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Christopher K. Rodesch

Researcher at University of Utah

Publications -  27
Citations -  2865

Christopher K. Rodesch is an academic researcher from University of Utah. The author has contributed to research in topics: Synaptic vesicle & Neurotransmission. The author has an hindex of 20, co-authored 27 publications receiving 2646 citations. Previous affiliations of Christopher K. Rodesch include University of Iowa & Vanderbilt University.

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Human ESCRT and ALIX proteins interact with proteins of the midbody and function in cytokinesis

TL;DR: The experiments suggest that the ESCRT pathway may be recruited to facilitate analogous membrane fission events during HIV budding, MVB vesicle formation, and the abscission stage of cytokinesis.
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Drosophila Unc-13 is essential for synaptic transmission

TL;DR: Dunc-13 is essential for a stage of neurotransmission following vesicle docking and before fusion and is comparable only to removal of the core complex proteins Syntaxin and Synaptobrevin.
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Impaired neutrophil extracellular trap (NET) formation: a novel innate immune deficiency of human neonates

TL;DR: It is found that neutrophils from term and preterm infants fail to form NETs when activated by inflammatory agonists-in contrast to leukocytes from healthy adults, and this deficiency in NET formation may be a critical facet of a common developmental immunodeficiency that predisposes newborn infants to infection.
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The Ubiquitin Proteasome System Acutely Regulates Presynaptic Protein Turnover and Synaptic Efficacy

TL;DR: It is demonstrated that the UPS functions locally within synaptic boutons to acutely control levels of presynaptic protein and that the rate of UPS-dependent protein degradation is a primary determinant of neurotransmission strength.
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Living synaptic vesicle marker: synaptotagmin-GFP.

TL;DR: Multiple lines of evidence indicate that syt-eGFP is present in SVs, with expression similar to the native syt, and at neuromuscular junction (NMJ) synapses, the sytThe fluorescence pattern of which colocalizes with native SV proteins at synapses perfectly matches the staining pattern seen with antibodies against SV-associated proteins, suggesting that syT-e GFP is tightly linked to SVs.