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Douglas K. Palmer

Researcher at Oklahoma State University–Stillwater

Publications -  66
Citations -  2818

Douglas K. Palmer is an academic researcher from Oklahoma State University–Stillwater. The author has contributed to research in topics: Coronatine & Antigen. The author has an hindex of 25, co-authored 66 publications receiving 2728 citations. Previous affiliations of Douglas K. Palmer include Iowa State University & University of Hull.

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Purification of the centromere-specific protein CENP-A and demonstration that it is a distinctive histone.

TL;DR: Partial sequence analysis of the purified protein indicates that CENP-A is a distinctive gene product, and some CENp-A sequences are highly similar to regions of histone H3.
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A 17-kD centromere protein (CENP-A) copurifies with nucleosome core particles and with histones

TL;DR: It is concluded that this 17-kD centromere-specific protein is a histone-like component of chromatin, and the data suggest that CENP-A functions as a centromer-specific core histone.
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The Phytotoxin Coronatine and Methyl Jasmonate Impact Multiple Phytohormone Pathways in Tomato

TL;DR: The results indicate that conjugation of CFA to an amino acid is required for optimal activity in tomato, including chlorosis, changes in chloroplast structure, cell wall thickening, accumulation of proteinase inhibitors, induction of anthocyanins, and root growth inhibition.
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Effects of Environmental and Nutritional Factors on Production of the Polyketide Phytotoxin Coronatine by Pseudomonas syringae pv. Glycinea

TL;DR: The results of the present study were used to formulate a medium which allowed for enhanced coronatine production in nearly all strains of P. syringae tested and a rapid method for extracting coron atine from small volumes of culture supernatant was developed.
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The centromere specific histone CENP-A is selectively retained in discrete foci in mammalian sperm nuclei.

TL;DR: It is shown here that CENP-A is present in tissue of bovine origin, and that it is quantitatively retained in mature spermatozoa, suggesting that C ENP- A is a functionally important component of centromeres and that pre-existing CENp-A: DNA interactions are likely to be important in organizing the centromres of the paternal genome during early embryogenesis.