19 results on '"Gámez, Gustavo"'
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2. Streptococcus pneumoniae two-component regulatory systems: The interplay of the pneumococcus with its environment
3. Molecular Characterization and Antibiotic Susceptibility of Non-PCV13 Pneumococcal Serotypes among Vaccinated Children in Cape Coast, Ghana
4. Atypical N-glycosylation of SARS-CoV-2 impairs the efficient binding of Spike-RBM to the human-host receptor hACE2
5. Genomic organization, structure, regulation and pathogenic role of pilus constituents in major pathogenic Streptococci and Enterococci
6. Molecular Epidemiology of Multidrug-Resistant Pneumococci among Ghanaian Children under Five Years Post PCV13 Using MLST
7. List of Contributors
8. Pneumococcal Pili and Adhesins
9. Factors Associated with Streptococcus pneumoniae Nasopharyngeal Carriage and Antimicrobial Susceptibility among Children Under the Age of 5 Years in the Southwestern Colombia
10. Atypical N-glycosylation of SARS-CoV-2 impairs the efficient binding of Spike-RBM to the human-host receptor hACE2
11. PROSECUCIÓN ACADÉMICA EN LA UNELLEZ VIPI, EN EL CONTEXTO DEL COVID 19
12. Post-Vaccination Streptococcus pneumoniae Carriage and Virulence Gene Distribution among Children Less Than Five Years of Age, Cape Coast, Ghana
13. Nasopharyngeal Colonization, Associated Factors and Antimicrobial Resistance ofStreptococcus pneumoniaeamong Children under 5 Years of Age in the Southwestern Colombia
14. PavB is a surface-exposed adhesin of Streptococcus pneumoniae contributing to nasopharyngeal colonization and airways infections
15. Pneumococcal Metabolic Adaptation and Colonization Are Regulated by the Two-Component Regulatory System 08
16. Pneumococcal metabolic adaptation and colonization is regulated by the two-component regulatory system 08
17. The variome of pneumococcal virulence factors and regulators
18. Atypical N-glycosylation of SARS-CoV-2 impairs the efficient binding of Spike-RBM to the human host receptor hACE2.
19. Atypical N-glycosylation of SARS-CoV-2 impairs the efficient binding of Spike-RBM to the human-host receptor hACE2
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