Jeremy Sullivan

Research Associate

20002015
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Fingerprint Dive into the research topics where Jeremy Sullivan is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

Astacoidea Medicine & Life Sciences
Neurons Medicine & Life Sciences
Neurogenesis Medicine & Life Sciences
Olfactory Pathways Medicine & Life Sciences
Neuropil Medicine & Life Sciences
Brain Medicine & Life Sciences
Decapoda (Crustacea) Medicine & Life Sciences
TRPV Cation Channels Medicine & Life Sciences

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Research Output 2000 2015

Novel mutations highlight the key role of the ankyrin repeat domain in TRPV4-mediated neuropathy

Sullivan, J., Zimanyi, C. M., Aisenberg, W., Bears, B., Chen, D. H., Day, J. W., Bird, T. D., Siskind, C. E., Gaudet, R. & Sumner, C., Dec 1 2015, In : Neurology: Genetics. 1, 4, e29.

Research output: Contribution to journalArticle

Ankyrin Repeat
Mutation
Missense Mutation
Peripheral Nerves
Immunoblotting

Structure of the Nervous System: General Design and Gross Anatomy

Sullivan, J. & Herberholz, J., May 8 2015, Functional Morphology and Diversity. Oxford University Press

Research output: Chapter in Book/Report/Conference proceedingChapter

nervous system
Nervous System
Anatomy
Crustacea
Thoracica

A TRPV channel in drosophila motor neurons regulates presynaptic resting Ca2+ levels, synapse growth, and synaptic transmission

Wong, C. O., Chen, K., Lin, Y., Chao, Y., Duraine, L., Lu, Z., Yoon, W., Sullivan, J., Broadhead, G. T., Sumner, C., Lloyd, T., Macleod, G. T., Bellen, H. J. & Venkatachalam, K., Nov 19 2014, In : Neuron. 84, 4, p. 764-777 14 p.

Research output: Contribution to journalArticle

Synaptic Vesicles
Motor Neurons
Synaptic Transmission
Microtubules
Synapses

Hereditary channelopathies caused by TRPV4 Mutations

Sullivan, J., Lloyd, T. & Sumner, C., Jan 1 2014, Pathologies of Calcium Channels. Springer Berlin Heidelberg, p. 413-440 28 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

Channelopathies
TRPV Cation Channels
Mutation
Genes
Spinal Muscular Atrophy

Phenotypic spectrum and incidence of TRPV4 mutations in patients with inherited axonal neuropathy

Sullivan, J. M., Landouré, G., Gaudet, R., Sumner, C. J., Echaniz-Laguna, A. & Latour, P., Nov 1 2014, In : Neurology. 83, 21, p. 1991 1 p.

Research output: Contribution to journalArticle

Hereditary Sensory and Autonomic Neuropathies
TRPV Cation Channels
Phenotype
Mutation
Incidence