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Rabbani, H.

Publications and source records attributed to Rabbani, H..

2 recordsLinked to original sources

A population readout of extrastriate activity reveals biased and smoothed temporal representations across saccades

Perception of visual time is transiently distorted around saccadic eye movements, yet the neuronal mechanisms constructing perisaccadic representations of time remain unclear. Here, we investigate how perisaccadic temporal information is encoded and read out in extrastriate cortex, by combining electrophysiological recordings in V4 and MT neuronal population in macaque monkeys under high spatiotemporal resolution visual stimulation, and a statistical modeling framework capturing perisaccadic response modulations at single-trial precision. Our analyses show that perisaccadic neuronal responses systematically shift the temporal representation of presaccadic stimuli within receptive fields-biasing them toward earlier times, and also reduce temporal sensitivity for presaccadic stimuli-impairing discrimination of stimulus onset times. Model-based readout using time-varying spatiotemporal sensitivity maps in neuronal ensembles enables quantitative characterization of these effects and identifies their specific neuronal response components at millisecond resolution. In silico manipulations further demonstrate a causal role of representational bias in reducing temporal sensitivity. These findings suggest that extrastriate cortex implements an active encoding strategy to stabilize presaccadic temporal information by favoring the most recent reliable input, revealing a fundamental tradeoff between temporal precision and robustness that supports a continuous visual percept across saccades. This finding also establishes a general role for extrastriate populations in constructing the perception of visual time.

neuroscience↗

A One-Step Plasma Assisted Synthesis of Gold Nanoparticles and Simultaneous Linker-Free Conjugation with Nestin: An In Vitro Study of Cellular toxicity.

We introduce a method for conjugating antigens to gold nanoparticles (GNPs) while synthesizing them using gas plasma, which eliminates the need for chemical linkers intended to facilitate the conjugation procedure for immunotherapy purposes. We report a physical approach to conjugate antigen Nestin (NES) as a marker in malignant tumors to GNPs. Two approaches were used to perform the conjugation of GNPs and NES. The first method involved using citrate to synthesize GNPs, and then NES was conjugated onto the GNPs surface by plasma. In the second method, GNPs were simultaneously synthesized and linker-freely conjugated to NES by plasma treatment. Enzyme-linked immunosorbent assay with the protocol defined in this study, Zeta-sizer, Ultraviolet-visible spectroscopy, and Transmission Electron Microscopy results confirmed NES conjugation to GNPs. In addition, the toxicity of the prepared samples was investigated in vitro using peripheral blood mononuclear cells (PBMCs) and flow cytometry, which proved the non-toxicity of the samples. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=113 SRC="FIGDIR/small/570950v2_ufig1.gif" ALT="Figure 1"> View larger version (32K): org.highwire.dtl.DTLVardef@1bffa43org.highwire.dtl.DTLVardef@c75811org.highwire.dtl.DTLVardef@166f4b3org.highwire.dtl.DTLVardef@4b4def_HPS_FORMAT_FIGEXP M_FIG C_FIG

biophysics↗