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

Courtney MacMullen

Showing results (1-10 of 20) with videos related to

Pageof 2
Sort By:
SLAS Discovery : Advancing Life Sciences R & D|March 16, 2021
High-Throughput Phenotypic Assay for Compounds That Influence Mitochondrial Health Using iPSC-Derived Human NeuronsCourtney MacMullen, Ronald L Davis
Brain : a Journal of Neurology|November 8, 2024
Mitochondrial dynamics and bioenergetics in Alzheimer's induced pluripotent stem cell-derived neuronsCourtney MacMullen, Neelam Sharma, Ronald L Davis
Neuron|June 7, 2016
Scribble Scaffolds a Signalosome for Active ForgettingIsaac Cervantes-Sandoval, Molee Chakraborty, Courtney MacMullen, et al.
The Journal of Biological Chemistry|December 8, 2005
A novel KCNJ11 mutation associated with congenital hyperinsulinism reduces the intrinsic open probability of beta-cell ATP-sensitive potassium channelsYu-Wen Lin, Courtney MacMullen, Arupa Ganguly, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|December 25, 2003
Histopathology of congenital hyperinsulinism: retrospective study with genotype correlationsMariko Suchi, Courtney MacMullen, Paul S Thornton, et al.
Diabetes|June 19, 2007
Congenital hyperinsulinism associated ABCC8 mutations that cause defective trafficking of ATP-sensitive K+ channels: identification and rescueFei-Fei Yan, Yu-Wen Lin, Courtney MacMullen, et al.
Diabetes|February 24, 2007
A mutation in the TMD0-L0 region of sulfonylurea receptor-1 (L225P) causes permanent neonatal diabetes mellitus (PNDM)Ricard Masia, Diva D De Leon, Courtney MacMullen, et al.
The Journal of Clinical Endocrinology and Metabolism|November 25, 2004
Genotype-phenotype correlations in children with congenital hyperinsulinism due to recessive mutations of the adenosine triphosphate-sensitive potassium channel genesMaria J Henwood, Andrea Kelly, Courtney Macmullen, et al.
The American Journal of Surgical Pathology|September 17, 2004
Congenital hyperinsulinism: intraoperative biopsy interpretation can direct the extent of pancreatectomyMariko Suchi, Paul S Thornton, N Scott Adzick, et al.
Cell Reports|November 23, 2017
Dopamine Receptor DAMB Signals via Gq to Mediate Forgetting in DrosophilaSophie Himmelreich, Ikuo Masuho, Jacob A Berry, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
SLAS Discovery : Advancing Life Sciences R & D|March 16, 2021
High-Throughput Phenotypic Assay for Compounds That Influence Mitochondrial Health Using iPSC-Derived Human NeuronsCourtney MacMullen, Ronald L Davis
Brain : a Journal of Neurology|November 8, 2024
Mitochondrial dynamics and bioenergetics in Alzheimer's induced pluripotent stem cell-derived neuronsCourtney MacMullen, Neelam Sharma, Ronald L Davis
Neuron|June 7, 2016
Scribble Scaffolds a Signalosome for Active ForgettingIsaac Cervantes-Sandoval, Molee Chakraborty, Courtney MacMullen, et al.
The Journal of Biological Chemistry|December 8, 2005
A novel KCNJ11 mutation associated with congenital hyperinsulinism reduces the intrinsic open probability of beta-cell ATP-sensitive potassium channelsYu-Wen Lin, Courtney MacMullen, Arupa Ganguly, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|December 25, 2003
Histopathology of congenital hyperinsulinism: retrospective study with genotype correlationsMariko Suchi, Courtney MacMullen, Paul S Thornton, et al.
Diabetes|June 19, 2007
Congenital hyperinsulinism associated ABCC8 mutations that cause defective trafficking of ATP-sensitive K+ channels: identification and rescueFei-Fei Yan, Yu-Wen Lin, Courtney MacMullen, et al.
Diabetes|February 24, 2007
A mutation in the TMD0-L0 region of sulfonylurea receptor-1 (L225P) causes permanent neonatal diabetes mellitus (PNDM)Ricard Masia, Diva D De Leon, Courtney MacMullen, et al.
The Journal of Clinical Endocrinology and Metabolism|November 25, 2004
Genotype-phenotype correlations in children with congenital hyperinsulinism due to recessive mutations of the adenosine triphosphate-sensitive potassium channel genesMaria J Henwood, Andrea Kelly, Courtney Macmullen, et al.
The American Journal of Surgical Pathology|September 17, 2004
Congenital hyperinsulinism: intraoperative biopsy interpretation can direct the extent of pancreatectomyMariko Suchi, Paul S Thornton, N Scott Adzick, et al.
Cell Reports|November 23, 2017
Dopamine Receptor DAMB Signals via Gq to Mediate Forgetting in DrosophilaSophie Himmelreich, Ikuo Masuho, Jacob A Berry, et al.
Pageof 2