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Charles K. Stover

Researcher at MedImmune

Publications -  64
Citations -  10387

Charles K. Stover is an academic researcher from MedImmune. The author has contributed to research in topics: Antigen & Epitope. The author has an hindex of 31, co-authored 63 publications receiving 9884 citations. Previous affiliations of Charles K. Stover include Pfizer & Walter Reed Army Institute of Research.

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New use of BCG for recombinant vaccines.

TL;DR: Extrachromosomal and integrative expression vectors carrying the regulatory sequences for major BCG heat-shock proteins have been developed and can elicit long-lasting humoral and cellular immune responses to foreign antigens in mice.
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Molecular analysis of genetic differences between Mycobacterium bovis BCG and virulent M. bovis.

TL;DR: The live attenuated bacillus Calmette-Guerin (BCG) vaccine for the prevention of disease associated with mycobacterium tuberculosis was derived from the closely related virulent tubercle bacilli, Mycobacteriaium bovis, and the precise junctions and DNA sequence of each deletion were determined as discussed by the authors.
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Protective immunity elicited by recombinant bacille Calmette-Guerin (BCG) expressing outer surface protein A (OspA) lipoprotein: a candidate Lyme disease vaccine.

TL;DR: Improved antibody responses were observed in heterogeneous mouse strains that vary in their immune responsiveness to OspA and sensitivity to BCG growth, and expression of protective antigens as chimeric membrane-associated lipoproteins on recombinant BCG may result in the generation of new candidate vaccines against Lyme borreliosis and other human or veterinary diseases where humoral immunity is the protective response.
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Staphylococcus aureus genetic loci impacting growth and survival in multiple infection environments

TL;DR: Signature‐tag transposon mutagenesis screening of a 1520‐member library identified numerous S. aureus genetic loci affecting growth and survival in four complementary animal infection models, providing insight into the complexities of human infection and on the molecular mechanisms that could be targeted by new antibacterial therapies.