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Bernardin, F.

Publications and source records attributed to Bernardin, F..

2 recordsLinked to original sources

Passage of time at the level of milliseconds: a new approach and a selective difficulty in individuals with schizophrenia

Background and HypothesisIndividuals with schizophrenia report that to them time sometimes feels discontinuous. Previous work has shown a link between the sense of self, and the ability to prepare to react to a target and to benefit from the passage of time, at the level of a few hundreds of milliseconds. However, the sense of time continuity requires a higher time resolution than examined in previous studies. Here we investigate to which extent individuals with schizophrenia and controls benefit from an increased delay when detecting asynchronies in the order of tens of milliseconds (stimulus onset asynchronies, i.e. SOA) between two successive visual stimuli. Study DesignWe re-analyzed three datasets and contrasted performance when the SOA increases, remains identical or decreases from trial t-1 to trial t. Study ResultsPerformance of all participants improved with an increase in the SOA, as the task became easier, but for controls more so than individuals with schizophrenia. These results are replicated across datasets, and were specific to the condition when SOA increased from one trial to the next. There was no significant group difference when the SOA decreased or remained identical. This was true even when the latter condition was more frequent, and when SOA magnitude was equalized across the conditions. Importantly, the difference between the two groups was specific to temporal judgements, and was not observed in a control masking task. ConclusionsWe suggest the results reveal a difficulty for individuals with schizophrenia to experience time at the level of milliseconds.

neuroscience↗

Highly multiplexed targeted plasma proteomics quantifies several hundred blood proteins in serum from colorectal carcinoma patients

The rapid analysis of human serum and plasma can provide deep insights into changes of the blood proteome in response to different patient treatments or diseases. Targeted proteomics techniques, like SRM and PRM, can be utilized to monitor proteins at high sensitivitym but so far were limited to smaller protein panels, which can be monitored in one experiment. The recently, on a Bruker tims-TOF pro mass spectrometer, developed parallel reaction monitoring-parallel accumulation - serial fragmentation (prm-PASEF) method expands the standard PRM method by using ion-mobility. The use of ion mobility as a fourth separation dimension increases the proteome coverage while reducing the length of the necessary chromatogeaphic separation. By combining an isotope-labeled reference standard, which covers 579 plasma proteins, we were able to quantify 565 proteins in plasma using prm-PASEF, with the least abundant protein being quantified at 7 amol. We continued the analysis by combining the isotype-labeled reference standard with dia-PASEF, which allowed the quantification of 549 proteins. Both methods were used to analyze 20 patient plasma samples from a colorectal cancer (CRC) cohort. The analysis identified 16 differentially regulated proteins between the CRC patient and control individual plasma samples. 15 of the 16 proteins showed a high correlation to the mRNA expression in CRC tumor samples, showing the technique s potential for the rapid identification of potential biomarkers in larger cohorts, abolishing the need for preselection of potential biomarker proteins. Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=68 SRC="FIGDIR/small/486663v1_ufig1.gif" ALT="Figure 1"> View larger version (15K): org.highwire.dtl.DTLVardef@eda5d4org.highwire.dtl.DTLVardef@220b01org.highwire.dtl.DTLVardef@1008757org.highwire.dtl.DTLVardef@1b56665_HPS_FORMAT_FIGEXP M_FIG C_FIG

biochemistry↗