Morefield, Garry L, Tammariello, Ralph F, Purcell, Bret K, Worsham, Patricia L, Chapman, Jennifer, Smith, Leonard A, ...
Abstract Background Combination vaccines reduce the total number of injections required for each component administered separately and generally provide the same level of disease protection. Yet,...
Identification and Characterization of Variable-Number Tandem Repeats in the Yersinia pestis Genome
Klevytska, Alexandra M., Price, Lance B., Schupp, James M., Worsham, Patricia L., Wong, Jane, Keim, Paul
Yersinia pestis, the infamous plague-causing pathogen, appears to have emerged in relatively recent history. Evidence of this fact comes from several studies that document a lack of nucleotide...
Identification of Nucleotide Sequences for the Specific and Rapid Detection of Yersinia pestis
Radnedge, Lyndsay, Gamez-Chin, Silvia, McCready, Paula M., Worsham, Patricia L., Andersen, Gary L.
Suppression subtractive hybridization, a cost-effective approach for targeting unique DNA, was used to identify a 41.7-kb Yersinia pestis-specific region. One primer pair designed from this region...
Motin, Vladimir L., Georgescu, Anca M., Elliott, Jeffrey M., Hu, Ping, Worsham, Patricia L., Ott, Linda L., ...
A PCR-based genotyping system that detects divergence of IS100 locations within the Yersinia pestis genome was used to characterize a large collection of isolates of different biovars and...
Identification and Characterization of Variable-Number Tandem Repeats in the Yersinia pestis Genome
Klevytska, Alexandra M., Price, Lance B., Schupp, James M., Worsham, Patricia L., Wong, Jane, Keim, Paul
Yersinia pestis, the infamous plague-causing pathogen, appears to have emerged in relatively recent history. Evidence of this fact comes from several studies that document a lack of nucleotide...
Identification of Nucleotide Sequences for the Specific and Rapid Detection of Yersinia pestis
Radnedge, Lyndsay, Gamez-Chin, Silvia, McCready, Paula M., Worsham, Patricia L., Andersen, Gary L.
Suppression subtractive hybridization, a cost-effective approach for targeting unique DNA, was used to identify a 41.7-kb Yersinia pestis-specific region. One primer pair designed from this region...
Motin, Vladimir L., Georgescu, Anca M., Elliott, Jeffrey M., Hu, Ping, Worsham, Patricia L., Ott, Linda L., ...
A PCR-based genotyping system that detects divergence of IS100 locations within the Yersinia pestis genome was used to characterize a large collection of isolates of different biovars and...