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Daniel E. Voth

Researcher at University of Arkansas for Medical Sciences

Publications -  55
Citations -  9729

Daniel E. Voth is an academic researcher from University of Arkansas for Medical Sciences. The author has contributed to research in topics: Coxiella burnetii & Secretion. The author has an hindex of 28, co-authored 52 publications receiving 8765 citations. Previous affiliations of Daniel E. Voth include National Institutes of Health & University of Oklahoma Health Sciences Center.

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Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

Daniel J. Klionsky, +2522 more
- 21 Jan 2016 - 
TL;DR: In this paper, the authors present a set of guidelines for the selection and interpretation of methods for use by investigators who aim to examine macro-autophagy and related processes, as well as for reviewers who need to provide realistic and reasonable critiques of papers that are focused on these processes.
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Clostridium difficile Toxins: Mechanism of Action and Role in Disease

TL;DR: There have been major advances in defining the role of these toxins in modulating the inflammatory events involving the disruption of cell junctions, neuronal activation, cytokine production, and infiltration by polymorphonuclear cells.
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Lounging in a lysosome: the intracellular lifestyle of Coxiella burnetii.

TL;DR: Current understanding of the cellular events that occur during parasitism of host cells by Coxiella, including deployment of a type IV secretion system to deliver effector proteins to the host cytosol is summarized.
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Dot/Icm Type IVB Secretion System Requirements for Coxiella burnetii Growth in Human Macrophages

TL;DR: It is proved that T4BSS function is required for productive infection of human macrophages by C. burnetii, the only bacterial pathogen known to replicate in a vacuole resembling a phagolysosome.
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Comparative Genomics Reveal Extensive Transposon-Mediated Genomic Plasticity and Diversity among Potential Effector Proteins within the Genus Coxiella

TL;DR: The observation that the attenuated Dugway isolate has the largest genome with the fewest pseudogenes and IS elements suggests that this isolate's lineage is at an earlier stage of pathoadaptation than the NM, K, and G lineages.