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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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The CpxR/CpxA two-component system up-regulates two Tat-dependent peptidoglycan amidases to confer bacterial resistance to antimicrobial peptide.

TL;DR: A new transcriptional regulation pathway is uncovered in which the Cpx envelope stress response system modulates the integrity of the cell envelope in part by controlling peptidoglycan amidase activity, which confers bacterial resistance to protamine and α-helical CAMPs.
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In silico Estimates of Tissue Components in Surgical Samples Based on Expression Profiling Data

TL;DR: Four large gene expression microarray data sets from prostate cancer, whose tissue components were estimated by pathologists, were used to test the performance of multivariate linear regression models for in silico prediction of major tissue components.
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Site-specific methylation: effect on DNA modification methyltransferases and restriction endonucleases

TL;DR: An updated list of the sensitivities of over 240 restriction endonucleases to the site-specific DNA modifications '14C, n-6C, h1"5C, and m6A, four modifications that are common in DNA prokaryotes, eukaryote, and their viruses is presented.
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Global Transcriptional Analysis of Dehydrated Salmonella enterica Serovar Typhimurium

TL;DR: The findings indicate the involvement of a relatively small fraction of the Salmonella genome in transcriptional adjustment from water to dehydration, with a high prevalence of genes belonging to the protein biosynthesis machinery.
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Electrophoretic separation of the three Rhizobium meliloti replicons.

TL;DR: The megaplasmids and the chromosome from the bacterium Rhizobium meliloti 1021 were separated in preparative quantities by using transverse alternating-field gel electrophoresis and the genetic content of each electrophoretically separated band was determined by Southern hybridization with replicon-specific probes and by comparison with Agrobacterium tumefaciens transconjugants harboring either pSym-a or p Sym-b megaplasmaids.