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Sina Bavari

Researcher at United States Army Medical Research Institute of Infectious Diseases

Publications -  353
Citations -  21495

Sina Bavari is an academic researcher from United States Army Medical Research Institute of Infectious Diseases. The author has contributed to research in topics: Ebola virus & Virus. The author has an hindex of 69, co-authored 349 publications receiving 18782 citations. Previous affiliations of Sina Bavari include University of Nebraska Medical Center & Walter Reed Army Institute of Research.

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Sorafenib Impedes Rift Valley Fever Virus Egress by Inhibiting Valosin-Containing Protein Function in the Cellular Secretory Pathway.

TL;DR: Detailed mechanism-of-action studies indicate that sorafenib causes a disruption in viral egress by targeting VCP and the secretory pathway, resulting in a buildup of virions within dilated ER vesicles.
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Validation of the Filovirus Plaque Assay for Use in Preclinical Studies.

TL;DR: The results demonstrated that the EBOV and MARV plaque assays are accurate, precise and robust for filovirus titration in samples associated with the performance of GLP animal model studies.
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Considerations for the development of Zika virus vaccines.

TL;DR: The broader research community’s extensive experience with dengue virus vaccine development and with the pros and cons of different vaccine platforms has led to speculation that a Zika virus vaccine can be accelerated, potentially with clinical trials initiating by the end of 2016.
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Mechanisms of Immunity in Post-Exposure Vaccination against Ebola Virus Infection

TL;DR: It is reported that VLPs protect Ebola virus-infected mice when given 24 hours post-infection and that the mechanisms of immune protection in this setting require both increased antibody production and generation of cytotoxic T cells, suggesting that a non-replicating Ebola virus vaccine can provide post-exposure protection.
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Heat fixation inactivates viral and bacterial pathogens and is compatible with downstream MALDI mass spectrometry tissue imaging

TL;DR: Heat fixation inactivates viral and bacterial pathogens and is compatible with proteomic analysis by MALDI-MSI, which will enable the use of infected tissue from studies performed in bio-safety level 3 laboratories with VEEV and Burkholderia to be safely used for proteomic, small molecule drug detection, and imaging mass spectrometry analysis.