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A Plasticity Framework for Hoarding Disorder: Cross-Disorder Genomic Comparisons Reveal Divergent Compulsivity Mechanisms
Ngo Cheung
Posted: 06 January 2026
The 3D Collagen Network as a Determinant of Tumor Progression and Drug Delivery Efficiency in Breast Adenocarcinoma
Mariana Hirata
,Rogerio Padovan Gonçalves
,Maria Eduarda Teixeira Pereira Cândido da Silva
,Geovanna de Castro Feitosa
,Caio Sérgio Galina Spilla
,Domingos Donizeti Roque
,Lisete Horn Belon Fernandes
,Virgínia Maria Cavallari Strozze Catharin
,Vitor Cavallari Strozze Catharin
,Leila Maria Guissoni Campos
+8 authors
Background/Objectives: Breast cancer is a biologically complex malignancy whose high prevalence and therapeutic resistance represent a continuous challenge for global health. The Tumor Microenvironment (TME) is a crucial component in disease progression, and the Extracellular Matrix (ECM), particularly its 3D collagen architecture, is recognized for mediating interactions that influence invasion, metastasis, and pharmacological response. This review aims to critically synthesize recent evidence to elucidate the multifaceted role of collagen in the progression and modulation of therapeutic response in breast adenocarcinoma. Methods: A comprehensive literature review was conducted, analyzing studies addressing specific collagen subtypes, ECM stiffening (fibrosis), biomechanical signaling, and its impact on drug transport kinetics and immunomodulatory effects. Results: The results demonstrate that structural alterations of collagen not only orchestrate a pro-tumoral microenvironment, fostering aggressive phenotypes and immune evasion, but also create a physical barrier that compromises drug delivery efficiency and promotes metastatic dissemination. The synthesis of the data reinforces collagen as a potent prognostic biomarker and a promising therapeutic target for overcoming stroma-mediated resistance. Conclusions: Targeting the collagen-rich stroma and its 3D network is a critical frontier for therapeutic innovation. Developing adjuvant strategies to modulate the ECM has the potential to enhance clinical outcomes and optimize the distribution of antineoplastic agents, especially in patients with high degrees of tumor fibrosis.
Background/Objectives: Breast cancer is a biologically complex malignancy whose high prevalence and therapeutic resistance represent a continuous challenge for global health. The Tumor Microenvironment (TME) is a crucial component in disease progression, and the Extracellular Matrix (ECM), particularly its 3D collagen architecture, is recognized for mediating interactions that influence invasion, metastasis, and pharmacological response. This review aims to critically synthesize recent evidence to elucidate the multifaceted role of collagen in the progression and modulation of therapeutic response in breast adenocarcinoma. Methods: A comprehensive literature review was conducted, analyzing studies addressing specific collagen subtypes, ECM stiffening (fibrosis), biomechanical signaling, and its impact on drug transport kinetics and immunomodulatory effects. Results: The results demonstrate that structural alterations of collagen not only orchestrate a pro-tumoral microenvironment, fostering aggressive phenotypes and immune evasion, but also create a physical barrier that compromises drug delivery efficiency and promotes metastatic dissemination. The synthesis of the data reinforces collagen as a potent prognostic biomarker and a promising therapeutic target for overcoming stroma-mediated resistance. Conclusions: Targeting the collagen-rich stroma and its 3D network is a critical frontier for therapeutic innovation. Developing adjuvant strategies to modulate the ECM has the potential to enhance clinical outcomes and optimize the distribution of antineoplastic agents, especially in patients with high degrees of tumor fibrosis.
