J
James E. Schoelz
Researcher at University of Missouri
Publications - 83
Citations - 2656
James E. Schoelz is an academic researcher from University of Missouri. The author has contributed to research in topics: Cauliflower mosaic virus & Virus. The author has an hindex of 29, co-authored 83 publications receiving 2434 citations. Previous affiliations of James E. Schoelz include Friedrich Miescher Institute for Biomedical Research & Cornell University.
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Resistance to Pseudomonas syringae conferred by an Arabidopsis thaliana coronatine‐insensitive (coi1) mutation occurs through two distinct mechanisms
Andrew P. Kloek,Michelle L. Verbsky,Shashi Sharma,James E. Schoelz,John P. Vogel,Daniel F. Klessig,Barbara N. Kunkel +6 more
TL;DR: These findings are consistent with the hypotheses that the P. syringae phytotoxin coronatine acts to promote virulence by inhibiting host defense responses and by promoting lesion formation.
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Intracellular Transport of Plant Viruses: Finding the Door out of the Cell
TL;DR: This review will discuss the strategies that viruses use for intracellular movement from the replication site to the PD, in particular focusing on the role of host membranes for intrACEllular transport and the coordinated interactions between virus proteins within cells that are necessary for successful virus spread.
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Intracellular Transport of Viruses and Their Components: Utilizing the Cytoskeleton and Membrane Highways
TL;DR: There is not sufficient information for any plant virus to create a complete model of its intracellular movement; thus, more research is needed to achieve that goal.
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Region VI of cauliflower mosaic virus encodes a host range determinant.
TL;DR: A domain of cauliflower mosaic virus which controls systemic spread in two solanaceous hosts was mapped to the first half of open reading frame 6 and suggests that the gene VI protein interacts with the plant to suppress hypersensitivity, the normal response of solanoidal hosts to CaMV infection.
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PCR amplification of species-specific DNA sequences can distinguish among Phytophthora species.
TL;DR: This is the first report on PCR-driven amplification with Phytophthora species-specific primers, which amplifiedDNAs from P. parasitica and P. citrophthora growing in infected tomato stem tissue were amplified as distinctly as DNAs from axenic cultures of each fungal species.