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cs.AI, q-bio.NC updates on arXiv.org
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DarkPatterns-LLM: A Multi-Layer Benchmark for Detecting Manipulative and Harmful AI Behavior
arXiv:2512.22470v1 Announce Type: new Abstract: The proliferation of Large Language Models (LLMs) has intensified concerns about manipulative or deceptive behaviors that can undermine user autonomy, trust, and well-being. Existing safety benchmarks predominantly rely on coarse binary labels and fail to capture the nuanced psychological and social mechanisms constituting manipulation. We introduce \textbf{DarkPatterns-LLM}, a comprehensive benchmark dataset and diagnostic framework for fine-grai
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cs.AI, q-bio.NC updates on arXiv.org
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Why AI Safety Requires Uncertainty, Incomplete Preferences, and Non-Archimedean Utilities
arXiv:2512.23508v1 Announce Type: new Abstract: How can we ensure that AI systems are aligned with human values and remain safe? We can study this problem through the frameworks of the AI assistance and the AI shutdown games. The AI assistance problem concerns designing an AI agent that helps a human to maximise their utility function(s). However, only the human knows these function(s); the AI assistant must learn them. The shutdown problem instead concerns designing AI agents that: shut down w
Why AI Safety Requires Uncertainty, Incomplete Preferences, and Non-Archimedean Utilities
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cs.AI, q-bio.NC updates on arXiv.org
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Interpretable Link Prediction in AI-Driven Cancer Research: Uncovering Co-Authorship Patterns
arXiv:2512.22181v1 Announce Type: cross Abstract: Artificial intelligence (AI) is transforming cancer diagnosis and treatment. The intricate nature of this disease necessitates the collaboration of diverse stakeholders with varied expertise to ensure the effectiveness of cancer research. Despite its importance, forming effective interdisciplinary research teams remains challenging. Understanding and predicting collaboration patterns can help researchers, organizations, and policymakers optimize
Interpretable Link Prediction in AI-Driven Cancer Research: Uncovering Co-Authorship Patterns
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cs.AI, q-bio.NC updates on arXiv.org
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LLM-Guided Exemplar Selection for Few-Shot Wearable-Sensor Human Activity Recognition
arXiv:2512.22385v1 Announce Type: cross Abstract: In this paper, we propose an LLM-Guided Exemplar Selection framework to address a key limitation in state-of-the-art Human Activity Recognition (HAR) methods: their reliance on large labeled datasets and purely geometric exemplar selection, which often fail to distinguish similar weara-ble sensor activities such as walking, walking upstairs, and walking downstairs. Our method incorporates semantic reasoning via an LLM-generated knowledge prior t
LLM-Guided Exemplar Selection for Few-Shot Wearable-Sensor Human Activity Recognition
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cs.AI, q-bio.NC updates on arXiv.org
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MedGemma vs GPT-4: Open-Source and Proprietary Zero-shot Medical Disease Classification from Images
arXiv:2512.23304v1 Announce Type: cross Abstract: Multimodal Large Language Models (LLMs) introduce an emerging paradigm for medical imaging by interpreting scans through the lens of extensive clinical knowledge, offering a transformative approach to disease classification. This study presents a critical comparison between two fundamentally different AI architectures: the specialized open-source agent MedGemma and the proprietary large multimodal model GPT-4 for diagnosing six different disease
MedGemma vs GPT-4: Open-Source and Proprietary Zero-shot Medical Disease Classification from Images
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cs.AI, q-bio.NC updates on arXiv.org
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Generating Verifiable Chain of Thoughts from Exection-Traces
arXiv:2512.00127v2 Announce Type: replace-cross Abstract: Teaching language models to reason about code execution remains a fundamental challenge. While Chain-of-Thought (CoT) prompting has shown promise, current synthetic training data suffers from a critical weakness: the reasoning steps are often plausible-sounding explanations generated by teacher models, not verifiable accounts of what the code actually does. This creates a troubling failure mode where models learn to mimic superficially c
Generating Verifiable Chain of Thoughts from Exection-Traces
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Cell Death Discovery nature.com science feeds
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Modeling hepatocellular carcinoma and its microenvironment on a chip
Cell Death Discovery, Published online: 29 December 2025; doi:10.1038/s41420-025-02917-8Modeling hepatocellular carcinoma and its microenvironment on a chip
Modeling hepatocellular carcinoma and its microenvironment on a chip
Cell Death Discovery, Published online: 29 December 2025; doi:10.1038/s41420-025-02917-8
Modeling hepatocellular carcinoma and its microenvironment on a chip-
(Multiomics OR Omics) AND (Lung OR gastric OR Hepatocellular)
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Metabolic signatures in gastroenteropancreatic neuroendocrine neoplasms: unraveling diagnostic and prognostic insights
Front Endocrinol (Lausanne). 2025 Dec 11;16:1676021. doi: 10.3389/fendo.2025.1676021. eCollection 2025.ABSTRACTGastroenteropancreatic neuroendocrine neoplasms (GEP-NENs) are a heterogeneous group of tumors characterized by diverse biological behaviors and variable clinical outcomes. Recent advances have highlighted the important role of metabolic reprogramming in tumorigenesis, progression, and therapeutic resistance in GEP-NENs. In this review, we synthesize the current evidence on metabolic bi
Metabolic signatures in gastroenteropancreatic neuroendocrine neoplasms: unraveling diagnostic and prognostic insights
Front Endocrinol (Lausanne). 2025 Dec 11;16:1676021. doi: 10.3389/fendo.2025.1676021. eCollection 2025.
ABSTRACT
Gastroenteropancreatic neuroendocrine neoplasms (GEP-NENs) are a heterogeneous group of tumors characterized by diverse biological behaviors and variable clinical outcomes. Recent advances have highlighted the important role of metabolic reprogramming in tumorigenesis, progression, and therapeutic resistance in GEP-NENs. In this review, we synthesize the current evidence on metabolic biomarkers and altered metabolic pathways-particularly those involving glucose, lipid, and amino acid metabolism. Key biomarkers such as GLUT-1, FASN, and enzymes involved in ferroptosis, cholesterol biosynthesis, and amino acid catabolism demonstrate strong associations with tumor aggressiveness, hypoxia, and mTOR signaling. Moreover, metabolomic profiling and functional studies suggest that metabolic markers may inform prognosis and predict response to targeted therapies such as Everolimus. Although promising, the clinical translation of these markers is still limited and requires further validation in large, subtype-specific cohorts. Our findings highlight the importance of integrating metabolic profiling into the diagnostic and therapeutic landscape of GEP-NENs. Future research should prioritize biomarker standardization, multi-omics integration, and the development of metabolism-based therapeutic strategies tailored to tumor subtype and differentiation grade.
PMID:41458541 | PMC:PMC12738315 | DOI:10.3389/fendo.2025.1676021