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Pharmacologic control of homeostatic and antigen-driven proliferation to target HIV-1 persistence.
Innis, E A; Levinger, C; Szaniawski, M A; Williams, E S C P; Alcamí, J; Bosque, A; Schiffer, J T; Coiras, M; Spivak, A M; Planelles, V.
Afiliación
  • Innis EA; Division of Microbiology and Immunology, Department of Pathology, University of Utah School of Medicine, Salt Lake City, UT, USA.
  • Levinger C; Department of Microbiology, Immunology and Tropical Medicine, George Washington University, Washington, USA.
  • Szaniawski MA; Division of Microbiology and Immunology, Department of Pathology, University of Utah School of Medicine, Salt Lake City, UT, USA.
  • Williams ESCP; Division of Microbiology and Immunology, Department of Pathology, University of Utah School of Medicine, Salt Lake City, UT, USA.
  • Alcamí J; AIDS Immunopathology Unit, National Center of Microbiology (CNM), Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
  • Bosque A; Department of Microbiology, Immunology and Tropical Medicine, George Washington University, Washington, USA.
  • Schiffer JT; Fred Hutchinson Cancer Research Center, Vaccine and Infectious Diseases Division, Seattle, WA 98109, USA.
  • Coiras M; AIDS Immunopathology Unit, National Center of Microbiology (CNM), Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
  • Spivak AM; Division of Infectious Diseases, Department of Medicine, University of Utah School of Medicine, Salt Lake City, UT, USA. Electronic address: adam.spivak@hsc.utah.edu.
  • Planelles V; Division of Microbiology and Immunology, Department of Pathology, University of Utah School of Medicine, Salt Lake City, UT, USA. Electronic address: vicente.planelles@path.utah.edu.
Biochem Pharmacol ; 194: 114816, 2021 12.
Article en En | MEDLINE | ID: mdl-34715067
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: VIH-1 / Sistemas de Liberación de Medicamentos / Inhibidores de Proteínas Quinasas / Proliferación Celular / Homeostasis / Antígenos Virales Tipo de estudio: Clinical_trials Límite: Humans Idioma: En Revista: Biochem Pharmacol Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
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PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: VIH-1 / Sistemas de Liberación de Medicamentos / Inhibidores de Proteínas Quinasas / Proliferación Celular / Homeostasis / Antígenos Virales Tipo de estudio: Clinical_trials Límite: Humans Idioma: En Revista: Biochem Pharmacol Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos