Publications by authors named "Veronique Massonneau"

Prion diseases are characterized by deposits of abnormal conformers of the PrP protein. Although large aggregates of proteinase K-resistant PrP (PrP(res)) are infectious, the precise relationships between aggregation state and infectivity remain to be established. In this study, we have fractionated detergent lysates from prion-infected cultured cells by differential ultracentrifugation and ultrafiltration and have characterized a previously unnoticed PrP species.

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Article Synopsis
  • Researchers looked at how melatonin helps rat brains that are hurt early in development.
  • They gave melatonin to baby rats and found it helped fix problems in their brain cells, making them more mature.
  • The study suggests melatonin could be useful for protecting brains in newborns with damage and could help with brain diseases in older people too.
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White-matter damage is a leading cause of neurological handicap. Although hypoxia-ischemia and excitotoxicity are major pathogenic factors, a role for genetic influences was suggested recently. Thus, protracted gestational hypoxia was associated with white-matter damage (WMD) in rat pups but not in mouse pups.

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Synopsis of recent research by authors named "Veronique Massonneau"

  • - Veronique Massonneau's research primarily focuses on the mechanisms and effects of prion diseases, particularly in relation to the aggregation and infectivity of PrP(res) protein, as highlighted in her 2011 study where she identified a previously unnoticed PrP species in prion-infected cultured cells.
  • - Another significant aspect of her work involves the impact of melatonin on oligodendroglial maturation in the context of neonatal white matter injury, suggesting potential therapeutic avenues for brain development issues arising from prenatal hypoxia, as demonstrated in her 2009 publication.
  • - Massonneau's studies also explore the vulnerability of white matter to antenatal hypoxia, revealing species-dependent regulatory mechanisms of glutamate receptor subunits that contribute to the pathogenesis of white-matter damage in her 2008 research, thereby underscoring the genetic influences on neurological outcomes following hypoxic events.