ArticleBrain structure & function2025
Identification and characterization of the thalamic ventral posterior complex by 11.7T ex vivo diffusion tensor imaging.
Article in Brain structure & function, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
2 citing papers in PubMed.
- Submillimeter postmortem and in vivo diffusion and susceptibility magnetic resonance imaging to characterize cortical micro- and meso-structures.Research square · 2026Article
- Machine learning for classification of pediatric bipolar disorder with and without psychotic symptoms based on thalamic subregional structural volume.BMC psychiatry · 2025Article
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Authors and funding
5 authors.
Funding
Abstract
The thalamic ventral posterior (VP) nuclear complex includes several subnuclei, including the VPM, VPL, VPI, and VMb, each with distinct inputs, axonal trajectories, and staining properties. Understanding the three-dimensional organization of neuronal fiber structures of the VP complex is crucial for understanding intra-thalamic and thalamocortical connections related to somatosensory processing. In this study, an ex vivo block of the human brain was scanned using mesoscopic Diffusion Tensor Imaging (DTI), and the four VP subnuclei were identified using existing histological atlases as references. The VP subnuclei were characterized using a mean diffusivity (MeanD) map, orientation-coded fractional anisotropy (FA) map, and tractography obtained from DTI. The results demonstrated differential patterns in MeanD and orientation-coded FA maps among the four subnuclei, underscoring the potential of mesoscale imaging to identify and differentiate these subnuclei. The tractography identified patterns of afferent and efferent fibers unique to each nucleus, offering insights into their functional roles in sensory processing. The findings highlighted the advantages of DTI in visualizing the direction of fibrous structures and conducting three-dimensional tractography, offering a foundation for further investigations into in vivo imaging applications and the neural mechanisms of somatosensory disorders, including central pain syndrome.
Indexed as
Identifiers
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.