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Patricia S. Estes

Researcher at University of Arizona

Publications -  17
Citations -  1902

Patricia S. Estes is an academic researcher from University of Arizona. The author has contributed to research in topics: Synaptic vesicle & Synaptic vesicle recycling. The author has an hindex of 14, co-authored 17 publications receiving 1797 citations.

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Staufen- and FMRP-containing neuronal RNPs are structurally and functionally related to somatic P bodies.

TL;DR: It is shown that staufen- and FMRP-containing RNPs in Drosophila neurons contain proteins also present in somatic "P bodies," including the RNA-degradative enzymes Dcp1p and Xrn1p/Pacman and crucial components of miRNA (argonaute), NMD (Upf1p), and general translational repression pathways.
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The Organization of Extrinsic Neurons and Their Implications in the Functional Roles of the Mushroom Bodies in Drosophila melanogaster Meigen

TL;DR: In this paper, a novel presynaptic reporter construct, UAS-neuronal synaptobrevin-green fluorescent protein (n-syb-GFP), was used to reveal the direction of information in the GAL4-labeled neurons.
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Traffic of dynamin within individual Drosophila synaptic boutons relative to compartment-specific markers.

TL;DR: The results suggest that dynamin is not a freely diffusible molecule in resting nerve terminals; rather, it appears localized to synaptic sites by association with yet uncharacterized presynaptic components.
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Nucleoside Diphosphate Kinase, a Source of GTP, Is Required for Dynamin-Dependent Synaptic Vesicle Recycling

TL;DR: It is demonstrated that NDK regulates synaptic vesicle internalization at the stage where function of the dynamin GTPase is required, and this connection between NDK and membrane internalization further strengthens an emerging hypothesis that endocytosis, probably of activated growth factor receptors, is an important tumor suppressing activity in vivo.
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Wild-type and A315T mutant TDP-43 exert differential neurotoxicity in a Drosophila model of ALS

TL;DR: It is found that when expressed at comparable levels, wild-type TDP-43 exerts more severe effects on neuromuscular junction architecture, viability and motor neuron loss compared with the A315T allele, and neuronal apoptosis does not require the cytoplasmic localization of T DP-43 and that its neurotoxicity is modulated by the proteasome, the HSP70 chaperone and the apoptosis pathway.