Publications by authors named "Chanyang Uhm"

Backgrounds & Aims: Since the Omicron variant emerged as a major severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variant, COVID-19-associated mortality has decreased remarkably. Nevertheless, patients with a history of SARS-CoV-2 infection have been suffering from an aftereffect commonly known as 'long COVID,' affecting diverse organs. However, the effect of SARS-CoV-2 on gastric cells and disease progression was not previously known.

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The accumulation of photosensitizers (PSs) in lesion sites but not in other organs is an important challenge for efficient image guiding in photodynamic therapy. Cancer cells are known to express a significant number of albumin-binding proteins that take up albumin as a nutrient source. Here, we converted albumin to a novel BODIPY-like PS by generating a tetrahedral boron environment via a flick reaction.

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Article Synopsis
  • Intranasal infection is a common method to study SARS-CoV-2 in mice, but it often results in high mortality rates, limiting research on non-fatal COVID-19 cases.
  • Substituting intranasal administration with aerosolized inhalation shows unique and milder pathological features that align better with COVID-19 symptoms seen in patients, such as chest CT patterns.
  • The research indicates that the inhalation model allows for the study of long COVID and related interventions by mimicking non-fatal COVID-19 conditions more effectively than the intranasal method.
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Unlabelled: The Organization for Economic Co-operation and Development approved a reconstructed human epidermis (RHE) model for skin irritation and corrosion tests as an alternative to animal testing for cosmetics, which has been banned in the European Union since 2013. However, RHE models have several limitations, such as high manufacturing costs, a loose skin barrier, and inability to simulate all cellular and non-cellular components of the human epidermis. Therefore, new alternative skin models are needed.

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Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causing coronavirus disease 2019 (COVID-19) has been a global health concern since 2019. The viral spike protein infects the host by binding to angiotensin-converting enzyme 2 (ACE2) expressed on the cell surface, which is then processed by type II transmembrane serine protease. However, ACE2 does not react to SARS-CoV-2 in inbred wild-type mice, which poses a challenge for preclinical research with animal models, necessitating a human ACE2 (hACE2)-expressing transgenic mouse model.

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Background: Keratohyalin granules (KHGs) supply the critical epidermal protein constituents such as filaggrin for maintaining skin barrier function during epidermal differentiation; however, their regulating mechanism remains largely unelucidated.

Methods: To investigate the role of Ras-related protein Rab-25 (RAB25) expression in skin disease, we utilized skin specimens of patients with moderate-to-severe atopic dermatitis (AD) and healthy controls. To investigate the susceptibility of Rab25 knockout mice to AD, we established an oxazolone-induced AD model.

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Article Synopsis
  • SARS-CoV-2 is the virus responsible for COVID-19, leading to serious respiratory disease and complications in humans.
  • Researchers used K18-hACE2 mice and Syrian golden hamsters to study how the virus impacts hosts, focusing on symptoms, disease progression, and immune responses.
  • The study found that while K18-hACE2 mice experienced severe and fatal disease, Syrian golden hamsters had milder, reversible symptoms with no fatalities, highlighting differences in how these models react to the virus.
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