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One or more keywords matched the following properties of Wormley Jr., Floyd L.
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overview Dr. Wormley received his B.S. degree in Cellular and Molecular Biology from Tulane University in New Orleans, LA and his M.S. and Ph.D. degrees from Louisiana State University Health Science Center also in New Orleans, LA. He then conducted his post-doctoral studies in Infectious Diseases at Duke University Medical Center in Durham, NC prior to joining the faculty in the Department of Biology at The University of Texas at San Antonio (UTSA) in 2005. Dr. Wormley’s research laboratory utilizes the human fungal pathogen Cryptococcus neoformans as a model organism to study host-fungal interactions for the purpose of developing novel immune therapies and/or vaccines to treat and/or prevent invasive fungal infections. C. neoformans infections are a significant cause of morbidity and mortality among AIDS patients. In sub-Saharan Africa, deaths due to cryptococcal meningitis (530,000) appear to be more frequent than tuberculosis (350,000). Dr. Wormley’s research is supported by two grants from the National Institute of Allergy and Infectious Diseases (NIAID) of the National Institutes of Health (NIH) and he is co-investigator on a training grant funded by the Department of Defense. He currently is a standing member of the AIDS-Associated Opportunistic Infections and Cancer (AOIC) NIH study section, a member of the Committee on Microbiological Issues Impacting Minorities for the American Society for Microbiology (ASM), Associate Director of the South Texas Center for Emerging Infectious Diseases, and Associate Dean for Research in the College of Sciences at UTSA.
One or more keywords matched the following items that are connected to Wormley Jr., Floyd L.
Item TypeName
Academic Article Identification and characterization of Cryptococcus neoformans protein fractions that induce protective immune responses.
Academic Article Protection against cryptococcosis by using a murine gamma interferon-producing Cryptococcus neoformans strain.
Concept Cryptococcus neoformans
Academic Article Evaluation of host immune responses to pulmonary cryptococcosis using a temperature-sensitive C. neoformans calcineurin A mutant strain.
Academic Article Immunology of infection caused by Cryptococcus neoformans.
Academic Article Identification and characterization of an SKN7 homologue in Cryptococcus neoformans.
Academic Article Biofilm formation by Cryptococcus neoformans under distinct environmental conditions.
Academic Article A proteomic-based approach for the identification of immunodominant Cryptococcus neoformans proteins.
Academic Article Insights into the mechanisms of protective immunity against Cryptococcus neoformans infection using a mouse model of pulmonary cryptococcosis.
Academic Article Pulmonary infection with an interferon-gamma-producing Cryptococcus neoformans strain results in classical macrophage activation and protection.
Academic Article Role of IL-17A on resolution of pulmonary C. neoformans infection.
Academic Article Interleukin-17 is not required for classical macrophage activation in a pulmonary mouse model of Cryptococcus neoformans infection.
Academic Article Protective immunity against experimental pulmonary cryptococcosis in T cell-depleted mice.
Academic Article Induction of protective immunity against cryptococcosis.
Academic Article Protective immunity against pulmonary cryptococcosis is associated with STAT1-mediated classical macrophage activation.
Academic Article Mechanisms of dendritic cell lysosomal killing of Cryptococcus.
Academic Article Depletion of neutrophils in a protective model of pulmonary cryptococcosis results in increased IL-17A production by ?d T cells.
Academic Article Characterization of IL-22 and antimicrobial peptide production in mice protected against pulmonary Cryptococcus neoformans infection.
Academic Article Cryptococcus neoformans hyperfilamentous strain is hypervirulent in a murine model of cryptococcal meningoencephalitis.
Academic Article Molecules at the interface of Cryptococcus and the host that determine disease susceptibility.
Academic Article Is Development of a Vaccine against Cryptococcus neoformans Feasible?
Academic Article Development of protective inflammation and cell-mediated immunity against Cryptococcus neoformans after exposure to hyphal mutants.
Academic Article STAT1 signaling is essential for protection against Cryptococcus neoformans infection in mice.
Academic Article Cryptococcal heat shock protein 70 homolog Ssa1 contributes to pulmonary expansion of Cryptococcus neoformans during the afferent phase of the immune response by promoting macrophage M2 polarization.
Academic Article STAT1 signaling within macrophages is required for antifungal activity against Cryptococcus neoformans.
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  • Cryptococcus neoformans
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