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Michael McClelland

Researcher at University of California, Irvine

Publications -  376
Citations -  29109

Michael McClelland is an academic researcher from University of California, Irvine. The author has contributed to research in topics: Salmonella enterica & Salmonella. The author has an hindex of 79, co-authored 372 publications receiving 27627 citations. Previous affiliations of Michael McClelland include University of Illinois at Chicago & University of Georgia.

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Web-based visualization tools for bacterial genome alignments

TL;DR: These web-based tools revealed that rffH, a gene involved in enterobacterial common antigen (ECA) biosynthesis, is partly deleted in one of the genomes, and were used to show that this deletion occurs sporadically in some strains of some serovars of S.enterica subspecies I but not in any strains tested from six other subspecies.
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Use of a promiscuous, constitutively-active bacterial enhancer-binding protein to define the σ54 (RpoN) regulon of Salmonella Typhimurium LT2

TL;DR: This work assesses the ability of a promiscuous, constitutively-active bEBP—the AAA+ ATPase domain of DctD from Sinorhizobium meliloti—to activate transcription from all σ54-dependent promoters for the characterization of the ρ54 regulon of Salmonella Typhimurium LT2.
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The frequency and distribution of methylatable DNA sequences in leguminous plant protein coding genes

TL;DR: An analysis of the distribution of di- and trinucleotides across functionally classified regions of genes showed CpG to be asymmetrically distributed, which may reflect a methylation-mediated regulatory role for this region in some legume genes.
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Solid tumors provide niche-specific conditions that lead to preferential growth of Salmonella

TL;DR: A high-throughput screening of single-gene deletion mutants of S. Typhimurium in an orthotopic, syngeneic murine mammary model of breast cancer shows that the chemotaxis gene cheY and the motility genes motAB confer an advantage for colonization of Salmonella within Orthotopic syngenesic breast tumors.