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

S-L Shyng

Showing results (11-20 of 21) with videos related to

Pageof 3
Sort By:
Proceedings of the National Academy of Sciences of the United States of America|February 28, 2001
Defective trafficking and function of KATP channels caused by a sulfonylurea receptor 1 mutation associated with persistent hyperinsulinemic hypoglycemia of infancyE A Cartier, L R Conti, C A Vandenberg, et al.
The Journal of Biological Chemistry|September 8, 2001
Transmembrane topology of the sulfonylurea receptor SUR1L R Conti, C M Radeke, S L Shyng, et al.
Biophysical Journal|April 25, 2000
The kinetic and physical basis of K(ATP) channel gating: toward a unified molecular understandingD Enkvetchakul, G Loussouarn, E Makhina, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 15, 1996
Depletion of intracellular polyamines relieves inward rectification of potassium channelsS L Shyng, Q Sha, T Ferrigni, et al.
Biochemistry|February 2, 1993
Processing of a cellular prion protein: identification of N- and C-terminal cleavage sitesD A Harris, M T Huber, P van Dijken, et al.
Diabetes|July 2, 1998
Functional analyses of novel mutations in the sulfonylurea receptor 1 associated with persistent hyperinsulinemic hypoglycemia of infancyS L Shyng, T Ferrigni, J B Shepard, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 19, 2000
Modulation of nucleotide sensitivity of ATP-sensitive potassium channels by phosphatidylinositol-4-phosphate 5-kinaseS L Shyng, A Barbieri, A Gumusboga, et al.
Human Molecular Genetics|June 9, 1998
Genetic heterogeneity in familial hyperinsulinismA Nestorowicz, B Glaser, B A Wilson, et al.
The Journal of Clinical Endocrinology and Metabolism|January 1, 2013
Genotype and phenotype correlations in 417 children with congenital hyperinsulinismK E Snider, S Becker, L Boyajian, et al.
Science (New York, N.Y.)|June 21, 1996
Adenosine diphosphate as an intracellular regulator of insulin secretionC G Nichols, S L Shyng, A Nestorowicz, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Proceedings of the National Academy of Sciences of the United States of America|February 28, 2001
Defective trafficking and function of KATP channels caused by a sulfonylurea receptor 1 mutation associated with persistent hyperinsulinemic hypoglycemia of infancyE A Cartier, L R Conti, C A Vandenberg, et al.
The Journal of Biological Chemistry|September 8, 2001
Transmembrane topology of the sulfonylurea receptor SUR1L R Conti, C M Radeke, S L Shyng, et al.
Biophysical Journal|April 25, 2000
The kinetic and physical basis of K(ATP) channel gating: toward a unified molecular understandingD Enkvetchakul, G Loussouarn, E Makhina, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 15, 1996
Depletion of intracellular polyamines relieves inward rectification of potassium channelsS L Shyng, Q Sha, T Ferrigni, et al.
Biochemistry|February 2, 1993
Processing of a cellular prion protein: identification of N- and C-terminal cleavage sitesD A Harris, M T Huber, P van Dijken, et al.
Diabetes|July 2, 1998
Functional analyses of novel mutations in the sulfonylurea receptor 1 associated with persistent hyperinsulinemic hypoglycemia of infancyS L Shyng, T Ferrigni, J B Shepard, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 19, 2000
Modulation of nucleotide sensitivity of ATP-sensitive potassium channels by phosphatidylinositol-4-phosphate 5-kinaseS L Shyng, A Barbieri, A Gumusboga, et al.
Human Molecular Genetics|June 9, 1998
Genetic heterogeneity in familial hyperinsulinismA Nestorowicz, B Glaser, B A Wilson, et al.
The Journal of Clinical Endocrinology and Metabolism|January 1, 2013
Genotype and phenotype correlations in 417 children with congenital hyperinsulinismK E Snider, S Becker, L Boyajian, et al.
Science (New York, N.Y.)|June 21, 1996
Adenosine diphosphate as an intracellular regulator of insulin secretionC G Nichols, S L Shyng, A Nestorowicz, et al.
Pageof 3