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Kaela Singleton
Kaela Singleton
Emory University School of Medicine
Підтверджена електронна адреса в emory.edu - Домашня сторінка
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Посилання
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Mutations in the BLOC-1 subunits dysbindin and muted generate divergent and dosage-dependent phenotypes
J Larimore, SA Zlatic, A Gokhale, K Tornieri, KS Singleton, AP Mullin, ...
Journal of Biological Chemistry 289 (20), 14291-14300, 2014
402014
Rare genetic diseases: nature's experiments on human development
CE Lee, KS Singleton, M Wallin, V Faundez
IScience 23 (5), 2020
392020
Dysbindin deficiency modifies the expression of GABA neuron and ion permeation transcripts in the developing hippocampus
J Larimore, SA Zlatic, M Arnold, KS Singleton, R Cross, H Rudolph, ...
Frontiers in genetics 8, 28, 2017
242017
A year in review: Are diversity, equity, and inclusion initiatives fixing systemic barriers?
KS Singleton, DSRK Murray, AJ Dukes, LNS Richardson
Neuron 109 (21), 3365-3367, 2021
212021
The endosome localized Arf-GAP AGAP1 modulates dendritic spine morphology downstream of the neurodevelopmental disorder factor dysbindin
M Arnold, R Cross, KS Singleton, S Zlatic, C Chapleau, AP Mullin, I Rolle, ...
Frontiers in Cellular Neuroscience 10, 218, 2016
152016
An open letter to past, current and future mentors of Black neuroscientists
KS Singleton, R Tesfaye, EN Dominguez, AJ Dukes
Nature Reviews Neuroscience 22 (2), 71-72, 2021
142021
Heterogeneous expression of nuclear encoded mitochondrial genes distinguishes inhibitory and excitatory neurons
ME Wynne, AR Lane, KS Singleton, SA Zlatic, A Gokhale, E Werner, ...
Eneuro 8 (4), 2021
72021
Reduced marker of vascularization in the anterior hippocampus in a female monkey model of depression
A Kalidindi, SD Kelly, KS Singleton, D Guzman, L Merrill, SL Willard, ...
Physiology & behavior 172, 12-15, 2017
42017
Systemic proteome phenotypes reveal defective metabolic flexibility in Mecp2 mutants
SA Zlatic, E Werner, V Surapaneni, CE Lee, A Gokhale, K Singleton, ...
Human Molecular Genetics 33 (1), 12-32, 2024
22024
Systemic Metabolic and Mitochondrial Defects in Rett Syndrome Models.
SA Zlatic, E Werner, V Surapaneni, CE Lee, A Gokhale, K Singleton, ...
Biorxiv: the Preprint Server for Biology, 2023
22023
Neuronal Endosomal Trafficking: One of the Common Molecular Pathways Disrupted in Autism Spectrum Disorders and Schizophrenia
H Rudolph, RD Cross, L Segura, KS Singleton, JL Larimore
J Neurol Psychol 4 (2), 11, 2016
22016
Xenopus Sox11 Partner Proteins and Functional Domains in Neurogenesis
KS Singleton, P Silva-Rodriguez, DD Cunningham, EM Silva
Genes 15 (2), 243, 2024
2024
Young researchers series# 2
CB Palavicino-Maggio, KS Singleton, K Challa
TRENDS IN CELL BIOLOGY 32 (5), 367-369, 2022
2022
Robustness and innovation along the endocytic route: Lessons from darkness
KS Singleton, V Faundez
Journal of Cell Biology 220 (7), e202105030, 2021
2021
Pairing your Sox: Identification of Sox11 partner proteins and interaction domains in the developing neural plate
KS Singleton, P Silva-Rodriguez, EM Silva
bioRxiv, 2020.04. 23.057919, 2020
2020
Characterization of SOX11 Partner Proteins and Interaction Domains in Xenopus Neurogenesis
KS Singleton
Georgetown University, 2020
2020
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