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Michael S. Chaussee

Researcher at University of South Dakota

Publications -  42
Citations -  2255

Michael S. Chaussee is an academic researcher from University of South Dakota. The author has contributed to research in topics: Streptococcus pyogenes & Virulence. The author has an hindex of 22, co-authored 42 publications receiving 2153 citations. Previous affiliations of Michael S. Chaussee include Rocky Mountain Laboratories & University of Minnesota.

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Genome sequence and comparative microarray analysis of serotype M18 group A Streptococcus strains associated with acute rheumatic fever outbreaks

TL;DR: DNA microarray analysis of 36 serotype M18 strains from diverse localities showed that most regions of variation were phages or phage-like elements, which provides a critical foundation for accelerated research into ARF pathogenesis and a molecular framework to study the plasticity of GAS genomes.
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Staphylococcus aureus aconitase inactivation unexpectedly inhibits post-exponential-phase growth and enhances stationary-phase survival.

TL;DR: The data suggest that carbon and energy for post-exponential-phase growth and virulence factor production are derived from the catabolism of acetate mediated by the TCA cycle, and aconitase inactivation enhanced stationary-phase survival relative to the wild-type strain.
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Bacterial Effector Binding to Ribosomal Protein S3 Subverts NF-κB Function

TL;DR: It is suggested that NleH may disrupt host innate immune responses by binding to a cofactor of host transcriptional complexes that is at least partially responsible for the inhibitory activity of Nleh1 toward RPS3.
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The rgg Gene of Streptococcus pyogenes NZ131 Positively Influences Extracellular SPE B Production

TL;DR: Complementation of the rgg mutant with an intactrgg gene copy in S. pyogenes NZ131 could restore SPE B production and confirmed that the rGG gene product is involved in the production of SPEB.
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Identification of Rgg-Regulated Exoproteins of Streptococcus pyogenes

TL;DR: Rgg regulates the transcription of several genes expressed primarily during the stationary phase of growth, including Mitogenic factor, DNA entry nuclease, and ORF 953, which has no known function.