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Santhosh Sethuramanujam

Researcher at University of Victoria

Publications -  18
Citations -  387

Santhosh Sethuramanujam is an academic researcher from University of Victoria. The author has contributed to research in topics: Retina & Excitatory postsynaptic potential. The author has an hindex of 8, co-authored 18 publications receiving 294 citations. Previous affiliations of Santhosh Sethuramanujam include University at Buffalo.

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Two transcription factors, Pou4f2 and Isl1, are sufficient to specify the retinal ganglion cell fate

TL;DR: It is reported that ectopic expression of Pou4f2 and Isl1 in the Atoh7-null retina using a binary knockin-transgenic system is sufficient for the specification of the RGC fate.
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A Central Role for Mixed Acetylcholine/GABA Transmission in Direction Coding in the Retina

TL;DR: It is found that ACh initiates responses to motion in natural scenes or under low-contrast conditions, and mixed transmission plays a central role in shaping directional responses of DSGCs.
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Specific Wiring of Distinct Amacrine Cells in the Directionally Selective Retinal Circuit Permits Independent Coding of Direction and Size

TL;DR: It is demonstrated that increasing ambient illumination leads to the recruitment of GABAergic wide-field amacrine cells (WACs) endowing the DS circuit with an additional feature: size selectivity, which permits high-fidelity direction coding over a range of ambient light levels, over which sizeSelectivity is adjusted.
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The Antipsychotic Drug Loxapine Is an Opener of the Sodium-Activated Potassium Channel Slack (Slo2.2)

TL;DR: In dorsal root ganglion neurons, loxapine was found to behave as an opener of native KNa channels and to increase the rheobase of action potential.
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Retinal direction selectivity in the absence of asymmetric starburst amacrine cell responses.

TL;DR: It is demonstrated that direction selectivity in downstream ganglion cells remains remarkably unaffected when starburst dendrites are rendered non-directional, using a novel strategy combining a conditional GABAA α2 receptor knockout mouse with optogenetics.