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PMID |
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1 |
25815330
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Our aim was to investigate the effects of hyperthermia, ultraviolet A rays (UVA), and ultraviolet C rays (UVC) as well as glucose and ascorbic acid (AA) on the regulation of human β-defensin 1 (DEFB1), cathelicidin (CAMP), and interferon-γ (IFNG) genes in normal human keratinocytes (NHK).
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2 |
25815330
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Our aim was to investigate the effects of hyperthermia, ultraviolet A rays (UVA), and ultraviolet C rays (UVC) as well as glucose and ascorbic acid (AA) on the regulation of human β-defensin 1 (DEFB1), cathelicidin (CAMP), and interferon-γ (IFNG) genes in normal human keratinocytes (NHK).
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3 |
25815330
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We found that AA is a more potent APE for DEFB1 than glucose in NHK.
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4 |
25815330
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We found that AA is a more potent APE for DEFB1 than glucose in NHK.
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5 |
25815330
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Glucose but not AA is an APE for CAMP.
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6 |
25815330
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Glucose but not AA is an APE for CAMP.
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7 |
25815330
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AA-dependent DEFB1 upregulation below 20 mM predicts in vitro antimicrobial activity as well as glucose- and AA-dependent CAMP and IFNG upregulation.
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8 |
25815330
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AA-dependent DEFB1 upregulation below 20 mM predicts in vitro antimicrobial activity as well as glucose- and AA-dependent CAMP and IFNG upregulation.
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9 |
25815330
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UVC upregulates CAMP and DEFB1 genes but UVA only upregulates the DEFB1 gene.
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10 |
25815330
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UVC upregulates CAMP and DEFB1 genes but UVA only upregulates the DEFB1 gene.
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11 |
25815330
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Our results suggest that glucose upregulates CAMP in an IFN-γ-independent manner.
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12 |
25815330
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Our results suggest that glucose upregulates CAMP in an IFN-γ-independent manner.
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