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At least 253 records · Page 14Linked to original sources
PubMed2006

A practical VEP-based brain-computer interface.

This paper introduces the development of a practical brain-computer interface at Tsinghua University. The system uses frequency-coded steady-state visual evoked potentials to determine the gaze direction of the user. To ensure more universal applicability of the system, approaches for reducing user variation on system performance have been proposed. The information transfer rate (ITR) has been evaluated both in the laboratory and at the Rehabilitation Center of China, respectively. The system has been proved to be applicable to > 90% of people with a high ITR in living environments.

Adult↗
PubMed2006

Implementation of talairach atlas based automated brain segmentation for radiation therapy dosimetry.

Radiotherapy for brain cancer inevitably results in irradiation of uninvolved brain. While it has been demonstrated that irradiation of the brain can result in cognitive deficits, dose-volume relationships are not well established. There is little work correlating a particular cognitive deficit with dose received by the region of the brain responsible for the specific cognitive function. One obstacle to such studies is that identification of brain anatomy is both labor intensive and dependent on the individual performing the segmentation. Automatic segmentation has the potential to be both efficient and consistent. Brains2 is a software package developed by the University of Iowa for MRI volumetric studies. It utilizes MR images, the Talairach atlas, and an artificial neural network (ANN) to segment brain images into substructures in a standardized manner. We have developed a software package, Brains2DICOM, that converts the regions of interest identified by Brains2 into a DICOM radiotherapy structure set. The structure set can be imported into a treatment planning system for dosimetry. We demonstrated the utility of Brains2DICOM using a test case, a 34-year-old man with diffuse astrocytoma treated with three-dimensional conformal radiotherapy. Brains2 successfully applied the Talairach atlas to identify the right and left frontal, parietal, temporal, occipital, subcortical, and cerebellum regions. Brains2 was not successful in applying the ANN to identify small structures, such as the hippocampus and caudate. Further work is necessary to revise the ANN or to develop new methods for identification of small structures in the presence of disease and radiation induced changes. The segmented regions-of-interest were transferred to our commercial treatment planning system using DICOM and dose-volume histograms were constructed. This method will facilitate the acquisition of data necessary for the development of normal tissue complication probability (NTCP) models that assess the probability of cognitive complications secondary to radiotherapy for intracranial and head and neck neoplasms.

Adult↗
PubMed2026

Cell type resolved MR based on brain single cell eQTLs corroborated by single cell RNA sequencing uncovers neuroimmune and vascular programs in intracerebral hemorrhage.

BACKGROUND: Intracerebral hemorrhage (ICH) lacks effective neuroprotective therapies. We integrated cell type–resolved genetic inference with single-cell profiling to map putative causal programs and multicellular circuitry relevant to ICH. METHODS: Cis-eQTLs from eight human brain cell types were used as instruments for two-sample Mendelian randomization (MR), with an ICH meta-analysis from large biobanks and a stroke consortium as the outcome. Instruments were LD-pruned and restricted to strong variants (F > 10). Inverse-variance weighting (IVW) was the primary estimator, supported by robustness methods, heterogeneity/pleiotropy diagnostics, and false discovery rate control. Experimental validation used mouse collagenase ICH single-cell RNA-seq at 24 h (n = 3 sham; n = 3 ICH) with Seurat integration, composition testing, Slingshot pseudotime, and CellChat. An independent mouse cohort underwent qRT–PCR for selected genes. RESULTS: The ICH meta-analysis showed acceptable genomic control, supporting downstream MR. We identified 524 nominal gene–cell type associations, with a glia-weighted signal landscape. Enrichment implicated autophagy/mitophagy, antigen processing, cytoskeletal and vesicular trafficking, endothelial matrix–adhesion programs, ferroptosis, and myelin stress pathways. In mouse scRNA-seq, disease-associated microglia expanded with reciprocal loss of homeostatic microglia and increased neutrophils and T cells. Prioritized genes showed directional concordance; qRT–PCR confirmed ARPC3 and EIF2AK2 upregulation and TBCK and SPECC1 downregulation in ICH versus sham. Pseudotime supported a shift toward disease-associated microglial states, and CellChat indicated increased network interaction strength with microglia and endothelium as hubs. CONCLUSIONS: Cell type–specific MR combined with single-cell validation highlights neuroimmune and neurovascular programs in ICH and links genetic signals to state transitions and inferred intercellular communication.

