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

Kaela S Singleton

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

Pageof 2
Sort By:
The Journal of Cell Biology|June 3, 2021
Robustness and innovation along the endocytic route: Lessons from darknessKaela S Singleton, Victor Faundez
Iscience|May 19, 2020
Rare Genetic Diseases: Nature's Experiments on Human DevelopmentChelsea E Lee, Kaela S Singleton, Melissa Wallin, et al.
Genes|February 24, 2024
Xenopus Sox11 Partner Proteins and Functional Domains in NeurogenesisKaela S Singleton, Pablo Silva-Rodriguez, Doreen D Cunningham, et al.
Neuron|August 6, 2021
A year in review: Are diversity, equity, and inclusion initiatives fixing systemic barriers?Kaela S Singleton, De-Shaine R K Murray, Angeline J Dukes, et al.
Physiology & Behavior|July 18, 2016
Reduced marker of vascularization in the anterior hippocampus in a female monkey model of depressionAnisha Kalidindi, Sean D Kelly, Kaela S Singleton, et al.
The Journal of Biological Chemistry|April 10, 2014
Mutations in the BLOC-1 subunits dysbindin and muted generate divergent and dosage-dependent phenotypesJennifer Larimore, Stephanie A Zlatic, Avanti Gokhale, et al.
Frontiers in Genetics|March 28, 2017
Dysbindin Deficiency Modifies the Expression of GABA Neuron and Ion Permeation Transcripts in the Developing HippocampusJennifer Larimore, Stephanie A Zlatic, Miranda Arnold, et al.
Eneuro|July 27, 2021
Heterogeneous Expression of Nuclear Encoded Mitochondrial Genes Distinguishes Inhibitory and Excitatory NeuronsMeghan E Wynne, Alicia R Lane, Kaela S Singleton, et al.
Frontiers in Cellular Neuroscience|October 8, 2016
The Endosome Localized Arf-GAP AGAP1 Modulates Dendritic Spine Morphology Downstream of the Neurodevelopmental Disorder Factor DysbindinMiranda Arnold, Rebecca Cross, Kaela S Singleton, et al.
Molecular Biology of the Cell|January 29, 2025
Adaptive protein synthesis in genetic models of copper deficiency and childhood neurodegenerationAlicia R Lane, Noah E Scher, Shatabdi Bhattacharjee, et al.
Pageof 2

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

Sort By:
Pageof 2
The Journal of Cell Biology|June 3, 2021
Robustness and innovation along the endocytic route: Lessons from darknessKaela S Singleton, Victor Faundez
Iscience|May 19, 2020
Rare Genetic Diseases: Nature's Experiments on Human DevelopmentChelsea E Lee, Kaela S Singleton, Melissa Wallin, et al.
Genes|February 24, 2024
Xenopus Sox11 Partner Proteins and Functional Domains in NeurogenesisKaela S Singleton, Pablo Silva-Rodriguez, Doreen D Cunningham, et al.
Neuron|August 6, 2021
A year in review: Are diversity, equity, and inclusion initiatives fixing systemic barriers?Kaela S Singleton, De-Shaine R K Murray, Angeline J Dukes, et al.
Physiology & Behavior|July 18, 2016
Reduced marker of vascularization in the anterior hippocampus in a female monkey model of depressionAnisha Kalidindi, Sean D Kelly, Kaela S Singleton, et al.
The Journal of Biological Chemistry|April 10, 2014
Mutations in the BLOC-1 subunits dysbindin and muted generate divergent and dosage-dependent phenotypesJennifer Larimore, Stephanie A Zlatic, Avanti Gokhale, et al.
Frontiers in Genetics|March 28, 2017
Dysbindin Deficiency Modifies the Expression of GABA Neuron and Ion Permeation Transcripts in the Developing HippocampusJennifer Larimore, Stephanie A Zlatic, Miranda Arnold, et al.
Eneuro|July 27, 2021
Heterogeneous Expression of Nuclear Encoded Mitochondrial Genes Distinguishes Inhibitory and Excitatory NeuronsMeghan E Wynne, Alicia R Lane, Kaela S Singleton, et al.
Frontiers in Cellular Neuroscience|October 8, 2016
The Endosome Localized Arf-GAP AGAP1 Modulates Dendritic Spine Morphology Downstream of the Neurodevelopmental Disorder Factor DysbindinMiranda Arnold, Rebecca Cross, Kaela S Singleton, et al.
Molecular Biology of the Cell|January 29, 2025
Adaptive protein synthesis in genetic models of copper deficiency and childhood neurodegenerationAlicia R Lane, Noah E Scher, Shatabdi Bhattacharjee, et al.
Pageof 2