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Gnodde, S.

Publications and source records attributed to Gnodde, S..

2 recordsLinked to original sources

Posterior but not frontal neural signatures of subjective visibility in report-independent EEG decoding

A central question in consciousness research is whether perceptual awareness arises predominantly from activity in posterior sensory regions or from later frontal processes associated with access and report. Empirical tests of these alternatives are challenging because most paradigms rely on explicit perceptual reports, introducing motor and decisional confounds. Here, we used an electroencephalography design combining two independent tasks to isolate neural signatures of subjective visibility while minimizing report-related activity. Participants viewed lateralized gratings in a backward-masking task and rated their subjective visibility, while in a separate no-report task they viewed unmasked gratings without reporting. Classifiers were trained on stimulus location in the no-report task and tested on masked trials sorted by subjective visibility in the masking task. This cross-decoding approach isolates stimulus-specific neural representations that generalize across tasks and are therefore independent of reporting and decision processes. Decoding revealed a reliable difference between subjectively visible and invisible stimuli in an early time window from 130 to 170 milliseconds, driven by posterior sensors over occipital, temporal, and parietal regions. No corresponding effects were observed over frontal sensors. These results indicate that subjective awareness is associated with early, posterior neural representations, whereas frontal activity observed in report-based paradigms likely reflects post-perceptual processing rather than awareness per se.

neuroscience↗

Single cell transcriptomics reveals correct developmental dynamics and high-quality midbrain cell types by improved hESC differentiation.

Stem cell technologies provide new opportunities for modeling cells in the healthy and diseased states and for regenerative medicine. In both cases developmental knowledge as well as the quality and molecular properties of the cells are essential for their future application. In this study we identify developmental factors important for the differentiation of human embryonic stem cells (hESCs) into midbrain dopaminergic (mDA) neurons. We found that Laminin-511, and dual canonical and non-canonical WNT activation followed by GSK3{beta} inhibition plus FGF8b, improved midbrain patterning. In addition, mDA neurogenesis and differentiation was enhanced by activation of liver X receptors and inhibition of fibroblast growth factor signaling. Moreover, single-cell RNA-sequencing analysis revealed a developmental dynamics similar to that of the endogenous human ventral midbrain and the emergence of high quality molecularly-defined midbrain cell types, including mDA neurons that become functional. Thus, our study identifies novel factors important for human midbrain development and opens the door for a future application of molecularly-defined hESC-derived midbrain cell types in Parkinsons disease.

neuroscience↗