Animals↗
PubMedDate not supplied

Frequency component selection for an ECoG-based brain-computer interface.

The aim of the present study was to investigate the most significant frequency components in electrocorticogram (ECoG) recordings in order to operate a brain computer interface (BCI). For this purpose the time-frequency ERD/ERS map and the distinction sensitive learning vector quantization (DSLVQ) are applied to ECoG from three subjects, recorded during a self-paced finger movement. The results show that the ERD/ERS pattern found in ECoG generally matches the ERD/ERS pattern found in EEG recordings, but has an increased prevalence of frequency components in the beta range.

Brain Mapping↗
PubMedDate not supplied

The Ca2+-dependent incorporation of nitrogenous bases into brain microsomal phospholipid subspecies in vitro.

The specificity of the Ca2+-stimulated choline and ethanolamine incorporation into the molecular subspecies of the correspondent choline and ethanolamine phosphoglycerides has been investigated in vitro in rat brain microsomes. In the presence of 5.0 mM Ca2+-ions and at pH 8.1, choline was incorporated 6 times faster into the tetraenoic diacyl-glycero-3-phosphorylcholines (diacyl-GPCs or lecithins) than into the saturated subspecies. The specific activities of the other species were intermediary, and decreased with increasing saturation. Hexaenoic species of lecithins were however weakly labelled. The rate of labelling of diacyl-GPC molecular subspecies was affected noticeably by changing the pH and the Ca2+-ion concentration of the incubation medium. Ethanolamine was incorporated in the presence of 2.5 mM Ca2+-ions and at pH 8.1 preferentially into the monoenoic species of total ethanolamine phosphoglycerides of rat brain microsomes. The rate of incorporation into the monoenoic species was twice that into the trienoic, tetraenoic and hexaenoic and 4 times faster that into the dienoic species. When the pattern of labelling was determined specifically for the molecular subspecies of diacyl-glycero-3-phosphorylethanolamines (diacyl-GPEs or phosphatidylethanolamines), the rate of incorporation of ethanolamine into the hexaenoic species resulted three times faster that into the saturated and monoenoic species and about twice that into the trienoic and tetraenoic species, in accordance with data for liver microsomes. The pattern of labelling of the molecular subspecies of ethanolamine phosphoglycerides and of diacyl-GPEs was not influenced by changing the pH and the Ca2+-ion concentration of the incubation medium.

Animals↗
PubMed1988

The anatomic and physiologic bases of brain stem auditory evoked potentials.

The generators of human BAEPs, as summarized in Table 1 and Figure 12, are more complex than has often been presumed. Most peaks reflect activity in several structures, though patterns of BAEP abnormality can be correlated with abnormalities in general areas of the brain stem. The phasic peaks originate in action potentials, whereas the SN reflects postsynaptic potentials within brain-stem auditory nuclei.

Acoustic Stimulation↗
PubMedDate not supplied

The Crib-O-Gram in the NICU: an evaluation based on brain stem electric response audiometry.

This study evaluated the Crib-O-Gram as a screening test for hearing loss in NICU infants using Brain Stem Electric Response Audiometry (BERA) as the standard. Two Crib-O-Gram tests were administered to 280 babies within 48 hours of BERA testing. An additional 26 babies received BERA and one Crib-O-Gram test. Correlation coefficients for the two Crib-O-Gram scalar scores were calculated separately for a group of preterm (31 to 37 weeks) and a group of full term and older (38 to 54 weeks) infants, with values of 0.36 and 0.52, respectively. This indicates that the Crib-O-Gram has poor reliability for a screening test, particularly for preterm babies. Approximately one-third of babies with normal BERA thresholds failed Crib-O-Gram screening. The identification of hearing loss by Crib-O-Gram increased with the severity of the loss. Crib-O-Gram was able to identify moderately severe hearing losses in full term and older babies.

Acoustic Stimulation↗