Posted: 06 January 2026
The Synthesis of Tetrakis(N,N-Dimethylaminomethyl)ferrocene and its Bimetallic Nickel(II) Dichloride Complex: Key Precursors for Methoxycarbonylation Ligands
Ian R. Butler
,Peter N. Horton
,William Clegg
,Simon J. Coles
,Lorretta Murphy
,Steven Elliott
The family of N,N-dimethylaminomethylferrocenes is one of the most important in ferrocene chemistry. They serve as precursors for a range of anti-malaria and anti-tumour medicinal compounds in addition to being key precursors for ferrocene ligands in the Lucite alpha process. A brief discussion on the importance of, and the synthesis of N,N-dimethylaminomethyl-substituted ferrocenes preludes the synthesis of the new ligand 1,1´,2,2´-tetrakis-(N,N-dimethylaminomethyl)ferrocene. The crystal structure of this compound is reported and a comparison is made with its disubstituted analogue, 1,2-bis-(N,N-dimethylaminomethyl)ferrocene. The tetrahedral nickel dichloride complexes of both these ligands have been crystallographically characterised. Finally, a pointer to future research in the area is given which includes a discussion of a new method to extract ferrocenylmethylamines from mixtures using additives and a new synthetic avenue from substituted cyclopentadiene itself.
The family of N,N-dimethylaminomethylferrocenes is one of the most important in ferrocene chemistry. They serve as precursors for a range of anti-malaria and anti-tumour medicinal compounds in addition to being key precursors for ferrocene ligands in the Lucite alpha process. A brief discussion on the importance of, and the synthesis of N,N-dimethylaminomethyl-substituted ferrocenes preludes the synthesis of the new ligand 1,1´,2,2´-tetrakis-(N,N-dimethylaminomethyl)ferrocene. The crystal structure of this compound is reported and a comparison is made with its disubstituted analogue, 1,2-bis-(N,N-dimethylaminomethyl)ferrocene. The tetrahedral nickel dichloride complexes of both these ligands have been crystallographically characterised. Finally, a pointer to future research in the area is given which includes a discussion of a new method to extract ferrocenylmethylamines from mixtures using additives and a new synthetic avenue from substituted cyclopentadiene itself.
Posted: 06 January 2026
Planck-Hubble-Hawking Universe: Light-Speed Rotation, No Shear, No Vorticity, 8 m/s Horizon Expansion
U.V. S. Seshavatharam
,S. Lakshminarayana
Posted: 06 January 2026
Divergent Inflammatory Profiles but No Predictive Biomarkers of Psychiatric Sequelae After Viral Infection: A 12-Month Cohort Study
Piotr Lorkiewicz
,Justyna Adamczuk
,Justyna Kryńska
,Mateusz Maciejczyk
,Małgorzata Żendzian-Piotrowska
,Robert Flisiak
,Anna Moniuszko – Malinowska
,Napoleon Waszkiewicz
Posted: 06 January 2026
Risks on Sustainable Supply Chain and Logistics
Batoul Modarress-Fathi
,Alexander Ansari
,Al Ansari
Posted: 06 January 2026
Soil Types and Degradation Pathways in Saudi Arabia: A Geospatial Approach for Sustainable Land Management
Saif Alharbi
,Khalid Al Rohily
Posted: 06 January 2026
PV Modules Stored on Farmlands after Repowering: Sustainability and Environmental Impact
Martin Kozelka
,Jiří Marcan
,Vladislav Poulek
,Václav Beránek
,Tomáš Finsterle
,Agnieszka Klimek-Kopyra
,Marcin Kopyra
,Martin Libra
,František Kumhála
Ground‑mounted photovoltaics, including agrivoltaic concepts, are increasingly deployed on agricultural land. In practice, damaged modules from repowering modules are sometimes stored on‑site for prolonged periods, creating localized vegetation suppression and land‑stewardship concerns that are rarely quantified. We present two anonymized case studies from Czechia (nominal capacities of 0.861 and 1.109 MWp; commissioned 2010 and 2009; repowered 2022 and 2021), where cracked backsheets and/or broken front‑glass modules were stacked and stored directly on grasslands within PV parcels. Using GIS delineation on orthophotos supported by field photographs, we quantified the land area (19,560 and 22,100 m²), PV panel area (plan‑ view; 4,960 and 5,080 m²), and stored PV module area (plan‑ view storage footprint; 109 and 100 m²). Stored module counts were estimated from visible stacks (≈1800 and ≈2000 modules). Using a conservative mass range of 18–25 kg/module, the stored masses were ~32–45 t and ~36–50 t, respectively. Although the storage footprints constitute <1% of the land area, they create persistent “dead zones” on agricultural land and concentrate tens of tonnes of material directly on the soil. We discuss regulatory and economic barriers to timely removal in the context of circular‑economic goals and propose practical reporting indicators for repowering projects on agricultural land: Astore (m²), Nstore (pcs), Mstore (t), storage duration, condition class, and storage interface.
