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Karla A. Fenton

Researcher at University of Texas Medical Branch

Publications -  69
Citations -  2191

Karla A. Fenton is an academic researcher from University of Texas Medical Branch. The author has contributed to research in topics: Ebola virus & Virus. The author has an hindex of 23, co-authored 55 publications receiving 1541 citations.

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Lipid nanoparticle siRNA treatment of Ebola-virus-Makona-infected nonhuman primates

TL;DR: It is shown that lipid-nanoparticle-encapsulated short interfering RNAs (siRNAs) rapidly adapted to target the Makona outbreak strain of Ebola virus are able to protect 100% of rhesus monkeys against lethal challenge when treatment was initiated at 3 days after exposure while animals were viraemic and clinically ill.
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Establishment of an African green monkey model for COVID-19 and protection against re-infection.

TL;DR: It is reported that African green monkeys infected with the SARS-CoV-2 virus develop disease symptoms that closely resemble those seen in infected humans, making this animal model a useful surrogate to investigate immune responses to coronavirus infection.
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Therapeutic Treatment of Nipah Virus Infection in Nonhuman Primates with a Neutralizing Human Monoclonal Antibody

TL;DR: Results represent the successful therapeutic in vivo efficacy by an investigational drug against Nipah virus in a nonhuman primate and highlight the potential impact that a monoclonal antibody can have on a highly pathogenic zoonotic human disease.
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A chikungunya fever vaccine utilizing an insect-specific virus platform

TL;DR: The EILV platform represents the first structurally native application of an insect-specific virus in preclinical vaccine development and highlights the potential application of such viruses in vaccinology.
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Pathogenic Differences between Nipah Virus Bangladesh and Malaysia Strains in Primates: Implications for Antibody Therapy.

TL;DR: Investigating pathogenic differences between strains of NiV suggests that postexposure treatments may need to be NiV strain specific for optimal efficacy and shows that NiVB is more pathogenic in AGMs under identical experimental conditions.