Showing 1,541 - 1,560 results of 15,421 for search 'F/LOSS~', query time: 3.20s Refine Results
  1. 1541

    Loss of pelagic fish and zooplankton density associated with subglacial upwelling in high Arctic estuaries may be mitigated by benthic habitat expansion following tidewater glacier retreat by Victor Gonzalez Triginer, Arunima Sen, Maxime Geoffroy, Børge Damsgård

    Published 2025-01-01
    “…In shallow fjords and areas with hard bottom substrate, it is expected that sea-ice and glacial retreat will promote macroalgal settlement, and we suggest that macroalgal expansion may compensate the loss of tidewater glacier-associated density of fish and zooplankton by the increase of benthic-driven density. …”
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  2. 1542

    Instruments for evaluating the parental emotional status and ecological support systems among parents who considered cochlear implantation for their children with hearing loss: A scoping review. by Tang Zhi Lim, Cila Umat, Pei-Hua Chen, Chun Hong Gan, Bee See Goh

    Published 2024-01-01
    “…<h4>Objectives</h4>Parents of children diagnosed with severe-to-profound sensorineural hearing loss may experience a range of emotions owing to a lack of knowledge and experience in dealing with such children. …”
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    Enhancing Thyroid Nodule Detection in Ultrasound Images: A Novel YOLOv8 Architecture with a C2fA Module and Optimized Loss Functions by Shidan Wang, Zi-An Zhao, Yuze Chen, Ye-Jiao Mao, James Chung-Wai Cheung

    Published 2025-01-01
    “…Building upon the YOLOv8 architecture, YOLO-Thyroid introduces the C2fA module—an extension of C2f that incorporates Coordinate Attention (CA)—to enhance feature extraction. Additionally, loss functions were incorporated, including class-weighted binary cross-entropy to alleviate class imbalance and SCYLLA-IoU (SIoU) to improve localization accuracy during boundary regression. …”
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  5. 1545

    Biallelic SLC13A1 loss-of-function variants result in impaired sulfate transport and skeletal phenotypes, including short stature, scoliosis, and skeletal dysplasia by Christina G. Tise, Katie Ashton, Lachlan de Hayr, Kun-Di Lee, Omkar L. Patkar, Emma Krzesinski, Jennifer A. Bassetti, Erin M. Carter, Cathleen Raggio, Andreas Zankl, Anas M. Khanshour, Kristhen N. Atala, Jonathan J. Rios, Carol A. Wise, Ying Zhu, Futao Zhang, Tony Roscioli, Michael Buckley, Robert J. Harvey, Paul A. Dawson

    Published 2025-01-01
    “…Functional studies were consistent with SLC13A1 variants resulting in the complete loss of sulfate transport activity. Conclusion: Biallelic loss-of-function variants in SLC13A1 are a novel cause of skeletal phenotypes in humans with a measurable biomarker. …”
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