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Purpose: Artificial intelligence (AI)-automated tumor delineation for pediatric gliomas would enable real-time volumetric evaluation to support diagnosis, treatment response assessment, and clinical decision-making. Auto-segmentation algorithms for pediatric tumors are rare, due to limited data availability, and algorithms have yet to demonstrate clinical translation.
Methods: We leveraged two datasets from a national brain tumor consortium (n=184) and a pediatric cancer center (n=100) to develop, externally validate, and clinically benchmark deep learning neural networks for pediatric low-grade glioma (pLGG) segmentation using a novel in-domain, stepwise transfer learning approach. The best model [via Dice similarity coefficient (DSC)] was externally validated and subject to randomized, blinded evaluation by three expert clinicians wherein clinicians assessed clinical acceptability of expert- and AI-generated segmentations via 10-point Likert scales and Turing tests.
Results: The best AI model utilized in-domain, stepwise transfer learning (median DSC: 0.877 [IQR 0.715-0.914]) versus baseline model (median DSC 0.812 [IQR 0.559-0.888]; <0.05). On external testing (n=60), the AI model yielded accuracy comparable to inter-expert agreement (median DSC: 0.834 [IQR 0.726-0.901] vs. 0.861 [IQR 0.795-0.905], =0.13). On clinical benchmarking (n=100 scans, 300 segmentations from 3 experts), the experts rated the AI model higher on average compared to other experts (median Likert rating: 9 [IQR 7-9]) vs. 7 [IQR 7-9], <0.05 for each). Additionally, the AI segmentations had significantly higher (<0.05) overall acceptability compared to experts on average (80.2% vs. 65.4%). Experts correctly predicted the origins of AI segmentations in an average of 26.0% of cases.
Conclusions: Stepwise transfer learning enabled expert-level, automated pediatric brain tumor auto-segmentation and volumetric measurement with a high level of clinical acceptability. This approach may enable development and translation of AI imaging segmentation algorithms in limited data scenarios.
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http://dx.doi.org/10.1101/2023.06.29.23292048 | DOI Listing |
Inorg Chem
September 2025
School of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang 212013, PR China.
Confronting the dual challenges of carbon neutrality and sustainable energy, photocatalytic CO reduction requires precise control over product selectivity. This study demonstrates that surface hydroxyl (-OH) density serves as a molecular switch for reaction pathways in graphene oxide/cobalt tetraphenylporphyrin (GO/CoTPP) hybrids. By tuning the reduction degree of GO supports via gradient hydrazine hydrate treatment (0-85%), we constructed catalysts with controlled -OH concentrations.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
Surface Science Laboratory, Department of Materials and Geosciences, Technical University of Darmstadt, Peter-Grünberg-Straße 4, 64287 Darmstadt, Germany.
The performance of NiO-based electrocatalysts for the oxygen evolution reaction (OER) is strongly influenced by the interface between the metal support (current collector) and the catalyst layer, which modulates electronic properties and electrochemical activity. This study systematically investigates the solid-solid interface behavior of NiO thin films prepared by reactive magnetron sputtering on Pt, Au, and Ni, followed by electrochemical characterization. Stepwise NiO deposition and X-ray photoelectron spectroscopy reveal distinct band alignment and electronic structure differences at the metal-catalyst interface.
View Article and Find Full Text PDFChemistry
September 2025
Department of Inorganic and Physical Chemistry, Indian Institute of Science, Bangalore, 560012, India.
Rigid and conformationally restricted dichalcogenides based on 1,8-naphthyl system have attracted significant interest as electron donors in charge transfer complexes and organic electrode materials. Recently, naphthalene-1,8-peri-diselenides have been shown to mimic the function of two major selenoenzymes - iodothyronine deiodinase (Dio) and glutathione peroxidase (GPx) - mainly through two-electron redox processes involving deiodination of thyroid hormones and thiol-mediated reduction of hydrogen peroxide, respectively. Herein, we report that naphthalene-1,8-peri-dichalcogenides can mediate a six-electron reduction of organic nitro compounds to produce the corresponding primary amines at physiologically relevant temperature (37 °C) using water as the solvent.
View Article and Find Full Text PDFChem Sci
August 2025
School of Chemistry and Chemical Engineering, Shandong University of Technology Zibo 255000 P. R. China
Natural photosynthesis, a quintessential energy conversion process sustaining life on Earth through its sophisticated multi-step energy transfer cascades, has inspired the development of artificial light-harvesting systems aimed at mimicking its efficiency and complexity. Here, we report a supramolecular energy transfer platform constructed electrostatic interactions between sodium polystyrene sulfonate (RSS) and a quaternary ammonium salt modified cyano-substituted phenylenevinylene derivative (PPTA) in HO medium, achieving a sequential four-step energy relay. Energy is sequentially transferred from the PPTA-RSS complex to eosin Y (EY), rhodamine B (RhB), sulforhodamine 101 (SR101), and cyanine 5 (Cy5), with stepwise enhancement in superoxide anion radical (O˙) generation efficiency.
View Article and Find Full Text PDFPlant Cell Physiol
August 2025
Department of Applied Chemistry, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8654, Japan.
Photosystem II (PSII) catalyzes the light-driven oxidation of water, progressing via sequential oxidation states (S-states) of the Mn4CaO5 cluster. Among structural snapshots of intermediate S-states obtained using X-ray free-electron laser (XFEL) crystallography, two-flash XFEL structures assigned to the S3 state reveal an additional oxygen atom (O6) near the O5 site of the cluster, leading to proposals that O6 is incorporated as a new substrate water molecule during the S2 to S3 transition. However, recent re-analyses of the XFEL data highlight potential complications, including conformational heterogeneity, refinement bias, and possible radiation-induced artifacts.
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