Publications by authors named "Karen Zeise"

Article Synopsis
  • The text discusses a specific fungus that survives in the acidic environment of the human stomach, potentially causing conditions like ulcers and gastritis.
  • In research on mice, it was found that this fungus can induce localized gastritis without affecting the intestine, highlighting the stomach's vulnerability to fungal infections.
  • The study identified immune responses and gene expressions linked to fungal infection in a specific stomach region, suggesting the importance of further research on how this infection interacts with the host's immune system and microbiota.
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Article Synopsis
  • Scientists studied how certain bacteria affect stomach inflammation in mice, which can be similar to humans.
  • They found that the bacteria caused only a little inflammation but made the stomach produce more helpful substances against infections.
  • When the mice had a food allergy, their stomachs showed a strong immune response, but the bacteria didn’t make this response worse.
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Noradrenaline (norepinephrine) is known to modulate many physiological functions and behaviors. In this study, we tested to what extent astrocytes, a type of glial cell, participate in noradrenergic signaling in mouse primary visual cortex (V1). Astrocytes are essential partners of neurons in the central nervous system.

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Emerging studies have highlighted the disproportionate role of Candida albicans in influencing both early community assembly of the bacterial microbiome and dysbiosis during allergic diseases and intestinal inflammation. Nonpathogenic colonization of the human gastrointestinal (GI) tract by C. albicans is common, and the role of this single fungal species in modulating bacterial community reassembly after broad-spectrum antibiotics can be readily recapitulated in mouse studies.

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MultiFlow® DNA Damage-p53, γH2AX, Phospho-Histone H3 is a miniaturized, flow cytometry-based assay that provides genotoxic mode of action information by distinguishing clastogens, aneugens, and nongenotoxicants. Work to date has focused on the p53-competent human cell line TK6. While mammalian cell genotoxicity assays typically supply exogenous metabolic activation in the form of concentrated rat liver S9, this is a less-than-ideal approach for several reasons, including 3Rs considerations.

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