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Seung Wook Oh

Researcher at Allen Institute for Brain Science

Publications -  20
Citations -  10906

Seung Wook Oh is an academic researcher from Allen Institute for Brain Science. The author has contributed to research in topics: Daf-16 & Caenorhabditis elegans. The author has an hindex of 17, co-authored 19 publications receiving 8494 citations. Previous affiliations of Seung Wook Oh include University of Massachusetts Medical School.

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A robust and high-throughput Cre reporting and characterization system for the whole mouse brain

TL;DR: A set of Cre reporter mice with strong, ubiquitous expression of fluorescent proteins of different spectra is generated and enables direct visualization of fine dendritic structures and axonal projections of the labeled neurons, which is useful in mapping neuronal circuitry, imaging and tracking specific cell populations in vivo.
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A mesoscale connectome of the mouse brain

TL;DR: A brain-wide, cellular-level, mesoscale connectome for the mouse, using enhanced green fluorescent protein-expressing adeno-associated viral vectors to trace axonal projections from defined regions and cell types, and high-throughput serial two-photon tomography to image the EGFP-labelled axons throughout the brain.
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The Allen Mouse Brain Common Coordinate Framework: A 3D Reference Atlas.

TL;DR: This work constructed an average template brain at 10 μm voxel resolution by interpolating high resolution in-plane serial two-photon tomography images with 100 μm z-sampling from 1,675 young adult C57BL/6J mice and parcellated the entire brain directly in 3D.
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JNK regulates lifespan in Caenorhabditis elegans by modulating nuclear translocation of forkhead transcription factor/DAF-16

TL;DR: This work demonstrates that c-Jun N-terminal kinase (JNK) is a positive regulator of DAF-16 in both lifespan regulation and stress resistance and defines an interaction between two well conserved proteins, JNK-1 and D AF-16, and provides a mechanism by which JNK regulates longevity and stress Resistance.
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Identification of direct DAF-16 targets controlling longevity, metabolism and diapause by chromatin immunoprecipitation.

TL;DR: The results show that the ChIP-based cloning strategy leads to greater enrichment for DAF-16 target genes than previous screening strategies, and it is demonstrated that Daf-16 is recruited to multiple promoters to coordinate regulation of its downstream targets.