Publications by authors named "K N Avery"

Background: Oesophago-gastric cancer surgery negatively affects quality of life with a high postoperative symptom burden. Several conditions that may be diagnosed and treated after surgery are recognised. However, consensus regarding their definition and management is lacking.

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  • Variably Protease Sensitive Prionopathy (VPSPr) is a rare, fatal human prion disease that differs from other prion diseases like Creutzfeldt-Jakob disease (CJD), particularly in the sensitivity of its prion proteins to digestion by proteinase.
  • The disease is characterized by distinctive protein fragments (23, 17, and 7 kDa) that arise after digestion, especially notable in cases with the codon 129 VV genotype, where a unique 7 kDa fragment can be harder to identify with traditional methods.
  • Researchers have found that using capillary electrophoresis (CE) offers a more sensitive and reproducible approach for detecting and analyzing these prion proteins, allowing for
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The recent occurrence of the Covid-19 pandemic and frequent wildfires have worsened pulmonary diseases and raised the urgent need for investigating host-pathogen interactions and advancing drug and vaccine therapies. Historically, research and experimental studies have relied on two-dimensional cell culture dishes and/or animal models, which suffer from physiological differences from the human lung. More recently, there has been investigation into the use of lung-on-a-chip models and organoids, while the use of bioprinting technologies has also emerged to fabricate three-dimensional constructs or lung models with enhanced physiological relevance.

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T-cell activation is a multistep process requiring T-cell receptor engagement by peptide-major histocompatibility complexes (Signal 1) coupled with CD28-mediated costimulation (Signal 2). Tumors typically lack expression of CD28 ligands, so tumor-specific Signal 1 (e.g.

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Background: Tumor heterogeneity is a main contributor of resistance to anti-cancer targeted agents though it has proven difficult to study. Unfortunately, model systems to functionally characterize and mechanistically study dynamic responses to treatment across coexisting subpopulations of cancer cells remain a missing need in oncology.

Methods: Using single cell cloning and expansion techniques, we established monoclonal cell subpopulations (MCPs) from a commercially available epidermal growth factor receptor (EGFR)-mutant non-small cell lung cancer cell line.

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