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Chris A. Whitehouse

Researcher at United States Army Medical Research Institute of Infectious Diseases

Publications -  72
Citations -  5793

Chris A. Whitehouse is an academic researcher from United States Army Medical Research Institute of Infectious Diseases. The author has contributed to research in topics: Virus & Monkeypox virus. The author has an hindex of 31, co-authored 64 publications receiving 4608 citations. Previous affiliations of Chris A. Whitehouse include University of Kentucky & United States Geological Survey.

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Crimean–Congo hemorrhagic fever

TL;DR: The history, epidemiology, ecology, clinical features, pathogenesis, diagnosis, and treatment of CCHF are reviewed, and issues related to its possible use as a bioterrorism agent are discussed.
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Genomic analysis of diversity, population structure, virulence, and antimicrobial resistance in Klebsiella pneumoniae, an urgent threat to public health

TL;DR: The DNA sequence of K. pneumoniae isolates from around the world is determined and it is shown that there is a wide spectrum of diversity, including variation within shared sequences and gain and loss of whole genes, and there is an unrecognized association between the possession of specific gene profiles associated with virulence and antibiotic resistance.
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Crimean-Congo hemorrhagic fever: history, epidemiology, pathogenesis, clinical syndrome and genetic diversity.

TL;DR: Current knowledge of CCHFV is summarized, summarizing its molecular biology, maintenance and transmission, epidemiology and geographic range, including an extensive discussion of C CHFV genetic diversity, including maps of the range of the virus with superimposed phylogenetic trees.
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Smallpox vaccine–induced antibodies are necessary and sufficient for protection against monkeypox virus

TL;DR: It is reported that vaccinia-specific B-cell responses are essential for protection of macaques from monkeypox virus, a variola virus ortholog, and vaccines able to induce long-lasting protective antibody responses may constitute realistic alternatives to the currently available smallpox vaccine.
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Campylobacter jejuni Cytolethal Distending Toxin Causes a G2-Phase Cell Cycle Block

TL;DR: Results indicated that CDT treatment results in a failure to activate CDC2, which leads to cell cycle arrest in G2, and provides a model for the generation of diarrheal disease by C. jejuni and other diarrheagenic bacteria that produce CDT.