Jeremy S. Duncan

University of Iowa, Iowa City, IA 
"Jeremy Duncan"
Mean distance: 17.69 (cluster 6)


Sign in to add mentor
Bernd Fritzsch grad student 2012 University of Iowa
 (Cochlear neurosensory specification and competence: You gata have Gata.)
BETA: Related publications


You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Stoner ZA, Ketchum EM, Sheltz-Kempf S, et al. (2022) Expression Within Inner Ear Afferent Neurons Is Necessary for Central Pathfinding. Frontiers in Neuroscience. 15: 779871
Duncan JS, Fritzsch B, Houston DW, et al. (2019) Topologically correct central projections of tetrapod inner ear afferents require Fzd3. Scientific Reports. 9: 10298
Fritzsch B, Elliott KL, Pavlinkova G, et al. (2019) Neuronal Migration Generates New Populations of Neurons That Develop Unique Connections, Physiological Properties and Pathologies. Frontiers in Cell and Developmental Biology. 7: 59
Elliott KL, Fritzsch B, Duncan JS. (2018) Evolutionary and Developmental Biology Provide Insights Into the Regeneration of Organ of Corti Hair Cells. Frontiers in Cellular Neuroscience. 12: 252
Duncan JS, Stoller ML, Francl AF, et al. (2017) Celsr1 Coordinates the Planar Polarity of Vestibular Hair Cells During Inner Ear Development. Developmental Biology
Fritzsch B, Duncan JS, Kersigo J, et al. (2016) Neuroanatomical Tracing Techniques in the Ear: History, State of the Art, and Future Developments. Methods in Molecular Biology (Clifton, N.J.). 1427: 243-62
Saito Y, Miranda-Rottmann S, Ruggiu M, et al. (2016) NOVA2-mediated RNA regulation is required for axonal pathfinding during development. Elife. 5
Saito Y, Miranda-Rottmann S, Ruggiu M, et al. (2016) Author response: NOVA2-mediated RNA regulation is required for axonal pathfinding during development Elife
Duncan JS, Elliott KL, Kersigo J, et al. (2015) Combining whole-mount in situ hybridization with neuronal tracing and immunohistochemistry Neuromethods. 99: 339-352
Cheng L, Desai J, Miranda CJ, et al. (2014) Human CFEOM1 mutations attenuate KIF21A autoinhibition and cause oculomotor axon stalling. Neuron. 82: 334-49
See more...