Ground‑mounted photovoltaics, including agrivoltaic concepts, are increasingly deployed on agricultural land. In practice, damaged modules from repowering modules are sometimes stored on‑site for prolonged periods, creating localized vegetation suppression and land‑stewardship concerns that are rarely quantified. We present two anonymized case studies from Czechia (nominal capacities of 0.861 and 1.109 MWp; commissioned 2010 and 2009; repowered 2022 and 2021), where cracked backsheets and/or broken front‑glass modules were stacked and stored directly on grasslands within PV parcels. Using GIS delineation on orthophotos supported by field photographs, we quantified the land area (19,560 and 22,100 m²), PV panel area (plan‑ view; 4,960 and 5,080 m²), and stored PV module area (plan‑ view storage footprint; 109 and 100 m²). Stored module counts were estimated from visible stacks (≈1800 and ≈2000 modules). Using a conservative mass range of 18–25 kg/module, the stored masses were ~32–45 t and ~36–50 t, respectively. Although the storage footprints constitute <1% of the land area, they create persistent “dead zones” on agricultural land and concentrate tens of tonnes of material directly on the soil. We discuss regulatory and economic barriers to timely removal in the context of circular‑economic goals and propose practical reporting indicators for repowering projects on agricultural land: Astore (m²), Nstore (pcs), Mstore (t), storage duration, condition class, and storage interface.
Posted: 06 January 2026
Bayesian Elastic‑Net Cox Models for Time‑to‑Event Prediction: Application with Breast‑Cancer Cohort
Ersin Yılmaz
,Syed Ejaz Ahmed
,Dursun Aydın
Posted: 06 January 2026
The Philosophy of Marriage in India: A Tripartite Analysis of Contract, Institution, and Moral Bond
Shashank Tiwari
Posted: 06 January 2026
Graphene Oxide Nanoparticles Mediated Protective Effect Against the Ethanol Induced Gut-Liver Axis by Targeting miRNA-203a and miRNA-122
Hiral Aghara
,Teja Naveen Sata
,Prashsti Chadha
,Manali Patel
,Md Ismail
,Deeksha Rajput
,Pooja Gori
,Sriram Kanvah
,Manan Raval
,Senthil Kumar Venugopal
+1 authors
Posted: 06 January 2026
Large Language Models for Continual Relation Extraction
Sefika Efeoglu
,Adrian Paschke
,Sonja Schimmler
Posted: 06 January 2026
Quantum-Enhanced Adaptive Graph Convolutional Networks for Sentiment Representation Learning
Mingrui Rao
,Zihan Long
Posted: 06 January 2026
AEP-M: AI-Enhanced Anonymous E-Payment for Mobile Devices Using ARM Trust Zone and Divisible E-Cash
Vimal Teja Manne
Posted: 06 January 2026
Novel Silicone-Polyol Antifoam Emulsions: Impact on Foam Control and Physiology of Diverse Microbial Cultures
Mikhail Frolov
,Trofim A. Lozhkarev
,Elmira A. Vasilieva
,Leysan A. Vasileva
,Almaz A. Zagidullin
,Lucia Ya. Zakharova
,Galim A. Kungurov
,Natalia V. Trachtmann
,Shamil Z. Validov
The selection of an optimal antifoam is critical for efficient fermentation, as industrial agents often have detrimental side effects like growth inhibition, while some can enhance productivity. This study presents a rational approach to developing and screening novel silicone-polyol antifoam emulsions. A key finding was the discovery of selective antibacterial activity in agent 3L10, which strongly inhibited Gram-positive bacteria (especially Corynebacterium glutamicum) but not Gram-negative strains. This specificity, likely mediated by interaction with the mycolic acid layer of C. glutamicum, highlights the necessity for strain-specific antifoam testing. A comprehensive