Publications by authors named "R Cloete"

Background: HIV-1 produces Tat, a crucial protein for transcription, viral replication, and CNS neurotoxicity. Tat interacts with TAR, enhancing HIV reverse transcription. Subtype C Tat variants (C31S, R57S, Q63E) are associated with reduced transactivation and neurovirulence compared to subtype B.

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Zinc (Zn) is vital to marine organisms. Its active uptake by phytoplankton results in a substantial depletion of dissolved Zn, and Zn bound to particulate organic matter replenishes dissolved Zn in the ocean through remineralization. However, we found that particulate Zn changes from Zn bound to phosphoryls in cells to recalcitrant inorganic pools that include biogenic silica, clays, and iron, manganese, and aluminum oxides in the Southern Ocean water column.

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Ebola viral disease (EVD) is a highly infectious and potentially fatal illness with a case fatality rate ranging from 25% to 90%. To effectively control its spread, there is a need for rapid, reliable and lowcost point-of-care (P OC) diagnostic tests. While various EVD diagnostic tests exist, few are P OC tests, and many are not cost-effective.

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Using a spatiotemporal dataset of dissolved lead (dPb) from the subtropical oceans surrounding South Africa, this study quantifies the exchange of dPb between the Indian and Atlantic Oceans. Despite the absence of a major Pb source within the South Atlantic sector and the complete phase-out of leaded petroleum in Southern Africa, the ecologically important southeast Cape Basin shows an elevated surface dPb concentration (21-30 pmol kg). We estimated up to 90% of the measured dPb in surface waters of the Cape Basin was delivered from the Indian Ocean via the Agulhas Current (AC).

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Article Synopsis
  • Parkinson's disease (PD) is a rapidly increasing neurological disorder with complex causes, and a specific genetic variant, p.G849D in NRXN2α, has been identified as potentially contributing to PD.
  • The research involved studying the effects of both normal and mutant NRXN2α proteins in SH-SY5Y cells, using mass spectrometry to analyze protein changes.
  • Results showed that the wild-type protein enhanced neurodegenerative-related proteins, while the mutant protein decreased ribosomal function proteins, suggesting that ribosome-related processes at synapses could be crucial in understanding PD mechanisms.
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