Publications by authors named "K E Kim"

Background: The recent introduction of generative artificial intelligence (AI) as an interactive consultant has prompted an interest in assessing its applicability in medical discussions and consultations, particularly in the domain of depression.

Objective: This study assessed the capability of Large Language Models (LLMs) in AI to generate responses to depression-related queries.

Methods: Utilizing the PubMedQA and QuoraQA datasets, we compared various LLMs, such as BioGPT, PMC-Llama, GPT-3.

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Sampling is a pivotal element in the design of metasurfaces, enabling a broad spectrum of applications. Despite its flexibility, sampling can result in reduced efficiency and unintended diffractions, which are more pronounced at high numerical aperture or shorter wavelengths, e.g.

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Recent studies have reported that monitoring spinal cord perfusion pressure (SCPP) using a pressure probe to measure "intraspinal pressure" (ISP) within the subdural space at the injury site may improve the hemodynamic management of acute spinal cord injury (SCI) patients. This study aimed to investigate, within a pig model of SCI, the relationship between the ISP measured within the subdural space and the "spinal cord pressure" (SCP) measured within the spinal cord itself. Specifically, we sought to characterize the changes to ISP and SCP over time, both rostral and caudal to the injury epicenter, and in relation to native spinal cord morphometry.

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To enhance the efficiency of vaccine manufacturing, this study focuses on optimizing the microfluidic conditions and lipid mix ratios of messenger RNA-lipid nanoparticles (mRNA-LNP). Different mRNA-LNP formulations ( = 24) were developed using an I-optimal design, where machine learning tools (XGBoost/Bayesian optimization and self-validated ensemble (SVEM)) were used to optimize the process and predict lipid mix ratio. The investigation included material attributes, their respective ratios, and process attributes.

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Spinal fusion surgery remains a significant challenge due to limitations in current bone graft materials, particularly in terms of bioactivity, integration, and safety. This study presents an innovative approach using an injectable hydroxyapatite/β-tricalcium phosphate (HA/β-TCP) hydrogel combined with stromal vascular fraction (SVF) and low-dose recombinant human BMP-2 (rhBMP-2) to enhance osteodifferentiation and angiogenesis. Through a series of in vitro studies and preclinical models involving rats and minipigs, we demonstrated that the hydrogel system enables the sustained release of rhBMP-2, resulting in significantly improved bone density and integration, alongside reduced inflammatory responses.

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