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  1. 1921
    “…To understand differences in host-Candida albicans interactions that occur during colonization of healthy or compromised hosts, production of phenotypic variants and colonization of healthy or immunodeficient mice by C. albicans were studied. …”
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  2. 1922
    “…However, we show that there is significant dislocation between the proteome and transcriptome in C. albicans. Glucose triggers the degradation of the ICL1 and PCK1 transcripts in C. albicans, yet isocitrate lyase (Icl1) and phosphoenolpyruvate carboxykinase (Pck1) are stable and are retained. …”
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  3. 1923
    “…Candida albicans, a common fungal pathogen which diverged from the baker’s yeast Saccharomyces cerevisiae has the unique ability to utilise N-acetylglucosamine, an amino sugar and exhibits phenotypic differences. …”
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  4. 1924
    “…Three of these opportunistic fungal pathogens: Aspergillus fumigatus, Candida albicans and Cryptococcus neoformans pose the biggest concern for the immune-compromised host. …”
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  5. 1925
    por Su, Chang, Lu, Yang, Liu, Haoping
    Publicado 2013
    “…Candida albicans is able to undergo reversible morphological changes between yeast and hyphal forms in response to environmental cues. …”
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  6. 1926
    “…Combination drug therapies are employed to treat patients with HIV, cancer, or tuberculosis, and has considerable promise in the treatment of fungal infections like cryptococcal meningitis and C. albicans infections. Our studies reported here demonstrate that posaconazole exhibits in vitro synergy with caspofungin or FK506 against drug susceptible or resistant C. albicans strains. …”
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  7. 1927
    “…The network is enriched with genes upregulated in C. albicans cells growing in the host. Our findings indicate that many aspects of commensalism and pathogenicity are intertwined and that the ability of this microorganism to colonize multiple niches relies on a large, integrated circuit.…”
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  8. 1928
    “…Oropharyngeal candidiasis (OPC) is an opportunistic infection caused by Candida albicans. Despite its prevalence, little is known about C. albicans-specific immunity in the oral mucosa. …”
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  9. 1929
  10. 1930
  11. 1931
    “…The high affinity iron uptake system of the opportunistic pathogenic yeast Candida albicans has been shown to be essential for virulence. …”
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  12. 1932
    “…Chitosan was shown to effectively augment the effect of PDI mediated by toluidine blue O (TBO) against C. albicans that were incubated with chitosan for 30 min following PDI. …”
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  13. 1933
  14. 1934
    “…The purpose of this study was to evaluate the time to positivity (TTP) of blood cultures in patients with Candida albicans BSIs and to assess its impact on clinical outcome. …”
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  15. 1935
    “…INTRODUCTION: An important consideration in endodontic treatment is the elimination of microorganisms, including fungi, from the complex three- dimensional root canal system. Candida Albicans (CA) has a major role in endodontic treatment failure as the most important fungus isolated from the root canal system. …”
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  16. 1936
    por Buu, Leh-Miauh, Chen, Yee-Chun
    Publicado 2013
    “…BACKGROUND: The polymorphic species Candida albicans is the major cause of candidiasis in humans. …”
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  17. 1937
    “…In this study, we demonstrated that a subset of murine J774A.1 macrophage cell line (8% to 17%) and peritoneal macrophages (8.5% to 15%) form METs-like structures (METs-LS) in response to Escherichia coli and Candida albicans challenge. We found only a portion of murine METs-LS, which are released by dying macrophages, showed detectable killing effects on trapped E. coli but not C. albicans. …”
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  18. 1938
    “…Here we show that the hyphae of the human fungal pathogen Candida albicans continue to extend throughout the whole of mitosis. …”
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  19. 1939
    por Bai, Feng-Yan
    Publicado 2014
    “…Candida albicans is a commensal microorganism in the mucosa of healthy individuals, but is also the most common opportunistic fungal pathogen of humans. …”
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  20. 1940
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