Publications by authors named "J J Bearss"

Coccidioidomycosis is a common cause of community-acquired pneumonia in endemic regions. Approximately 20 000 cases of coccidioidomycosis occur annually; however, this statistic is limited by a widespread lack of testing. Here, we analyze emergency medicine provider attitudes toward coccidioidal testing and assess the effect of an intervention to improve testing rates.

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Smallpox was the most rampant infectious disease killer of the 20th century, yet much remains unknown about the pathogenesis of the variola virus. Using archived tissue from a study conducted at the Centers for Disease Control and Prevention we characterized pathology in 18 cynomolgus macaques intravenously infected with the Harper strain of variola virus. Six macaques were placebo-treated controls, six were tecovirimat-treated beginning at 2 days post-infection, and six were tecovirimat-treated beginning at 4 days post-infection.

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Introduction: Pemigatinib is a selective small-molecule inhibitor of the fibroblast growth factor receptor (FGFR) 1-3. FGFR is associated with increased cell division, proliferation, and survival. Inhibition of this receptor is an effective treatment against tumors driven by activated fusions in FGFR2.

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Introduction: The treatment landscape of biliary cancers is rapidly changing. Inhibitors against the actionable targets FGFR and IDH1 are now being included in the treatment guidelines of multiple countries for patients with advanced cholangiocarcinoma. However, there remains an unmet need in identifying the mechanisms of resistance and treatment strategies involving possible tumor sequencing.

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Article Synopsis
  • Compound VBT-5445 is an inhibitor that blocks the interaction of Pim and EDC3, which helps regulate mRNA decay, and it also targets the Pim and mTORC protein kinases.
  • Structural modifications led to a series of VBT analogs that effectively reduce the growth of various cancers, such as pancreatic, prostate, breast, lung, and leukemia.
  • Notably, the GRG-1-34 derivative showed low toxicity in mice and has a suitable pharmacokinetic profile, suggesting it could be a promising candidate for future cancer treatment development.
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