Publications by authors named "M Reynders"

Article Synopsis
  • - The Human Respiratory Syncytial Virus (HRSV) significantly impacts young children and the elderly, with two main subtypes (A and B) and various genotypes, making it a focus of surveillance in Belgium.
  • - This study analyzed HRSV circulation in Belgium over eight seasons (2011-2019) prior to the COVID-19 pandemic, testing nearly 27,400 respiratory samples for HRSV using advanced PCR techniques.
  • - Findings showed a consistent winter pattern of HRSV with both subtypes co-existing; notably, subtype A strains with a specific genetic duplication replaced other strains from the 2014-2015 season onwards.
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Background: Prematurity remains one of the main causes of neonatal morbidity and mortality. Approximately two thirds of preterm births are spontaneous, i.e.

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Background: Reactive case detection (RCD) aims to reduce malaria transmission stemming from asymptomatic carriers. Symptomatic individuals diagnosed with malaria at a health centre are followed to their households, where members of the index case and neighbouring households are tested and treated for malaria. An RCD programme was tested in the Ashanti region of Ghana in order to study diagnostic accuracy in the hospital and household settings, assess the prevalence of subclinical infections and possible clustering in index case households, and identify operational challenges for future RCD programmes.

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Retinoic acid receptor-related orphan receptor γ (RORγ) is a nuclear hormone receptor with multiple biological functions in circadian clock regulation, inflammation, and immunity. Its cyclic temporal role in circadian rhythms, and cell-specific activity in the immune system, make it an intriguing target for spatially and temporally localised pharmacology. To create tools that can study RORγ biology with appropriate spatiotemporal resolution, we designed light-dependent inverse RORγ agonists by building azobenzene photoswitches into ligand consensus structures.

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Azobenzene analogues of the tubulin polymerisation inhibitor combretastatin A4 (PSTs) were previously developed to optically control microtubule dynamics in living systems, with subsecond response time and single-cell spatial precision, by reversible photoswitching of their bioactivity with near-UV/visible light. First-generation PSTs were sufficiently potent and photoswitchable for use in live cells and embryos. However, the link between their seconds-scale and hours-scale bioactivity remained untested.

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