Lee Chae
Carnegie Institution for Science
9 Papers
Lee Chae is an academic researcher from Carnegie Institution for Science. The author has contributed to research in topics: Gene & Biology. The author has an hindex of 6, co-authored 7 publications. Previous affiliations of Lee Chae include San Francisco State University & University of California, Berkeley.
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Papers
Genome-Wide Prediction of Metabolic Enzymes, Pathways, and Gene Clusters in Plants
Pascal Schläpfer,Peifen Zhang,Chuan Wang,Taehyong Kim,Michael Banf,Lee Chae,Kate Dreher,Arvind K. Chavali,Ricardo Nilo-Poyanco,Thomas Bernard,Daniel Kahn,Seung Y. Rhee +11 more
TL;DR: A computational pipeline is presented to identify metabolic enzymes, pathways, and gene clusters from a sequenced genome that implicate local gene duplication and single gene transposition as playing roles in the evolution of plant metabolic gene clusters.
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Genomic Signatures of Specialized Metabolism in Plants
TL;DR: It is found that, relative to their primary metabolic counterparts, genes coding for specialized metabolic functions have proliferated to a much greater degree and by different mechanisms and display lineage-specific patterns of physical clustering within the genome and coexpression, which illustrate the differential evolution of specialized metabolism in plants.
Tissue-Specific and Developmentally Regulated Expression of a Cluster of Tandemly Arrayed Cell Wall-Associated Kinase-Like Kinase Genes in Arabidopsis
TL;DR: The characterization of group 2 members that are composed of a cluster of seven tandemly arrayed WAKL genes is described, suggesting that they, like some WAK members, are wound inducible and can be defined as pathogenesis-related genes.
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Towards understanding how molecular networks evolve in plants.
TL;DR: Progress is discussed being made to elucidate the nature of these forces and their impact on the composition and structure of molecular networks in plant network analysis.
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Impact of selected novel plant bioactives on improvement of impaired gut barrier function using human primary cell intestinal epithelium
TL;DR: In this article , N-trans caffeoyltyltyramine (NCT) was co-administered with tumor necrosis factor (TNF) along with NCT, NFT or NCT/NFT (2.2 ratio) post-differentiation, over a 48-hour period to induce inflammation and observe the effects of NCT and NFT.
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