Abstract Renal pathology relies on multiple special stains—including H0.85. Virtual stains restored key elements—including basement membranes, mesangial matrix, tubular epithelium, and interstitial collagen—closely matching chemical references. Large-region predictions preserved coherent architecture. Virtual PAS and AFOG highlighted basement membranes, glycogen-rich areas, collagen deposition, and casts, supporting interpretation of glomerular injury and interstitial fibrosis. Robust performance was maintained in thick tissues (10–50 μm), where chemical stains often show uneven penetration; virtual stains preserved uniform contrast and delineated overlapping structures. Multiplexing enabled consistent visualization of basement membrane thickening, mesangial expansion, and inflammation within the same section, removing serial-section artifacts.Holotomography with generative translation enables reliable, label-free virtual multiplexed staining, producing H Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 1450.
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Jeong et al. (Fri,) studied this question.
www.synapsesocial.com/papers/69d1fd13a79560c99a0a2df0 — DOI: https://doi.org/10.1158/1538-7445.am2026-1450
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:
Siwon Jeong
J. I. Park
Hyun-Seok Min
Cancer Research
Yonsei University
Korea Advanced Institute of Science and Technology
Korea Atomic Energy Research Institute
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