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In this paper, we study a stochastic susceptible-infected-susceptible (SIS) epidemic model that includes an additional immigration process. In the presence of multiplicative noise, generated by environmental perturbations, the model exhibits noise-induced transitions. The bifurcation diagram has two distinct regions of unimodality and bimodality in which the steady-state probability distribution has one and two peaks, respectively. Apart from first-order transitions between the two regimes, a critical-point transition occurs at a cusp point with the transition belonging to the mean-field Ising universality class. The epidemic model shares these features with the well-known Horsthemke-Lefever model of population genetics. The effect of vaccination on the spread/containment of the epidemic in a stochastic setting is also studied. We further propose a general vaccine-hesitancy model, along the lines of Kirman's ant model, with the steady-state distribution of the fraction of the vaccine-willing population given by the Beta distribution. The distribution is shown to give a good fit to the COVID-19 data on vaccine hesitancy and vaccination. We derive the steady-state probability distribution of the basic reproduction number, a key parameter in epidemiology, based on a beta-distributed fraction of the vaccinated population. Our study highlights the universal features that epidemic and vaccine models share with other dynamical models.
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http://dx.doi.org/10.1103/11qy-2gc3 | DOI Listing |
Medicine (Baltimore)
September 2025
Department of Pediatrics, Affiliated Hospital of Jining Medical University, Jining, Shandong Province, China.
Rationale: Weaver syndrome is a rare congenital overgrowth disorder characterized by a wide spectrum of clinical manifestations that often overlap with other overgrowth syndromes. It is primarily caused by pathogenic variants in the Enhancer of Zeste Homolog 2 (EZH2) gene on chromosome 7q36.1.
View Article and Find Full Text PDFCancer Sci
September 2025
Laboratory of Ploidy Pathology, Graduate School of Frontier Biosciences, The University of Osaka, Osaka, Japan.
Polyploid giant cancer cells (PGCCs) represent a unique and distinct subset of cancer cells, characterized by either an abnormally large nucleus or the presence of multiple nuclei within a single cell. An increasing body of evidence indicates that PGCCs are closely linked to cancer progression, therapeutic resistance, and poor clinical prognosis. However, despite their distinctive morphology, no universal marker has been identified to reliably distinguish PGCCs from other cancer cell populations.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Department of Chemical and Biomolecular Engineering, Department of Chemistry, Department of Materials Science and Engineering, Beckman Institute for Advanced Science and Technology, University of Illinois Urbana-Champaign,Urbana, Illinois 61801, United States.
Spontaneous chiral symmetry breaking remains a fascination in chemistry, biology, materials science, and even astronomy. Chiral symmetry breaking usually requires intrinsic molecular chirality or extrinsic chiral sources but remains rare in nonchiral systems. Here, we reveal a ubiquitous, entropy-driven chiral symmetry breaking mechanism observed in 22 out of 35 conjugated polymers in the absence of any chiral source─a phenomenon overlooked for decades.
View Article and Find Full Text PDFJ Vis Exp
August 2025
Department of Oncology, Division of Pediatric Oncology and Institute for Cell Engineering, The Johns Hopkins University School of Medicine;
Human cord blood (CB) myeloid progenitor reprogramming to a high-fidelity human induced pluripotent stem cell (hiPSC) state can be achieved using non-integrating episomal vectors and stromal signals. These conventional, primed CB-hiPSC lines can subsequently be chemically reverted with high efficiencies to a blastomere-like Tankyrase/PARP Inhibitor-Regulated Naive Stem Cell (TIRN-SC) state with functional totipotency. PARP-regulated TIRN-SCs are human stem cells with high epigenetic plasticity, stable epigenomic imprints, and have greater differentiation potency than conventional, lineage-primed hiPSCs.
View Article and Find Full Text PDFIEEE J Biomed Health Inform
September 2025
Short peptides and their structural modifications have demonstrated significant potential in the field of therapeutic drug development. During the research and development process, peptide-protein interaction plays a crucial role for screening highly effective peptides. Although traditional experimental methods can identity peptide-protein interactions, their time-consuming and resource-intensive nature make researchers develop various of computational alternatives.
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