterization of the region containing the BCHE geneT Zelinski, G Coghlan, J Mauthe, et al.
Molecular and Cellular Biochemistry|April 12, 1995
PCR-based analysis of voltage-gated K+ channels in vascular smooth muscleP Zahradka, K D Harris, B Triggs-Raine, et al.
American Journal of Human Genetics|April 1, 1995
Mutational analyses of Tay-Sachs disease: studies on Tay-Sachs carriers of French Canadian background living in New EnglandB Triggs-Raine, M Richard, N Wasel, et al.
Molecular and Cellular Biochemistry|July 1, 1997
Identification of proteins that interact with a protein of interest: applications of the yeast two-hybrid systemR D Gietz, B Triggs-Raine, A Robbins, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 26, 1999
Mutations in HYAL1, a member of a tandemly distributed multigene family encoding disparate hyaluronidase activities, cause a newly described lysosomal disorder, mucopolysaccharidosis IXB Triggs-Raine, T J Salo, H Zhang, et al.
Human Mutation|May 29, 1998
W474C amino acid substitution affects early processing of the alpha-subunit of beta-hexosaminidase A and is associated with subacute G(M2) gangliosidosisE Petroulakis, Z Cao, J T Clarke, et al.
Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire|March 10, 2001
Human growth factor receptor bound 14 binds the activated insulin receptor and alters the insulin-stimulated tyrosine phosphorylation levels of multiple proteinsR Hemming, R Agatep, K Badiani, et al.
Genomics|July 1, 1993
A homoallelic Gly317-->Asp mutation in ALPL causes the perinatal (lethal) form of hypophosphatasia in Canadian mennonitesC R Greenberg, C L Taylor, J C Haworth, et al.
Pageof 2