evaluation protocol—combining chemical design, cytotoxicity screening across diverse microorganisms, determination of minimum effective concentrations (MEC), and validation in model bioreactor fermentations—was established. Through this process, agent 6T80 was identified as a promising candidate. It exhibited low MEC, high emulsion stability, no cytotoxicity, and did not impair growth or recombinant protein production in B. subtilis or P. putida fermentations. The study concludes that agent 6T80 is suitable for further application in processes involving Gram-negative and certain Gram-positive hosts, whereas agent 3L10 serves as a valuable tool for studying surfactant-membrane interactions. The developed methodology enables the targeted selection of highly efficient and biocompatible antifoams for specific biotechnological processes.
The selection of an optimal antifoam is critical for efficient fermentation, as industrial agents often have detrimental side effects like growth inhibition, while some can enhance productivity. This study presents a rational approach to developing and screening novel silicone-polyol antifoam emulsions. A key finding was the discovery of selective antibacterial activity in agent 3L10, which strongly inhibited Gram-positive bacteria (especially Corynebacterium glutamicum) but not Gram-negative strains. This specificity, likely mediated by interaction with the mycolic acid layer of C. glutamicum, highlights the necessity for strain-specific antifoam testing. A comprehensive evaluation protocol—combining chemical design, cytotoxicity screening across diverse microorganisms, determination of minimum effective concentrations (MEC), and validation in model bioreactor fermentations—was established. Through this process, agent 6T80 was identified as a promising candidate. It exhibited low MEC, high emulsion stability, no cytotoxicity, and did not impair growth or recombinant protein production in B. subtilis or P. putida fermentations. The study concludes that agent 6T80 is suitable for further application in processes involving Gram-negative and certain Gram-positive hosts, whereas agent 3L10 serves as a valuable tool for studying surfactant-membrane interactions. The developed methodology enables the targeted selection of highly efficient and biocompatible antifoams for specific biotechnological processes.
Posted: 06 January 2026
Comparative Evaluation of DeepLabCut Convolutional Neural Network Architectures for High-Precision Markerless Tracking in the Mouse Staircase Test
Valentin Fernandez
,Landoline Bonnin
,Christine Fernandez-Maloigne
Posted: 06 January 2026
Workflow for Buried Pipe Detection and Geotechnical Characterization in Conductive Clay–Marl Environments
Pedro Carrasco-García
,Arturo Zevallos
,Javier Carrasco-García
,Juan Ignacio Canelo-Perez
Posted: 06 January 2026
A Novel anti-Cadherin 19 Monoclonal Antibody (Ca19Mab-8) for Flow Cytometry, Western Blotting, and Immunohistochemistry
Guanjie Li
,Hiroyuki Suzuki
,Mika K. Kaneko
,Yukinari Kato
Posted: 06 January 2026
Breast Cancer Patient Attitudes Towards Oncology Drug Costs in Ireland
Matthew Cronin
,Ruth Kieran
,Clara Steele
,Katie Cooke
,Seamus O’Reilly
Posted: 06 January 2026
Genome-Scale Modeling–Guided Metabolic Engineering Enables Heterologous Production of 3,4-amino-4-hydroxybenzoic Acid in Streptomyces thermoviolaceus
Togo Yamada
,Pamella Apriliana
,Prihardi Kahar
,Tomoya Kobayashi
,Yutaro Mori
,Chiaki Ogino
Posted: 06 January 2026
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