Yonis Bare

Yonis Bare
CNRS Montpellier · IRIM - Research Institute in Infectiology of Montpellier

PhD

About

6
Publications
551
Reads
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24
Citations
Citations since 2017
6 Research Items
24 Citations
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201720182019202020212022202301234567
201720182019202020212022202301234567
201720182019202020212022202301234567
Education
October 2016 - October 2019
King's College London
Field of study
  • Cell Biology

Publications

Publications (6)
Preprint
Full-text available
Transmigration of circulating monocytes from the bloodstream toward the central nervous system (CNS) represents a hallmark of neuroinflammation and plays an important role during viral encephalitis and HIV-associated neurocognitive disorders (HAND). The molecular mechanisms involved in monocyte transmigration through endothelia has been extensively...
Article
Full-text available
The morphogen Sonic Hedgehog (SHH) plays an important role in coordinating embryonic development. Short- and long-range SHH signalling occurs through a variety of membrane-associated and membrane-free forms. However, the molecular mechanisms that govern the early events of the trafficking of neosynthesised SHH in mammalian cells are still poorly un...
Article
Full-text available
Background and aims: Numerous HCV entry factors have been identified, and yet information regarding their spatiotemporal dynamics is still limited. Specifically, one of the main entry factors of HCV is occludin (OCLN), a protein clustered at tight junctions (TJs), away from the HCV landing site. Thus, whether HCV particles slide toward TJs or, con...
Preprint
Full-text available
SARS-CoV-2 (CoV2) is the viral agent responsible for the pandemic of the coronavirus disease 2019 (COVID-19). Vaccines are being deployed all over the world with good efficacy, but there is no approved antiviral treatment to date. This is particularly needed since the emergence of variants and the potential immune escape may prolong pandemic spread...
Article
Slac2-b, also known as exophilin-5, is a Rab27b effector protein with a role in exosome transport and is encoded by the exophilin-5 (EXPH5) gene. We previously described biallelic loss-of-function mutations in EXPH5 in an autosomal recessive form of epidermolysis bullosa simplex. However, how loss of Slac2-b expression leads to skin fragility and e...

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