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Digital pathology has made significant advances in tumor diagnosis and segmentation; however, image variability resulting from tissue preparation and digitization - referred to as domain shift - remains a significant challenge. Variations caused by heterogeneous scanners introduce color inconsistencies that negatively affect the performance of segmentation algorithms. To address this issue, we have developed a joint multitask U-net architecture trained for both segmentation and stain separation. This model isolates the stain matrix and stain density, allowing it to handle color variations and improve generalization across different scanners. On 180 stain images from three different scanners, our model achieved a Dice score of 0.898 and an Intersection Over Union (IoU) score of 0.816, outperforming conventional supervised learning methods by +1.5% and +2.5%, respectively. On external datasets containing images from six different scanners, our model averaged a Dice score and IoU of 0.792. By leveraging our novel approach to stain separation, we improved segmentation accuracy and generalization across diverse histopathological samples. These advances may pave the way for more reliable and consistent diagnostic tools for breast adenocarcinoma.
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http://dx.doi.org/10.3233/SHTI250272 | DOI Listing |
Mikrochim Acta
September 2025
Department of Public Health Laboratory Sciences, College of Public Health, Hengyang Medical School, University of South China, 28 Changsheng West Road, Hengyang, 421001, Hunan, China.
We systematically evaluated the DNA adsorption and desorption efficiencies of several nanoparticles. Among them, titanium dioxide (TiO₂) nanoparticles (NPs), aluminum oxide (Al₂O₃) NPs, and zinc oxide (ZnO) NPs exhibited strong DNA-binding capacities under mild conditions. However, phosphate-mediated DNA displacement efficiencies varied considerably, with only TiO₂ NPs showing consistently superior performance.
View Article and Find Full Text PDFCytoskeleton (Hoboken)
September 2025
Department of Biology, Lakeland Community College, Kirtland, Ohio, USA.
Elastic tethers connect telomeres of separating chromosomes in anaphase of animal cells. Immunofluorescence staining of titin in crane-fly spermatocytes, using 4 different antibodies, shows that the giant elastic protein titin seems to be a component of mitotic tethers: titin "strands" extend between separating chromosomes, connecting their telomeres, just as tethers do. Since titin is responsible for elastic forces in myofibrils, we suggest that titin is responsible for the backwards forces exerted on chromosome arms during anaphase.
View Article and Find Full Text PDFiScience
September 2025
Department of Animal Science, University of Connecticut, 1390 Storrs Road, Storrs, CT 06269-4163, USA.
Recent studies suggested that treating sperm with R848, a ligand for the X-linked Toll-like receptors 7 and 8 (TLR7/8) in mice, goats, and cattle, could selectively reduce the motility of X chromosome bearing sperm (X-sperm). This reduction enables the separation of X- and Y-sperm and thereby sex selection. However, through three species and multiple methods, our results challenged prior published data.
View Article and Find Full Text PDFEnviron Pollut
September 2025
Department of Aquatic Life Medicine, Jeju National University, Jeju 63243, Republic of Korea; Department of Marine Life Science, Jeju National University, Jeju 63243, Republic of Korea. Electronic address:
In this study, Cyprinus carpio nudus were exposed for 2 weeks to polyethylene microplastics (MPs) of two particle sizes (125 μm and 34 μm) at concentrations of 0, 40, 80, 160, 320, and 640 ppm. The experiment involved 11 treatment groups, each with triplicate tanks, and evaluated MPs accumulation in tissues, hematological profiles, plasma components, and antioxidant responses. Accumulation in the gill, intestine, and liver were quantified using Nile red staining and fluorescence microscopy, showing the highest accumulation in the intestine, followed by the gill and liver, with smaller MPs accumulated significantly more than larger MPs.
View Article and Find Full Text PDFSpecific protein detection plays a crucial role in biological analysis and clinical diagnostics, serving as an essential tool for disease diagnosis, therapeutic monitoring, and biological research. However, conventional methods such as immunofixation electrophoresis (IFE) and western blotting (WB) suffer from complex workflows, time-consuming operations, and limited quantification capabilities owing to intricate staining and de-staining procedures. In addition, these traditional immunological detection methods require extensive manual handling and specialized expertise, while low levels of automation restrict their applicability to high-throughput or large-scale analysis scenarios.
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